Answers to FOUR FREQUENTLY ASKED QUESTIONS ABOUT THE ELMIRON LAWSUIT BY A NASHVILLE ELMIRON LAWYER5/23/2023
If you suffered from Elmiron side effects, call a Nashville Elmiron lawyer, you may be eligible for a Elmiron lawsuit
The Firm is reviewing claims on behalf of Interstitial Cystitis (IC) patients who took the prescription drug Elmiron and now may be suffering from a severe eye disease called maculopathy or has suffered vision impairment as a result. If you developed malculopathy or a vision impairment and took Elmiron, or have additional questions, give Nashville Elmiron Lawyer Timothy L. Miles a call today for a free case evaluation, you could be entitled to significantly compensation if you meet the Elmiron Lawsuit Criteria and file an Elmiron lawsuit.
Read on for answer to four frequently asked questions about an Elmiron lawsuit and see if you are eligible for an Elmiron lawsuit. WHAT IS ELMIRON AND WHY DOES IT CAUSE ELMIRON EYE DAMAGE?
Since 1996, millions of patients have been prescribed Elmiron in order to treat their interstitial cystitis (IC), otherwise known as painful bladder syndrome. But there is now reason to believe that this drug may cause a serious eye condition in those taking it, one that may result in blindness.
This condition is a form of maculopathy – the degeneration of the macula, the central part of the retina. Maculopathy’s first symptoms are blurred vision, dark spots, trouble focusing, and other impairments: as it progresses, it may lead to total blindness. As the evidence has piled up, the manufacturer of Elmiron – Janssen Pharmaceuticals – has failed to warn the public about these risks. Millions of people are taking a drug that may one day rob them of their vision, and an untold number may have already suffered serious health conditions. Elmiron eye damage lawsuits on behalf of the injured have already begun claiming their maculopathy was caused by Elmiron. If you or a loved one took Elmiron and has since been diagnosed with maculopathy, or vision impairment or other serious Elmiron side effects, you may be eligible for compensation. Contact a Nashville Elmiron Lawyer today to have your case reviewed for free and see if you meet the Elmiron lawsuit criteria. IS MACULOPATHY CAUSED BY LONG-TERM USE OF ELMIRON?![]()
In 2018, researchers at the Emory Eye Center at the Emory School of Medicine in Atlanta alerted the public that taking Elmiron is linked to the retinal condition, maculopathy. Pentosan polysulfate sodium can cause severe vision problems and side effects, including interstitial cytitis, and even blindness.
Nieraj Jain, M.D., of Emory Eye Center in Atlanta, Ga., reported that six Elmiron patients who had been taking Elmiron for about 15 years had developed unusual changes in their macula. Because nothing in the patients’ medical history or diagnostic tests explained the subtle, but striking pattern of abnormalities, Dr. Jain and his colleagues raised a warning flag that long-term use of Elmiron may damage the retina. The retina is a thin layer of tissue that lines the back of the eye on the inside. It is located near the optic nerve. The retina receives light that the lens has focused and converts the light into neural signals. It then sends these signals on to the brain for visual recognition All patients in the study reportedly showed signs of retinal disease and that the youngest patient in the study was diagnosed with interstitial cystitis at 23 years of age. That patient began taking the medication daily and began showing visual symptoms by the age of 30. In addition, three ophthalmologists conducted a review of patients at Kaiser Permanente in Northern California and found that approximately one-quarter of patients with significant exposure to Elmiron showed definite signs of eye damage. It also found the medication could potentially be linked to retinal conditions, such as age-related macular degeneration or pattern dystrophy. Patients who have used or are using the pentosan polysulfate sodium drug Elmiron are advised to be screened by ophthalmologists if they are experiencing any unusual eye symptoms. They are also advised to cease pentosan therapy if eye disease is present. WHAT ARE THE SYMPTOMS OF ELMIRON EYE DAMAGE RELATED TO RELATED RETINAL MACULOPATHY?
A newly discovered condition has come to light, and it is presently unknown how many symptoms there actually are, or how serious this can end up being for those suffering from it.
The currently known symptoms associated with this eye condition include:
IF I SUFFERED ELMIRON EYE DAMAGE, HOW DO I KNOW IF I AM ELIGIBLE FOR AN ELMIRON LAWSUIT?
You may be eligible for an Elmiron lawsuit if meet the following criteria:
The criteria are based upon the medical studies linking the drug to eye disease and vision impairment, including interstitial cytitis and maculopathy. However, there may be exceptions to the Elmiron lawsuit criteria. There may be other eye damage claims available for you to pursue and you still may be eligible for an Elmiron lawsuit. IF YOU SUFFERED ELMIRON EYE DAMAGE, OR ELMIRON SIDE EFFECTS, CALL A NASHVILLE ELMIRON LAWYER TODAY TO SEE IF YOU ARE ELIGIBLE FOR AN ELMIRON LAWSUIT?
If you were diagnosed with maculopathy or vision impairment caused by Elmiron, or other serious Elmiron Side Effects, contact a Nashville Elmiron Lawyer today as you most likely meet the Elmiron lawsuit criteria and are eligible for an Elmiron lawsuit and possibly recover substantial compensation. The call is free and so is the fee unless we will you case. So, call today and see what a Nashville Elmiron lawyer can do for you.
So, give a Nashville Elmiron Lawyer call today or submit the free case evaluation form if you suffered Elmiron Side Effects and see if you and are eligible to file an Elmiron lawsuit. nashville elmiron lawyer timothy l. milesTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Onglyza Side Effects contact Nashville Onglyza lawyer Timothy L. Miles, you could be eligible for an Onglyza lawsuit
Onglyza (saxagliptin) and Kombiglyze XR (saxagliptin and metformin) belong to a new class of diabetic drugs known as DPP-4 inhibitors. Onglyza gained federal drug approval by the U.S. Food & Drug Administration (FDA) despite initial concerns over the cardiovascular safety of the drug.
These concerns were echoed in a post-marketing safety study that found Onglyza may be associated with an increased risk of heart failure and an increased risk of death. If you or a loved one took Onglyza as directed and suffered from Onglyza side effects including heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, after starting Onglyza therapy, contact Nashville Onglyza lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for an Onglyza lawsuit and possibly entitled to substantial compensation. WHAT IS ONGLYZA?
Onglyza (saxagliptin) is an add-on medication to diet and exercise to improve blood sugar control in people with type 2 diabetes. It is a is a dipeptidyl peptidase-4 (DPP-4) inhibitor that increases the amount of insulin your body makes. Onglyza comes in tablets in dosages of 2.5 mg and 5 mg taken once by mouth daily.
WHO SHOULD NOT TAKE ONGLYZA?
You should not take Onglyza if you are allergic to any of its ingredients. Serious allergic reactions can occur with Onglyza including swelling of the face, throat, lips and difficulty breathing, among others. Your doctor should test your blood to measure how well your kidneys work before and during treatment with Onglyza. You may need a lower dose of Onglyza if your kidneys are not working well.
WHAT IS THE PROBLEM WITH ONGLYZA, DOES IT CAUSE ONGLYZA SIDE EFFECTS?![]()
Type 2 diabetes patients have a significantly increased risk of cardiovascular complications, and the majority of diabetics die from such complications. Amid growing concerns over the safety of many diabetes drugs, in 2008 the FDA recommended that the makers of new type 2 diabetes drugs provide evidence that the drugs do not increase the risk of cardiovascular events such as heart attacks.
Onglyza met the FDA's cardiovascular safety criteria. Though the FDA approved the new diabetic drug, it had reservations about the sufficiency of Onglyza clinical trials and ordered AstraZeneca to perform a post-marketing study. As a result, AstraZeneca completed a 16,000-patient cardiovascular outcomes trial called SAVOR. The results of that trial were published in the New England Journal of Medicine and raised major Onglyza safety concerns. SAVOR found that Onglyza patients were 27% more likely to be hospitalized for heart failure. The study also found a significant increase in the rate of “all-cause mortality” among Onglyza patients. The warning signs of heart failure include:
Following the release of SAVOR, the FDA issued an Onglyza drug safety communication and convened an advisory committee meeting to analyze the results and recommend further action. The committee voted 14-to-1 to add information to Onglyza’s label warning about heart failure risks. The other member voted to withdraw Onglyza from the U.S. market. The committee, however, did not advise updating the warning label to address the measured increase in all-cause mortality among Onglyza patients and did not recommend any restrictions on prescribing the drug. In an April 2016 drug safety communication, the FDA announced that Onglyza and Kombiglyze XR are now required to carry warnings about heart failure risk. Other FDA warnings about saxagliptin include:
WHAT ARE THE ONGLYZA SIDE EFFECTS?
In addition to heart failure, Onglyza is linked to these adverse Onglyza side effects:
IF I SUFFERED ONGLYZA SIDE EFFECTS, HOW DO I KNOW IF I MEET THE REQUIREMENTS FOR AN ONGLYZA LAWSUIT?
If you or a loved one took Onglyza as directed and suffered suffered heart failure, death, or another serious cardiovascular injury, after starting Onglyza therapy, you may meet the requirements for an Onglyza lawsuit and possibly be entitled to substantial compensation. Call a Nashville Onglyza lawyer for free today who can tell you if you are eligible for an Onglyza lawsuit.
if i suffered onglyza side effects and i am eligible for an onglyza lawsuit, What Can I Get Out of an Onglyza Lawsuit?
If you meet the requirements for an Onglyza lawsuit and are successful you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff who is eligible for an Onglyza lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they meet the requirements for an Onglyza lawsuit and are successful. IF I AM ELIGIBLE FOR AN ONGLYZA LAWSUIT, HOW MUCH DOES IT COST TO HIRE A NASHVILLE ONGLYZA LAWYER
It does not cost anything to hire a Nashville Onglyza lawyer. We take all cases on a contingency basis which means we do not get paid unless we win your case. A Nashville Onglyza lawyer can explain the process and answer any questions you may have including whether you are eligible for an Onglyza lawsuit. Call a Nashville Onglyza lawyer today for a free case evaluation.
if you suffered onglyza side effects, Contact a Nashville Onglyza Lawyer to See if You Are Eligible for an Onglyza Lawsuit?
If you or a loved one took Onglyza as directed and suffered from Onglyza Side Effects, specifically: heart failure, death or another serious cardiovascular injury —such as congestive heart failure or myocardial infarction, after starting Onglyza therapy, contact Nashville Onglyza lawyer Timothy L. Miles today to see if you are eligible for a Onglyza lawsuit and possibly entitled to substantial compensation.
nashville onglyza lawyer timothy l. milesTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Valsartan side effects, contact Nashville Valsartan lawyer Timothy L. Miles today
Patients who have taken Valsartan and have been diagnosed with cancer, as a result, should read on to learn more about how they can hold the drug makers accountable.
Valsartan has been recalled due to possible nitrosamine contamination. Nitrosamines can cause tumors in the liver and other organs in lab animals and are thought to be carcinogenic in humans as well. It is believed that these blood pressure drugs were tainted during flawed manufacturing processes. The U.S. Food and Drug Administration (FDA) stated that these contaminants “are of special concern to global regulators because, unlike most impurities in drugs, they have the potential to cause harm at very low levels.” The recalls began in July when the FDA found that some Valsartan products contained a potentially cancer-causing chemical. European regulators had already made the same discovery. The substance can form during manufacturing if the chemical reactions used to make the drug are not carefully controlled and monitored, the FDA said. Valsartan is made by Chinese manufacturer Zhejiang Huahai Pharmaceuticals. These recalls are a product of greater FDA scrutiny of foreign drug imports, but FDA warnings alone will not ensure safe medications. In a culture where the profit motive exists, drug companies must be held accountable to cutting corners and sacrificing consumer safety. If you or a loved one took Valsartan and later were diagnosed with cancer or other serious Valsartan Side Effects, contact Nashville Valsartan lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Valsartan lawsuit and possibly entitled to substantial compensation. Read on for the answers to five frequently asked questions about a Valsartan lawsuit by a Nashville Valsartan lawyer. DID THE VALSARTAN SIDE EFFECTS PROMPT THE VALSARTAN RECALL?![]()
In July 2018, the FDA announced the Valsartan Recall due to contamination. The recall was prompted because of the discovery of a cancer-causing agent in the drug. The FDA launched an investigation into the cause and impact of the contamination which led to several additional recalls over the following year. The FDA also found that other blood pressure drugs contained impurities.
The first recall was prompted by the finding of the impurity N-nitrosodimethylamine (NDMA). Later, the FDA later discovered the second impurity, N-Nitrosodiethylamine (NDEA). While neither compound has been studied in humans, both have been shown to cause cancer in animal studies. WHAT ARE THE VALSARTAN SIDE EFFECTS?
In addition to cancer, sources say other Valsartan Side Effects include:
IF I SUFFERED VALSARTAN SIDE EFFECTS, AM I ELIGIBLE FOR A VALSARTAN LAWSUIT?
If you took Valsartan and subsequently were diagnosed with cancer, or experienced other serious Valsartan side effects, then you may be eligible for a Valsartan lawsuit possibly may be entitled to substantial compensation. Contact Nashville Valsartan Lawyer Timothy L. Miles today and see if are eligible for a Valsartan lawsuit.
IF I AM ELIGIBLE FOR A VALSARTAN LAWSUIT, HOW MUCH CAN I GET OUT OF A VALSARTAN LAWSUIT?
If you are eligible for a Valsartan lawsuit and are successful, you can recover money for some of the following damages:
Broadly speaking, a plaintiff in a Valsartan lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they are eligible for a Valsartan lawsuit and are successful. IF I AM ELIGIBLE FOR A VALSARTAN LAWSUIT, WHAT CAN A NASHVILLE VALSARTAN LAWYER DO FOR ME?
While it is possible for individuals whom these products might have injured to go it alone without knowledgeable representation, those who do so run the risk of receiving an unfair settlement — if they get anything at all. Because drug makers have large amounts of money to spend on lawyers, going up against them as an individual can be intimidating and difficult. With an experienced Nashville Valsartan Lawyer, you can have the best chance to stand up to these large companies and optimize your chances of being fully compensated. Call Nashville Valsartan lawyer Timothy L. Miles today and see if you are eligible for a Valsartan lawsuit.
IF YOU SUFFERED VALSARTAN SIDE EFFECTS, CALL A NASHVILLE VALSARTAN LAWYER AND SEE IF YOU ARE ELIGIBLE FOR A VALSARTAN LAWSUIT
If you or a loved one has received a cancer diagnosis or experienced other serious Valsartan side effects after taking Valsartan, contact us for a free, no-risk case evaluation to see if you meet the Valsartan lawsuit criteria. We might be able to help you pursue compensation for the harm you and your loved ones have suffered if you meet the Valsartan lawsuit criteria.
Call Nashville Valsartan Lawyer Timothy L. Miles today to see how he can help you. A Nashville Valsartan Lawyer can explain the process and answer any questions you may have including whether you meet the Valsartan lawsuit criteria. While there is still time to file a lawsuit, be mindful that these cases are time sensitive, and give us a call today. nashville valsartan lawyer timothy l. milesTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Elmiron Eye Damage contact a Nashville Elmiron lawyer today, you could be eligible for an Elmiron lawsuit
The Firm is reviewing claims on behalf of Interstitial Cystitis (IC) patients who took the prescription drug Elmiron and now may be suffering from a severe eye disease called maculopathy or has suffered vision impairment as a result. If you developed malculopathy or a vision impairment and took Elmiron, or have additional questions, give Nashville Elmiron Lawyer Timothy L. Miles a call today for a free case evaluation, you could be entitled to significantly compensation if you meet the Elmiron Lawsuit Criteria and file an Elmiron lawsuit.
Get started by filling out a free case evaluation form or calling a Nashville Elmiron Lawyer. (855) Tim-M-Law (855-846-6529). Read on for everything you need to know about an Elmiron lawsuit from a Nashville Elmiron lawyer. WHAT IS ELMIRON AND WHY DOES IT CAUSE ELMIRON EYE DAMAGE?
Since 1996, millions of patients have been prescribed Elmiron in order to treat their interstitial cystitis (IC), otherwise known as painful bladder syndrome. But there is now reason to believe that this drug may cause a serious eye condition in those taking it, one that may result in blindness.
This condition is a form of maculopathy – the degeneration of the macula, the central part of the retina. Maculopathy’s first symptoms are blurred vision, dark spots, trouble focusing, and other impairments: as it progresses, it may lead to total blindness. As the evidence has piled up, the manufacturer of Elmiron – Janssen Pharmaceuticals – has failed to warn the public about these risks. Millions of people are taking a drug that may one day rob them of their vision, and an untold number may have already suffered serious health conditions. Elmiron eye damage lawsuits on behalf of the injured have already begun claiming their maculopathy was caused by Elmiron. If you or a loved one took Elmiron and has since been diagnosed with maculopathy, or vision impairment you may be eligible for compensation. Contact a Nashville Elmiron Lawyer today to have your case reviewed for free and see if you meet the Elmiron lawsuit criteria. IS MACULOPATHY CAUSED BY LONG-TERM USE OF ELMIRON?![]()
In 2018, researchers at the Emory Eye Center at the Emory School of Medicine in Atlanta alerted the public that taking Elmiron is linked to the retinal condition, maculopathy. Pentosan polysulfate sodium can cause severe vision problems and side effects, including interstitial cytitis, and even blindness.
Nieraj Jain, M.D., of Emory Eye Center in Atlanta, Ga., reported that six Elmiron patients who had been taking Elmiron for about 15 years had developed unusual changes in their macula. Because nothing in the patients’ medical history or diagnostic tests explained the subtle, but striking pattern of abnormalities, Dr. Jain and his colleagues raised a warning flag that long-term use of Elmiron may damage the retina. The retina is a thin layer of tissue that lines the back of the eye on the inside. It is located near the optic nerve. The retina receives light that the lens has focused and converts the light into neural signals. It then sends these signals on to the brain for visual recognition All patients in the study reportedly showed signs of retinal disease and that the youngest patient in the study was diagnosed with interstitial cystitis at 23 years of age. That patient began taking the medication daily and began showing visual symptoms by the age of 30. In addition, three ophthalmologists conducted a review of patients at Kaiser Permanente in Northern California and found that approximately one-quarter of patients with significant exposure to Elmiron showed definite signs of eye damage. It also found the medication could potentially be linked to retinal conditions, such as age-related macular degeneration or pattern dystrophy. Patients who have used or are using the pentosan polysulfate sodium drug Elmiron are advised to be screened by ophthalmologists if they are experiencing any unusual eye symptoms. They are also advised to cease pentosan therapy if eye disease is present. WHAT ARE THE SYMPTOMS OF ELMIRON EYE DAMAGE RELATED TO RELATED RETINAL MACULOPATHY?
A newly discovered condition has come to light, and it is presently unknown how many symptoms there actually are, or how serious this can end up being for those suffering from it.
The currently known symptoms associated with this eye condition include:
IF I SUFFERED ELMIRON EYE DAMAGE, HOW DO I KNOW IF I AM ELIGIBLE FOR AN ELMIRON LAWSUIT?
You may be eligible for an Elmiron lawsuit if meet the following criteria:
The criteria are based upon the medical studies linking the drug to eye disease and vision impairment, including interstitial cytitis and maculopathy. However, there may be exceptions to the Elmiron lawsuit criteria. There may be other eye damage claims available for you to pursue and you still may be eligible for an Elmiron lawsuit. SHOULD I REPORT ANY ELMIRON EYE DAMAGE I SUFFERED?
Yes, the FDA encourages people who had a problem related to the devices or drug to report the problem through the MedWatch Voluntary Reporting Form or call 1-800-332-1088 for more information. Make sure to provide all information about your Elmiron Eye Damage along with a detailed description of any othre problems you suffered from the long-term use of Elmiron.
HOW DO I GET STARTED IF I SUFFERED ELMIRON EYE DAMAGE AND BELIEVE I AM ELIGIBLE FOR AN ELMIRON LAWSUIT?
If you suffered Elmiron Eye Damage fill out and submit this form for a Free Case Evaluation with a Nashville Elmiron Lawyer to see if you are eligible for a Elmiron lawsuit and possibly entitled to substantial compensation.
IS A ELMIRON LAWSUIT TO GET MONEY FOR ELMIRON EYE DAMAGE?
An Elmiron Lawsuit is a demand from the defendants for monetary compensation by patients who took Elmiron and subsequently developed Elmiron Eye Damage. The lawsuits allege the defendants made a defective drug and failed to warn physicians about its serious side effects including Elmiron Eye Damage. If you suffered Elmiron Eye Damage and are eligible an Elmiron lawsuit, you may possibly be entitled to substantial compensation. A Nashville Elmiron Lawyer can answer these questions and is available anytime just give us a call or submit the form below for a free case evaluation to see if you areeligible for an Elmiron lawsuit.
IF I SUFFERED ELMIRON EYE DAMAGE AND I AM ELIGIBLE FOR AN ELMIRON LAWSUIT, HOW MUCH COMPENSATION CAN I GET IN A ELMIRON LAWSUIT?
If you are eligible for an Elmiron lawsuit, a successful plaintiff is entitled to compensatory damages which would include compensation for things such as:
If your case proceeds to trial it is also possible the court could impose punitive damages, intended to punish the defendant for their actions. HOW CAN A NASHVILLE ELMIRON LAWYER HELP ME IF I SUFFERED ELMIRON EYE DAMAGE OR ELMIRON SIDE EFFECTS?
First, a Nashville Elmiron Lawyer can determine if you are eligible for an Elmiron lawsuit. More importantly, because of the complexity of the cases and the need to hire experts, a products liability attorney is the go-to attorney when you have been injured by a product that is defective like Elmiron. A Nashville Elmiron Lawyer, who is an experienced products liability attorney, can help you by putting you in the best possible position to win your Elmiron Eye Damage lawsuit and recover the most compensation.
IF I AM ELIGIBLE FOR AN ELMIRON LAWSUIT, HOW MUCH DOES IT COST TO HIRE A NASHVILLE ELMIRON LAWYER?
It does not cost anything to hire a Nashville Elmiron lawyer. We take all cases on a contingency basis which means we do not get paid unless we win your case, so contact us today. A Nashville Elmiron lawyer can explain the process and answer any questions you may have. So, the call is free and so is the fee unless we win your case. If you suffered Elmiron Eye damage, contact us today for a free case evaluation, you may be eligible for an Elmiron lawsuit and possibly entitled to substantial compensation.
HOW DOES A ELMIRON LAWSUIT WORK IF I SUFFERED ELMIRON EYE DAMAGE OR ELMIRON SIDE EFFECTS?
If you suffered Elmiron side effects or Elmiron Eye Damange and you are eligible for an Elmiron lawsuit, your Nashville Elmiron Lawyer will fully explain the process and will then need to ask you a few questions concerning the circumstances of you diagnoses, how long you have been taking Elmiron and your medical history including your Elmiron side effects orElmiron Eye Damage.
Your Nashville Elmiron Lawyer will then draft what is known as a complaint. This will be a multi-page document explaining why the defendant is responsible for your injuries and what damages (that is, compensation) you are seeking. Once your complaint is filed with the court, your Elmiron Lawsuit officially begins. From here, it will be a lot of back and forth between your Nashville Elmiron lawyer and the attorney(s) for the defendant in an attempt to resolve the matter. The attorneys may take review documents, take depositions, issue subpoenas, hire experts, calculate damages, attend hearings, and file motions, briefs, evidence or other documents with the court during the stages of the lawsuit. If your Elmiron lawsuit is not dismissed and a settlement cannot be reached, the case will proceed to a jury trial. IF YOU SUFFERED ELMIRON EYE DAMAGE, OR ELMIRON SIDE EFFECTS, CALL A NASHVILLE ELMIRON LAWYER TODAY TO SEE IF YOU ARE ELIGIBLE FOR AN ELMIRON LAWSUIT?
If you were diagnosed with maculopathy or vision impairment caused by Elmiron, or other serious Elmiron Side Effects, contact a Nashville Elmiron Lawyer today as you most likely meet the Elmiron lawsuit criteria and are eligible to file an Elmiron lawsuit and possibly recover substantial compensation. The call is free and so is the fee unless we will you case. So, call today and see what a Nashville Elmiron lawyer can do for you.
So, give a Nashville Elmiron Lawyer call today or submit the free case evaluation form if you suffered Elmiron Side Effects and see if you and are eligible to file an Elmiron lawsuit. NASHVILLE ELMIRON LAWYER TIMOTHY L. MILESTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Meridia side effects, contact a Nashville Meridia lawyer to see if you meet the requirements for a Meridia lawsuit
Meridia, made by Abbott Laboratories, was approved in 1997 for weight loss and weight loss maintenance for obese patients, and also very obese individuals who already had other health risk factors for cardiovascular disease. Meridia was approved after clinical studies showed that more patients taking Meridia lost at least 5 percent of their body weight than members of the placebo group who relied solely on diet and exercise.
However, the U.S. Food & Drug Administration (FDA) has now requested that Meridia be recalled following a nearly year-long safety review of the drug which was initiated after researchers published the results of a study known as SCOUT (Sibutramine Cardiovascular Outcomes Trial). The study, which prompted a Meridia recall in Europe, showed a 16% percent increase in the risk of serious Meridia side effects, including:
SCOUT monitored 10,000 obese patients over the age of 55 who had a history of heart disease, and type 2 diabetes or similar risk factors. The initial purpose of the study was to show that weight loss through Meridia use lowered the risk of heart problems. However, that was not the case. In fact, the results suggested that those taking the weight loss drug had an increased chance of suffering Meridia cardiovascular side effects. Doctors have been advised to stop prescribing Meridia and begin discussing weight loss alternatives with their patients. If you or a loved one suffered serious Meridia side effects including a heart attack, stroke or even death, contact Nashville Meridia lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Meridia lawsuit and possibly entitled to substantial compensation. We hope you find this beneficial and enjoy the video on "Who is eligible for a Meridia lawsuit." WHAT IS MERIDIA?![]()
Meridia is a medication which requires a prescription and is used to treat the symptoms of obesity, weight loss, and maintenance of weight loss. It may be used alone or with other medications. Meridia belongs to a class of drugs called Schedule IV controlled substances and can cause severe Meridia side effects in some people. If you or a loved one suffered severe Meridia side effects call Nashville Meridia Lawyer Timothy L. Miles for a free case evaluation to see if you are eligible for a Meridia lawsuit and possibly entitled to substantial damages.
IS MERIDIA STILL ON THE MARKET BECAUSE OF MERIDA SIDE EFFECTS?
Because of the seriousness of the Meridia side effects including the risk of a heart attack or stroke, Abbott agreed to voluntarily withdraw Meridia from the U.S. market because of clinical trial data indicating an increased risk of heart attack and stroke, according to the FDA.
The FDA requested the market withdrawal after reviewing data from the Sibutramine Cardiovascular Outcomes Trial (SCOUT). SCOUT was initiated as part of a postmarket requirement to look at cardiovascular safety of sibutramine after the European approval of this drug. The trial demonstrated a 16 percent increase in the risk of serious heart events, including non-fatal heart attack, non-fatal stroke, the need to be resuscitated once the heart stopped, and death, in a group of patients given sibutramine compared to another given placebo. There was a small difference in weight loss between the placebo group and the group that received sibutramine. SERIOUS MERIDIA SIDE EFFECTS
In the beginning, Meridia seemed to be a booming success as it was used by millions of individuals around the world. However, hundreds of users began reporting serious Meridia side effects including:
Patients taking Meridia have also experienced these Merida side effects:
Additionally, approximately 30 deaths were caused by Merida in the United States. Researchers looked at 10,000 patients who were obese, over the age of 55 with a history of risk factors and found that 11.4% of patients using Meridia suffered heart problems, compared to 10% given a sugar pill. As of June 30, 2009, the FDA Adverse Event Reactions (AERS) database indicates that at least 84 Meridia deaths from cardiovascular causes have been reported to the FDA.' If you suffered severe Meridia side effects call Nashville Meridia Lawyer Timothy L. Miles for a free case evaluation to see if you are eligible for a Meridia lawsuit. MERIDIA RECALLED AFTER SERIOUS MERIDIA SIDE EFFECTS REPORTED
The limited benefits provided by Meridia are outweighed by the increased risk of cardiovascular problems which prompted federal regulators to issue the recall for Meridia in October 2010. Lawyers are investigating and considering potential lawsuits against Abbott on behalf of individuals who suffered a:
If you took Meridia as directed and suffered serious Meridia side effects including a heart attack or stroke, then you may meet the requirements for a Merida lawsuit and possibly be entitled to substantial compensation. Contact Nashville Merida Lawyer Timothy L. Miles today to see if you are eligible for a Merida lawsuit. IF I SUFFERED MERIDA SIDE EFFECTS AND AM ELIGIBLE FOR A MERIDIA LAWSUIT, WHAT CAN I GET OUT OF A MERIDIA LAWSUIT?
If you meet the requirements for a Meridia lawsuit and are successful you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff who is eligible for a Meridia lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they meet the requirements for a Meridia lawsuit and are successful. Call today to see if you are eligible for a Meridia lawsuit. IF YOU SUFFERED MERIDIA SIDE EFFECTS, CALL A NASHVILLE MERIDIA LAWYER TODAY TO SEE IF YOU ARE ELIGIBLE FOR A MERIDIA LAWSUIT
If you or a loved one suffered serious Meridia side effects including a heart attack, stroke or even death, contact Nashville Meridia lawyer Timothy L. Miles today to see if you are eligible for a Meridia lawsuit and possibly entitled to substantial compensation. While there is still time to file a lawsuit, be mindful that these cases are time sensitive, and give us a call today and see if you meet the requirements for a Meridia lawsuit.
NASHVILLE MERIDiA LAWYER TIMOTHY L. MILESTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you took Kombiglyze XR and suffered Kombiglyze XR side effects call a Nashville Kombiglyze XR lawyer you may be eligible for a Kombiglyze XR lawsuit
Kombiglyze XR is a combination of metformin (a biguanide) and saxagliptin (a DPP4 inhibitor). Kombiglyze XR works by lowering the amount of sugar made by your liver, decreasing the amount of sugar absorbed by your intestine, increasing the amount of insulin your body makes, and helps your body respond better to insulin.
However, research shows that type 2 diabetes drug Kombiglyze XR (saxagliptin and metformin) may cause heart failure or other cardiovascular injuries in some patients. According to the Centers for Disease Control and Prevention (CDC), 30 million Americans have diabetes and 84 million have pre-diabetes. Metformin—one of the drugs found in combination in Kombiglyze—is among the top 10 most popular prescription drugs taken by Americans. Analysts also predict that Onglyza (saxagliptin), Kombiglyze’s sister drug, could reach $1.8 billion in sales in 2018. In 2015, roughly 386,000 people were prescribed Onglyza or Kombiglyze XR, the U.S. Food and Drug Administration (FDA) reported. Given that so many people take these drugs, any side effects they may cause that are severe enough to hospitalize patients should be treated with concern. Dozens of patients are filing lawsuits against Kombiglyze’s manufacturer AstraZeneca and its previous partner Bristol-Myers Squibb alleging that the companies failed to adequately test the drugs’ safety prior to selling it, which ultimately caused their cardiovascular injuries. If you or a loved one took Kombiglyze XR as directed and suffered from Kombiglyze XR side effects including heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, after starting Kombiglyze XR therapy, contact Nashville Kombiglyze XR lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation. We hope you enjoy and find the video helpful on: Who is Eligible for a Kombiglyze XR lawsuit. IF YOU SUFFERED FROM KOMBIGLYZE XR SIDE EFFECTS, CALL A NASHVILLE KOMBIGLYZE XR LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A KOMBIGLYZE XR LAWSUIT
If you or a loved one took Kombiglyze XR as directed and suffered from Kombiglyze XR Side Effects, specifically: heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, after starting Kombiglyze XR therapy, contact Nashville Kombiglyze XR lawyer Timothy L. Miles today to see if you are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation.
nashville kombiglyze xr lawyer timothy l. milesTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website. the tasigna side effects and who is eligible for a tasigna lawsuit by a nashville tasigna lawyer5/18/2023
Call a Nashville Tasigna lawyer if you took Tasigna and developed Tasigna side effects to see if you are eligible for a Tasigna lawsuit
First approved in 2007, Tasigna (nilotinib), is a prescription medication used to treat chronic myeloid leukaemia (CML). Tasigna is part of a class of drugs known as tyrosine kinase inhibitors (TKIs). Other TKI drugs include Gleevec (imatinib), also made by Novartis, and Sprycel (dasatinib), made by Bristol-Myers Squibb.
These drugs help treat leukemia by blocking the protein tyrosine kinases—a protein that stimulates the growth of cancer cells. In blocking this protein, TKI drugs like Tasigna help stop leukemia from spreading. Tasigna is prescribed as a twice daily drug and is taken orally in capsule form. If you suffered Tasigna side effects, including Tasigna cardiovascular side effects, call Nashville Tasigna lawyer Timothy L. Miles today for a free case evaluation and see if you qualify for a Tasigna lawsuit and are eligible for a Tasigna lawsuit. WHAT IS THE PROBLEM WITH TASIGNA AND WHY DOES IT CAUSE TASIGNA SIDE EFFECTS?
Injured patients and their families are now filing lawsuits against Tasigna manufacturer Novartis, on the grounds that the company failed to warn of the drug’s cardiovascular risks including Tasigna side effects. Studies have allegedly linked the drug to serious cardiovascular side effects like Long QT syndrome, a condition involving irregular heartbeats, and atherosclerosis, a disease that causes plaque to build up in the arteries.
The FDA issued a black box warning (the highest warning they can issue) for Tasigna’s link to QT interval prolongation and sudden death. If you suffered Tasigna side effects, contact a Nashville Tasigna lawyer today as you may be eligible for a Tasigna lawsuit. WHAT ARE THE TASIGNA SIDE EFFECTS?![]()
To date, approximately 15,500 Tasigna related adverse events and 2,786 deaths have allegedly been reported to the FDA to date. These include serious Tasigna side effects including cardiovascular side effects, like Long QT syndrome, myocardial ischemia, and atherosclerosis.
Tasigna has one black box warning—the highest warning the FDA can issue—for Long QT syndrome, or QT interval prolongation, and sudden death. It is a condition that affects heart rhythm, resulting in fast, irregular heartbeats. If left untreated, it can result in fainting, seizures, and sudden death. Tasigna may also been linked to myocardial ischemia, a condition involving reduced blood flow to the heart, causing a decreased amount of oxygen sent to the heart. Myocardial ischemia is usually caused by a blockage of the coronary arteries. Recent lawsuits have also been filed over the drug’s alleged connection to atherosclerosis, a disease that causes fatty deposits to build up and eventually clog arteries. This serious condition gradually reduces blood flow and oxygen to cells. Atherosclerosis is currently the leading cause of death in the developed world. It may eventually cause the following complications:
WHAT ARE SOME OF THE ADDITIONAL TASIGNA SIDE EFFECTS?
Novartis warns of the following Tasigna side effects:
If you suffered Tasigna side effects, including Tasigna cardiovascular side effects call Nashville Tasigna lawyer Timothy L. Miles for a free case evaluation to see if you are eligible for a Tasigna lawsuit and may be entitled to substantial compensation for suffering Tasigna side effects, including Tasigna cardiovascular side effects. IF I SUFFERED TASIGNA SIDE EFFECTS AND I AM ELIGIBLE FOR TASIGNA LAWSUIT, WHAT IS A TASIGNA LAWSUIT?
A Tasigna Lawsuit is a demand from the defendant for monetary compensation by patients who took Tasigna and subsequently suffered heart or circulation problems (including complications like blocked arteries, heart attacks, or strokes). The lawsuits allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties. If eligible you may participate in a Tasigna lawsuit and possibly be entitled to substantial compensation. A Nashville Tasigna Lawyer can answer these questions and is available anytime just give us a call or submit the form below for a free case evaluation. If you are eligible for a Tasigna lawsuit and may be entitled to substantial compensation for suffering Tasigna side effects, including Tasigna cardiovascular side effects.
IF I SUFFERED TASIGNA SIDE EFFECTS, AM I ELIGIBLE FOR A TASIGNA LAWSUIT?
If you or a loved one took Tasigna and suffered heart or circulation problems (including complications like blocked arteries, heart attacks, or strokes), you could be eligible for a Tasigna lawsuit and possible entitled to substantial compensation. Call Nashville Tasigna lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Tasigna lawsuit and may be entitled to substantial compensation for suffering Tasigna side effects, including Tasigna cardiovascular side effects.
IF YOU SUFFERED TASIGNA SIDE EFFECTS, CALL A NASHVILLE TASIGNA LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A TASIGNA LAWSUIT?
If you or a loved one took Tasigna and suffered heart or circulation problems (including complications like blocked arteries, heart attacks, or strokes), you could be eligible for a Tasigna Lawsuit. If you suffered Tasigna side effects, including Tasigna cardiovascular side effects, call Nashville Tasigna lawyer Timothy L. Miles today for a free case evaluation and see if you qualify for a Tasigna lawsuit.
NASHVILLE TASIGNA LAWYER TIMOTHY L. MILESTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website. ACTEMRA SIDE EFFECTS AND WHO IS ELIGIBLE FOR AN ACTEMRA LAWSUIT BY A NASHVILLE ACTEMRA LAWYER5/17/2023
Call a Nashville Actemra lawyer today if you suffered serious Actemra side effects, you may be eligible for an Actemra lawsuit
Roche’s Actemra was heralded as a breakthrough therapy for rheumatoid arthritis when it was introduced in 2010.
The drug’s website proclaims that “Actemra works differently” and shows a patient happily scuba diving and walking on a tropical beach. But nowhere does Roche mention certain side effects that may have contributed to more than 1,100 patient deaths. Research suggests that Actemra patients, compared to those taking competing rheumatoid arthritis drugs, face similar risks for heart attacks, heart failure, strokes, lung disease, and pancreatitis. But unlike the competition, Actemra’s label does not warn about these side effects. If you or a loved one suffered serious Actemra side effects including heart, lung, or pancreatic side effects while taking Actemra, contact Nashville Actemra lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for an Actemra lawsuit. If you meet the requirements for an Actemra lawsuit you may be entitled to substantial compensation. WHAT ARE THE ACTEMRA SIDE EFFECTS TO THE HEART AND LUNGS?![]()
A STAT News report and postmarketing studies raise questions about the adequacy of Actemra's safety warnings.
STAT reviewed more than 500,000 adverse event reports on leading rheumatoid arthritis drugs, including Actemra, Humira, and Remicade. STAT found evidence that Roche downplayed Actemra’s cardiovascular, pancreatic, and lung side effects. According to STAT, from 2010 to 2016 the U.S. Food and Drug Administration (FDA) logged more than 13,500 Actemra adverse event reports, including 1,128 patients who died after taking Actemra. While safety data indicate the risks of heart attacks, strokes, heart failure, and interstitial lung disease are as high or higher for Actemra patients than for patients taking some similar drugs, Actemra’s warning label—unlike its competition's—does not reflect these risks. For example, Actemra patients reported more cases of interstitial lung disease than Remicade patients, and nearly the same number as Humira patients. But while Remicade and Humira have interstitial lung disease warnings, Actemra does not. STAT’s findings are supported by postmarketing studies—clinical studies conducted after a pharmaceutical product goes on the market to better understand drug risks. The FDA ordered Actemra postmarketing studies because premarket testing revealed potentially worrisome side effects. One such study compared Actemra to another arthritis drug, Enbrel, and found rates of stroke and heart failure were about 1.5 times higher in Actemra users. Enbrel has strong warnings for patients with cardiovascular disease. Actemra does not have similar warnings despite similar or worse cardiovascular risks. The takeaway from these findings is that doctors and patients may not be getting a complete picture of Actemra’s risk-benefit profile. IF I SUFFERED ACTEMRA SIDE EFFECTS, AM I ELIGIBLE FOR AN ACTEMRA LAWSUIT?
We are looking into claims that Genetech/Roche failed to warn about the following Actemra side effects:
Actemra patients who suffered any of these side effects may be eligible for an Actemra lawsuit. IF I SUFFERED ACTEMRA SIDE EFFECTS AND MEET THE REQUIREMENTS FOR AN ACTEMRA LAWSUIT, WHAT CAN I GET?
If you meet the requirements for an Actemra lawsuit and are successful you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff who is eligible for an Actemra lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they meet the requirements for an Actemra lawsuit and are successful. HOW MUCH DOES IT COST TO HIRE A NASHVILLE ACTEMRA LAWYER IF I SUFFERED ACTEMRA SIDE EFFECTS AND MEET THE REQUIREMENTS FOR AN ACTEMRA LAWSUIT?
It does not cost anything to hire a Nashville Actemra lawyer. We take all cases on a contingency basis which means we do not get paid unless we win your case. A Nashville Actemra lawyer can explain the process and answer any questions you may have including whether you are eligible for an Actemra lawsuit.
IF YOU SUFFERED ACTEMRA SIDE EFFECTS, CALL A NASHVILLE ACTEMRA LAWYER TODAY IF YOU SUFFERED SERIOUS ACTEMRA SIDE EFFECTS?
If you or a loved one suffered serious Actemra side effects including heart, lung, or pancreatic side effects while taking Actemra, contact Nashville Actemra lawyer Timothy L. Miles today to see if you are eligible for an Actemra lawsuit. If you meet the requirements for an Actemra lawsuit you may be entitled to substantial compensation.
nashville actemra lawyer timothy l. milesTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you sufferd Xeljanz side effects, contact a Nashville Xeljanx lawyer today you could be eligible for a Xeljanx lawsuit
Pharmaceutical companies and suppliers have both an ethical and legal responsibility to properly disclose the risks and side effects of a drug before bringing it to market, but all too often those warnings are withheld in the name of profit.
However, in just the last two years, the U.S. Food and Drug Administration (FDA) has warned that Xeljanz (Tofacitinib) can be associated with heart problems, blood clots, and even cancer. But the question remains: why didn’t Pfizer warn consumers about these potential risks sooner? Xeljanz lawsuits claim that Pfizer failed to give adequate warning about the Xeljanz's side effects, which caused preventable harm to patients who suffered blood clots in the lungs, heart attacks, strokes, breast and colon cancer, and other severe health problems. We are accepting these cases on a contingency-fee basis. That means our clients don’t pay unless we win. If you need to discuss a lawsuit with a Nashville Xeljanz lawyer, free of charge, please contact a Nashville Xeljanz lawyer for a free case evaluation. (855) Tim-M-Law (855-846-6529). Read on to learn more about the Xeljanx side effects and see if you may be eligible for a Xeljanx lawsuit if you suffered Xeljanz side effects. ABOUT XELJANZ![]()
Xeljanz belongs to a class of drugs known as Janus kinase (JAK) inhibitors. As Pfizer explains, our body has signaling proteins called cytokines that regulate immune system responses. The production of cytokines is increased when our body fights infection. Cytokine production is thought to play a role in chronic inflammatory conditions, such as rheumatoid arthritis, psoriatic arthritis, and ulcerative colitis. Xeljanz disrupts signaling that produces some of the cytokines, reducing inflammation. Specifically, Xeljanz blocks—or inhibits—the release of cytokines in the JAK signal pathway.
Xeljanz has been approved for several different uses:
Xeljanz has been approved for several different uses:
WHAT ARE THE XELJANZ SIDE EFFECTS?
The Xeljanz Side Effects include:
If you suffered serious Xeljanz side effects, contact Nashville Xeljanz lawyer Timothy L. Miles today. SOME PATIENTS TOOK XELJANZ AND DEVELOPED BLOOD CLOTS AS XELJANZ SIDE EFFECTS
In February 2019, the FDA warned that the ongoing Xeljanz safety trial found an increased risk of taking Xeljanz and developing blood clots in the lungs and death. In July 2019, the FDA announced that it had approved new warnings about thrombosis and death in patients treated with a 10 mg twice-daily dose of Xeljanz.
Thrombosis occurs when a blood clot blocks a vein or artery. Deep vein thrombosis, pulmonary embolism, and arterial thrombosis have all been reported in Xeljanz patients. A blood clot in a deep vein is known as a deep vein thrombosis (DVT). DVT usually occurs in the legs. A blood clot that travels to the lungs is called a pulmonary embolism (PE). PE is usually caused by a blood clot that starts in the arm or the leg. Arterial thrombosis is a blood clot in an artery. This type of thrombosis can stop blood from reaching vital organs. Blood clots can lead to a heart attack, stroke, organ damage, and even death. Symptoms of a blood clot include:
XELJANZ AND CANCER AS ANOTHER OF THE XELJANZ SIDE EFFECTS
The next major safety news to come out of the Xeljanz post-marketing study was equally concerning because of Xeljanz and Cancer. The FDA alerted the public in February 2021 that preliminary results showed an increased risk of cancer with Xeljanz.
Pfizer reports in a press release that malignancies observed in Xeljanz studies include (but are not limited to):
Also in February 2021, the FDA warned about serious heart-related problems that may result from Xeljanz use. Pfizer refers to these in its press release as “major adverse cardiovascular events” (MACE). Pfizer reports that a total of 135 patients in the study had a major adverse cardiovascular event, although the full results have not yet been released. The most frequently reported event was myocardial infarction (i.e. heart attack).
We are currently speaking to clients across the country about Xeljanz side effects including Xeljanz cancer, blood clot, and cardiovascular lawsuits. Patients who took Xeljanz as prescribed and developed a malignancy, thrombosis, or heart-related issues may qualify for a Xeljanz lawsuit. Lawsuits against Pfizer can recover compensation for medical bills, lost wages, pain and suffering, reduced quality of life, and more. XELJANZ AND MAJOR CARDIOVASCULAR EVENTS AS ANOTHER ONE OF THE XELJANZ SIDE EFFECTS
The latest results from the ORAL Surveillance study were released in early 2021 and led to an FDA safety communication about increased risk of serious heart-related problems, or “major adverse cardiovascular events” (MACE).
Pfizer reported 135 patient subjects with MACE. The most frequently reported such event was myocardial infarction (heart attack), but the full data has not yet been released. Other major cardiac events and Xeljanx side effects that may be linked to Xeljanz include:
IF I SUFFERED XELJANZ SIDE EFFECTS, AM I ELIGIBLE FOR A XELJANZ LAWSUIT?
If you took Xeljanz and have been diagnosed with cancer, a major adverse cardiovascular event, or venous thromboembolism (such as a pulmonary embolism or deep vein thrombosis) or other serious Xeljanz side effects, you may be eligible for a Xeljanz lawsuit and possibly be entitled to substantial compensation. Call today for a free case evaluation with a Nashville Xeljanz lawyer and see if you meet the Xeljanz Lawsuit Criteria.
IF I SUFFERED XELJANZ SIDE EFFECTS AND I AM ELIGIBLE FOR A XELJANZ LAWSUIT, WHAT CAN I GET OUT OF A XELJANZ LAWSUIT?
If you are eligible for a Xeljanz lawsuit, a successful plaintiff is entitled to compensatory damages which would include compensation for things such as:
If your case proceeds to trial it is also possible the court could impose punitive damages, intended to punish the defendant for their actions. IF YOU SUFFERED XELJANZ SIDE EFFECTS, CONTACT A NASHVILLE XELJANZ LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A XELJANZ LAWSUIT
Xeljanz, while marketed as a safe medication, increases the risk of blood clots, cancer, and cardiovascular problems for its users. The FDA approved the drug upon release, but a post-marketing safety study revealed serious safety concerns and concluded that the side effects are more detrimental than initially believed. The company responsible for the medication, Pfizer, knew about the side effects prior to the safety study but failed to disclose this information to the public in an attempt to retain their profits. This unethical behavior exposed thousands of consumers to an elevated risk of harm, making their actions unacceptable by any means.
Unfortunately, some users of Xeljanz have developed cancer as a result of their medication use, including but not limited to lymphoma, melanoma, and lung cancer. Pfizer, already knowing the risk of the Xeljanz side effects, sold it to consumers anyway, causing many innocent individuals to develop and suffer from a life-threatening disease. Their reluctance to disclose the risk of their product is not just unethical, it’s illegal, and our attorneys are here to help hold them accountable to the fullest extent of the law. Contact a Nashville Xeljanz Lawyer today at (855) 846-6529 or [email protected] or by submitting this form and see if you meet the Xeljanz lawsuit criteria if you suffered Xeljanz side effects. Someone will promptly get in touch with you. We are here to help! nashville xeljanz lawyer timothy l. miles, esq.Timothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website. a closer look at the side effects of kombiglyze xr and by a nashville kombiglyze xr lawyer5/17/2023
If you took Kombiglyze XR and suffered Kombiglyze XR side effects call a Nashville Kombiglyze XR lawyer you may be eligible for a Kombiglyze XR lawsuit
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Kombiglyze XR is a combination of metformin (a biguanide) and saxagliptin (a DPP4 inhibitor). Kombiglyze XR works by lowering the amount of sugar made by your liver, decreasing the amount of sugar absorbed by your intestine, increasing the amount of insulin your body makes, and helps your body respond better to insulin.
However, research shows that type 2 diabetes drug Kombiglyze XR (saxagliptin and metformin) may cause heart failure or other cardiovascular injuries in some patients. According to the Centers for Disease Control and Prevention (CDC), 30 million Americans have diabetes and 84 million have pre-diabetes. Metformin—one of the drugs found in combination in Kombiglyze—is among the top 10 most popular prescription drugs taken by Americans. Analysts also predict that Onglyza (saxagliptin), Kombiglyze’s sister drug, could reach $1.8 billion in sales in 2018. In 2015, roughly 386,000 people were prescribed Onglyza or Kombiglyze XR, the U.S. Food and Drug Administration (FDA) reported. Given that so many people take these drugs, any side effects they may cause that are severe enough to hospitalize patients should be treated with concern. Dozens of patients are filing lawsuits against Kombiglyze’s manufacturer AstraZeneca and its previous partner Bristol-Myers Squibb alleging that the companies failed to adequately test the drugs’ safety prior to selling it, which ultimately caused their cardiovascular injuries. If you or a loved one took Kombiglyze XR as directed and suffered from Kombiglyze XR side effects including heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, after starting Kombiglyze XR therapy, contact Nashville Kombiglyze XR lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation. Read on to learn more about the Kombiglyze XR side effects and see if you may be eligible for a Kombiglyze XR lawsuit if you suffered Kombiglyze side effects. WHAT ARE THE KOMBIGLYZE XR SIDE EFFECTS?
The following are some of the common Kombiglyze XR side effects:
Additionally, dozens of lawsuits allege other Kombiglyze XR side effects including serious cardiovascular injury. If you suffered Kombiglyze XR side effects call a Nashville Kombiglyze XR lawyer today. DOES KOMBIGLYZE XR PUT PATIENTS AT RISK OF HEART FAILURE?
A clinical trial funded by AstraZeneca and Bristol-Myers Squibb was one of the first studies to report cardiovascular health risks associated with these drugs.
Saxagliptin Assessment of Vascular Outcomes Recorded in Patients with Diabetes Mellitus, or the SAVOR trial, found that patients with a history of heart problems who took Onglyza or Kombiglyze XR had a 27% greater chance of being hospitalized for heart failure than patients who took a placebo. Patients with chronic kidney disease and / or previous heart failure were more likely to be hospitalized. When an FDA panel reviewed the results from the SAVOR study, 14 out of 15 panelists voted to require a safety warning on all Onglyza and Kombiglyze XR bottles that the drugs could result in cardiovascular injury. Patients are filing lawsuits against AstraZeneca and Bristol-Myers Squibb alleging that Kombiglyze XR caused their cardiovascular injuries. Complaints allege that AstraZeneca and Bristol-Myers Squibb failed to adequately test the drug prior to their sale. In February 2018, more than 80 Onglyza and Kombiglyze XR lawsuits were centralized in Lexington, Kentucky. Plaintiffs' attorneys said that centralization is key to reducing inconsistencies since these lawsuits were "just the tip of the iceberg" and the number of filed complaints was expected to grow. In a complaint filed in January 2018, Illinois plaintiff Jerald Adams alleged that after being exposed to saxagliptin after taking both Onglyza and Kombiglyze XR, the diagnosis of his heart failure was “directly related to taking these drugs.” In the complaint, Mr. Adams alleged that the manufacturers not only knew of the cardiovascular injury risk associated with saxagliptin, but that they also failed to warn or mitigate this risk despite their knowledge including the Kombiglyze side effects. "At all relevant times, defendants had knowledge that there was a significantly increased risk of adverse events associated with saxagliptin, including heart failure, congestive heart failure, cardiac failure, and death related to those events, and despite this knowledge, defendants continued to manufacture, market, distribute, sell, and profit from sales of saxagliptin," the complaint alleges. Some lawsuits filed in New Jersey claim that Bristol-Myers and AstraZeneca did not just do a poor job of testing the safety of their drugs, but that they also did not conduct the clinical trials recommended by the FDA in 2008 prior to Onglyza’s sale debut in 2009. In 2008, the FDA Endocrinologic and Metabolic Drugs Advisory Committee "determined that concerns about cardiovascular risk should be more thoroughly addressed during drug development." Bristol-Myers and AstraZeneca failed to do so and began marketing Onglyza in 2009. HOW DO I KNOW IF I AM ELIGIBLE OR A KOMBIGLYZE XR LAWSUIT?
If you or a loved one took Kombiglyze XR as directed and suffered from heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, or other serious Kombiglyze XR side effects, after starting Kombiglyze XR therapy, you may meet the requirements for a Kombiglyze XR lawsuit and possibly be entitled to substantial compensation. Call a Nashville Kombiglyze XR lawyer for free today who can tell you if you are eligible for a Kombiglyze XR lawsuit.
IF I MEET THE REQUIREMENTS FOR A KOMBIGLYZE XR LAWSUIT, WHAT CAN I GET?
If you meet the requirements for a Kombiglyze XR lawsuit and are successful you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff who is eligible for a Kombiglyze XR lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they meet the requirements for a Kombiglyze XR lawsuit and are successful. IF YOU SUFFERED FROM KOMBIGLYZE XR SIDE EFFECTS, CALL A NASHVILLE KOMBIGLYZE XR LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A KOMBIGLYZE XR LAWSUIT
If you or a loved one took Kombiglyze XR as directed and suffered from Kombiglyze XR Side Effects, specifically: heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, after starting Kombiglyze XR therapy, contact Nashville Kombiglyze XR lawyer Timothy L. Miles today to see if you are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation.
NASHVILLE KOMBIGLYZE XR LAWYER TIMOTHY L. MILESTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Onglyza Side Effects contact Nashville Onglyza lawyer Timothy L. Miles, you could be eligible for an Onglyza lawsuit
Onglyza (saxagliptin) and Kombiglyze XR (saxagliptin and metformin) belong to a new class of diabetic drugs known as DPP-4 inhibitors. Onglyza gained federal drug approval by the U.S. Food & Drug Administration (FDA) despite initial concerns over the cardiovascular safety of the drug.
These concerns were echoed in a post-marketing safety study that found Onglyza may be associated with an increased risk of heart failure and an increased risk of death. If you or a loved one took Onglyza as directed and suffered from Onglyza side effects including heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, after starting Onglyza therapy, contact Nashville Onglyza lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for an Onglyza lawsuit and possibly entitled to substantial compensation. Read on for more information on who is eligible for an Onglyza lawsuit and if you suffered Onglyza side effects, see if you are eligible for an Onglyza lawsuit. WHAT IS ONGLYZA?
Onglyza (saxagliptin) is an add-on medication to diet and exercise to improve blood sugar control in people with type 2 diabetes. It is a is a dipeptidyl peptidase-4 (DPP-4) inhibitor that increases the amount of insulin your body makes. Onglyza comes in tablets in dosages of 2.5 mg and 5 mg taken once by mouth daily.
WHAT IS THE PROBLEM WITH ONGLYZA, DOES IT CAUSE ONGLYZA SIDE EFFECTS?![]()
Type 2 diabetes patients have a significantly increased risk of cardiovascular complications, and the majority of diabetics die from such complications. Amid growing concerns over the safety of many diabetes drugs, in 2008 the FDA recommended that the makers of new type 2 diabetes drugs provide evidence that the drugs do not increase the risk of cardiovascular events such as heart attacks.
Onglyza met the FDA's cardiovascular safety criteria. Though the FDA approved the new diabetic drug, it had reservations about the sufficiency of Onglyza clinical trials and ordered AstraZeneca to perform a post-marketing study. As a result, AstraZeneca completed a 16,000-patient cardiovascular outcomes trial called SAVOR. The results of that trial were published in the New England Journal of Medicine and raised major Onglyza safety concerns. SAVOR found that Onglyza patients were 27% more likely to be hospitalized for heart failure. The study also found a significant increase in the rate of “all-cause mortality” among Onglyza patients. The warning signs of heart failure include:
Following the release of SAVOR, the FDA issued an Onglyza drug safety communication and convened an advisory committee meeting to analyze the results and recommend further action. The committee voted 14-to-1 to add information to Onglyza’s label warning about heart failure risks. The other member voted to withdraw Onglyza from the U.S. market. The committee, however, did not advise updating the warning label to address the measured increase in all-cause mortality among Onglyza patients and did not recommend any restrictions on prescribing the drug. In an April 2016 drug safety communication, the FDA announced that Onglyza and Kombiglyze XR are now required to carry warnings about heart failure risk. Other FDA warnings about saxagliptin include:
WHAT ARE THE ONGLYZA SIDE EFFECTS?
In addition to heart failure, Onglyza is linked to these adverse Onglyza side effects:
IF I SUFFERED ONGLYZA SIDE EFFECTS, HOW DO I KNOW IF I MEET THE REQUIREMENTS FOR AN ONGLYZA LAWSUIT?
If you or a loved one took Onglyza as directed and suffered suffered heart failure, death, or another serious cardiovascular injury, after starting Onglyza therapy, you may meet the requirements for an Onglyza lawsuit and possibly be entitled to substantial compensation. Call a Nashville Onglyza lawyer for free today who can tell you if you are eligible for an Onglyza lawsuit.
IF I SUFFERED ONGLYZA SIDE EFFECTS AND I AM ELIGIBLE FOR AN ONGLYZA LAWSUIT, WHAT CAN I GET OUT OF AN ONGLYZA LAWSUIT?
If you meet the requirements for an Onglyza lawsuit and are successful you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff who is eligible for an Onglyza lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they meet the requirements for an Onglyza lawsuit and are successful. IF I SUFFERED ONGLYZA SIDE EFFECTS, HOW DOES AN ONGLYZA LAWSUIT WORK?
If you are eligible for a Onglyza lawsuit, before it is filed with the court, your Nashville Onglyza lawyer will fully explain the process and will then need to ask you a few questions concerning the circumstances of you diagnoses, how long you have been taking Onglyza and your medical history including your Onglyza side effects.
Your Nashville Onglyza lawyer will then draft what is known as a complaint. This will be a multi-page document explaining why the defendant is responsible for your injuries and what damages (that is, compensation) you are seeking. Once your complaint is filed with the court, your Onglyza Lawsuit officially begins. From here, it will be a lot of back and forth between your Nashville Onglyza lawyer and the attorney(s) for the defendant in an attempt to resolve the matter. The attorneys may take review documents, take depositions, issue subpoenas, hire experts, calculate damages, attend hearings, and file motions, briefs, evidence or other documents with the court during the stages of the lawsuit. If your Onglyza lawsuit is not dismissed and a settlement cannot be reached, the case will proceed to a jury trial. IF YOU SUFFERED ONGLYZA SIDE EFFECTS, CONTACT A NASHVILLE ONGLYZA LAWYER TO SEE IF YOU ARE ELIGIBLE FOR AN ONGLYZA LAWSUIT?
If you or a loved one took Onglyza as directed and suffered from Onglyza Side Effects, specifically: heart failure, death or another serious cardiovascular injury —such as congestive heart failure or myocardial infarction, after starting Onglyza therapy, contact NashvilleOnglyza lawyer Timothy L. Miles today to see if you are eligible for a Onglyza lawsuit and possibly entitled to substantial compensation.
nashville onglyza lawyer timothy l. milesTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Elmiron Eye Damage contact a Nashville Elmiron lawyer today, you could be eligible for an Elmiron lawsuit
The Firm is reviewing claims on behalf of Interstitial Cystitis (IC) patients who took the prescription drug Elmiron and now may be suffering from a severe eye disease called maculopathy or has suffered vision impairment as a result.
If you developed malculopathy or a vision impairment and took Elmiron, or have additional questions, give Nashville Elmiron Lawyer Timothy L. Miles a call today for a free case evaluation, you could be entitled to significantly compensation if you meet the Elmiron Lawsuit Criteria and file an Elmiron lawsuit. Get started by filling out a free case evaluation form or calling a Nashville Elmiron Lawyer. (855) Tim-M-Law (855-846-6529). Read on to learn more on who is eligible for an Elmiron lawsuit, and if you suffered Elmiron side effects, see if you areeligible for an Elmiron lawsuit. WHAT IS ELMIRON AND WHY DOES IT CAUSE ELMIRON EYE DAMAGE?
Since 1996, millions of patients have been prescribed Elmiron in order to treat their interstitial cystitis (IC), otherwise known as painful bladder syndrome. But there is now reason to believe that this drug may cause a serious eye condition in those taking it, one that may result in blindness.
This condition is a form of maculopathy – the degeneration of the macula, the central part of the retina. Maculopathy’s first symptoms are blurred vision, dark spots, trouble focusing, and other impairments: as it progresses, it may lead to total blindness. As the evidence has piled up, the manufacturer of Elmiron – Janssen Pharmaceuticals – has failed to warn the public about these risks. Millions of people are taking a drug that may one day rob them of their vision, and an untold number may have already suffered serious health conditions. Elmiron eye damage lawsuits on behalf of the injured have already begun claiming their maculopathy was caused by Elmiron. If you or a loved one took Elmiron and has since been diagnosed with maculopathy, or vision impairment you may be eligible for compensation. Contact a Nashville Elmiron Lawyer today to have your case reviewed for free and see if you meet the Elmiron lawsuit criteria and are eligible for an Elmiron lawsuit. IS MACULOPATHY CAUSED BY LONG-TERM USE OF ELMIRON?
In 2018, researchers at the Emory Eye Center at the Emory School of Medicine in Atlanta alerted the public that taking Elmiron is linked to the retinal condition, maculopathy. Pentosan polysulfate sodium can cause severe vision problems and side effects, including interstitial cytitis, and even blindness.
Nieraj Jain, M.D., of Emory Eye Center in Atlanta, Ga., reported that six Elmiron patients who had been taking Elmiron for about 15 years had developed unusual changes in their macula. Because nothing in the patients’ medical history or diagnostic tests explained the subtle, but striking pattern of abnormalities, Dr. Jain and his colleagues raised a warning flag that long-term use of Elmiron may damage the retina. The retina is a thin layer of tissue that lines the back of the eye on the inside. It is located near the optic nerve. The retina receives light that the lens has focused and converts the light into neural signals. It then sends these signals on to the brain for visual recognition All patients in the study reportedly showed signs of retinal disease and that the youngest patient in the study was diagnosed with interstitial cystitis at 23 years of age. That patient began taking the medication daily and began showing visual symptoms by the age of 30. In addition, three ophthalmologists conducted a review of patients at Kaiser Permanente in Northern California and found that approximately one-quarter of patients with significant exposure to Elmiron showed definite signs of eye damage. It also found the medication could potentially be linked to retinal conditions, such as age-related macular degeneration or pattern dystrophy. Patients who have used or are using the pentosan polysulfate sodium drug Elmiron are advised to be screened by ophthalmologists if they are experiencing any unusual eye symptoms. They are also advised to cease pentosan therapy if eye disease is present. WHAT ARE THE SYMPTOMS OF ELMIRON EYE DAMAGE RELATED TO RELATED RETINAL MACULOPATHY?
A newly discovered condition has come to light, and it is presently unknown how many symptoms there actually are, or how serious this can end up being for those suffering from it.
The currently known symptoms associated with this eye condition include:
IF I SUFFERED ELMIRON EYE DAMAGE, HOW DO I KNOW IF I AM ELIGIBLE FOR AN ELMIRON LAWSUIT?
You may be eligible for an Elmiron lawsuit if meet the following criteria:
The criteria are based upon the medical studies linking the drug to eye disease and vision impairment, including interstitial cytitis and maculopathy. However, there may be exceptions to the Elmiron lawsuit criteria. There may be other eye damage claims available for you to pursue and you still may be eligible for an Elmiron lawsuit. HOW DO I GET STARTED IF I SUFFERED ELMIRON EYE DAMAGE AND BELIEVE I AM ELIGIBLE FOR AN ELMIRON LAWSUIT?
If you suffered Elmiron Eye Damage fill out and submit this form for a Free Case Evaluation with a Nashville Elmiron Lawyer to see if you are eligible for a Elmiron lawsuit and possibly entitled to substantial compensation.
IF YOU SUFFERED ELMIRON EYE DAMAGE, OR ELMIRON SIDE EFFECTS, CALL A NASHVILLE ELMIRON LAWYER TODAY TO SEE IF YOU ARE ELIGIBLE FOR AN ELMIRON LAWSUIT?
If you were diagnosed with maculopathy or vision impairment caused by Elmiron, or other serious Elmiron Side Effects, contact a Nashville Elmiron Lawyer today as you most likely meet the Elmiron lawsuit criteria and are eligible for an Elmiron lawsuit and possibly recover substantial compensation. The call is free and so is the fee unless we will you case. So, call today and see what a Nashville Elmiron lawyer can do for you.
So, give a Nashville Elmiron Lawyer call today or submit the free case evaluation form if you suffered Elmiron Side Effects and see if you and are eligible for an Elmiron lawsuit. nashville elmiron lawyer timothy l. milesTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Tepezza hearing loss or other Tepezza side effects, contact a Nashville Tepezza lawyer today
Tepezza (teprotumumab-trbw) is a prescription drug that was developed by Horizon Therapeutics® for a condition known as Graves' eye disease and the treatment of thyroid eye disease (TED). TED is a condition that occurs when the eye muscles, tear glands, eyelids, and the fatty tissue behind the eyes become inflamed. The eye inflammation is triggered through an abnormal autoimmune response and can cause the eyes to swell and obstruct vision.
Tepezza works by blocking a specific protein that is believed to be the cause of the development of TED. The eye treatment drug is administered through injection about every three weeks for roughly five months. Approved by the Food and Drug Administration (FDA) in January 2020, it was the first medication approved for TED. Victims of Tepezza are now filing lawsuits after taking the drug and suffering from Tepezza hearing loss. According to the lawsuits, the labels on the drug did not warn patients or doctors about the potential risk for hearing loss nor did it warn how these issues could be permanent to those taking the eye drug. If you suffered Tepezza hearing loss or other serious Tepezza side effects, contact Nashville Tepezza lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Tepezza lawsuit and possibly entitled to substantial compensation. Read on to learn more on who exactly is eligible for a Tepezza lawsuit. TEPEZZA HEARING LOSS
In January 2020, the FDA approved Tepezza, the only drug known to treat TED, based on clinical trials that documented only 10% of patients reporting Tepezza hearing loss issues. However, a 2021 study found that patients taking Tepezza are at a 65% higher risk for developing temporary and even permanent hearing issues, making it over six times higher than the original estimated risk of hearing loss disclosed by Horizon during the FDA approval process.
WHAT ARE THE TEPEZZA SIDE EFFECTS?
The Tepezza side effects include:
If you suffered Tepezza side effects including Tepezza hearing loss, call a Nashville Tepezza lawyer today. IF I SUFFERED TEPEZZA HEARING LOSS, DO I QUALIFY FOR A TEPEZZA LAWSUIT?
In order to qualify for a Tepezza lawsuit, you must have taken the drug and have experienced permanent or persistent Tepezza hearing loss. The best way to understand if you qualify to file a Tepezza lawsuit against Horizon Therapeutics is by speaking to a Nashville Tepezza lawyer as soon as possible. Depending on your state, there may be a statute of limitations for filing a claim, ranging from two to four years on average depending on the State. If you suspect that you may have lost your hearing after taking Tepezza, do not wait to speak with an attorney.
IF I SUFFERED TEPEZZA HEARING LOSS, WHAT IS A TEPEZZA LAWSUIT?
A Tepezza Lawsuit is a demand from the defendants for monetary compensation by patients who took Tepezza and subsequently developed Tepezza Hearing Loss and other Tepezza side effects. The lawsuits allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties.
If you suffered Tepezza Hearing Loss and are eligible a Tepezza lawsuit, you may possibly be entitled to substantial compensation. A Nashville Tepezza Lawyer can answer these questions and is available anytime just give us a call or submit this form below for a free case evaluation to see if you areeligible for a Tepezza lawsuit. IF YOU SUFFERED TEPEZZA HEARING LOSS, CALL A NASHVILLE TEPEZZA LAWYER TODAY AND SEE IF YOU ARE ELIGIBLE FOR A TEPEZZA LAWSUIT
If you or your loved one received Tepezza (teprotumumab) infusions and later experienced Tepezza hearing loss or tinnitus, contact Nashville Tepezza lawyer Timothy L. Miles today for a free case evaluation to see if you qualify for a Tepezza Lawsuit and are possibly entitled to significant compensation.
NASHVILLE TEPEZZA LAWYER TIMOTHY L. MILESTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Valsartan side effects, contact Nashville Valsartan lawyer Timothy L. Miles today
Valsartan has been recalled due to possible nitrosamine contamination. Nitrosamines can cause tumors in the liver and other organs in lab animals and are thought to be carcinogenic in humans as well. It is believed that these blood pressure drugs were tainted during flawed manufacturing processes. The U.S. Food and Drug Administration (FDA) stated that these contaminants “are of special concern to global regulators because, unlike most impurities in drugs, they have the potential to cause harm at very low levels.”
The recalls began in July when the FDA found that some Valsartan products contained a potentially cancer-causing chemical. European regulators had already made the same discovery. The substance can form during manufacturing if the chemical reactions used to make the drug are not carefully controlled and monitored, the FDA said. Valsartan is made by Chinese manufacturer Zhejiang Huahai Pharmaceuticals. These recalls are a product of greater FDA scrutiny of foreign drug imports, but FDA warnings alone will not ensure safe medications. In a culture where the profit motive exists, drug companies must be held accountable to cutting corners and sacrificing consumer safety. If you or a loved one took Valsartan and later were diagnosed with cancer or other serious Valsartan Side Effects, contact Nashville Valsartan lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Valsartan lawsuit and possibly entitled to substantial compensation. Read on to learn more on who is eligible for a Valsartan lawsuit. WHAT IS VALSARTAN?![]()
Valsartan belongs to a class of drugs called angiotensin II receptor blockers (ARB). Valsartan is a blood pressure medication used to treat high blood pressure and heart failure. It is also prescribed after a heart attack to lower blood pressure and help the patient live a longer life. The medication should not be taken while pregnant because it may be harmful to an unborn child.
WHAT ARE THE VALSARTAN SIDE EFFECTS?
In addition to cancer, sources say other ValsartanValsartan Side Effects include:
IF I SUFFERED VALSARTAN SIDE EFFECTS, AM I ELIGIBLE FOR A VALSARTAN LAWSUIT?
If you took Valsartan and subsequently were diagnosed with cancer, or experienced other serious Valsartan side effects, then you may be eligible for a Valsartan lawsuit possibly may be entitled to substantial compensation. Contact Nashville Valsartan Lawyer Timothy L. Miles today and see if are eligible for a Valsartan lawsuit.
IF I AM ELIGIBLE FOR A VALSARTAN LAWSUIT, HOW MUCH CAN I GET OUT OF A VALSARTAN LAWSUIT?
If you are eligible for a Valsartan lawsuit and are successful, you can recover money for some of the following damages:
Broadly speaking, a plaintiff in a Valsartan lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they are eligible for a Valsartan lawsuit and are successful. IF YOU SUFFERED VALSARTAN SIDE EFFECTS, CALL A NASHVILLE VALSARTAN LAWYER AND SEE IF YOU ARE ELIGIBLE FOR A VALSARTAN LAWSUIT
If you or a loved one has received a cancer diagnosis or experienced other serious Valsartan side effects after taking Valsartan, contact us for a free, no-risk case evaluation to see if you meet the Valsartan lawsuit criteria. We might be able to help you pursue compensation for the harm you and your loved ones have suffered if you meet the Valsartan lawsuit criteria.
Call Nashville Valsartan Lawyer Timothy L. Miles today to see how he can help you. A Nashville Valsartan Lawyer can explain the process and answer any questions you may have including whether you meet the Valsartan lawsuit criteria. While there is still time to file a lawsuit, be mindful that these cases are time sensitive, and give us a call today. NASHVILLE VALSARTAN LAWYER TIMOTHY L. MILESTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Merida side effects, contact a Nashville Merida lawyer to see if you meet the requirements for a Merida lawsuit
Meridia, made by Abbott Laboratories, was approved in 1997 for weight loss and weight loss maintenance for obese patients, and also very obese individuals who already had other health risk factors for cardiovascular disease. Meridia was approved after clinical studies showed that more patients taking Meridia lost at least 5 percent of their body weight than members of the placebo group who relied solely on diet and exercise.
However, the U.S. Food & Drug Administration (FDA) has now requested that Meridia be recalled following a nearly year-long safety review of the drug which was initiated after researchers published the results of a study known as SCOUT (Sibutramine Cardiovascular Outcomes Trial). The study, which prompted a Meridia recall in Europe, showed a 16% percent increase in the risk of serious Meridia side effects, including:
SCOUT monitored 10,000 obese patients over the age of 55 who had a history of heart disease, and type 2 diabetes or similar risk factors. The initial purpose of the study was to show that weight loss through Meridia use lowered the risk of heart problems. However, that was not the case. In fact, the results suggested that those taking the weight loss drug had an increased chance of suffering Meridia cardiovascular side effects. Doctors have been advised to stop prescribing Meridia and begin discussing weight loss alternatives with their patients. If you or a loved one suffered serious Meridia side effects including a heart attack, stroke or even death, contact Nashville Meridia lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Meridia lawsuit and possibly entitled to substantial compensation. Read on to learn more about the requirements for a Merida lawsuit and if you suffered Merida side effects, see if you are eligible for a Merida lawsuit. WHAT IS MERIDIA?![]()
Meridia is a medication which requires a prescription and is used to treat the symptoms of obesity, weight loss, and maintenance of weight loss. It may be used alone or with other medications. Meridia belongs to a class of drugs called Schedule IV controlled substances and can cause severe Meridia side effects in some people. If you or a loved one suffered severe Meridia side effects call Nashville Meridia Lawyer Timothy L. Miles for a free case evaluation to see if you are eligible for a Meridia lawsuit and possibly entitled to substantial damages.
SERIOUS MERIDIA SIDE EFFECTS
In the beginning, Meridia seemed to be a booming success as it was used by millions of individuals around the world. However, hundreds of users began reporting serious Meridia side effects including:
Patients taking Meridia have also experienced these Merida side effects:
Additionally, approximately 30 deaths were caused by Merida in the United States. Researchers looked at 10,000 patients who were obese, over the age of 55 with a history of risk factors and found that 11.4% of patients using Meridia suffered heart problems, compared to 10% given a sugar pill. As of June 30, 2009, the FDA Adverse Event Reactions (AERS) database indicates that at least 84 Meridia deaths from cardiovascular causes have been reported to the FDA.' If you suffered severe Meridia side effects call Nashville Meridia Lawyer Timothy L. Miles for a free case evaluation to see if you are eligible for a Meridia lawsuit. if i meet the requirements for a merida lawsuit, what can i get out of a merida lawsuit?
If you meet the requirements for a Meridia lawsuit and are successful you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff who is eligible for a Meridia lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they meet the requirements for a Meridia lawsuit and are successful. Call today to see if you are eligible for a Meridia lawsuit. IF I SUFFERED MERIDA SIDE EFFECTS AND DECIDE TO FILE A MERIDA LAWSUIT, HOW INVOLVED WILL I HAVE TO BE?
If you suffered Merida side effects and are eligible for a Meridia Lawsuit and decide to file a Meridia Lawsuit, your primary responsibilities as a plaintiff are as follows:
While this may not be every single thing you are required to do, it is the bulk of your responsibilities as a plaintiff. When you meet with your Nashville Meridia lawyer, he will explain your responsibilities in greater detail. IF YOU SUFFERED MERIDIA SIDE EFFECTS, CALL A NASHVILLE MERIDIA LAWYER TODAY TO SEE IF YOU ARE ELIGIBLE FOR A MERIDIA LAWSUIT
If you or a loved one suffered serious Meridia side effects including a heart attack, stroke or even death, contact Nashville Meridia lawyer Timothy L. Miles today to see if you are eligible for a Meridia lawsuit and possibly entitled to substantial compensation. While there is still time to file a lawsuit, be mindful that these cases are time sensitive, and give us a call today and see if you meet the requirements for a Meridia lawsuit.
NASHVILLE MERIDA LAWYER TIMOTHY L. MILESTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
Call a Nashville Belviq lawyer if you suffered Belviq side effects to see if you are eligible for a Belviq lawsuit
Belviq (generic name: lorcaserin) is a popular prescription weight-loss drug made by Eisai Inc. to help people experiencing obesity and weight-related health issues curb their hunger. While it is not known exactly how Belviq works, the drug targets a hunger receptor in the brain and helps people fee full after easting smaller amounts of food and also seems to help people fee full longer.
Alarmingly, a U.S. Food and Drug Administration (FDA) safety trial concluded that the drug could increase the risk of several different types of cancer, including pancreatic, lung, and colorectal cancer. Those individuals who participated in the clinical trial reported certain types of cancer with some types occurring more frequently in the lorcaserin group, including pancreatic, colorectal, and lung. The trial was conducted between January 2014 and June 2018 and consisted of 12,000 men and women who were overweight or obese, according to the FDA’s February 2020 Drug Safety Communication. While researchers were looking into cardiovascular safety, they also noted more diagnoses of cancer among people who took Belviq versus those who took placebo. “There was a numerical imbalance in the number of patients with malignancies, with one additional cancer observed per 470 patients treated for one year … Imbalances in specific cancers including pancreatic, colorectal, and lung contributed to the observed overall imbalance in cancer cases. There was no apparent difference in the incidence of cancer over the initial months of treatment, but the imbalance increased with longer duration on lorcaserin,” the agency said. Among patients treated with lorcaserin, 462 (7.7 percent) patients were diagnosed with 520 primary cancers compared to the placebo group, in which 423 (7.1 percent) patients were diagnosed with 470 cancers. As a result, Eisai Inc. announced that it was withdrawing Belviq from the U.S. market on Feb. 13, 2020, after the FDA requested the withdrawal. In response, numerous Belviq lawsuits have been filed including a Belviq class action. If you or a loved one took Belviq, Belviq XR, or another brand of lorcaserin, and you were diagnosed with cancer, or other serios Belviq side effects, you may be eligible for a Belviq lawsuit or be included in a Belviq class action lawsuit and receive compensation from the drug’s manufacturer. Fill out a free case evaluation review form to find out if you are owed money for damages and talk to a Nashville Belviq Lawyer about whether you meet the Belviq Lawsuit Criteria and are eligible for a Belviq lawsuit or to be a part of the Belviq class action lawsuit today at no charge. Call us today for more information or if you have additional questions. Read on to lear more about a Belviq lawsuit from a Nashville Belviq lawyer. WHAT KIND OF DRUG IS BELVIQ?![]()
Belviq belongs to a class of drugs which includes Central Nervous System (CNS) Stimulants; Anorexiants; and Serotonin 5HT2C-Receptor Agonist. The drug is used by certain overweight people, such as those who are obese or have weight-related medical problems. Losing weight and keeping it off can lessen the many health risks that come with obesity, including heart disease, diabetes, high blood pressure, and a shorter life, among others. Belviq is thought to work by affecting a certain part of the brain that helps control your appetite.
Belviq was available by prescription in its original form and in an extended-release version, Belviq XR. Both versions are the subject of Belviq lawsuits. Arena Pharmaceuticals manufactures Belviq at its facility in Switzerland. Eisai Inc. marketed and distributed Belviq in the United States. Both companies are named defendants in lawsuits. WHAT ARE THE BELVIQ SIDE EFFECTS?
The most common Belviq side effects include headache, dizziness and nausea. People with diabetes also commonly suffered hypoglycemia, back pain and cough. Other common Belviq side effects include:
IS CANCER ONE OF THE BELVIQ SIDE EFFECTS?
Weight-loss drugs are not known for their safety; unfortunately, Belviq is no exception resulting in a Belviq recall. In a five-year, double-blind study of 12,000 patients, those taking Belviq were more likely to be diagnosed with cancer than those taking a placebo (sugar pill). At the end of the five-years, the FDA found 7.1% of people in the placebo group developed cancer compared to 7.7% of people in the Belviq group who developed cancer. The FDA stated, “A range of cancer types was reported, with several different types of cancers occurring more frequently in the lorcaserin group,” including: Pancreatic cancer, colorectal cancer; and Lung cancer.
IS A BELVIQ LAWSUIT TO GET MONEY FOR BELVIQ SIDE EFFECTS?
A Belviq Lawsuit is a demand from the defendant for monetary compensation by patients who took Belviq and subsequently developed cancer or other severe Belviq side effects. The lawsuits allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties. If eligible you may participate in a Belviq class action lawsuit or file an individual Belviq lawsuit. A Nashville Belviq Lawyer can answer these questions and is available anytime just give us a call or submit the form below for a free case evaluation with a Nashville Belviq Lawyer to see if you are eligible for a Belviq lawsuit.
WHAT IS THE CRITERIA FOR A BELVIQ LAWSUIT?
If you took Belviq or its generic equivalent and were diagnosed with cancer, you should consider taking legal action against the drug’s manufacturer. If you meet these criteria, you may be eligible for a Belviq lawsuit and able file a Belviq class action.
-Over the age of 18 -Diagnosed with cancer after taking Belviq, Belviq XR, or another brand of lorcaserin If a loved one took this weight loss drug and was diagnosed with cancer, you may also contact a Nashville Belviq Lawyer on their behalf about a Belviq class action lawsuit. Call Nashville Belviq Lawyer Timothy L. Miles today (855-Tim-M-Law) for a free and confidential case evaluation and see if you are eligible for a Belviq lawsuit. IF YOU SUFFERED BELVIQ SIDE EFFECTS, CALL A NASHVILLE BELVIQ LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A BELVIQ LAWSUIT
If you took Belviq and have been diagnosed with cancer, you could be owed significant compensation for medical costs, pain and suffering, lost wages, and other damages. You should speak with Nashville Belviq lawyer Timothy L. Miles as soon as possible to determine the best course of action including filing a Belviq class action lawsuit or an individual Belviq Lawsuit if you were diagnosed with cancer or experienced other severeBelviq side effects.
These cases are time-sensitive, including the Belviq class action lawsuit, so do not wait. Fill out a case review form to receive a free, no-obligation case evaluation. It costs nothing to get started, a Nashville Belviq lawyer can explain the process and answer any questions you may have. We take all cases on a contingency basis which means we do not get paid unless we win your case. Call today and see what a Nashville Belviq Lawyer can do for you. NASHVILLE BELVIQ LAWYER TIMOTHY L. MILESTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
Call a Nashville Actemra lawyer today if you suffered serious Actemra side effects, you may be eligible for an Actemra lawsuit
Roche’s Actemra was heralded as a breakthrough therapy for rheumatoid arthritis when it was introduced in 2010.
The drug’s website proclaims that “Actemra works differently” and shows a patient happily scuba diving and walking on a tropical beach. But nowhere does Roche mention certain side effects that may have contributed to more than 1,100 patient deaths. Research suggests that Actemra patients, compared to those taking competing rheumatoid arthritis drugs, face similar risks for heart attacks, heart failure, strokes, lung disease, and pancreatitis. But unlike the competition, Actemra’s label does not warn about these Actemra side effects. If you or a loved one suffered serious Actemra side effects including heart, lung, or pancreatic side effects while taking Actemra, contact Nashville Actemra lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for an Actemra lawsuit. If you meet the requirements for an Actemra lawsuit you may be entitled to substantial compensation. Read on to learn more about the Actemra lawsuit from a Nashville Actemra lawyer. WHAT ARE THE ACTEMRA SIDE EFFECTS TO THE HEART AND LUNGS?![]()
A STAT News report and postmarketing studies raise questions about the adequacy of Actemra's safety warnings and Actemra side effects.
STAT reviewed more than 500,000 adverse event reports on leading rheumatoid arthritis drugs, including Actemra, Humira, and Remicade. STAT found evidence that Roche downplayed Actemra’s cardiovascular, pancreatic, and lung side effects as well as other Actemra side effects. According to STAT, from 2010 to 2016 the U.S. Food and Drug Administration (FDA) logged more than 13,500 Actemra adverse event reports, including 1,128 patients who died after taking Actemra. While safety data indicate the risks of heart attacks, strokes, heart failure, and interstitial lung disease are as high or higher for Actemra patients than for patients taking some similar drugs, Actemra’s warning label—unlike its competition's—does not reflect these risks or other Actemra side effects. For example, Actemra patients reported more cases of interstitial lung disease than Remicade patients, and nearly the same number as Humira patients. But while Remicade and Humira have interstitial lung disease warnings, Actemra does not. STAT’s findings are supported by postmarketing studies—clinical studies conducted after a pharmaceutical product goes on the market to better understand drug risks. The FDA ordered Actemra postmarketing studies because premarket testing revealed potentially worrisome side effects. One such study compared Actemra to another arthritis drug, Enbrel, and found rates of stroke and heart failure were about 1.5 times higher in Actemra users. Enbrel has strong warnings for patients with cardiovascular disease. Actemra does not have similar warnings despite similar or worse cardiovascular risks. The takeaway from these findings is that doctors and patients may not be getting a complete picture of Actemra’s risk-benefit profile. DRUG MANUFACTURERS HAVE A DUTY TO WARN ABOUT ACTEMRA SIDE EFFECTS
Pharmaceutical products are not expected to be completely without harmful side effects. But if a drugmaker understands that a drug presents a certain risk, it has a duty to put an appropriate warning label on the product. That way patients and their doctors can evaluate all known risks and benefits and make an educated decision about whether a medication is right for them.
While the FDA has authority to demand warning labels, the responsibility ultimately falls on drug manufacturers. Actemra has garnered FDA attention since it was approved in 2010. At one point the agency considered a pancreatitis warning label. But Genetech/Roche talked the FDA out of the warning. The agency then approved broader use of Actemra for giant cell arteritis. Conflicts of interest between manufacturers and regulators plague the drug safety system. The STAT report details how all 11 authors of an Actemra postmarketing study had financial ties to Roche or Genetech. And a former FDA manager who oversaw Actemra’s approval for rheumatoid arthritis now works for Roche, where he helps gain FDA approval for new uses of the drug. The drug safety system, in other words, cannot always be trusted to put patient safety first. That’s why, when patients suffer harm from drug side effects, they often must turn to the legal system such as in the case of Actemra side effects. IF I SUFFERED ACTEMRA SIDE EFFECTS, AM I ELIGIBLE FOR AN ACTEMRA LAWSUIT?
We are looking into claims that Genetech/Roche failed to warn about the following Actemra side effects:
Actemra patients who suffered any of these Actemra side effects may be eligible for an Actemra lawsuit. IF I SUFFERED ACTEMRA SIDE EFFECTS AND MEET THE REQUIREMENTS FOR AN ACTEMRA LAWSUIT, WHAT CAN I GET?
If you meet the requirements for an Actemra lawsuit and are successful you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff who is eligible for an Actemra lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they meet the requirements for an Actemra lawsuit and are successful. IF I AM SUFFERED ACTEMRA SIDE EFFECTS AND AM ELIGIBLE FOR AN ACTEMRA LAWSUIT, HOW DOES AN ACTEMRA LAWSUIT WORK?
Your Nashville Actemra lawyer will first determine that you are eligible for an Actemra lawsuit and then ask you some questions about your medical history and Actemra side effects. Your Nashville Actemra lawyer will then draft what is known as a complaint. This will be a multi-page document explaining why the defendant is responsible for your injuries and what damages (that is, compensation) you are seeking.
Once your complaint is filed with the court, your Actemra Lawsuit officially begins. From here, it will be a lot of back and forth between your Nashville Actemra lawyer and the attorney(s) for the defendant in an attempt to resolve the matter. The attorneys may take review documents, take depositions, issue subpoenas, hire experts, calculate damages, attend hearings, and file motions, briefs, evidence or other documents with the court during the stages of the lawsuit. If your Actemra lawsuit is not dismissed and a settlement cannot be reached, the case will proceed to a jury trial. IF YOU SUFFERED ACTEMRA SIDE EFFECTS, CALL A NASHVILLE ACTEMRA LAWYER TODAY IF YOU SUFFERED SERIOUS ACTEMRA SIDE EFFECTS?
If you or a loved one suffered serious Actemra side effects including heart, lung, or pancreatic side effects while taking Actemra, contact Nashville Actemra lawyer Timothy L. Miles today to see if you are eligible for an Actemra lawsuit. If you meet the requirements for an Actemra lawsuit you may be entitled to substantial compensation.
nashville actemra lawyer timothy l. milesTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you suffered Zostavax side effects call a Nashville Zostavax lawyer, you may be eligible for a Zostavaz lawsuit
In an attempt to prevent shingles, some patients may have unintentionally contracted the virus from their shingles vaccination.
The shingles vaccine Zostavax may cause serious injuries, including shingles, blindness, and even death. Injured patients are now filing lawsuits against Zostavax’s manufacturer Merck (and its owner, Bayer) for failing to warn about the potential Zostavax side effects. If you or a loved one suffered serious Zostavax side effects including shingles, blindness or even death, contact Nashville Zostavax lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Zostavax lawsuit and possibly entitled to substantial compensation. Read on for answers to four frequently asked questions about the Zostavax lawsuit from a Nashville Zostavax lawyer and if you suffered Zostavax side effects, see if you are eligible for a Zostavax lawsuit. WHAT IS A ZOSTAVAX?![]()
Zostavax became the first shingles vaccine to be approved by the U.S. Food and Drug Administration (FDA) in 2006. FDA. Zostavax is administered as a shot to the upper and works using a live, but weakened form, of the varicella-zoster virus to decrease the risk of shingles. The varicella-zoster virus also causes chickenpox in children.
It was thought to be highly effective at the time and Zostavax seemed to be an important breakthrough in the containment of the disease. Zostavax would help Merck earn nearly $750 million in profits over the next 12 years. WHAT ARE THE ZOSTAZAX SIDE EFFECTS?
The FDA reports that Zostavax side effects can include the following:
But some plaintiffs allege that Zostavax side effects caused even more serious complications, like blindness, hearing loss, paralysis, brain damage, and fatal liver failure. If you suffered Zostavax side effects, call a Nashville Zostavax lawyer today as you are probably eligible for a Zostavax lawsuit. IF I SUFFERED ZOSTAVAX SIDE EFFECTS, AM I ELIGIBLE FOR A ZOSTAVAX LAWSUIT?
If you or a loved one received the Zostavax vaccine after 2006 and were diagnosed with shingles, you may be eligible for a Zostavax lawsuit. Please note that shingles must have appeared at least three weeks after the vaccination date but within one year from receiving Zostavax.
besides suffering zostavax side effects, Who Else May Meet the Requirements for a Zostavax Lawsuit?
In addition to serious Zostavax side effects, if you or a loved one suffered from one of the following injuries within two years from the vaccination date, you may also be eligible for a Zostavax lawsuit:
IF YOU SUFFERED ZOSTAVAX SIDE EFFECTS, CONTACT A NASHVILLE ZOSTAVAZ LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A NASHVILLE ZOSTAVAX LAWSUIT
If you or a loved one suffered serious Zostavax side effects including shingles, blindness or even death, contact Nashville Zostavax lawyer Timothy L. Miles today to see if you are eligible for a Zostavax lawsuit and possibly entitled to substantial compensation. While there is still time to file a lawsuit, be mindful that these cases are time sensitive, and give a Nashville Zostavax lawyer a call today.
nashville zostavax lawyer timothy l. milesTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you sufferd Xeljanz side effects, contact a Nashville Xeljanx lawyer today you could be eligible for a Xeljanx lawsuit
Pharmaceutical companies and suppliers have both an ethical and legal responsibility to properly disclose the risks and side effects of a drug before bringing it to market, but all too often those warnings are withheld in the name of profit.
However, in just the last two years, the U.S. Food and Drug Administration (FDA) has warned that Xeljanz (Tofacitinib) can be associated with heart problems, blood clots, and even cancer. But the question remains: why didn’t Pfizer warn consumers about these potential risks sooner? Xeljanz lawsuits claim that Pfizer failed to give adequate warning about the Xeljanz side effects, which caused preventable harm to patients who suffered blood clots in the lungs, heart attacks, strokes, breast and colon cancer, and other severe health problems. We are accepting these cases on a contingency-fee basis. That means our clients don’t pay unless we win. If you need to discuss a lawsuit with a Nashville Xeljanz lawyer, free of charge, please contact a Nashville Xeljanz lawyer for a free case evaluation. (855) Tim-M-Law (855-846-6529). Read on for answers to four frequently asked questions by Nashville Xeljanz Lawyer Timothy L. Miles about the Xeljanx lawsuits, and if you suffered Xeljanx side effects, see if you are eligible for a Xeljanx lawsuit. We hope you find this helpful! What is xeljanz?![]()
Xeljanz belongs to a class of drugs known as Janus kinase (JAK) inhibitors. As Pfizer explains, our body has signaling proteins called cytokines that regulate immune system responses. The production of cytokines is increased when our body fights infection. Cytokine production is thought to play a role in chronic inflammatory conditions, such as rheumatoid arthritis, psoriatic arthritis, and ulcerative colitis. Xeljanz disrupts signaling that produces some of the cytokines, reducing inflammation. Specifically, Xeljanz blocks—or inhibits—the release of cytokines in the JAK signal pathway.
Xeljanz has been approved for several different uses:
Xeljanz has been approved for several different uses:
WHAT ARE THE XELJANZ SIDE EFFECTS?
The Xeljanz Side Effects include:
If you suffered serious Xeljanz side effects, contact Nashville Xeljanz lawyer Timothy L. Miles today. IF I SUFFERED XELJANZ SIDE EFFECTS, AM I ELIGIBLE FOR A XELJANZ LAWSUIT?
If you took Xeljanz and have been diagnosed with cancer, a major adverse cardiovascular event, or venous thromboembolism (such as a pulmonary embolism or deep vein thrombosis) or other serious Xeljanz side effects, you may be eligible for a Xeljanz lawsuit and possibly be entitled to substantial compensation. Call today for a free case evaluation with a Nashville Xeljanz lawyer and see if you meet the Xeljanz Lawsuit Criteria.
IF I SUFFERED XELJANZ SIDE EFFECTS AND I AM ELIGIBLE FOR A XELJANZ LAWSUIT, WHAT CAN I GET OUT OF A XELJANZ LAWSUIT?
If you are eligible for a Xeljanz lawsuit, a successful plaintiff is entitled to compensatory damages which would include compensation for things such as:
If your case proceeds to trial it is also possible the court could impose punitive damages, intended to punish the defendant for their actions. IF YOU SUFFERED XELJANZ SIDE EFFECTS, CONTACT A NASHVILLE XELJANZ LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A XELJANZ LAWSUIT
Xeljanz, while marketed as a safe medication, increases the risk of blood clots, cancer, and cardiovascular problems for its users. The FDA approved the drug upon release, but a post-marketing safety study revealed serious safety concerns and concluded that the side effects are more detrimental than initially believed. The company responsible for the medication, Pfizer, knew about the side effects prior to the safety study but failed to disclose this information to the public in an attempt to retain their profits. This unethical behavior exposed thousands of consumers to an elevated risk of harm, making their actions unacceptable by any means.
Unfortunately, some users of Xeljanz have developed cancer as a result of their medication use, including but not limited to lymphoma, melanoma, and lung cancer. Pfizer, already knowing the risk of the Xeljanz side effects, sold it to consumers anyway, causing many innocent individuals to develop and suffer from a life-threatening disease. Their reluctance to disclose the risk of their product is not just unethical, it’s illegal, and our attorneys are here to help hold them accountable to the fullest extent of the law. Contact a Nashville Xeljanz Lawyer today at (855) 846-6529 or [email protected] or by submitting this form and see if you meet the Xeljanz lawsuit criteria if you suffered Xeljanz side effects. Someone will promptly get in touch with you. We are here to help! nashville xeljanz lawyer timothy l. miles, esq.Timothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
If you took Kombiglyze XR and suffered Kombiglyze XR side effects call a Nashville Kombiglyze XR lawyer you may be eligible for a Kombiglyze XR lawsuit
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Kombiglyze XR is a combination of metformin (a biguanide) and saxagliptin (a DPP4 inhibitor). Kombiglyze XR works by lowering the amount of sugar made by your liver, decreasing the amount of sugar absorbed by your intestine, increasing the amount of insulin your body makes, and helps your body respond better to insulin.
However, research shows that type 2 diabetes drug Kombiglyze XR (saxagliptin and metformin) may cause heart failure or other cardiovascular injuries in some patients. According to the Centers for Disease Control and Prevention (CDC), 30 million Americans have diabetes and 84 million have pre-diabetes. Metformin—one of the drugs found in combination in Kombiglyze—is among the top 10 most popular prescription drugs taken by Americans. Analysts also predict that Onglyza (saxagliptin), Kombiglyze’s sister drug, could reach $1.8 billion in sales in 2018. In 2015, roughly 386,000 people were prescribed Onglyza or Kombiglyze XR, the U.S. Food and Drug Administration (FDA) reported. Given that so many people take these drugs, any side effects they may cause that are severe enough to hospitalize patients should be treated with concern. Dozens of patients are filing lawsuits against Kombiglyze’s manufacturer AstraZeneca and its previous partner Bristol-Myers Squibb alleging that the companies failed to adequately test the drugs’ safety prior to selling it, which ultimately caused their cardiovascular injuries. If you or a loved one took Kombiglyze XR as directed and suffered from Kombiglyze XR side effects including heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, after starting Kombiglyze XR therapy, contact Nashville Kombiglyze XR lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation. Read on for the answers to four frequently asked questions by Nashville Kombiglyze XR lawyer Timothy L. Miles about the Kombiglyze XR lawsuit and if you used Kombiglyze XR and suffered Kombiglyze XR side effects, see if you are eligible for a Kombiglyze XR lawsuit. WHAT ARE THE KOMBIGLYZE XR SIDE EFFECTS?
The following are some of the common Kombiglyze XR side effects:
Additionally, dozens of lawsuits allege other Kombiglyze XR side effects including serious cardiovascular injury. If you suffered Kombiglyze XR side effects call a Nashville Kombiglyze XR lawyer today. DOES KOMBIGLYZE XR PUT PATIENTS AT RISK OF HEART FAILURE?
A clinical trial funded by AstraZeneca and Bristol-Myers Squibb was one of the first studies to report cardiovascular health risks associated with these drugs and as another of the Kombiglyze XR side effects.
Saxagliptin Assessment of Vascular Outcomes Recorded in Patients with Diabetes Mellitus, or the SAVOR trial, found that patients with a history of heart problems who took Onglyza or Kombiglyze XR had a 27% greater chance of being hospitalized for heart failure than patients who took a placebo. Patients with chronic kidney disease and / or previous heart failure were more likely to be hospitalized. When an FDA panel reviewed the results from the SAVOR study, 14 out of 15 panelists voted to require a safety warning on all Onglyza and Kombiglyze XR bottles that the drugs could result in cardiovascular injury. Patients are filing lawsuits against AstraZeneca and Bristol-Myers Squibb alleging that Kombiglyze XR caused their cardiovascular injuries. Complaints allege that AstraZeneca and Bristol-Myers Squibb failed to adequately test the drug prior to their sale and did not disclose the Kombiglyze XR side effects. In February 2018, more than 80 Onglyza and Kombiglyze XR lawsuits were centralized in Lexington, Kentucky. Plaintiffs' attorneys said that centralization is key to reducing inconsistencies since these lawsuits were "just the tip of the iceberg" and the number of filed complaints was expected to grow. In a complaint filed in January 2018, Illinois plaintiff Jerald Adams alleged that after being exposed to saxagliptin after taking both Onglyza and Kombiglyze XR, the diagnosis of his heart failure was “directly related to taking these drugs.” In the complaint, Mr. Adams alleged that the manufacturers not only knew of the cardiovascular injury risk associated with saxagliptin, but that they also failed to warn or mitigate this risk despite their knowledge. "At all relevant times, defendants had knowledge that there was a significantly increased risk of adverse events associated with saxagliptin, including heart failure, congestive heart failure, cardiac failure, and death related to those events, and despite this knowledge, defendants continued to manufacture, market, distribute, sell, and profit from sales of saxagliptin," the complaint alleges. Some lawsuits filed in New Jersey claim that Bristol-Myers and AstraZeneca did not just do a poor job of testing the safety of their drugs, but that they also did not conduct the clinical trials recommended by the FDA in 2008 prior to Onglyza’s sale debut in 2009. In 2008, the FDA Endocrinologic and Metabolic Drugs Advisory Committee "determined that concerns about cardiovascular risk should be more thoroughly addressed during drug development." Bristol-Myers and AstraZeneca failed to do so and began marketing Onglyza in 2009. HOW DO I KNOW IF I AM ELIGIBLE OR A KOMBIGLYZE XR LAWSUIT?
If you or a loved one took Kombiglyze XR as directed and suffered from heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, or other serious Kombiglyze side effects after starting Kombiglyze XR therapy, you may meet the requirements for a Kombiglyze XR lawsuit and possibly be entitled to substantial compensation. Call a Nashville Kombiglyze XR lawyer for free today who can tell you if you are eligible for a Kombiglyze XR lawsuit.
IF I MEET THE REQUIREMENTS FOR A KOMBIGLYZE XR LAWSUIT, WHAT CAN I GET?
If you meet the requirements for a Kombiglyze XR lawsuit and are successful you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff who is eligible for a Kombiglyze XR lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they meet the requirements for a Kombiglyze XR lawsuit and are successful. IF YOU SUFFERED FROM KOMBIGLYZE XR SIDE EFFECTS, CALL A NASHVILLE KOMBIGLYZE XR LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A KOMBIGLYZE XR LAWSUIT
If you or a loved one took Kombiglyze XR as directed and suffered from Kombiglyze XR Side Effects, specifically: heart failure or other cardiovascular injuries—such as congestive heart failure or myocardial infarction, after starting Kombiglyze XR therapy, contact Nashville Kombiglyze XR lawyer Timothy L. Miles today to see if you are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation.
nashville kombiglyze xr lawyer timothy l. miles, esq.Timothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website. answers to four frequently asked questionS about the elmiron lawsuit from a nashville elmiron lawyer5/15/2023
If you suffered Elmiron Eye Damage contact a Nashville Elmiron lawyer today, you could be eligible for an Elmiron lawsuit
The Firm is reviewing claims on behalf of Interstitial Cystitis (IC) patients who took the prescription drug Elmiron and now may be suffering from a severe eye disease called maculopathy or has suffered vision impairment as a result.
If you developed malculopathy or a vision impairment and took Elmiron, or have additional questions, give Nashville Elmiron Lawyer Timothy L. Miles a call today for a free case evaluation, you could be entitled to significantly compensation if you meet the Elmiron Lawsuit Criteria and are eligible for an Elmiron lawsuit. Read on for the answers to four frequently asked questions by Nashville Elmiron lawyer Timothy L. Miles about the Elmiron lawsuit and if you used Elmiron and suffered Elmiron eye damage or other serious Elmiron side effects, see if you are eligible for a Elmiron lawsuit. WHAT IS ELMIRON AND WHY DOES IT CAUSE ELMIRON EYE DAMAGE?
Since 1996, millions of patients have been prescribed Elmiron in order to treat their interstitial cystitis (IC), otherwise known as painful bladder syndrome. But there is now reason to believe that this drug may cause a serious eye condition in those taking it, one that may result in blindness.
This condition is a form of maculopathy – the degeneration of the macula, the central part of the retina. Maculopathy’s first symptoms are blurred vision, dark spots, trouble focusing, and other impairments: as it progresses, it may lead to total blindness. As the evidence has piled up, the manufacturer of Elmiron – Janssen Pharmaceuticals – has failed to warn the public about these risks. Millions of people are taking a drug that may one day rob them of their vision, and an untold number may have already suffered serious health conditions. Elmiron eye damage lawsuits on behalf of the injured have already begun claiming their maculopathy was caused by Elmiron. If you or a loved one took Elmiron and has since been diagnosed with maculopathy, or vision impairment or serious Elmiron Side Effects you may be eligible for an Elmiron lawsuit. Contact a Nashville Elmiron Lawyer today to have your case reviewed for free and see if you meet the Elmiron lawsuit criteria. IS MACULOPATHY CAUSED BY LONG-TERM USE OF ELMIRON?
In 2018, researchers at the Emory Eye Center at the Emory School of Medicine in Atlanta alerted the public that taking Elmiron is linked to the retinal condition, maculopathy. Pentosan polysulfate sodium can cause severe vision problems and side effects, including interstitial cytitis, and even blindness.
Nieraj Jain, M.D., of Emory Eye Center in Atlanta, Ga., reported that six Elmiron patients who had been taking Elmiron for about 15 years had developed unusual changes in their macula. Because nothing in the patients’ medical history or diagnostic tests explained the subtle, but striking pattern of abnormalities, Dr. Jain and his colleagues raised a warning flag that long-term use of Elmiron may damage the retina. The retina is a thin layer of tissue that lines the back of the eye on the inside. It is located near the optic nerve. The retina receives light that the lens has focused and converts the light into neural signals. It then sends these signals on to the brain for visual recognition All patients in the study reportedly showed signs of retinal disease and that the youngest patient in the study was diagnosed with interstitial cystitis at 23 years of age. That patient began taking the medication daily and began showing visual symptoms by the age of 30. In addition, three ophthalmologists conducted a review of patients at Kaiser Permanente in Northern California and found that approximately one-quarter of patients with significant exposure to Elmiron showed definite signs of eye damage. It also found the medication could potentially be linked to retinal conditions, such as age-related macular degeneration or pattern dystrophy. Patients who have used or are using the pentosan polysulfate sodium drug Elmiron are advised to be screened by ophthalmologists if they are experiencing any unusual eye symptoms. They are also advised to cease pentosan therapy if eye disease is present. WHAT ARE THE SYMPTOMS OF ELMIRON EYE DAMAGE RELATED TO RELATED RETINAL MACULOPATHY?
A newly discovered condition has come to light, and it is presently unknown how many symptoms there actually are, or how serious this can end up being for those suffering from it.
The currently known symptoms associated with this eye condition include:
IF I SUFFERED ELMIRON EYE DAMAGE, HOW DO I KNOW IF I AM ELIGIBLE FOR AN ELMIRON LAWSUIT?
You may be eligible for an Elmiron lawsuit if meet the following criteria:
The criteria are based upon the medical studies linking the drug to eye disease and vision impairment, including interstitial cytitis and maculopathy. However, there may be exceptions to the Elmiron lawsuit criteria. There may be other eye damage claims available for you to pursue and you still may be eligible for an Elmiron lawsuit if you suffered other serious Elmiron side effects. IF YOU SUFFERED ELMIRON EYE DAMAGE, CALL A NASHVILLE ELMIRON LAWYER TODAY TO SEE IF YOU ARE ELIGIBLE FOR AN ELMIRON LAWSUIT?
If you were diagnosed with maculopathy or vision impairment caused by Elmiron, or suffered serious Elmiron side effects, contact a Nashville Elmiron Lawyer today as you most likely meet the Elmiron lawsuit criteria and are eligible for an Elmiron lawsuit and possibly entitled to recover substantial compensation. The call is free and so is the fee unless we will you case. So, call today and see what a Nashville Elmiron lawyer can do for you.
So, give a Nashville Elmiron Lawyer call today or submit the free case evaluation form and see if you and are eligible for an Elmiron lawsuit. NASHVILLE ELMIRON LAWYER TIMOTHY L. MILES, ESQ.Timothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website. answers to four frequently asked quESTIONS about a victoza lawsuit from a nashville victoza lawyer5/15/2023
Contact a Nashville Victoza Lawyer today if you suffered Victoza side effects, you may be eligible for a Victoza lawsuit
Hundreds of Victoza lawsuits filed by victims from across the country allege that Victoza, which is an incretin mimetic drug used to treat type 2 diabetes, may cause pancreatic cancer and that the manufacturer of Victoza, Novo Nordisk, failed to warn them of this risk and many people have been diagnosed with pancreatic cancer after taking Victoza.
Other incretin mimetic drugs have also been linked to this dangerous side effect. As a result, Januvia, Janumet, and Byetta have also been linked to pancreatic cancer. Manufacturers Novo Nordisk, Merck & Co., Eli Lilly, and Amylin Pharmaceuticals now hundreds of lawsuits that have been coordinated for pretrial proceedings in a multidistrict litigation (MDL) in Southern California while further research continues on the question of does Victoza cause pancreatic cancer continues and cause someone to be diagnosed with pancreatic cancer. If you or a loved one took Victoza were later diagnosed with pancreatic cancer, or suffered other serious Victoza side effects, contact Nashville Victoza Lawyer Timothy L. Miles today for a free case evaluation and see if you are eligible for a Victoza lawsuit and possibly entitled to substantial compensation. Read on for the answers to four frequently asked questions by Nashville Victoza lawyer Timothy L. Miles about the Victoza lawsuit and if you used Victoza and suffered Victoza side effects, see if you are eligible for a Victoza lawsuit. WHAT IS THE PROBLEM WITH VICTOZA, DOES IT CAUSE VICTOZA SIDE EFFECTS?![]()
Incretin mimetic drugs such as Victoza regulate the production of incretin, a type of hormone that stimulates the release of insulin in the body. Victoza does this by injecting patients with a substance that mimics a particular incretin called Glucagon-Like Peptide-1 (GLP-1). Victoza cancer lawsuits allege this process overstimulates the pancreas causing cells in the pancreas to multiply resulting in pancreatic cancer.
Researchers suspect that the process used by Victoza, and other incretin mimetic drugs may overstimulate the pancreas, and in some cases, cause pancreas cells to multiply. One expert in this area, Dr. Peter Butler, who is a diabetes expert at UCLA, discovered a growth of precancerous lesions in the pancreas when this process occurred. Additionally, according to the U.S. Food & Drug Administration's (FDA) adverse event database, patients taking Januvia, a similar drug to Victoza, are 10 times more likely to be diagnosed with pancreatic cancer. Beyond these observations though, the research is still unclear if and how incretin mimetic drugs cause pancreatic cancer. In 2013, the FDA requested that researchers investigate the correlation in greater detail. However, as more evidence is gathered for a more detailed review on the question of does Victoza cause pancreatic cancer, patients are continuing to file lawsuits asserting they got pancreatic cancer after taking their type 2 diabetes medication. In fact, over 2,500 Victoza patients have registered complaints with the FDA also asserting that the medication caused them to have pancreatic side effects and some to be diagnosed with pancreatic cancer. The vast majority (more than 2,300) allege pancreatitis, both acute and chronic. Moreover, similar reports have been made for other incretin mimetics: Roughly 2,400 Januvia patients and more than 3,000 Byetta patients have similarly complained of pancreatitis and filed lawsuits with claims similar to the Victoza cancer lawsuits. Finally, the American Cancer Society warns that patients with chronic pancreatitis (inflammation of the pancreas) may have an increased risk of being diagnosed with pancreatic cancer. If you or a loved one suffered the side effects of Victoza, or were diagnosed with pancreatic cancer, contact Nashville Victoza Lawyer Timothy L. Miles today and see if you are eligible for a Victoza cancer lawsuit. IF I SUFFERED VICTOZA SIDE EFFECTS, HOW DO I KNOW IF I AM ELIGIBLE FOR A VICTOZA LAWSUIT?
If you or a loved one took Victoza and were diagnosed with pancreatic cancer in 2005 or later, or suffered serious Victoza side effects, you may be eligible for a Victoza lawsuit against Novo Nordisk and may be entitled to substantial compensation.
IF I AM ELIGIBLE FOR A VICTOZA CANCER LAWSUIT, WHAT CAN I GET OUT OF A VICTOZA CANCER LAWSUIT?
If you are eligible for a Victoza lawsuit and are successful, you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff in a Victoza lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they qualify for a Victoza lawsuit and are successful. IF I SUFFERED VICTOZA SIDE EFFECTS, HOW MUCH DOES IT COST TO HIRE A NASHVILLE VICTOZA LAWYER?
It does not cost anything to hire a Nashville Victoza lawyer. We take all cases on a contingency basis which means we do not get paid unless we win your case. If you suffered Victoza side effects, contact Nashville Victoza lawyer Timothy L. Miles who can explain the process and answer any questions you may have including whether you are eligible for a Victoza lawsuit.
CALL A NASHVILLE VICTOZA LAWYER AND SEE IF YOU ARE ELIGIBLE FOR A VICTOZA CANCER LAWSUIT?
If you or a loved one took Victoza and were diagnosed with pancreatic cancer in 2005 or later, or suffered other serious Victoza side effects you may be eligible for a Victoza lawsuit. Contact Nashville Victoza lawyer Timothy L. Miles today and see if you qualify for a Victoza lawsuit and could be eligible for substantial compensation. While there is still time to file a lawsuit, be mindful that these cases are time sensitive, and give us a call today.
CONTACT The Law Offices of Timothy L. Miles Tapestry at Brentwood Town Center 300 Centerview Dr., #247 Brentwood, TN 37027 Phone: (855) 846-6529 Email: [email protected] Nashville Victoza lawyer TIMOTHY L. MILES, ESQ.Timothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website. answers to four freqently asked queSTIONS about a tasigna lawsuit from a nashville tasigna lawyer5/15/2023
Call a Nashville Tasigna lawyer if you took Tasigna and developed Tasigna side effects to see if you are eligible for a Tasigna lawsuit
First approved in 2007, Tasigna (nilotinib), is a prescription medication used to treat chronic myeloid leukaemia (CML). Tasigna is part of a class of drugs known as tyrosine kinase inhibitors (TKIs). Other TKI drugs include Gleevec (imatinib), also made by Novartis, and Sprycel (dasatinib), made by Bristol-Myers Squibb.
These drugs help treat leukemia by blocking the protein tyrosine kinases—a protein that stimulates the growth of cancer cells. In blocking this protein, TKI drugs like Tasigna help stop leukemia from spreading. Tasigna is prescribed as a twice daily drug and is taken orally in capsule form. If you suffered Tasigna side effects, including Tasigna cardiovascular side effects, call Nashville Tasigna lawyer Timothy L. Miles today for a free case evaluation and see if you qualify for a Tasigna lawsuit. Read on for the answers to four frequently asked questions by Nashville Tasigna lawyer Timothy L. Miles about the Tasigna lawsuit and if you used Tasigna and suffered Tasigna side effects, see if you are eligible for a Tasigna lawsuit. WHAT ARE THE TASIGNA SIDE EFFECTS?![]()
To date, approximately 15,500 Tasigna related adverse events and 2,786 deaths have allegedly been reported to the FDA to date. These include serious Tasigna side effects including cardiovascular side effects, like Long QT syndrome, myocardial ischemia, and atherosclerosis.
Tasigna has one black box warning—the highest warning the FDA can issue—for Long QT syndrome, or QT interval prolongation, and sudden death. It is a condition that affects heart rhythm, resulting in fast, irregular heartbeats. If left untreated, it can result in fainting, seizures, and sudden death. Tasigna may also been linked to myocardial ischemia, a condition involving reduced blood flow to the heart, causing a decreased amount of oxygen sent to the heart. Myocardial ischemia is usually caused by a blockage of the coronary arteries. Recent lawsuits have also been filed over the drug’s alleged connection to atherosclerosis, a disease that causes fatty deposits to build up and eventually clog arteries. This serious condition gradually reduces blood flow and oxygen to cells. Atherosclerosis is currently the leading cause of death in the developed world. It may eventually cause the following complications:
WHAT ARE SOME OF THE ADDITIONAL TASIGNA SIDE EFFECTS?
Novartis warns of the following Tasigna side effects:
IF I SUFFERED TASIGNA SIDE EFFECTS AND I AM ELIGIBLE FOR TASIGNA LAWSUIT, WHAT IS A TASIGNA LAWSUIT?
A Tasigna Lawsuit is a demand from the defendant for monetary compensation by patients who took Tasigna and subsequently suffered heart or circulation problems (including complications like blocked arteries, heart attacks, or strokes). The lawsuits allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties. If you are eligible for a Tasigna lawsuit you possibly may be entitled to substantial compensation. A Nashville Tasigna Lawyer can answer these questions and is available anytime just give us a call or submit the form below for a free case evaluation.
IF I SUFFERED TASIGNA SIDE EFFECTS, AM I ELIGIBLE FOR A TASIGNA LAWSUIT?
If you or a loved one took Tasigna and suffered heart or circulation problems (including complications like blocked arteries, heart attacks, or strokes), or other serious Tasigna side effects, you could be eligible for a Tasigna lawsuit and possible entitled to substantial compensation. Call Nashville Tasigna lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Tasigna lawsuit.
IF YOU SUFFERED TASIGNA SIDE EFFECTS, CALL A NASHVILLE TASIGNA LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A TASIGNA LAWSUIT?
If you or a loved one took Tasigna and suffered heart or circulation problems (including complications like blocked arteries, heart attacks, or strokes), you could be eligible for a Tasigna Lawsuit. If you suffered Tasigna side effects, including Tasigna cardiovascular side effects, call Nashville Tasigna lawyer Timothy L. Miles today for a free case evaluation and see if you qualify for a Tasigna lawsuit.
NASHVILLE TASIGNA LAWYER TIMOTHY L. MILES, ESQ.Timothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website. answers to four frequently asked queSTIONS abouT THE tepezza lawsuit by a nashville tepezza lawyer5/15/2023
![]() Tepezza (teprotumumab-trbw) is a prescription drug that was developed by Horizon Therapeutics® for a condition known as Graves' eye disease and the treatment of thyroid eye disease (TED). TED is a condition that occurs when the eye muscles, tear glands, eyelids, and the fatty tissue behind the eyes become inflamed. The eye inflammation is triggered through an abnormal autoimmune response and can cause the eyes to swell and obstruct vision. Victims of Tepezza are now filing lawsuits after taking the drug and suffering from Tepezza hearing loss. According to the lawsuits, the labels on the drug did not warn patients or doctors about the potential risk for hearing loss nor did it warn how these issues could be permanent to those taking the eye drug. If you suffered Tepezza hearing loss or other serious Tepezza side effects, contact Nashville Tepezza lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for a Tepezza lawsuit and possibly entitled to substantial compensation. Read on for the answers to four frequently asked questions by Nashville Tepezza lawyer Timothy L. Miles about the Tepezza lawsuit and you used Tepezza and suffered Tepezza hearing loss or other Tepezza side effects, see if you are eligible for a Tepezza lawsuit. WHAT ARE THE TEPEZZA SIDE EFFECTS?The Tepezza side effects include:
If you suffered Tepezza side effects including Tepezza hearing loss, call a Nashville Tepezza lawyer today. IF I SUFFERED TEPEZZA HEARING LOSS, DO I QUALIFY FOR A TEPEZZA LAWSUIT?![]() In order to qualify for a Tepezza lawsuit, you must have taken the drug and have experienced permanent or persistent Tepezza hearing loss or other severe Tepezza side effects. The best way to understand if you qualify to file a Tepezza lawsuit against Horizon Therapeutics is by speaking to a Nashville Tepezza lawyer as soon as possible. Depending on your state, there may be a statute of limitations for filing a claim, ranging from two to four years on average depending on the State. If you suspect that you may have lost your hearing after taking Tepezza, do not wait to speak with an attorney. IF I SUFFERED TEPEZZA SIDE EFFECTS, AM I ELIGIBLE FOR A TEPEZZA LAWSUIT, HOW MUCH DOES IT COST TO HIRE A NASHVILLE TEPEZZA LAWYER?It does not cost anything to hire a Nashville Tepezza lawyer if you are eligible for a Tepezza lawsuit. We take all cases on a contingency basis which means we do not get paid unless we win or settle your case. A Nashville Tepezza lawyer can explain the process of a Tepezza lawsuit and answer any questions you may have free of charge, so contact Nashville Tepezza lawyer Timothy L. Miles today for a free case evaluation and see if you qualify for a Tepezza lawsuit. WHAT CAN I GET IF I SUFFERED TEPEZZA HEARING LOSS AND BELIEVE I AM ELIGIBLE FOR A TEPEZZA LAWSUIT?Every case is unique, but people who successfully file drug or medical device lawsuits can recover money for some of the following damages: • Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff in a Tepezza lawsuit could be entitled to compensation for any past and future costs associated with their Tepezza hearing loss hearing loss diagnosis or their severe Tepezza side effects. IF YOU SUFFERED TEPEZZA HEARING LOSS, CALL A NASHVILLE TEPEZZA LAWYER TODAY AND SEE IF YOU ARE ELIGIBLE FOR A TEPEZZA LAWSUITIf you or your loved one received Tepezza (teprotumumab) infusions and later experienced Tepezza hearing loss or tinnitus, or other serious Tezezza side effects, contact Nashville Tepezza lawyer Timothy L. Miles today for a free case evaluation to see if you qualify for a Tepezza Lawsuit and are eligible for a Tepezza lawsuit. NASHVILLE TEPEZZA LAWYER TIMOTHY L. MILESTimothy L. Miles is a nationally recognized shareholder and consumer rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2023 Top Ranked Lawyer, 2023 Top Rated Litigator. and a 2023 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, securities fraud, civil procedure, corporate formation, corporate takeover litigation, derivative lawsuits, and more. Visit out website.
Contact a Nashville Victoza Lawyer today if you suffered Victoza side effects, you may be eligible for a Victoza lawsuit
Hundreds of Victoza lawsuits filed by victims from across the country allege that Victoza, which is an incretin mimetic drug used to treat type 2 diabetes, may cause pancreatic cancer and that the manufacturer of Victoza, Novo Nordisk, failed to warn them of this risk and many people have been diagnosed with pancreatic cancer after taking Victoza.
Other incretin mimetic drugs have also been linked to this dangerous side effect. As a result, Januvia, Janumet, and Byetta have also been linked to pancreatic cancer. Manufacturers Novo Nordisk, Merck & Co., Eli Lilly, and Amylin Pharmaceuticals now hundreds of lawsuits that have been coordinated for pretrial proceedings in a multidistrict litigation (MDL) in Southern California while further research continues on the question of does Victoza cause pancreatic cancer continues and cause someone to be diagnosed with pancreatic cancer. If you or a loved one took Victoza were later diagnosed with pancreatic cancer, contact Nashville Victoza Lawyer Timothy L. Miles today for a free case evaluation and see if you are eligible for a Victoza lawsuit and possibly entitled to substantial compensation. Call Nashville Victoza Lawyer Timothy L. Miles for a free case evaluation. WHAT KIND OF DRUG IS VICTOZA?![]()
Victoza (liraglutide) is a medicine used to treat type 2 diabetes. It is glucagon-like peptide-1 (GLP-1) receptor agonist. A receptor agonist drug means that it binds to a certain receptor and causes the same action as the substance that normally binds to that receptor. Victoza, by binding to and activating the GLP-1 receptor, tells your body to release more insulin, stops the body from releasing more sugar, and slows down digestion.
Victoza is a solution for injection available in pre‑filled pens. The shots are given by the patient once a day by injection under the skin in the abdomen, thigh or upper arm. The starting dose of Victoza is 0.6 mg, and after at least one week, the dose is then increased to 1.2 mg. In certain patients, the dose can be further increased to 1.8 mg one week later, if necessary, achieve better control of blood glucose. WHAT IS THE PROBLEM WITH VICTOZA, DOES IT CAUSE VICTOZA SIDE EFFECTS?
Incretin mimetic drugs such as Victoza regulate the production of incretin, a type of hormone that stimulates the release of insulin in the body. Victoza does this by injecting patients with a substance that mimics a particular incretin called Glucagon-Like Peptide-1 (GLP-1). Victoza cancer lawsuits allege this process overstimulates the pancreas causing cells in the pancreas to multiply resulting in pancreatic cancer.
Researchers suspect that the process used by Victoza, and other incretin mimetic drugs may overstimulate the pancreas, and in some cases, cause pancreas cells to multiply. One expert in this area, Dr. Peter Butler, who is a diabetes expert at UCLA, discovered a growth of precancerous lesions in the pancreas when this process occurred. Additionally, according to the U.S. Food & Drug Administration's (FDA) adverse event database, patients taking Januvia, a similar drug to Victoza, are 10 times more likely to be diagnosed with pancreatic cancer. Beyond these observations though, the research is still unclear if and how incretin mimetic drugs cause pancreatic cancer. In 2013, the FDA requested that researchers investigate the correlation in greater detail. However, as more evidence is gathered for a more detailed review on the question of does Victoza cause pancreatic cancer, patients are continuing to file lawsuits asserting they got pancreatic cancer after taking their type 2 diabetes medication. In fact, over 2,500 Victoza patients have registered complaints with the FDA also asserting that the medication caused them to have pancreatic side effects and some to be diagnosed with pancreatic cancer. The vast majority (more than 2,300) allege pancreatitis, both acute and chronic. Moreover, similar reports have been made for other incretin mimetics: Roughly 2,400 Januvia patients and more than 3,000 Byetta patients have similarly complained of pancreatitis and filed lawsuits with claims similar to the Victoza cancer lawsuits. Finally, the American Cancer Society warns that patients with chronic pancreatitis (inflammation of the pancreas) may have an increased risk of being diagnosed with pancreatic cancer. If you or a loved one suffered the side effects of Victoza, and were later diagnosed with pancreatic cancer, contact Nashville Victoza Lawyer Timothy L. Miles today and see if you are eligible for a Victoza cancer lawsuit. WHAT IS THE STATUS OF THE VICTOZA CANCER LAWSUITS?
The Judicial Panel on Multidistrict Litigation (MDL) ordered that 749 incretin mimetic cases filed against leading manufacturers Novo Nordisk, Merck & Co., and Eli Lilly & Co be coordinated for pretrial proceedings in one multi-district litigation (MDL) and transferred the MDL cases to the Southern District of California and assigned to Judge Anthony Battaglia. The Victoza cancer lawsuits, all allege the drugs cause pancreatic cancer and that the manufacturers failed to warn doctors and patients of the risk.
In 2015, Federal Battaglia dismissed the then 744 lawsuits alleging a failure-to-warn in favor of the defendants' argument that the FDA would have prevented them from putting a pancreatic cancer warning on their drug labels, and since the FDA is a federal agency, it overrides state laws. In September 2016, plaintiffs asserted that Judge Battaglia had misinterpreted federal preemption law. In December 2017, a Ninth Circuit judicial panel agreed, and ruled in favor of plaintiffs, claiming that Judge Battaglia misinterpreted the Supreme Court ruling in Buckman Co. v. Plaintiffs' Legal Committee which states that private parties cannot pursue state law tort claim alleging violations of the Food, Drug, and Cosmetic Act (FDCA). The court of appeals also ruled that consumers claimed defendants violated the common law duty to warn, which falls outside the FDCA. SHOULD I REPORT ANY VICTOZA SIDE EFFECTS?
Yes, the FDA urges consumers who experience adverse advents to any medication or product to report it via the MedWatch Online Voluntary Reporting Form. When reporting your Victoza side effect make sure to be through and give as many details as possible about your experience taking the drug including all Victoza side effects you suffered, and any other symptoms you suffered especially if you were diagnosed with pancreatic cancer that you believe was cause by Victoza use.
IF I AM ELIGIBLE FOR A VICTOZA CANCER LAWSUIT, WHAT CAN I GET OUT OF A VICTOZA CANCER LAWSUIT?
If you are eligible for a Victoza lawsuit and are successful you can recover money for some of the following damages:
• Past and future medical bills (including medication, hospital stays, and in-home care) • Pain and suffering • Lost wages • Loss of earning capacity • Funeral expenses (in the event of a loved one’s death) Broadly speaking, a plaintiff in a Victoza lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they qualify for a Victoza lawsuit and are successful. IF I AM ELIGIBLE FOR A VICTOZA LAWSUIT, HOW CAN A NASHVILLE VICTOZA LAWYER HELP ME?
Because of the complexity of the cases and the need to hire experts, a products liability attorney is the go-to attorney when you have been injured by a drug or a product that is defective like Victoza. A Nashville Victoza Lawyer, who is an experienced products liability attorney, can determine if you are eligible for a Victoza lawsuit, and if so, can help you by putting you in the best possible position to win your Victoza Lawsuit and recover the most compensation.
CALL A NASHVILLE VICTOZA LAWYER AND SEE IF YOU ARE ELIGIBLE FOR A VICTOZA CANCER LAWSUIT?
If you or a loved one took Victoza and were diagnosed with pancreatic cancer in 2005 or later, or suffered other serious Victoza side effects you may be eligible for a Victoza lawsuit. Contact Nashville Victoza lawyer Timothy L. Miles today and see if you qualify for a Victoza lawsuit and could be eligible for substantial compensation. While there is still time to file a lawsuit, be mindful that these cases are time sensitive, and give us a call today.
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CONTACT
The Law Offices of Timothy L. Miles Tapestry at Brentwood Town Center 300 Centerview Dr., #247 Brentwood, TN 37027 Phone: (855) 846-6529 Email: [email protected] HOURS OF OPERATION Mon-Fri: 24/7 Sat-Sun: 24/7 |
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