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
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. |
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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