If you sufferd Xeljanz side effects, contact a Nashville Xeljanx lawyer today you could be eligible for a Xeljanx lawsuit
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). I hope you find this helpful! 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. POST-MARKETING XELJANZ STUDY REVEALS SERIOUS SAFETY CONCERNS ABOUT XELJANZ SIDE EFFECTS
Most Americans assume that if a drug is approved by the FDA, it has been thoroughly evaluated for safety and efficacy. However, this isn’t always the case. In addition to pre-approval clinical testing, the FDA may order post-marketing studies as a condition of drug approval. These trials gather more information about a drug’s safety, efficacy, or optimal use. Here, the Xeljanz study reveals serious safety concerns.
When the FDA first approved Xeljanz in 2012, it ordered a post-marketing Xeljanz safety study known as ORAL Surveillance. But rather than confirming the safety of Xeljanz, the post-marketing Xeljanz Study Revealed Serious Safety Concerns and has led to new health alerts and warnings about serious Xeljanz side effects. 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 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 that may be linked to Xeljanz include:
SHOULD I STOP TAKING XELJANZ IF I SUFFERED XELJANZ SIDE EFFECTS?
Anyone who is currently using Xeljanz should speak with their doctor about terminating their prescription to avoid the dangerous Xeljanz side effects. Not only will they help you stop the drug, but they can also advise you on safe medication alternatives for your condition.
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.
HOW CAN A NASHVILLE XELJANX LAWYER HELP ME IF I SUFFERED XELJANZ SIDE EFFECTS AND AM ELIGIBLE FOR A XELJANZ LAWSUIT?
`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 Xeljanz Lawyer, you can have the best chance to stand up to these large companies and optimize your chances of being fully compensated. Call Nashville Xeljanz lawyer Timothy L. Miles today and see if you are eligible for a Xeljanz lawsuit.
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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 suffered Byetta side effects contact a Nashville Byetta lawyer today you may be eligible for a Byettta lawsuit
Byetta (exenatide) was the first of a new class drugs used to treat type 2 diabetes drugs known as glucagon-like peptide 1 (GLP-1) receptor agonists which generated a lot of early excitement with added benefits including a low risk of hypoglycemia and successful weight loss. However, early optimism was halted by reports that Byetta and similar drugs were a possible risk factor for pancreatitis and pancreatic cancer.
There have been hundreds of pancreatic cancer lawsuits filed against the manufacturers of Byetta, Victoza, Janument, and Januvia. These lawsuits were all transferred the Southern District of California by the Judicial Panel on Multidistrict Litigation for coordinated and pretrial discovery and proceedings. A ruling by the trial judge in 2015 appeared to end the case until a recent court of appeals decision in favor of the Byetta plaintiffs holding their claims may proceed in federal court. If you or a loved one took Byetta and were diagnosed with pancreatic cancer, or another o of the major Byetta side effects, contact Nashville Byetta lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for Byetta lawsuit and possible entitled to substantial damages. (855) Tim-M-Law (855-846-6529). See what a Nashville Byetta Lawyer can do for you! Read on as Nashville Byetta Lawyer Timothy L. Miles breaks down the requirements for a Byetta lawsuit and takes a look at who is eligible for a Byetta lawsuit. We hope you find this helpful! WHAT IS BYETTA?
Byetta (exenatide) 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. Byetta, 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.
Byetta is a solution for injection available in pre‑filled pens of 5mcg or 10 mcg. The shots are given by the patient twice a day by injection under the skin in the abdomen, thigh or upper arm. The starting dose of Byetta is 5 mcg, twice a day before a meal. After four weeks, the dose can be increased to 10 mcg depending on how well your blood sugar levels respond to Byetta injections. WHAT IS THE PROBLEM WITH BYETTA, DOES IT CAUSE SERIOUS BYETTA SIDE EFFECTS?
Incretin mimetic drugs such as Byetta regulate the production of incretin, a type of hormone that stimulates the release of insulin in the body. Byetta does this by injecting patients with a substance that mimics a particular incretin called Glucagon-Like Peptide-1 (GLP-1). Byetta lawsuits allege this process overstimulates the pancreas causing cells in the pancreas to multiply resulting in pancreatic cancer.
BYETTA SIDE EFFECTS Byetta side effects include, among others:
With other Byetta side effects, a more severe allergic reaction to Byetta is rare but possible. The symptoms of a severe allergic reaction can include:
IF I SUFFERED BYETTA SIDE EFFECTS, AND I AM ELIGIBLE FOR A BYETTA LAWSUIT, WHAT IS A BYETTA LAWSUIT?
A Byetta Lawsuit is a demand from the defendants for monetary compensation by patients who took Byetta and subsequently developed serious Byetta Side Effects. The lawsuits allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties. If you suffered Byetta Side Effects and are eligible for a Byetta lawsuit, you may possibly be entitled to substantial compensation. A Nashville Byetta Lawyer can answer these questions and is available anytime just give us a call or submit this form for a free case evaluation to see if you are eligible for a Byetta lawsuit.
IF I SUFFERED BYETTA SIDE EFFECTS, AM I ELIGIBLE FOR A BYETTA LAWSUIT?
If you meet the following criteria, you may be eligible for a Byetta lawsuit:
Plaintiffs eligible for a Byetta lawsuit may also seek claims related to the wrongful death of a loved one who was prescribed Byetta and developed fatal pancreatic cancer. A Nashville Byetta lawyer can explain in further detail so give a Nashville Byetta lawyer a call today. IF I SUFFERED BYETTA SIDE EFECTS AND I AM ELIGIBLE FOR A BYETTA LAWSUIT, HOW MUCH DOES IT COST TO HIRE A NASHVILLE BYETTA LAWYER?
It does not cost anything to hire a Nashville Byetta Lawyer. We take all cases on a contingency basis which means we do not get paid unless we win your case. A Nashville Byetta Lawyer can explain the process and answer any questions you may have including whether you are eligible for a Byetta lawsuit.
IF I SUFFERED BYETTA SIDE EFFECTS AND I AM ELIGIBLE FOR A BYETTA LAWSUIT, HOW DOES A BYETTA LAWSUIT WORK?
If you meet the requirements for a Byetta lawsuit, and are eligible for a Byetta lawsuit, before it is filed with the court, your Nashville Byetta 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 Byetta, your medical history and how your Byetta side effects have affected your life.
Your Nashville Byetta 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 Byetta Lawsuit officially begins. From here, it will be a lot of back and forth between your Nashville Byetta 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 Byetta lawsuit is not dismissed and a settlement cannot be reached, the case will proceed to a jury trial. A Nashville Byetta lawyer will be fully prepared to try your Byetta lawsuit. IF I AM ELIGIBLE FOR A BYETTA LAWSUIT AND I DECIDE TO FILE A BYETTA LAWSUIT, HOW INVOLVED WILL I HAVE TO BE
If you suffered Byetta side effects and you are eligible for a Byetta Lawsuit and decide to file a Byetta 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 Byetta lawyer, he will explain your responsibilities in greater detail. IF YOU SUFFERED BYETTA SIDE EFFECTS, CALL A NASHVILLE BYETTA LAWYER IF YOU TOOK BYETTA AND WERE DIAGNOSED WITH PANCREATIC CANCER
If you or a loved one took Byetta and were diagnosed with pancreatic cancer, you may be eligible to file a Byetta lawsuit. Contact Nashville Byetta lawyer Timothy L. Miles today and see if you meet the requirements for a Byetta lawsuit and could be eligible for a Byetta Byetta lawsuit and possibly substantial compensation. (855) Tim-M-Law (855-846-6529).
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 or other Elmiron side effects.
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. Get started by filling out a free case evaluation form or calling a Nashville Elmiron Lawyer. (855) Tim-M-Law (855-846-6529). If you suffered Elmiron Eye Damage or other serious Elmiron side effects, Read on to learn more on how an Elmiron lawsuit works if you are eligible for an Elmiron lawsuit. We hope you find this helpful. 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 Elmiron lawsuit 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 and other Elmiron side effects 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 or other Elmiron side effects fill out and submit the form below 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 I SUFFERED ELMIRON EYE DAMAGE, WHY SHOULD I FILE AN ELMIRON EYE DAMAGE LAWSUIT?
If you or a loved one suffered Elmiron Eye Damage, or other serious Elmiron side effects, you have a right to file a claim for compensation for your pain and suffering and other damages such as lost wages, hospital and medical bills. A Nashville Elmiron lawyer will investigate your claim free of charge to determine if you are eligible for an Elmiron lawsuit.
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 or other serious Elmiron side effects. 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 are eligible 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. 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?
If you are eligible for an Elmiron lawsuit, before it is filed with the court, 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.
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 I AM ELIGIBLE FOR AN ELMIRON LAWSUIT AND I DECIDE TO FILE AN ELMIRON LAWSUIT, HOW INVOLVED WILL I HAVE TO BE
If you are eligible for an Elmiron Lawsuit and decide to file an Elmiron 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 Elmiron lawyer he will explain your responsibilities in greater detail. 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, 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 and see if you and are eligible to file 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. HOW A MERIDA LAWSUIT WORKS IF YOU ARE ELIGIBLE FOR A MERIDA LAWSUIT BY A NASHVILLE MERIDA LAWYER5/14/2023
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 and other Merida 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 how a Merida lawsuit works if you are eligible for a Merida lawsuit from Nashville Merida lawyer Timothy L. Miles. Did you suffer 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 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. HOW MUCH DOES IT COST TO HIRE A NASHVILLE MERIDA LAWYER IF I SUFFERED MERIDA SIDE EFFECTS AND MEET THE REQUIREMENTS FOR A MERIDA LAWSUITIt does not cost anything to hire a Nashville Meridia lawyer. We take all cases on a contingency basis which means we do not get paid unless we win your case. A Nashville Meridia lawyer can explain the process and answer any questions you may have including whether you are eligible for a Meridia lawsuit. So, call today and see if you meet the requirements for a Meridia lawsuit. If eligible for a Meridia lawsuit, you may be entitled to substantial compensation as a result of suffering Meridia side effects. IF I SUFFERED MERIDA SIDE EFFECTS, WHAT IS A MERIDA LAWSUIT?A Meridia Lawsuit is a demand from the defendants for monetary compensation by patients who took Meridia and subsequently developed Meridia Side Effects including a heart attack, stroke or even death. The lawsuits allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties. If you suffered Meridia Side Effects and are eligible a Meridia lawsuit, you may possibly be entitled to substantial compensation. A Nashville Meridia 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 are eligible for a Meridia lawsuit. IF I SUFFERED MERIDA SIDE EFFECTS AND AM ELIGIBLE FOR A MERIDA LAWSUIT, HOW DOES A MERIDA LAWSUIT WORK?If you suffered Merida side effects and are eligible for an Meridia lawsuit, before it is filed with the court, your Nashville Meridia 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 Meridia and your medical history and about your Merida side effects. Your Nashville Meridia 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 Nashville Meridia Lawsuit officially begins. From here, it will be a lot of back and forth between your Nashville Meridia 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 Meridia lawsuit is not dismissed and a settlement cannot be reached, the case will proceed to a jury trial. 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 LAWSUITIf 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 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 to learn four things about the Onglyza lawsuit from a Nashville Onglyza lawyer. 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 and additional Onglyza side effects.
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 over Onglyza side effects. 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 as another of the Onglyza side effects. 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, or another of the serious Onglyza side effects after starting Onglyza therapy, you may meet the requirements for an Onglyza lawsuit and possibly be eligible for an Onglyza lawsuit and possibly 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 A NASHVILLE ONGLYZA LAWSUIT, HOW MUCH DOES IT COST TO HIRE AN 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 NashvilleOnglyza lawyer can explain the process and answer any questions you may have including whether you are eligible for an Onglyza lawsuit.
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 meet the requirements for an Onglyza lawsuit and are eligible for a Onglyza lawsuit and possibly entitled to substantial compensation.
nashville onglyza 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 suffered Onglyza Side Effects contact 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 what you need to know about the Onglyza lawsuits by Nashville Onglyza lawyer Timothy L. Miles. 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, other another of the serious Onglyza side effects 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 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. 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 Valsartan and developed Valsartan side effects, call a Nashville Valsartan lawyer
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 four things you should know about the Valsartan lawsuits from a Nashville Valsartan lawyer. 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.
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 for Valsartan side effects. 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?
ValsartanIn 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 and 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 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. 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. 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. HOW DOES TEPEZZA WORK?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. ARE TEPEZZA LAWSUITS ABOUT TEPEZZA HEARING LOSS?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 what a Nashville Tepezza lawyer can do for you. TEPEZZA HEARING LOSSIn 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. 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 in addition to tepezza hearing loss?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 for 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 suffered Tepezza hearing loss or other Tapezza side effects, do not wait to speak with an attorney. 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, 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. 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 from Kombiglyze XR side effects contact Nashville Kombiglyze XR lawyer Timothy L. Miles today
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 meet the requirements for a Kombiglyze XR lawsuit are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation. Read on to learn more about the requirements for a Kombiglyze XR lawsuit and who is eligible for a Kombiglyze XR lawsuit by Nashville Kombiglyze XR lawyer Timothy L. Miles. Please visit our full Kombiglyze XR page on our website by clicking here. 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. 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 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 as another one of the Kombiglyze XR side effects. 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. "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 fOR 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. WHAT CAN A NASHVILLE KOMBIGLYZE XR LAWYER DO FOR ME IF I AM ELIGIBLE FOR A KOMBIGLYZE XR LAWSUIT?
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 Kombiglyze XR. A Nashville Kombiglyze XR Lawyer, who is an experienced products liability attorney, can help you by putting you in the best possible position to win your Kombiglyze XR Lawsuit and recover the most compensation if you are eligible for a Kombiglyze XR lawsuit.
HOW DOES A KOMBIGLYZE XR LAWSUIT WORK?
If you meet the requirements for a Kombiglyze XR lawsuit, before it is filed with the court, your Nashville Kombiglyze XR 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 Kombiglyze XR and your medical history including you Kombiglyze XR side effects.
Your Nashville Kombiglyze XR 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 Kombiglyze XR Lawsuit officially begins. From here, it will be a lot of back and forth between your Nashville Kombiglyze XR 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 Kombiglyze XR lawsuit. is not dismissed and a settlement cannot be reached, the case will proceed to a jury trial. 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.
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. If eligible for a Tasigna lawsuit, you may be entitled to substantial compensation. 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. Studies have allegedly linked the drug to Tasigna side effects including 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, you may beeligible 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 other Tasigna side effects including 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, another of the Tasigna side effects, and 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, 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. If eligible for a Tasigna lawsuit, you could be entitled to substantial compensation.
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. 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 about the requirements for a Merida lawsuit and who is eligible for a Merida lawsuit by a Nashville Merida lawyer. SERIOUS MERIDIA SIDE EFFECTSIn 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 meet the requirements for a Merida lawsuit and are eligible for a Meridia 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. HOW MUCH DOES IT COST TO HIRE A NASHVILLE MERIDA LAWYER IF I SUFFERED MERIDA SIDE EFFECTS AND MEET THE REQUIREMENTS FOR A MERIDA LAWSUITIt does not cost anything to hire a Nashville Meridia lawyer. We take all cases on a contingency basis which means we do not get paid unless we win your case. A Nashville Meridia lawyer can explain the process and answer any questions you may have including whether you are eligible for a Meridia lawsuit. So, call today and see if you meet the requirements for a Meridia lawsuit. If eligible for a Meridia lawsuit, you may be entitled to substantial compensation as a result of suffering Meridia side effects. IF YOU SUFFERED MERIDIA SIDE EFFECTS, CALL A NASHVILLE MERIDIA LAWYER TODAY TO SEE IF YOU ARE ELIGIBLE FOR A MERIDIA LAWSUITIf 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. 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.
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. Read on to learn three things you should know about an Actemra lawsuit by 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.
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 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 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. 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. 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 entitled to file 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 as Nashville Belviq Lawyer Timothy L. Miles explains who is eligible for a Belviq lawsuit. 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. 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 lawsuit. -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 LAWSUITIf 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 severe Belviq 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. 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. 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. HOW DOES TEPEZZA WORK?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. ARE TEPEZZA LAWSUITS ABOUT TEPEZZA HEARING LOSS?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. TEPEZZA HEARING LOSSIn 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. 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 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, 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. 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.
Call a Nashville Byetta lawyer today if you suffered Byetta side effects, you could be eligible for a Byetta lawsuit
Byetta (exenatide) was the first of a new class drugs used to treat type 2 diabetes drugs known as glucagon-like peptide 1 (GLP-1) receptor agonists which generated a lot of early excitement with added benefits including a low risk of hypoglycemia and successful weight loss. However, early optimism was halted by reports that Byetta and similar drugs were a possible risk factor for pancreatitis and pancreatic cancer.
There have been hundreds of pancreatic cancer lawsuits filed against the manufacturers of Byetta, Victoza, Janument, and Januvia. These lawsuits were all transferred the Southern District of California by the Judicial Panel on Multidistrict Litigation for coordinated and pretrial discovery and proceedings. A ruling by the trial judge in 2015 appeared to end the case until a recent court of appeals decision in favor of the Byetta plaintiffs holding their claims may proceed in federal court. If you or a loved one took Byetta and were diagnosed with pancreatic cancer, contact Nashville Byetta lawyer Timothy L. Miles today for a free case evaluation to see if you are eligible for Byetta lawsuit and possible entitled to substantial damages. (855) Tim-M-Law (855-846-6529). Read on to learn five things you should know about a Byetta lawsuit from a Nashville Byetta Lawyer. WHAT IS BYETTA?
Byetta (exenatide) 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. Byetta, 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.
Byetta is a solution for injection available in pre‑filled pens of 5mcg or 10 mcg. The shots are given by the patient twice a day by injection under the skin in the abdomen, thigh or upper arm. The starting dose of Byetta is 5 mcg, twice a day before a meal. After four weeks, the dose can be increased to 10 mcg depending on how well your blood sugar levels respond to Byetta injections. WHAT IS THE PROBLEM WITH BYETTA?
Incretin mimetic drugs such as Byetta regulate the production of incretin, a type of hormone that stimulates the release of insulin in the body. Byetta does this by injecting patients with a substance that mimics a particular incretin called Glucagon-Like Peptide-1 (GLP-1). Byetta lawsuits allege this process overstimulates the pancreas causing cells in the pancreas to multiply resulting in pancreatic cancer.
BYETTA SIDE EFFECTS
Byetta side effects include, among others:
A more severe allergic reaction to Byetta is rare but possible. The symptoms of a severe allergic reaction can include:
IF I SUFFERED BYETTA SIDE EFFECTS, AM I ELIGIBLE FOR A BYETTA LAWSUIT?
If you meet the following criteria, you may be eligible for a Byetta lawsuit:
Plaintiffs eligible for a Byetta lawsuit may also seek claims related to the wrongful death of a loved one who was prescribed Byetta and developed fatal pancreatic cancer. IF I SUFFERED BYETTA SIDE EFECTS AND I AM ELIGIBLE FOR A BYETTA LAWSUIT, HOW MUCH DOES IT COST TO HIRE A NASHVILLE BYETTA LAWYER?
It does not cost anything to hire a Nashville Byetta lawyer. We take all cases on a contingency basis which means we do not get paid unless we win your case. A Nashville Byetta lawyer can explain the process and answer any questions you may have including whether you are eligible for a Byetta lawsuit.
IF YOU SUFFERED BYETTA SIDE EFFECTS, CALL A NASHVILLE BYETTA LAWYER IF YOU TOOK BYETTA AND WERE DIAGNOSED WITH PANCREATIC CANCER
If you or a loved one took Byetta and were diagnosed with pancreatic cancer, you may be eligible to file a Byetta lawsuit. Contact Nashville Byetta lawyer Timothy L. Miles today and see if you meet the requirements for a Byetta lawsuit and could be eligible for substantial compensation. (855) Tim-M-Law (855-846-6529).
nashville byetta lawyer timothy l. milesHomeTimothy 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 AVPreeminent 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 our website.
If you took Xeljanz and developed Xeljanz side effects, call a Xeljanx lawyer to see if you are eligible for an Xeljanz lawsuit
What should you do when a medication makes you feel worse, not better? Whether it is over-the-counter medicine or a prescription from a doctor, drugs are meant to treat a patient. However, when the side effects exceed the benefits, medicines can become very dangerous and sometimes lethal.
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 and other Xeljanz side effects. 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 and other Xeljanz side effects. 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 Xeljanz lawyer, free of charge, please contact us for a free case evaluation. (855) Tim-M-Law (855-846-6529). Read on to learn more about the Xeljanz side effects and whether you my be eligible for a Xeljanz lawsuit. 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 Xeljanz lawyer Timothy L. Miles today. POST-MARKETING XELJANZ STUDY REVEALS SERIOUS SAFETY CONCERNS ABOUT XELJANZ SIDE EFFECTS
Most Americans assume that if a drug is approved by the FDA, it has been thoroughly evaluated for safety and efficacy. However, this isn’t always the case. In addition to pre-approval clinical testing, the FDA may order post-marketing studies as a condition of drug approval. These trials gather more information about a drug’s safety, efficacy, or optimal use. Here, the Xeljanz study reveals serious safety concerns including Xeljanz side effects.
When the FDA first approved Xeljanz in 2012, it ordered a post-marketing Xeljanz safety study known as ORAL Surveillance. But rather than confirming the safety of Xeljanz, the post-marketing Xeljanz Study Revealed Serious Safety Concerns and has led to new health alerts and warnings about the Xeljanz side effects. 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 as another of the Xeljanz side effects. 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 2Xeljanz 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 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) as another of the Xeljanz side effects.
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 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 Xeljanz lawyer and see if you meet the Xeljanz Lawsuit Criteria.
IF YOU SUFFERED XELJANZ SIDE EFFECTS, CONTACT A 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 Xeljanz 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 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! xeljanz 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 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 Tasigna lawyer Timothy L. Miles today for a free case evaluation and see if you qualify for a Tasigna lawsuit. Read on to learn more on the Tasigna side effects and how you may be 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 and other 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. 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 side effects 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 and another of the Tasigna side effects. 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:
ARE THERE STUDIES LINKING TASIGNA TO CARDIOVASCULAR EVENTS AS A TASIGNA SIDE EFFECT?
Two recent studies have connected Tasigna with cardiovascular events:
The FDA’s adverse event reporting database has received more than 100 reports of Tasigna-related myocardial ischemia diagnoses. Myocardial ischemia is a condition that is usually caused by a blockage of the coronary arteries. It results in reduced blood flow to the heart, decreasing the amount of oxygen to the heart. In an FDA post-market review, 5.8% of patients taking Tasigna allegedly suffered ischemic heart. Atherosclerosis is 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 may eventually cause coronary artery disease, peripheral arterial disease, blood clots, heart attacks, or strokes. It’s currently the leading cause of death in the developed world. Since 2013, Tasigna products sold in Canada come with a warning of the drug’s connection to atherosclerosis. This label change came after Canadian health officials warned that 277 cases of atherosclerosis were allegedly reported worldwide. Lawsuits allege that Novartis never warned of the risk of atherosclerosis in the U.S. though, despite these reports. Other serious Tasigna side effects noticed by the FDA that may be linked to Tasigna include low blood cell counts; decreased blood flow to the heart, lungs, or brain; pancreatitis; and Tumor Lysis Syndrome, a condition that can occur when cancer cells are broken down quickly, resulting in kidney failure or an abnormal heartbeat. Lawsuits have been filed some patients against Novartis. who took Tasigna and subsequently suffered a heart or circulation problem. The lawsuits allege Novartis failed to properly warn of these Tasigna side effects. 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 and Tasigna side effects. If eligible you may participate in a Tasigna lawsuit and possibly be entitled to substantial compensation. A Tasigna Lawyer can answer these questions and is available anytime just give us a call or submit this form for a free case evaluation.
IF YOU SUFFERED TASIGNA SIDE EFFECTS, CALL A 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), or other serious Tasigna side effects you could be eligible for a Tasigna Lawsuit. If you suffered Tasigna side effects, including Tasigna cardiovascular side effects, call Tasigna lawyer Timothy L. Miles today for a free case evaluation and see if you qualify for a Tasigna lawsuit.
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.
If you suffered Onglyza side effects, contact a Onglyza lawyer today 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 and other Onglyza side effects. If you or a loved one took Onglyza as directed and suffered from Onglyza side effects including heart failure or other cardiovascular injuries after starting Onglyza therapy, contact 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 to learn about the Onglza side effects and if you could be eligible for an Onglyza lawsuit. WHAT IS 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 including Onglyza side effects. 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 and other Onglyza side effects. 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, or other Onglyza side effects after starting Onglyza therapy, you may meet the requirements for an Onglyza lawsuit and possibly be entitled to substantial compensation. Call an 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 YOU SUFFERED ONGLYZA SIDE EFFECTS, CONTACT AN 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 Onglyza lawyer Timothy L. Miles today to see if you are eligible for a Onglyza lawsuit and possibly entitled to substantial compensation.
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. 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 Tepezza hearing loss nor did it warn how these issues and other serious Tepezza side effects could be permanent to those taking the eye drug. If you suffered Tepezza hearing loss or other serious Tepezza side effects, contact 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 how if you suffered Tepezza hearing loss or other Tepezza side effects, you could be eligible for a Tepezza lawsuit and possibly substantial compensation. TEPEZZA HEARING LOSSIn January 2020, the FDA approved Tepezza, the only drug known to treat TED, based on clinical trials that documented only 10% of patients reporting hearing issues. However, a 2021 study found that patients taking Tepezza are at a 65% higher risk for developing temporary and even permanent hearing issues, including Tepezza hearing loss 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 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 for a Tepezza lawsuit against Horizon Therapeutics is by speaking to a 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 TEPEZZA LAWYER?It does not cost anything to hire a 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 Tepezza lawyer can explain the process of a Tepezza lawsuit and answer any questions you may have free of charge, so contact Tepezza lawyer Timothy L. Miles today for a free case evaluation and see if you qualify for a Tepezza lawsuit. HOW DO I GET STARTED IF I SUFFERED TEPEZZA HEARING LOSS AND BELIEVE I AM ELIGIBLE FOR A TEPEZZA LAWSUIT?If you suffered Tepezza hearing loss fill out and submit this form for a Free Case Evaluation with a Tepezza lawyer to see if you are eligible for a Tepezza lawsuit and possibly entitled to substantial compensation. 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 diagnosis. IF YOU SUFFERED TEPEZZA HEARING LOSS, CALL A 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, contact 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. 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 suffered Zostavax side effects call a 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 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 to see if you meet the requirements for a Zostavax lawsuit and may be eligible for a Zostavax lawsuit. 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. HOW DO I KNOW IF I AM 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.
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. WHO ELSE MAY MEET THE REQUIREMENTS FOR A ZOSTAVAX LAWSUIT?
If you or a loved one suffered from one of the following injuries within two years from the vaccination date, you may also meet the requirements for a Zostavax lawsuit:
WHAT IS A ZOSTAXAX LAWSUIT?
An Zostavax Lawsuit is a demand from the defendants for monetary compensation by patients who took Zostavax and serious Zostavax side effects. The lawsuit would allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties. If you are eligible for a Zostavax lawsuit you could possibly be entitled to substantial compensation. A Zostavax Lawyer can answer these questions including whether you meet the requirements for a Zostavax lawsuit and is available anytime. Just give us a call or submit the form below for a free case evaluation and see if you are eligible for a Zostavax Lawsuit.
WHO CAN FILE A ZOSTAVAX LAWSUIT?
Individuals of all ages who have experienced severe or debilitating Zostavax side effects as a result of receiving Zostavax may be eligible for a Zostavax lawsuit and receive compensation for damages related to the vaccine. Zostavax is approved for people who are at least 50 years of age, but some people in their 40s have also been prescribed it. When deciding whether to apply for the vaccine, it is important to weigh the benefits against the potential side effects and risks. Not everyone who is at risk is a good candidate for the vaccine. Because Zostavax is a live vaccine, it is not appropriate for people who are immunocompromised or pregnant. Most of the Zostavax lawsuits focus on individuals who have experienced serious Zostavax side effects.
If you or a loved one suffered serious Zostavax side effects including shingles, blindness or even death, contact us today. (855) Tim-M-Law (855-846-6529). WHAT CAN I GET IN A ZOSTAVAX LAWSUIT?
If you meet the requirements for a Zostavax 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 Zostavax lawsuit could be entitled to compensation for any past and future costs associated with their diagnosis if they meet the requirements for a Zostavax lawsuit and are successful. IF I DECIDE TO FILE A ZOSTAVAZ LAWSUIT, HOW INVOLVED WILL I HAVE TO BE
If you are eligible for a Zostavax Lawsuit and decide to file a Zostavax 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 Zostavax lawyer, he will explain your responsibilities in greater detail. CONTACT A ZOSTAVAZ LAWYER ABOUT A ZOSTAVAX IF YOU SUFFERED ZOSTAVAZ SIDE EFFECTS
If you or a loved one suffered serious Zostavax side effects including shingles, blindness or even death, contact 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 us a call today.
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.
Call a Byetta lawyer to see if you are eligible for a Byetta lawsuit if you sufferered Byetta side effects
Byetta (exenatide) was the first of a new class drugs used to treat type 2 diabetes drugs known as glucagon-like peptide 1 (GLP-1) receptor agonists which generated a lot of early excitement with added benefits including a low risk of hypoglycemia and successful weight loss. However, early optimism was halted by reports that Byetta and similar drugs were a possible risk factor for pancreatitis and pancreatic cancer.
There have been hundreds of pancreatic cancer lawsuits filed against the manufacturers of Byetta, Victoza, Janument, and Januvia. These lawsuits were all transferred the Southern District of California by the Judicial Panel on Multidistrict Litigation for coordinated and pretrial discovery and proceedings. A ruling by the trial judge in 2015 appeared to end the case until a recent court of appeals decision in favor of the Byetta plaintiffs holding their claims may proceed in federal court. If you or a loved one took Byetta and were diagnosed with pancreatic cancer OR or other serious Byetta side effects, contact Byetta lawsuit lawyer Timothy L. Miles today for a free case evaluation to see if you meet the requirements for a Byetta lawsuit and are eligible for Byetta lawsuit and possibly entitled to substantial damages. (855) Tim-M-Law (855-846-6529). WHAT IS THE PROBLEM WITH BYETTA?
Incretin mimetic drugs such as Byetta regulate the production of incretin, a type of hormone that stimulates the release of insulin in the body. Byetta does this by injecting patients with a substance that mimics a particular incretin called Glucagon-Like Peptide-1 (GLP-1). Byetta lawsuits allege this process overstimulates the pancreas causing cells in the pancreas to multiply resulting in pancreatic cancer.
BYETTA SIDE EFFECTS
Byetta side effects include, among others:
A more severe allergic reaction to Byetta is rare but possible. The symptoms of a severe allergic reaction can include:
WHAT DO THE BYETTA LAWSUITS ALLEGE?
The specific claims against Eli Lilly/Amylin and other drug companies include:
HOW DO I KNOW IF I AM ELIGIBLE FOR A BYETTA LAWSUIT?
If you meet the following requirements for a Byetta lawsuit, you may be eligible for Byetta lawsuit:
Plaintiffs may also seek claims related to the wrongful death of a loved one who was prescribed Byetta and developed fatal pancreatic cancer. What is a Byetta Lawsuit?
A Byetta Lawsuit is a demand from the defendants for monetary compensation by patients who took Byetta and subsequently developed serious Byetta Side Effects. The lawsuits allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties. If you suffered Byetta Side Effects and are eligible for a Byetta lawsuit, you may possibly be entitled to substantial compensation. A Byetta Lawsuit Lawyer can answer these questions and is available anytime just give us a call or submit the form for a free case evaluation to see if you are eligible for a Byetta lawsuit.
HOW DOES A BYETTA LAWSUIT WORK?
If you meet the requirements for a Byetta lawsuit, before it is filed with the court, your Byetta Lawsuit 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 Byetta and your medical history including your Byetta side effects.`
Your Byetta Lawsuit 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 Byetta Lawsuit officially begins. From here, it will be a lot of back and forth between your Byetta Lawsuit 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 Byetta lawsuit is not dismissed and a settlement cannot be reached, the case will proceed to a jury trial. IF I DECIDE TO FILE A BYETTA LAWSUIT, HOW INVOLVED WILL I HAVE TO BE
If you meet the requirements for a Byetta lawsuit and are eligible for a Byetta Lawsuit and decide to file a Byetta 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 Byetta lawyer, he will explain your responsibilities in greater detail. CALL A BYETTA LAWSUIT LAWYER IF YOU TOOK BYETTA AND WERE DIAGNOSED WITH PANCREATIC CANCER
If you or a loved one took Byetta and were diagnosed with pancreatic cancer, or suffered other serious Byetta side effects you may be eligible to file a Byetta lawsuit. Contact Byetta lawsuit lawyer Timothy L. Miles today and see if you meet the requirements for a Byetta lawsuit and could be eligible for substantial compensation. (855) Tim-M-Law (855-846-6529).
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 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 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 see if you may be eligible for a Kombiglyze XR lawsuit and possibly entitled to to subtantial compensation. 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. WHAT DO THE KOMBIGLYZE XR LAWSUITS ALLEGE?
Kombiglyze XR lawsuits allege that AstraZeneca and Bristol-Myers Squibb failed to:
SHOULD I REPORT ANY SIDE EFFECTS OF KOMBIGLYZE XR?
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 Kombiglyze XR side effects make sure to be through and give as many details as possible about your experience taking the drug including all Kombiglyze XR side effects you suffered, and any other symptoms you suffered that you believe were cause by Kombiglyze XR use.
What is a Kombiglyze XR Lawsuit?
A Kombiglyze XR Lawsuit is a demand from the defendants for monetary compensation by patients who took Kombiglyze XR and subsequently developed Kombiglyze XR Side Effects including cardiovascular injuries. The lawsuits allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties. If you suffered Kombiglyze XR Side Effects and are eligible a Kombiglyze XR lawsuit, you may possibly be entitled to substantial compensation. A Kombiglyze XR Lawyer can answer these questions and is available anytime just give us a call or submit this form for a free case evaluation to see if you are eligible for a Kombiglyze XR lawsuit.
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, after starting Kombiglyze XR therapy, you may meet the requirements for a Kombiglyze XR lawsuit and possibly be entitled to substantial compensation. Call a 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. HOW DOES A KOMBIGLYZE XR LAWSUIT WORK?
If you meet the requirements for a Kombiglyze XR lawsuit, before it is filed with the court, your Kombiglyze XR 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 Kombiglyze XR and your medical history including your Kombiglyze XR side effects.
Your Kombiglyze XR 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 Kombiglyze XR Lawsuit officially begins. From here, it will be a lot of back and forth between your Kombiglyze XR 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 Kombiglyze XR Lawsuit is not dismissed and a settlement cannot be reached, the case will proceed to a jury trial. IF I DECIDE TO FILE A KOMBIGLYZE XR LAWSUIT, HOW INVOLVED WILL I HAVE TO BE
If you meet the requirements for a Kombiglyze XR lawsuit and are eligible for a Kombiglyze XR Lawsuit and decide to file a Kombiglyze XR 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 Kombiglyze XR lawyer he will explain your responsibilities in greater detail. IF YOU SUFFERED FROM KOMBIGLYZE XR SIDE EFFECTS, CALL A 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 Kombiglyze XR lawyer Timothy L. Miles today to see if you meet the requirements for a Kombiglyze XR lawsuit and are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation.
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. 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 Belviq Lawsuit 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. Read on to see if you meet the Belviq Lawsuit Criteria and may be eligible for a Belviq lawsuit. 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:
DOES BELVIQ CAUSE CANCER?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. WHAT IS THE RISK IN TAKING BELVIQ?In February 2020, the FDA requested the Belviq Recall and for to Eisai pull all Belviq and Belviq XR products from the market due to Belviq Side Effects. Eisai has complied with this request. As a result, Belviq is no longer commercially available. WHAT IS A BELVIQ LAWSUIT?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 Belviq Lawsuit 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 Belviq Lawsuit 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 Belviq Lawsuit Lawyer on their behalf about a Belviq class action lawsuit. Call 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 I SUFFERED BYETTA SIDE EFFECTS, WHAT CAN I RECOVER FROM A BELVIQ 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 Belviq lawsuit could be entitled to compensation for any past and future costs associated with their cancer diagnosis if eligible for a Belviq lawsuit. IF I AM ELIGIBLE FOR AN BELVIQ LAWSUIT, HOW DOES A BELVIQ LAWSUIT WORK?If you are eligible for an Belviq lawsuit, before it is filed with the court, your Belviq 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 Belviq and your medical history. Your Belviq 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 Belviq Lawsuit officially begins. From here, it will be a lot of back and forth between your Belviq 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 Belviq lawsuit is not dismissed and a settlement cannot be reached, the case will proceed to a jury trial. CALL A BELVIQ LAWSUIT LAWYER TO SEE IF YOU ARE ELIGIBLE FOR A BELVIQ LAWSUITIf 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 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 severe Belviq 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 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 Belviq Lawyer can do for you. 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 Kombiglyze XR lawyer
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 Kombiglyze XR lawyer Timothy L. Miles today for a free case evaluation to see if you meet the requirements for a Kombiglyze XR lawsuit and are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation. Read on to see if you may meet the requirements for a Kombiglyze XR lawsuit and if so, whether may be 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, there are dozens of lawsuits that allege other Kombiglyze XR side effects including serious cardiovascular injury. What Do the Kombiglyze XR Lawsuits Allege?
Kombiglyze XR lawsuitsKOMBIGLYZE allege that AstraZeneca and Bristol-Myers Squibb failed to:
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, after starting Kombiglyze XR therapy, or any other serious Kombiglyze XR side effects you may meet the requirements for a Kombiglyze XR lawsuit and possibly be entitled to substantial compensation. Call a 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 I DECIDE TO FILE A KOMBIGLYZE XR LAWSUIT, HOW INVOLVED WILL I HAVE TO BE
If you are eligible for a Kombiglyze XR Lawsuit and decide to file a Kombiglyze XR 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 Kombiglyze XR lawyer he will explain your responsibilities in greater detail. IF YOU SUFFERED FROM KOMBIGLYZE XR SIDE EFFECTS, CALL A 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 Kombiglyze XR lawyer Timothy L. Miles today to see if you are eligible for a Kombiglyze XR lawsuit and possibly entitled to substantial compensation.
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. 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) highlighting Merida side effects. The study, which prompted a Meridia recall in Europe, showed a 16% percent increase in the risk of serious Meridia side effects, including:
To gauge the Merida side effects, 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 and other serious Merida 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 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 what you need to know about the serious Merida side effects. SERIOUS MERIDIA SIDE EFFECTSIn 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 the following Merida side effects:
Additionally, approximately 30 deaths were caused by serious Merida side effects 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 serious Merida side effects including 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 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 REPORTEDThe 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:
SHOULD I REPORT MERIDIA 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 Merida side effects make sure to be through and give as many details as possible about your experience taking the drug including all Merida side effects your suffered, and any other symptoms you suffered that you believe was caused by Merida use. IF YOU SUFFERED MERIDIA SIDE EFFECTS, CALL A MERIDIA LAWYER TODAY TO SEE IF YOU ARE ELIGIBLE FOR A MERIDIA LAWSUITIf you or a loved one suffered serious Meridia side effects including a heart attack, stroke or even death, contact 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. 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. |
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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