NEW YORK – The U.S. Food and Drug Administration (FDA) has expanded its voluntary Valsartan recall; a medication prescribed to treat high blood pressure and heat complications. According to our personal injury lawyers, New York pharmacies are pulling a number of medications containing Valsartan off their shelves.
The FDA recently discovered traces of a chemical known to cause cancer in the drug, sparking the massive recall.
Officials with the FDA first issued recall notices in July when doctors discovered traces of N-nitrosodimethylamine, a known carcinogen, in over 70 different medications, all of which contained Valsartan. The recall does not affect the United States alone, as the European Medicines Agency has issued a similar recall.
Personal injury attorneys in New York say this global recall effort has also put drug manufacturers under a microscope. Generic valsartan is commonly produced by Chinese companies, which are often the subjects of controversy due to the production of defective drugs or counterfeit drugs.
If you have been taking valsartan and have experienced odd side-effects or have been diagnosed with cancer, you may be eligible for compensation, which can help pay for your medical bills, lost time at work, pain and suffering, and more. Make a FREE call to the experienced medical malpractice attorneys at Cellino & Barnes to find out if a Valsartan Recall Lawsuit is right for you.
What To Do If I’ve Taken Valsartan
The expanded recall includes dozens of different prescription medications, but many drugs containing Valsartan are NOT in this recall (See The Drugs Not Included in Valsartan Recall Here). Whether it’s been recalled or not, here are some steps to follow if you’ve been prescribed valsartan.
If you’ve been prescribed any medication that contains Valsartan, contact your physician immediately.
Because valsartan is used to treat serious medical conditions, DO NOT stop taking the medicine until you’re prescribed a replacement product.
If you aren’t sure if your medicine is on the latest recall list, contact your pharmacy. They will have the most up-to-date recall list, and should be able to inform you if the drug(s) you’re taking are affected.
Finally, talk to the New York medical malpractice lawyers at Cellino & Barnes for a FREE consultation.
Valsartan may be considered a dangerous drug, and those who’ve suffered damaging side-effects as a result may be owed compensation for any injuries or illnesses caused by the medication.
Medical malpractice law firms like Cellino & Barnes have experienced lawyers and former doctors on staff who can assess your situation and help determine a proper legal course of action for you and your family.
Since valsartan can affect the cardiovascular system, the side-effects could include cancer, brain injuries, heart complications, or even wrongful death.
Our team has years of experience battling the big drug companies in court, and our malpractice attorneys can help you get the best result possible from a case involving valsartan.
NEW YORK – A new bipartisan measure aims to create uniform safety regulations and protect the health of all Americans who use personal care products.
Introduced by U.S. Sens. Susan Collins (R-Maine) and Dianne Feinstein (D-Calif.), The Personal Care Products Safety Act is a bipartisan bill that would set rules and guidelines for pharmaceutical companies and other industries creating personal care items such as baby powder, lotions and hair products.
Market experts now estimate that the industry collects over $60 billion in revenue, but a New York talcum powder attorney at Cellino & Barnes says federal rules haven’t been updated since before World War II.
According to New York talcum powder attorneys, there are questions surrounding many personal care products and the ingredients they contain. Over the last 80 years, there have been few official studies on these ingredients, and testing is rare.
Under the new bill, the U.S. Food and Drug Administration (FDA) would be required to evaluate at least five ingredients per year to determine whether they are safe, and how these ingredients can be used appropriately.
The bill also outlines a process in which consumers are warned about dangerous ingredients, if federal researchers find evidence of negative health impacts.
Sens. Feinstein and Collins hope to pass their bill this year, as it could provide important information and resources to both consumers and companies.
Recently, several Johnson & Johnson products containing talc have been linked to ovarian cancer. Independent studies on this connection have been conducted with mixed results, but several women who filed complaints have won large jury verdicts.
If you or a loved one has been diagnosed with ovarian cancer and you suspect talc may have played a role in its development, a New York talcum powder lawyer at Cellino & Barnes could help. Our attorneys are former physicians and legal advocates with years of experience handling cases involving medicines, dangerous products and more.
NEW YORK – Lawsuits against major drug companies and their testosterone supplements are piling up in courts across the nation. Almost 2,000 cases are accusing drug manufacturers of causing serious injuries with supplements such as Axiron, Testim and Androgel, according to the U.S. Judicial Panel on Mulidistrict Litigation (MDL).
Most lawsuits claim the drug makers failed to warn consumers of serious risks like blood clots and heart attacks. Some cases allege the pharmaceutical products were improperly marketed.
New York dangerous drug attorneys at Cellino & Barnes say thousands of men may have been exposed to high-risk topical treatments.
“Some of these drugs were widely-marketed to men in New York,” dangerous drug attorney Ross Cellino said. “Some of these men may not have needed these topical treatments but it still exposed them to unnecessary side effects.”
A number of cases are currently being prepared for early trial, which could measure how juries will consider the evidence and arguments of both sides, allowing attorneys to prepare for the bulk of the cases currently being reviewed.
Data suggests physicians wrote millions of prescriptions for testosterone replacement medications and, some cases allege, to many men who did not need the topical treatment.
If you believe you’ve been injured by a testosterone gel or other treatment, contact an attorney who focuses on handling these cases.
NEW YORK – The U.S. Food and Drug Administration is asking companies for more safety data on testosterone drugs after a patient broke out in hives during a mid-stage trial.
According to Reuters, the FDA is becoming more cautious with testosterone drugs since it discovered a large percentage of patients didn’t get their hormone levels tested before or during treatment.
Reuters reports the FDA requested data on 350 patients exposed to QuickShot Testosterone, a drug introduced by Antares Pharma Inc. The pharmaceutical company reports it may have to submit more data based on its ongoing late-stage trial.
Antares is currently in the testing phase of QuickShot Testosterone and the government’s request for more data could delay its regulatory and marketing applications.
I would like to thank your firm for representing our family on behalf of my late husband. This whole process was, at times, difficult for us and sometimes painful. But, we were always in good hands as Brian and Maria are two of the hardest working and sincerest people I have ever had the pleasure of meeting. They did a tremendous job.