https://www.medlegal360.com/amiodarone-lawsuits/
Amiodarone is an anti-arrhythmic drug that helps people with life-threatening ventricular arrhythmias, including ventricular fibrillation and ventricular tachycardia, regulate their heartbeats. In cases where previous medications have failed to control the condition and life-threatening cardiac rhythm abnormalities are present, patients may be given amiodarone.
Amiodarone should only be used as a last resort when other drugs or treatments have failed, according to the FDA. This is because the medication has fatal side effects, such as liver damage, blindness, depression, damage to the spinal cord nerves, and lung failure. Many people filed wrongful death lawsuits against the drug manufacturers.
Amiodarone has been sold under the trade names Cordarone, Pacerone, and Nexterone. Many pharmaceutical companies, including Teva Pharmaceuticals, Wyeth-Ayerst Laboratories, Upsher-Smith Pharmaceuticals, etc., have marketed it. Wyeth initially produced and distributed amiodarone, but in 1998, the FDA authorised Sandoz and Upsher-Smith to market and sell generic copies of the drug. While Upsher-Smith branded its medicine Pacerone, Sandoz referred to its medication as amiodarone hydrochloride, which is also its generic name.
The FDA reports that Mylan has recalled four lots of both tranexamic acid injection and amiodarone HCl injection. Between April and July 2020, these lots were awarded to hospitals and nursing facilities in the United States. The vials were intended for medical purposes.
You might be entitled to compensation for your pain and suffering, medical costs, lost wages, and more if you meet the requirements to take part in amiodarone lawsuits. Participating in amiodarone lawsuits could help you hold the producer of the medication responsible for alleged negligence and failing to warn patients about the medication's hazards.
Most lawsuits involving amiodarone brought against the manufacturer involve personal injury allegations. You must provide evidence that your personal harm was brought on by the product's inferior design, negative side effects, or misleading marketing. Additionally, you must demonstrate that you received insufficient information regarding the risks associated with the medication.
It is critical that your doctor updates your medical record if you experience side effects that call for modifying your prescription or reducing the dosage. You can verify medical records with the assistance of a company that reviews medical records, which is vital in injury claims.
