According to a recent drug safety communication issues by the Food and Drug Administration (FDA) the use of Nizoral (Ketoconazole) can result in severe medical side effects including damage to the liver and adrenal glands. Liver injury caused by the use of Nizoral can be so severe as to require a liver transplant and can result in death. The attorneys form our drug defect law firm are currently investigating legal option for individuals who have suffered medical complications due to the use on Nizoral. To report you incident to our law firm for investigation and a thorough case evaluation contact our law offices toll free by calling (855)385-2529. All consultations are free of charge.
Ketoconazole (sold under the trade names Nizoral, Extina, Xolegel and Kuric) is an anti-fungal medication developed for the prevention and reduction in the growth of fungus. The FDA originally approved the use of the anti fungus medication in 1981.
Some of the most Severe Side Effects from the Used of Nizoral Are As Follows:
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FDA Warning Limited Use of Nizoral: The FDA has recommended the elimination of the use of Nizoral as a first-line treatment for most fungal infections. According to the FDA, Nizoral tablets should be used only for the treatment of certain life-threatening mycoses when the potential benefits outweigh the risks and alternative therapeutic options are not available or tolerated.” For more information regarding FDA warnings regarding Nizoral see here.
Lawsuits filed against giant pharmaceutical drug makers for unsafe drugs are usually predicated on a product liability tort action. Defective product cases wrest on proving one of three distinct causes of action.
1. Defect in the original design of the drug: Evidence of the failure of the drug manufacturers to implement current drug designs with a substantially lower risk of severe side effects is an important factor in proving the presence of a design defect in the court of law.
2. Defect in the manufacturing process of the drug: Manufacturing defect can be established when the final produced and distributed drug is markedly different and as a result substantially more dangerous than the original safer design.
3. Labeling defect also known as failure to warn: Drug manufacturers owe a duty to warn consumers of their products of all known and knowable risk factors associated with the use if their products. All too often drug companies intentionally fail to place proper warning information on their product in an attempt to maintain the sale of their product.
A statute of limitations is a time period an individual have to file a claim against at fault parties in the court of law. The specific statute of limitations for your case will depend in the jurisdiction where you live. Failure to file a claim within the time period can eliminate your right to recovery in the court of law. For the statute of limitations for all 50 states and jurisdictions across the country see here.
Victims of dangerous drug side effects are entitled to full and just compensation for all their losses. The potential value of a lawsuit for injuries caused by the use of Nizoral are based on several significant factors including
Legal Assistance: If you wish to discuss your case against the manufacturers of Nizoral contact our attorneys toll free by calling (855)385-2529. All consultations are free of charge and confidential.
Further Information: Nizoral Lawsuit – Class Action Claim Infomration
Over $500 Million Recovered
for Our Clients
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