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drug_recall aravaMedWatch is the FDA''s program that allows consumers to report serious reactions and problems with medical products. So far, there have been at least 130 cases of severe liver problems (hepatoxicity) and 22 deaths since Arava''s arrival to the market in 1998. It is estimated that there is a 10-100 fold of underreporting that occurs with a drug''s adverse effects. Not reporting serious adverse Arava side effects can result in continued instances of death and serious health conditions that may have been prevented. If you, or a family member, have suffered the serious and potentially deadly Arava side effects, it is encouraged for you to report it, and there are several different reporting options available./p>
Your health care provider or the FDA online reporting form allows consumers to notify the FDA of important and useful information regarding patient safety. The FDA''s MedWatch has outlined the injuries that constitute a serious adverse event. If you, or a family member, have experienced any of these adverse Arava side effects you are encouraged to report it to the FDA. To learn your legal rights regarding Arava, contact us to receive your free consultation with an expert Arava attorney.
When FDA medical reviewer David Graham told lawmakers during a congressional hearing on the recall of Vioxx that drugs require stricter safety evaluations, he didn''t stop there. Graham named five other drugs currently on the market that he belie...