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Arava was approved by the U.S. Food and Drug Administration on September 11, 1998 for the treatment of active rheumatoid arthritis in adults.
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Arthritis Drug Should Be Removed From Market Arava Linked to Liver Complications and Deaths, Public Citizen Tells FDA WASHINGTON, D.C.
Adverse event resulted in: hospitalization. Suspect drug(s): Arava Administration route: Oral Indication: Rheumatoid Arthritis Start date: 2008-05-08. End date:
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Approved by the Food and Drug Administration in September 1998, Arava is used to treat rheumatoid arthritis. It is known as a disease modifying antirheumatic
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Following a Food and Drug Administration review of possible side effects related to the arthritis drug Arava, the drug's maker, Sanofi-Aventis,
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FDA Panel Scrutinizes Safety Of 4 Rheumatoid Arthritis Drugs. The risk versus benefit of Arava, Enbrel, Remicade, and Humira is reconsidered. By Carol Eustice
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