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Tylenol Recall
Motrin Recall
FDA Stevens Johnson Syndrome Ibuprofen Citizen Petition
FDA Recommended Changes to the Ibuprofin/Motrin Labels
Motrin Prescription Label Never Published by McNeil or J&J
Report adverse events to FDA's MedWatch reporting system by completing a form on line at FDA's MedWatch
Faxing (1-800-FDA-0178) Mail using the postage-paid address form provided on line (5600 Fishers Lane, Rockville, MD 20853-9787) Telephone (1-800-FDA-1088)
Preventable Adverse Drug Reactions
Over 2 MILLION serious ADRs yearly
100,000 DEATHS yearly
ADRs 4th leading cause of death ahead of pulmonary disease, diabetes, AIDS, pneumonia, accidents and automobile deaths
Nursing home patients
ADR rate 350,000 yearly
Institute of Medicine, National Academy Press, 2000
Stevens-Johnson Info:
Dangerous Prescription
Watch the Full Program Online
FRONTLINE: Dangerous Prescription
Producer, writer and director Andy Liebman was online (washingtonpost.com) to discuss the film and the likelihood of harmful drugs making it through the FDA approval process. View their discussion
FAQs & Links
Frequently asked questions about the FDA and drug safety, with links to resources for consumers and further reading.
