SARAFEM Safety Questions, SARAFEM Answers
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SARAFEM Safety Reports
Total SARAFEM reports: 2.SARAFEM FDA safety alerts: No.
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Consumer or non-health professional from UNITED STATES reported SARAFEM problem on June 04, 2007. Female patient, 25 years of age, weighting 110.0 lb, was diagnosed with prophylaxis, stress and was treated with SARAFEM. After drug was administered, patient experienced the following problems/side effects: anorexia, feeling abnormal, insomnia, irritability, suicidal ideation, weight decreased. SARAFEM dosage: unknown. Patient recovered.
SARAFEM problem was reported by a Health Professional from UNITED STATES on Aug 09, 2006. Female patient, 46 years of age, weighting 130.0 lb, was diagnosed with premenstrual syndrome, attention deficit/hyperactivity disorder and was treated with SARAFEM. After drug was administered, patient experienced the following problems/side effects: apathy, blepharospasm, dyskinesia, eyelid function disorder, facial pain, feeling abnormal, hallucination, visual, headache. SARAFEM dosage: 10 MG 1X DAILY PO. During the same period patient was treated with CONCERTA, MAXALT, NAPROXEN, RENOVA, EXCEDRINE EXTRA STRENGTH. Patient recovered.