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Femigoa FDA adverse reports: 1. View All Femigoa FDA Adverse Reports

Femigoa FDA safety alerts: No

Reported hospitalizations: 1

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Femigoa Side Effects Report: 4602834-7,Blood Creatine Phosphokinase Increased, Intentional Misuse
on Feb 28, 2005 Female patient from , , 17 years of age, was treated with Femigoa. After Femigoa was administered, patient had the following side effects: Femigoa and blood creatine phosphokinase increased, Femigoa and intentional misuse. Femigoa dosage: Oral. During the same period patient was treated with ALCOHOL, COTRIMTE, IBUPROFEN, PARACETAMOL, PENICILLIN. Patient was hospitalized.


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