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Madopar Side Effects submitted to FDA
Total Madopar reports: 3.Madopar FDA safety alerts: No.
Reported deaths: 3 Reported hospitalizations: 1.
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FDA Reported Madopar Side Effects: liver disorder, leukopenia, blood lactate dehydrogenase increased, aspartate aminotransferase increased, anorexia, alanine aminotransferase increased,
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Madopar Side Effects Report #5486282-6
Consumer or non-health professional from ITALY reported MADOPAR problem on Oct 11, 2007. Male patient, 70 years of age, was diagnosed with parkinson's disease and was treated with MADOPAR. After drug was administered, patient experienced the following problems/side effects: completed suicide. MADOPAR dosage: 1025 MG/DAY. During the same period patient was treated with APOMORPHINE HYDROCHLORIDE, LEXOTAN, COMTAN. Patient died.
Madopar Side Effects Report #5497033-3
MADOPAR problem was reported by a Consumer or non-health professional from ITALY on Oct 22, 2007. Male patient, 70 years of age, was diagnosed with parkinson's disease and was treated with MADOPAR. After drug was administered, patient experienced the following problems/side effects: completed suicide. MADOPAR dosage: 1025 MG/DAY. During the same period patient was treated with APOMORPHINE HYDROCHLORIDE, LEXOTAN, COMTAN. Patient died.
Madopar Side Effects Report #5502581-3
Consumer or non-health professional from ITALY reported MADOPAR problem on Oct 26, 2007. Male patient, 70 years of age, was diagnosed with parkinson's disease and was treated with MADOPAR. After drug was administered, patient experienced the following problems/side effects: completed suicide. MADOPAR dosage: 1025 MG/DAY. During the same period patient was treated with APOMORPHINE HYDROCHLORIDE, LEXOTAN, COMTAN. Patient died.
Madopar Side Effects


