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Maintate Side Effects submitted to FDA
Total Maintate reports: 2.Maintate FDA safety alerts: No.
Reported hospitalizations: 2.
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Maintate Side Effects Report #5661617-X
Physician from JAPAN reported MAINTATE problem on Mar 03, 2008. Female patient, 68 years of age, weighting 141.1 lb, was diagnosed with hypertension, lipids abnormal, lacunar infarction and was treated with MAINTATE. After drug was administered, patient experienced the following problems/side effects: anti-platelet antibody positive, bleeding time prolonged, blood pressure increased, epistaxis, haemoptysis, haemorrhage subcutaneous, megakaryocytes decreased, platelet count decreased, thrombocytopenia. MAINTATE dosage: 2.5 MG/DAY. During the same period patient was treated with FLUVASTATIN, NORVASC, ASPIRIN, DIOVAN, DEPAS. Patient was hospitalized. Patient recovered.
Maintate Side Effects Report #5713844-0
MAINTATE problem was reported by a Consumer or non-health professional from JAPAN on Apr 07, 2008. Male patient, 39 years of age, was treated with MAINTATE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, continuous haemodiafiltration, oliguria, pleural effusion, pulmonary congestion, renal failure, shock, somnolence. MAINTATE dosage: 150 MG (150 MG, 1 IN 1 D). During the same period patient was treated with AMLODIPINE. Patient was hospitalized. Patient recovered.
Maintate Side Effects


