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ULCEX Safety Reports

Total ULCEX reports: 1.
ULCEX FDA safety alerts: 2005 2006 .
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Health Professional from ITALY reported ULCEX problem on June 07, 2007. Male patient, 64 years of age, was diagnosed with dyslipidaemia and was treated with ULCEX. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood creatinine increased, blood urea increased, haemoglobinuria, proteinuria, renal failure. ULCEX dosage: 150 MG/D. During the same period patient was treated with DIURESIX, CARDURA, ASPIRIN, LESCOL. Patient recovered.

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