RENITEC Safety Questions, RENITEC Answers
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RENITEC Safety Reports
Total RENITEC reports: 2.RENITEC FDA safety alerts: No.
Reported hospitalizations: 2.
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Consumer or non-health professional from SWEDEN reported RENITEC problem on Mar 27, 2007. Female patient, 80 years of age, was treated with RENITEC. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood potassium increased, chest pain, depressed level of consciousness, dialysis, hypoglycaemia, lactic acidosis, nausea, pyrexia. RENITEC dosage: unknown. During the same period patient was treated with ZOCOR, GLUCOPHAGE, ALLOPURINOL, LANACRIST, GLYBURIDE, IMDUR. Patient was hospitalized. Patient recovered.
RENITEC problem was reported by a Consumer or non-health professional from FRANCE on Aug 31, 2006. Female patient, child 10 years of age, was diagnosed with hypertension, facial neuralgia and was treated with RENITEC. After drug was administered, patient experienced the following problems/side effects: fall, fluid intake restriction, hyponatraemia, pain. RENITEC dosage: 5 MG, QD. During the same period patient was treated with TEGRETOL, ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.