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UNIRETIC Safety Reports
Total UNIRETIC reports: 2.UNIRETIC FDA safety alerts: No.
Reported hospitalizations: 2.
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Consumer or non-health professional from UNITED STATES reported UNIRETIC problem on Nov 28, 2005. Female patient, 77 years of age, was diagnosed with hypertension, dementia alzheimer's type and was treated with UNIRETIC. After drug was administered, patient experienced the following problems/side effects: hyponatraemia. UNIRETIC dosage: unknown. During the same period patient was treated with MEMANTINE, DONEPEZIL, CLOPIDOGREL BISULPHATE, ACETYLSALICYLIC. Patient was hospitalized. Patient recovered.
UNIRETIC problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 24, 2007. Female patient, 57 years of age, weighting 280.0 lb, was diagnosed with hypertension and was treated with UNIRETIC. After drug was administered, patient experienced the following problems/side effects: asthenia, chest pain, condition aggravated, dyspnoea, feeling abnormal, heart rate irregular, hypertension, tinnitus. UNIRETIC dosage: unknown. Patient was hospitalized. Patient recovered.