HYGROTON Safety Questions, HYGROTON Answers
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HYGROTON Safety Reports
Total HYGROTON reports: 2.HYGROTON FDA safety alerts: No.
Reported hospitalizations: 1.
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Consumer or non-health professional from SWITZERLAND reported HYGROTON problem on Aug 19, 2005. Male patient, 75 years of age, was diagnosed with hypertension, back pain, calcium metabolism disorder, nail tinea and was treated with HYGROTON. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, dehydration, diarrhoea, focal glomerulosclerosis, hypovolaemia, nephrosclerosis, rash macular, renal failure acute, renal failure chronic. HYGROTON dosage: 75 MG,/ WEEK UNK. During the same period patient was treated with VOLTAREN, AREDIA, LAMISIL, BRUFEN, ENATEC, NOVALGIN, ALLOPURINOL, TRYPTIZOL. Patient was hospitalized. Patient recovered.
HYGROTON problem was reported by a Consumer or non-health professional from CROATIA (local name: Hrvatska) on July 02, 2007. Male patient, 45 years of age, was diagnosed with hypertension and was treated with HYGROTON. After drug was administered, patient experienced the following problems/side effects: vision blurred. HYGROTON dosage: 1 X 12.5 MG, ORAL. Patient recovered.