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DIART Safety Reports
Total DIART reports: 3.DIART FDA safety alerts: No.
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Health Professional from JAPAN reported DIART problem on Feb 05, 2007. Male patient, weighting 135.9 lb, was treated with DIART. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, glycosylated haemoglobin increased, renal impairment. DIART dosage: 45 MG. During the same period patient was treated with MEILAX, AMOBAN, AZUCURENIN S, NITOROL, COMELIAN, TENAXIL, DIACORT. Patient recovered.
DIART problem was reported by a Health Professional from JAPAN on Apr 13, 2007. Male patient, weighting 135.9 lb, was treated with DIART. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, glycosylated haemoglobin increased, renal impairment. DIART dosage: 45 MG. During the same period patient was treated with MEILAX, AMOBAN, AZUCURENIN S, NITOROL, COMELIAN, TENAXIL, DIACORT. Patient recovered.
Health Professional from JAPAN reported DIART problem on May 28, 2007. Male patient, weighting 135.9 lb, was treated with DIART. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, glycosylated haemoglobin increased, renal impairment. DIART dosage: 45 MG. During the same period patient was treated with MEILAX, AMOBAN, AZUCURENIN S, NITOROL, COMELIAN, TENAXIL, DIACORT. Patient recovered.