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DIGITEK Safety Reports
Total DIGITEK reports: 2.DIGITEK FDA safety alerts: No.
Reported hospitalizations: 2.
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Pharmacist from UNITED STATES reported DIGITEK problem on May 25, 2007. Female patient, 88 years of age, was diagnosed with atrial fibrillation, hypertension and was treated with DIGITEK. After drug was administered, patient experienced the following problems/side effects: bradycardia, hyperkalaemia, oral intake reduced, renal failure acute, therapeutic agent toxicity. DIGITEK dosage: 0.125MG DAILY PO. During the same period patient was treated with METOPROLOL SUCCINATE, SYNTHROID, CELEBREX, COUMADIN, ALLOPURINOL, METOPROLOL SUCCINATE, SIMETHICONE. Patient was hospitalized. Patient recovered.
DIGITEK problem was reported by a Physician from UNITED STATES on Feb 16, 2006. Male patient, 70 years of age, weighting 174.0 lb, was diagnosed with blood iron increased and was treated with DIGITEK. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood bilirubin increased, blood creatinine increased, blood glucose abnormal, blood urea increased, blood urine present, brain natriuretic peptide abnormal, cardiac failure congestive, dehydration. DIGITEK dosage: unknown. During the same period patient was treated with METFORMIN, LISINOPRIL, PANTOPRAZOLE, LASIX, COREG, EXJADE. Patient was hospitalized. Patient recovered.