Takepron and malaise Patient Reports February 13, 2012

Takepron Side Effects Report #5728425-2
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Apr 24, 2008. Female patient, 76 years of age, was diagnosed with gastric ulcer, osteoporosis  and was treated with Takepron. After drug was administered, patient experienced the following side effects: agranulocytosis, disseminated intravascular coagulation, hepatic necrosis, hepatitis acute, malaise, neutrophil count decreased, septic shock, staphylococcal infection , white blood cell count decreased. Takepron dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with FOSAMAC, PREDNISOLONE, MAGNESIUM OXIDE. Patient died.

Takepron Side Effects Report #4976154-5
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Mar 28, 2006. Male patient, 63 years of age, was diagnosed with gastric ulcer, gastric disorder, prophylaxis and was treated with Takepron. After drug was administered, patient experienced the following side effects: facial palsy, haematuria, haemodialysis, malaise, nephrosclerosis, renal failure acute, tubulointerstitial nephritis. Takepron dosage: 30 MG (30 MG, 1 IN 1 D). During the same period patient was treated with RABEPRAZOLE. Patient recovered.