Takepron and condition aggravated Patient Reports February 09, 2010

Takepron Side Effects Report #5147199-X
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Oct 31, 2006. Male patient, 78 years of age, was diagnosed with gastrointestinal haemorrhage and was treated with Takepron. After drug was administered, patient experienced the following side effects: condition aggravated, diabetic nephropathy, disease progression, renal impairment. Takepron dosage: 15 MG PER ORAL. During the same period patient was treated with FERROMIA, AMINOFLUID, LACTEC. Patient recovered.

Takepron Side Effects Report #4758070-7
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Aug 25, 2005. Female patient, 79 years of age, was diagnosed with gastritis erosive, helicobacter infection and was treated with Takepron. After drug was administered, patient experienced the following side effects: acidosis, blood pressure decreased, condition aggravated, depressed level of consciousness, gastritis erosive, haemolytic anaemia, no therapeutic response, pneumonia , respiratory disorder. Takepron dosage: unknown. During the same period patient was treated with TAKEPRON OD, TAKEPRON OD, TAKEPRON OD, CLARITHROMYCIN, SAWASILLIN. Patient was hospitalized. Patient died.

Takepron Side Effects Report #4573917-5
Takepron side effect was reported by a Physician from on Jan 27, 2005. Male patient, 72 years of age, was diagnosed with gastric cancer, gastric ulcer haemorrhage and was treated with Takepron. After drug was administered, patient experienced the following side effects: abdominal pain upper, anuria, ascites, blood pressure increased, blood urine present, condition aggravated, gastric haemorrhage, haemodialysis. Takepron dosage: 30 MG (15 MG 2 IN 1 D). During the same period patient was treated with ACTOS, GLIMEPIRIDE, BROTIZOLAM. Patient recovered.