Takepron and altered state of consciousness Patient Reports February 13, 2012

Takepron Side Effects Report #6068803-8
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Jan 26, 2009. Male patient, 81 years of age, was diagnosed with helicobacter infection, diabetes mellitus and was treated with Takepron. After drug was administered, patient experienced the following side effects: altered state of consciousness, blood glucose increased, diarrhoea, duodenal ulcer perforation, gastrointestinal ulcer, glycosylated haemoglobin increased, heart rate decreased, hyperhidrosis. Takepron dosage: 30 MG (30 MG, 1 OM 1 D) PER ORAL, 60 MG MG (30 MG, 2 IN 1 D) PER ORAL. During the same period patient was treated with TAKEPRON OD, TAKEPRON OD, GLYBURIDE, CLARITIN. Patient was hospitalized. Patient recovered.

Takepron Side Effects Report #5603402-0
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Jan 16, 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, altered state of consciousness, blood culture positive, disseminated intravascular coagulation, faecal incontinence, neutrophil count decreased, septic shock, staphylococcal infection , urinary incontinence . Takepron dosage: 30 MG (30 MG, 1 - 2) 35 MG (35 MG, 1 - 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 #5676750-6
Takepron side effect was reported by a Health Professional from JAPAN on Mar 12, 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, altered state of consciousness, antinuclear antibody positive, blood pressure decreased, disseminated intravascular coagulation, faecal incontinence, hepatic necrosis, hepatitis acute, malaise. Takepron dosage: 30 MG (30 MG,1 IN 1 D). During the same period patient was treated with FOSAMAX, PREDNISOLONE, MAGNESIUM OXIDE. Patient died.

Takepron Side Effects Report #5912838-X
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Sept 26, 2008. Male patient, 81 years of age, was diagnosed with duodenal ulcer, helicobacter infection, diabetes mellitus and was treated with Takepron. After drug was administered, patient experienced the following side effects: altered state of consciousness, blood glucose increased, diarrhoea, duodenal perforation, heart rate decreased, helicobacter infection, hyperhidrosis, hypoglycaemia, hypophagia. Takepron dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with TAKEPRON OD, GLYBURIDE, CLARITHROMYCIN, SWACILLIN. Patient was hospitalized. Patient recovered.