Takepron and blood pressure decreased Patient Reports February 09, 2010

Takepron Side Effects Report #4749209-8
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Aug 12, 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, depressed level of consciousness, exchange blood transfusion, haemolytic anaemia, infection in an immunocompromised host, pneumonia , pyrexia, respiratory disorder. Takepron dosage: 60 MG (60 MG, 1 D), PER ORAL. During the same period patient was treated with TAKEPRON OD, CLARITHROMYCIN, SAWASILLIN. Patient was hospitalized. Patient died.

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 #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.