Takepron and blood creatine phosphokinase increased Patient Reports February 13, 2012

Takepron Side Effects Report #5269674-X
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Mar 09, 2007. Female patient, 68 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, myalgia. Takepron dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with NEUROTROPIN. Patient was hospitalized. Patient recovered.

Takepron Side Effects Report #5020490-3
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on May 22, 2006. Male patient, 61 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, muscular weakness. Takepron dosage: 15 MG (15 MG, 1 - 1 D) PER ORAL. During the same period patient was treated with OMEPRAZOLE, ASPIRIN, PLETAL, MUCOSTA. Patient was hospitalized. Patient recovered.

Takepron Side Effects Report #5402854-9
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on July 23, 2007. Male patient, 56 years of age, was diagnosed with gastric ulcer and was treated with Takepron. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, oedema peripheral. Takepron dosage: 15 MG (15 MG, 1 IN 1 D); PER ORAL. During the same period patient was treated with LANSAP. Patient was hospitalized. Patient recovered.