Didronel and haematemesis Patient Reports February 12, 2012

Didronel Side Effects Report #5043228-2
Didronel side effect was reported by a Health Professional from UNITED KINGDOM on June 19, 2006. Female patient, 83 years of age, was diagnosed with osteoporosis  and was treated with Didronel. After drug was administered, patient experienced the following side effects: haematemesis, nausea , ulcer . Didronel dosage: unknown. During the same period patient was treated with BENDROFLUMETHIAZIDE, OMACOR, RAMIPRIL. Patient was hospitalized. Patient recovered.

Didronel Side Effects Report #6128781-X
Didronel side effect was reported by a Pharmacist from GERMANY on Mar 09, 2009. Female patient, 69 years of age, weighting 108.0 lb, was diagnosed with osteoporosis , hepatic cirrhosis and was treated with Didronel. After drug was administered, patient experienced the following side effects: abdominal distension, activated partial thromboplastin time prolonged, gastrointestinal ulcer haemorrhage, haematemesis, haematocrit decreased, haemoglobin decreased, heart rate increased, hiatus hernia, melaena. Didronel dosage: 200 MG, 1 /DAY ORAL. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ALLOPURINOL, CALCIUM, SPIRONOLACTONE, XIPAMIDE. Patient was hospitalized. Patient recovered.