Actonel and dehydration Patient Reports February 13, 2012

Actonel Side Effects Report #5087203-0
Actonel side effect was reported by a Physician from ESTONIA on Aug 07, 2006. Female patient, 68 years of age, weighting 154.3 lb, was diagnosed with osteoporosis postmenopausal and was treated with Actonel. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, alveolitis, aspartate aminotransferase increased, asthenia, blood creatinine increased, blood potassium increased, blood sodium decreased, dehydration, dementia . Actonel dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with CARDACE, GASEC, MEDROL, IMURAN. Patient was hospitalized. Patient died on 07/11/2006.

Actonel Side Effects Report #6055924-9
Actonel side effect was reported by a Health Professional from FRANCE on Jan 15, 2009. Female patient, 72 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: abdominal pain upper, dehydration, dysphagia, haematemesis, malnutrition, necrotising oesophagitis, vomiting. Actonel dosage: 35 MG, 1 /WEEK, ORAL. During the same period patient was treated with PAROXETINE HYDROCHLORIDE, MYLASTAN, ZOLPIDEM TARTRATE, TANAKAN, XYZALL, OROCAL D, NAFTIDROFURYL, PRAVASTATIN. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5726063-9
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on May 01, 2008. Female patient, 64 years of age, weighting 135.0 lb, was diagnosed with osteopenia and was treated with Actonel. After drug was administered, patient experienced the following side effects: abdominal pain upper, arthralgia, body temperature increased, dehydration, feeling abnormal, malaise, myalgia, nausea . Actonel dosage: 1 - 35 MG 1X/WEEK. Patient was hospitalized and became disabled. Patient recovered.

Actonel Side Effects Report #5708953-6
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 14, 2008. Female patient, 51 years of age, weighting 270.0 lb, was diagnosed with osteopenia and was treated with Actonel. After drug was administered, patient experienced the following side effects: dehydration, hypertension, migraine , nausea , tinnitus . Actonel dosage: unknown. Patient was hospitalized. Patient recovered.


Actonel Side Effects Report #5737037-6
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on May 12, 2008. Female patient, weighting 128.0 lb, was diagnosed with colitis ulcerative, osteoporosis prophylaxis and was treated with Actonel. After drug was administered, patient experienced the following side effects: anaemia, blood pressure decreased, dehydration, diarrhoea, frequent bowel movements, muscle spasms, rectal haemorrhage, weight decreased. Actonel dosage: 5 MG. ONE DAILY. During the same period patient was treated with MORPHINE, CLINORIL, NITROGLYCERIN, PENTASA. Patient recovered.

Actonel Side Effects Report #5483172-X
Actonel side effect was reported by a Health Professional from FRANCE on Sept 27, 2007. Female patient, 93 years of age, was treated with Actonel. After drug was administered, patient experienced the following side effects: blood creatine increased, blood urea increased, dehydration, eating disorder , hypernatraemia, somnolence. Actonel dosage: unknown. During the same period patient was treated with OLMESARTAN MEDOXOMIL, RISPERDAL, KARDEGIC. Patient was hospitalized. Patient died on 08/02/2007.