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Index of reports
> Serious Events (5)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Glucophage XR (Metformin) serious events. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Glucophage XR side effects in female
Reported by a consumer/non-health professional from United States on 2012-07-03
Patient: female
Reactions: Weight Decreased, Flatulence, Adrenal Neoplasm, Cardiac Disorder
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Glucophage XR
Other drugs received by patient: Metoprolol Succinate
Possible Glucophage XR side effects in female
Reported by a consumer/non-health professional from United States on 2012-05-22
Patient: female
Reactions: Vomiting, Syncope, Anaemia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Glucophage XR
Possible Glucophage XR side effects in 84 year old female
Reported by a consumer/non-health professional from United States on 2012-02-08
Patient: 84 year old female, weighing 77.0 kg (169.4 pounds)
Reactions: Diarrhoea, Anaemia, Feeling Hot, Rash Pruritic
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Aspirin
Dosage: 1 df : 2 nos
Glucophage XR
Dosage: several years ago,1000-1500 mg/daily,2 pills in mrng, 1 pill in evening
Administration route: Oral
Indication: Type 2 Diabetes Mellitus
Start date: 2002-08-05
Other drugs received by patient: Lotrel; Vitamin; Lipitor
Possible Glucophage XR side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2011-11-23
Patient: female, weighing 71.7 kg (157.7 pounds)
Reactions: Product Quality Issue, Drug Ineffective, Blood Glucose Increased
Drug(s) suspected as cause:
Glucophage XR
Possible Glucophage XR side effects in 40 year old male
Reported by a consumer/non-health professional from Germany on 2011-10-20
Patient: 40 year old male, weighing 89.0 kg (195.8 pounds)
Reactions: Hypersensitivity, Upper Respiratory Tract Infection, Abasia, Chromaturia, Drug Interaction
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Glucophage XR
Dosage: 1df:1 tabs of 500mg
Administration route: Oral
Indication: Metabolic Disorder
Start date: 2011-01-01
Cefuroxime
Dosage: stopped
Administration route: Oral
Indication: Respiratory Tract Infection
Start date: 2011-01-01
Other drugs received by patient: Losartan Potassium
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