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Index of reports
> Hospitalization (2)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Bextra (Valdecoxib) hospitalization. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Bextra side effects in male
Reported by a consumer/non-health professional from United States on 2012-05-24
Patient: male
Reactions: Nausea, Suicidal Ideation, Weight Increased, Mood Altered, Heart Rate Increased, Chest Pain, Dizziness, Depression, Heart Rate Irregular, Myocardial Infarction
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Bextra
Dosage: unk
Indication: Arthritis
Start date: 2003-11-05
End date: 2004-10-22
Bextra
Dosage: 10 mg, 1x/day
Bextra
Dosage: 20 mg, 1x/day
Possible Bextra side effects in female
Reported by a consumer/non-health professional from United States on 2012-02-14
Patient: female
Reactions: Pneumonia, Coronary Artery Disease, Bundle Branch Block Left, Congestive Cardiomyopathy, Cardiomegaly, Respiratory Failure, Mitral Valve Incompetence, Left Atrial Dilatation, Cardiac Failure Congestive
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Bextra
Dosage: 20 mg, 2x/day
Indication: Antiinflammatory Therapy
Start date: 2004-03-24
Bextra
Dosage: 20 mg, 2x/day
Indication: Musculoskeletal Pain
Start date: 2004-05-20
Bextra
Dosage: 20 mg, 2x/day
Indication: Back Pain
Start date: 2004-10-08
Other drugs received by patient: Levoxyl; Glucophage; Amaryl; Neurontin
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