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Index of reports
> Serious Events (3)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Aplenzin (Bupropion) serious events. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Aplenzin side effects in male
Reported by a consumer/non-health professional from United States on 2012-05-31
Patient: male, weighing 97.5 kg (214.6 pounds)
Reactions: Atrial Fibrillation
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Diltiazem HCL
Dosage: (120 mg, daily oral), (240 mg, daily oral)
Administration route: Oral
Indication: Atrial Fibrillation
Start date: 2011-09-01
Aplenzin
Dosage: (522 mg qd)
Indication: Depression
Start date: 2009-12-01
Other drugs received by patient: Ramipril; Simvastatin; Zolpidem; Atorvastatin Calcium
Possible Aplenzin side effects in female
Reported by a physician from United States on 2012-02-27
Patient: female
Reactions: Product Substitution Issue, NO Therapeutic Response, Condition Aggravated, Depression
Drug(s) suspected as cause:
Wellbutrin
Dosage: 300mg qd
Aplenzin
Dosage: 348 q day
Other drugs received by patient: Lamictal
Possible Aplenzin side effects in 55 year old female
Reported by a consumer/non-health professional from United States on 2011-10-17
Patient: 55 year old female, weighing 68.0 kg (149.7 pounds)
Reactions: Photosensitivity Reaction, Urticaria, Rash
Drug(s) suspected as cause:
Aplenzin
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