|
Index of reports
> Cases resulting in life threatening events (12)
> Cases with Pharmaceutical Product Complaint (3)
Below is the selection of adverse event reports related to Wellbutrin XL (Bupropion) that includes cases resulting in life threatening events where reactions include pharmaceutical product complaint.
Adverse event in 48 year old female receiving Wellbutrin XL (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-10-22
Patient: 48 year old female
Adverse reactions / side effects: Dysarthria, Pharyngeal Oedema, Swollen Tongue, Pharmaceutical Product Complaint
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Wellbutrin XL (Bupropion)
Other drugs received by patient: Celexa
Adverse event in 48 year old female receiving Wellbutrin XL (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-10-02
Patient: 48 year old female
Adverse reactions / side effects: Dysarthria, Pharyngeal Oedema, Swollen Tongue, Pharmaceutical Product Complaint
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Wellbutrin XL (Bupropion)
Other drugs received by patient: Celexa
Adverse event in 33 year old female receiving Wellbutrin XL (Bupropion)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-01
Patient: 33 year old female, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Drug Ineffective, Therapeutic Response Unexpected With Drug Substitution, Depression, Drug Withdrawal Syndrome, Pharmaceutical Product Complaint, Suicidal Ideation
Adverse event resulted in: life threatening event
Suspect drug(s):
Bupropion HCL
Dosage: 300 mg 1x per day po
Administration route: Oral
Indication: Depression
Start date: 2006-12-27
End date: 2007-01-30
Wellbutrin XL
|
