Index of reports
> Cases with Product Quality Issue (2)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Parnate (Tranylcypromine) where reactions include product quality issue. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Parnate side effects in female
Reported by a consumer/non-health professional from Brazil on 2011-12-29
Patient: female, weighing 95.0 kg (209.0 pounds)
Reactions: Product Quality Issue, Nightmare, Nausea, Drug Ineffective, Somnolence, Hunger, Weight Increased, Anxiety, Depression, Depressed Mood, Panic Reaction, Crying
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Parnate
Dosage: 10mg twice per day
Administration route: Oral
Start date: 2011-05-30
Parnate
Dosage: 10mg three times per day
Administration route: Oral
Start date: 2011-07-02
Parnate
Dosage: 10mg four times per day
Administration route: Oral
Start date: 2011-08-01
Parnate
Indication: Depression
Start date: 2010-01-01
Other drugs received by patient: Dolamin; Clonazepam
Possible Parnate side effects in female
Reported by a consumer/non-health professional from Brazil on 2011-12-22
Patient: female, weighing 95.0 kg (209.0 pounds)
Reactions: Product Quality Issue, Nightmare, Nausea, Drug Ineffective, Somnolence, Hunger, Anxiety, Weight Increased, Depression, Depressed Mood, Panic Reaction, Crying
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Parnate
Dosage: 10mg three times per day
Administration route: Oral
Start date: 2011-07-02
Parnate
Dosage: 10mg four times per day
Administration route: Oral
Start date: 2011-08-01
Parnate
Indication: Depression
Start date: 2010-01-01
Parnate
Dosage: 10mg twice per day
Administration route: Oral
Start date: 2011-05-30
Other drugs received by patient: Dolamin; Clonazepam
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