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Index of reports
> Disability (4)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Prolixin (Fluphenazine) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Prolixin side effects in female
Reported by a consumer/non-health professional from United States on 2012-03-30
Patient: female, weighing 86.2 kg (189.6 pounds)
Reactions: Weight Increased, Syncope, Visual Acuity Reduced, Mental Retardation, Unevaluable Event, Unemployment
Adverse event resulted in: life threatening event, disablity
Drug(s) suspected as cause:
Prolixin
Risperidol / Alonzopin
Dosage: 25mg- fried me shots
Start date: 1983-01-01
End date: 1984-01-01
Depakote
Haldol
Dosage: 25 mg - 100mg fried me shots
Start date: 1997-01-01
End date: 1998-01-01
Possible Prolixin side effects in male
Reported by a consumer/non-health professional from United States on 2012-03-11
Patient: male
Reactions: Hypersensitivity, Drug Interaction, Cardiac Disorder, Brain Injury, Mental Impairment, Overdose, Mental Disability, Nervous System Disorder, Tardive Dyskinesia, Neuroleptic Malignant Syndrome, Myocardial Infarction
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Fluphenazine
Indication: Mental Disorder
Seroquel
Indication: Mental Disorder
Fluphenazine
Indication: Anxiety Disorder
Seroquel
Indication: Anxiety Disorder
Prolixin
Indication: Mental Disorder
Prolixin
Indication: Anxiety Disorder
Possible Prolixin side effects in male
Reported by a consumer/non-health professional from United States on 2012-03-09
Patient: male, weighing 100.7 kg (221.5 pounds)
Reactions: Medication Error, Paralysis
Adverse event resulted in: life threatening event, hospitalization, disablity
Drug(s) suspected as cause:
Haldol
Dosage: 1/st injec
Start date: 1986-01-01
End date: 1987-01-01
Prolixin
Dosage: 2 times inject
Start date: 1987-01-01
Possible Prolixin side effects in female
Reported by a individual with unspecified qualification from United States on 2011-12-15
Patient: female
Reactions: Dyskinesia, Drug Hypersensitivity
Adverse event resulted in: life threatening event, disablity
Drug(s) suspected as cause:
Benadryl
Dosage: 100 mg once shot
Indication: Dysphonia
Start date: 2011-11-21
Prolixin
Dosage: 10 mg. once shot
Indication: Dysphonia
Start date: 2011-11-21
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