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Index of reports
> Cases resulting in disability (10)
Below is the selection of adverse event reports related to Prozac (Fluoxetine) that includes cases resulting in disability.
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a physician from United States on 2007-05-22
Patient: female
Adverse reactions / side effects: Vomiting, HIP Dysplasia, Dyslexia, Constipation, Drug Exposure During Pregnancy, Developmental Delay, Learning Disability, Enamel Anomaly, Hypotonia, Feeding Disorder Neonatal
Adverse event resulted in: disablity
Suspect drug(s):
Prozac (Fluoxetine)
Other drugs received by patient: Paxil
Adverse event in 44 year old male receiving Prozac (Fluoxetine)
Reported by a physician from United Kingdom on 2007-05-09
Patient: 44 year old male
Adverse reactions / side effects: Flat Affect, Sexual Dysfunction
Adverse event resulted in: disablity
Suspect drug(s):
Prozac
Dosage: 20 mg, unk
Administration route: Oral
Indication: Depression
Start date: 1999-03-26
End date: 1999-08-31
Prozac
Dosage: 20 mg, unk
Administration route: Oral
Start date: 1999-11-16
End date: 2000-08-11
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from United States on 2007-05-02
Patient: female
Adverse reactions / side effects: Vomiting, Abasia, Dyslexia, Constipation, Eating Disorder, Developmental Delay, Drug Exposure During Pregnancy, Learning Disability, Hypotonia, Enamel Anomaly
Adverse event resulted in: disablity
Suspect drug(s):
Paxil
Dosage: 20mg per day
Start date: 1999-01-01
End date: 2000-01-01
Prozac
Dosage: 10mg per day
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from United States on 2007-04-09
Patient: female, weighing 75.3 kg (165.7 pounds)
Adverse reactions / side effects: Condition Aggravated, Depression
Adverse event resulted in: disablity
Suspect drug(s):
Prozac (Fluoxetine)
Adverse event in 48 year old female receiving Prozac (Fluoxetine)
Reported by a physician from France on 2007-03-19
Patient: 48 year old female
Adverse reactions / side effects: Tendonitis
Adverse event resulted in: disablity
Suspect drug(s):
Prozac (Fluoxetine)
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a individual with unspecified qualification from United States on 2007-02-15
Patient: female, weighing 73.5 kg (161.7 pounds)
Adverse reactions / side effects: Wrist Fracture, Fracture, Osteopenia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Prozac (Fluoxetine)
Adverse event in 47 year old female receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from Brazil on 2007-02-05
Patient: 47 year old female
Adverse reactions / side effects: Tumour Necrosis, Hypersensitivity, Drug Ineffective, Flatulence, Abasia, Urinary Incontinence, Constipation, Erythema, Obstructive Uropathy, Abdominal Pain Upper, Weight Increased, Oral Mucosal Discolouration, Malaise, Dyspepsia, Depression, Kidney Infection, Thrombocytopenia, Metastases TO Lung, Immunosuppression, Bladder Cancer, Disease Recurrence, Alopecia, Insomnia
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
CO-Renitec
Dosage: df
Indication: Hypertension
Start date: 1996-01-01
End date: 2006-12-01
Mylanta Plus
Dosage: df po
Administration route: Oral
Indication: Abdominal Pain Upper
Start date: 1996-01-01
Mylanta Plus
Dosage: var prn po
Administration route: Oral
Indication: Abdominal Pain Upper
Start date: 2006-04-01
End date: 2006-11-01
Alimta
Dosage: df
Indication: Lung Neoplasm Malignant
Start date: 2006-04-01
Chemotherapy NOS
Dosage: df
Indication: Drug USE FOR Unknown Indication
Start date: 2004-01-01
Chemotherapy NOS
Dosage: 1 df qwk
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-01
Prozac
Dosage: df
Indication: Depression
Start date: 2001-01-01
Other drugs received by patient: Tagamet; Antibiotic Drugs; Filgrastim
Adverse event in 64 year old female receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from France on 2007-01-25
Patient: 64 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Mitral Valve Disease, Visual Acuity Reduced, Mitral Valve Stenosis, Mitral Valve Calcification, Retinal Artery Thrombosis
Adverse event resulted in: disablity
Suspect drug(s):
Rivotril
Administration route: Oral
End date: 2006-07-02
Arthrotec
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2006-07-02
Prozac
Administration route: Oral
End date: 2006-07-02
Kerlone
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2006-07-02
Piascledine
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2006-07-02
Adverse event in 64 year old female receiving Prozac (Fluoxetine)
Reported by a physician from France on 2007-01-25
Patient: 64 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Visual Acuity Reduced, Macular Degeneration, Mitral Valve Stenosis, Retinal Artery Thrombosis
Adverse event resulted in: disablity
Suspect drug(s):
Prozac (Fluoxetine)
Other drugs received by patient: Rivotril / NOR /; Piascledine; Kerlone; Arthrotec
Adverse event in 64 year old female receiving Prozac (Fluoxetine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-25
Patient: 64 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Cataract, Visual Acuity Reduced, Maculopathy, Retinal Artery Thrombosis
Adverse event resulted in: disablity
Suspect drug(s):
Arthrotec
Dosage: text:2 df
Administration route: Oral
Piascledine
Dosage: text:1 df
Administration route: Oral
Rivotril
Administration route: Oral
Indication: Depression
Kerlone
Dosage: text:0.5 df
Administration route: Oral
Prozac
Dosage: text:1 df
Administration route: Oral
Indication: Depression
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