|
Index of reports
> Cases resulting in life threatening events (12)
Below is the selection of adverse event reports related to Prozac (Fluoxetine) that includes cases resulting in life threatening events.
Adverse event in 35 year old female receiving Prozac (Fluoxetine)
Reported by a individual with unspecified qualification from United States on 2007-10-30
Patient: 35 year old female, weighing 52.2 kg (114.8 pounds)
Adverse reactions / side effects: Thinking Abnormal, Impaired Work Ability, Abnormal Behaviour, Somnolence
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Cymbalta
Dosage: 40 mg once a day po
Administration route: Oral
Indication: Depression
Start date: 2007-10-08
End date: 2007-10-17
Prozac
Dosage: 30 mg once a day po
Administration route: Oral
Indication: Depression
Adverse event in 76 year old male receiving Prozac (Fluoxetine)
Reported by a physician from Netherlands on 2007-06-13
Patient: 76 year old male, weighing 87.0 kg (191.4 pounds)
Adverse reactions / side effects: Pneumonia, Pulmonary Fibrosis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Prozac
Dosage: 20 mg, unknown
Administration route: Oral
Indication: Depression
Start date: 2003-08-18
End date: 2006-02-17
Prozac
Dosage: 40 mg, unk
Start date: 2004-01-01
Adverse event in 18 year old male receiving Prozac (Fluoxetine)
Reported by a individual with unspecified qualification from United States on 2007-05-29
Patient: 18 year old male, weighing 71.7 kg (157.7 pounds)
Adverse reactions / side effects: Homicide, Hostility, Physical Assault, Abnormal Behaviour, Aggression
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Prozac (Fluoxetine)
Adverse event in 21 year old male receiving Prozac (Fluoxetine)
Reported by a physician from United States on 2007-05-16
Patient: 21 year old male
Adverse reactions / side effects: Intentional Overdose, Suicide Attempt, Ejaculation Disorder
Adverse event resulted in: life threatening event
Suspect drug(s):
Invega
Administration route: Oral
Indication: Schizophrenia
Prozac
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Wellbutrin
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-05-02
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Hypotonia, Bradycardia, Respiratory Distress
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax
Largactil
Prozac
Dosage: daily dose:20mg-freq:once daily
Trandate
Indication: Complication of Pregnancy
Loxen
Indication: Complication of Pregnancy
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a physician from United Kingdom on 2007-03-29
Patient: female, weighing 2.8 kg (6.2 pounds)
Adverse reactions / side effects: Hypoventilation, Drug Exposure During Pregnancy, Neonatal Disorder, Floppy Infant
Adverse event resulted in: life threatening event
Suspect drug(s):
Prozac (Fluoxetine)
Adverse event in 53 year old male receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from United States on 2007-03-29
Patient: 53 year old male, weighing 126.1 kg (277.4 pounds)
Adverse reactions / side effects: Suicidal Behaviour
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Prozac (Fluoxetine)
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a physician from France on 2007-03-22
Patient: female
Adverse reactions / side effects: Neonatal Respiratory Distress Syndrome, Drug Exposure During Pregnancy, Hypotonia Neonatal, Bradycardia Neonatal
Adverse event resulted in: life threatening event
Suspect drug(s):
Prozac (Fluoxetine)
Other drugs received by patient: Largactil; Atarax; Loxen; Trandate
Adverse event in male receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from United States on 2007-03-16
Patient: male, weighing 2.7 kg (6.0 pounds)
Adverse reactions / side effects: Premature Baby, Multiple Congenital Abnormalities, Drug Exposure Before Pregnancy, Transposition of THE Great Vessels, Cardiac Disorder, Respiratory Syncytial Virus Infection, Drug Exposure During Pregnancy, Psychomotor Skills Impaired, Chronic Respiratory Disease, Ankyloglossia Congenital
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Prozac (Fluoxetine)
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a individual with unspecified qualification from France on 2007-02-16
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Hypotonia, Bradycardia, Respiratory Distress
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax
Largactil
Prozac
Dosage: daily dose:20mg-freq:once daily
Trandate
Indication: Complication of Pregnancy
Loxen
Indication: Complication of Pregnancy
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 health professional (non-physician/pharmacist) from France on 2007-01-24
Patient: 64 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Visual Acuity Reduced, Retinal Artery Occlusion
Adverse event resulted in: life threatening event
Suspect drug(s):
Kerlone
Dosage: 10 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2006-07-02
Rivotril
Dosage: unk
Administration route: Oral
Indication: Depression
End date: 2006-07-02
Piascledine
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2006-07-02
Arthrotec
Dosage: 2 unit
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2006-07-02
Prozac
Administration route: Oral
Indication: Depression
End date: 2006-07-02
|
