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Index of reports
> Cases resulting in other serious reactions (92)
> Cases with Depression (12)
Below is the selection of adverse event reports related to Prozac (Fluoxetine) that includes cases resulting in other serious reactions where reactions include depression.
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a physician from United States on 2007-10-30
Patient: female, weighing 77.0 kg (169.4 pounds)
Adverse reactions / side effects: Drug Effect Decreased, Therapeutic Response Unexpected With Drug Substitution, Condition Aggravated, Depression, Crying
Suspect drug(s):
Prozac (Fluoxetine)
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from United States on 2007-06-22
Patient: female
Adverse reactions / side effects: Intentional Self-Injury, Suicidal Ideation, Drug Toxicity, Social Avoidant Behaviour, Anger, Depression, Hypersomnia, Crying, Violent Ideation, Nausea, Abnormal Behaviour, Apallic Syndrome, Aggression, Logorrhoea, Limb Injury, Pseudodementia, Depressed Level of Consciousness, Memory Impairment
Suspect drug(s):
Lamictal
Administration route: Oral
Indication: Bipolar II Disorder
Start date: 2007-06-01
Paroxetine Hydrochloride
Administration route: Oral
Indication: Depression
Prozac
Dosage: 60mg per day
Indication: Depression
Wellbutrin
Dosage: 200mg per day
Administration route: Oral
Indication: Depression
Other drugs received by patient: Tranxene
Adverse event in 44 year old female receiving Prozac (Fluoxetine)
Reported by a individual with unspecified qualification from United States on 2007-06-19
Patient: 44 year old female, weighing 70.3 kg (154.7 pounds)
Adverse reactions / side effects: Drug Ineffective, Therapeutic Response Unexpected With Drug Substitution, Screaming, Depression, Feeling Abnormal, Pharmaceutical Product Complaint, Crying
Suspect drug(s):
Prozac
Dosage: 1 pill daily po
Administration route: Oral
Indication: Depression
Start date: 2007-04-15
End date: 2007-06-05
Wellbutrin
Dosage: 1 pill daily po
Administration route: Oral
Indication: Depression
Start date: 2007-04-15
End date: 2007-06-05
Adverse event in 64 year old female receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from United States on 2007-06-12
Patient: 64 year old female
Adverse reactions / side effects: Polyp Colorectal, Unresponsive TO Stimuli, Somnolence, Sensation of Foreign Body, Hypokinesia, Fatigue, Aspiration, Depression, Oxygen Saturation Decreased, Decreased Appetite, Dyspnoea, Nasal Congestion, Stress, Anxiety, Gait Disturbance, Memory Impairment, Hypertension, Frustration, Adrenal Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Humatrope
Dosage: 0.3 mg, daily (1/d)
Indication: Hypopituitarism
Start date: 1998-05-01
Prozac
Dosage: unk, unknown
Indication: Depression
Start date: 1997-06-01
End date: 1997-08-01
Other drugs received by patient: Prilosec; Levoxyl; Premarin; Climara; Multi-Vitamin; Calcium W / Vitamin D NOS; Fibercon
Adverse event in 31 year old female receiving Prozac (Fluoxetine)
Reported by a physician from United States on 2007-04-23
Patient: 31 year old female
Adverse reactions / side effects: Abdominal Pain, Agitation, Ketonuria, Tachycardia, Constipation, Hyperhidrosis, Malaise, Irritable Bowel Syndrome, Depression, Muscle Spasms, Blood Glucose Increased, Blood Urine Present, Nausea, Muscular Weakness, Cholecystitis Chronic, Hepatic Enzyme Increased, Hepatic Steatosis, Insomnia, Memory Impairment, Depressed Mood, Feeling Abnormal
Suspect drug(s):
Cymbalta
Dosage: 30 mg, daily (1/d)
Indication: Depression
Start date: 2006-01-04
End date: 2006-02-28
Cymbalta
Dosage: 60 mg, unk
Start date: 2006-08-21
End date: 2007-01-01
Cymbalta
Dosage: 30 mg, each evening
Start date: 2006-03-28
End date: 2006-08-20
Cymbalta
Dosage: 20 mg, unk
Start date: 2007-02-05
End date: 2007-02-19
Cymbalta
Dosage: 30 mg, unk
Start date: 2007-01-01
End date: 2007-02-04
Cymbalta
Dosage: unk mg, unk
Cymbalta
Dosage: unk mg, unk
Start date: 2006-03-01
End date: 2006-03-27
Prozac
Dosage: 20 mg, daily (1/d)
Indication: Muscle Spasms
Start date: 2006-03-02
End date: 2006-03-01
Prozac
Dosage: unk mg, unk
Start date: 2007-03-01
Prozac
Dosage: unk mg, unk
End date: 2006-01-04
Other drugs received by patient: Trazodone HCL; Trazodone HCL; Trazodone HCL; Trazodone HCL; Trazodone HCL; Trazodone HCL; Lithium Carbonate; Restoril; Restoril; Lithobid; Flexeril; Zelnorm; Mineral OIL Emulsion
Adverse event in male receiving Prozac (Fluoxetine)
Reported by a lawyer from United States on 2007-04-11
Patient: male
Adverse reactions / side effects: Drug Ineffective, Alcohol Poisoning, Suicidal Ideation, Grand MAL Convulsion, Hallucination, Visual, Insomnia, Hypoxia, Suicide Attempt, Multiple Drug Overdose Intentional, Depression
Adverse event resulted in: hospitalization
Suspect drug(s):
Alcohol
Dilantin
Administration route: Oral
Effexor
Neurontin
Administration route: Oral
Indication: Neuralgia
Neurontin
Indication: Convulsion
Omeprazole
Oxycontin
Prozac
Remeron
Other drugs received by patient: Wellbutrin SR; Lexapro; Lisinopril; Humalog; Lantus
Adverse event in 54 year old female receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from United States on 2007-03-27
Patient: 54 year old female
Adverse reactions / side effects: Agitation, Eyelid Oedema, Drug Ineffective, Skin Burning Sensation, Headache, Pyrexia, Hyperhidrosis, Abdominal Pain Upper, Haematemesis, Skin Ulcer, Skin Discolouration, Oedema Peripheral, Anger, Raynaud's Phenomenon, Depression, Vomiting, Swelling Face, Feeling Hot and Cold, Abnormal Behaviour, Rash, Aggression, Irritability, Joint Swelling
Adverse event resulted in: hospitalization
Suspect drug(s):
Prozac (Fluoxetine)
Other drugs received by patient: Inderal; Ativan; Klonopin; Buspar; Chlor-Trimeton; Pletal; Norvasc; Tramadol HCL
Adverse event in female receiving Prozac (Fluoxetine)
Reported by a physician from United States on 2007-03-20
Patient: female
Adverse reactions / side effects: Drug Toxicity, Anxiety, Agitation, Sedation, Drug Interaction Potentiation, Prescribed Overdose, Depression, Feeling Abnormal
Suspect drug(s):
Prozac
Dosage: 120 mg, unk
Indication: Depression
Prozac
Dosage: 80 mg, unk
Prozac
Dosage: 60 mg, unk
Prozac
Dosage: 40 mg, unk
Start date: 2006-01-01
Other drugs received by patient possibly interacting with the suspect drug: Cymbalta
Dosage: 30 mg, unk
Indication: Depression
Start date: 2006-11-01
Cymbalta
Dosage: 30 mg, 2/d
Other drugs received by patient: Nortriptyline HCL; Insulin
Adverse event in 46 year old male receiving Prozac (Fluoxetine)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-15
Patient: 46 year old male
Adverse reactions / side effects: Condition Aggravated, Apathy, Sleep Disorder, Huntington's Chorea, Depression, Asthenia, Tearfulness, Decreased Appetite
Suspect drug(s):
Prozac (Fluoxetine)
Other drugs received by patient: Haloperidol; Clomipramine HCL; Risperidone
Adverse event in 46 year old male receiving Prozac (Fluoxetine)
Reported by a physician from United Kingdom on 2007-03-13
Patient: 46 year old male
Adverse reactions / side effects: Sleep Disorder, Huntington's Chorea, Depression, Tearfulness, Depressed Mood, Decreased Appetite
Suspect drug(s):
Prozac (Fluoxetine)
Other drugs received by patient: Clomipramine HCL; Haloperidol; Risperidone
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):
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
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
Prozac
Dosage: df
Indication: Depression
Start date: 2001-01-01
Other drugs received by patient: Tagamet; Antibiotic Drugs; Filgrastim
Adverse event in 57 year old female receiving Prozac (Fluoxetine)
Reported by a consumer/non-health professional from Brazil on 2007-01-22
Patient: 57 year old female
Adverse reactions / side effects: General Physical Condition Abnormal, Hypersensitivity, Flatulence, Urinary Incontinence, Constipation, Abdominal Pain Upper, Weight Increased, Malaise, Dyspepsia, Ureteric Obstruction, Lung Neoplasm Malignant, Depression, Thrombocytopenia, Bladder Cancer, Cough, Blood Urine Present, Kidney Enlargement, Urinary Tract Infection, Alopecia, Insomnia
Adverse event resulted in: hospitalization
Suspect drug(s):
Alimta
Dosage: unk, unknown
Indication: Lung Neoplasm Malignant
Start date: 2006-04-01
Prozac
Dosage: unk, unknown
Indication: Depression
Start date: 2001-01-01
Other drugs received by patient: Mylanta Plus; Mylanta Plus; Enalapril Maleate and Hydrochlorothiazide; Antibiotics
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