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Prozac (Fluoxetine) - Adverse Event Reports - Other Serious Reactions

 



Index of reports > Cases resulting in other serious reactions (92)

     Depression (12)Anxiety (11)Drug Ineffective (10)Drug Exposure During Pregnancy (10)Suicidal Ideation (8)Nausea (7)Agitation (6)Aggression (6)Malaise (6)Abnormal Behaviour (5)

Below is the selection of adverse event reports related to Prozac (Fluoxetine) that includes cases resulting in other serious reactions.

 Reports 1 - 25 of 92   Next >>

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 42 year old male receiving Prozac (Fluoxetine)

Reported by a physician from United Kingdom on 2007-10-23

Patient: 42 year old male, weighing 92.0 kg (202.4 pounds)

Adverse reactions / side effects: Rash Erythematous, Mental Disorder, Rash Maculo-Papular

Suspect drug(s):
Prozac (Fluoxetine)

Other drugs received by patient: Aripiprazole; Gaviscon; Paracetamol; Zopiclone



Adverse event in 62 year old female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-10-23

Patient: 62 year old female

Adverse reactions / side effects: Anxiety, Initial Insomnia, Irritability, Weight Increased, Knee Arthroplasty, Somnolence, Nervousness

Suspect drug(s):
Cymbalta
    Dosage: 60 mg, daily (1/d)
    Administration route: Oral
    Indication: Neck Pain
    Start date: 2006-01-01

Prozac
    Start date: 2001-01-01

Other drugs received by patient: Meclizine; Naprosyn; Diovan; Lipitor; Nexium; Diazepam



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a individual with unspecified qualification from United States on 2007-10-18

Patient: female

Adverse reactions / side effects: Fatigue, Activities of Daily Living Impaired, Balance Disorder, Visual Disturbance, Memory Impairment

Suspect drug(s):
Esomeprazole (Esomeprazole)

Neurontin
    Indication: Dyskinesia
    Start date: 2005-12-01
    End date: 2006-05-01

Prozac

Sleep AID (Scopolamine Aminoxide Hydrobromide)



Adverse event in male receiving Prozac (Fluoxetine)

Reported by a physician from United States on 2007-10-18

Patient: male

Adverse reactions / side effects: Overdose, Supraventricular Extrasystoles, Drug Ineffective

Suspect drug(s):
Cymbalta
    Dosage: 60 mg, each morning
    Indication: Depression
    Start date: 2007-09-01

Cymbalta
    Dosage: 30 mg, each evening
    Start date: 2007-09-01

Prozac
    Dosage: 160 mg, daily (1/d)
    Indication: Depression



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a physician from United States on 2007-10-17

Patient: female

Adverse reactions / side effects: Status Epilepticus

Adverse event resulted in: hospitalization

Suspect drug(s):
Forteo
    Dosage: unk, unk
    Indication: Fibromyalgia
    Start date: 2007-06-01

Prozac
    Dosage: 60 mg, daily (1/d)
    Indication: Depression

Other drugs received by patient: Betagan



Adverse event in 27 year old male receiving Prozac (Fluoxetine)

Reported by a physician from Spain on 2007-10-17

Patient: 27 year old male

Adverse reactions / side effects: Respiratory Rate Increased, Psychomotor Hyperactivity, Tachycardia, Drug Interaction, Hyperreflexia, Disorientation, Pyrexia, Serotonin Syndrome, Hyperhidrosis, Myoclonus, Salivary Hypersecretion, Hypertension, Respiratory Tract Infection

Adverse event resulted in: hospitalization

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a physician from Canada on 2007-10-16

Patient: female

Adverse reactions / side effects: Panic Attack, Drug Withdrawal Syndrome, Hydrocephalus, Amnesia, Crying

Suspect drug(s):
Prozac (Fluoxetine)

Other drugs received by patient: Ativan; Atacand; Singulair; Losec; Vitamin B-12



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-10-12

Patient: female

Adverse reactions / side effects: Fatigue, Nausea, Lymphoma

Suspect drug(s):
Cymbalta
    Dosage: 60 mg, daily (1/d)
    Indication: Depression
    Start date: 2007-02-01

Prozac
    Dosage: unk mg, unk
    Indication: Depression
    Start date: 1998-01-01

Other drugs received by patient: Xanax; Synthroid



Adverse event in 56 year old male receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-10-11

Patient: 56 year old male, weighing 90.7 kg (199.6 pounds)

Adverse reactions / side effects: Therapeutic Response Unexpected With Drug Substitution, Formication, Mental Disorder

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in 23 year old female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-10-11

Patient: 23 year old female

Adverse reactions / side effects: Anxiety, Hallucination, Auditory, Hallucination, Visual, Palpitations, Pain

Suspect drug(s):
Geodon
    Dosage: daily dose:60mg-freq:for 2 weeks

Prozac
    Dosage: daily dose:20mg-freq:for 2 weeks



Adverse event in male receiving Prozac (Fluoxetine)

Reported by a physician from United States on 2007-10-04

Patient: male

Adverse reactions / side effects: Drug Ineffective

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in 84 year old female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-07-27

Patient: 84 year old female, weighing 49.9 kg (109.7 pounds)

Adverse reactions / side effects: Weight Decreased, Nausea, Drug Abuser, Fall, Ulcer, Herpes Zoster, HIP Fracture, Ageusia, Anorexia, Dizziness, Immune System Disorder, Depressed Mood

Adverse event resulted in: hospitalization

Suspect drug(s):
Cymbalta
    Dosage: 30 mg, daily (1/d)
    Indication: Pain
    Start date: 2005-01-01
    End date: 2007-02-01

Prozac
    Dosage: 20 mg, daily (1/d)
    Indication: Depression
    Start date: 2007-02-01

Prozac
    Dosage: 20 mg, daily (1/d)
    Administration route: Oral
    End date: 2005-01-01

Other drugs received by patient: Omeprazole; Ensure / 00472201 /



Adverse event in 18 year old male receiving Prozac (Fluoxetine)

Reported by a physician from United Kingdom on 2007-07-26

Patient: 18 year old male

Adverse reactions / side effects: Dyskinesia, Epilepsy

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in 38 year old male receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-07-25

Patient: 38 year old male

Adverse reactions / side effects: Dysarthria, Dysstasia, Road Traffic Accident, Miosis, Muscle Twitching

Suspect drug(s):
Ambien
    Dosage: unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Prozac
    Dosage: unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Wellbutrin
    Dosage: unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Zyprexa
    Dosage: unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a physician from United Kingdom on 2007-07-24

Patient: female

Adverse reactions / side effects: Umbilical Cord Around Neck, Intra-Uterine Death, Drug Exposure During Pregnancy, Pregnancy

Adverse event resulted in: death

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a physician from United States on 2007-07-20

Patient: female

Adverse reactions / side effects: Drug Withdrawal Syndrome Neonatal

Suspect drug(s):
Invega
    Indication: Drug Exposure During Pregnancy

Nicotine
    Indication: Unevaluable Event

Prozac
    Indication: Drug Exposure During Pregnancy



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-07-12

Patient: female

Adverse reactions / side effects: Tooth Loss, Overdose, Drug Ineffective, Drug Exposure During Pregnancy, Tooth Discolouration, Dental Caries, DRY Mouth, Mastectomy, Toothache

Suspect drug(s):
Prozac
    Dosage: 20 mg, daily (1/d)
    Administration route: Oral
    Indication: Depression

Prozac
    Dosage: 120 mg, daily (1/d)
    Administration route: Oral

Zyprexa
    Indication: Depression

Other drugs received by patient: Alprazolam; Lorazepam



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-07-12

Patient: female

Adverse reactions / side effects: Nausea, Drug Ineffective, Anorexia, Ulcer, Abdominal Pain Upper, Gallbladder Perforation, Suicidal Ideation

Suspect drug(s):
Cymbalta
    Dosage: 30 mg, unk
    Indication: Depression
    Start date: 2006-12-01
    End date: 2007-01-01

Cymbalta
    Dosage: 30 mg, unk
    Start date: 2007-01-01

Prozac
    Dosage: 40 mg, unk
    Indication: Depression
    Start date: 1999-01-01
    End date: 2006-12-01

Other drugs received by patient: Aciphex; Trazodone HCL; Hormones and Related Agents



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a physician from United States on 2007-07-10

Patient: female

Adverse reactions / side effects: Foreign Body Aspiration

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a physician from United States on 2007-07-10

Patient: female

Adverse reactions / side effects: Foreign Body Aspiration

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in 60 year old female receiving Prozac (Fluoxetine)

Reported by a physician from France on 2007-07-10

Patient: 60 year old female

Adverse reactions / side effects: Grand MAL Convulsion, Renal Failure, Sciatica, Gait Disturbance, Respiratory Distress

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Gemzar
    Dosage: 2400 mg, other
    Indication: non-Small Cell Lung Cancer
    Start date: 2007-04-25

Prozac
    Dosage: unk, unknown
    Administration route: Oral
    Indication: Depression

Other drugs received by patient: Cisplatin; Other Antineoplastic Agents; Valium; Stilnox / FRA /; Xanax; Voltaren; Dafalgan / FRA /; Primperan / SCH /; Solu-Medrol; Zofran



Adverse event in male receiving Prozac (Fluoxetine)

Reported by a physician from United States on 2007-07-06

Patient: male, weighing 90.7 kg (199.5 pounds)

Adverse reactions / side effects: Abnormal Dreams, Agitation, Nightmare, Dyspnoea, Hypoventilation, Pruritus, Rash

Suspect drug(s):
Chantix
    Dosage: daily dose:1mg
    Indication: Smoking Cessation Therapy
    Start date: 2007-04-01
    End date: 2007-05-04

Chantix
    Indication: Tobacco User

Prozac
    Indication: Depression

Other drugs received by patient: Diazepam; SAW Palmetto; Fluoxetine



Adverse event in 60 year old female receiving Prozac (Fluoxetine)

Reported by a physician from France on 2007-06-29

Patient: 60 year old female

Adverse reactions / side effects: Grand MAL Convulsion, Renal Failure, Sciatica, Gait Disturbance

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Gemzar
    Dosage: 2400 mg, other
    Indication: non-Small Cell Lung Cancer
    Start date: 2007-04-25

Prozac
    Dosage: unk, unknown
    Administration route: Oral
    Indication: Depression

Other drugs received by patient: Cisplatin; Other Antineoplastic Agents; Valium; Stilnox / FRA /; Xanax; Voltaren; Dafalgan / FRA /; Primperan / SCH /; Solu-Medrol; Zofran



Adverse event in female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-06-29

Patient: female

Adverse reactions / side effects: Agitation, Akathisia, Flat Affect, Depersonalisation, Pain, Abnormal Behaviour, Suicidal Ideation, Tremor, Anxiety, Social Avoidant Behaviour, Suicide Attempt, Injury

Suspect drug(s):
Paxil
    Start date: 1999-11-01
    End date: 2004-06-01

Prozac
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 1999-11-01
    End date: 2004-06-01



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