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

 



Index of reports > Cases resulting in other serious reactions (92) > Cases with Anxiety (11)

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

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 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 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



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 female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-06-11

Patient: female, weighing 90.3 kg (198.6 pounds)

Adverse reactions / side effects: Anxiety, Road Traffic Accident, Pain in Extremity, Insomnia, Blood Cholesterol Increased, Dizziness, Oedema, Hypertension

Suspect drug(s):
Duragesic-100
    Dosage: 2 x 75 ug/hr patches
    Indication: Pain

Prozac
    Administration route: Oral
    Indication: Anxiety

Other drugs received by patient: Estrace; Micronase; Oxycontin



Adverse event in 17 year old female receiving Prozac (Fluoxetine)

Reported by a individual with unspecified qualification from United States on 2007-06-07

Patient: 17 year old female, weighing 52.6 kg (115.7 pounds)

Adverse reactions / side effects: Anxiety, Malaise, Pharmaceutical Product Complaint

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in 14 year old female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-05-22

Patient: 14 year old female, weighing 72.6 kg (159.6 pounds)

Adverse reactions / side effects: Conversion Disorder, Headache, Loss of Consciousness, Dysarthria, Anxiety, Dysstasia, Syncope, Vertigo, Dizziness, Hypoxia, Syncope Vasovagal

Adverse event resulted in: hospitalization

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in 14 year old female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-05-21

Patient: 14 year old female, weighing 72.6 kg (159.6 pounds)

Adverse reactions / side effects: Conversion Disorder, Headache, Loss of Consciousness, Dysarthria, Anxiety, Dysstasia, Syncope, Vertigo, Dizziness, Hypoxia, Syncope Vasovagal

Adverse event resulted in: hospitalization

Suspect drug(s):
Prozac (Fluoxetine)



Adverse event in 14 year old female receiving Prozac (Fluoxetine)

Reported by a consumer/non-health professional from United States on 2007-05-01

Patient: 14 year old female, weighing 72.6 kg (159.6 pounds)

Adverse reactions / side effects: Conversion Disorder, Loss of Consciousness, Dysarthria, Anxiety, Dysstasia, Syncope, Dizziness, Vertigo, Syncope Vasovagal

Adverse event resulted in: hospitalization

Suspect drug(s):
Prozac (Fluoxetine)



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 female receiving Prozac (Fluoxetine)

Reported by a lawyer from United States on 2007-01-19

Patient: female, weighing 38.6 kg (84.9 pounds)

Adverse reactions / side effects: Intentional Overdose, Pain, Laceration, Suicidal Ideation, Haemothorax, Anxiety, Fracture, Completed Suicide, Multiple Injuries, Suicide Attempt, Acute Respiratory Failure, RIB Fracture

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Ambien
    Administration route: Oral
    Indication: Insomnia

Ativan
    Administration route: Oral
    Indication: Anxiety

Ativan
    Indication: Agitation

Lithium Carbonate
    Administration route: Oral
    Indication: Bipolar Disorder

Neurontin
    Administration route: Oral
    Indication: Movement Disorder

Neurontin
    Indication: Depression

Neurontin
    Indication: Fatigue

Neurontin
    Indication: Arthralgia

Prozac
    Administration route: Oral

Xanax
    Administration route: Oral

Other drugs received by patient: Tequin; Restoril; Valium; Zyprexa; Pepcid

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