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Zyprexa (Olanzapine) - Adverse Event Reports - Disability - Loss of Consciousness

 



Index of reports > Cases resulting in disability (42) > Cases with Loss of Consciousness (4)

Below is the selection of adverse event reports related to Zyprexa (Olanzapine) that includes cases resulting in disability where reactions include loss of consciousness.

Adverse event in 54 year old male receiving Zyprexa (Olanzapine)

Reported by a consumer/non-health professional from United States on 2007-07-09

Patient: 54 year old male

Adverse reactions / side effects: Diabetes Mellitus, Abasia, Coma, Lower Limb Fracture, Liver Disorder, Loss of Consciousness, Weight Increased, Overdose, Sedation, Injury, Back Injury

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Zyprexa
    Dosage: 5 mg, 2/d
    Administration route: Oral
    Indication: Schizoaffective Disorder
    Start date: 2004-05-11
    End date: 2005-04-05

Zyprexa
    Dosage: 5 mg, 2/d
    Administration route: Oral
    Start date: 2006-12-21

Zyprexa
    Dosage: 20 mg, daily (1/d)
    Start date: 1997-01-01

Zyprexa
    Dosage: 30 mg, daily (1/d)

Zyprexa
    Dosage: 10 mg, daily (1/d)

Zyprexa
    Dosage: 50 mg, daily (1/d)

Zyprexa Zydis
    Dosage: 10 mg, 2/d
    Administration route: Oral
    Indication: Schizoaffective Disorder
    Start date: 2003-08-01

Zyprexa Zydis
    Dosage: 15 mg, 2/d
    Administration route: Oral
    Start date: 2004-02-26
    End date: 2004-03-12

Zyprexa Zydis
    Dosage: 5 mg, 2/d
    Administration route: Oral
    Start date: 2005-11-08

Zyprexa Zydis
    Dosage: 10 mg, other
    Administration route: Oral
    Start date: 2004-01-21

Zyprexa Zydis
    Dosage: 10 mg, each evening
    Administration route: Oral
    Start date: 2006-04-18
    End date: 2006-04-25

Zyprexa Zydis
    Dosage: 5 mg, 2/d
    Administration route: Oral
    Start date: 2006-04-25
    End date: 2006-05-30

Zyprexa Zydis
    Dosage: 10 mg, each evening
    Administration route: Oral
    Start date: 2006-05-30
    End date: 2006-07-03

Zyprexa Zydis
    Dosage: 5 mg, 2/d
    Administration route: Oral
    Start date: 2006-07-03
    End date: 2006-12-21

Other drugs received by patient: Ativan; Ativan; Risperidone; Risperidone; Risperidone; Risperidone; Risperdal Consta; Risperdal Consta; Haldol; Cogentin; Cogentin; Trazodone HCL; Lexapro; Lexapro; Multi-Vitamin



Adverse event in male receiving Zyprexa (Olanzapine)

Reported by a consumer/non-health professional from United States on 2007-05-24

Patient: male

Adverse reactions / side effects: Diabetes Mellitus, Abasia, Prescribed Overdose, Coma, Lower Limb Fracture, Liver Disorder, Loss of Consciousness, Weight Increased, Injury, Back Injury

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Zyprexa
    Dosage: 20 mg, daily (1/d)
    Start date: 1997-01-01

Zyprexa
    Dosage: 30 mg, daily (1/d)

Zyprexa
    Dosage: 10 mg, daily (1/d)

Zyprexa
    Dosage: 50 mg, daily (1/d)



Adverse event in male receiving Zyprexa (Olanzapine)

Reported by a consumer/non-health professional from United States on 2007-04-24

Patient: male

Adverse reactions / side effects: Abasia, Prescribed Overdose, Coma, Lower Limb Fracture, Liver Disorder, Loss of Consciousness, Weight Increased, Injury, Back Injury

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Zyprexa
    Dosage: 20 mg, daily (1/d)

Zyprexa
    Dosage: 30 mg, daily (1/d)



Adverse event in male receiving Zyprexa (Olanzapine)

Reported by a consumer/non-health professional from Canada on 2007-01-10

Patient: male

Adverse reactions / side effects: Feeling of Despair, Tinnitus, Frontal Lobe Epilepsy, Glaucoma, Body Temperature Increased, Dyskinesia, Impaired Work Ability, Fall, Loss of Consciousness, Impaired Driving Ability, Dysarthria, Brain Damage, Musculoskeletal Stiffness

Adverse event resulted in: disablity

Suspect drug(s):
Zyprexa (Olanzapine)

Other drugs received by patient: Loxapine; Fluanxol ^lundbeck^

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