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Zyprexa (Olanzapine) - Adverse Event Reports - Life Threatening Events - Overdose

 



Index of reports > Cases resulting in life threatening events (87) > Cases with Overdose (5)

Below is the selection of adverse event reports related to Zyprexa (Olanzapine) that includes cases resulting in life threatening events where reactions include overdose.

Adverse event in 51 year old male receiving Zyprexa (Olanzapine)

Reported by a physician from Switzerland on 2007-07-05

Patient: 51 year old male

Adverse reactions / side effects: Waldenstrom's Macroglobulinaemia, Agranulocytosis, Overdose, Left Ventricular Hypertrophy

Adverse event resulted in: life threatening event

Suspect drug(s):
Zyprexa (Olanzapine)

Other drugs received by patient: Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Lorazepam; Lorazepam; Lorazepam; Lorazepam; Cyclophosphamide; Pantozol



Adverse event in 51 year old male receiving Zyprexa (Olanzapine)

Reported by a physician from Switzerland on 2007-05-24

Patient: 51 year old male

Adverse reactions / side effects: Overdose, Agranulocytosis, Left Ventricular Hypertrophy

Adverse event resulted in: life threatening event

Suspect drug(s):
Zyprexa (Olanzapine)

Other drugs received by patient: Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Clozapine; Lorazepam; Lorazepam; Lorazepam; Lorazepam; Endoxan; Pantozol



Adverse event in 43 year old female receiving Zyprexa (Olanzapine)

Reported by a physician from Switzerland on 2007-04-24

Patient: 43 year old female, weighing 73.0 kg (160.6 pounds)

Adverse reactions / side effects: Cogwheel Rigidity, Fatigue, Overdose, Balance Disorder, Fall, Asphyxia, Convulsion

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Zyprexa
    Dosage: 10 mg, daily (1/d)
    Administration route: Oral
    Indication: Psychotic Disorder
    Start date: 2007-03-14
    End date: 2007-03-15

Zyprexa
    Dosage: 15 mg, daily (1/d)
    Administration route: Oral
    Start date: 2007-03-16
    End date: 2007-03-18

Zyprexa
    Dosage: 20 mg, daily (1/d)
    Administration route: Oral
    Start date: 2007-03-19
    End date: 2007-03-19

Zyprexa
    Dosage: 30 mg, other

Other drugs received by patient: Tolvon; Tolvon; Tolvon; Temesta; Temesta; Temesta; Temesta; Emselex; Pantozol; Risperdal; Risperdal; Risperdal



Adverse event in 47 year old female receiving Zyprexa (Olanzapine)

Reported by a physician from United Kingdom on 2007-02-19

Patient: 47 year old female, weighing 62.0 kg (136.4 pounds)

Adverse reactions / side effects: Agitation, Hyperthermia, Tachycardia, Liver Disorder, Blood Osmolarity Decreased, Overdose, Musculoskeletal Stiffness, Depression, Neuroleptic Malignant Syndrome, White Blood Cell Count Increased, Posturing, Fluid Imbalance, Blood Pressure Increased, Trismus, Abnormal Behaviour, Delirium, Tremor, Renal Impairment, Communication Disorder, Escherichia Infection

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zyprexa
    Dosage: 15 mg, each evening
    Indication: Psychotic Disorder
    End date: 2007-01-01

Zyprexa
    Dosage: 7.5 mg, each evening
    Start date: 2007-01-01
    End date: 2007-01-01

Zyprexa
    Dosage: 2.5 mg, each evening
    Administration route: Oral
    Start date: 2007-01-11
    End date: 2007-01-24

Other drugs received by patient: Sertraline; Lithium Carbonate; Paracetamol; Senna; Lactulose; Lactulose; Cefaclor; Procyclidine Hydrochloride 2MG TAB



Adverse event in 41 year old female receiving Zyprexa (Olanzapine)

Reported by a health professional (non-physician/pharmacist) from Germany on 2007-02-07

Patient: 41 year old female

Adverse reactions / side effects: Fatigue, Overdose, Vomiting, Suicide Attempt

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Tavor / 00273201 /
    Dosage: 30 mg once po
    Administration route: Oral
    Start date: 2007-01-20
    End date: 2007-01-20

Zyprexa
    Dosage: 50 mg once po
    Administration route: Oral
    Start date: 2007-01-20
    End date: 2007-01-20

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