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Trileptal (Oxcarbazepine) - Adverse Event Reports - Death - Completed Suicide

 



Index of reports > Cases resulting in death (12) > Cases with Completed Suicide (3)

Below is the selection of adverse event reports related to Trileptal (Oxcarbazepine) that includes cases resulting in death where reactions include completed suicide.

Adverse event in 14 year old female receiving Trileptal (Oxcarbazepine)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-19

Patient: 14 year old female, weighing 83.9 kg (184.6 pounds)

Adverse reactions / side effects: Completed Suicide

Adverse event resulted in: death

Suspect drug(s):
Keppra
    Dosage: 250 mg, bid
    Administration route: Oral
    Indication: Convulsion
    Start date: 2006-11-28
    End date: 2006-12-05

Keppra
    Dosage: 500 mg, bid
    Administration route: Oral
    Start date: 2006-12-05
    End date: 2007-01-04

Trileptal
    Dosage: 600 mg, tid
    Indication: Convulsion
    Start date: 2005-11-11
    End date: 2007-01-04



Adverse event in 14 year old female receiving Trileptal (Oxcarbazepine)

Reported by a consumer/non-health professional from United States on 2007-02-06

Patient: 14 year old female, weighing 81.6 kg (179.6 pounds)

Adverse reactions / side effects: Completed Suicide

Adverse event resulted in: death

Suspect drug(s):
Keppra
    Dosage: 500mg bid po
    Administration route: Oral
    Indication: Convulsion
    Start date: 2006-11-28
    End date: 2007-01-10

Trileptal
    Dosage: 600mg tid po
    Administration route: Oral
    Indication: Convulsion
    Start date: 2005-11-15
    End date: 2007-01-10



Adverse event in 14 year old female receiving Trileptal (Oxcarbazepine)

Reported by a individual with unspecified qualification from United States on 2007-02-01

Patient: 14 year old female

Adverse reactions / side effects: Completed Suicide

Adverse event resulted in: death

Suspect drug(s):
Keppra
    Indication: Convulsion
    Start date: 2006-11-29

Trileptal
    Dosage: 600 mg, tid
    Indication: Convulsion
    Start date: 2006-08-01

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