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Zarontin (Ethosuximide) - Stevens-Johnson Syndrome - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Stevens-Johnson Syndrome (2)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Zarontin (Ethosuximide) where reactions include stevens-johnson syndrome. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Zarontin side effects in male

Reported by a lawyer from United States on 2012-06-29

Patient: male, weighing 41.0 kg (90.2 pounds)

Reactions: Atelectasis, Oral Infection, Toxic Epidermal Necrolysis, Mycoplasma Infection, Abdominal Discomfort, Lymphadenitis, Systemic Inflammatory Response Syndrome, Stevens-Johnson Syndrome

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Zarontin
    Dosage: one 250mg capsule every morning and 2 capsules every night
    Administration route: Oral
    Indication: Epilepsy
    Start date: 2010-11-28
    End date: 2010-12-16

Zarontin
    Dosage: 250 mg, 2x/day
    Administration route: Oral
    Indication: Partial Seizures
    Start date: 2010-11-23
    End date: 2010-11-27

Other drugs received by patient: Depakote; Ciprodex



Possible Zarontin side effects in male

Reported by a lawyer from United States on 2012-06-22

Patient: male, weighing 41.0 kg (90.2 pounds)

Reactions: Atelectasis, Abdominal Discomfort, Oral Infection, Toxic Epidermal Necrolysis, Systemic Inflammatory Response Syndrome, Stevens-Johnson Syndrome, Mycoplasma Infection

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Zarontin
    Dosage: 750 mg (250mg capsules, 1 capsule every morning and 2 capsules every night)
    Administration route: Oral
    Indication: Partial Seizures
    Start date: 2010-11-22
    End date: 2010-12-16

Zarontin
    Indication: Epilepsy

Other drugs received by patient: Depakote; Ciprodex

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