Index of reports
> Life Threatening Events (4)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Depakote ER (Divalproex) life threatening events. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Depakote ER side effects in male
Reported by a consumer/non-health professional from Brazil on 2012-07-05
Patient: male, weighing 143.0 kg (314.6 pounds)
Reactions: Procedural Pain, Vomiting, Hepatic Steatosis
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Depakote ER
Possible Depakote ER side effects in male
Reported by a consumer/non-health professional from Brazil on 2012-07-02
Patient: male, weighing 143.0 kg (314.6 pounds)
Reactions: Vomiting, Hepatic Steatosis
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Depakote ER
Possible Depakote ER side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2011-12-16
Patient: female
Reactions: Product Substitution Issue, Status Epilepticus, Convulsion
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Depakote ER
Possible Depakote ER side effects in 62 year old male
Reported by a health professional (non-physician/pharmacist) from United States on 2011-10-03
Patient: 62 year old male, weighing 87.5 kg (192.6 pounds)
Reactions: Weight Decreased, Migraine, Insomnia, Hypophagia, Visual Impairment, Gait Disturbance
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Depakote ER
Other drugs received by patient: Topamax
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