Does PHENOBARBITAL Cause Intentional product use issue? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Intentional product use issue have been filed in association with PHENOBARBITAL (Phenobarbital Sodium). This represents 0.5% of all adverse event reports for PHENOBARBITAL.
32
Reports of Intentional product use issue with PHENOBARBITAL
0.5%
of all PHENOBARBITAL reports
9
Deaths
21
Hospitalizations
How Dangerous Is Intentional product use issue From PHENOBARBITAL?
Of the 32 reports, 9 (28.1%) resulted in death, 21 (65.6%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PHENOBARBITAL. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does PHENOBARBITAL Cause?
Drug ineffective (1,686)
Off label use (781)
Seizure (620)
Multiple-drug resistance (406)
Toxicity to various agents (392)
Status epilepticus (317)
Drug reaction with eosinophilia and systemic symptoms (274)
Foetal exposure during pregnancy (266)
Hypotension (256)
Epilepsy (253)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which PHENOBARBITAL Alternatives Have Lower Intentional product use issue Risk?
PHENOBARBITAL vs PHENOLPHTHALEIN
PHENOBARBITAL vs PHENOTHIAZINE
PHENOBARBITAL vs PHENPROCOUMON
PHENOBARBITAL vs PHENTERMINE
PHENOBARBITAL vs PHENTERMINE\TOPIRAMATE