Does PHENOBARBITAL Cause Wrong patient received product? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Wrong patient received product have been filed in association with PHENOBARBITAL (Phenobarbital Sodium). This represents 0.3% of all adverse event reports for PHENOBARBITAL.
17
Reports of Wrong patient received product with PHENOBARBITAL
0.3%
of all PHENOBARBITAL reports
0
Deaths
17
Hospitalizations
How Dangerous Is Wrong patient received product From PHENOBARBITAL?
Of the 17 reports, 17 (100.0%) required hospitalization, and 14 (82.4%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PHENOBARBITAL. However, 17 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 Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which PHENOBARBITAL Alternatives Have Lower Wrong patient received product Risk?
PHENOBARBITAL vs PHENOLPHTHALEIN
PHENOBARBITAL vs PHENOTHIAZINE
PHENOBARBITAL vs PHENPROCOUMON
PHENOBARBITAL vs PHENTERMINE
PHENOBARBITAL vs PHENTERMINE\TOPIRAMATE