Does ZOLPIDEM Cause Product prescribing error? 56 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 56 reports of Product prescribing error have been filed in association with ZOLPIDEM (Zolpidem Tartrate). This represents 0.3% of all adverse event reports for ZOLPIDEM.
56
Reports of Product prescribing error with ZOLPIDEM
0.3%
of all ZOLPIDEM reports
6
Deaths
36
Hospitalizations
How Dangerous Is Product prescribing error From ZOLPIDEM?
Of the 56 reports, 6 (10.7%) resulted in death, 36 (64.3%) required hospitalization, and 1 (1.8%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZOLPIDEM. However, 56 reports have been filed with the FAERS database.
What Other Side Effects Does ZOLPIDEM Cause?
Drug ineffective (2,419)
Drug abuse (2,252)
Toxicity to various agents (2,157)
Completed suicide (1,842)
Intentional overdose (1,468)
Somnolence (1,308)
Suicide attempt (1,231)
Drug dependence (1,104)
Insomnia (1,049)
Overdose (981)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which ZOLPIDEM Alternatives Have Lower Product prescribing error Risk?
ZOLPIDEM vs ZOLPIDEM\ZOLPIDEM
ZOLPIDEM vs ZOMETA
ZOLPIDEM vs ZONISAMIDE
ZOLPIDEM vs ZOPICLONE
ZOLPIDEM vs ZOTEPINE