Does ZOLPIDEM Cause Product administration error? 58 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 58 reports of Product administration error have been filed in association with ZOLPIDEM (Zolpidem Tartrate). This represents 0.3% of all adverse event reports for ZOLPIDEM.
58
Reports of Product administration error with ZOLPIDEM
0.3%
of all ZOLPIDEM reports
5
Deaths
46
Hospitalizations
How Dangerous Is Product administration error From ZOLPIDEM?
Of the 58 reports, 5 (8.6%) resulted in death, 46 (79.3%) required hospitalization, and 3 (5.2%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZOLPIDEM. However, 58 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which ZOLPIDEM Alternatives Have Lower Product administration error Risk?
ZOLPIDEM vs ZOLPIDEM\ZOLPIDEM
ZOLPIDEM vs ZOMETA
ZOLPIDEM vs ZONISAMIDE
ZOLPIDEM vs ZOPICLONE
ZOLPIDEM vs ZOTEPINE