Does ZOLPIDEM Cause Incorrect product administration duration? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Incorrect product administration duration have been filed in association with ZOLPIDEM (Zolpidem Tartrate). This represents 0.3% of all adverse event reports for ZOLPIDEM.
57
Reports of Incorrect product administration duration with ZOLPIDEM
0.3%
of all ZOLPIDEM reports
0
Deaths
14
Hospitalizations
How Dangerous Is Incorrect product administration duration From ZOLPIDEM?
Of the 57 reports, 14 (24.6%) required hospitalization, and 4 (7.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZOLPIDEM. However, 57 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ZOLPIDEM Alternatives Have Lower Incorrect product administration duration Risk?
ZOLPIDEM vs ZOLPIDEM\ZOLPIDEM
ZOLPIDEM vs ZOMETA
ZOLPIDEM vs ZONISAMIDE
ZOLPIDEM vs ZOPICLONE
ZOLPIDEM vs ZOTEPINE