Does ZOLPIDEM Cause Suspected product quality issue? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Suspected product quality issue have been filed in association with ZOLPIDEM (Zolpidem Tartrate). This represents 0.1% of all adverse event reports for ZOLPIDEM.
10
Reports of Suspected product quality issue with ZOLPIDEM
0.1%
of all ZOLPIDEM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Suspected product quality issue From ZOLPIDEM?
Of the 10 reports, 1 (10.0%) required hospitalization.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZOLPIDEM. However, 10 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 Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
LEVOTHYROXINE (37)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
IOPROMIDE (25)
Which ZOLPIDEM Alternatives Have Lower Suspected product quality issue Risk?
ZOLPIDEM vs ZOLPIDEM\ZOLPIDEM
ZOLPIDEM vs ZOMETA
ZOLPIDEM vs ZONISAMIDE
ZOLPIDEM vs ZOPICLONE
ZOLPIDEM vs ZOTEPINE