Does ZOLPIDEM Cause Recalled product administered? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Recalled product administered have been filed in association with ZOLPIDEM (Zolpidem Tartrate). This represents 0.2% of all adverse event reports for ZOLPIDEM.
35
Reports of Recalled product administered with ZOLPIDEM
0.2%
of all ZOLPIDEM reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product administered From ZOLPIDEM?
Of the 35 reports.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZOLPIDEM. However, 35 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which ZOLPIDEM Alternatives Have Lower Recalled product administered Risk?
ZOLPIDEM vs ZOLPIDEM\ZOLPIDEM
ZOLPIDEM vs ZOMETA
ZOLPIDEM vs ZONISAMIDE
ZOLPIDEM vs ZOPICLONE
ZOLPIDEM vs ZOTEPINE