Does ZOPICLONE Cause Product dose omission issue? 95 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 95 reports of Product dose omission issue have been filed in association with ZOPICLONE. This represents 0.7% of all adverse event reports for ZOPICLONE.
95
Reports of Product dose omission issue with ZOPICLONE
0.7%
of all ZOPICLONE reports
13
Deaths
91
Hospitalizations
How Dangerous Is Product dose omission issue From ZOPICLONE?
Of the 95 reports, 13 (13.7%) resulted in death, 91 (95.8%) required hospitalization, and 10 (10.5%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZOPICLONE. However, 95 reports have been filed with the FAERS database.
What Other Side Effects Does ZOPICLONE Cause?
Toxicity to various agents (1,697)
Coma (1,405)
Drug ineffective (1,279)
Somnolence (1,269)
Intentional overdose (1,247)
Off label use (1,243)
Headache (1,039)
Overdose (894)
Fatigue (830)
Drug interaction (750)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which ZOPICLONE Alternatives Have Lower Product dose omission issue Risk?
ZOPICLONE vs ZOTEPINE
ZOPICLONE vs ZUCLOPENTHIXOL
ZOPICLONE vs ZUCLOPENTHIXOL DECANOATE
ZOPICLONE vs ZURANOLONE
ZOPICLONE vs ZYPREXA