Does SUVOREXANT Cause Product dose omission? 78 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 78 reports of Product dose omission have been filed in association with SUVOREXANT (BELSOMRA). This represents 0.8% of all adverse event reports for SUVOREXANT.
78
Reports of Product dose omission with SUVOREXANT
0.8%
of all SUVOREXANT reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission From SUVOREXANT?
Of the 78 reports, 3 (3.8%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUVOREXANT. However, 78 reports have been filed with the FAERS database.
What Other Side Effects Does SUVOREXANT Cause?
Drug ineffective (2,855)
Nightmare (723)
Somnolence (639)
Abnormal dreams (588)
Insomnia (529)
Feeling abnormal (427)
Headache (421)
Hallucination (338)
No adverse event (327)
Fatigue (231)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which SUVOREXANT Alternatives Have Lower Product dose omission Risk?
SUVOREXANT vs SUZETRIGINE
SUVOREXANT vs SYMBICORT
SUVOREXANT vs SYNAGIS
SUVOREXANT vs SYNTHROID
SUVOREXANT vs TACROLIMUS