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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SUVOREXANT Cause Product dose omission issue? 189 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 189 reports of Product dose omission issue have been filed in association with SUVOREXANT (BELSOMRA). This represents 2.0% of all adverse event reports for SUVOREXANT.

189
Reports of Product dose omission issue with SUVOREXANT
2.0%
of all SUVOREXANT reports
1
Deaths
6
Hospitalizations

How Dangerous Is Product dose omission issue From SUVOREXANT?

Of the 189 reports, 1 (0.5%) resulted in death, 6 (3.2%) required hospitalization.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SUVOREXANT. However, 189 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 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 SUVOREXANT Alternatives Have Lower Product dose omission issue Risk?

SUVOREXANT vs SUZETRIGINE SUVOREXANT vs SYMBICORT SUVOREXANT vs SYNAGIS SUVOREXANT vs SYNTHROID SUVOREXANT vs TACROLIMUS

Related Pages

SUVOREXANT Full Profile All Product dose omission issue Reports All Drugs Causing Product dose omission issue SUVOREXANT Demographics