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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 LEMBOREXANT Cause Hepatic function abnormal? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Hepatic function abnormal have been filed in association with LEMBOREXANT (DAYVIGO). This represents 1.5% of all adverse event reports for LEMBOREXANT.

15
Reports of Hepatic function abnormal with LEMBOREXANT
1.5%
of all LEMBOREXANT reports
1
Deaths
9
Hospitalizations

How Dangerous Is Hepatic function abnormal From LEMBOREXANT?

Of the 15 reports, 1 (6.7%) resulted in death, 9 (60.0%) required hospitalization.

Is Hepatic function abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LEMBOREXANT. However, 15 reports have been filed with the FAERS database.

What Other Side Effects Does LEMBOREXANT Cause?

Drug ineffective (225) Suicide attempt (98) Somnolence (90) Suicidal ideation (86) Sleep paralysis (80) Condition aggravated (74) Nightmare (71) Altered state of consciousness (45) Off label use (45) Adverse drug reaction (44)

What Other Drugs Cause Hepatic function abnormal?

NIVOLUMAB (1,131) PEMBROLIZUMAB (1,079) METHOTREXATE (1,054) CABOZANTINIB S-MALATE (912) CYCLOPHOSPHAMIDE (824) BEVACIZUMAB (769) PACLITAXEL (603) LENVATINIB (528) ATORVASTATIN (520) CYCLOSPORINE (508)

Which LEMBOREXANT Alternatives Have Lower Hepatic function abnormal Risk?

LEMBOREXANT vs LENACAPAVIR LEMBOREXANT vs LENALIDOMIDE LEMBOREXANT vs LENIOLISIB LEMBOREXANT vs LENOGRASTIM LEMBOREXANT vs LENVATINIB

Related Pages

LEMBOREXANT Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal LEMBOREXANT Demographics