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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 DULAGLUTIDE Cause Hepatic function abnormal? 27 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Hepatic function abnormal have been filed in association with DULAGLUTIDE (Trulicity). This represents 0.0% of all adverse event reports for DULAGLUTIDE.

27
Reports of Hepatic function abnormal with DULAGLUTIDE
0.0%
of all DULAGLUTIDE reports
0
Deaths
14
Hospitalizations

How Dangerous Is Hepatic function abnormal From DULAGLUTIDE?

Of the 27 reports, 14 (51.9%) 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 DULAGLUTIDE. However, 27 reports have been filed with the FAERS database.

What Other Side Effects Does DULAGLUTIDE Cause?

Injection site pain (9,474) Nausea (9,137) Blood glucose increased (9,119) Incorrect dose administered (5,207) Diarrhoea (5,036) Vomiting (4,880) Inappropriate schedule of product administration (3,606) Extra dose administered (3,047) Injection site haemorrhage (3,028) Weight decreased (3,000)

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 DULAGLUTIDE Alternatives Have Lower Hepatic function abnormal Risk?

DULAGLUTIDE vs DULERA DULAGLUTIDE vs DULOXETINE DULAGLUTIDE vs DUPILUMAB DULAGLUTIDE vs DURAGESIC DULAGLUTIDE vs DUROGESIC

Related Pages

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