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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 Subdural haematoma? 18 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Subdural haematoma have been filed in association with DULAGLUTIDE (Trulicity). This represents 0.0% of all adverse event reports for DULAGLUTIDE.

18
Reports of Subdural haematoma with DULAGLUTIDE
0.0%
of all DULAGLUTIDE reports
12
Deaths
5
Hospitalizations

How Dangerous Is Subdural haematoma From DULAGLUTIDE?

Of the 18 reports, 12 (66.7%) resulted in death, 5 (27.8%) required hospitalization, and 1 (5.6%) were considered life-threatening.

Is Subdural haematoma Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DULAGLUTIDE. However, 18 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 Subdural haematoma?

RIVAROXABAN (1,423) ASPIRIN (1,181) APIXABAN (1,025) WARFARIN (1,012) CLOPIDOGREL BISULFATE (809) DABIGATRAN ETEXILATE (648) IBRUTINIB (342) HEPARIN (201) ENOXAPARIN (156) CYCLOPHOSPHAMIDE (146)

Which DULAGLUTIDE Alternatives Have Lower Subdural haematoma Risk?

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

Related Pages

DULAGLUTIDE Full Profile All Subdural haematoma Reports All Drugs Causing Subdural haematoma DULAGLUTIDE Demographics