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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 Wrong patient received product? 100 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 100 reports of Wrong patient received product have been filed in association with DULAGLUTIDE (Trulicity). This represents 0.1% of all adverse event reports for DULAGLUTIDE.

100
Reports of Wrong patient received product with DULAGLUTIDE
0.1%
of all DULAGLUTIDE reports
0
Deaths
7
Hospitalizations

How Dangerous Is Wrong patient received product From DULAGLUTIDE?

Of the 100 reports, 7 (7.0%) required hospitalization.

Is Wrong patient received product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DULAGLUTIDE. However, 100 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 Wrong patient received product?

INSULIN LISPRO (334) CLOZAPINE (198) RISPERIDONE (176) OXAZEPAM (152) BISOPROLOL (150) LEVETIRACETAM (126) ACETAMINOPHEN (123) METFORMIN (116) INSULIN GLARGINE (114) CLONAZEPAM (112)

Which DULAGLUTIDE Alternatives Have Lower Wrong patient received product Risk?

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

Related Pages

DULAGLUTIDE Full Profile All Wrong patient received product Reports All Drugs Causing Wrong patient received product DULAGLUTIDE Demographics