Does DULAGLUTIDE Cause Wrong product administered? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Wrong product administered have been filed in association with DULAGLUTIDE (Trulicity). This represents 0.1% of all adverse event reports for DULAGLUTIDE.
50
Reports of Wrong product administered with DULAGLUTIDE
0.1%
of all DULAGLUTIDE reports
0
Deaths
9
Hospitalizations
How Dangerous Is Wrong product administered From DULAGLUTIDE?
Of the 50 reports, 9 (18.0%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULAGLUTIDE. However, 50 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 product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which DULAGLUTIDE Alternatives Have Lower Wrong product administered Risk?
DULAGLUTIDE vs DULERA
DULAGLUTIDE vs DULOXETINE
DULAGLUTIDE vs DUPILUMAB
DULAGLUTIDE vs DURAGESIC
DULAGLUTIDE vs DUROGESIC