Does DULAGLUTIDE Cause Intentional product misuse? 58 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 58 reports of Intentional product misuse have been filed in association with DULAGLUTIDE (Trulicity). This represents 0.1% of all adverse event reports for DULAGLUTIDE.
58
Reports of Intentional product misuse with DULAGLUTIDE
0.1%
of all DULAGLUTIDE reports
2
Deaths
17
Hospitalizations
How Dangerous Is Intentional product misuse From DULAGLUTIDE?
Of the 58 reports, 2 (3.4%) resulted in death, 17 (29.3%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULAGLUTIDE. However, 58 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which DULAGLUTIDE Alternatives Have Lower Intentional product misuse Risk?
DULAGLUTIDE vs DULERA
DULAGLUTIDE vs DULOXETINE
DULAGLUTIDE vs DUPILUMAB
DULAGLUTIDE vs DURAGESIC
DULAGLUTIDE vs DUROGESIC