Does DULAGLUTIDE Cause Incorrect product storage? 62 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Incorrect product storage have been filed in association with DULAGLUTIDE (Trulicity). This represents 0.1% of all adverse event reports for DULAGLUTIDE.
62
Reports of Incorrect product storage with DULAGLUTIDE
0.1%
of all DULAGLUTIDE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product storage From DULAGLUTIDE?
Of the 62 reports, 1 (1.6%) resulted in death, 2 (3.2%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULAGLUTIDE. However, 62 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which DULAGLUTIDE Alternatives Have Lower Incorrect product storage Risk?
DULAGLUTIDE vs DULERA
DULAGLUTIDE vs DULOXETINE
DULAGLUTIDE vs DUPILUMAB
DULAGLUTIDE vs DURAGESIC
DULAGLUTIDE vs DUROGESIC