Does DULAGLUTIDE Cause Product storage error? 555 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 555 reports of Product storage error have been filed in association with DULAGLUTIDE (Trulicity). This represents 0.8% of all adverse event reports for DULAGLUTIDE.
555
Reports of Product storage error with DULAGLUTIDE
0.8%
of all DULAGLUTIDE reports
0
Deaths
25
Hospitalizations
How Dangerous Is Product storage error From DULAGLUTIDE?
Of the 555 reports, 25 (4.5%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULAGLUTIDE. However, 555 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 Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which DULAGLUTIDE Alternatives Have Lower Product storage error Risk?
DULAGLUTIDE vs DULERA
DULAGLUTIDE vs DULOXETINE
DULAGLUTIDE vs DUPILUMAB
DULAGLUTIDE vs DURAGESIC
DULAGLUTIDE vs DUROGESIC