Does DULAGLUTIDE Cause Product dose omission? 653 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 653 reports of Product dose omission have been filed in association with DULAGLUTIDE (Trulicity). This represents 0.9% of all adverse event reports for DULAGLUTIDE.
653
Reports of Product dose omission with DULAGLUTIDE
0.9%
of all DULAGLUTIDE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Product dose omission From DULAGLUTIDE?
Of the 653 reports, 24 (3.7%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULAGLUTIDE. However, 653 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which DULAGLUTIDE Alternatives Have Lower Product dose omission Risk?
DULAGLUTIDE vs DULERA
DULAGLUTIDE vs DULOXETINE
DULAGLUTIDE vs DUPILUMAB
DULAGLUTIDE vs DURAGESIC
DULAGLUTIDE vs DUROGESIC