Does TEDUGLUTIDE Cause Product use issue? 406 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 406 reports of Product use issue have been filed in association with TEDUGLUTIDE (Gattex). This represents 4.6% of all adverse event reports for TEDUGLUTIDE.
406
Reports of Product use issue with TEDUGLUTIDE
4.6%
of all TEDUGLUTIDE reports
31
Deaths
291
Hospitalizations
How Dangerous Is Product use issue From TEDUGLUTIDE?
Of the 406 reports, 31 (7.6%) resulted in death, 291 (71.7%) required hospitalization, and 4 (1.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 406 reports have been filed with the FAERS database.
What Other Side Effects Does TEDUGLUTIDE Cause?
Vascular device infection (1,009)
Weight decreased (991)
Product dose omission issue (937)
Diarrhoea (779)
Abdominal pain (714)
Nausea (682)
Weight increased (631)
Dehydration (615)
Vomiting (585)
Death (527)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which TEDUGLUTIDE Alternatives Have Lower Product use issue Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL