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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TEDUGLUTIDE Cause Unevaluable event? 26 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Unevaluable event have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.3% of all adverse event reports for TEDUGLUTIDE.

26
Reports of Unevaluable event with TEDUGLUTIDE
0.3%
of all TEDUGLUTIDE reports
4
Deaths
14
Hospitalizations

How Dangerous Is Unevaluable event From TEDUGLUTIDE?

Of the 26 reports, 4 (15.4%) resulted in death, 14 (53.8%) required hospitalization, and 1 (3.8%) were considered life-threatening.

Is Unevaluable event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 26 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 Unevaluable event?

ADALIMUMAB (4,242) ETANERCEPT (3,902) LENALIDOMIDE (3,331) OXYCODONE (3,145) AMBRISENTAN (2,336) SODIUM OXYBATE (2,328) CARBIDOPA\LEVODOPA (1,632) DUPILUMAB (1,410) MORPHINE (1,161) ACETAMINOPHEN\HYDROCODONE (1,118)

Which TEDUGLUTIDE Alternatives Have Lower Unevaluable event Risk?

TEDUGLUTIDE vs TEDUGLUTIDE\WATER TEDUGLUTIDE vs TEGAFUR TEDUGLUTIDE vs TEGAFUR\URACIL TEDUGLUTIDE vs TEGASEROD TEDUGLUTIDE vs TEGRETOL

Related Pages

TEDUGLUTIDE Full Profile All Unevaluable event Reports All Drugs Causing Unevaluable event TEDUGLUTIDE Demographics