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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 Device failure? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device failure have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.1% of all adverse event reports for TEDUGLUTIDE.

5
Reports of Device failure with TEDUGLUTIDE
0.1%
of all TEDUGLUTIDE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Device failure From TEDUGLUTIDE?

Of the 5 reports, 4 (80.0%) required hospitalization.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 5 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 Device failure?

EPINEPHRINE (1,344) SOMATROPIN (1,141) PEGFILGRASTIM (829) TREPROSTINIL (713) BACLOFEN (691) BUDESONIDE\FORMOTEROL (686) ETANERCEPT (576) GOLIMUMAB (487) LEVONORGESTREL (332) ACLIDINIUM (304)

Which TEDUGLUTIDE Alternatives Have Lower Device failure Risk?

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

Related Pages

TEDUGLUTIDE Full Profile All Device failure Reports All Drugs Causing Device failure TEDUGLUTIDE Demographics