Does TEDUGLUTIDE Cause Complication associated with device? 133 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 133 reports of Complication associated with device have been filed in association with TEDUGLUTIDE (Gattex). This represents 1.5% of all adverse event reports for TEDUGLUTIDE.
133
Reports of Complication associated with device with TEDUGLUTIDE
1.5%
of all TEDUGLUTIDE reports
5
Deaths
122
Hospitalizations
How Dangerous Is Complication associated with device From TEDUGLUTIDE?
Of the 133 reports, 5 (3.8%) resulted in death, 122 (91.7%) required hospitalization, and 4 (3.0%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 133 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
AMBRISENTAN (125)
Which TEDUGLUTIDE Alternatives Have Lower Complication associated with device Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL