Does TEDUGLUTIDE Cause Device related infection? 372 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 372 reports of Device related infection have been filed in association with TEDUGLUTIDE (Gattex). This represents 4.2% of all adverse event reports for TEDUGLUTIDE.
372
Reports of Device related infection with TEDUGLUTIDE
4.2%
of all TEDUGLUTIDE reports
15
Deaths
317
Hospitalizations
How Dangerous Is Device related infection From TEDUGLUTIDE?
Of the 372 reports, 15 (4.0%) resulted in death, 317 (85.2%) required hospitalization, and 16 (4.3%) were considered life-threatening.
Is Device related infection Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 372 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 related infection?
TREPROSTINIL (1,005)
EPOPROSTENOL (841)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (638)
AMBRISENTAN (492)
METHOTREXATE (437)
CYCLOPHOSPHAMIDE (431)
RITUXIMAB (361)
MACITENTAN (339)
DEXAMETHASONE (313)
ADALIMUMAB (305)
Which TEDUGLUTIDE Alternatives Have Lower Device related infection Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL