Does TEDUGLUTIDE Cause Device related sepsis? 226 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 226 reports of Device related sepsis have been filed in association with TEDUGLUTIDE (Gattex). This represents 2.6% of all adverse event reports for TEDUGLUTIDE.
226
Reports of Device related sepsis with TEDUGLUTIDE
2.6%
of all TEDUGLUTIDE reports
12
Deaths
213
Hospitalizations
How Dangerous Is Device related sepsis From TEDUGLUTIDE?
Of the 226 reports, 12 (5.3%) resulted in death, 213 (94.2%) required hospitalization, and 17 (7.5%) were considered life-threatening.
Is Device related sepsis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 226 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 sepsis?
TREPROSTINIL (225)
CYCLOPHOSPHAMIDE (130)
RITUXIMAB (113)
EPOPROSTENOL (89)
CYCLOSPORINE (82)
METHYLPREDNISOLONE (82)
BORTEZOMIB (79)
MACITENTAN (55)
DEXAMETHASONE (53)
ADALIMUMAB (49)
Which TEDUGLUTIDE Alternatives Have Lower Device related sepsis Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL