Does TEDUGLUTIDE Cause Device leakage? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Device leakage have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.5% of all adverse event reports for TEDUGLUTIDE.
45
Reports of Device leakage with TEDUGLUTIDE
0.5%
of all TEDUGLUTIDE reports
1
Deaths
27
Hospitalizations
How Dangerous Is Device leakage From TEDUGLUTIDE?
Of the 45 reports, 1 (2.2%) resulted in death, 27 (60.0%) required hospitalization, and 2 (4.4%) were considered life-threatening.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 45 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
Which TEDUGLUTIDE Alternatives Have Lower Device leakage Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL