Does TEDUGLUTIDE Cause Device dislocation? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Device dislocation have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.6% of all adverse event reports for TEDUGLUTIDE.
52
Reports of Device dislocation with TEDUGLUTIDE
0.6%
of all TEDUGLUTIDE reports
2
Deaths
47
Hospitalizations
How Dangerous Is Device dislocation From TEDUGLUTIDE?
Of the 52 reports, 2 (3.8%) resulted in death, 47 (90.4%) required hospitalization, and 4 (7.7%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 52 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 dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
Which TEDUGLUTIDE Alternatives Have Lower Device dislocation Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL