Does TEDUGLUTIDE Cause Excessive granulation tissue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Excessive granulation tissue have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.1% of all adverse event reports for TEDUGLUTIDE.
7
Reports of Excessive granulation tissue with TEDUGLUTIDE
0.1%
of all TEDUGLUTIDE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Excessive granulation tissue From TEDUGLUTIDE?
Of the 7 reports, 6 (85.7%) required hospitalization.
Is Excessive granulation tissue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 7 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 Excessive granulation tissue?
CARBIDOPA\LEVODOPA (117)
ADALIMUMAB (38)
BACLOFEN (31)
ZOLEDRONIC ACID (29)
ZOMETA (27)
AREDIA (21)
METHOTREXATE (19)
RITUXIMAB (13)
BECAPLERMIN (11)
PAMIDRONATE (11)
Which TEDUGLUTIDE Alternatives Have Lower Excessive granulation tissue Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL