Does TEDUGLUTIDE Cause Post procedural complication? 73 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 73 reports of Post procedural complication have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.8% of all adverse event reports for TEDUGLUTIDE.
73
Reports of Post procedural complication with TEDUGLUTIDE
0.8%
of all TEDUGLUTIDE reports
9
Deaths
61
Hospitalizations
How Dangerous Is Post procedural complication From TEDUGLUTIDE?
Of the 73 reports, 9 (12.3%) resulted in death, 61 (83.6%) required hospitalization, and 2 (2.7%) were considered life-threatening.
Is Post procedural complication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 73 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 Post procedural complication?
ADALIMUMAB (2,494)
ETANERCEPT (318)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (244)
UPADACITINIB (241)
RISANKIZUMAB-RZAA (232)
INFLIXIMAB (217)
METHOTREXATE (188)
TREPROSTINIL (174)
HUMAN IMMUNOGLOBULIN G (159)
PREDNISONE (157)
Which TEDUGLUTIDE Alternatives Have Lower Post procedural complication Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL