Does TEDUGLUTIDE Cause Product dose omission issue? 937 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 937 reports of Product dose omission issue have been filed in association with TEDUGLUTIDE (Gattex). This represents 10.7% of all adverse event reports for TEDUGLUTIDE.
937
Reports of Product dose omission issue with TEDUGLUTIDE
10.7%
of all TEDUGLUTIDE reports
65
Deaths
728
Hospitalizations
How Dangerous Is Product dose omission issue From TEDUGLUTIDE?
Of the 937 reports, 65 (6.9%) resulted in death, 728 (77.7%) required hospitalization, and 4 (0.4%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 937 reports have been filed with the FAERS database.
What Other Side Effects Does TEDUGLUTIDE Cause?
Vascular device infection (1,009)
Weight decreased (991)
Diarrhoea (779)
Abdominal pain (714)
Nausea (682)
Weight increased (631)
Dehydration (615)
Vomiting (585)
Death (527)
Abdominal distension (515)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which TEDUGLUTIDE Alternatives Have Lower Product dose omission issue Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL