Does TEDUGLUTIDE Cause Intentional product use issue? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Intentional product use issue have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.4% of all adverse event reports for TEDUGLUTIDE.
32
Reports of Intentional product use issue with TEDUGLUTIDE
0.4%
of all TEDUGLUTIDE reports
6
Deaths
20
Hospitalizations
How Dangerous Is Intentional product use issue From TEDUGLUTIDE?
Of the 32 reports, 6 (18.8%) resulted in death, 20 (62.5%) required hospitalization, and 2 (6.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 32 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which TEDUGLUTIDE Alternatives Have Lower Intentional product use issue Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL