Does TEDUGLUTIDE Cause Product use complaint? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Product use complaint have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.4% of all adverse event reports for TEDUGLUTIDE.
31
Reports of Product use complaint with TEDUGLUTIDE
0.4%
of all TEDUGLUTIDE reports
4
Deaths
16
Hospitalizations
How Dangerous Is Product use complaint From TEDUGLUTIDE?
Of the 31 reports, 4 (12.9%) resulted in death, 16 (51.6%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 31 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 Product use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which TEDUGLUTIDE Alternatives Have Lower Product use complaint Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL