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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TEDUGLUTIDE Cause Nephrolithiasis? 193 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 193 reports of Nephrolithiasis have been filed in association with TEDUGLUTIDE (Gattex). This represents 2.2% of all adverse event reports for TEDUGLUTIDE.

193
Reports of Nephrolithiasis with TEDUGLUTIDE
2.2%
of all TEDUGLUTIDE reports
6
Deaths
124
Hospitalizations

How Dangerous Is Nephrolithiasis From TEDUGLUTIDE?

Of the 193 reports, 6 (3.1%) resulted in death, 124 (64.2%) required hospitalization, and 3 (1.6%) were considered life-threatening.

Is Nephrolithiasis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 193 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 Nephrolithiasis?

ADALIMUMAB (2,416) ETANERCEPT (1,292) INFLIXIMAB (981) METHOTREXATE (979) ABATACEPT (788) TOPIRAMATE (768) CERTOLIZUMAB PEGOL (735) RITUXIMAB (709) TOFACITINIB (699) SODIUM OXYBATE (698)

Which TEDUGLUTIDE Alternatives Have Lower Nephrolithiasis Risk?

TEDUGLUTIDE vs TEDUGLUTIDE\WATER TEDUGLUTIDE vs TEGAFUR TEDUGLUTIDE vs TEGAFUR\URACIL TEDUGLUTIDE vs TEGASEROD TEDUGLUTIDE vs TEGRETOL

Related Pages

TEDUGLUTIDE Full Profile All Nephrolithiasis Reports All Drugs Causing Nephrolithiasis TEDUGLUTIDE Demographics