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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 Blood creatinine increased? 65 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 65 reports of Blood creatinine increased have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.7% of all adverse event reports for TEDUGLUTIDE.

65
Reports of Blood creatinine increased with TEDUGLUTIDE
0.7%
of all TEDUGLUTIDE reports
11
Deaths
50
Hospitalizations

How Dangerous Is Blood creatinine increased From TEDUGLUTIDE?

Of the 65 reports, 11 (16.9%) resulted in death, 50 (76.9%) required hospitalization.

Is Blood creatinine increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 65 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 Blood creatinine increased?

EMTRICITABINE\TENOFOVIR DISOPROXIL (1,966) TENOFOVIR DISOPROXIL (1,460) TACROLIMUS (1,439) METHOTREXATE (1,401) SACUBITRIL\VALSARTAN (1,389) RITUXIMAB (1,265) EFAVIRENZ\EMTRICITABINE\TENOFOVIR DISOPROXIL (1,112) METFORMIN (986) ECULIZUMAB (967) LENALIDOMIDE (959)

Which TEDUGLUTIDE Alternatives Have Lower Blood creatinine increased Risk?

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

Related Pages

TEDUGLUTIDE Full Profile All Blood creatinine increased Reports All Drugs Causing Blood creatinine increased TEDUGLUTIDE Demographics