Does TEDUGLUTIDE Cause Hypokalaemia? 100 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 100 reports of Hypokalaemia have been filed in association with TEDUGLUTIDE (Gattex). This represents 1.1% of all adverse event reports for TEDUGLUTIDE.
100
Reports of Hypokalaemia with TEDUGLUTIDE
1.1%
of all TEDUGLUTIDE reports
5
Deaths
69
Hospitalizations
How Dangerous Is Hypokalaemia From TEDUGLUTIDE?
Of the 100 reports, 5 (5.0%) resulted in death, 69 (69.0%) required hospitalization, and 5 (5.0%) were considered life-threatening.
Is Hypokalaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 100 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 Hypokalaemia?
FUROSEMIDE (2,503)
HYDROCHLOROTHIAZIDE (1,152)
CARBOPLATIN (1,118)
PREDNISONE (967)
DEXAMETHASONE (876)
CYCLOPHOSPHAMIDE (864)
OMEPRAZOLE (851)
RITUXIMAB (822)
AMLODIPINE (815)
PANTOPRAZOLE (811)
Which TEDUGLUTIDE Alternatives Have Lower Hypokalaemia Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL