Does TEDUGLUTIDE Cause Hypomagnesaemia? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Hypomagnesaemia have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.6% of all adverse event reports for TEDUGLUTIDE.
55
Reports of Hypomagnesaemia with TEDUGLUTIDE
0.6%
of all TEDUGLUTIDE reports
2
Deaths
38
Hospitalizations
How Dangerous Is Hypomagnesaemia From TEDUGLUTIDE?
Of the 55 reports, 2 (3.6%) resulted in death, 38 (69.1%) required hospitalization, and 3 (5.5%) were considered life-threatening.
Is Hypomagnesaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 55 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 Hypomagnesaemia?
OMEPRAZOLE (1,766)
PANTOPRAZOLE (1,246)
PANITUMUMAB (611)
ESOMEPRAZOLE (591)
CARBOPLATIN (586)
LANSOPRAZOLE (504)
FUROSEMIDE (501)
FLUOROURACIL (477)
METFORMIN (415)
CISPLATIN (395)
Which TEDUGLUTIDE Alternatives Have Lower Hypomagnesaemia Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL