Does TEDUGLUTIDE Cause Hepatic function abnormal? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Hepatic function abnormal have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.2% of all adverse event reports for TEDUGLUTIDE.
14
Reports of Hepatic function abnormal with TEDUGLUTIDE
0.2%
of all TEDUGLUTIDE reports
3
Deaths
12
Hospitalizations
How Dangerous Is Hepatic function abnormal From TEDUGLUTIDE?
Of the 14 reports, 3 (21.4%) resulted in death, 12 (85.7%) required hospitalization, and 1 (7.1%) were considered life-threatening.
Is Hepatic function abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 14 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 Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which TEDUGLUTIDE Alternatives Have Lower Hepatic function abnormal Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL