Does TEDUGLUTIDE Cause Product solubility abnormal? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product solubility abnormal have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.1% of all adverse event reports for TEDUGLUTIDE.
6
Reports of Product solubility abnormal with TEDUGLUTIDE
0.1%
of all TEDUGLUTIDE reports
1
Deaths
5
Hospitalizations
How Dangerous Is Product solubility abnormal From TEDUGLUTIDE?
Of the 6 reports, 1 (16.7%) resulted in death, 5 (83.3%) required hospitalization.
Is Product solubility abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 6 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 Product solubility abnormal?
BUPRENORPHINE (498)
BUPRENORPHINE\NALOXONE (274)
POLYETHYLENE GLYCOL 3350 (220)
CHOLESTYRAMINE (193)
PATIROMER (107)
LEVOTHYROXINE (100)
SOMATROPIN (98)
EXENATIDE (97)
ESTRADIOL (94)
NITROGLYCERIN (81)
Which TEDUGLUTIDE Alternatives Have Lower Product solubility abnormal Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL