Does TEDUGLUTIDE Cause Product preparation error? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product preparation error have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.2% of all adverse event reports for TEDUGLUTIDE.
14
Reports of Product preparation error with TEDUGLUTIDE
0.2%
of all TEDUGLUTIDE reports
1
Deaths
9
Hospitalizations
How Dangerous Is Product preparation error From TEDUGLUTIDE?
Of the 14 reports, 1 (7.1%) resulted in death, 9 (64.3%) required hospitalization.
Is Product preparation error 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 Product preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which TEDUGLUTIDE Alternatives Have Lower Product preparation error Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL