Does TEDUGLUTIDE Cause Product packaging quantity issue? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Product packaging quantity issue have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.3% of all adverse event reports for TEDUGLUTIDE.
30
Reports of Product packaging quantity issue with TEDUGLUTIDE
0.3%
of all TEDUGLUTIDE reports
0
Deaths
22
Hospitalizations
How Dangerous Is Product packaging quantity issue From TEDUGLUTIDE?
Of the 30 reports, 22 (73.3%) required hospitalization.
Is Product packaging quantity issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 30 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 packaging quantity issue?
LEUPROLIDE (523)
ALBUTEROL (431)
BUDESONIDE\FORMOTEROL (301)
FENTANYL (286)
BUPRENORPHINE (225)
CYCLOSPORINE (206)
ESTRADIOL (201)
BIMATOPROST (177)
RIVAROXABAN (174)
EXENATIDE (154)
Which TEDUGLUTIDE Alternatives Have Lower Product packaging quantity issue Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL