Does TEDUGLUTIDE Cause Device related bacteraemia? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Device related bacteraemia have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.5% of all adverse event reports for TEDUGLUTIDE.
40
Reports of Device related bacteraemia with TEDUGLUTIDE
0.5%
of all TEDUGLUTIDE reports
2
Deaths
38
Hospitalizations
How Dangerous Is Device related bacteraemia From TEDUGLUTIDE?
Of the 40 reports, 2 (5.0%) resulted in death, 38 (95.0%) required hospitalization, and 3 (7.5%) were considered life-threatening.
Is Device related bacteraemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 40 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 Device related bacteraemia?
CYCLOPHOSPHAMIDE (29)
PREDNISONE (23)
CYTARABINE (21)
MYCOPHENOLATE MOFETIL (20)
TACROLIMUS (20)
METHOTREXATE (19)
RITUXIMAB (19)
DINUTUXIMAB BETA (17)
ISOTRETINOIN (17)
SARGRAMOSTIM (17)
Which TEDUGLUTIDE Alternatives Have Lower Device related bacteraemia Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL