Does TEDUGLUTIDE Cause Haemoglobin decreased? 76 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Haemoglobin decreased have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.9% of all adverse event reports for TEDUGLUTIDE.
76
Reports of Haemoglobin decreased with TEDUGLUTIDE
0.9%
of all TEDUGLUTIDE reports
8
Deaths
62
Hospitalizations
How Dangerous Is Haemoglobin decreased From TEDUGLUTIDE?
Of the 76 reports, 8 (10.5%) resulted in death, 62 (81.6%) required hospitalization.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 76 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which TEDUGLUTIDE Alternatives Have Lower Haemoglobin decreased Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL