Does VEDOLIZUMAB Cause Wrong product administered? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Wrong product administered have been filed in association with VEDOLIZUMAB (ENTYVIO). This represents 0.0% of all adverse event reports for VEDOLIZUMAB.
16
Reports of Wrong product administered with VEDOLIZUMAB
0.0%
of all VEDOLIZUMAB reports
1
Deaths
5
Hospitalizations
How Dangerous Is Wrong product administered From VEDOLIZUMAB?
Of the 16 reports, 1 (6.3%) resulted in death, 5 (31.3%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VEDOLIZUMAB. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does VEDOLIZUMAB Cause?
Off label use (21,017)
Colitis ulcerative (13,455)
Crohn's disease (9,759)
Drug ineffective (8,424)
Diarrhoea (7,493)
Abdominal pain (6,401)
Fatigue (5,477)
Haematochezia (5,215)
Frequent bowel movements (4,527)
Arthralgia (4,028)
What Other Drugs Cause Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which VEDOLIZUMAB Alternatives Have Lower Wrong product administered Risk?
VEDOLIZUMAB vs VELAGLUCERASE ALFA
VEDOLIZUMAB vs VELCADE
VEDOLIZUMAB vs VELETRI
VEDOLIZUMAB vs VELIPARIB
VEDOLIZUMAB vs VEMURAFENIB