Does VEDOLIZUMAB Cause Device leakage? 136 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 136 reports of Device leakage have been filed in association with VEDOLIZUMAB (ENTYVIO). This represents 0.2% of all adverse event reports for VEDOLIZUMAB.
136
Reports of Device leakage with VEDOLIZUMAB
0.2%
of all VEDOLIZUMAB reports
3
Deaths
28
Hospitalizations
How Dangerous Is Device leakage From VEDOLIZUMAB?
Of the 136 reports, 3 (2.2%) resulted in death, 28 (20.6%) required hospitalization.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VEDOLIZUMAB. However, 136 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 Device leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
Which VEDOLIZUMAB Alternatives Have Lower Device leakage Risk?
VEDOLIZUMAB vs VELAGLUCERASE ALFA
VEDOLIZUMAB vs VELCADE
VEDOLIZUMAB vs VELETRI
VEDOLIZUMAB vs VELIPARIB
VEDOLIZUMAB vs VEMURAFENIB