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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does VEDOLIZUMAB Cause Device breakage? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Device breakage have been filed in association with VEDOLIZUMAB (ENTYVIO). This represents 0.0% of all adverse event reports for VEDOLIZUMAB.

9
Reports of Device breakage with VEDOLIZUMAB
0.0%
of all VEDOLIZUMAB reports
0
Deaths
3
Hospitalizations

How Dangerous Is Device breakage From VEDOLIZUMAB?

Of the 9 reports, 3 (33.3%) required hospitalization.

Is Device breakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VEDOLIZUMAB. However, 9 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 breakage?

COPPER (9,201) SOMATROPIN (7,761) ETONOGESTREL (4,140) LEVONORGESTREL (2,726) ETHINYL ESTRADIOL\ETONOGESTREL (741) CARBIDOPA\LEVODOPA (634) TREPROSTINIL (396) ADALIMUMAB (375) ALBUTEROL (256) EPOPROSTENOL (240)

Which VEDOLIZUMAB Alternatives Have Lower Device breakage Risk?

VEDOLIZUMAB vs VELAGLUCERASE ALFA VEDOLIZUMAB vs VELCADE VEDOLIZUMAB vs VELETRI VEDOLIZUMAB vs VELIPARIB VEDOLIZUMAB vs VEMURAFENIB

Related Pages

VEDOLIZUMAB Full Profile All Device breakage Reports All Drugs Causing Device breakage VEDOLIZUMAB Demographics