Does VEDOLIZUMAB Cause Product storage error? 336 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 336 reports of Product storage error have been filed in association with VEDOLIZUMAB (ENTYVIO). This represents 0.5% of all adverse event reports for VEDOLIZUMAB.
336
Reports of Product storage error with VEDOLIZUMAB
0.5%
of all VEDOLIZUMAB reports
2
Deaths
27
Hospitalizations
How Dangerous Is Product storage error From VEDOLIZUMAB?
Of the 336 reports, 2 (0.6%) resulted in death, 27 (8.0%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VEDOLIZUMAB. However, 336 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 Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which VEDOLIZUMAB Alternatives Have Lower Product storage error Risk?
VEDOLIZUMAB vs VELAGLUCERASE ALFA
VEDOLIZUMAB vs VELCADE
VEDOLIZUMAB vs VELETRI
VEDOLIZUMAB vs VELIPARIB
VEDOLIZUMAB vs VEMURAFENIB