Does MEPOLIZUMAB Cause Intentional product use issue? 540 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 540 reports of Intentional product use issue have been filed in association with MEPOLIZUMAB (Nucala). This represents 1.3% of all adverse event reports for MEPOLIZUMAB.
540
Reports of Intentional product use issue with MEPOLIZUMAB
1.3%
of all MEPOLIZUMAB reports
518
Deaths
430
Hospitalizations
How Dangerous Is Intentional product use issue From MEPOLIZUMAB?
Of the 540 reports, 518 (95.9%) resulted in death, 430 (79.6%) required hospitalization, and 442 (81.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEPOLIZUMAB. However, 540 reports have been filed with the FAERS database.
What Other Side Effects Does MEPOLIZUMAB Cause?
Asthma (11,033)
Dyspnoea (9,192)
Wheezing (6,093)
Product dose omission issue (5,873)
Cough (4,577)
Pneumonia (4,107)
Therapeutic product effect incomplete (4,106)
Drug ineffective (3,880)
Loss of personal independence in daily activities (3,566)
Fatigue (2,656)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which MEPOLIZUMAB Alternatives Have Lower Intentional product use issue Risk?
MEPOLIZUMAB vs MEPROBAMATE
MEPOLIZUMAB vs MERCAPTOPURINE
MEPOLIZUMAB vs MEROPENEM
MEPOLIZUMAB vs MEROPENEM ANHYDROUS
MEPOLIZUMAB vs MESALAMINE