Does MEPOLIZUMAB Cause Device use error? 153 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 153 reports of Device use error have been filed in association with MEPOLIZUMAB (Nucala). This represents 0.4% of all adverse event reports for MEPOLIZUMAB.
153
Reports of Device use error with MEPOLIZUMAB
0.4%
of all MEPOLIZUMAB reports
1
Deaths
4
Hospitalizations
How Dangerous Is Device use error From MEPOLIZUMAB?
Of the 153 reports, 1 (0.7%) resulted in death, 4 (2.6%) required hospitalization.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEPOLIZUMAB. However, 153 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 Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which MEPOLIZUMAB Alternatives Have Lower Device use error Risk?
MEPOLIZUMAB vs MEPROBAMATE
MEPOLIZUMAB vs MERCAPTOPURINE
MEPOLIZUMAB vs MEROPENEM
MEPOLIZUMAB vs MEROPENEM ANHYDROUS
MEPOLIZUMAB vs MESALAMINE