Does MEPOLIZUMAB Cause Wrong product administered? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Wrong product administered have been filed in association with MEPOLIZUMAB (Nucala). This represents 0.0% of all adverse event reports for MEPOLIZUMAB.
16
Reports of Wrong product administered with MEPOLIZUMAB
0.0%
of all MEPOLIZUMAB reports
0
Deaths
2
Hospitalizations
How Dangerous Is Wrong product administered From MEPOLIZUMAB?
Of the 16 reports, 2 (12.5%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEPOLIZUMAB. However, 16 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which MEPOLIZUMAB Alternatives Have Lower Wrong product administered Risk?
MEPOLIZUMAB vs MEPROBAMATE
MEPOLIZUMAB vs MERCAPTOPURINE
MEPOLIZUMAB vs MEROPENEM
MEPOLIZUMAB vs MEROPENEM ANHYDROUS
MEPOLIZUMAB vs MESALAMINE