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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 MEPOLIZUMAB Cause Device use issue? 24 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Device use issue have been filed in association with MEPOLIZUMAB (Nucala). This represents 0.1% of all adverse event reports for MEPOLIZUMAB.

24
Reports of Device use issue with MEPOLIZUMAB
0.1%
of all MEPOLIZUMAB reports
1
Deaths
3
Hospitalizations

How Dangerous Is Device use issue From MEPOLIZUMAB?

Of the 24 reports, 1 (4.2%) resulted in death, 3 (12.5%) required hospitalization.

Is Device use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MEPOLIZUMAB. However, 24 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 issue?

SOMATROPIN (2,571) LEVONORGESTREL (2,489) COPPER (1,318) BUDESONIDE\FORMOTEROL (1,236) EXENATIDE (992) BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976) DUPILUMAB (528) ALIROCUMAB (471) INSULIN GLARGINE (469) BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)

Which MEPOLIZUMAB Alternatives Have Lower Device use issue Risk?

MEPOLIZUMAB vs MEPROBAMATE MEPOLIZUMAB vs MERCAPTOPURINE MEPOLIZUMAB vs MEROPENEM MEPOLIZUMAB vs MEROPENEM ANHYDROUS MEPOLIZUMAB vs MESALAMINE

Related Pages

MEPOLIZUMAB Full Profile All Device use issue Reports All Drugs Causing Device use issue MEPOLIZUMAB Demographics