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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 MUPIROCIN Cause Condition aggravated? 100 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 100 reports of Condition aggravated have been filed in association with MUPIROCIN (MUPIROCIN). This represents 2.9% of all adverse event reports for MUPIROCIN.

100
Reports of Condition aggravated with MUPIROCIN
2.9%
of all MUPIROCIN reports
1
Deaths
6
Hospitalizations

How Dangerous Is Condition aggravated From MUPIROCIN?

Of the 100 reports, 1 (1.0%) resulted in death, 6 (6.0%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MUPIROCIN. However, 100 reports have been filed with the FAERS database.

What Other Side Effects Does MUPIROCIN Cause?

Drug ineffective (1,036) Product use in unapproved indication (793) Macular degeneration (771) Off label use (451) Pain (277) Product use issue (257) Therapeutic product effect incomplete (256) Nausea (240) Pyrexia (230) Malaise (226)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which MUPIROCIN Alternatives Have Lower Condition aggravated Risk?

MUPIROCIN vs MUPIROCIN\MUPIROCIN MUPIROCIN vs MUROMONAB-CD3 MUPIROCIN vs MYCOPHENOLATE MUPIROCIN vs MYCOPHENOLATE MOFETIL MUPIROCIN vs MYCOPHENOLATE MOFETIL\MYCOPHENOLATE MOFETIL

Related Pages

MUPIROCIN Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated MUPIROCIN Demographics