Does MUPIROCIN Cause Product use in unapproved indication? 793 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 793 reports of Product use in unapproved indication have been filed in association with MUPIROCIN (MUPIROCIN). This represents 22.9% of all adverse event reports for MUPIROCIN.
793
Reports of Product use in unapproved indication with MUPIROCIN
22.9%
of all MUPIROCIN reports
3
Deaths
17
Hospitalizations
How Dangerous Is Product use in unapproved indication From MUPIROCIN?
Of the 793 reports, 3 (0.4%) resulted in death, 17 (2.1%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MUPIROCIN. However, 793 reports have been filed with the FAERS database.
What Other Side Effects Does MUPIROCIN Cause?
Drug ineffective (1,036)
Macular degeneration (771)
Off label use (451)
Pain (277)
Product use issue (257)
Therapeutic product effect incomplete (256)
Nausea (240)
Pyrexia (230)
Malaise (226)
Weight decreased (225)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which MUPIROCIN Alternatives Have Lower Product use in unapproved indication Risk?
MUPIROCIN vs MUPIROCIN\MUPIROCIN
MUPIROCIN vs MUROMONAB-CD3
MUPIROCIN vs MYCOPHENOLATE
MUPIROCIN vs MYCOPHENOLATE MOFETIL
MUPIROCIN vs MYCOPHENOLATE MOFETIL\MYCOPHENOLATE MOFETIL