Does MUPIROCIN\MUPIROCIN Cause Product use in unapproved indication? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Product use in unapproved indication have been filed in association with MUPIROCIN\MUPIROCIN. This represents 9.2% of all adverse event reports for MUPIROCIN\MUPIROCIN.
31
Reports of Product use in unapproved indication with MUPIROCIN\MUPIROCIN
9.2%
of all MUPIROCIN\MUPIROCIN reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product use in unapproved indication From MUPIROCIN\MUPIROCIN?
Of the 31 reports, 1 (3.2%) resulted in death, 1 (3.2%) required hospitalization.
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\MUPIROCIN. However, 31 reports have been filed with the FAERS database.
What Other Side Effects Does MUPIROCIN\MUPIROCIN Cause?
Drug ineffective (90)
Macular degeneration (71)
Drug hypersensitivity (58)
Off label use (48)
Toxic epidermal necrolysis (38)
Malaise (25)
Pruritus (22)
Erythema (21)
Nausea (19)
Pain (18)
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\MUPIROCIN Alternatives Have Lower Product use in unapproved indication Risk?
MUPIROCIN\MUPIROCIN vs MUROMONAB-CD3
MUPIROCIN\MUPIROCIN vs MYCOPHENOLATE
MUPIROCIN\MUPIROCIN vs MYCOPHENOLATE MOFETIL
MUPIROCIN\MUPIROCIN vs MYCOPHENOLATE MOFETIL\MYCOPHENOLATE MOFETIL
MUPIROCIN\MUPIROCIN vs MYCOPHENOLIC ACID