Does MUPIROCIN Cause Recalled product administered? 53 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Recalled product administered have been filed in association with MUPIROCIN (MUPIROCIN). This represents 1.5% of all adverse event reports for MUPIROCIN.
53
Reports of Recalled product administered with MUPIROCIN
1.5%
of all MUPIROCIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product administered From MUPIROCIN?
Of the 53 reports.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MUPIROCIN. However, 53 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which MUPIROCIN Alternatives Have Lower Recalled product administered Risk?
MUPIROCIN vs MUPIROCIN\MUPIROCIN
MUPIROCIN vs MUROMONAB-CD3
MUPIROCIN vs MYCOPHENOLATE
MUPIROCIN vs MYCOPHENOLATE MOFETIL
MUPIROCIN vs MYCOPHENOLATE MOFETIL\MYCOPHENOLATE MOFETIL