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Drug overview for MUPIROCIN (mupirocin calcium):
Generic name: mupirocin calcium (mue-PIR-oh-sin)
Drug class: Topical Antibiotics
Therapeutic class: Dermatological
Mupirocin is a pseudomonic acid antibiotic produced by Pseudomonas fluorescens.
No enhanced Uses information available for this drug.
Generic name: mupirocin calcium (mue-PIR-oh-sin)
Drug class: Topical Antibiotics
Therapeutic class: Dermatological
Mupirocin is a pseudomonic acid antibiotic produced by Pseudomonas fluorescens.
No enhanced Uses information available for this drug.
DRUG IMAGES
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The following indications for MUPIROCIN (mupirocin calcium) have been approved by the FDA:
Indications:
Staph aureus traumatic skin lesion infection
Traumatic skin lesion Streptococcus pyogenes infection
Professional Synonyms:
Skin infection due to Staphylococcus aureus
Skin infection due to Staphylococcus pyogenes aureus
Skin infection due to Streptococcus pyogenes
Indications:
Staph aureus traumatic skin lesion infection
Traumatic skin lesion Streptococcus pyogenes infection
Professional Synonyms:
Skin infection due to Staphylococcus aureus
Skin infection due to Staphylococcus pyogenes aureus
Skin infection due to Streptococcus pyogenes
The following dosing information is available for MUPIROCIN (mupirocin calcium):
No enhanced Dosing information available for this drug.
No enhanced Administration information available for this drug.
DRUG LABEL | DOSING TYPE | DOSING INSTRUCTIONS |
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MUPIROCIN 2% CREAM | Maintenance | Adults apply a small amount to the affected area by topical route 3 times per day for 10 days |
DRUG LABEL | DOSING TYPE | DOSING INSTRUCTIONS |
---|---|---|
MUPIROCIN 2% CREAM | Maintenance | Adults apply a small amount to the affected area by topical route 3 times per day for 10 days |
The following drug interaction information is available for MUPIROCIN (mupirocin calcium):
There are 0 contraindications.
There are 0 severe interactions.
There are 0 moderate interactions.
The following contraindication information is available for MUPIROCIN (mupirocin calcium):
Drug contraindication overview.
No enhanced Contraindications information available for this drug.
No enhanced Contraindications information available for this drug.
There are 0 contraindications.
There are 0 severe contraindications.
There are 1 moderate contraindications.
Clinically significant contraindication, where the condition can be managed or treated before the drug may be given safely.
Moderate List |
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No disease contraindications |
The following adverse reaction information is available for MUPIROCIN (mupirocin calcium):
Adverse reaction overview.
No enhanced Common Adverse Effects information available for this drug.
No enhanced Common Adverse Effects information available for this drug.
There are 3 severe adverse reactions.
More Frequent | Less Frequent |
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None. | None. |
Rare/Very Rare |
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Anaphylaxis Angioedema Clostridioides difficile infection |
There are 15 less severe adverse reactions.
More Frequent | Less Frequent |
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Headache disorder Nausea Skin rash |
Dry skin Erythema Pruritus of skin Skin inflammation Skin swelling Stinging of skin Treatment site sequelae |
Rare/Very Rare |
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Acute abdominal pain Aphthous stomatitis Dizziness Pain Urticaria |
The following precautions are available for MUPIROCIN (mupirocin calcium):
No enhanced Pediatric Use information available for this drug.
Contraindicated
Severe Precaution
Management or Monitoring Precaution
Contraindicated
None |
Severe Precaution
None |
Management or Monitoring Precaution
None |
Data are insufficient to determine whether there is a drug-associated risk with use of mupirocin ointment for dermatologic use, mupirocin calcium cream for dermatologic use, or mupirocin calcium ointment for intranasal use in pregnant women. One manufacturer states that mupirocin ointment for dermatologic use should be used during pregnancy only if clearly needed. Systemic absorption of mupirocin following topical application to intact skin is minimal.
Although systemic absorption of mupirocin was reported to be negligible following intranasal application of mupirocin calcium ointment for intranasal use in adults, the dosage regimen used in this study did not mimic the recommended intranasal dosage. Reproduction studies in rats or rabbits using subcutaneous mupirocin in dosages up to 22 or 43 times, respectively, the usual human topical dosage or up to 65 or 130 times, respectively, the usual human intranasal dosage have not revealed evidence of developmental toxicity.
Although systemic absorption of mupirocin was reported to be negligible following intranasal application of mupirocin calcium ointment for intranasal use in adults, the dosage regimen used in this study did not mimic the recommended intranasal dosage. Reproduction studies in rats or rabbits using subcutaneous mupirocin in dosages up to 22 or 43 times, respectively, the usual human topical dosage or up to 65 or 130 times, respectively, the usual human intranasal dosage have not revealed evidence of developmental toxicity.
It is not known whether systemically absorbed mupirocin is distributed into human milk, affects milk production, or affects the breast-fed infant. Because systemic absorption of mupirocin is minimal following topical application to skin and negligible following intranasal administration, the manufacturers state that mupirocin exposure in breast-feeding infants is unlikely. The benefits of breast-feeding and the importance of mupirocin to the woman should be considered along with potential adverse effects on the breast-fed child from the drug or from the underlying maternal condition.
One manufacturer states that mupirocin ointment for dermatologic use should be used with caution in nursing women. If a breast and/or nipple is being treated with mupirocin ointment for dermatologic use or mupirocin calcium cream for dermatologic use, the treated area should be thoroughly washed prior to breast-feeding to minimize oral exposure to the drug in the breast-feeding infant.
One manufacturer states that mupirocin ointment for dermatologic use should be used with caution in nursing women. If a breast and/or nipple is being treated with mupirocin ointment for dermatologic use or mupirocin calcium cream for dermatologic use, the treated area should be thoroughly washed prior to breast-feeding to minimize oral exposure to the drug in the breast-feeding infant.
No enhanced Geriatric Use information available for this drug.
The following prioritized warning is available for MUPIROCIN (mupirocin calcium):
No warning message for this drug.
No warning message for this drug.
The following icd codes are available for MUPIROCIN (mupirocin calcium)'s list of indications:
Staph aureus traumatic skin lesion infection | |
B95.6 | Staphylococcus aureus as the cause of diseases classified elsewhere |
B95.61 | Methicillin susceptible staphylococcus aureus infection as the cause of diseases classified elsewhere |
B95.62 | Methicillin resistant staphylococcus aureus infection as the cause of diseases classified elsewhere |
Traumatic skin lesion strep pyogenes infection | |
B95.0 | Streptococcus, group a, as the cause of diseases classified elsewhere |
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