Medically reviewed by Drugs.com. Last updated on Mar 3, 2020.
(MA fe nide)
- Mafenide Acetate
Excipient information presented when available (limited, particularly for generics); consult specific product labeling.
Cream, External, as acetate [strength expressed as base]:
Sulfamylon: 85 mg/g (56.7 g, 113.4 g, 453.6 g) [contains methylparaben, propylparaben, sodium metabisulfite]
Packet, External, as acetate:
Sulfamylon: 50 g (1 ea, 5 ea)
Generic: 50 g (1 ea, 5 ea)
Brand Names: U.S.
- Antibiotic, Topical
As a sulfonamide, mafenide interferes with bacterial folic acid synthesis through competitive inhibition of para-aminobenzoic acid. Spectrum of activity encompasses both gram positive and negative organisms, including Pseudomonas and some anaerobes.
Diffuses through devascularized areas and is rapidly absorbed from burned surface
To para-carboxybenzene sulfonamide; mafenide and metabolite are carbonic anhydrase inhibitors
Urine (as metabolites)
Time to Peak
Serum: Cream 11%: 2 to 4 hours; Burn tissue: Cream 11%: 2 hours, Solution 5%: 4 hours
Use: Labeled Indications
Burn treatment: For adjunctive therapy of patients with second- and third-degree burns (cream); for use as an adjunctive topical antimicrobial agent to control bacterial infection when used under moist dressings over meshed autografts on excised burn wounds (powder for solution)
Hypersensitivity to mafenide or any component of the formulation
Burn treatment: Topical:
Cream: Apply once or twice daily with a sterile-gloved hand; apply to a thickness of approximately 1/16 inch (thicker application is not recommended). The burned area should be covered with cream at all times. Continue treatment until healing is progressing well or the burn site is ready for grafting.
Powder for solution: Wet an 8-ply burn dressing with solution and cover graft area. Keep dressing wet using syringe or irrigation tubing every 4 hours (or as necessary) or by moistening dressing every 6 to 8 hours (or as necessary). Continue treatment until autograft vascularization occurs and healing is progressing; may leave dressings in place for ≤5 days.
Dosage adjustment for concomitant therapy: Significant drug interactions exist, requiring dose/frequency adjustment or avoidance. Consult drug interactions database for more information.
Refer to adult dosing.
Cream: Infants, Children, and Adolescents: Apply once or twice daily with a sterile-gloved hand; apply to a thickness of approximately 1/16 inch; the burned area should be covered with cream at all times.
Solution (5%): Infants ≥3 months, Children, and Adolescents: Cover graft area with 1 layer of fine mesh gauze. Wet an 8-ply burn dressing with mafenide solution and cover graft area. Keep dressing wet using syringe or irrigation tubing every 4 hours (or as necessary), or by moistening dressing every 6 to 8 hours (or as necessary). Irrigation dressing should be secured with bolster dressing and wrapped as appropriate. May leave dressings in place for up to 5 days.
Dosing: Adjustment for Toxicity
Acidosis: When acidosis becomes difficult to control, discontinuing treatment for 24 to 48 hours may aid in restoring acid-base balance
Powder for solution: To prepare a 5% topical solution, add mafenide 50 g to 1000 mL of NS for irrigation or sterile water for irrigation. Mix until dissolved.
Cream: For external use only. Keep burn area covered with cream at all times. Dressings are typically not required however if necessary only a thin layer of dressings should be used. Apply to clean debrided area with a sterile gloved hand. Apply to a thickness of approximately 1/16 inch (thicker application is not recommended). Do not discontinue therapy if there is a possibility of infection. If possible, patient should bathe daily to aid debridement (eg, whirlpool bath, shower, or bathed in bed).
Powder for solution: For external use only. Cover graft area with 1 layer of fine mesh gauze. Wet an 8-ply burn dressing with solution until leaking is noticeable and cover graft area. Keep dressing wet using syringe or irrigation tubing or by moistening dressing. Irrigation tubing should be placed over burn dressing in contact with the wound; use an additional 8-ply dressing to cover. Irrigation dressing should be secured with bolster dressing and wrapped as appropriate.
Cream: Avoid exposure to excessive heat (>40°C [>104°F]).
Powder for solution: Prior to reconstitution, store powder at 15°C to 30°C (59°F to 86°F). Store prepared solution at 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F and 86°F). May store at 15°C to 30°C (59°F to 86°F) for limited periods. Solution may be stored in unopened containers for up to 28 days; once container is open, discard unused portion within 48 hours.
BCG (Intravesical): Antibiotics may diminish the therapeutic effect of BCG (Intravesical). Avoid combination
BCG Vaccine (Immunization): Antibiotics may diminish the therapeutic effect of BCG Vaccine (Immunization). Monitor therapy
Dapsone (Topical): May enhance the adverse/toxic effect of Methemoglobinemia Associated Agents. Monitor therapy
Local Anesthetics: Methemoglobinemia Associated Agents may enhance the adverse/toxic effect of Local Anesthetics. Specifically, the risk for methemoglobinemia may be increased. Monitor therapy
Nitric Oxide: May enhance the adverse/toxic effect of Methemoglobinemia Associated Agents. Combinations of these agents may increase the likelihood of significant methemoglobinemia. Monitor therapy
Prilocaine: Methemoglobinemia Associated Agents may enhance the adverse/toxic effect of Prilocaine. Combinations of these agents may increase the likelihood of significant methemoglobinemia. Management: Monitor patients for signs of methemoglobinemia (e.g., hypoxia, cyanosis) when prilocaine is used in combination with other agents associated with development of methemoglobinemia. Avoid lidocaine/prilocaine in infants receiving such agents. Monitor therapy
Sodium Nitrite: Methemoglobinemia Associated Agents may enhance the adverse/toxic effect of Sodium Nitrite. Combinations of these agents may increase the likelihood of significant methemoglobinemia. Monitor therapy
Sodium Picosulfate: Antibiotics may diminish the therapeutic effect of Sodium Picosulfate. Management: Consider using an alternative product for bowel cleansing prior to a colonoscopy in patients who have recently used or are concurrently using an antibiotic. Consider therapy modification
Frequency not defined.
Cardiovascular: Edema, facial edema
Dermatologic: Erythema, maceration, pruritus, rash, urticaria
Endocrine & metabolic: Hyperchloremia, metabolic acidosis
Gastrointestinal: Diarrhea (following accidental ingestion)
Hematologic: Bleeding, bone marrow suppression, DIC, eosinophilia, hemolytic anemia, porphyria
Local: Blisters, burning sensation, excoriation, pain
Respiratory: Dyspnea, hyperventilation, pCO2 decreased, tachypnea
Concerns related to adverse effects:
• Acid-base imbalance: Mafenide and its metabolite inhibit carbonic anhydrase; metabolic acidosis may occur. Symptoms may include compensatory hyperventilation; risk is increased in patients with impaired renal function. Some patients experience masked hyperventilation and respiratory alkalosis; etiology is unknown. Monitor acid-base balance, especially in patients with extensive second-degree or partial-thickness burns and in patients with pulmonary or renal dysfunction.
• Sulfonamide allergy: Chemical similarities are present among sulfonamides, sulfonylureas, carbonic anhydrase inhibitors, thiazides, and loop diuretics (except ethacrynic acid). Use in patients with sulfonamide allergy is specifically contraindicated in product labeling, however, a risk of cross-reaction exists in patients with allergy to any of these compounds; avoid use when previous reaction has been severe.
• Superinfection: Prolonged use may result in fungal or bacterial superinfection, including C. difficile-associated diarrhea (CDAD) and pseudomembranous colitis; CDAD has been observed >2 months postantibiotic treatment.
• G6PD deficiency: Use caution in patients with G6PD deficiency; hemolytic anemia with DIC (including fatalities) has been reported with use, presumably related to G6PD deficiency.
• Renal impairment: Use with caution in burn patients with acute renal impairment; accumulation of parent drug and metabolite may enhance carbonic anhydrase inhibition and increase risk of metabolic acidosis.
Dosage forms specific issues:
• Sulfites: Some dosage forms contain sulfites which may cause allergic-type reactions (including anaphylaxis) as well as life-threatening or less severe asthmatic episodes in certain individuals; consider discontinuation of therapy if allergic reactions occur.
Acid base balance; signs of infection; signs of healing
The manufacturer does not recommend use of the cream in women of childbearing potential unless the burn area covers >20% of the total body surface.
The manufacturer does not recommend use of the cream unless the benefits of treatment outweigh possible risks to the fetus.
What is this drug used for?
• It is used to avoid or treat skin infections in patients with burns.
All drugs may cause side effects. However, many people have no side effects or only have minor side effects. Call your doctor or get medical help if any of these side effects or any other side effects bother you or do not go away:
• Short-term pain
WARNING/CAUTION: Even though it may be rare, some people may have very bad and sometimes deadly side effects when taking a drug. Tell your doctor or get medical help right away if you have any of the following signs or symptoms that may be related to a very bad side effect:
• Acidosis like confusion, fast breathing, fast heartbeat, abnormal heartbeat, severe abdominal pain, nausea, vomiting, fatigue, shortness of breath, or loss of strength and energy
• Severe skin irritation
• Hemolytic anemia like severe loss of strength and energy, dark urine, or yellow skin
• Signs of an allergic reaction, like rash; hives; itching; red, swollen, blistered, or peeling skin with or without fever; wheezing; tightness in the chest or throat; trouble breathing, swallowing, or talking; unusual hoarseness; or swelling of the mouth, face, lips, tongue, or throat.
Note: This is not a comprehensive list of all side effects. Talk to your doctor if you have questions.
Consumer Information Use and Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only the healthcare provider has the knowledge and training to decide which medicines are right for a specific patient. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a limited summary of general information about the medicine's uses from the patient education leaflet and is not intended to be comprehensive. This limited summary does NOT include all information available about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not intended to provide medical advice, diagnosis or treatment and does not replace information you receive from the healthcare provider. For a more detailed summary of information about the risks and benefits of using this medicine, please speak with your healthcare provider and review the entire patient education leaflet.
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
More about mafenide topical
- Side Effects
- During Pregnancy
- Dosage Information
- Pricing & Coupons
- En Español
- Drug class: topical antibiotics
Other brands: Sulfamylon