Fusidic Acid Gel (Fusidic Acid Hydrate)
Fusidic Acid Hydrate 20mg
OTC medication
Dongwha Pharmaceutical Co., Ltd.
MFDS item code 200001087 · Notified 2000.04.07
Treatment of skin infections and pyoderma such as Staphylococcus aureus
This medication is used to treat osteomyelitis caused by Staphylococcus aureus, wound infections of the skin, skin infections such as furuncle and abscess, sepsis, cystic fibrosis, endocarditis, and bronchopneumonia in syrup form. Cream and gel formulations are utilized for the treatment of pyoderma (impetigo and infectious eczema, etc.), common acne, folliculitis, boils, pyogenic granuloma, and secondary infections caused by burns, trauma, surgical wounds, and skin abrasions. Therefore, this medicine is effective in alleviating various skin and internal infections.
Syrup: administer 15mL [750mg (potency)] orally 3 times a day. Cream or gel: apply an appropriate amount to the affected area 3 to 4 times a day. However, if bandaging, it is advisable to reduce the frequency to 1 to 2 times a day.
Children aged 5 to 12 years: administer 10mL [500mg (potency)] orally 3 times a day. Infants aged 1 to 5 years: administer 5mL [250mg (potency)] orally 3 times a day. Infants under 1 year of age
This drug should not be used in certain patients. Those who are allergic to fusidic acid or its salts should not take this medication. It is advisable to avoid use in patients with Staphylococcus infections of the urinary tract that are not caused by renal disease. Patients with poor liver function should also avoid this drug. While taking this medication, gastrointestinal symptoms such as nausea, vomiting, diarrhea, anorexia, stomach ache, abdominal pain, or dyspepsia may occur. Abnormal blood conditions such as granulocytopenia, thrombocytopenia, and bone marrow suppression may arise, so caution is warranted. Liver dysfunction may lead to an increase in bilirubin levels or jaundice; in such cases, discontinuation of the medication will improve symptoms. Rarely, allergic reactions such as skin rashes may occur. It is recommended to perform sensitivity testing to prevent the development of resistant bacteria and use it only for the necessary minimum duration. Patients on high doses or long-term treatment, and those with weak liver function, should undergo regular liver function tests. Caution is required for neonates, premature infants, and infants with jaundice, and it is preferable to use this along with other medications in severe infections. This medication is mainly excreted through bile, so dose adjustment is not necessary for patients with impaired kidney function. Caution should also be exercised when using it in conjunction with other antibiotics such as lincomycin or rifampicin, which share similar biliary excretion pathways. Pregnant women should only use it if the benefits of treatment outweigh the risks, as this medication can cross the placenta. Nursing mothers should either discontinue breastfeeding or use this medication carefully since it can pass into breast milk. Children or neonates should be monitored closely for liver function due to their immature liver function. In cases of overdose, liver enzyme levels may temporarily rise, or symptoms such as jaundice, upper abdominal discomfort, and diarrhea may appear. In such cases, treatment should focus on alleviating symptoms, and dialysis is not recommended as it is ineffective. This medication should be stored away from direct sunlight and heat, shaken well before use, and should not be diluted. When used topically, careful observation is necessary for any skin allergic reactions, and it is advisable not to use it on the inner face areas such as the eyes or eyelids. Long-term or widespread application should be avoided, and to prevent the development of resistant bacteria, it is wise to use it only for the necessary minimum duration after confirming sensitivity. Pregnant or nursing women should consult a physician before using it topically. Caution is required for premature or newborn infants, as they may experience liver dysfunction with extensive or prolonged use. If rashes, itching, swelling, or blisters as allergic symptoms appear while using this drug, usage should be discontinued immediately and professional consultation sought. This medication should be kept out of reach of children and stored in its original container tightly closed, as transferring to another container may degrade the quality or risk misuse.
Symptoms of liver abnormalities (hyperbilirubinemia, jaundice), severe allergic reactions (hypersensitivity reactions)
Nausea, vomiting, diarrhea, anorexia, stomach pain, abdominal pain, dyspepsia, blood system abnormalities (granulocytopenia, thrombocytopenia, bone marrow suppression), skin rashes, temporary burning sensation, mild pain and irritation, pain
Not everyone experiences these, and they can vary from person to person.
This drug should be stored in a tightly sealed container to prevent air or moisture from entering. It is important to maintain a storage temperature between 1 and 30 degrees Celsius. This ensures the medication remains effective for an extended period and can be used safely.
White gel preparation
10 grams/tube, 15 grams/tube
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Fusidic Acid Hydrate 20mg
OTC medication
Dongwha Pharmaceutical Co., Ltd.
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Prescription medication
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Fusidic Acid Hydrate 20mg
OTC medication
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.