Viewing nowEnrisone SR Sustained-Release Tablet (Eperisone Hydrochloride)
Eperisone Hydrochloride 75mg
Tablet · Prescription medication
NBK Pharmaceutical Co., Ltd.

MFDS item code 201908698 · Approved 2019.12.30 · Insurance code 054800620
Relief of painful muscle spasms associated with musculoskeletal disorders (cervical myofascial syndrome, periarthritis of the shoulder)
Used for painful muscle spasms associated with musculoskeletal disorders such as cervical myofascial syndrome, periarthritis of the shoulder, and low back pain.
This medication is in a sustained-release tablet form and should be taken whole without crushing, splitting, or chewing. Adults take 1 tablet (75 mg of eperisone hydrochloride) orally after meals, twice daily. The dosage may be adjusted appropriately based on age and symptoms.
This medication should not be used by patients with known allergies to this drug or by patients with severe myasthenia gravis. Patients with a history of drug allergies or those with liver dysfunction should use this medication cautiously, as liver function may worsen. During treatment, serious allergic reactions or symptoms such as skin rash, fever, itching, blisters, eye redness, and stomatitis may occur, in which case treatment should be discontinued immediately and medical assistance sought. Additionally, various side effects such as headache, dizziness, drowsiness, indigestion, nausea, vomiting, constipation, diarrhea, and abdominal pain may occur, so it is important to monitor your condition closely. During treatment, symptoms such as weakness, staggering, and drowsiness may appear, so it is advisable to reduce the dosage or discontinue use if these symptoms occur. Drowsiness and reduced concentration may occur, so activities such as driving or operating hazardous machinery should be avoided during treatment. Women who are pregnant or may become pregnant should only use this medication after consulting with a physician, as the safety profile has not been established, weighing the treatment benefits against the risks. Breastfeeding women should ideally avoid this medication, and if unavoidable, it is recommended to discontinue breastfeeding while on treatment. Safety in children has not been sufficiently established, thus special caution is needed when administering to children. Elderly patients may have reduced physiological function, so dosage adjustments and careful monitoring are necessary.
Hives, severe swelling (edema), difficulty breathing, shock, anaphylactic reactions, toxic epidermal necrolysis, Stevens-Johnson syndrome, severe fever, severe rash, blisters, peeling skin, pain in mucous membranes of the mouth/eyes, extreme lethargy, jaundice, sudden and severe headache, thunderclap headache, seizures, altered consciousness, vision abnormalities, paralysis, markedly reduced urination, severe generalized swelling accompanied by elevated blood pressure.
Not everyone experiences these, and they can vary from person to person.
This medicine should be stored in a tightly sealed container to avoid exposure to air or moisture, and the storage temperature should be maintained at room temperature between 1°C and 30°C. Storing it this way will help maintain the effectiveness of the medication safely.
White to almost white round sustained-release film-coated tablet
30 tablets/bottle, 500 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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.