Medication info
Myrikson Sustained Release Tablet (Eperisone Hydrochloride)

Myrikson Sustained Release Tablet (Eperisone Hydrochloride)

Prescription medicationTablet경구
Ingredient · strength
Eperisone Hydrochloride›75mg / 1 tablet
Manufacturer / importer
(주)라이트팜텍
Appearance
White to nearly white round sustained release film-coated tablet
Packaging
30 tablets/bottle, 500 tablets/bottle
Approval status
Active

MFDS item code 201905953 · Approved 2019.08.22 · Insurance code 690301550

Summary

Main use
Relief of painful muscle spasms in musculoskeletal diseases (cervical shoulder syndrome, periarthritis of the shoulder)
Who takes it
Adults
Adult dose
This medication is a sustained release tablet, and it should be taken whole without crushing, splitting, or chewing. Adults should take 1 tablet (75mg of eperisone hydrochloride) twice a day after meals. Dosage may be adjusted according to age and symptoms.

Ingredients

Manufacturer
(주)라이트팜텍

Efficacy & effects

Relief of painful muscle spasms in musculoskeletal diseases (cervical shoulder syndrome, periarthritis of the shoulder)

  • Painful muscle spasms
  • cervical shoulder syndrome
  • periarthritis of the shoulder
  • low back pain
View approved original text

This medication is used to relieve muscle spasms associated with pain in musculoskeletal disorders. It is effective for conditions such as cervical shoulder syndrome, periarthritis of the shoulder, and low back pain. It can help patients who experience discomfort due to these symptoms. It alleviates muscle tension and reduces pain, improving comfort in daily life. This drug helps alleviate pain from muscle spasms and increase activity levels. Therefore, it is used for relief of musculoskeletal pain.

How to take

Adult dose

This medication is a sustained release tablet, and it should be taken whole without crushing, splitting, or chewing. Adults should take 1 tablet (75mg of eperisone hydrochloride) twice a day after meals. Dosage may be adjusted according to age and symptoms.

Precautions

This drug should not be used in patients with hypersensitivity to this medication or in patients with severe myasthenia gravis. Patients with a history of hypersensitivity to the drug or with liver function problems should use this drug with caution, as liver function may deteriorate. Allergic reactions such as redness, itching, hives, swelling, and dyspnea may rarely occur, and if these symptoms appear, use should be discontinued immediately and appropriate treatment should be received. Additionally, serious skin adverse reactions such as toxic epidermal necrolysis and Stevens-Johnson syndrome may occur, so symptoms such as fever, skin rash, blisters, itching, conjunctival hyperemia, and stomatitis should be carefully monitored, and if any of these symptoms occur, the use of the medication should be discontinued immediately. Various adverse reactions such as abnormalities in liver or kidney function, anemia, insomnia, drowsiness, headaches, indigestion, nausea, vomiting, constipation, diarrhea, urinary retention, may occur occasionally, so the body's condition should be observed carefully. During treatment with this drug, symptoms such as weakness, staggering, and drowsiness may appear, so if these symptoms occur, it is advisable to reduce the dosage or discontinue use. Drowsiness or decreased attention may occur, so it is safe to avoid driving or operating dangerous machinery. Pregnant women or those who may become pregnant should only use this medication when the benefit of treatment outweighs the risks, as its safety has not been established. Breastfeeding women should avoid use if possible, and if unavoidable, breastfeeding should be discontinued. In children, safety has not been fully established, so caution is required in use. Elderly patients may have decreased physical function, so careful attention to dosage adjustment is needed.

Side effects and when to seek care immediately

Serious side effects

Hives, swelling, dyspnea, shock and anaphylactic reactions, toxic epidermal necrolysis (Lyell's syndrome), mucosal epidermal necrolysis (Stevens-Johnson syndrome), fever, erythema, blisters, conjunctival hyperemia, stomatitis, anaphylactic reactions, angioedema

Mild side effects

  • Headache
  • drowsiness
  • insomnia
  • dizziness
  • nausea
  • vomiting
  • loss of appetite
  • stomach discomfort
  • dry mouth
  • constipation
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  • diarrhea
  • abdominal pain
  • abdominal bloating
  • stomatitis
  • urinary retention
  • urinary incontinence
  • sensation of residual urine
  • weakness
  • staggering
  • general fatigue
  • muscle tone reduction
  • facial flushing
  • sweating
  • palpitations
  • hiccups
  • indigestion
  • upper respiratory infection
  • nasopharyngitis
  • localized swelling
  • ligament sprains
  • arthralgia
  • heartburn
  • discomfort in the chest
  • neck/shoulder pain
  • sore throat
  • cough
  • upper abdominal discomfort

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a sealed container to protect it from air and moisture. It is best to keep it at room temperature between 1 to 30 degrees Celsius. This helps maintain the drug's efficacy and safety for a long time.

Appearance and packaging

Appearance

White to nearly white round sustained release film-coated tablet

Package unit

30 tablets/bottle, 500 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.