Medication info
Alfeson Sustained Release Tablets (Eperisone Hydrochloride)

Alfeson Sustained Release Tablets (Eperisone Hydrochloride)

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

MFDS item code 201905951 · Approved 2019.08.22 · Insurance code 649507910

Summary

Main use
Relief of painful muscle spasms associated with musculoskeletal disorders (shoulder humeral syndrome, adhesive capsulitis)
Who takes it
Adults
Adult dose
As this medication is a sustained release tablet, it should be taken whole without crushing, splitting, or chewing. Adults: 1 tablet (75 mg of eperisone hydrochloride) taken orally twice daily after meals. Adjustment may be made based on age and symptoms.

Ingredients

Manufacturer
유니메드제약(주)

Efficacy & effects

Relief of painful muscle spasms associated with musculoskeletal disorders (shoulder humeral syndrome, adhesive capsulitis)

  • Painful muscle spasms
  • shoulder humeral syndrome
  • adhesive capsulitis
  • low back pain
View approved original text

This medication is used to relieve painful muscle spasms associated with musculoskeletal disorders such as shoulder humeral syndrome, adhesive capsulitis, and low back pain.

How to take

Adult dose

As this medication is a sustained release tablet, it should be taken whole without crushing, splitting, or chewing. Adults: 1 tablet (75 mg of eperisone hydrochloride) taken orally twice daily after meals. Adjustment may be made based on age and symptoms.

Precautions

This medication should not be used in patients with hypersensitivity or severe myasthenia gravis. It should be used cautiously in patients with a history of hypersensitivity to the drug or impaired liver function, as liver function may deteriorate. When using this medication, there is a rare possibility of serious allergic reactions such as shock or anaphylaxis, so if symptoms such as redness, itching, hives, swelling, or shortness of breath occur, use should be discontinued immediately and medical attention sought. Also, serious skin conditions such as toxic epidermal necrolysis or Stevens-Johnson syndrome may occur, so if symptoms such as fever, erythema, blisters, itching, conjunctival injection, or stomatitis appear, the medication should be discontinued immediately and medical advice should be sought. Side effects such as abnormal liver function, renal dysfunction, anemia, rash, insomnia, drowsiness, headache, dyspepsia, nausea, vomiting, constipation, diarrhea, abdominal pain, urinary retention, weakness, dizziness, and muscle stiffness may occasionally occur, so if any unusual symptoms arise, consult a doctor. During treatment with this drug, drowsiness or decreased concentration may occur, so it is advisable to avoid driving or operating hazardous machinery. For women who are pregnant or may become pregnant, the safety of this medication has not been established, and it should only be used when the benefits of treatment are deemed greater than the risks, and during breastfeeding, it should be avoided if possible or breastfeeding should be discontinued if absolutely necessary. Safety in children has not been sufficiently confirmed, so it should be administered cautiously to children. In elderly patients, caution is needed due to possible decline in physical function, including dose reduction.

Side effects and when to seek care immediately

Serious side effects

  • Hives
  • severe swelling
  • edema
  • shortness of breath
  • shock
  • anaphylaxis
  • toxic epidermal necrolysis
  • Lyell's syndrome
  • mucocutaneous syndrome
  • Stevens-Johnson syndrome
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  • fever
  • erythema
  • blisters
  • conjunctival injection
  • stomatitis
  • jaundice
  • profound malaise
  • severe edema
  • elevated blood pressure
  • severe allergic reactions
  • severe skin adverse reactions
  • respiratory issues
  • liver abnormalities
  • severe edema
  • or urinary problems.

Mild side effects

  • Nausea
  • vomiting
  • loss of appetite
  • gastrointestinal discomfort
  • thirst
  • constipation
  • diarrhea
  • abdominal pain
  • abdominal fullness
  • stomatitis
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  • insomnia
  • drowsiness
  • headache
  • limb paralysis
  • rigidity
  • limb tremors
  • dizziness
  • decreased muscle tone
  • facial flushing
  • sweating
  • palpitations
  • hiccups
  • localized swelling
  • weakness
  • unsteadiness
  • general malaise
  • sensory abnormalities
  • decreased sensation
  • worsening headache
  • slowed reactions
  • chest discomfort
  • leg pain
  • sleep disturbances
  • eczematous dermatitis
  • erythematous rash

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

Storage

This medication should be stored in a tightly closed container to prevent exposure to air and moisture. It is best to maintain room temperature between 1 degree and 30 degrees Celsius. This helps to preserve the effectiveness of the medication and prevent degradation.

Appearance and packaging

Appearance

White to almost white round sustained release film-coated tablets

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.