Medication info
Aperson SR Extended Release Tablet (Eperisone Hydrochloride)

Aperson SR Extended Release Tablet (Eperisone Hydrochloride)

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

MFDS item code 201905622 · Approved 2019.08.08 · Insurance code 663607890

Summary

Main use
Relief of painful muscle spasms associated with musculoskeletal disorders (cervical spondylosis syndrome, periarthritis of the shoulder)
Who takes it
Adults
Adult dose
This medication is an extended-release tablet and should be taken whole without crushing, splitting, or chewing. Administer 1 tablet (75mg of Eperisone Hydrochloride) orally after meals twice a day. Adjust as necessary according to age and symptoms.

Ingredients

Manufacturer
한국프라임제약(주)

Efficacy & effects

Relief of painful muscle spasms associated with musculoskeletal disorders (cervical spondylosis syndrome, periarthritis of the shoulder)

  • Painful muscle spasms associated with musculoskeletal disorders
  • cervical spondylosis syndrome
  • periarthritis of the shoulder
  • low back pain
View approved original text

This medication is used to relieve painful muscle spasms associated with musculoskeletal disorders. It is effective for symptoms such as cervical spondylosis syndrome, periarthritis of the shoulder, and low back pain. It helps improve these symptoms, reducing discomfort for patients and enhancing their quality of daily life.

How to take

Adult dose

This medication is an extended-release tablet and should be taken whole without crushing, splitting, or chewing. Administer 1 tablet (75mg of Eperisone Hydrochloride) orally after meals twice a day. Adjust as necessary according to age and symptoms.

Precautions

This medication should not be used by individuals with an allergy to this medication or those with myasthenia gravis. Patients with a history of hypersensitivity to the drug or impaired liver function should use this medication cautiously as it may worsen liver function. If allergic symptoms such as redness, itching, hives, swelling, or shortness of breath occur while taking this medication, discontinue use immediately and consult healthcare professionals. Severe skin reactions, such as toxic epidermal necrolysis or Stevens-Johnson syndrome, may occur, so symptoms such as fever, skin rash, blisters, itching, eye redness, or oral inflammation should be monitored closely. Rarely, there may be increases in liver enzymes, proteinuria, blood abnormalities, gastrointestinal symptoms (nausea, vomiting, constipation, diarrhea, etc.), neurological symptoms (insomnia, drowsiness, headache, dizziness, etc.), or urinary symptoms (urinary retention, incontinence), so any abnormal symptoms should be reported to a doctor. Drowsiness or decreased concentration may occur while taking this medication, so it is advisable to avoid driving or operating hazardous machinery. Women who are pregnant or may become pregnant should carefully consider the benefits and risks of treatment when taking this medication, and nursing mothers should ideally avoid taking it or discontinue breastfeeding. The safety for children has not been adequately confirmed, so it should be used with caution in children. Elderly patients may have decreased bodily functions, so careful dose adjustment is needed when using this medication. Caution should be exercised when taking this medication with other drugs with similar components as it may cause visual disturbances.

Side effects and when to seek care immediately

Serious side effects

Urticaria, severe swelling (edema), shortness of breath, shock and anaphylactic reactions, toxic epidermal necrolysis (Lyell's syndrome), mucocutaneous syndrome (Stevens-Johnson syndrome), severe rash with fever, blistering, peeling skin, pain in oral/ocular mucosa, deterioration of liver function, anaphylactic reactions, angioedema

Mild side effects

  • Skin itching
  • rash
  • insomnia
  • drowsiness
  • headache
  • nausea
  • vomiting
  • decreased appetite
  • gastrointestinal discomfort
  • dryness of the mouth
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  • constipation
  • diarrhea
  • abdominal pain
  • bloating
  • stomatitis
  • urinary retention
  • incontinence
  • feelings of residual urine
  • weakness
  • staggering
  • general malaise
  • dizziness
  • muscle hypotonia
  • facial flushing
  • sweating
  • palpitations
  • hiccups
  • indigestion
  • heartburn
  • gastrointestinal disturbances
  • chest discomfort
  • neck/shoulder pain
  • sore throat
  • cough
  • localized swelling
  • sprain
  • nasopharyngitis

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

Storage

This medication may be sensitive to air and moisture, so it should be stored in a tightly closed container. Additionally, avoid storing it in extremely hot or cold environments, and it is safe to store it at room temperature between 1°C and 30°C.

Appearance and packaging

Appearance

White to nearly white, round extended 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.