Medication info
Epison SR Extended Release Tablet (Eperisone Hydrochloride)

Epison SR Extended Release Tablet (Eperisone Hydrochloride)

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

MFDS item code 201905621 · Approved 2019.08.08 · Insurance code 669907650

Summary

Main use
Relief of muscular spasms associated with musculoskeletal disorders (cervical spondylosis, periarthritis of the shoulder)
Who takes it
Adults
Adult dose
As this medicine is an extended-release tablet, it should be swallowed whole without crushing, dividing, or chewing. Adults should take 1 tablet (75 mg of Eperisone Hydrochloride) by mouth twice a day after meals. Dosage may be adjusted appropriately according to age and symptoms.

Ingredients

Manufacturer
대한뉴팜(주)

Efficacy & effects

Relief of muscular spasms associated with musculoskeletal disorders (cervical spondylosis, periarthritis of the shoulder)

  • Painful muscular spasms
  • cervical spondylosis
  • periarthritis of the shoulder
  • low back pain
View approved original text

This medicine is used to relieve painful muscular spasms accompanying musculoskeletal disorders such as cervical spondylosis, periarthritis of the shoulder, and low back pain.

How to take

Adult dose

As this medicine is an extended-release tablet, it should be swallowed whole without crushing, dividing, or chewing. Adults should take 1 tablet (75 mg of Eperisone Hydrochloride) by mouth twice a day after meals. Dosage may be adjusted appropriately according to age and symptoms.

Precautions

This medicine should not be used in patients with an allergic reaction to this drug or those with myasthenia gravis. Care should be taken when administering to patients with a history of hypersensitivity to the drug or poor liver function, as liver function may worsen. During the course of taking this drug, rare allergic reactions or serious skin adverse effects may occur; if symptoms such as redness, itching, rash, swelling, difficulty breathing, fever, blistering, or eye congestion develop, use should be discontinued immediately and consult a healthcare professional. Various side effects may occur, including abnormalities in liver or kidney function, blood disorders, neurological symptoms, gastrointestinal disturbances, urinary problems, and systemic symptoms; if any unusual symptoms appear, they should be reported immediately. Clinical trials and post-marketing studies have reported symptoms such as dizziness, headache, drowsiness, indigestion, and diarrhea; if these symptoms are severe, discontinuation of use and consultation with a physician are advised. Weakness, staggering, and drowsiness may occur during use, and if these symptoms arise, it may be necessary to reduce or discontinue the dosage. Drowsiness or decreased attention may occur, so driving or operating dangerous machinery should be avoided while taking this medication. Interactions may occur when taken with other medications, especially similar ones, so caution is advised. Women who are pregnant or may become pregnant should only use this medication when the benefit outweighs the risk, as its safety has not been established; breastfeeding should be avoided if possible during treatment. Safety has not been sufficiently established for children, and there is limited experience with its use, so it should be administered with caution; elderly patients may require dose adjustments due to decreased physiological functions.

Side effects and when to seek care immediately

Serious side effects

  • Urticaria
  • swelling
  • difficulty breathing
  • redness
  • itching
  • shock
  • anaphylactic reactions
  • toxic epidermal necrolysis
  • Stevens-Johnson syndrome
  • fever
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  • erythema
  • blistering
  • eye congestion
  • stomatitis
  • anaphylaxis
  • angioedema

Mild side effects

  • Headache
  • drowsiness
  • insomnia
  • nausea
  • vomiting
  • loss of appetite
  • abdominal discomfort
  • thirst
  • constipation
  • diarrhea
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  • abdominal pain
  • abdominal bloating
  • stomatitis
  • urinary retention
  • incontinence
  • residual urine sensation
  • weakness
  • staggering
  • general malaise
  • dizziness
  • decreased muscle tone
  • facial flushing
  • sweating
  • palpitations
  • hiccups
  • indigestion
  • sensory abnormalities
  • decreased sensation
  • slowed reactions
  • heartburn
  • chest discomfort
  • leg pain
  • peripheral edema
  • limb pain
  • increased purulent discharge from wounds
  • facial swelling
  • pelvic pain

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

Storage

This medicine should be stored in a tightly closed container to prevent air or moisture entry. Additionally, avoid storing the medication in places that are too hot or too cold, and it is advisable to keep it at room temperature between 1 degree and 30 degrees Celsius.

Appearance and packaging

Appearance

White to almost white round extended-release film-coated tablets

Package unit

30 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.