Medication info
Perison SR Sustained-Release Tablet (Eperisone Hydrochloride)

Perison SR Sustained-Release Tablet (Eperisone Hydrochloride)

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

MFDS item code 201905615 · Approved 2019.08.08 · Insurance code 670608290

Summary

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

Ingredients

Manufacturer
(주)휴온스

Efficacy & effects

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

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

This medication is used to relieve painful muscle spasms associated with musculoskeletal disorders. For example, it is effective for symptoms such as cervical spondylosis, periarthritis of the shoulder, and low back pain. It helps reduce pain and muscle stiffness caused by these conditions and improves the discomfort in daily life. Therefore, this medication is used to treat muscle pain and discomfort around the joints.

How to take

Adult dose

This medication is a sustained-release tablet, so it should be taken whole without crushing, splitting, or chewing. Take 1 tablet (75mg of eperisone hydrochloride) orally after meals, twice a day. Adjust according to age and symptoms as appropriate.

Precautions

This medicine should not be administered to certain patients. First, it should not be used in patients who have an allergy to the medication or have severe muscle weakness symptoms. In addition, it should be administered with caution to patients with a history of hypersensitivity to medications or those with liver function problems. Caution is required as liver function may deteriorate. While rare, serious allergic reactions or skin reactions may occur when using this medication, so if symptoms such as redness, itching, hives, difficulty breathing, fever, blisters, or stomatitis appear, discontinuation should be immediate, and a medical consultation sought. Some patients have reported abnormal liver enzymes, renal function issues, blood abnormalities, neurological symptoms, gastrointestinal issues, and urinary symptoms, so it is important to notify immediately if any unusual symptoms occur. During the use of this medication, symptoms such as weakness, dizziness, or drowsiness may appear, and in such cases, the dosage should be reduced or the administration should be discontinued. Due to drowsiness or decreased concentration, it is advisable to avoid driving or operating dangerous machinery. Moreover, caution should be exercised when taking this medication in combination with other muscle relaxants, as visual disturbances may arise. Women who are pregnant or may become pregnant should use this medication only when the benefits outweigh the risks, as its safety has not been established, and nursing mothers should avoid it if possible and discontinue breastfeeding if unavoidable. The safety for children has not been adequately established, so caution should be exercised when administering to children. For elderly patients, as physical functions may be declined, careful administration and dosage adjustment are necessary.

Side effects and when to seek care immediately

Serious side effects

Shock and anaphylactic reactions (redness, itching, hives, swelling, difficulty breathing), toxic epidermal necrolysis (Lyell's syndrome), Stevens-Johnson syndrome (mucous membrane syndrome), fever, erythema, blisters, conjunctival injection, stomatitis, anaphylaxis, angioedema

Mild side effects

  • Redness
  • itching
  • hives
  • swelling
  • dizziness
  • headache
  • drowsiness
  • nausea
  • vomiting
  • loss of appetite
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  • abdominal discomfort
  • thirst
  • constipation
  • diarrhea
  • abdominal pain
  • bloating
  • stomatitis
  • urinary retention
  • incontinence
  • residual urine sensation
  • weakness
  • staggering
  • generalized fatigue
  • muscle tone reduction
  • facial flushing
  • sweating
  • palpitations
  • hiccups
  • dyspepsia
  • upper abdominal pain
  • dry mouth
  • colitis
  • gastritis
  • numbness
  • paresthesia
  • skin tingling
  • decreased sensation
  • headache

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

Storage

This medication should be stored in a sealed container to prevent air and moisture from entering and kept at room temperature between 1 degree and 30 degrees Celsius. Storing it this way helps maintain the effectiveness of the medication.

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.