Medication info
Roperisone Tablet (Eperisone Hydrochloride)

Roperisone Tablet (Eperisone Hydrochloride)

Prescription medicationTablet경구
Ingredient · strength
Eperisone Hydrochloride›50mg / 1 tablet
Manufacturer / importer
(주)인트로바이오파마
Appearance
White, round film-coated tablets
Packaging
30 tablets/bottle, 500 tablets/bottle
Approval status
Active

MFDS item code 201603481 · Approved 2016.06.15 · Insurance code 052400050

Summary

Main use
Treatment of musculoskeletal disorders (painful muscle spasms, etc.) and neurological disorders (spastic paralysis, etc.)
Who takes it
Adults
Adult dose
Administer orally 50 mg three times a day after meals as efarison hydrochloride. Adjust dosage appropriately based on age and symptoms.

Ingredients

Manufacturer
(주)인트로바이오파마

Efficacy & effects

Treatment of musculoskeletal disorders (painful muscle spasms, etc.) and neurological disorders (spastic paralysis, etc.)

  • painful muscle spasms
  • rotator cuff syndrome
  • periarthritis of the shoulder
  • low back pain
  • spastic paralysis
  • cerebrovascular disorders
  • spastic spinal paralysis
  • cervical spondylosis
  • postoperative sequelae
  • post-traumatic sequelae
  • amyotrophic lateral sclerosis
  • cerebral palsy
View approved original text

This medication is used for symptoms associated with painful muscle spasms accompanying musculoskeletal disorders, such as rotator cuff syndrome, periarthritis of the shoulder, and low back pain. It is also effective in alleviating spastic symptoms caused by various neurological disorders, such as spastic paralysis, cerebrovascular disorders, spastic spinal paralysis, post-surgical and post-traumatic sequelae, and cerebral palsy. It is used to improve muscle stiffness and pain occurring in musculoskeletal and neurological diseases.

How to take

Adult dose

Administer orally 50 mg three times a day after meals as efarison hydrochloride. Adjust dosage appropriately based on age and symptoms.

Precautions

This medication should not be used in patients with allergic reactions or those suffering from myasthenia gravis. Additionally, it should not be administered to patients with genetic conditions such as galactose intolerance, lactase deficiency, or glucose-galactose malabsorption. Careful use is required for patients with a history of hypersensitivity to this drug and those with liver function issues. This medication may rarely cause severe side effects such as shock, liver dysfunction, kidney dysfunction, and anemia, so symptoms should be closely monitored. Various side effects may occur, including skin rash, itching, insomnia, drowsiness, headache, dyspepsia, urinary retention, lethargy, and others. If symptoms of serious skin reactions such as Stevens-Johnson syndrome appear, medication should be stopped immediately and treatment sought. Drowsiness or decreased concentration may occur during the use of this drug; therefore, it is advisable to avoid driving or operating hazardous machinery. Additionally, caution is required when using this medication alongside similar drugs or specific muscle relaxants, as it may cause visual disturbances. Women who are pregnant or may become pregnant should only use this medication if the benefits outweigh the risks, as its safety has not been established, and breastfeeding women should preferably avoid it or discontinue breastfeeding. There is insufficient confirmation of safety in pediatric patients, so caution is necessary when using it. Elderly patients may have weakened physical functions, so special care should be taken, such as reducing the dosage.

Side effects and when to seek care immediately

Serious side effects

Shock (severe allergic reaction due to hypersensitivity), anaphylaxis, angioedema, toxic epidermal necrolysis and mucocutaneous ocular syndrome (Stevens-Johnson syndrome), liver dysfunction (ALT, AST, ALP elevation), kidney abnormalities (proteinuria, BUN elevation).

Mild side effects

  • Occasionally rash
  • rarely itchiness
  • insomnia
  • drowsiness
  • headache
  • limb paralysis
  • muscle rigidity
  • limb tremors
  • nausea
  • vomiting
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  • loss of appetite
  • discomfort in the upper abdomen
  • thirst
  • constipation
  • diarrhea
  • abdominal pain
  • abdominal bloating
  • stomatitis
  • urinary retention
  • incontinence
  • sensation of residual urine
  • lethargy
  • staggering
  • general malaise
  • dizziness
  • muscle tone reduction
  • facial flushing
  • sweating
  • edema.

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

Storage

This medication should be stored in a tightly sealed container to prevent air exposure and kept at room temperature between 1 and 30 degrees Celsius for safety. Proper storage will help maintain the effectiveness of the medication and prevent deterioration.

Appearance and packaging

Appearance

White, round 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.