Medication info
Murex Tablets (Eperisone Hydrochloride)

Murex Tablets (Eperisone Hydrochloride)

Prescription medicationTablet경구
Ingredient · strength
Eperisone Hydrochloride›50mg / 1 tablet
Manufacturer / importer
초당약품공업(주)
Appearance
White, round tablet
Packaging
(Domestic use) 30 tablets/bottle, 500 tablets/bottle (For export) 100 tablets/box (10 tablets/PTP x 10)
Approval status
Active

MFDS item code 198902330 · Notified 1989.05.22 · Insurance code 670700310

Summary

Main use
Treatment of musculoskeletal disorders (painful muscle spasms) and neurological diseases (spastic paralysis)
Who takes it
Adults
Adult dose
For adults, as hydrochloride eperisone, 50 mg is taken orally three times a day after meals. The dosage may be adjusted appropriately according to age and symptoms.

Ingredients

Manufacturer
초당약품공업(주)

Efficacy & effects

Treatment of musculoskeletal disorders (painful muscle spasms) and neurological diseases (spastic paralysis)

  • Painful muscle spasms accompanying musculoskeletal disorders
  • adhesive capsulitis
  • 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 helps relieve muscle spasms and pain associated with musculoskeletal disorders. It is particularly effective in improving pain and muscle stiffness around the shoulder and arm, and is also effective for lower back pain. Additionally, it is used to alleviate spastic paralysis symptoms caused by neurological disorders such as cerebrovascular accidents or spinal cord injuries. This medication aids in alleviating muscle stiffness due to various sequelae of central nervous system diseases such as cerebral palsy and spinal muscular atrophy. It contributes to reducing discomfort in daily life by alleviating muscle stiffness and pain.

How to take

Adult dose

For adults, as hydrochloride eperisone, 50 mg is taken orally three times a day after meals. The dosage may be adjusted appropriately according to age and symptoms.

Precautions

This medication should not be administered to certain patients. For example, it should not be used in patients with allergies to this medication or those with myasthenia gravis. Additionally, this medication contains lactose, so it should not be administered to patients with genetic conditions such as lactose intolerance, lactase deficiency, or glucose-galactose malabsorption. Caution is advised in patients with a history of drug hypersensitivity or those with impaired liver function. It may pose a risk of worsening liver function, so careful observation is necessary. During the use of this medication, rare side effects such as acute shock, liver dysfunction, kidney dysfunction, and anemia may occur, so symptoms should be closely monitored. Various side effects such as skin rashes or itching, insomnia, drowsiness, headaches, dyspepsia, urinary problems, weakness, and dizziness may occur; if any abnormal symptoms appear, immediate consultation with healthcare professionals is advised. In particular, serious skin adverse reactions such as toxic epidermal necrolysis and mucous membrane-epidermal-eye syndrome may occur, so if symptoms such as fever, erythema, blisters, itching, conjunctival injection, or stomatitis appear, administration should be stopped immediately. Drowsiness or decreased concentration may occur while taking this medication, so it is advisable to avoid driving or operating hazardous machinery. Additionally, caution is required when combined with similar medications or certain muscle relaxants, as it may cause visual disturbances. Women who are pregnant or may become pregnant should use this medication only when absolutely necessary as its safety has not been established, and nursing mothers should avoid administration or stop breastfeeding while using this medication. Safety has not been fully established for children, so caution is required in its use. Elderly patients may have reduced physiological function, and therefore should use with caution, including adjustment of dosage.

Side effects and when to seek care immediately

Serious side effects

Shock, elevated ALT, elevated AST, elevated ALP, proteinuria, elevated BUN, anemia, anaphylactic reaction, angioedema, toxic epidermal necrolysis, and mucous membrane-epidermal-eye syndrome (Stevens-Johnson syndrome)

Mild side effects

  • Rash
  • itching
  • insomnia
  • drowsiness
  • headache
  • body stiffness
  • limb tremors
  • nausea
  • vomiting
  • loss of appetite
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  • discomfort in the upper abdomen
  • thirst
  • constipation
  • diarrhea
  • abdominal pain
  • abdominal distension
  • stomatitis
  • urinary retention
  • urinary incontinence
  • sensation of residual urine
  • weakness
  • staggering
  • general malaise
  • dizziness
  • reduced muscle tone
  • flushing
  • sweating

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 or moisture from entering, and it is recommended to keep it at room temperature, avoiding direct sunlight. Proper storage will help maintain the effectiveness of the medication for a longer period.

Appearance and packaging

Appearance

White, round tablet

Package unit

(Domestic use) 30 tablets/bottle, 500 tablets/bottle (For export) 100 tablets/box (10 tablets/PTP x 10)

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.

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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.