Medication info
Epira Tablet (Eperisone Hydrochloride)

Epira Tablet (Eperisone Hydrochloride)

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

MFDS item code 201404981 · Approved 2014.10.28 · Insurance code 657805490

Summary

Main use
Treatment of musculoskeletal pain-related muscle spasms and neurological spastic paralysis
Who takes it
Adults
Adult dose
Eperisone hydrochloride 50mg orally after meals three times a day. Adjust the dose appropriately based on age and symptoms.

Ingredients

Manufacturer
하나제약(주)

Efficacy & effects

Treatment of musculoskeletal pain-related muscle spasms and neurological spastic paralysis

  • Painful muscle spasms
  • cervicobrachial syndrome
  • periarthritis of the shoulder
  • low back pain
  • spastic paralysis
  • cerebrovascular disorders
  • spastic spinal paralysis
  • cervical spondylosis
  • postoperative aftereffects
  • traumatic aftereffects
  • amyotrophic lateral sclerosis
  • cerebral palsy
View approved original text

This medication is used for painful muscle spasms accompanying musculoskeletal disorders, such as cervicobrachial syndrome, periarthritis of the shoulder, and low back pain. It also helps alleviate muscle stiffness caused by various central nervous system diseases, such as spastic paralysis due to neurological disorders, cerebrovascular disorders, spastic spinal paralysis, aftereffects of spinal cord injury or brain/spinal cord tumor surgery, traumatic aftereffects, and cerebral palsy. This drug is effective in reducing excessive tension in the muscles, improving pain and stiffness. Therefore, it is used to improve muscle function and relieve pain in various conditions related to musculoskeletal and neurological systems.

How to take

Adult dose

Eperisone hydrochloride 50mg orally after meals three times a day. Adjust the dose appropriately based on age and symptoms.

Precautions

This medication should never be administered to certain patients. For instance, it should not be used in patients who are allergic to this drug or have myasthenia gravis. Additionally, patients with genetic disorders that prevent the breakdown of lactose should not take this medicine. When using this drug, particular caution should be exercised in patients with drug hypersensitivity or liver function issues. Liver function may deteriorate, so the state should be closely monitored. Rarely, during the use of this medication, side effects such as shock or abnormalities in liver and kidney functions, anemia, etc., may appear. Various symptoms including skin rash or itching, neurological symptoms, digestive disturbances, urinary problems, and generalized weakness may occur, so careful monitoring is necessary. If serious skin reactions, such as Stevens-Johnson syndrome, appear, the medication should be discontinued immediately and medical advice should be sought. Drowsiness, weakness, or unsteadiness may occur during the use of this medication, so if these symptoms arise, the dosage should be reduced or discontinued. Additionally, since attention and reflex abilities may decrease, it is advisable to avoid driving or operating dangerous machinery. Caution is necessary when taking this medication in combination with other muscle relaxants, as side effects may be exacerbated. Pregnant women or those who may become pregnant should only take this medication when the benefits outweigh the risks, as its safety has not been established. Nursing mothers should avoid taking this medication if possible, and if unavoidable, discontinuing breastfeeding is preferable. The safety of this medication in children has not been sufficiently confirmed, so it should be used with caution due to limited experience.

Side effects and when to seek care immediately

Serious side effects

Shock (severe allergic reaction), anaphylaxis (severe allergic reaction), angioedema (severe swelling), toxic epidermal necrolysis and mucosal-skin-eye syndrome (severe skin reactions), severe rash with fever, blisters, skin peeling, pain in mouth/eye mucosa, liver function abnormalities (potential jaundice due to elevated ALT, AST, ALP), proteinuria, elevated BUN (kidney abnormalities), anemia (blood abnormalities).

Mild side effects

  • Rash
  • itching
  • insomnia
  • drowsiness
  • headache
  • limb paralysis
  • stiffness of the body
  • limb tremors
  • nausea
  • vomiting
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  • loss of appetite
  • abdominal discomfort
  • thirst
  • constipation
  • diarrhea
  • abdominal pain
  • bloating
  • stomatitis
  • urinary retention
  • urinary incontinence
  • post-void dribbling
  • weakness
  • unsteadiness
  • generalized fatigue
  • dizziness
  • decreased muscle tone
  • facial flushing
  • sweating
  • drowsiness
  • decreased attention span
  • decreased concentration
  • reduced reflex capability.

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

Storage

This medication should be stored in a tightly sealed container that does not allow air to pass through, and it is best to keep it at room temperature between 1°C and 30°C. Proper storage will help maintain the drug's effectiveness for a longer time.

Appearance and packaging

Appearance

White round 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.