Medication info
Limarif Tablet (Limaprost Alpha-Dex)

Limarif Tablet (Limaprost Alpha-Dex)

Prescription medicationTablet
Ingredient · strength
Limaprost Alfadex›166.67μg / 1 tablet
Manufacturer / importer
Medica Korea Co., Ltd.
Appearance
White round tablets
Packaging
84 tablets (21 tablets/PTPX4)
Approval status
Active

MFDS item code 201702413 · Approved 2017.05.16 · Insurance code 646004320

Summary

Main use
Improvement of symptoms and walking ability in lumbar spinal stenosis, and ischemic symptoms in Buerger’s disease
Who uses it
Adults
Adult dosage
For improvement of ischemic symptoms such as ulcers, pain, and coldness caused by thromboangiitis obliterans (Buerger's disease), the usual adult dose is 2 tablets orally 3 times daily. For improvement of subjective symptoms (lower limb pain and numbness) and walking ability associated with acquired lumbar spinal stenosis (patients with normal SLR test results and bilateral intermittent claudication), the usual adult dose is 1 tablet orally 3 times daily. The dose may be adjusted appropriately according to age and symptoms.

Ingredients

Manufacturer
Medica Korea Co., Ltd.

Efficacy & effects

Improvement of symptoms and walking ability in lumbar spinal stenosis, and ischemic symptoms in Buerger’s disease

  • Ulcers
  • pain
  • cold sensations
  • leg pain
  • leg numbness
View approved original text

This medication helps improve ischemic symptoms such as ulcers, pain, and cold sensations caused by occlusive thromboangiitis (Buerger's disease). It is also effective in relieving leg pain and numbness in patients with acquired lumbar spinal stenosis and improving walking ability. In other words, it is used to enhance blood circulation and alleviate symptoms, thereby improving the quality of life for patients.

Dosage and Administration

Adult dosage

For improvement of ischemic symptoms such as ulcers, pain, and coldness caused by thromboangiitis obliterans (Buerger's disease), the usual adult dose is 2 tablets orally 3 times daily. For improvement of subjective symptoms (lower limb pain and numbness) and walking ability associated with acquired lumbar spinal stenosis (patients with normal SLR test results and bilateral intermittent claudication), the usual adult dose is 1 tablet orally 3 times daily. The dose may be adjusted appropriately according to age and symptoms.

Precautions

This medication should not be used by women who are pregnant or may become pregnant. Due to the presence of lactose, individuals with genetic issues such as lactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption should not take this medication. Patients with a tendency for bleeding or those taking antiplatelet agents, thrombolytics, or anticoagulants must exercise caution when using this medication. During usage, hypersensitivity reactions such as rash or itching may occur, and if these symptoms appear, stop taking the medication immediately. Bleeding may occur rarely, so if abnormal symptoms arise, discontinue use and observe the situation. Gastrointestinal side effects such as diarrhea, nausea, abdominal pain, loss of appetite, and heartburn may occur. Liver function abnormalities may arise, so it is advisable to regularly monitor liver status. Symptoms such as rapid heartbeat, cold extremities, and low blood pressure may occur; hence, caution is necessary. Rarely, headaches, facial flushing, dizziness, tremors, swelling, and anemia may occur. Patients with lumbar spinal stenosis should carefully observe symptom progression and make decisions about continuing use. Safety during pregnancy has not been established, so pregnant women should not use this drug; uterine contraction effects have been reported in animal tests. Safety for children has not been confirmed, and there is no usage experience. Elderly patients should take caution as bodily functions may decline, and dosage adjustments may be necessary. Administering a large amount to healthy adults may temporarily lower blood pressure, so caution is also needed.

Side effects

  • rash
  • itching
  • bleeding
  • diarrhea
  • nausea
  • abdominal discomfort
  • abdominal pain
  • loss of appetite
  • heartburn
  • vomiting
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  • abdominal bloating
  • elevated AST (GOT)
  • elevated ALT (GPT)
  • palpitations
  • peripheral cyanosis
  • hypotension
  • headache
  • facial flushing
  • dizziness
  • feeling of warmth
  • general fatigue
  • edema
  • breast engorgement
  • body tremors
  • hirsutism
  • anemia

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

Storage

This medication should be stored in a tightly closed container to protect it from air and moisture. It is safe to store at room temperature, i.e., between 1 and 30 degrees Celsius.

Appearance and packaging

Appearance

White round tablets

Package unit

84 tablets (21 tablets/PTPX4)

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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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.