Medication info
Frost Tablet (Limaprost Alpadex)

Frost Tablet (Limaprost Alpadex)

Prescription medicationTabletOral
Ingredient · strength
Limaprost Alfadex›166.67μg / 1 tablet
Manufacturer / importer
Ixu Pharmaceutical Co., Ltd.
Appearance
White round tablets
Packaging
84 tablets/Alu-Alu (21 tablets/Alu-Alu X4)
Approval status
Active

MFDS item code 201901399 · Approved 2019.03.07 · Insurance code 658502120

Summary

Main use
Improvement of symptoms and walking ability in lumbar spinal stenosis, and ischemic symptoms of Buerger disease
Who takes it
Adults
Adult dose
1. 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. 2. For improvement of subjective symptoms (lower-limb pain and numbness) and walking ability caused by acquired lumbar spinal canal stenosis (in 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
Ixu Pharmaceutical Co., Ltd.

Efficacy & effects

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

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

This medication helps improve blood circulation disorder symptoms such as ulcers, pain, and cold sensations caused by obstructive thromboangiitis. Additionally, it alleviates leg pain and numbness in patients with acquired lumbar spinal stenosis and enhances walking ability. By improving blood circulation and neurological symptoms, it allows for a more comfortable daily life for patients.

How to take

Adult dose

1. 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. 2. For improvement of subjective symptoms (lower-limb pain and numbness) and walking ability caused by acquired lumbar spinal canal stenosis (in 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. This medication contains lactose and should not be administered to patients with genetic conditions such as galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption. Caution should be exercised in patients with a tendency to bleed or those taking antiplatelet agents, thrombolytics, or anticoagulants. During the use of this medication, hypersensitivity reactions such as rash or itching may occur, and if these symptoms appear, it should be discontinued immediately. Bleeding may rarely occur, so symptoms should be closely monitored, and if abnormalities arise, administration should be stopped. Gastrointestinal symptoms such as diarrhea, nausea, abdominal discomfort, abdominal pain, loss of appetite, heartburn, vomiting, and abdominal bloating may occur. Liver function abnormalities may occur, so it is advisable to periodically check liver enzymes (AST, ALT). Cardiovascular symptoms such as palpitations, cyanosis of hands and feet, and hypotension may occur. Headaches, facial flushing, dizziness, heat sensation, general fatigue, edema, glandular swelling, tremors, hirsutism, and anemia may occur rarely. Patients with lumbar spinal stenosis should observe the progression of symptoms to decide whether to continue use, and for severe cases requiring surgery, the effectiveness of this medication is uncertain. Safety during pregnancy has not been established, and contraction effects have been reported in animal studies, so pregnant women or those who may become pregnant should not take this medication. Safety in children has not been confirmed, so it is advisable not to use it in children. In elderly patients, caution should be taken as physiological function may be decreased, and the dosage should be reduced accordingly.

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
  • limb cyanosis
  • hypotension
  • headache
  • facial flushing
  • dizziness
  • warmth
  • generalized fatigue
  • edema
  • lymphadenopathy
  • tremors
  • hirsutism
  • anemia

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 exposure to air or moisture. It is important to maintain a storage temperature between 1 degree and 30 degrees Celsius.

Appearance and packaging

Appearance

White round tablets

Package unit

84 tablets/Alu-Alu (21 tablets/Alu-Alu X4)

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.