Medication info
Limadex Tablets (Limaprost Aldex)

Limadex Tablets (Limaprost Aldex)

Prescription medicationTablet
Ingredient · strength
Limaprost Alfadex›166.67μg / 1 tablet
Manufacturer / importer
Allico Pharmaceuticals Co., Ltd.
Appearance
White round tablets
Packaging
84 tablets (21 tablets/PTP x 4)
Approval status
Active

MFDS item code 201602341 · Approved 2016.04.26 · Insurance code 656004180

Summary

Main use
Symptoms of Buerger's disease (ulcers, coldness, etc.), symptoms of lumbar spinal stenosis, and improved walking ability
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 per dose, 3 times daily, taken orally. For improvement of subjective symptoms (lower-limb pain and numbness) and walking ability caused by acquired lumbar spinal stenosis (patients with a normal SLR test and bilateral intermittent claudication), the usual adult dose is 1 tablet per dose, 3 times daily, taken orally. The dose may be adjusted appropriately according to age and symptoms.

Ingredients

Manufacturer
Allico Pharmaceuticals Co., Ltd.

Efficacy & effects

Symptoms of Buerger's disease (ulcers, coldness, etc.), symptoms of lumbar spinal stenosis, and improved walking ability

  • Ulcer
  • pain
  • coldness
  • lower limb pain
  • lower limb numbness
View approved original text

This medication helps improve ischemic symptoms such as ulcers, pain, and coldness occurring due to obstructive thromboangiitis. It also alleviates subjective symptoms like lower limb pain and numbness caused by acquired lumbar spinal stenosis and enhances walking ability. It is used effectively to improve vascular and nerve-related symptoms, thereby enhancing the quality of life.

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 per dose, 3 times daily, taken orally. For improvement of subjective symptoms (lower-limb pain and numbness) and walking ability caused by acquired lumbar spinal stenosis (patients with a normal SLR test and bilateral intermittent claudication), the usual adult dose is 1 tablet per dose, 3 times daily, taken orally. The dose may be adjusted appropriately according to age and symptoms.

Precautions

This medication must not be administered to pregnant women or women who may become pregnant. This medication contains lactose and should not be used by patients with genetic disorders that prevent lactose digestion. Patients with a tendency to bleed or those taking medications affecting blood coagulation should exercise caution when using this medication. This medication may cause hypersensitivity reactions such as skin rashes or itching; if such symptoms occur, the medication should be discontinued immediately. Bleeding may occur rarely; if bleeding symptoms appear, discontinue the medication and consult a healthcare professional immediately. Gastrointestinal side effects such as diarrhea, nausea, abdominal pain, loss of appetite, and heartburn may occur, so caution is advised. There may be a potential for liver dysfunction, so it is advisable to periodically check liver health. Symptoms such as increased heart rate or lowered blood pressure may occur; if these symptoms appear, inform your healthcare professional. Various side effects such as headaches, facial redness, dizziness, tremors, and swelling may occur, so report any unusual symptoms immediately. Patients with lumbar spinal stenosis should closely monitor changes in symptoms and decide whether to continue using this medication. The effectiveness of this medication is not confirmed in cases of severe spinal stenosis that require surgery. Safety during pregnancy has not been established; therefore, this medication should not be used by pregnant women. Animal studies have reported uterine contractions. Safety in children has not been confirmed; therefore, it should not be used in pediatric patients. Older patients may have decreased physical function, so dosage adjustments and careful use are required. High doses in healthy adults may lead to temporarily lowered blood pressure, so caution is necessary.

Side effects

  • Rash
  • itching
  • bleeding
  • diarrhea
  • nausea
  • abdominal discomfort
  • abdominal pain
  • loss of appetite
  • heartburn
  • vomiting
Show 16 more
  • abdominal bloating
  • AST (GOT) elevation
  • ALT (GPT) elevation
  • palpitations
  • peripheral cyanosis
  • hypotension
  • headache
  • facial flushing
  • dizziness
  • feeling of warmth
  • generalized fatigue
  • edema
  • mastitis
  • 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 avoid exposure to light and air, and it is safest to store it at room temperature between 1°C and 30°C. Storing it this way helps maintain the effectiveness of the medication.

Appearance and packaging

Appearance

White round tablets

Package unit

84 tablets (21 tablets/PTP x 4)

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.