Medication info

Kaypro Tablet (Limaprost Aldex)

Prescription medicationTabletApproval withdrawn
Ingredient · strength
Limaprost Alfadex›166.67μg / 1 tablet
Manufacturer / importer
Genewon Science Co., Ltd.
Appearance
White, round tablets
Packaging
84 tablets/Alu-Alu [21 tablets/Alu-Alu x 4]
Approval status
Approval withdrawn

MFDS item code 202002838 · Approved 2020.04.22

This product's status changed to Approval withdrawn on 2024.10.25. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improvement of ischemic symptoms of Buerger's disease and symptoms and walking ability in lumbar spinal stenosis
Who uses it
Adults
Adult dosage
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 (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
Genewon Science Co., Ltd.

Efficacy & effects

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

  • Ulcers
  • pain
  • cold sensation
  • lower limb pain
  • numbness in the lower limbs
View approved original text

Used to improve ischemic symptoms such as ulcers, pain, and cold sensations caused by occlusive thromboangiitis, as well as subjective symptoms like lower limb pain and numbness caused by acquired lumbar spinal stenosis, and to enhance walking ability.

Dosage and Administration

Adult dosage

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 (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 drug should not be used by women who are pregnant or may become pregnant. This drug contains lactose, so it should not be used in patients with genetic problems that prevent the digestion of lactose. Patients with a tendency to bleed or those taking medications that may cause bleeding should be cautious when using this drug. An allergic reaction such as skin rash or itching may occur when taking this drug; if such symptoms appear, discontinue use immediately. Rarely, bleeding may occur, so if bleeding symptoms appear, stop taking the medication immediately and consult a healthcare provider. Gastrointestinal symptoms such as diarrhea, nausea, abdominal pain, and loss of appetite may occur, so it is advisable to consult a doctor if these symptoms persist. Since it may affect liver function, liver enzyme levels should be monitored carefully if abnormalities arise. Symptoms such as rapid heartbeat or low blood pressure may occur rarely, so inform a healthcare provider immediately if such symptoms occur. Headaches, dizziness, and facial flushing may occur, so caution should be exercised if these symptoms are severe. Patients with lumbar spinal stenosis should carefully monitor changes in their symptoms to decide whether to continue using this drug. Safety during pregnancy has not been established, and uterine contractions have been reported in animal studies, so pregnant women should avoid using this drug. The safety in children has not been confirmed, so it is preferable not to use it in children. Elderly patients may have diminished physical function, so caution should be exercised regarding dosage adjustments.

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
  • cyanosis of extremities
  • hypotension
  • headache
  • facial flushing
  • dizziness
  • fever
  • general malaise
  • edema
  • mastitis
  • tremors
  • hirsutism
  • anemia

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

Storage

Store this medication in a tightly closed container to protect it from air and moisture. Additionally, it is recommended to keep the medication at room temperature, which is between 1 degree and 30 degrees Celsius, avoiding extremes of temperature.

Appearance and packaging

Appearance

White, round tablets

Package unit

84 tablets/Alu-Alu [21 tablets/Alu-Alu 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.