Medication info
Limastad Tablets (Limaprost Alpha-dex)

Limastad Tablets (Limaprost Alpha-dex)

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

MFDS item code 201208875 · Approved 2012.11.29 · Insurance code 665506340

Summary

Main use
Improvement of symptoms and walking ability in acquired lumbar spinal stenosis; improvement of ischemic symptoms in Buerger disease
Who takes it
Adults
Adult dose
1. For improvement of ischemic symptoms such as ulcers, pain, and coldness due to 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 due to acquired lumbar spinal stenosis (in patients with a normal SLR test and bilateral intermittent claudication), the usual adult dose is 1 tablet orally 3 times daily. The dose may be adjusted as appropriate according to age and symptoms.

Ingredients

Manufacturer
Korea Union Pharmaceutical Co., Ltd.

Efficacy & effects

Improvement of symptoms and walking ability in acquired lumbar spinal stenosis; improvement of ischemic symptoms in Buerger disease

  • Ulcers
  • pain
  • coldness
  • lower limb pain
  • lower limb tingling
View approved original text

This medication is used to improve ischemic symptoms such as ulcers, pain, and coldness caused by occlusive thromboangiitis, and to alleviate symptoms of pain and tingling in the lower limbs and decreased walking ability caused by acquired lumbar spinal stenosis.

How to take

Adult dose

1. For improvement of ischemic symptoms such as ulcers, pain, and coldness due to 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 due to acquired lumbar spinal stenosis (in patients with a normal SLR test and bilateral intermittent claudication), the usual adult dose is 1 tablet orally 3 times daily. The dose may be adjusted as appropriate 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 individuals with genetic disorders that affect lactose digestion should not take it. Patients at risk of bleeding or taking blood-thinning medications should use this drug cautiously. Allergic reactions such as skin rash or itching may occur, so if these symptoms arise, discontinue use immediately. Bleeding may rarely occur; if bleeding symptoms manifest, stop taking the medication and consult a healthcare professional. Gastrointestinal discomfort may occur, including diarrhea, nausea, abdominal pain, decreased appetite, and heartburn. Liver function may be adversely affected; if liver enzyme levels become abnormal, inform a healthcare professional. Be cautious as increased heart rate, rarely, bluish discoloration of the extremities, or low blood pressure may occur. Headaches, facial flushing, dizziness, warmth sensation, fatigue, swelling, tremors, increased body hair in the legs, and anemia may occur. Patients with lumbar spinal stenosis should monitor symptom changes and decide whether to continue use. This drug has not been proven effective in severe cases of spinal stenosis requiring surgery. Safety during pregnancy has not been established; therefore, pregnant women should not take this medication. Animal studies have reported uterine contractions, posing risks to pregnant women. There is insufficient safety data for children, and there is no experience using it in this population. Elderly patients may experience decreased physical function, so dosage should be adjusted accordingly. Healthy adults taking a large amount may experience a temporary drop in blood pressure, so caution is necessary.

Side effects

  • Rash
  • itching
  • bleeding
  • diarrhea
  • nausea
  • abdominal discomfort
  • abdominal pain
  • loss of appetite
  • heartburn
  • vomiting
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  • abdominal distension
  • elevated AST (GOT)
  • elevated ALT (GPT)
  • palpitations
  • cyanosis
  • hypotension
  • headache
  • facial flushing
  • dizziness
  • warmth sensation
  • 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 sealed container to protect it from air and moisture. The recommended storage temperature is between 1 and 30 degrees Celsius. Proper storage will help maintain the effectiveness of the medication over time.

Appearance and packaging

Appearance

White round tablet

Package unit

84 tablets/PTP (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.

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.