Medication info
Rimapalmone Tablet (Rimaprost alpha dex)

Rimapalmone Tablet (Rimaprost alpha dex)

Prescription medicationTablet
Ingredient · strength
Limaprost Alfadex›166.67μg / 1 tablet
Manufacturer / importer
Hanwha Pharmaceutical Co., Ltd.
Appearance
White round tablet
Packaging
84 tablets/Alu-Alu (21 tablets * 4 Alu-Alu)
Approval status
Active

MFDS item code 201603514 · Approved 2016.06.15 · Insurance code 651602070

Summary

Main use
Improvement of symptoms and walking ability in lumbar spinal stenosis, and ischemic symptoms of Buerger disease
Who uses it
Adults
Adult dosage
1. For improvement of ischemic symptoms such as ulcers, pain, and coldness due to thromboangiitis obliterans (Buerger 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 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 according to age and symptoms.

Ingredients

Manufacturer
Hanwha Pharmaceutical Co., Ltd.

Efficacy & effects

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

  • Ulcer
  • pain
  • cold sensation
  • subjective symptoms
  • leg pain
  • leg numbness
View approved original text

It is used to improve ischemic symptoms such as ulcers, pain, and cold sensations caused by occlusive thromboangiitis, specifically Buerger's disease. In addition, it alleviates subjective symptoms such as leg pain, numbness, and decreased walking ability that occur in patients with acquired lumbar spinal canal stenosis, aiding comfort in daily life. This medication is effective in improving the patient's symptoms by facilitating blood circulation.

Dosage and Administration

Adult dosage

1. For improvement of ischemic symptoms such as ulcers, pain, and coldness due to thromboangiitis obliterans (Buerger 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 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 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, so individuals with genetic disorders that prevent lactose digestion should not take it. Patients with a tendency to bleed or those taking medications that can easily cause bleeding should use this medication with caution. Skin rashes or itching may occur during the course of this medication. If these symptoms appear, stop taking the medication immediately and consult a doctor. Bleeding may occur infrequently, so if bleeding symptoms are observed, stop taking the medication immediately and seek medical attention. It may affect the gastrointestinal tract, causing diarrhea, nausea, abdominal pain, decreased appetite, and heartburn. It can affect liver function, and liver enzyme levels may rise in blood tests, so regular testing may be necessary. Symptoms such as increased heart rate, cold extremities, and low blood pressure may occur infrequently. Various symptoms such as headache, facial flushing, dizziness, warmth, general fatigue, swelling, body tremors, increased body hair, and anemia may occur. Patients with lumbar spinal canal stenosis should closely monitor symptoms to decide whether to continue using the medication. The effectiveness of this medication in severe cases of lumbar spinal canal stenosis that require surgery is not certain. There is insufficient research on safety during pregnancy, so pregnant women should not take it. Animal studies have shown that this medication induces uterine contractions. Safety has not been established in children, and there is no experience of use. Elderly patients may have decreased bodily functions, so caution is required regarding dosage adjustment, such as reducing the dose. Healthy adults taking a large amount of this medication may experience a temporary drop in blood pressure, so caution is warranted.

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
  • hypotension
  • headache
  • facial flushing
  • dizziness
  • warm sensation
  • general malaise
  • edema
  • mastitis
  • tremors
  • hirsutism
  • anemia

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

Storage

This medication is sensitive to air and moisture, so it must be stored in a sealed container. It is also best to store it at room temperature, that is, between 1 to 30 degrees Celsius, rather than in extremely hot or cold locations.

Appearance and packaging

Appearance

White round tablet

Package unit

84 tablets/Alu-Alu (21 tablets * 4 Alu-Alu)

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.