Medication info
Rimapam Tablets (Rimaprost Alpha-Dex)

Rimapam Tablets (Rimaprost Alpha-Dex)

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

MFDS item code 201603132 · Approved 2016.05.31 · Insurance code 659901160

Summary

Main use
Improves ischemic symptoms of Buerger disease (e.g., ulcers and pain) 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 due to thromboangiitis obliterans (Buerger's disease), the usual adult dose is 2 tablets per dose, administered orally 3 times daily. 2. For improvement of subjective symptoms (lower limb pain and numbness) and walking ability due to acquired lumbar spinal stenosis (patients with a normal SLR test and bilateral intermittent claudication), the usual adult dose is 1 tablet per dose, administered orally 3 times daily. Adjust the dose as appropriate according to age and symptoms.

Ingredients

Manufacturer
Korea Pharma Bio Co., Ltd.

Efficacy & effects

Improves ischemic symptoms of Buerger disease (e.g., ulcers and pain) and symptoms and walking ability in lumbar spinal stenosis

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

This medication is effective in improving ischemic symptoms such as ulcers, pain, and cold sensation due to occlusive thromboangiitis. It also helps relieve leg pain and numbness experienced by patients with acquired lumbar spinal stenosis, and improves walking ability. Therefore, this drug is used to alleviate discomfort related to vascular symptoms and spinal stenosis.

Dosage and Administration

Adult dosage

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 per dose, administered orally 3 times daily. 2. For improvement of subjective symptoms (lower limb pain and numbness) and walking ability due to acquired lumbar spinal stenosis (patients with a normal SLR test and bilateral intermittent claudication), the usual adult dose is 1 tablet per dose, administered orally 3 times daily. Adjust the dose as appropriate 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 taken by individuals with a genetic condition that prevents them from digesting lactose. Patients with a tendency to bleed or who are taking blood-thinning medications should use this drug with caution. Adverse reactions such as skin rash or itching may occur when taking this medication, and it should be discontinued immediately if such symptoms arise. Bleeding may occur rarely, so if any bleeding symptoms appear, stop taking the medication and consult a physician. It can affect the digestive system, resulting in symptoms such as diarrhea, nausea, abdominal pain, and heartburn. It may affect liver function, and liver enzyme levels may rise. Cardiovascular symptoms such as an increased heart rate or low blood pressure may occur. Headache, facial flushing, dizziness, and tremors have also been reported. Patients with lumbar spinal stenosis should closely monitor changes in symptoms and decide whether to continue taking this medication. Safety during pregnancy has not been established, and uterine contractions have been reported in animal studies, so pregnant women should avoid taking it. Safety for children has not been confirmed, so it is advisable not to use it in pediatric patients. Elderly patients may have reduced physical function, so caution is needed to adjust the dosage accordingly. If a healthy adult takes a large amount, it may cause a temporary drop in blood pressure, so caution is advised.

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
  • fever
  • general malaise
  • edema
  • mastitis
  • tremors
  • hirsutism
  • anemia

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

Storage

This medication may be sensitive to air or moisture, so it should be stored in a tightly sealed container. Additionally, it is recommended to store the medication at room temperature, between 1 degrees and 30 degrees Celsius, away from extreme heat or cold.

Appearance and packaging

Appearance

White round tablet

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.

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.