Medication info
Rimaglan Tablet (Rimaprost Alpha Dextrin)

Rimaglan Tablet (Rimaprost Alpha Dextrin)

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

MFDS item code 201602284 · Approved 2016.04.25 · Insurance code 669906720

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 associated with 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 associated with acquired lumbar spinal stenosis (patients with a normal SLR test and bilateral intermittent claudication), the usual adult dose is 1 tablet orally 3 times daily. Adjust the dose as appropriate according to age and symptoms.

Ingredients

Manufacturer
Daehan New Pharm 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
  • leg pain
  • leg numbness
View approved original text

This medication helps improve ischemic symptoms such as ulcers, pain, and cold sensation caused by obstructive thromboangiitis, specifically Buerger's disease. It also has the effect of improving leg pain and numbness caused by acquired lumbar spinal canal stenosis, as well as enhancing walking ability. Through these effects, patients' daily lives can become more comfortable and symptoms can be alleviated. Therefore, it is used for the improvement of symptoms related to obstructive thromboangiitis and lumbar spinal canal stenosis.

Dosage and Administration

Adult dosage

1. For improvement of ischemic symptoms such as ulcers, pain, and coldness associated with 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 associated with acquired lumbar spinal stenosis (patients with a normal SLR test and bilateral intermittent claudication), the usual adult dose is 1 tablet orally 3 times daily. Adjust the dose as appropriate according to age and symptoms.

Precautions

This medication should not be used by women who are pregnant or may become pregnant. Since this medication contains lactose, it should not be used in patients with genetic diseases that impair the digestion of lactose. It should be used with caution in patients with a tendency to bleed or at risk of bleeding, and care should also be taken with patients taking antiplatelet agents, thrombolytics, or anticoagulants. While taking this medication, allergic reactions such as skin rash or itching may occasionally occur, and if such symptoms appear, use should be stopped immediately. Bleeding may occur infrequently, so body conditions should be closely monitored, and if any unusual symptoms arise, medication should be discontinued. It can affect the gastrointestinal system, resulting in diarrhea, nausea, abdominal discomfort, decreased appetite, and heartburn. It may also affect liver function possibly leading to elevated liver enzyme levels in blood tests, so periodic testing is required. Cardiovascular symptoms such as increased heart rate, cyanosis of the extremities, and hypotension may occur. Various side effects may appear, including headache, facial flushing, dizziness, warmth, generalized malaise, edema, tremors, hypertrichosis, and anemia, so caution is advised. Patients with lumbar spinal canal stenosis should observe changes in symptoms and decide whether to continue medication, as the effects of this medication are not certain in severe cases requiring surgery. The safety during pregnancy has not been established, and uterine contractions have been reported in animal experiments, so women who may become pregnant should not take it. Safety in children has not been verified due to lack of experience, so it is advisable not to administer it to children. Elderly patients may have diminished bodily functions, so special care, such as reducing the dosage, is required. Caution is advised as administering a large amount to healthy adults may temporarily lower blood pressure.

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
  • feeling of warmth
  • general malaise
  • 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 sealed container to prevent exposure to air or moisture. It is important to maintain a storage temperature between 1 and 30 degrees Celsius to ensure the medication's efficacy remains safe.

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.

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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.