Medication info
Limamax Tablets (Rimaprost Alpha-Dex)

Limamax Tablets (Rimaprost Alpha-Dex)

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

MFDS item code 201902806 · Approved 2019.04.30 · Insurance code 073000070

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 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 (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 appropriately according to age and symptoms.

Ingredients

Manufacturer
Geonil Biopharm 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 occlusive thromboangiitis (Buerger's disease). Additionally, it assists in alleviating subjective symptoms like leg pain and numbness and improving walking ability in patients with acquired lumbar spinal canal stenosis. Thus, this drug is used to enhance the quality of life of patients by alleviating discomfort associated with vascular and spinal disorders.

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 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 orally 3 times daily. The dose may be adjusted appropriately according to age and symptoms.

Precautions

This medicine should not be used by women who are pregnant or may become pregnant. This medication contains lactose and should not be administered to individuals with genetic problems that prevent lactose digestion. Patients with tendencies for bleeding or those taking antiplatelet agents, thrombolytics, or anticoagulants should exercise caution when using this drug. Taking this medicine may result in allergic reactions such as skin rashes or itching; if such symptoms occur, discontinue use immediately. Rarely, bleeding can occur; if unusual symptoms arise, stop taking the medication and consult a physician. Gastrointestinal symptoms may include diarrhea, nausea, abdominal discomfort, loss of appetite, and heartburn. It may affect liver function, leading to elevated liver enzyme levels; thus, regular testing may be required. Symptoms such as rapid heartbeat or blue discoloration of the extremities and low blood pressure may occur. Headache, facial flushing, dizziness, warmth, shaking, edema, and anemia may also occur infrequently. Patients with lumbar spinal canal stenosis should carefully monitor changes in symptoms to determine whether to continue taking the medication. The effectiveness of this drug is not certain for patients with severe spinal canal stenosis who require surgery. Safety during pregnancy has not been established; therefore, it should not be administered to pregnant individuals. Uterine contractions have been reported in animal studies. Safety in pediatric patients has not been confirmed, and there is no experience using it in children. Elderly patients may have diminished physiological function, so dosage adjustments and additional caution are necessary. Administration of high doses to healthy adults may temporarily lower 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
  • flushing
  • dizziness
  • heat sensation
  • general fatigue
  • edema
  • mastitis
  • body 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 humidity. Additionally, avoid extremely hot or cold environments, and store at room temperature between 1 and 30 degrees Celsius.

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.