Medication info
Omaphron Tablets (Limaprost Aldex)

Omaphron Tablets (Limaprost Aldex)

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

MFDS item code 201602185 · Approved 2016.04.19 · Insurance code 662503390

Summary

Main use
Relief of ischemic symptoms of Buerger disease and improvement of leg 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 (in patients with normal SLR test results 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
Nexpam Korea Co., Ltd.

Efficacy & effects

Relief of ischemic symptoms of Buerger disease and improvement of leg symptoms and walking ability in lumbar spinal stenosis

  • Ulcers
  • pain
  • cold sensation
  • subjective symptoms
  • lower limb pain
  • lower limb paresthesia
View approved original text

This medication effectively improves ischemic symptoms such as ulcers, pain, and cold sensation caused by obliterative thromboangiitis, also known as Buerger's disease. It also helps alleviate lower limb pain, tingling symptoms, and decreased walking ability due to acquired lumbar spinal stenosis. It is expected to have a positive effect on the patient's blood circulation and the relief of neurological symptoms.

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 (in patients with normal SLR test results 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 in women who are pregnant or may become pregnant. This medication contains lactose, and should not be administered to patients with a genetic disorder that impairs lactose digestion. Caution should be exercised when using this medication in patients with a tendency to bleed or those taking antiplatelet agents, thrombolytic agents, or anticoagulants. Hypersensitivity reactions such as rash or itching may occur while taking this medication; if such symptoms occur, usage should be discontinued immediately. Bleeding symptoms may rarely occur, so if any signs of bleeding appear, the medication should be stopped and the physician consulted. Gastrointestinal discomfort may occur, including diarrhea, nausea, abdominal pain, loss of appetite, and heartburn, so caution is necessary. Liver function abnormalities may occur, thus monitoring for liver-related symptoms is required. Palpitations, hypotension, and bluish discoloration of the hands and feet may rarely occur; caution should be exercised. Headaches, facial flushing, dizziness, a feeling of heat, tremors, and anemia may also occur; if any unusual symptoms arise, the physician should be informed. Patients with lumbar spinal stenosis should carefully observe changes in symptoms while deciding on the continuation of medication. The effectiveness of this medication is not certain for patients with severe lumbar spinal stenosis who require surgery. The safety during pregnancy has not been confirmed, and uterine contractions have been reported in animal studies, so it should not be administered to pregnant women. Safety for children has not been confirmed, and there is no experience using it. Elderly patients may have diminished physical function, so caution should be exercised in usage and dosage should be reduced if necessary. Healthy adults who take a large quantity may experience transient hypotension, and care should be taken.

Side effects

  • Rash
  • itching
  • bleeding
  • diarrhea
  • nausea
  • abdominal discomfort
  • abdominal pain
  • poor appetite
  • heartburn
  • vomiting
Show 16 more
  • abdominal bloating
  • increased AST (GOT)
  • increased ALT (GPT)
  • palpitations
  • cyanosis
  • low blood pressure
  • headache
  • facial flushing
  • dizziness
  • warmth
  • generalized weakness
  • 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 closed container to prevent exposure to air or moisture. Additionally, it is important to store the medication at room temperature, ideally between 1 to 30 degrees Celsius, avoiding extremes of hot or cold.

Appearance and packaging

Appearance

White round tablets

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

No questions yet.

For anything that needs medical judgment, consult a doctor or pharmacist.

Related searches

Search tags

Suggested searches

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.