Medication info
Bivorhin Rimaprostan Tablet (Rimaprostan Alpha-Dex)

Bivorhin Rimaprostan Tablet (Rimaprostan Alpha-Dex)

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

MFDS item code 201603596 · Approved 2016.06.20 · Insurance code 658203180

Summary

Main use
Improves symptoms and walking ability in lumbar spinal stenosis, and improves 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's disease), the usual adult dose is 2 tablets orally 3 times daily. 2. For improvement of subjective symptoms (lower-extremity 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. The dose may be adjusted according to age and symptoms.

Ingredients

Manufacturer
Bivorhin Pharmaceuticals Co., Ltd.

Efficacy & effects

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

  • Ulcers
  • pain
  • coldness
  • subjective symptoms
  • leg pain
  • leg numbness
View approved original text

This medication helps to alleviate ischemic symptoms such as ulcers, pain, and coldness caused by occlusive thromboangiitis (Buerger's disease). It also alleviates subjective symptoms such as leg pain and numbness that occur in patients with acquired lumbar spinal stenosis, improving walking ability. In summary, this medication is used to effectively improve various symptoms related to vascular and nerve issues.

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-extremity 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. 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. It contains lactose, and should not be administered to patients with genetic disorders that prevent them from digesting lactose. Patients who are at risk of bleeding or taking medications that may cause bleeding should use this medication with caution. It may cause hypersensitivity reactions such as skin rash or itching; if such symptoms occur, use should be discontinued immediately. Bleeding symptoms may rarely occur, so if any unusual signs appear, stop taking the medication and consult a doctor. Gastrointestinal side effects such as diarrhea, nausea, abdominal pain, loss of appetite, and heartburn may occur. Liver function abnormalities may arise, so it is advisable to periodically check liver health. Symptoms such as rapid heartbeat or low blood pressure may occur, so caution should be exercised if these symptoms are present. Headaches, facial flushing, dizziness, warmth, systemic fatigue, swelling, tremors, increased body hair on legs, and anemia may occur. Patients with spinal stenosis should observe for symptom changes and decide whether to continue using this medication. The effectiveness of this medication has not been proven in severe cases that require spinal stenosis surgery. Safety during pregnancy has not been established, and uterine contractions have been reported in animal studies, so women who may become pregnant should not use it. Safety in children has not been established, therefore it is not recommended for pediatric use. Elderly patients may have reduced bodily functions and should use a reduced dosage with caution.

Side effects

  • Rash
  • itching
  • bleeding
  • diarrhea
  • nausea
  • abdominal discomfort
  • abdominal pain
  • loss of appetite
  • heartburn
  • vomiting
Show 16 more
  • abdominal bloating
  • elevated AST (GOT)
  • elevated ALT (GPT)
  • palpitations
  • peripheral cyanosis
  • hypotension
  • headache
  • facial 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 moisture, and it is best stored at room temperature between 1 to 30 degrees Celsius. By storing it this way, the effectiveness of the medication can be maintained for a longer period.

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

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.