Omaris Tablets (Limaprost Aldex)

Adult dose

1. For improvement of ischemic symptoms such as ulcers, pain, and coldness caused by thromboangiitis obliterans (Buerger's disease), the usual adult dosage 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 canal stenosis (in patients with normal SLR test results and bilateral intermittent claudication), the usual adult dosage is 1 tablet orally 3 times daily. The dose may be increased or decreased appropriately according to age and symptoms.

This medication should not be used by women who are pregnant or may become pregnant. Due to the presence of lactose in this medication, it should not be administered to patients with a hereditary condition that prevents the digestion of lactose. Caution should be exercised when administering this medication to patients with a tendency to bleed or those taking anticoagulant medications. Hypersensitivity reactions such as skin rashes or itching may occur; if such symptoms appear, the medication should be discontinued immediately. Rarely, bleeding may occur; if bleeding symptoms manifest, the use of the medication should be stopped and medical consultation sought. Gastrointestinal discomfort, such as diarrhea, nausea, abdominal pain, decreased appetite, and heartburn may occur. Liver function may be affected, leading to elevated liver enzymes; regular testing is necessary. Rapid heartbeat or cold extremities may occur, and blood pressure may drop, requiring caution. Headaches, facial flushing, dizziness, warmth, fatigue, or swelling may also be present. Patients with lumbar spinal stenosis should closely monitor symptom changes and decide whether to continue medication use. The efficacy of this medication has not been sufficiently proven in cases where severe spinal stenosis surgery is required. Safety during pregnancy has not been established, and animal studies have indicated the potential to induce uterine contractions, hence it should not be taken by pregnant women. The safety in children has not been established, and there is no experience of use. Elderly patients may have decreased physical function, so caution should be exercised in dosing, including possible reduction. Caution is required when administering large doses to healthy adults, as temporary hypotension may occur.

• rash
• itching
• bleeding
• diarrhea
• nausea
• abdominal discomfort
• abdominal pain
• loss of appetite
• heartburn
• vomiting

This medication should be stored in a tightly sealed container to prevent exposure to air and moisture. It is important to maintain storage temperatures between 1 and 30 degrees Celsius to preserve the medication's efficacy safely.

Appearance

White round tablets

Package unit

84 tablets (21 tablets/Alu-Alu x 4)