Euromon Tablet (Limaprost Aldex)

Adult dose

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 a normal SLR test and bilateral intermittent claudication), the usual adult dose is 1 tablet orally 3 times daily. Adjust the dose appropriately according to age and symptoms.

This medication should not be used in women who are pregnant or may become pregnant. This medication contains lactose, so it should not be administered to patients with genetic disorders such as galactose intolerance, lactose deficiency, or glucose-galactose malabsorption. It should be administered with caution to patients at a high risk of bleeding or those taking antiplatelet agents, thrombolytics, or anticoagulants. While taking this medication, hypersensitivity symptoms such as rash or itching may occur; if these symptoms appear, use should be discontinued immediately, and appropriate measures should be taken. Additionally, bleeding may occur rarely, so if bleeding symptoms are present, administration should be stopped, and medical consultation should be sought. Gastrointestinal side effects may include diarrhea, nausea, abdominal pain, loss of appetite, and heartburn, while vomiting or abdominal distension may occur rarely. Since this medication may affect liver function, it is necessary to periodically check liver enzyme levels (AST, ALT). Cardiovascular symptoms such as palpitations, hypotension, and limb cyanosis may also occur rarely. Other side effects reported include headache, facial flushing, dizziness, feeling of warmth, general fatigue, swelling, tremors, excessive body hair on the legs, and anemia. In patients with lumbar spinal stenosis, the decision to continue medication should be made after closely observing symptom changes. The effectiveness of this medication is uncertain in patients with severe lumbar spinal stenosis who require surgery. The safety of administration during pregnancy has not been confirmed, and uterine contraction effects have been reported in animal studies, so it should not be used in pregnant women. The safety in children has not been established, and it is advisable not to use it in pediatric patients. Elderly patients may have decreased physical function, so care should be taken and dosages adjusted accordingly. Administering high doses to healthy adults may cause temporary decreases in blood pressure, so caution is advised.

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

This medication may be sensitive to air and moisture, so it should be stored in a tightly sealed container. It is best to maintain storage temperatures between 1 degree and 30 degrees Celsius at room temperature. Proper storage will secure the efficacy of the medication.

Appearance

White round tablet

Package unit

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