Viewing nowSafogre Tablet 100 mg (Sarpogrelate Hydrochloride)
Sarpogrelate Hydrochloride 100mg
Tablet · Prescription medication
Hwail Pharmaceutical Co., Ltd.

MFDS item code 201906564 · Approved 2019.09.19 · Insurance code 684501670
Improvement of ischemic symptoms in chronic peripheral arterial occlusive disease (ulcers, pain, etc.)
This medication is used to improve ischemic symptoms such as ulcers, pain, and cold sensitivity caused by chronic peripheral arterial occlusive disease. It helps alleviate symptoms occurring in conditions where blood vessels narrow or become blocked, such as Buerger's disease, obstructive arterial sclerosis, and diabetic peripheral vascular disease. It is effective in reducing discomfort due to blood circulation problems experienced by patients and improving symptoms.
Adults: Administer 100 mg of Sarpogrelate Hydrochloride orally after meals, three times a day. Adjust the dose appropriately according to symptoms.
This medication should not be administered to patients with bleeding, as it may increase the risk of further bleeding. Women who are pregnant or may become pregnant are advised not to use this medication, as it may harm the fetus. Patients who are genetically unable to digest lactose should not take this medication, as it contains lactose. Women menstruating or patients with a tendency to bleed should use this medication cautiously, as it may exacerbate bleeding. Patients taking anticoagulants or antiplatelet agents should be cautious when using this medication together, as the risk of bleeding may be increased. Patients with severely impaired kidney function should use this medication with caution, as there may be issues with its excretion. Elderly patients may have reduced kidney and liver function, increasing the risk of drug concentration elevation, so starting at a lower dose and monitoring their condition is recommended. During the use of this medication, careful observation for symptoms of bleeding or liver function abnormalities is advised, and if any abnormal symptoms occur, consultation with a doctor should be sought immediately. Hypersensitivity reactions such as vomiting, stomatitis, urticaria, rash, and pruritus may occur during treatment, and the medication should be discontinued if these symptoms arise. Regular blood tests to monitor the physical condition during treatment with this medication is advisable. It is preferably avoided by women who are pregnant or breastfeeding, and if it must be used, breastfeeding should be avoided. Safety for pediatric use has not been established, so this medication should be administered to children with caution. This medication should be kept out of the reach of children, and transferring it to another container should be avoided as it may adversely affect the quality.
Gastrointestinal bleeding (hematemesis and hematochezia, etc.), cerebral hemorrhage, subcutaneous bleeding, agranulocytosis, anemia, thrombocytopenia, leukopenia, acute hepatitis, liver failure, jaundice, urticaria
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to air and moisture, so it should be stored in a tightly sealed container. The storage temperature should be maintained between 1 and 30 degrees Celsius to preserve its effectiveness.
White round film-coated tablet
30 tablets/bottle, 100 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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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For anything that needs medical judgment, consult a doctor or pharmacist.
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.