Anapralate Sustained Release Tablet 300 mg (Sarpogrelate Hydrochloride)
Sarpogrelate Hydrochloride 200mg
Tablet · Prescription medication
Youngpharm Co., Ltd.
MFDS item code 201904324 · Approved 2019.06.24
This product's status changed to Expired on 2024.06.24. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Improvement of ischemic symptoms such as ulcers and pain in chronic arterial occlusion
This medication is used to improve ischemic symptoms such as ulcers, pain, and cold sensations caused by chronic arterial occlusion. It alleviates ischemic symptoms resulting from various causes such as Buerger's disease, obstructive arteriosclerosis, and diabetic peripheral vascular disease, aiding in the blood circulation of patients and improving their quality of life.
Administer 300 mg of Sarpogrelate Hydrochloride sustained release tablet orally once daily after meals. The tablet should be swallowed whole and not chewed or crushed.
This medication should not be used in patients with bleeding. It can aggravate bleeding risks in conditions such as hemophilia, gastrointestinal ulcers, and urinary tract bleeding. Women who are pregnant or may become pregnant should not use this medication, as it may pose risks to the fetus. Women during menstruation or those with tendencies for bleeding should use this medication cautiously due to the risk of increased bleeding. Patients on anticoagulants or antiplatelet agents may experience an increased risk of bleeding when using this medication together; therefore, caution is advised. Patients with severely impaired kidney function or the elderly should be monitored closely when using this medication, as it may affect drug excretion. While taking this medication, side effects such as urticaria, dyspepsia, headaches, cough, and blood pressure changes may occur, and patients should inform their healthcare provider of any symptoms. If symptoms of bleeding or severe allergic reactions occur, use of the medication should be stopped immediately, and the patient should visit a hospital. Regular blood tests during treatment are important to monitor for bleeding tendencies or blood abnormalities. Pregnant or nursing women are advised not to use this medication, and if absolutely necessary, should discuss with healthcare professionals about avoiding breastfeeding. Safety in children has not been established, so it is recommended not to use this medication in pediatric patients. This medication should be kept out of reach of children, and transferring it to other containers may jeopardize its quality, so caution is necessary.
Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, paleness, severe rashes with high fever, blisters, mucosal pain in the mouth/eyes, shortness of breath or difficulty breathing, asthma attacks, respiratory changes accompanied by cough and fever, jaundice (yellowing of skin or eyes), extreme lethargy, sudden and severe headaches, thunderclap headaches, seizures, altered consciousness, visual disturbances, paralysis, urinary retention
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to avoid exposure to air or moisture. It is advisable to maintain a storage temperature between 1 degree and 30 degrees Celsius. This will help preserve the medication's effectiveness for a longer time.
White oblong film-coated tablet
100 tablets/bottle, 30 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.