Viewing nowPravixen Tablets (Clopidogrel Hydrogen Sulfate)
Clopidogrel Bisulfate 97.875mg
Tablet · Prescription medication
Teragen Etex Co., Ltd.

MFDS item code 201206953 · Approved 2012.09.26 · Insurance code 698502340
Improvement of atherosclerotic symptoms such as ischemic stroke and myocardial infarction, improvement of acute coronary syndrome (cardiovascular abnormalities), reduction of stroke and thromboembolism risk in patients with atrial fibrillation.
This medication is used to improve symptoms resulting from atherosclerosis in adult patients with ischemic stroke, myocardial infarction, or peripheral arterial disease. Additionally, it reduces the risk of cardiovascular complications such as death, myocardial infarction, and stroke due to cardiovascular abnormalities in patients with acute coronary syndrome, for example, unstable angina or non-Q-wave myocardial infarction, after receiving drug therapy, percutaneous coronary intervention, or coronary artery bypass surgery. Moreover, it is effective in reducing the risk of stroke and thromboembolism in patients with atrial fibrillation who have one or more vascular risk factors and where vitamin K antagonists are not appropriate and there is a low risk of bleeding. Thus, this medication is used to effectively improve atherosclerosis and thrombotic symptoms in patients with various cardiovascular diseases and to prevent the occurrence of complications.
1. In patients with ischemic stroke, myocardial infarction, or peripheral arterial disease, Clopidogrel should be taken orally at a dose of 75 mg once daily. 2. In patients with acute coronary syndrome (unstable angina or non-Q-wave myocardial infarction), initiate treatment with a loading dose of 300 mg orally once on the day of administration, followed by a maintenance dose of 75 mg orally once daily. 3. In patients with atrial fibrillation, administer 75 mg orally once daily.
This medication helps prevent platelets from clumping together, facilitating better blood flow. This drug is activated into its effective form by a specific enzyme, CYP2C19, in the liver. If a person genetically has a reduced function of this enzyme, the efficacy of this medication may be diminished, prompting a reconsideration of treatment options. Furthermore, taking this medication with drugs that activate CYP2C19 enzyme may increase the risk of bleeding, so it is recommended not to use them together. Patients allergic to this medication or those with active bleeding, severely impaired liver function, and nursing mothers should not take this medication. Moreover, patients who are genetically unable to digest lactose should also refrain from taking this medication. Patients with a high risk of bleeding, issues with blood coagulation, or those who have had recent surgeries should use this medication cautiously. In cases of planned surgery, this medication should be discontinued 5 to 7 days prior, and resumed after hemostasis has been achieved. During the course of this medication, watch for signs of bleeding, and inform your doctor about this medication if you are prescribed new medication or prior to surgery. This medication may increase the risk of bleeding, so extra caution is needed when taken with aspirin or other drugs that affect blood coagulation. Rarely, severe side effects may occur, characterized by a drastic drop in blood cell count; if symptoms of infection or bleeding arise, immediate medical consultation is advised. Pregnant women should only use this medication for severe cardiovascular disease treatment, and should discontinue it during delivery because of the risk of bleeding. Nursing mothers should consider discontinuing breastfeeding or the use of this medication due to the potential for drug transmission to the infant through breast milk. Safety in infants has not been established. Elderly patients should use it cautiously, as impaired kidney or liver function may increase bleeding risk and should follow a doctor's instructions. In case of overdose, bleeding may worsen, and since there is no specific antidote, platelet transfusion may be needed to stop the bleeding. This medication should be stored out of reach of children, and care should be taken not to transfer it to another container as this may compromise its quality.
Hives, severe swelling (angioedema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with fever, blisters, peeling skin, pain in oral/ocular mucosa, breathlessness or difficulty breathing, asthma attack, respiratory abnormalities with cough + fever, yellowing of the skin or eyes (jaundice), profound lethargy, sudden severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis,
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container to prevent air from entering and preferably at room temperature between 1 and 30 degrees Celsius. Storing it this way will help maintain the medication's effectiveness for a long time.
Pink round film-coated tablets
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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Tablet · Prescription medication
Teragen Etex Co., Ltd.

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Tablet · Prescription medication
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Tablet · Prescription medication
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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.