Clopidogrel hydrogen sulphate
Clopidogrel Hydrogen Sulphate is a pharmaceutical compound widely used in the prevention of blood clots. This medication falls under the category of antiplatelet agents, which work by preventing platelets from clumping together and forming clots that can lead to heart attacks, strokes, and other serious vascular conditions. Clopidogrel is particularly prescribed to individuals who have experienced heart attacks, strokes, or have been diagnosed with peripheral artery disease.
Mechanism of Action[edit | edit source]
Clopidogrel hydrogen sulphate inhibits the binding of adenosine diphosphate (ADP) to its platelet receptor and the subsequent ADP-mediated activation of the glycoprotein GPIIb/IIIa complex, thereby inhibiting platelet aggregation. This action is irreversible, and the platelet's ability to aggregate will not return until new platelets are produced, which typically takes about 7 to 10 days.
Indications[edit | edit source]
Clopidogrel is indicated for the reduction of atherosclerotic events in patients with a history of recent myocardial infarction, acute coronary syndrome (without ST-segment elevation), stroke, or established peripheral arterial disease.
Administration and Dosage[edit | edit source]
The drug is administered orally, and the standard dosage is often a single daily dose of 75 mg. However, dosages may vary based on specific conditions or in combination with other medications.
Side Effects[edit | edit source]
Common side effects of clopidogrel include, but are not limited to, bleeding, bruising, diarrhea, and indigestion. Severe bleeding, allergic reactions, and liver enzyme changes are less common but more serious side effects that require immediate medical attention.
Contraindications[edit | edit source]
Clopidogrel should not be used by individuals with active pathological bleeding such as peptic ulcer or intracranial hemorrhage. It is also contraindicated in patients with known hypersensitivity to the drug or any of its components.
Pharmacokinetics[edit | edit source]
Clopidogrel is rapidly absorbed by the gastrointestinal tract, and its active metabolite (which provides the antiplatelet effect) is produced by liver metabolism. The onset of action is within 2 hours of oral administration, and its half-life is approximately 6 hours, though the antiplatelet effect lasts for the lifetime of the platelet.
Interactions[edit | edit source]
Clopidogrel can interact with several other medications, including proton pump inhibitors (PPIs), anticoagulants, and nonsteroidal anti-inflammatory drugs (NSAIDs), potentially reducing its effectiveness or increasing the risk of bleeding.
Conclusion[edit | edit source]
Clopidogrel hydrogen sulphate plays a crucial role in the management and prevention of thrombotic vascular events. Its use, however, must be carefully balanced with the risk of bleeding and considered in the context of individual patient profiles and concomitant medications.
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Contributors: Prab R. Tumpati, MD