Here’s a **complete and structured overview** of **antiplatelet drugs, anticoagulants, and fibrinolytic drugs**, including **mechanism, examples, clinical uses, and adverse effects** — perfect for revision or notes.
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## 🩸 **1. ANTIPLATELET DRUGS**
### 🔹 **Mechanism of Action**
They **inhibit platelet aggregation** by interfering with platelet activation pathways — used mainly in **arterial thrombosis** (where platelets play a major role).
### 🔹 **Major Classes & Examples**
| Class | Drugs | Mechanism | Key Uses |
| ----------------------------------- | --------------------------------------------------------------- | ------------------------------------------------------- | ------------------------------------------------------------ |
| **COX Inhibitors** | **Aspirin (Acetylsalicylic acid)** | Irreversibly inhibits COX-1 → ↓ Thromboxane A₂ (TXA₂) | MI prevention, unstable angina, post-stent |
| **ADP Receptor (P2Y₁₂) Blockers** | **Clopidogrel**, **Prasugrel**, **Ticagrelor**, **Ticlopidine** | Inhibit ADP binding → prevent GPIIb/IIIa activation | After PCI, ACS, stroke prevention |
| **GPIIb/IIIa Receptor Blockers** | **Abciximab**, **Eptifibatide**, **Tirofiban** | Block fibrinogen binding → prevent platelet aggregation | During PCI, unstable angina |
| **Phosphodiesterase Inhibitors** | **Dipyridamole**, **Cilostazol** | ↑ cAMP → ↓ platelet aggregation, vasodilation | Stroke prophylaxis (with aspirin), intermittent claudication |
| **Thromboxane Synthase Inhibitors** | **Picotamide**, **Ridogrel** | Block TXA₂ synthesis/action | Experimental/rarely used |
### ⚠️ **Adverse Effects**
* Bleeding (GI, intracranial)
* Gastritis (esp. aspirin)
* Thrombocytopenia (esp. ticlopidine, abciximab)
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## 🧬 **2. ANTICOAGULANTS**
### 🔹 **Mechanism of Action**
They **inhibit clotting factors** (mainly fibrin formation) — used in **venous thrombosis** and **embolism prevention**.
### 🔹 **Major Types & Examples**
| Class | Drugs | Mechanism | Route | Monitoring | Antidote |
| ------------------------------------- | ----------------------------------------------------------------------------------------------------- | -------------------------------------------------------------------------------- | ------------ | -------------- | ----------------------------- |
| **Heparins** | **Unfractionated Heparin (UFH)**, **Low Molecular Weight Heparin (LMWH)** e.g. Enoxaparin, Dalteparin | Activate **antithrombin III** → inhibit **Factor Xa & IIa (thrombin)** | IV, SC | aPTT (for UFH) | Protamine sulfate |
| **Factor Xa Inhibitors** | **Fondaparinux**, **Apixaban**, **Rivaroxaban**, **Edoxaban** | Directly inhibit **Factor Xa** | Oral (DOACs) | Not needed | Andexanet alfa |
| **Direct Thrombin Inhibitors (DTIs)** | **Dabigatran**, **Argatroban**, **Bivalirudin** | Directly inhibit **thrombin (Factor IIa)** | Oral/IV | Not needed | Idarucizumab (for dabigatran) |
| **Vitamin K Antagonist** | **Warfarin** | Inhibits **Vitamin K epoxide reductase** → ↓ synthesis of Factors II, VII, IX, X | Oral | PT/INR | Vitamin K, FFP |
### ⚠️ **Adverse Effects**
* **Bleeding** (major)
* **Heparin-induced thrombocytopenia (HIT)** (UFH)
* **Teratogenicity (Warfarin)** — contraindicated in pregnancy
* **Skin necrosis (Warfarin early therapy)**
### 💉 **Clinical Uses**
* DVT, PE
* Atrial fibrillation
* Mechanical heart valves (warfarin)
* MI, unstable angina (with antiplatelets)
* During surgery (thromboprophylaxis)
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## 🧫 **3. FIBRINOLYTIC (THROMBOLYTIC) DRUGS**
### 🔹 **Mechanism of Action**
They **lyse existing fibrin clots** by converting **plasminogen → plasmin**, which breaks down fibrin.
### 🔹 **Major Agents**
| Drug | Source | Mechanism | Key Use |
| --------------------------- | -------------------- | ----------------------------------------- | ----------------------------------------------- |
| **Streptokinase** | Streptococci-derived | Activates plasminogen | MI, PE (cheap but antigenic) |
| **Urokinase** | Human-derived | Directly activates plasminogen | PE, DVT |
| **Alteplase (tPA)** | Recombinant | Fibrin-specific activation of plasminogen | Acute MI, ischemic stroke (within 3–4.5 hr), PE |
| **Reteplase, Tenecteplase** | Modified tPA | Longer half-life, more specific | Same as above |
### ⚠️ **Adverse Effects**
* **Severe bleeding**
* **Allergic reactions** (streptokinase)
* **Reperfusion arrhythmias** (post-MI)
### 💉 **Contraindications**
* Active bleeding
* Recent surgery/trauma
* History of hemorrhagic stroke
* Severe uncontrolled hypertension
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## 🧾 **Quick Summary Table**
| Type | Mechanism | Examples | Used For | Antidote |
| ----------------- | ---------------------------- | ------------------------ | ------------------- | ---------------------------------- |
| **Antiplatelet** | Inhibit platelet aggregation | Aspirin, Clopidogrel | Arterial thrombosis | None (supportive) |
| **Anticoagulant** | Inhibit clotting factors | Heparin, Warfarin, DOACs | Venous thrombosis | Protamine, Vit K |
| **Fibrinolytic** | Dissolve existing clots | tPA, Streptokinase | MI, Stroke, PE | Aminocaproic acid, Tranexamic acid |
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