Indications |
Oral Prophylaxis of thrombotic stroke Adult: >18 yr: 250 mg bid. Renal impairment: Dose reduction or discontinuance if haemorrhagic or haematopoietic complications occur. Hepatic impairment: Severe: contraindicated. Oral Ischaemic heart disease Adult: >18 yr: 250 mg bid. Renal impairment: Dose reduction or discontinuance if haemorrhagic or haematopoietic complications occur. Hepatic impairment: Severe: contraindicated. Oral Intermittent claudication Adult: >18 yr: 250 mg bid. Renal impairment: Dose reduction or discontinuance if haemorrhagic or haematopoietic complications occur. Hepatic impairment: Severe: contraindicated. Oral Prophylaxis of subacute stent occlusion after intracoronary stenting Adult: >18 yr: 250 mg bid for 4 wk, in conjunction with aspirin, starting at the time of stent placement. Renal impairment: Dose reduction or discontinuance if haemorrhagic or haematopoietic complications occur. Hepatic impairment: Severe: contraindicated. |
Contraindications |
Pre-existing or history of blood dyscrasias; haemostatic disorder or active pathological bleeding (eg. bleeding peptic ulcer, intracranial bleeding); severe hepatic dysfunction. Hypersensitivity. Lactation. |
Warnings / Precautions |
Patients with increased risk of bleeding from trauma, surgery or pathological disorder. Moderate to severe renal impairment. May need to stop therapy 10-14 days before elective surgery. Full blood counts should be performed prior to therapy and every 2 wk during the first 3 mth of treatment. Pregnancy. |
Adverse Reactions |
Diarrhoea, nausea, dyspepsia, bleeding, pupura, skin rash, increase in serum cholesterol concentration, elevation of LFTs, hepatitis, cholestatic jaundice. Potentially Fatal: Neutropenia, agranulocytosis, thrombotic thrombocytopenic purpura and aplastic anaemia. |
Overdose Reactions |
GI haemorrhage, convulsions, hypothermia, dyspnoea, loss of equilibrium and abnormal gait. |
Drug Interactions |
Reduced clearance with cimetidine; corticosteroid may antagonise effects on bleeding time. Avoid concurrent use with clopidogrel. Potentially Fatal: Risk of haemorrhage increased with NSAIDs and oral anticoagulants; decreased metabolism of theophylline, phenytoin and bupropion. See Below for More ticlopidine Drug Interactions |
Food Interactions |
Increased risk of bleeding with Ginkgo biloba and Kangen-karyu. |
Mechanism of Actions |
Ticlopidine inhibits adenosine diphosphate-mediated platelet aggregation. Absorption: Rapidly and almost completely absorbed from the GI tract (oral). Oral bioavailability increased by 20% when taken after meals. Distribution: Protein-binding: Extensive. Metabolism: Hepatic: Extensive. Excretion: As metabolites; via urine (60%), via faeces (25%). Terminal half-life: 30-50 hr. |
Administration |
Should be taken with food. |
ATC Classification |
B01AC05 - ticlopidine ; Belongs to the class of platelet aggregation inhibitors excluding heparin. Used in the treatment of thrombosis. |
Available As |
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Ticlopidine
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Ticlopidine Containing Brands
Ticlopidine is used in following diseases
Drug - Drug Interactions of Ticlopidine
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