AURO-CLOPIDOGREL is a brand name for Clopidogrel, supplied as a tablet. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: AURO-CLOPIDOGREL (clopidogrel bisulfate) is indicated: for the secondary prevention of atherothrombotic events (myocardial infarction, stroke and vascular death) in patients with atherosclerosis documented by stroke, myocardial infarction, or established peripheral arterial disease. in combination with…
Verbatim from this product's HC label. Tap a section to expand.
2 Recommended Dose and Dosage Adjustment MI, Stroke or Established Peripheral Arterial Disease The recommended dose of AURO-CLOPIDOGREL is 75 mg once daily long term with or without food. Acute Coronary Syndrome For patients with non-ST-segment elevation acute coronary syndrome (unstable angina/non-Q-wave MI), AURO-CLOPIDOGREL should be initiated with a 300 mg loading dose and continued long term at 75 mg once a day with ASA (80 mg-325 mg daily) (see 14 CLINICAL TRIALS).
For patients with ST-segment elevation acute myocardial infarction, the recommended dose of AURO-CLOPIDOGREL is 75 mg once daily, administered in combination with ASA, with or without thrombolytics. AURO-CLOPIDOGREL may be initiated with or without a loading dose (300 mg was used in CLARITY; see 14 CLINICAL TRIALS).
No dosage adjustment is necessary for elderly patients or patients with renal impairment (see 10 CLINICAL PHARMACOLOGY). Atrial Fibrillation For patients with atrial fibrillation who have at least one risk factor for vascular events, who have a low risk of bleeding, and who are unsuitable for anticoagulation therapy, the recommended dose of AURO-CLOPIDOGREL is 75 mg once daily, administered in combination with ASA (75-100 mg daily) (see 14 CLINICAL TRIALS).
Pharmacogenetics CYP2C19 poor metaboliser status is associated with diminished antiplatelet response to AURO-CLOPIDOGREL Product Monograph Page No: 6 of 59 clopidogrel. Although a higher dose regimen in poor metaboliser healthy subjects increases antiplatelet response, an appropriate dose regimen for this patient population has not been established in clinical outcome trials (see 10 CLINICAL PHARMACOLOGY).
4 Administration For oral use. 5 Missed Dose If a dose of AURO-CLOPIDOGREL is missed, it should be taken as soon as possible. However, if it is close to the time of the next dose, disregard the missed dose and return to the regular dosing schedule.
Do not double doses.
). Patients should be told that it may take longer than usual to stop bleeding when they take AURO- CLOPIDOGREL alone or in combination with ASA, and that they should re port any unusual bleeding (site or duration) to their physician.
Patients should inform physicians and dentists that they are taking AURO-CLOPIDOGREL before any surgery is scheduled and before any new drug is taken. In patients with recent TIA or stroke and who are at high risk of recurrent ischemic events, the combination of ASA and clopidogrel has not been shown to be more effective than clopidogrel alone, but the combination has been shown to increase major bleeding (see
2 Geriatrics 05/2021 TABLE OF CONTENTS Sections or subsections that are not applicable at the time of authorization are not listed. RECENT MAJOR LA BEL CHANGES ............................................................................................
2 TABLE OF CONTENTS .............................................................................................................. 2 PART I: HEALTH PROFESSIONAL INFO RMATION ......................................................................
4 1 INDICATIONS ....................................................................................................................... 1 Pedi atri cs ..............................................................................................................
2 Geri atri cs ............................................................................................................... 4 2 CONTRAINDICATIONS..........................................................................................................
4 4 DOSAGE AND ADMINISTRATION.......................................................................................... 2 Re commended Dose and Dosage Adjustme nt......................................................... 4 Admi ni strati on ......................................................................................................
5 Mi ssed Dose ........................................................................................................... 5 5 OVERDOSAGE ......................................................................................................................
5 6 DOSAGE FORMS, ST RENGT HS, COMPOSITION AND PACKAGING .......................................... 6 7 WARNINGS AND PRECAUTIONS........................................................................................... 1 Speci al Popul ations................................................................................................
AURO-CLOPIDOGREL (clopidogrel bisulfate) is contraindicated in: Patients who are hypersensitive to this drug or to any ingredient in the formulation, including any non-medicinal ingredient, or component of the container. For a complete listing, see the 6 DOSAGE FORMS, STRENGTHS, COMPOSITION AND PACKAGING section of the product monograph.
Patients with active bleeding such as peptic ulcer and intracranial hemorrhage (ICH). Patients with significant liver impairment or cholestatic jaundice. Patients who are using repaglinide (see 9 DRUG INTERACTIONS).
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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1 Pregnant Wome n................................................................................................ 2 Bre ast-fee di ng.....................................................................................................
3 Pe di atrics……………….. ......................................................................................... 10 8 ADVERS E REACTIONS .........................................................................................................
1 Adve rse Re acti on Ove rvi ew .................................................................................. 2 Cl i ni cal Tri al Adve rse Re acti ons .............................................................................
5 Post-Market Adverse Re acti ons ............................................................................. 17 9 DRUG INTE RACTIONS .........................................................................................................
1 Se ri ous Drug Interacti ons ..................................................................................... 2 Drug Inte racti ons Ove rview .................................................................................. 4 Drug-Drug Interacti ons .........................................................................................
5 Drug-Food Interacti ons ........................................................................................ 6 Drug-He rb Interacti ons ......................................................................................... 7 Drug-Laboratory Test Inte racti ons .........................................................................
26 10 CLINICAL PHA RMACOLOGY .............................................................................................. 1 Mechani sm of Acti on ...........................................................................................
2 Pharmacodynami cs ............................................................................................ 3 Pharmacoki ne ti cs .............................................................................................. 28 11 STORAGE, STABILITY AND DISPOSAL ................................................................................
31 12 SPECIAL HANDLING INSTRUCTIONS .................................................................................. 31 PART II: SCIENTIFIC INFORMATION .......................................................................................
32 13 PHARMACEUTICAL INFO RMATION ................................................................................... 32 14 CLINICAL TRIALS ...............................................................................................................
1 Cl i ni cal Tri al s by Indi cati on ................................................................................. 3 Comparati ve Bi oavail abili ty Studie s ....................................................................
50 15 MICROBIOLOGY ............................................................................................................... 50 16 NON-CLINICAL TOXICOLOGY ............................................................................................
50 17 SUPPORTING PRODUCT MONOGRAPHS ........................................................................... 51 PATIENT MEDICATION INFO RMATION .................................................................................. 52 AURO-CLOPIDOGREL Product Monograph Page No: 4 of 59 PART I: HEALTH PROFESSIONAL INFORMATION 1 INDICATIONS AURO-CLOPIDOGREL (clopidogrel bisulfate) is indicated: for the secondary prevention of atherothrombotic events (myocardial infarction, stroke and vascular death) in patients with atherosclerosis documented by stroke, […]