Clopidogrel: Difference between revisions

(added adult dosing/indications)
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==Adult Dosing==
==Adult Dosing==
'''acute coronary syndrome''':
===[[Acute coronary syndrome]]===
*Unstable Angina, NSTEMI: Start 300 mg PO x 1, then 75 mg PO qd
*[[Unstable angina]], [[NSTEMI]]: Start 300 mg PO x 1, then 75 mg PO qd
*[[STEMI]]: 75 mg/day PO (in combination with [[aspirin]] 162-325 mg/day  
*[[STEMI]]: 75 mg/day PO (in combination with [[aspirin]] 162-325 mg/day  
*Recent MI, [[Stroke]], or [[Peripheral Arterial Disease]]: 75 mg PO qd
*Recent MI, [[Stroke]], or [[Peripheral Arterial Disease]]: 75 mg PO qd


'''thrombotic event prevention''': 75 mg PO qd
===Thrombotic event prevention===
*75 mg PO qd


==Pediatric Dosing==
==Pediatric Dosing==
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*bleeding, severe,
*bleeding, severe,
*hemorrhage
*hemorrhage
*TTP
*[[TTP]]
*agranulocytosis
*agranulocytosis
*hypersensitivity rxn
*hypersensitivity reaction
*anaphylactoid rxn
*anaphylactoid reaction
*Stevens-Johnson syndrome
*[[Stevens-Johnson syndrome]]
*toxic epidermal necrolysis
*[[toxic epidermal necrolysis]]
*erythema multiforme
*[[erythema multiforme]]
*drug rash w/ eosinophilia and systemic sx
*drug rash with eosinophilia and systemic sx
*pneumonia, eosinophilic
*Eosinophilic pneumonia


===Common===
===Common===

Revision as of 13:13, 4 August 2015

General

  • Type: Antiplatelet
  • Dosage Forms: 75, 300 PO
  • Common Trade Names: Plavix

Adult Dosing

Acute coronary syndrome

Thrombotic event prevention

  • 75 mg PO qd

Pediatric Dosing

  • Not Recommended

Special Populations

  • Pregnancy Rating: B
  • Lactation: Safety Unknown
  • Renal Dosing
    • Adult: not defined
    • Pediatric
  • Hepatic Dosing
    • Adult: no adjustment
    • Pediatric

Contraindications

  • Allergy to class/drug
  • active bleeding
  • caution if trauma
  • caution if elective surgery w/in 5 days
  • caution if GI disorder
  • caution if ocular dz
  • caution if poor or intermediate CYP2C19 metabolizer
  • caution if renal impairment, mod-severe

Adverse Reactions

Serious

Common

  • bleeding
  • pruritus

Pharmacology

  • Half-life: 8h
  • Metabolism: liver, CYP450: 1A2, 2C9, 2C19 (primary), 3A4 substrate
  • Excretion: urine 50%, feces 46%
  • Mechanism of Action: irreversibly binds to P2Y12 adenosine diphosphate receptors, reducing platelet activation and aggregation

See Also

Sources