Baker WL, White CM (2009). “Role of prasugrel, a novel P2Y(12) receptor antagonist, in the management of acute coronary syndromes”. 《American Journal of Cardiovascular Drugs》 9 (4): 213–229. doi:10.2165/1131209-000000000-00000. PMID19655817. S2CID37160513.
Chew DP, Scott IA, Cullen L, French JK, Briffa TG, Tideman PA 외 (August 2016). “National Heart Foundation of Australia and Cardiac Society of Australia and New Zealand: Australian clinical guidelines for the management of acute coronary syndromes 2016”. 《The Medical Journal of Australia》 205 (3): 128–133. doi:10.5694/mja16.00368. PMID27465769. S2CID13014429.
Montalescot G, Bolognese L, Dudek D, Goldstein P, Hamm C, Tanguay JF 외 (September 2013). “Pretreatment with prasugrel in non-ST-segment elevation acute coronary syndromes”. 《The New England Journal of Medicine》 369 (11): 999–1010. doi:10.1056/NEJMoa1308075. PMID23991622. S2CID205095981.
John J, Koshy SK (2012). “Current oral antiplatelets: focus update on prasugrel”. 《Journal of the American Board of Family Medicine》 25 (3): 343–349. doi:10.3122/jabfm.2012.03.100270. PMID22570398.
O'Donoghue ML, Braunwald E, Antman EM, Murphy SA, Bates ER, Rozenman Y 외 (September 2009). “Pharmacodynamic effect and clinical efficacy of clopidogrel and prasugrel with or without a proton-pump inhibitor: an analysis of two randomised trials”. 《Lancet》 374 (9694): 989–997. doi:10.1016/S0140-6736(09)61525-7. PMID19726078. S2CID205956050.
Rehmel JL, Eckstein JA, Farid NA, Heim JB, Kasper SC, Kurihara A 외 (April 2006). “Interactions of two major metabolites of prasugrel, a thienopyridine antiplatelet agent, with the cytochromes P450”. 《Drug Metabolism and Disposition》 34 (4): 600–607. doi:10.1124/dmd.105.007989. PMID16415119. S2CID1698598.
Kurokawa T, Fukami T, Yoshida T, Nakajima M (March 2016). “Arylacetamide Deacetylase is Responsible for Activation of Prasugrel in Human and Dog”. 《Drug Metabolism and Disposition》 44 (3): 409–416. doi:10.1124/dmd.115.068221. PMID26718653.
Brandt JT, Payne CD, Wiviott SD, Weerakkody G, Farid NA, Small DS 외 (January 2007). “A comparison of prasugrel and clopidogrel loading doses on platelet function: magnitude of platelet inhibition is related to active metabolite formation”. 《American Heart Journal》 153 (1): 66.e9–66.16. doi:10.1016/j.ahj.2006.10.010. PMID17174640.
Wiviott SD, Trenk D, Frelinger AL, O'Donoghue M, Neumann FJ, Michelson AD 외 (December 2007). “Prasugrel compared with high loading- and maintenance-dose clopidogrel in patients with planned percutaneous coronary intervention: the Prasugrel in Comparison to Clopidogrel for Inhibition of Platelet Activation and Aggregation-Thrombolysis in Myocardial Infarction 44 trial”. 《Circulation》 116 (25): 2923–2932. doi:10.1161/CIRCULATIONAHA.107.740324. PMID18056526. S2CID8226182.
Baker WL, White CM (2009). “Role of prasugrel, a novel P2Y(12) receptor antagonist, in the management of acute coronary syndromes”. 《American Journal of Cardiovascular Drugs》 9 (4): 213–229. doi:10.2165/1131209-000000000-00000. PMID19655817. S2CID37160513.
Chew DP, Scott IA, Cullen L, French JK, Briffa TG, Tideman PA 외 (August 2016). “National Heart Foundation of Australia and Cardiac Society of Australia and New Zealand: Australian clinical guidelines for the management of acute coronary syndromes 2016”. 《The Medical Journal of Australia》 205 (3): 128–133. doi:10.5694/mja16.00368. PMID27465769. S2CID13014429.
Montalescot G, Bolognese L, Dudek D, Goldstein P, Hamm C, Tanguay JF 외 (September 2013). “Pretreatment with prasugrel in non-ST-segment elevation acute coronary syndromes”. 《The New England Journal of Medicine》 369 (11): 999–1010. doi:10.1056/NEJMoa1308075. PMID23991622. S2CID205095981.
John J, Koshy SK (2012). “Current oral antiplatelets: focus update on prasugrel”. 《Journal of the American Board of Family Medicine》 25 (3): 343–349. doi:10.3122/jabfm.2012.03.100270. PMID22570398.
O'Donoghue ML, Braunwald E, Antman EM, Murphy SA, Bates ER, Rozenman Y 외 (September 2009). “Pharmacodynamic effect and clinical efficacy of clopidogrel and prasugrel with or without a proton-pump inhibitor: an analysis of two randomised trials”. 《Lancet》 374 (9694): 989–997. doi:10.1016/S0140-6736(09)61525-7. PMID19726078. S2CID205956050.
Rehmel JL, Eckstein JA, Farid NA, Heim JB, Kasper SC, Kurihara A 외 (April 2006). “Interactions of two major metabolites of prasugrel, a thienopyridine antiplatelet agent, with the cytochromes P450”. 《Drug Metabolism and Disposition》 34 (4): 600–607. doi:10.1124/dmd.105.007989. PMID16415119. S2CID1698598.
Kurokawa T, Fukami T, Yoshida T, Nakajima M (March 2016). “Arylacetamide Deacetylase is Responsible for Activation of Prasugrel in Human and Dog”. 《Drug Metabolism and Disposition》 44 (3): 409–416. doi:10.1124/dmd.115.068221. PMID26718653.
Brandt JT, Payne CD, Wiviott SD, Weerakkody G, Farid NA, Small DS 외 (January 2007). “A comparison of prasugrel and clopidogrel loading doses on platelet function: magnitude of platelet inhibition is related to active metabolite formation”. 《American Heart Journal》 153 (1): 66.e9–66.16. doi:10.1016/j.ahj.2006.10.010. PMID17174640.
Wiviott SD, Trenk D, Frelinger AL, O'Donoghue M, Neumann FJ, Michelson AD 외 (December 2007). “Prasugrel compared with high loading- and maintenance-dose clopidogrel in patients with planned percutaneous coronary intervention: the Prasugrel in Comparison to Clopidogrel for Inhibition of Platelet Activation and Aggregation-Thrombolysis in Myocardial Infarction 44 trial”. 《Circulation》 116 (25): 2923–2932. doi:10.1161/CIRCULATIONAHA.107.740324. PMID18056526. S2CID8226182.
Baker WL, White CM (2009). “Role of prasugrel, a novel P2Y(12) receptor antagonist, in the management of acute coronary syndromes”. 《American Journal of Cardiovascular Drugs》 9 (4): 213–229. doi:10.2165/1131209-000000000-00000. PMID19655817. S2CID37160513.
Chew DP, Scott IA, Cullen L, French JK, Briffa TG, Tideman PA 외 (August 2016). “National Heart Foundation of Australia and Cardiac Society of Australia and New Zealand: Australian clinical guidelines for the management of acute coronary syndromes 2016”. 《The Medical Journal of Australia》 205 (3): 128–133. doi:10.5694/mja16.00368. PMID27465769. S2CID13014429.
Montalescot G, Bolognese L, Dudek D, Goldstein P, Hamm C, Tanguay JF 외 (September 2013). “Pretreatment with prasugrel in non-ST-segment elevation acute coronary syndromes”. 《The New England Journal of Medicine》 369 (11): 999–1010. doi:10.1056/NEJMoa1308075. PMID23991622. S2CID205095981.
O'Donoghue ML, Braunwald E, Antman EM, Murphy SA, Bates ER, Rozenman Y 외 (September 2009). “Pharmacodynamic effect and clinical efficacy of clopidogrel and prasugrel with or without a proton-pump inhibitor: an analysis of two randomised trials”. 《Lancet》 374 (9694): 989–997. doi:10.1016/S0140-6736(09)61525-7. PMID19726078. S2CID205956050.
Rehmel JL, Eckstein JA, Farid NA, Heim JB, Kasper SC, Kurihara A 외 (April 2006). “Interactions of two major metabolites of prasugrel, a thienopyridine antiplatelet agent, with the cytochromes P450”. 《Drug Metabolism and Disposition》 34 (4): 600–607. doi:10.1124/dmd.105.007989. PMID16415119. S2CID1698598.
Wiviott SD, Trenk D, Frelinger AL, O'Donoghue M, Neumann FJ, Michelson AD 외 (December 2007). “Prasugrel compared with high loading- and maintenance-dose clopidogrel in patients with planned percutaneous coronary intervention: the Prasugrel in Comparison to Clopidogrel for Inhibition of Platelet Activation and Aggregation-Thrombolysis in Myocardial Infarction 44 trial”. 《Circulation》 116 (25): 2923–2932. doi:10.1161/CIRCULATIONAHA.107.740324. PMID18056526. S2CID8226182.