CardioSource WorldNews | Page 27

Despite this paradox, diabetes is most certainly a risk multiplier in atherosclerosis. Despite this paradox, diabetes is most certainly a risk multiplier in atherosclerosis. It increases the risk of developing atherosclerosis and the incidence of complications of atherosclerosis, and is associated with poorer outcomes from these events. They noted that health care professionals have the benefit of a wide variety of clinical trial data supporting specific treatments and targets for HELPING PATIENTS START AND STAY ON THERAPY 12 months of FREE§ Effient therapy with the $avings Card for commercially insured patients – This offer is invalid for cash-paying patients and those whose prescription claims are eligible to be reimbursed, in whole or in part, by any governmental program § Out-of-pocket cost for patient is free. Restrictions may apply. Learn more at EffientHCP.com Effient is indicated to reduce the rate of thrombotic cardiovascular (CV) events (including stent thrombosis) in patients with acute coronary syndrome (ACS) who are to be managed with percutaneous coronary intervention (PCI) as follows: [1] patients with unstable angina (UA) or non–ST-elevation myocardial infarction (NSTEMI); [2] patients with ST-elevation myocardial infarction (STEMI) when managed with primary or delayed PCI. The loading dose (LD) of Effient is 60 mg and the maintenance dose (MD) is 10 mg once daily. Effient is available in 5-mg and 10-mg tablets. IMPORTANT SAFETY INFORMATION WARNING: BLEEDING RISK Effient® (prasugrel) can cause significant, sometimes fatal, bleeding. Do not use Effient in patients with active pathological bleeding or a history of transient ischemic attack or stroke. In patients ≥75 years of age, Effient is generally not recommended, because of the increased risk of fatal and intracranial bleeding and uncertain benefit, except in high-risk situations (patients with diabetes or a history of prior myocardial infarction [MI]) where its effect appears to be greater and its use may be considered. Do not start Effient in patients likely to undergo urgent coronary artery bypass graft surgery (CABG). When possible, discontinue Effient at least 7 days prior to any surgery. Additional risk factors for bleeding include: body weight <60 kg propensity to bleed concomitant use of medications that increase the risk of bleeding (eg, warfarin, heparin, fibrinolytic therapy, chronic use of nonsteroidal anti-inflammatory drugs [NSAIDs]) Suspect bleeding in any patient who is hypotensive and has recently undergone coronary angiography, percutaneous coronary intervention (PCI), CABG, or other surgical procedures in the setting of Effient. If possible, manage bleeding without discontinuing Effient. Discontinuing Effient, particularly in the first few weeks after acute coronary syndrome, increases the risk of subsequent cardiovascular events. Please see Brief Summary of Prescribing Information, including Boxed Warning regarding bleeding risk, on subsequent pages. CONTRAINDICATIONS Effient is contraindicated in patients with active pathological bleeding, such as from a peptic ulcer or intracranial hemorrhage (ICH), or a history of transient ischemic attack (TIA) or stroke, and in patients with hypersensitivity to prasugrel or any component of the product WARNINGS AND PRECAUTIONS Patients who experience a stroke or TIA while on Effient generally should have therapy discontinued. Effient should also be discontinued for active bleeding and elective surgery Premature discontinuation of Effient increases risk of stent thrombosis, MI, and death Thrombotic thrombocytopenic purpura (TTP), a rare but serious condition that can be fatal, has been reported with Effient, sometimes after a brief exposure (<2 weeks), and requires urgent treatment, including plasmapheresis Hypersensitivity, including angioedema, has been reported in patients receiving Effient, including patients with a history of hypersensitivity reaction to other thienopyridines ADVERSE REACTIONS Bleeding, including life-threatening and fatal bleeding, is the most commonly reported adverse reaction Represents commercial plans: HMO, PBM, POS, PPO, Employer, Insurer, and Health Insurance Exchange (HIX) formulary data. ‡ Represents MA-PD and PDP formulary data. Underlying enrollment values developed by Managed Markets Insight & Technology (MMIT), LLC as of June 2015 using a combination of third-party and public sources as well as a proprietary allocation methodology. The values may not be representative of an individual physician’s patient population. † Effient and the Effient logo are registered trademarks of Eli Lilly and Company. ©Daiichi Sankyo, Inc. and Lilly USA, LLC 12/2015. All Rights Reserv