Biologics

Non-Medical Switching May Increase Health Care Costs, New Study Finds

August 10, 2017

Opting for cheaper prescription drugs seems like an obvious way to cut health care costs.  The assumption has led health plans to employ utilization management techniques with increasing frequency in recent years.  And it’s given rise to a newer phenomenon known as “non-medical switching,” where health plans exclude a drug from coverage or increase patients’ out-of-pocket burden in hopes of persuading patients to take a less expensive drug.

Fast Facts: Co-Pay Coupons

August 1, 2017

People are living longer, healthier lives today with the help of advanced medicine. But innovative drugs can be expensive. Insurance…

Drug Safety Data Underscores Need for Pharmacovigilance

May 16, 2017

One in every three new drugs triggers side effects discovered only after Food and Drug Administration approval, new data reveals.  And that statistic begs a crucial question: How can we really ensure patients’ safety in an age of sophisticated medications and accelerated approval processes?

Access Issues Loom Large at Munich Workshop on Biologics and Biosimilars

May 10, 2017

When should patients switch from one medicine to another for non-medical reasons?  How can pharmacovigilance processes successfully monitor patients’ reactions to a medicine? And, perhaps most importantly, how do we ensure that patients are informed participants in decisions about their medication?

Summit on Biologics and Biosimilars Tackles Choice, Switching & Patient Access

April 10, 2017

Physicians and patients are no longer asking if a biological medicine is the best choice, but – more likely – which biological medicine is the best choice.  This opening thought from Alliance for Patient Access Chairman David Charles, MD, set the tone for the organization’s second annual National Policy and Advocacy Summit on Biologics and Biosimilars, held Thursday in Washington, DC.