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That’s the assertion a Philadelphia-area pharmacist is making in a federal class action suit filed recently at the U.S. District Court for the Eastern District of Pennsylvania.

The factor Xa inhibitor edoxaban (Savaysa, Daiichi Sankyo) has been approved by FDA to lower the risk of stroke and systemic embolism in patients with nonvalvular atrial fibrillation (AF), according to a January 8 announcement.

Prosecutors seized $18 million from accounts linked to the owners of the defunct New England Compounding Center, whose tainted products led to the 2012 meningitis outbreak that killed at least 64 people and sickened about 750.

The U.S. Centers for Disease Control and Prevention and the American Pharmacists Association Foundation recently announced a partnership intended to integrate pharmacy into public health efforts to manage hypertension.

As her first major initiative, State Attorney General-Elect Maura Healey plans to create a taskforce to combat Massachusetts’ heroin and prescription drug crisis.

A pharmacy-led prior authorization service can generate additional hospital revenues through increased reimbursements and decreased write-offs, according to a case study to be published in the American Journal of Health-System Pharmacy.

According to the most recent update from the U.S. Centers for Disease Control and Prevention (CDC), 15 children in the United States have died thus far this flu season as influenza has reached epidemic levels.

The American Diabetes Association (ADA) is calling for all patients with diabetes who are at high risk for cardiovascular disease (CVD) to be treated with statins and lifestyle therapy, according to its recently published guidance in the January issue of Diabetes Care.

Agents from the Drug Enforcement Administration recently searched records at a Virginia hospital pharmacy in connection with stolen narcotics with an estimated street value close to $1.4 million.

David Webster, associate director of pharmacy operations, University of Rochester Medical Center (URMC), explains URMC’s decision to transition to in-sourced IV compounding.

The committee is comprised of 14 members-12 voting and two non-voting-who will provide advice on scientific, technical, and medical issues concerning drug compounding under sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act.