Last week, Senator Claire McCaskill, D-Missouri, together with the minority staff of the Senate Homeland Security and Government Affairs Committee (HSGAC), released a report on prescription drug price increases that affect the 20 products most commonly prescribed to seniors.
Last week, Senator Claire McCaskill, D-Missouri, together with the minority staff of the Senate Homeland Security and Government Affairs Committee (HSGAC), released a report on prescription drug price increases that affect the 20 products most commonly prescribed to seniors.
According to the report, which used data from CMS and the IQVIA National Sales Perspectives information service, prices increased over the last 5 years for all 20 drugs in question, which include the diabetes medications insulin glargine (Lantus) and insulin aspart (NovoLog).
On average, prices for these drugs increased by 12% every year for the past 5 years, a rate that is approximately 10 times higher than the average annual rate of inflation. The percent change in price between 2012 and 2017 ranged from a low of 31% (for the shingles vaccine Zostavax) to a high of 477% (for the brand-name nitroglycerin, Nitrostat).
According to the report, these continual increases in price are keeping healthcare costs high despite reduced use of many of these drugs; while prescriptions rose for treatments including the blood-thinner rivaroxaban (Xarelto) and the dry-eye drug cyclosporine (Restasis), many of the 20 most-prescribed drugs saw sharp declines in prescribing from 2012 to 2017; prescriptions for rosuvastatin (Crestor) dropped by 94%, and nitroglycerine by 93%, for example.
“These findings underscore the need for further investigation by the Committee and other policymakers into dramatic price spikes and their impact on healthcare system costs and financial burdens for the growing US senior population,” conclude the authors.
In a statement, McCaskill added, “Can you imagine if you went to an auto dealership and last year’s exact model was being sold at a [20%] mark-up, and then you went back the next year and it had happened again? That’s exactly what’s happening in the prescription drug industry, where the cost of identical drugs skyrockets year after year.”
Juliet Johnson, a representative of the Pharmaceutical Research and Manufacturers of America (PhRMA) told CNN that the document is “yet another misleading report that ignores the robust negotiation that occurs between Medicare Part D plans, middlemen and biopharmaceutical companies.” Johnson added that PhRMA agrees that “…more can be done to make Part D more affordable and predictable for seniors. One way to do that is to ensure seniors benefit from the significant negotiated savings when they pick up their medicine at the pharmacy.”
Senators Introduce Bipartisan Legislation to Protect Skinny Labeling
January 2nd 2025To close out the year, 4 senators came together to introduce a new bipartisan bill to protect biosimilar and generic drug manufacturers from patent litigation when obtaining “skinny label” approvals for their products.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
How Vertical Integration Drives Innovation and Access in Biosimilars
December 27th 2024Elie Bahou, PharmD, highlights how vertical integration in the biosimilar industry streamlines costs, improves supply reliability, accelerates market adoption, and enhances patient access, while emphasizing the value of collaboration, quality control, and value-based contracts for sustainable health care delivery.
13 Strategies to Avoid the Nocebo Effect During Biosimilar Switching
December 18th 2024A systematic review identified 13 strategies, including patient and provider education, empathetic communication, and shared decision-making, to mitigate the nocebo effect in biosimilar switching, emphasizing the need for a multifaceted approach to improve patient perceptions and therapeutic outcomes.
BioRationality: Withdrawal of Proposed Terminal Disclaimer Rule Spells Major Setback for Biosimilars
December 10th 2024The United States Patent and Trademark Office (USPTO)’s withdrawal of its proposed terminal disclaimer rule is seen as a setback for biosimilar developers, as it preserves patent prosecution practices that favor originator companies and increases costs for biosimilar competition, according to Sarfaraz K. Niazi, PhD.