Summary: High prices of brand name drugs block patient access. Far too many patients across the country struggle to afford their medications. A 2021 survey found that nearly 40 percent of patients did not take their drugs as prescribed due to high costs, and 20 percent of patients took on debt to pay for their medications. It’s estimated that more than 5 million Medicare beneficiaries had trouble affording their medications in 2019, with rates highest among Black and Latino seniors. If current trends continue, 1.1 million beneficiaries could die this decade because they can’t afford the drugs they need.
The Inflation Reduction Act will increase access to prescription drugs by lowering drug prices and out-of-pocket costs for millions of Americans. The $2,000 out-of-pocket cap that takes effect in 2025 is estimated to help more than 1 million enrollees each year and many millions over time, making prescriptions more affordable and accessible. The $35 insulin copay cap that takes effect in 2023 is expected to help 2.7 million Medicare beneficiaries afford the insulin they need to survive. And thanks to the Medicare negotiation and inflationary rebate provisions, patients will be paying their cost-sharing based on lower prices without the risk of outrageous price increases each year. More affordable and consistent medication costs will lead to more access, not less.
Patient Perspectives: Katherine Pepper, a Washington patient who lives with an autoimmune disease, takes Humira, a medication that has a monthly price of $6,409. As Congress was considering the Inflation Reduction Act, Katherine wrote, “As a senior living on a fixed income, I’ve had to choose between filling my Humira prescription or buying groceries. That’s a decision no one should have to make.”
Therese Humphrey Ball, an Indiana patient living with multiple sclerosis, shared about a time when she couldn’t access her medication at all because of its price. “In 2017, I was forced to go off of Copaxone entirely because I simply could not pay its $6,000 monthly cost,” she writes. “Without the medication I needed, I began having difficulty with my cognitive function. I work really hard to keep my life in order and my memory intact even with MS, so this was devastating. I lost something that is so valuable to me.”
Vanessa Ladson, a Delaware patient living with lupus and fibromyalgia, wrote, “I am on a fixed income, and I have to scrimp and save just to be able to eat. I can’t afford all of my prescriptions, including the blood thinner Eliquis, which is priced at $500 per month. Instead, I take a cheaper drug that gives me a higher risk of bleeding.”