Latest News | Mar 29, 2021

The Week in Review in Prescription Drug Pricing

Get your vaccine now, a donut tomorrow, and a $175 booster next year?

Welcome to the Week in Review.

  1. A Lesson From COVID-19 Vaccines

2.  This Is The Moment

3. Coast To Coast

4. “Not The Life That I Want For My Son”

5. Drugs Don’t Work If People Can’t Afford Them

One more thing: This week, P4AD Founder David Mitchell pushed back against the idea that Big Pharma deserves all the credit for COVID-19 vaccines in a Wall Street Journal letter. He breaks down just how much publicly funded research and the government are to thank for the vaccines. 

AUGUSTA, Maine — Today, Patients For Affordable Drugs Now endorsed the Making Health Care Work for Maine package, a sweeping new package of bills aimed at taking on drug companies and lowering prescription drug prices for Mainers. The pieces of legislation were introduced by Maine Senate President Troy Jackson, along with Senate Majority Leader Eloise Vitelli, Senator Cathy Breen, and Senator Ned Claxton.

“We applaud Senators Jackson, Vitelli, Breen, and Claxton for this comprehensive drug price reform package,” said Sheila McLean, executive director of Patients For Affordable Drugs Now. “Patients For Affordable Drugs Now is proud to lend its endorsement of this legislation that would bring relief to Mainers suffering from the high price of prescription drugs.”

The package includes five pieces of legislation that would hold Big Pharma accountable by expanding pharmaceutical drug price transparency requirements, prohibiting unwarranted price hikes on both brand-name and generic prescription drugs, and providing support to the Maine prescription drug affordability board established by 2019’s LD 1499. The package would also provide relief to Mainers living with diabetes by creating emergency access to insulin at affordable prices.  

In Old Town, Maine, Sabrina Burbeck knows all too well the impact that high-priced insulin has on families. Her 8-year-old son, Dakota, lives with type 1 diabetes and relies on insulin to survive. Humalog, the type of insulin that Dakota is prescribed, is priced at $350 for a month’s supply. 

“No mother should have to worry if the life of her bright, loving, and curious child will be cut short because the price of their medication spikes overnight or they simply can’t afford it one month,” Burbeck explained at today’s press conference held by Senator Jackson. “The Making Health Care Work for Mainepackage is about reining in health care costs while providing immediate access to life-saving medication. It’s about making health care work for families like mine.”

The Making Health Care Work for Maine package includes the following legislation:  

  1. LD 675, led by Senator Ned Claxton, would clamp down on unsupported price increases by fining pharmaceutical manufacturers that increase drug prices without justification. 
  2. LD 1117, led by Senate President Troy Jackson, would prohibit price gouging on generic and off-patent drugs and give the state attorney general authority to bring penalties against drug companies that refuse to lower prices. 
  3. LD 673, led by Senator Cathy Breen, would create an insulin safety net program to provide emergency access to affordable insulin for Mainers needing immediate relief. 
  4. LD 686, led by Senate Majority Leader Eloise Vitelli, would strengthen prescription drug pricing transparency by requiring the Maine Health Data Organization to share information collected from drug companies with the public. 
  5. LD 120, led by Senate President Troy Jackson, would establish the Office of Affordable Health Care to help examine the factors contributing to rising prices. 

The legislature’s Health Coverage, Insurance and Financial Services Committee will hold public hearings on all five bills in the coming weeks. 

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SALEM, Ore. — Today, Oregon patient advocates Joanna Olson, Janet Bacon, and Mike Nielsen will testify in front of the Oregon Senate Health Care Committee in support of Senate Bill 844, which would establish a prescription drug affordability board and stakeholder council in an effort to rein in high drug prices for Oregonians. 

Joanna Olson of Beaverton, Oregon, suffers from a blood clotting condition and was prescribed Eliquis, which costs her $430 for a month’s supply. “Every time I pick up the prescription, I think about leaving without the drug,” Olson, 86, will explain. “A common medicine needed by millions like Eliquis shouldn’t break the bank for seniors like me, who live on a fixed income.”

In Happy Valley, Oregon, Janet Bacon’s inhaler Spiriva is priced at $478 a month. “If my drug prices continue to go up, I don’t know how I will get by — I worry about needing to sell my home and property to afford the medications I need,” Bacon, a retiree and a Medicare beneficiary, will say. “A prescription drug affordability board would hold Big Pharma accountable for its outrageous pricing practices and bring much needed relief to me and patients across our state. I urge you to vote in support of Senate Bill 844.”

SB 844 would establish a prescription drug affordability board and stakeholder council designed to review prices for prescription drugs that meet specified cost criteria. The board would:

Mike Nielsen’s wife, Jacki, was diagnosed with the potentially fatal disease hepatitis C. Her doctor prescribed her the curative drug Mavyret, which costs over $13,000 for a 90-day supply — or $433 per pill. That was unaffordable for the couple. “It’s wrong what the drug companies are allowed to get away with by playing the system and preventing more affordable generics from coming to market,” Mike Nielsen, a 69-year-old Vietnam veteran in Bend, Oregon, will tell the committee. “I am asking our legislators to fight for patients like us.”

The hearing and Olson, Bacon, and Nielsen’s testimonies can be watched hereat 1:00 PM PT. 

Senate Bill 844 is one of three bills taking on high drug prices. The Senate Health Care Committee also held a hearing on pharmaceutical reform Senate Bills 764 and 763, which are now moving through amendments for a final vote.

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Hello! I’m thrilled to be joining P4ADNow and all of you in the fight to lower drug prices. 

Welcome to the Week in Review.

  1. It’s Official: Secretary Becerra

2.  Winning The Battle In Minnesota

3. The Price Is Never Right

WASHINGTON, D.C. — The following statement was issued today by David Mitchell, a cancer patient and the founder of Patients For Affordable Drugs Now, on the confirmation of Xavier Becerra as Secretary of the U.S. Department of Health and Human Services: 

“Congratulations to HHS Secretary Xavier Becerra. President Biden made a great choice to lead HHS, and Becerra’s confirmation is a win for patients across the country who are struggling with high drug prices. We look forward to working together to restore balance to our system by ensuring patients get the innovation they need at prices they can afford. We know we can have both.”

BACKGROUND: 

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As The Fight To Lower Drug Prices Ramps Up, Audrey Baker Will Lead P4AD’s Communications Efforts

WASHINGTON, D.C. — The bipartisan advocacy organization Patients For Affordable Drugs, and its sister organization Patients For Affordable Drugs Now, today named Audrey Baker as its communications director. Audrey will take leadership of overall communications, including media relations. Audrey has worked in advocacy communications for over five years, most recently at the communications firm M+R, where she led media strategy for reproductive rights, criminal justice, housing, food advocacy, and humanitarian campaigns. 

“Audrey’s sharp communications skills, storytelling, and advocacy experience will be pivotal to our efforts to achieve meaningful drug pricing reform,” said Sheila McLean, executive director of Patients For Affordable Drugs and Patients For Affordable Drugs Now.

In addition to her communications and media relations experience, Audrey has worked as an organizer for local, state, and federal campaigns. 

“With Congress and the White House turning to drug pricing legislation, now is the time to ramp up our advocacy efforts to win the fight for affordable drugs,” McLean added. 

Patients For Affordable Drugs is a not-for-profit 501(c)(3) organization. It is the only independent national patient organization focused exclusively on policy changes to lower prescription drug prices. Patients For Affordable Drugs Now is a not-for-profit 501(c)(4) organization focused on advancing policies to lower drug prices. Both are independent and bipartisan and neither accepts funding from any organizations that profit from the development or distribution of prescription drugs.

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Hey Britain, pharma ads horrify us, too.
Welcome to the Week in Review.

  1. Cashing In On A Crisis

2.  Double Talk

3. Colorado Clamps Down

4. Greed, Not Need

5. Small Businesses Call For Lower Drug Prices

SAINT PAUL, Minn. — Eveleth patient Travis Paulson, who lives with type 1 diabetes, will testify in front of the Minnesota House State Government Finance and Elections Committee this afternoon in support of the bipartisan legislation HF 801, which would establish a prescription drug affordability board designed to address the high prices of prescription drugs for Minnesotans. 

Paulson was diagnosed with type 1 diabetes at age 14 and has struggled to keep up with the high price of insulin in recent years. His insulin, which he needs to survive, currently costs $300 a vial, which comes to $1,500 per month. Paulson has had to work odd jobs, living paycheck to paycheck in order to stay alive. 

“Unfortunately for me, years of rationing insulin has caused long-term complications that never would have occurred if I had access to affordable insulin,” Paulson will tell the committee. 

“These out-of-control drug prices have serious consequences for Minnesota patients and contribute to excessive costs for the state. We need our state government to pass House File 801, which would rein in drug prices while increasing transparency around the pricing practices of drug companies. Because drugs don’t work if people can’t afford them.”

HF 801 would:  

The hearing and Paulson’s testimony can be watched here at 6:00 PM CT. 

The bill was previously heard in the House Commerce Finance and Policy Committee, where patient advocate Ramae Hamrin testified in support of the bill. It passed out of committee on a 11 to 7 vote.

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