Source: United States Senator for West Virginia Shelley Moore Capito
WASHINGTON, D.C. – Last week, U.S. Senator Shelley Moore Capito (R-W.Va.) joined a bipartisan group of senators – led by U.S. Senator Martin Heinrich (D-N.M.) – in calling on the Drug Enforcement Administration (DEA) to take further action to remove barriers to buprenorphine, a lifesaving drug used to treat opioid use disorder.
Specifically, the senators are urging the DEA to initiate a multi-agency evaluation of buprenorphine with the Food and Drug Administration (FDA) and Substance Abuse and Mental Health Services Administration (SAMSHA) to eliminate access gaps to the prescription drug to reduce overdose and death from opioid use disorder.
“According to the Centers for Disease Control and Prevention (CDC), more than 106,000 Americans died from a drug overdose in the past year alone. Now more than ever, it is critical that the best treatments are made widely available and barriers to interventions are broken down,” the senators said.
The push from the senators comes as prescribers and patients across the country continue to report difficulty filling buprenorphine prescriptions, despite recent passage of the Mainstreaming Addiction Treatment (MAT) Act in the Consolidated Appropriations Act of 2023 that increased the number of medical professionals authorized to prescribe buprenorphine.
“We recognize that the Department of Justice (DOJ) and the DEA Diversion Control Division jointly published a Suspicious Orders Q&A on January 20, 2023, which explains that the agency does not place quantitative thresholds or limits on the amounts of controlled substances that a pharmacy can order. However, more is needed,” the senators continued. “Without formal guidance from the DEA, the absence of quantitative thresholds has created chilling effects on access to buprenorphine due to the perceived risks of crossing an undefined threshold by the DEA.”
The senators concluded, “The opioid epidemic remains one of the greatest public health crises our nation has ever faced. We must ensure the necessary resources and policies are in place so that every American who needs it can find treatment and lifesaving care.”
Senators Capito and Heinrich were joined in sending the letter by U.S. Senators Maggie Hassan (D-N.H.), Lisa Murkowski (R-Alaska), Sheldon Whitehouse (D-R.I.), Thom Tillis (R-N.C.), Elizabeth Warren (D-Mass.), Angus King (I-Maine), Chris Van Hollen (D-Md.), Tim Kaine (D-Va.), Ed Markey (D-Mass.), Ben Ray Luján (D-N.M.), Bob Menendez (D-N.J.), Amy Klobuchar (D-Minn.), Jeff Merkley (D-Ore.), Sherrod Brown (D-Ohio), and Cory Booker (D-N.J.).
The full text of the letter is available here or below:
Dear Administrator Milgram,
We write to request that the Drug Enforcement Administration (DEA) take further action to remove barriers to access buprenorphine. In December 2022, Congress directed the DEA to clarify the difference between suspicious orders of opioids and suspicious orders of buprenorphine in the Suspicious Orders Report System (SORS). We are concerned that the DEA has failed to develop and provide sufficiently clear guidance for pharmacists, wholesalers, distributors, and patients for accessing buprenorphine. We request that the DEA immediately initiate a multi-agency evaluation of buprenorphine with the Food and Drug Administration (FDA) and Substance Abuse and Mental Health Services Administration (SAMSHA) to eliminate access gaps to buprenorphine to reduce overdose and death from opioid use disorder.
The recent passage of the Mainstreaming Addiction Treatment (MAT) Act in the Consolidated Appropriations Act of 2023 has dramatically expanded our ability to treat opioid use disorder with buprenorphine. The Act increased the number of medical professionals who can prescribe buprenorphine for opioid use disorder from 130,000 to 1.8 million with the removal of the X waiver. However, prescribers and patients across the country continue to report difficulty filling buprenorphine prescriptions. A recent study of more than 5,000 pharmacies reported that less than half stocked buprenorphine, while another survey found that only one in five pharmacies were willing to fill buprenorphine prescriptions. An additional survey of addiction treatment providers found that 84% of their patients experienced a time delay in accessing their buprenorphine; a delay that can mean life or death for these patients.
According to the Centers for Disease Control and Prevention (CDC), more than 106,000 Americans died from a drug overdose in the past year alone. Now more than ever, it is critical that the best treatments are made widely available and barrier to interventions are broken down. The data clearly demonstrates that prescriptions of medications for opioid use disorders (MOUDs) significantly reduce the risk of overdose deaths – a recent study of individuals with opioid use disorder found they were 82% less likely to die from an opioid overdose when they received treatment with buprenorphine or methadone than when they did not. Despite the demonstrated effectiveness of MOUDs, approximately 87% of individuals with opioid use disorder, who may benefit from lifesaving MOUDs treatment, do not receive it.
A survey on pharmacy access published by the American Society of Addiction Medicine found the most-commonly cited reasons for not filling buprenorphine prescriptions included supplier shortages, the pharmacy’s wholesaler limiting the amount of the medication they may order, corporate policies restricting the dispensing of buprenorphine, and an assumption that the DEA has a cap on the quantity of buprenorphine that can be dispensed. A recent survey of pharmacists found that 31% of pharmacy respondents did not stock buprenorphine due to perceived ordering limits imposed by the DEA. We recognize that the Department of Justice (DOJ) and the DEA Diversion Control Division jointly published a Suspicious Orders Q&A on January 20, 2023, which explains that the agency does not place quantitative thresholds or limits on the amounts of controlled substances that a pharmacy can order. However, more is needed. Without formal guidance from the DEA, the absence of quantitative thresholds has created chilling effects on access to buprenorphine due to the perceived risks of crossing an undefined threshold by the DEA.
In report language included in the 2023 Consolidated Appropriations bill, Congress expressed its concern that the DEA’s lack of clarity is contributing to buprenorphine stocking issues. The report directs the DEA to “clarify the difference between suspicious orders of opioids and suspicious orders of buprenorphine, clarify the difference between suspicious orders and caps or quotas, clarify that the DEA has no quotas or caps on buprenorphine, and clarify how distributor-imposed quotas or caps on opioids or buprenorphine do or do not satisfy suspicious order regulations.” While the DEA has made public comments supporting increased buprenorphine prescribing, it is imperative that the DEA update its policies around suspicious orders and the dispensing of buprenorphine for opioid use disorder. This clarity and transparency is important for the public, pharmacies, manufacturers, and distributors, and also for the DEA field and office staff to ensure that policies are implemented equitably across all regions.
The opioid epidemic remains one of the greatest public health crises our nation has ever faced. We must ensure the necessary resources and policies are in place so that every American who needs it can find treatment and lifesaving care. Thank you for your prompt attention to this critical matter.
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