Ways and Means Committee, Energy and Commerce Committee
Introduced
In Committee
On Floor
Passed Chamber
Enacted
The Alternatives to PAIN Act seeks to enhance access to qualifying non-opioid pain management drugs under the Medicare Part D program. For plan years beginning on or after January 1, 2026, the bill mandates that the deductible will not apply to these specific drugs, and they must be placed on the lowest cost-sharing tier available. Furthermore, the legislation prohibits prescription drug plans and MA-PD plans from imposing certain utilization management requirements. Specifically, plans cannot require step therapy where an opioid must be used first, nor can they require prior authorization for these non-opioid pain management drugs. A qualifying non-opioid pain management drug is defined as an FDA-approved drug or biological product for acute pain that does not act on opioid receptors, lacks a therapeutically equivalent generic, and meets certain wholesale acquisition cost criteria.
Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.
Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.
Drug therapyHealth care costs and insuranceMedicarePrescription drugs
Alternatives to PAIN Act
USA119th CongressHR-1227| House
| Updated: 2/12/2025
The Alternatives to PAIN Act seeks to enhance access to qualifying non-opioid pain management drugs under the Medicare Part D program. For plan years beginning on or after January 1, 2026, the bill mandates that the deductible will not apply to these specific drugs, and they must be placed on the lowest cost-sharing tier available. Furthermore, the legislation prohibits prescription drug plans and MA-PD plans from imposing certain utilization management requirements. Specifically, plans cannot require step therapy where an opioid must be used first, nor can they require prior authorization for these non-opioid pain management drugs. A qualifying non-opioid pain management drug is defined as an FDA-approved drug or biological product for acute pain that does not act on opioid receptors, lacks a therapeutically equivalent generic, and meets certain wholesale acquisition cost criteria.
Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.
Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.