

Advocates: Probe Medicare impact on drug compounding
A consumer advocacy group is wondering if Medicare policy contributed to the rise of large-scale drug compounding, the practice behind the current national outbreak of meningitis.
Public Citizen, a left-leaning group, urged Health and Human Services (HHS) Secretary Kathleen Sebelius to review Medicare drug reimbursement policies in light of the outbreak, which has killed at least 33 people.
The Medicare agency "appears to have created inadvertent financial incentives for inappropriate use of compounded drugs," the group wrote to Sebelius.
In its letter, the group criticized the Centers for Medicare and Medicaid Services (CMS) for not using its authority to discourage wide-scale drug compounding conducted outside of parameters set by the Food and Drug Administration (FDA).
Public Citizen also slammed CMS guidance on compounded drugs as "ambiguous and conflicting."
Drug compounders customize medications for patients with special needs. Most operate on a small scale, but some firms have taken advantage of regulatory ambiguity to mass produce drugs that do not meet FDA safety standards.
So far, lawmakers have focused on the FDA's role in overseeing compounders and whether the agency could have used its current powers to prevent the outbreak. Discussion of Medicare policy as it relates to compounding has been limited.
In its letter to Sebelius, Public Citizen said that federal officials should be taken to task for the meningitis scare.
"This investigation must identify all CMS officials whose actions and decisions contributed to the agency's failure to prevent this public health catastrophe," the group wrote. "Ultimately, the senior leadership within the agency must be held accountable."
Public Citizen distributed the letter to a wide range of congressional leaders now probing the outbreak.
The compounder behind the deaths, the New England Compounding Center, is the firm behind the deaths. It shuttered this fall and faces several federal investigations.








