Dem chair asks FDA for documents on powerful new opioid

Democratic lawmakers are requesting documents from the Food and Drug Administration as they probe the agency’s controversial decision to approve a powerful new opioid.

Rep. Diana DeGetteDiana Louise DeGetteOvernight Energy: EPA to reconsider cost benefit analysis of air pollution rules | Interior gets new rules on free concert tickets | Dem challenges EPA for skipping hearing House Democrats press leaders to start Trump impeachment WHIP LIST: Democrats who support an impeachment inquiry against President Trump MORE (D-Colo.), the chairwoman of the Energy and Commerce oversight subcommittee, and Sen. Ed MarkeyEdward (Ed) John MarkeyHillicon Valley: Assange hit with 17 more charges | Facebook removes record 2.2B fake profiles | Senate passes anti-robocall bill | Senators offer bill to help companies remove Huawei equipment Senate passes anti-robocall bill The Hill's 12:30 Report: Pelosi fires back in feud with Trump MORE (D-Mass.) on Tuesday wrote to the FDA asking for documents that the agency relied on in approving the new opioid.

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The approval of the drug, called Dsuvia, in November, was controversial because advocates and some lawmakers had warned against approving a powerful new opioid amid the epidemic of opioid overdoses.

Dsuvia is 10 times more powerful than fentanyl and 1,000 times more powerful than morphine.

DeGette and Markey expressed concern the drug could be abused, saying it can “deliver a potency that has been known to be lethal in small dosages.”

In November when announcing the approval of the drug, FDA Commissioner Scott Gottlieb acknowledged its potential dangers but said it could be beneficial to the military.

He noted that the drug can be administered under the tongue, which could be helpful on the battlefield in situations where injecting a drug is difficult.  

“It fills a specific and important, but limited, unmet medical need in treating our nation’s soldiers on the battlefield,” Gottlieb said.