Relatives of Painkiller Overdose Patients Speak at FDA Hearing
Relatives of patients who overdosed on painkillers told
federal regulators Thursday they want changes on the labels of narcotic
painkillers, The Wall Street Journal reports. Pain patients concerned such action could limit their access to the medications spoke against the proposed changes.
They spoke at a Food and Drug Administration (FDA) hearing on the use of opioids
in the treatment of chronic pain. The FDA said it wants to gather
scientific evidence on issues including diagnosis and understanding of
patient pain, understanding and adhering to the labels of pain-treating
products, limiting opioid prescriptions and use, and abuse and misuse of
opioid medicines.
The FDA is considering a petition by Physicians for Responsible
Opioid Prescribing, a group of doctors and pain specialists, to include a
recommended upper daily dose on the medications’ label, and to limit
opioid treatment to 90 days, the article notes. The doctors’ group is
also recommending that opioids be indicated for severe pain, not
moderate pain, except in cancer patients.
Last month, a FDA advisory panel voted to strengthen restrictions
on hydrocodone combination drugs, such as Vicodin. The panel
recommended the FDA make the drugs more difficult to prescribe. If the
FDA accepts the panel’s recommendation, it will be sent to the
Department of Health and Human Services, which will make the final
decision.
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