Hello. I'm Dr John Whyte, director of Professional Affairs and Stakeholder Engagement (PASE) at the US Food and Drug Administration (FDA) Center for Drug Evaluation and Research. You're watching this video commentary as part of the FDA's collaboration with Medscape. I'd like to talk to you about a serious safety concern regarding the co-prescribing and combining of benzodiazepines and opioids. The dangerous drug combination is leading to increased overdoses and deaths throughout the United States.
A recent FDA review found that the growing combined use of opioid medicines with benzodiazepines or other drugs that depress the central nervous system (CNS) has resulted in serious, sometimes fatal side effects, including slowed or difficult breathing and death. The FDA concluded that from 2004 to 2011, the rate of emergency department visits involving nonmedical use of both drug classes increased significantly, with overdose deaths nearly tripling during that period. In addition, the number of patients who were prescribed both an opioid analgesic and benzodiazepine increased by 41% between 2002 and 2014, which translates to an increase of more than 2.5 million patients taking opioid analgesics while also receiving benzodiazepines.
In an effort to decrease the combined use of opioids and benzodiazepines or opioids and other CNS depressants, the FDA is requiring that its strongest warning, a Boxed Warning, appear on the drug labeling for these drug classes and patient-focused Medication Guides for several related products: prescription opioid analgesics, opioid-containing cough products, and benzodiazepines. That's nearly 400 products in total.
We recommend that healthcare professionals limit prescribing opioid pain medicines with benzodiazepines or other CNS depressants only to patients for whom alternative treatment options are inadequate. If these medicines are prescribed together, limit the dosages and duration of each drug to the minimum possible while achieving the desired clinical effect. Talk to your patient about the risk for slowed or difficult breathing and sedation, and the associated signs and symptoms. Avoid prescribing prescription opioid cough medicines for patients taking benzodiazepines or other CNS depressants, including alcohol. As always, we recommend that you talk to your patients to limit their alcohol use and discuss the interactions when alcohol is combined with the medications they are taking.
We recommend that you reset the prescribing of these two classes together and thoroughly evaluate, on a patient-by-patient basis, whether the benefits of using opioids and benzodiazepines or CNS depressants together outweigh these serious risks. Clinical guidelines from the Centers for Disease Control and Prevention (CDC) and existing label warnings regarding combined use caution prescribers about co-prescribing opioids and benzodiazepines to avoid potential serious health outcomes. The actions of the FDA in updating the labels are consistent with the CDC. To help inform the public, the FDA issued a Drug Safety Communication, which is available on our website. Thank you.
Please listen to the new podcast from Dr. Janet Woodcock, Director of the FDA's Center for Drug Evaluation and Research, as she discusses the FDA's actions to implement the Opioid Action Plan. You can download the podcast here.