News Release: Research
Dec. 1, 2010
Inconsistent Dosing Directions and Measuring Devices Found in Over-the-Counter Liquid Children's Medicines
A year-long study of 200 top-selling oral liquid over-the-counter medications for children found that most contained variable and inconsistent dosing directions and measuring devices. Nearly all the products had directions that did not match what was marked on the measuring device.
Results of the study are published online and will appear in the December 15 issue of JAMA.
A standardized measuring device was included with 148 of the products examined. Confusing information in these products included inconsistencies between dosing directions and markings on the measuring device (98.6 percent); missing markings on measuring devices (24.3 percent); superfluous markings (81.1 percent); atypical units of measurement (5.5 percent); nonstandard abbreviations; and lack of definitions for abbreviations. One-fourth of the products did not contain a dosing device at all, which means parents could have trouble selecting the right amount of medicine.
The study was conducted for the 52 weeks ending October 30, 2009, and included 99 percent of the U.S. market of analgesic, cough/cold, allergy and gastrointestinal OTC oral liquid products with dosing information for children younger than 12.
In November 2009, in response to reports of unintentional drug overdoses among children given over-the-counter medicines, the U.S. Food and Drug Administration (FDA) released new voluntary industry guidelines that recommended greater consistency and clarity in dosing directions for OTC medications and their measuring devices.
“This is an issue of patient safety and needs urgent attention,” says Ruth Parker, MD, professor of medicine at Emory University School of Medicine, who co-led the study. “Given how many products are affected, it seems unlikely that the voluntary guidelines alone set by the FDA and industry will fix this problem. The current guidance does not contain a timeline for compliance or specify consequences for non-compliance. Standards and regulatory oversight will likely be needed to ensure that all products contain label information and dosing device markings that match and are understandable and useful. This is an issue of patient safety."
The FDA voluntary guidelines recommended that all OTC liquid medications include a measuring device, the product’s device and directions should use the same abbreviations and units of measurement, devices should have only necessary markings and should not hold much more than the largest dose described, abbreviations should be standard and defined and decimals or fractions should be used carefully. They also recommended more research to confirm accurate use of this information by consumers.
Researchers included senior author Ruth M. Parker, MD, professor of medicine, Emory University School of Medicine and lead author H. Shonna Yin, MD, MD, New York University School of Medicine. Other authors were Michael S. Wolf, PhD, MPH, Feinberg School of Medicine, Northwestern University, Benard P. Dreyer, MD, NYU School of Medicine, and Lee M. Sanders, MD, MPH, Miller School of Medicine, University of Miami.
A related JAMA editorial by Darren A. DeWalt, MD, MPH, of the University of North Caroline at Chapel is entitled “Ensuring Safe and Effective Use of Medication and Health Care.”
On December 1 the Institute of Medicine will release a related document, proceedings from “The Safe Use Initiative and Health Literacy: A Workshop,” held April 27, 2010, in Washington, DC.