FDA drops plan for drug watch list.FDA FDA abbr. Food and Drug Administration FDA, n.pr See Food and Drug Administration. FDA, n.pr the abbreviation for the Food and Drug Administration. announced March 2 it has dropped plans to keep a public list of prescription drugs prescription drug Prescription medication Pharmacology An FDA-approved drug which must, by federal law or regulation, be dispensed only pursuant to a prescription–eg, finished dose form and active ingredients subject to the provisos of the Federal Food, Drug, with emerging safety concerns, one of the measures proposed after Merck's 2004 withdrawal of its arthritis drug Vioxx, Reuters reported. Instead of a "Drug Watch" list, FDA will place red asterisks next to the names of the medicines on an existing Web page that lists dozens of prescription drugs. Consumers can click on the drug name to link to FDA advisories and other information. FDA made the change because there was concern about potential confusion between "Drug Watch" and "MedWatch," an FDA program that provides alerts about new information on medical products. Sidney Wolfe, M.D., director of Public Citizen Health Research Group, said it sounded like the information would be hard for consumers and doctors to find, noting that they would need to scroll To continuously move forward, backward or sideways through the text and images on screen or within a window. Scrolling implies continuous and smooth movement, a line, character or pixel at a time, as if the data were on a paper scroll being rolled behind the screen. See auto scroll. through a long list. Drug makers are pleased FDA abandoned Drug Watch and is embracing a more balanced approach, said Alan Goldhammer, associate vice president for science and regulatory affairs Regulatory Affairs (RA), also called Government Affairs, is a profession within regulated industries, such as pharmaceuticals, medical devices, energy, and banking. Regulatory Affairs professionals usually have responsibility for the following general areas: The Drug Watch proposal was one of several the agency issued following Merck's withdrawal of Vioxx when research showed the arthritis medicine doubled heart attack and stroke risk in people who took it for at least 18 months. FDA also created a drug safety oversight
Oversight may refer to:
Effects of a proposed project on other parts of the firm. to the public. Details on various drugs can be found at http://www.fda.gov/cder/drug/DrugSafety/DrugIndex.htm. |
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