$Unique_ID{BRK02047} $Pretitle{} $Title{Reasons for the Increased Availability of Over the Counter Medications and the Importance of Following the Directions on the Label} $Subject{OTC's over the counter medications medicine medicines prescription drugs prescription drug prescriptions OTC Nonprescription Drug Manufacturers Association Food and Drug Administration FDA over-the-counter dose dosage dosages} $Volume{} $Log{} Copyright (c) 1993 Tribune Media Services, Inc. Reasons for the Increased Availability of Over the Counter Medications and the Importance of Following the Directions on the Label ------------------------------------------------------------------------------ QUESTION: There certainly are a lot of medicines now available on the shelves of my pharmacy that don't require a prescription, although that used to be the case. My friend says that they do not contain the same amount of medicine that was formerly in the capsules or tablets before the change. Can you tell me if this is true, which would mean I would have to take more of the new pills to get the same affect as before? ------------------------------------------------------------------------------ ANSWER: You are right about the increasing numbers of OTC (over the counter) medications that are now available. According to the Nonprescription Drug Manufacturers Association, there may be as many as 200 OTC drugs that have made the switch from prescription-only medications during the last ten years. But your analysis of the contents, and particularly your interpretation of their use, is way off the mark. Back in 1972, under the impetus of new amendments to the drug law, the FDA began to examine all the active ingredients in OTC products for safety and proven effectiveness. As a result, many of those products were taken off the market when they failed to meet the newly imposed standard for effectiveness, or when they were banned for safety reasons. The new amendment specified that a prescription drug was primarily a medication that would be unsafe unless used under professional supervision, while an OTC preparation could be used with safety if the patient carefully followed all the warnings and directions that were required on the label. Since many prescription medications had a low risk of causing harm and a high margin of safety, they were considered as good candidates for the switch from prescription-only to OTC. Many of the medications made the transition, with the same dosage indications as were used when prescribed. In some cases, dosages were reduced. Now to the most important part of this answer. OTC medications can be a very valuable part of your personal health care, but only, let me stress ONLY, used exactly as indicated on the label. Doubling the indicated dosage is a very big "no-no". All the cautions should be carefully observed, and if the symptoms you are trying to control fail to disappear after several days of taking the preparation, it is most important that you consult with your doctor. ---------------- The material contained here is "FOR INFORMATION ONLY" and should not replace the counsel and advice of your personal physician. Promptly consulting your doctor is the best path to a quick and successful resolution of any medical problem.