Silver Spring, MD/PRNewswire-USNewswire/ --The U.S. Food and Drug Administration today released its final guidance to firms that manufacture, market, or distribute over-the-counter (OTC) liquid drug products packaged with cups, droppers, syringes, and spoons to measure and dispense the doses of medication.
The guidance, titled Dosage Delivery Devices for Orally Ingested OTC Liquid Drug Products, describes how easy-to-use dosage delivery devices and devices that minimize the risk of unintentional overdose can be provided for OTC medicines such as liquid pain relievers, cold medicine, cough syrups, and digestion aids.
"Accidental medication overdose in young children is an increasingly common, but preventable public health problem," said Karen Weiss, M.D., program director for the Center for Drug Evaluation and Research's Safe Use Initiative.The FDA issued the guidance because of ongoing concerns about
the potential accidental drug overdoses that can result from the use of dosage delivery devices with markings that are confusing, unclear or inconsistent with the labeled dosage directions.
Key recommendations in the guidance include:
According to the FDA, parents and caregivers should follow 10 tips when giving medicine to an infant or child:
1.Always read and follow the Drug Facts label on your OTC medicine.
2.Know the 'active ingredient' in your child's medicine.
3.Give the right medicine, in the right amount, to your child.
4.Talk to your doctor, pharmacist, or nurse to find out what mixes well and what doesn't.
5.Use the dosing tool that comes with the medicine, such as a dropper or a dosing cup.
6.Know the difference between a tablespoon and a teaspoon.
7.Know your child's weight.
8.Prevent a poison emergency by always using a child-resistant cap.
9.Store all medicines in a safe place.
10.Check the medicine three times.
The FDA recommends that anyone with questions about dosage delivery devices or how to measure liquid OTC medicines contact a physician, pharmacist, or other health care professional.
Health care professionals and patients are encouraged to report adverse events, side effects, or product quality problems to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:
For more information:
Dosage Delivery Devices for Orally Ingested OTC Liquid Drug Products
Kids Aren't Just Small Adults
FDA's Safe Use Initiative: Collaborating to Reduce Preventable Harm from Medications
The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation's food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.
SOURCE: U.S. Food and Drug Administration
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