The FDA says that some topical pain relievers "should not be on the market" in a new alert
The agency has issued warning letters to six different companies on unregulated products.
Pharmacy cabinets are a tote for essential skin care, antibiotics and Common pain relief products . But when you launch spring cleaning at high speed, there are some topical pain relievers that the United States Food and Drug Administration (FDA) urges consumers to throw their stock due to illegally high quantities of a potentially ingredient dangerous.
On March 26, the government agency has issued a new warning For 19 over -the -counter analgesic products (OTC) (pain relief) which contain higher concentrations of lidocaine than what is authorized by the federal government for duty relief of topical pain. These products are in the form of gels, creams and sprays, and are announced as current affairs for tattoos, piercings, laser hair removal, microdermabrasion and other cosmetic procedures, explained the FDA .
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When used correctly, topical lidocaine products can Check, relieve and prevent Pain and itching, according to Mayo Clinic. For those who have undergone greater cosmetic procedures, the topical solution can cause "numbness or loss of feeling" near the affected area, they add.
However, when unregulated quantities of lidocaine are applied, you can put yourself in danger of serious health effects, in particular the "irregular heart rate, breathing seized and difficulties", according to the FDA opinion. Without forgetting, they can have negative interaction with other drugs and food supplements.
This is not the first time that the FDA has alerted consumers of topical anesthetics made with Lidocaine. In A 2009 opinion For patients and health professionals, the agency stressed that "if topical anesthesia is applied to a large area of the skin, if a large quantity is applied, if applied to irritated or broken, broken skin, Or if the skin temperature increases, "the probability that the drug passing through the blood circulation increases considerably. Once in the bloodstream, the over -the -counter medication can cause comas or even death.
But even again, topical pain relievers with high concentrations of lidocaine still exist - and some may even be in your home. The FDA has distributed warning letters to TKTX Company, Seenext Venture, Tattoo Numbing CREAM CO., Painless Tattoo Co., Derma Source Inc. and Inkeeze, companies with products that violate federal law. A detailed list of illegal products from each company is in the FDA version.
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There have been several reports of harmful effects on health in conjunction with these products, the FDA of which has been informed. The FDA requests those who have experienced serious side effects to report their file Medwatch adverse events program .
"These products have unacceptable risks for consumers and should not be on the market," said Jill Furman , JD, director of the compliance office at the FDA medication assessment and research center. "We are committed to using all the tools available to stop the sale of these high -risk illegal products."
In the future, the FDA advises consumers to avoid over -the -counter topical analgesics which contain more than four percent of Lidocaine. If you use a lidocaine product, the agency requests that patients do not apply quantities on large areas of skin or on irritated / broken skin. Finally, absorb to pack the treated areas with dressings, as this may increase the chances of harmful effects on health.
Best Life offers the most up -to -date information for high -level experts, new research and health agencies, but our content is not supposed to replace professional advice. Regarding the medication you take or any other health issue you have, always consult your health care provider directly.
