new structure

April 5 Office of the U.S. Food and Drug Administration USA (Food and Drug Administration - FDA) announced approval of a new drug to control the release of the active substance OxyContin ® (oxycodone, «Purdue Pharma LP»). The drug is designed to help prevent misuse and abuse, thus potentially reducing the risk of the likelihood of overdose.

As noted by Bob Rappaport (Bob Rappaport), director of product to be used in anesthesia and analgesia of the Centre for Evaluation and Research Medicines (Center for Drug Evaluation and Research) FDA, despite the fact that the new drug OxyContin accounts for only some of the benefits compared with the last version, it is a step in the right direction.

Company «Purdue Pharma» will be required postmarketing study on whether the new version of the drug can not cope with the incorrect use or abuse of the analgesic, says FDA.

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OxyContin - a drug with a slow-release narcotic painkiller oxycodone, designed to treat patients in need of continuous round the clock use of opiates for a long period of time. Each tablet contains a large amount of OxyContin oxycodone, which allows patients to take medication less often. However, when used incorrectly, or abuse of the drug could be released from his more active substance and as a result lead to a fatal overdose and drug abuse.

The new structure eliminates the possibility of chewing or any other violation of the integrity of the funds that could determine the release of high doses of the drug. Advanced composition can reduce the risk of overdose and possibly lead to a decrease in drug abuse, for example, by parenteral administration. However, the new structure does not exclude all possibilities of abuse, for example taking more pills than recommended by your doctor.