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NIDA Club Drug Research Funding To Jump 40%, Education Effort Underway

This article was originally published in The Tan Sheet

Executive Summary

The National Institute on Drug Abuse is accelerating its research efforts on the risks of "club drugs," including methamphetamine and GHB, through a 40% funding increase. The institute will now dedicate $54 mil. to study the abuse of these substances.

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GHB Analog-Containing Product Demand High, NEJM Researchers Report

Extensive industrial use of the GHB analog 1,4-butanediol (BD), in conjunction with the flexibility and anonymity of Internet marketing, "ensures a continued supply that is almost impossible to regulate," researchers say in the Jan. 11 New England Journal of Medicine.

GBL

Senate passes by voice vote the "Samantha Reid and Hillory J. Farias Date-Rape Drug Prohibition Act of 1999" (S 1561) Nov. 19 and returns it to the House; slightly different companion legislation had passed the House 423-1 on Oct. 12 ("The Tan Sheet" Oct. 18, In Brief). Introduced by Sen. Spencer Abraham (R-Mich.), the bill would classify gamma hydroxybutyric acid (GHB) and gamma butyrolactone (GBL) as controlled substances, would require the HHS secretary to develop a national awareness campaign educating consumers about such products and would establish a special unit at DEA to deal with drugs used for sexual assault. Certain regulatory exemptions are provided for researchers studying GHB for the treatment of narcolepsy. FDA first asked companies manufacturing dietary supplements containing GBL, a GHB precursor, to recall their products in a Jan. 21 "Talk Paper" ("The Tan Sheet" Jan. 25, p. 6)

Pseudoephedrine and PPA

Senate passes legislation Nov. 19 limiting the amount of the ingredients that could be sold at retail by a voice vote. Introduced by Sen. John Ashcroft (R-Mo.), the DEFEAT Meth Act (S 486) was the subject of an Aug. 5 Senate Judiciary Committee hearing ("The Tan Sheet" Aug. 16, p. 8). As passed, the bill would set the single transaction limit for non-safe harbor products containing pseudoephedrine or phenylpropanolamine at 9 g. Safe harbor packaging, which would be exempt, is defined as blister packs containing less than a 3 g base of either ingredient with no more than two doses per blister. In addition, the bill requires the Attorney General's office to conduct a study on the practice of converting OTC products containing the ingredients into meth, instructing the office to use information provided by federal and state agencies as well as by pharmaceutical firms. If the AG report finds a "significant number" of OTCs containing the ingredients are used for conversion to meth, a single transaction limit of no less than 24 g could be enacted after a notice and comment period. Mail order exemptions also are included in the measure. Companion legislation (HR 2987) was introduced in the House Sept. 30 by Rep. Chris Cannon (R-Utah)

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