United States Drugs

YEARS 1 United States Drug B 1 M 2003-04-12T10 00 CAUCASIAN... 

XT802 802101001 101 802101001 DM 2003-01-10T12 52 1975-02-26 2003-01-10 27 YEARS 1 United States Drug B 1 M 2003-04- 12T10 00 CAUCAS IAN... 

XT802 802101002 101 802101002 DM 2003-01-10T18 40 1950-01-30 2003-01-10 52 YEARS 1 United States Drug A 0 F 2003-04-11T12 33 CAUCAS IAN... 

XT802 802101007 101 802101007 DM 2003-03-01T19 42 1969-06-22 2003-03-01 33 YEARS 1 United States Drug B 1 F 2003-06- 04T11 47 CAUCAS IAN... 

XT802 802101008 101 802101008 DM 2003-03-02T12 33 1949-05-14 2003-03-02 53 YEARS 1 United States Drug A 0 M 2003-06- 12T12 52 CAUCAS IAN... 

Kottke, M.K., Scientific and regulatory aspects of nutraceutical products in the United States, Drug Dev Ind Pharm, 24, 1177, 1998. 

The United States Drug Export Amendment Act of 1986. Permitted the export of... 

Young, F., Nightingale, S., Mitchell, W., and Beaver, L. (1989). The United States Drug Export Amendment Act of 1986 Perspectives from the Food and Drug Administration. International Digest of Health Legislation 40 246-252. 

Chyka, P.A. and McEommon, S.W. (2000). Reporting of adverse drug reactions by poison control centers in the United States. Drug Safety 23 87-93. 

Statement of Michael Braun, Chief of Operations, United States Drug Enforcement Agency, before the House International Relations Committee, Subcommittee on the Western Hemisphere, 9 November 2005 National Drug Intelligence Centre, National Drug Threat Assessment... 

Cicero, T. et al., A postmarketing surveillance program to monitor Ultram (tramadol hydrochloride) abuse in tire United States, Drug Alcohol Depend., 57, 7, 1999. 

United States Drug Free Communities Act offers federal money to communities to help educate citizens on the dangers on methamphetamine use and production. 

According to the United States Drug Enforcement Agency (DEA), drug abusers favor short and intermediate-acting barbiturates. Barbiturate users often refer to the pills they take in terms of the color of the capsule. These street names include blues or blue devils for Amytal reds, red birds and red devils for Seconal yellow jackets for Nembutal purple hearts for Luminal and rainbows and Christmas trees for Tuinal. 

At the start of the twenty-first century, the United States Drug Enforcement Agency said that barbiturates accounted for 20% of depressant prescriptions. Barbiturate use had declined so much that researchers no longer compiled separate statistics about the drug. Instead, barbiturates were placed in the sedative category that included tranquilizers. 

Ephedra is subject to the Dietary Supplement Health and Education Act (DSHEA), which was passed in 1994. The act essentially protects dietary supplements like ephedra. That is, while U.S. federal agencies can regulate prescription drug and food additives, DSHEA exempts herbal products and supplements from federal regulation. The law states that the United States Food and Drug Administration (FDA) cannot regulate dietary supplements unless, or until, they are proven to be unsafe and pose a risk to users. The United States Drug Enforcement Administration (DEA) monitors ephedrine because it can be used to make methamphetamine. 

Phencyclidine, commonly known as PCP, is a difficult drug to categorize. The United States Drug Enforcement Administration (DEA) categorizes it as a hallucinogen, like LSD, because it can make people see, hear,... 

In the United States, drug GMPs were formally introduced in 1963 and included the regulation of computer systems. 21 CFR Part 211.2(b) emphasized computer backups and documentation, including keeping hardcopy of master formulas, specifications, test records, master production and control records, batch production records (batch production and control records), and calculations. 

United States Drug Enforcement Administration Congressional Testimony, July 16, 1996. 

In the UK, the principle legislative documents are the Misuse of Drugs Act, 1971, plus its amendment orders, and the Misuse of Drugs (Regulations), 2001. In the United States, drugs are controlled at the Federal level by the Controlled Substances Act. Control also exists at the State and County levels. An analogous... 

Eierman, H.J. Regulatory requirements for marketing cosmetics in the United States. Drug Inf. J. 1987,21, 387-391. 

Reekie, W.D. Price and quality competition in the united states drug industry (Mimeographed). In Pricing New Pharmaceutical Products, Croom Helm London, 1977. 

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