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Drug report

United Nations on Dings and Crime (UNODC) (2008) World Drug Report 2008... [Pg.224]

The prices for raw materials were obtained from the Oil, Paint and Drug Reporter, Aug. 9, 1971,... [Pg.325]

Specific adverse effects of rimonabant have not yet been released to the public, although the company that makes the drug reports that their incidence is low. Pending the completion of more safety and efficacy studies, rimonabant is expected to be available in the United States in the next couple of years. This drug may prove to be especially ideal for obese individuals who smoke, since it should help with both problems. [Pg.102]

United Nations Office on Drugs and Crime, UNODC. World drug report 2009. Available at http //www.unodc.org/documents/wdrAVDR 2009AVDR2009 eng web.pdf... [Pg.205]

Food and Drug Administration, USA. Improving Public Health through Human Drugs. Report 2001. http /www.fda.gov/cder/cder.org.htm ... [Pg.140]

The most commonly abused drug reported by those admitted was cocaine (38.4%), followed by heroin (25.5%) and marijuana (19.1%). [Pg.41]

European Union (EU). The European Agency for the Evaluation of Medical Products (EMEA) established January 2002 as the deadline for all electronically filed single case reports to be coded in MedDRA. All ADR drug reporting must be coded in MedDRA by January 2003. [Pg.853]

Source Biologic Drug Report, http //www.biologicdrugreport.com/leading.htni [accessed May 25, 2007]. [Pg.7]

Table 1.2 MISCELLANEOUS DRUGS REPORTED TO INHIBIT 5-LIPOXYGENASE... Table 1.2 MISCELLANEOUS DRUGS REPORTED TO INHIBIT 5-LIPOXYGENASE...
All drugs will pose some degree of risk, and completed clinical trials are the primary source of information in this subject. Clinical trials do, of course, have limitations. The principal one concerns the everpresent problem of sample size. Rare side effects, if they exist, cannot generally be detected in clinical trials involving limited numbers of patients. Adverse drug reports and case-reports provide early clues to such effects so-called pharmacoepidemiology studies may be mounted to evaluate such risks. [Pg.249]

United Nations Office Drug Crime (UNODC) (2006) 2006 World Drug Report, vol 1-2. UN Publications, Geneva... [Pg.460]

United Nation Office on Drug And Crime (2007) 2007 World Drug Report. United Nations Publications, Geneva... [Pg.460]

Committee on Safety of Drugs. Report of the Committee on Safety of Drugs for the year ended December 31, 1964. Her Majesty s Stationery Office, London, 1965. [Pg.488]

The Secretary of HHS is a Cabinet position, appointed by the President with the advice and consent of the Senate. The Commissioner of Food and Drugs reports to the Secretary of HHS. [Pg.567]

The comparison of the two sets of %ILS values allows us to conclude that MYKOMET 63 appears to be actually as active as MYKO 63, but not more active. In other words, the graft of methylated aziridinyl ligands on a six-membered cyclophosphazene ring does not significantly improve the antitumoral activity with respect to the non-methylated isologues. However, because MYKOMET 63 possesses only a slight toxicity compared to MYKO 63, the new drug reported here may be of interest for eventual clinical use, no matter what difficulties are encountered in its synthesis. [Pg.47]

Hypersensitivity to fluoroquinolones or the quinolone group tendinitis or tendon rupture associated with quinolone use patients receiving disopyramide and amiodarone or other QTc-prolonging antiarrhythmic drugs reported to cause torsade... [Pg.1572]

Pharmaceutical Starting Materials/Essential Drugs Report. Details over 273 active ingredients. Issued by WHO and the International Trade Centre, a joint WTO-UNCTAD Centre. [Pg.82]

WHO. The rational use of drugs. Report of the conference of experts. Geneva World Health Organization 1985. [Pg.96]

Male patients must always use a latex condom during sexual contact with women of childbearingpotential even if a successful vasectomy has been performed. Thalidomide is present in the semen of patients taking the drug. Report suspected fetal exposure to thalidomide to FDA (1-800-FDA-1088). [Pg.1198]

Darke S, Topp L Ross f (2002). The injection of methadone and benzodiazepines among Sydney injecting drug users 1996-2000 5-year monitoring of trends from the Illicit Drug Reporting System. Drug and Alcohol Review, 21, 27-32... [Pg.153]


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See also in sourсe #XX -- [ Pg.86 ]




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Adverse drug events, reporting

Adverse drug reactions patient reports

Adverse drug reactions reporting

Adverse drug reactions reporting requirements

Adverse drug reactions reporting systems

Adverse drug reactions reports

Adverse drug reports

Australian Adverse Drug Reaction Advisory reporting reactions

Canada drug reports

Drug Data Report

Drug Experience Report

Drug Product Problem Reporting Program

Drug misuse reporting

Drug reaction reporting

Drug reaction reports

Evidence From the Food and Drug Administrations Spontaneous Reporting System

FDA Perspectives on the Use of Postmarketing Reporting Systems to Evaluate Drug Interactions with CAHP

Food and Drug Administration Adverse Events Reporting System

Johns Wort Drug Interaction Reports from FDAs Postmarketing AERS

MACCS Drug Data Report

MACCS Drug Data Report database

MACCS-II drug data report

MDL Drug Data Report database

MDL Drug Data Report, MDDR

MDL Drug Data report

Molecular Drug Data Report

Oil, Paint and Drug Reporter

Orphan-Drug Annual Reports

Pharmaceutical regulation adverse drug reports

Postmarketing Safety Evaluation Monitoring, Assessing, and Reporting of Adverse Drug Responses (ADRs)

Report of the Indian Hemp Drug Commission

Report on Drug Safety

Spontaneous Reporting of Adverse Reactions to Drugs

Under-reporting adverse drug

Under-reporting adverse drug reactions

World Drug Report

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