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Drug organizations

If financially feasible, suggest the use of commerdally available drug organizers. If the patient cannot afford drug organizers, egg cartons or a muffin tin can be labeled and used as drug organize s. [Pg.57]

Isoniazid and rifampin are the two most important tuberculosis drugs organisms resistant to both these drugs [multidrug-resistant tuberculosis (MDR-TB)] are much more difficult to treat. [Pg.1105]

Medlicott,N. J., Foster, K. A., Audus, K. L., Gupta, S., and Stella, V. J. (1998), Comparison of the effects of potential parenteral vehicles for poorly water soluble anticancer drugs (organic cosolvents and cyclodextrin solutions) on cultured endothelial cells (HUV-EC), J. Pharm. Sci., 87,1138-1143. [Pg.435]

Laboratory culture plates provide an ideal environment for the drug-organism interactions. In clinical cases, the local environment at the infection site has a large effect on antimicrobial action. In diseases characterized by abscess formation, treatment failure may occur when the chosen antimicrobial agent is ineffective in acidic, anaerobic and hyperosmolar environments. The action of many antimicrobial drugs is decreased in milk. [Pg.19]

Partial change of the drug fund for side effects relief and research promotion Law (called Drug Organization Law). [Pg.271]

In accordance with the reorganization of the health authority (MHW, Drug Organization and NIHS) which Wcis effective in July 1997, the procedure has been chcinged as shown in Figure 1. [Pg.273]

In accordance with the revision of the PAL in 1996, the decision was made to reorganize the MHW, Drug Organization and National Institute of Health Sciences (NIHS) for intensifying the review cind approved system of drugs and medical devices. [Pg.276]

The Drug Organization is responsible for consultation on drug development, raw data check, GLP/GCP/GPMSP inspections and reviews on equivalency. [Pg.277]

Figure 2. Organization of the MHW, Drug Organization, NIHS and CPAC. [Pg.278]

A copy of documents confirming GLP complicince issued by the Drug Organization on the testing facility... [Pg.301]

With the enforcement of the revised Drug Organization Law in April 1994, the Drug Organization carries out a survey of GLP compliance. Confirmation of GLP compliance with domestic testing facilities is in principle done bcised on the results of the survey. When GLP studies are performed in foreign countries, the MHW may make a GLP inspection if necessary. [Pg.302]

Inspections to sponsors and institutes/investigators are done by the staff of the Drug Organization. [Pg.309]

When an applicant applies for approval of new indications, change of dose and dosage, etc., of the approved drug, it is necessary to submit the data on a copy of the approval form, review reports at the approved time, the outline of data, list of attached data, etc., of the approved drug. It is also required to attach the consultation records if ein applicant consulted on trials to the Drug Organization. [Pg.326]

Table 13-4. Examples of studies using zebrafish embryos for the evaluation of drug organ toxicity... Table 13-4. Examples of studies using zebrafish embryos for the evaluation of drug organ toxicity...
Scheme 6 Similar to the process in Scheme 5, where emulsification of the polymer/drug organic solution takes place forming an oil-in-water system. The alternative is the dissolution of the polymer and drag in an aqueous phase, which is added to an organic phase to form a water-in-oil emulsion. In both cases, the internal phase is then evaporated leaving the polymer-drag particles. Scheme 6 Similar to the process in Scheme 5, where emulsification of the polymer/drug organic solution takes place forming an oil-in-water system. The alternative is the dissolution of the polymer and drag in an aqueous phase, which is added to an organic phase to form a water-in-oil emulsion. In both cases, the internal phase is then evaporated leaving the polymer-drag particles.
The only sure way to tell if your LSD is pure is to have it analyzed with a sympathetic drug organization, doctor or chemist. A good point to remember, though, is that since acid is tasteless, and some adulterants have a bitter taste, you can sometimes taste speed, etc., by testing a miniscule amount on your finger. This test, however, is far from thorough. [Pg.13]

This review is limited to high resolution techniques for the analysis of proteins, but the use of analytical ITP has no such limitations. Such widely differing substances as ionizable lipids, halogen ions, trace metals, drugs, organic acids, nucleotides, and proteins can be analyzed by ITP (Al, E7). However, it is perhaps in the field of protein analysis that both the greatest potential and the greatest problems lie, because of the complexity of most natural protein mixtures. [Pg.252]


See other pages where Drug organizations is mentioned: [Pg.271]    [Pg.279]    [Pg.671]    [Pg.192]    [Pg.143]    [Pg.35]    [Pg.32]    [Pg.32]    [Pg.34]    [Pg.286]    [Pg.837]    [Pg.2387]    [Pg.915]    [Pg.43]    [Pg.394]    [Pg.272]    [Pg.272]    [Pg.273]    [Pg.274]    [Pg.274]    [Pg.279]    [Pg.279]    [Pg.490]    [Pg.23]    [Pg.670]    [Pg.22]    [Pg.102]    [Pg.24]    [Pg.24]   
See also in sourсe #XX -- [ Pg.38 ]




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