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Clinical Actions of Specific Agents
Clinical Actions of Specific Agents

... for local anesthetics and no longer adjusts them for inclusion of a vasoconstrictor -Changes in liver function, plasma protein binding, blood volume and other important physiological functions influence the manner in which local anesthetics are distributed and biotransformed in the body -The half li ...
Plant Profile, Phytochemistry and Pharmacology of Ashoka (Saraca
Plant Profile, Phytochemistry and Pharmacology of Ashoka (Saraca

... also gathered. Saraca asoca is the ideal candidate for screening of its endophytes for pharmaceutical related compounds.It is hoped that this review will provide sufficient, ideal and unique information under one umbrella and also give new direction for the researchers and pharmaceutical industry to ...
NIH Public Access
NIH Public Access

... fear. These results are of great interest, because the reduction of acquired fear associations is critical in therapies for anxiety disorders. We tested whether findings with respect to the Nmethyl-D-aspartate (NMDA) and cannabinoid receptor (CB) systems in animals carry over to healthy human subjec ...
Chloral hydrate
Chloral hydrate

... methyl ethyl ketone [1]. Trichloroethanol (an active metabolite of chloral hydrate) MF: Cl3CCH2OH MW: 149.4 Solubility: soluble in 12 parts water; miscible with ethanol or ether [2]. Major uses Chloral hydrate (synthesized in 1832 and introduced into medicine 1869) is the oldest member of sedative-h ...
NBER WORKING PAPER SERIES CHARACTERIZING MARKETS FOR BIOPHARMACEUTICAL INNOVATIONS:
NBER WORKING PAPER SERIES CHARACTERIZING MARKETS FOR BIOPHARMACEUTICAL INNOVATIONS:

... Genentech in 1976, and Genzyme in 1981. The first U.S. sales of a major recombinant therapeutic—human insulin—occurred in 1982. A decade later in 1992 Amgen became the first biotech Fortune 500 company, driven by the sales of Epogen (epoietin alfa). A decade later, just after the millennium, the hum ...
7_Kuffner-Improving Patient`s Awareness of Acetaminophen
7_Kuffner-Improving Patient`s Awareness of Acetaminophen

... computer systems and on the pharmacy label, often prevent the use of complete generic names 1 • If only a Rx brand name is used the label may not list acetaminophen or “APAP” at all1 • Acetaminophen portion of the name is commonly abbreviated as “APAP” which patients may not recognize as acetaminoph ...
Administrative Rules of the Board of Pharmacy
Administrative Rules of the Board of Pharmacy

... patient or the ultimate user. “AMDS” includes a device that prepares and packages a drug for unit dose dispensing, that prepares and packages a drug into outpatient prescription vials, and that dispenses pre-packaged drugs. (3) “Alternative evidence of the individual’s identity” as referred to in 18 ...
Chemistry - Bulletin < Brown
Chemistry - Bulletin < Brown

... The Chemistry concentration offers courses and research opportunities that range from fundamental studies involving the characterization and preparation of synthetic and naturally occurring molecules, to interdisciplinary studies at the interfaces of chemistry with biology, medicine, physics, engine ...
oral cyclosporine use in dogs
oral cyclosporine use in dogs

... majority of dogs with atopy.15–17 Therapeutic drug monitoring of cyclosporine in dogs being treated for atopy is not typically recommended. ...
Administrative Rules of the Board of Pharmacy
Administrative Rules of the Board of Pharmacy

... patient or the ultimate user. “AMDS” includes a device that prepares and packages a drug for unit dose dispensing, that prepares and packages a drug into outpatient prescription vials, and that dispenses pre-packaged drugs. (3) “Alternative evidence of the individual’s identity” as referred to in 18 ...
Effects of phenytoin and carbamazepine on calcium transport in
Effects of phenytoin and carbamazepine on calcium transport in

... absorption. Several studies have failed to Wnd a consistent correlation between altered vitamin D levels and anti-epileptic drug treatment; but induction of vitamin D catabolism may be involved in combination with other mechanisms (Gough et al., 1986; Verrotti et al., 2000). Studies in rats have sug ...
A Solid-State Approach to Enable Early Development Compounds
A Solid-State Approach to Enable Early Development Compounds

... compounds into the following four quadrants: high solubility and extensive metabolism (Class 1), low solubility and extensive metabolism (Class 2), high solubility and poor metabolism (Class 3), and low solubility and poor metabolism (Class 4). The use of different solid forms (e.g., salts, co-cryst ...
distribution of brimonidine into anterior and posterior tissues of
distribution of brimonidine into anterior and posterior tissues of

... by a progressive optic neuropathy and loss of retinal ganglion nerve cells (Adkins and Balfour, 1998). One of the primary risk factors for glaucoma is elevated intraocular pressure. When applied to the eye, brimonidine activates ␣2-adrenergic receptors, resulting in decreased aqueous humor productio ...
Drug Testing Appropriateness Document
Drug Testing Appropriateness Document

... This document focuses on clinical drug testing for identification, treatment and recovery of patients with, or at risk for, addiction. ASAM recognizes that drug testing is used in other contexts (for example, criminal justice, workplace and pain management settings). ASAM’s intent with this document ...
An Introduction to Medicinal Chemistry
An Introduction to Medicinal Chemistry

... woolly one and is not really relevant to our discussion of medicinal chemistry. All drugs have their good points and their bad points. Some have more good points than bad and vice versa, but like people, they all have their own individual characteristics. So how are we to define a drug in general? O ...
FOOD AND DRUG ADMINISTRATION, et al
FOOD AND DRUG ADMINISTRATION, et al

... (same). n10 These figures are based on a search of the FDCA and its regulations on West PREMISE 3.7 CD-ROM (updated June 1, 1999) using the query "intend! w/4 use." The "intended use" concept originated in the Pure Food and Drugs Act of 1906, which focused on manufacturer statements on the product l ...
Inhibitors of HIV-1 Reverse Transcriptase—Associated
Inhibitors of HIV-1 Reverse Transcriptase—Associated

... are RT active site-directed nucleoside analogs that require metabolic activation (phosphorylation) for antiviral activity. Once activated, NRTI-triphosphates and NtRTI-diphosphates compete with cellular deoxynucleotides for binding to the RT polymerase active site. More importantly, N(t)RTIs lack a ...
Substance Use Prevention Screening, Education, and Referral Resource Guide
Substance Use Prevention Screening, Education, and Referral Resource Guide

... Individuals who are deaf, hard of hearing, or have speech disabilities, and wish to file either an EEO or program complaint, please contact USDA through the Federal Relay Service at (800) 877-8339 or (800) 845-6136 (in Spanish). Persons with disabilities who wish to file a program complaint, please ...
Inhibitors of HIV-1 Reverse Transcriptase—Associated
Inhibitors of HIV-1 Reverse Transcriptase—Associated

... are RT active site-directed nucleoside analogs that require metabolic activation (phosphorylation) for antiviral activity. Once activated, NRTI-triphosphates and NtRTI-diphosphates compete with cellular deoxynucleotides for binding to the RT polymerase active site. More importantly, N(t)RTIs lack a ...
Covariate Analysis of QTc and T
Covariate Analysis of QTc and T

... This study adds the dimension of a T-wave morphology composite score (MCS) to the QTc interval–based evaluation of drugs that affect cardiac repolarization. Electrocardiographic recordings from 62 subjects on placebo and 400 mg moxifloxacin were compared with those from 21 subjects on 160 and 320 mg ...
SHPA Medicines Information Procedure Manual
SHPA Medicines Information Procedure Manual

... therapeutics related committees. Medicines information pharmacists usually work in an MIC which is a knowledge hub within their host organisation. Providing reliable information on the appropriate use of medicines is an essential component of pharmacy practice and patient care.1 High quality informa ...
Evaluation of Quality Control Parameters of Two Brands of
Evaluation of Quality Control Parameters of Two Brands of

... therapeutically active and standard drug. It can be achieved by following some parameters that are specified in the respective monograph of the drug. This research work was aimed to investigate the quality control parameters of two brands of diazepam (Seduxen®, Sedil®) which are available in market. ...
UNITED STATES DISTRICT COURT FOR THE NORTHERN
UNITED STATES DISTRICT COURT FOR THE NORTHERN

... Massachusetts-based employee welfare benefit plan, established and maintained pursuant to § 1002(1) and (3) of ERISA, for the purpose of providing health benefits to approximately 22,000 eligible participants and beneficiaries located throughout New England. Carpenters is a jointlyadministered Taft- ...
Ferrario A, Kanavos P, Managed entry agreements for pharmaceuticals: the European experience. EMiNet, Brussels, Belgium
Ferrario A, Kanavos P, Managed entry agreements for pharmaceuticals: the European experience. EMiNet, Brussels, Belgium

... reimbursement lists need to demonstrate that their drugs can provide additional benefit in relation to current therapies and value-for-money in order to obtain coverage. Data and the overall evidence base available at registration are often insufficient to accurately estimate the clinical and cost-e ...
Salvia divinorum use and phenomenology: results from an online
Salvia divinorum use and phenomenology: results from an online

... which lends support to assertions that it phenomenologically differs from other hallucinogens with primary serotonergic activity. The functions of use changed with greater experiences with the drug, and although many respondents reported use of S. divinorum as an alternative to illegal drugs it, was ...
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Drug discovery



In the fields of medicine, biotechnology and pharmacology, drug discovery is the process by which new candidate medications are discovered. Historically, drugs were discovered through identifying the active ingredient from traditional remedies or by serendipitous discovery. Later chemical libraries of synthetic small molecules, natural products or extracts were screened in intact cells or whole organisms to identify substances that have a desirable therapeutic effect in a process known as classical pharmacology. Since sequencing of the human genome which allowed rapid cloning and synthesis of large quantities of purified proteins, it has become common practice to use high throughput screening of large compounds libraries against isolated biological targets which are hypothesized to be disease modifying in a process known as reverse pharmacology. Hits from these screens are then tested in cells and then in animals for efficacy.Modern drug discovery involves the identification of screening hits, medicinal chemistry and optimization of those hits to increase the affinity, selectivity (to reduce the potential of side effects), efficacy/potency, metabolic stability (to increase the half-life), and oral bioavailability. Once a compound that fulfills all of these requirements has been identified, it will begin the process of drug development prior to clinical trials. One or more of these steps may, but not necessarily, involve computer-aided drug design. Modern drug discovery is thus usually a capital-intensive process that involves large investments by pharmaceutical industry corporations as well as national governments (who provide grants and loan guarantees). Despite advances in technology and understanding of biological systems, drug discovery is still a lengthy, ""expensive, difficult, and inefficient process"" with low rate of new therapeutic discovery. In 2010, the research and development cost of each new molecular entity (NME) was approximately US$1.8 billion. Drug discovery is done by pharmaceutical companies, with research assistance from universities. The ""final product"" of drug discovery is a patent on the potential drug. The drug requires very expensive Phase I, II and III clinical trials, and most of them fail. Small companies have a critical role, often then selling the rights to larger companies that have the resources to run the clinical trials.Discovering drugs that may be a commercial success, or a public health success, involves a complex interaction between investors, industry, academia, patent laws, regulatory exclusivity, marketing and the need to balance secrecy with communication. Meanwhile, for disorders whose rarity means that no large commercial success or public health effect can be expected, the orphan drug funding process ensures that people who experience those disorders can have some hope of pharmacotherapeutic advances.
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