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The buccal/sublingual route
The buccal/sublingual route

... Variable gastric emptying (factors). Possibility of irregular or poor absorption ( low bioavailability). Drug solubility may be altered by some substances in the GIT (e.g. Ca+2). Destruction of certain drugs in the GIT (due to enzymes or secretions). First pass effect (i.e. presystemic metaboli ...
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... Financing and Coordination. The work of this group, its findings and methods, will be available via the WHO Public Health, Innovation and Intellectual Property website. It is due to report to the World Health Assembly in 2012 as one part of WHO’s actions under the global strategy and plan of action ...
Dothiepin Hydrochloride - Apollo Pharmaceuticals API
Dothiepin Hydrochloride - Apollo Pharmaceuticals API

... treatment of chronic and ongoing pain disorders, particularly where insomnia and/or loss of appetite are present. It can take between two and four weeks of regular usage to become effective; it is often started at a low level and the dosage increased if this is ineffective. The drug causes drowsines ...
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Safety of the Subject - The University of Iowa
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... signs informed consent until 28 days after the last dose of Drug A, 90 days after the last dose of Drug B ...
Federal Register/Vol. 77, No. 49/Tuesday, March 13, 2012/Notices
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... and Budget (OMB) for each collection of information that they conduct or sponsor. ‘‘Collection of information’’ is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c), and includes Agency requests or requirements that members of the public submit reports, keep records, or provide information to a third ...
For synthetic chemicals tested in both mice and rats
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... Canadian Status: Prostanozol is not currently listed in the CDSA. The substance has been reported to be an ingredient in an nutritional supplement known as Win 50 and which marketed by Double Dragon pharmaceuticals2. “Anabolic steroids and their derivatives” are currently controlled under item 23 of ...
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SUSPECTED ADVERSE DRUG REACTIONS ADR
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... into Singapore in the recent 5 years, regardless of their nature and severity. Please do not be deterred from reporting because some details are not known. You may send the completed ADR Report Form (through your respective hospital pharmacies, if applicable) to the Vigilance Branch, Health Products ...
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... Given the drug’s extreme potency and narrow safety window, accurate measurement of doses is critical. Even a dose a few milligrams off can be life-threatening. Also, the slow onset of the high may lead some users to re-dose, which can result in death. Mislabeling of Bromo-Dragonfly as its far-less-p ...
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... separates from the solution is known as a precipitate. 4. Color change ...
Predicting Products online assistance #3
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... 1. synthesis - two reactants combine to form one product 2. decomposition - one reactant decomposes, or breaks apart, into two or more products. 3. single replacement - an element replaces another in a compound. 4. double replacement - the elements in two compounds switch partners to form two new co ...
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Illustrated Drug interaction By Mohie Al

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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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