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How Drugs Enter The Body (1)
How Drugs Enter The Body (1)

Drugs
Drugs

... Adverse Effects  Side Effects that can occur if medication is taken  e.g. Adverse Effect of Tylenol is hepatotoxicity. ...
Pharmacology DRUGS2014-11-19 09:1841 KB
Pharmacology DRUGS2014-11-19 09:1841 KB

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... Diazon Pharmaceutical’s anti-cancer agent DZ-2384 mechanism for high activity and low neurotoxicity published by McGill researchers in Science Translational Medicine Montreal, QC, November 16th 2016 – Diazon Pharmaceuticals Inc. today announced the publication of a preclinical oncology study identif ...
9BYO3IvgcQkevbgH5m4MVg5J_nF9t8U45TqcqcBmrETKoHMWh
9BYO3IvgcQkevbgH5m4MVg5J_nF9t8U45TqcqcBmrETKoHMWh

... 15. Tinea Pedis is commonly known as:a. Athlete's foot b. corns c. calluses d. warts e. blackheads 16. Signs and symptoms of "Caffeinism " may include all of the following except : a. Anxiety b. Muscle twitching c. Agitation d. Restlessness e. Cough 17. Parenteral drug products undergo what type of ...
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Basic PHARMACOLOGY Review

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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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