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Pharmacy history
Pharmacy history

... congress to pass the pure food and drug act in 1906.  In Germany, new discoveries in organic chemistry were making ...
Managing Medication Use
Managing Medication Use

... systems often use rules to determine when pop-ups will occur. These pop-ups may contain clinical information about medication use, potential drug interactions, recommended monitoring, etc. ■■ Stop orders: Physician orders that are automatically terminated. The P&T committee may establish stop orders ...
Highlights of PET studies on chiral radiotracers and drugs at
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... animal species. It also enables the assessment of drug behavior in diseases where there are no animal models. This information is not available with other methods and places PET in a unique position to streamline the process of drug development and evaluation. PET has also found increased applicatio ...
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Chemistry 11 Lab booklet # ___
Chemistry 11 Lab booklet # ___

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Stimulants - CAP Members
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... sensation known as a “rush” or a “flash.” Abuse is often associated with a pattern of binge use —sporadically consuming large doses of stimulants over a short period of time. Heavy users may inject themselves every few hours, continuing until they have depleted their drug supply or reached a point o ...
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Setor 11. Farmacologia Clínica, Farmacocinética
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Common Drugs of Abuse
Common Drugs of Abuse

... which a baby can suffer from dependence and withdrawal symptoms after birth. Pregnancy-related issues are listed in the chart below for drugs where there is enough scientific evidence to connect the drug use to negative effects. However, most drugs could potentially harm an unborn baby. In the chart ...
Straight Facts About Drugs and Drug Abuse
Straight Facts About Drugs and Drug Abuse

... major social concern. The widespread availability and use of drugs means that drug-related problems will impact all Canadians in one way or another. As a result, there is a need for accurate information about different types of drugs and their effects, how people use them, and how they can affect ou ...
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... recommended. On the other hand, for large therapeutic range drugs, such as oral antibiotics, antacids, antihistaminic agents and some analgesics, more flexible limits have been suggested.13 Literature shows that assessing bioequivalence for drugs with a high pharmacokinetic variability, such as vera ...
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... will transmit an infectious agent to humans has been reduced by the testing and inactivation of certain viruses during manufacturing, there is a theoretical risk for transmission of viral disease, including diseases caused by novel or unidentified viruses. The presence of porcine viruses that might ...
Chemistry
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... technological world rather than focusing on large quantities of factual material which may have only short term relevance. Experimental work is an important component and should underpin the teaching and learning of Chemistry. ...
Non-Clinical Investigation of the Dependence Potential of Medicinal
Non-Clinical Investigation of the Dependence Potential of Medicinal

... Whether a medicinal product may cause a dependence syndrome or lead to drug abuse is also influenced by other factors, for instance clinical (e.g. the occurrence of side-effects), social (acceptability of use), economic (availability and costs), chemical (ease of synthesis) and pharmaceutical. As th ...
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... • RNA therapeutics as a platform is a revolutionary approach to discover new and important therapeutic agents for treating human diseases • RNA as a class of molecules plays a major role in the regulation of biological processes and in human diseases • Therapeutic approaches against RNA are generall ...
Balancing the outcomes: reporting adverse events
Balancing the outcomes: reporting adverse events

... ITT methods should be routinely reported, and data for treatment actually received should be added, with an explanation as to why, if there are high rates of non-compliance. Treatment withdrawal after adverse events Adverse events resulting in withdrawals from treatment should also be adequately des ...
ANISOCHILUS CARNOSUS TETRA CHLORIDE –INDUCED HEPATOTOXICITY IN ALBINO RATS Full Proceeding Paper
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... lining the biliary ducts of the liver synthesise the enzyme Alkaline phosphatase (ALP). Bile duct obstruction or diseases of the liver result in an elevated level of ALP in the plasma. The increased activity of alkaline phosphatase, may be due to de novo synthesis by liver cells and is a reliable ma ...
Benzodiazepines
Benzodiazepines

... depressants that are commonly known as tranquilizers, sedatives, or anxiolytics  Due to the sedative effects they produce, they are often used as “date rape” drugs  Approximately 2,000 benzodiazepines have been produced but only 15 are marketed in the U.S  Schedule IV  Twice as many women as men ...
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... Always need to use the lowest possible dose and review frequently Most patients need these medications only for short periods (few months) ...
Prescribing Information
Prescribing Information

... buspirone, and St. John’s Wort [see Drug Interactions (7.1)]. Amphetamines and amphetamine derivatives are known to be metabolized, to some degree, by cytochrome P450 2D6 (CYP2D6) [see Clinical Pharmacology 12.3]. The potential for a pharmacokinetic interaction exists with the coadministration of CY ...
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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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