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REDUCING OF ERROR IN THE MEDICATION PROCESS OF A PRIVATE... NORTHEAST OF THAILAND  Original Article
REDUCING OF ERROR IN THE MEDICATION PROCESS OF A PRIVATE... NORTHEAST OF THAILAND Original Article

... considered to make hospital guidelines. The hospital guidelines were already constructed such as high alert drug manual, LASA drug list, and injectable drug manual. In addition, the hospital drug list including generic name, trade name, and drug strength was categorized and inform to doctors in docu ...
54 What does “off-label use” mean?
54 What does “off-label use” mean?

... The FDA-approved use or uses for a medication are narrowly defined in the professional product label. These include the disease being treated, the dose, the duration of treatment, and the age group of patients for which the medication is intended. The professional product label, or package insert, i ...
effect of slimming product - Perpustakaan Negara Malaysia
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... loss, slimming and/or diabetes, ConsumerLab.com focused its testing on products containing the following ingredients: chromium, CLA, and/or pyruvate. In addition to the uses indicated above, these ingredients have other potential actions and uses. There is mixed clinical evidence that chromium may h ...
Histopathological study of the liver of Alloxan
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... health problem that challenges not only health care professionals but also the pharmaceutical industry and drug regulatory agencies. Liver cell injury caused by various toxic chemicals (certain anti-biotic, chemotherapeutic agents, carbon tetrachloride (CCL4), thioacetamide (TAA) etc.), excessive al ...
General Notices - Indian Pharmacopoeia Commission
General Notices - Indian Pharmacopoeia Commission

... Water-bath. A bath of boiling water unless water at another temperature is indicated. Other methods of heating may be used provided the required temperature is approximately maintained but not exceeded. Provisions Applicable To Monographs and Test Methods Expression of Contents. Where the content of ...
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... Peptic ulcer diseases (PUD) are the disorder of the gastrointestinal system and millions of people suffer from this disease globally. The main causes of peptic ulcers are hyperacidity, excessive intake of alcohol, overeating, high intake of spicy foods, food poisoning, high intake of coffee, smoking ...
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Scandinavian Journal of Infectious Diseases
Scandinavian Journal of Infectious Diseases

... among 4 antibiotics (Table I). By E-test, the combinations with RIF (TIG-RIF and DOX-RIF) were synergistic for all strains. TIGSTR and DOX-STR combinations revealed additive activity in 6.25% and 12.5%, indifference in 81.25% and 68.75%, and antagonism in 12.5% and 18.75% of the isolates, respective ...
Alkaloids Derived from Phenylalanine and Tyrosine
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The Physics, Chemistry and Perception of Colored Flames
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... elements forming molecules. Use of that shorthand will simplify our discussions as well as shorten this paper significantly. For chemical elements in their natural atomic state, the shorthand notation is just to use the chemical symbol, instead of writing out the full chemical name. Thus, the symbol ...
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`Spice` Wars - Cayman Chemical
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... series, including CP 47,497 and CP 55,940, which proved to be 20 to 100 times more potent than THC in certain tests. With the discovery of two receptors for cannabinoids, it was hypothesized that compounds could be produced that selectively activated receptors to produce certain effects (e.g., pain ...
(BE) Study Reports
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... − The US regulations require quarterly reports during the first 3 years, then annual reports. The FDA has recently published proposed rules1 which take into account the CIOMS Working Group II proposals2. − In the EU, Council Directive 93/39/EEC and Council Regulation 2309/93 require reports with a p ...
Yanyan Cui, Mona I. Churchwell, Letha H. Couch, Daniel
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conclusions and regulatory obligations
conclusions and regulatory obligations

... combination of hydrocarbons obtained from the vacuum distillation of the products from a thermal cracking process. It is made up mainly of hydrocarbons with a number of carbon atoms predominantly greater than C34 and a boiling point above ~495 °C. The composition of the crude petroleum may vary betw ...
What`s New? - American Association of Diabetes Educators of Utah
What`s New? - American Association of Diabetes Educators of Utah

... • Alkaloid contained in several different plants • Has insulin sensitizing and AGI activity • May ↑ SDCs of drugs metabolized by CYP 3A4 (CyA, some statins, CCBs, etc.) • Constipation is main side effect • Should not be used in pregnancy • Has shown benefit on A1C, FPG, PPG, lipids, weight, and even ...
DIFFERENT TECHNIQUES USED FOR THE PREPARATION OF NANOPARTICLES USING  NATURAL POLYMERS AND THEIR APPLICATION 
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... antiinfectives  such  as  antibacterial,  antiviral,  antifungal  and  antiparasitic  drugs,  is  another  common  use  of  nanoparticles.  The  low therapeutic index of antifungal drugs, short half‐life of antivirals  and  the  limited  ability  of  antibiotics  to  penetrate  infected  cells  in  ...
Reporting adverse drug reactions
Reporting adverse drug reactions

... medicine-related problem.’ If ADRs that are not discovered during clinical trials are to be detected, investigated and communicated, and the appropriate action taken, then it is vital that post-marketing pharmacovigilance of all medicines is comprehensive. Effective pharmacovigilance should take int ...
The Generic Patient Controlled Analgesia Pump Model
The Generic Patient Controlled Analgesia Pump Model

... facilitate illustration of how model-based development techniques can be employed to develop software for a PCA pump. They are not intended to prescribe any particular implementation of an infusion pump. The GPCA model provides a reference PCA pump implementation that can be verified against safety ...
Lipid Nanoparticulate Drug Delivery Systems: A
Lipid Nanoparticulate Drug Delivery Systems: A

... obvious advantages of higher degree of biocompatibility and versatility. These systems are commercially viable to formulate pharmaceuticals for topical, oral, pulmonary or parenteral delivery. Lipid nano formulations can be tailored to meet a wide range of product requirements dictated by disease co ...
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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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