A Global Review of the Harm Reduction Response to Amphetamines
... pregnancy. Harm reduction measures to deal with this set of risks, along with drug treatment, ...
... pregnancy. Harm reduction measures to deal with this set of risks, along with drug treatment, ...
91391 Sample Assessment Schedule
... This compound is oxidised by Cr2O72-/H+ to an acid so it has to be a primary alcohol (or an aldehyde – rejected as too many H atoms). The OH has to be on an end C. It’s a branched chain molecule so there is a CH3 on the 2nd C atom. Hence: (c) ...
... This compound is oxidised by Cr2O72-/H+ to an acid so it has to be a primary alcohol (or an aldehyde – rejected as too many H atoms). The OH has to be on an end C. It’s a branched chain molecule so there is a CH3 on the 2nd C atom. Hence: (c) ...
Screening of Methanol Extract and Ethyl Acetate Fraction of Abies
... of Abies webbiana aerial parts and its ethyl acetate fraction. Properly identified aerial parts were defatted with petroleum ether and then extracted with methanol in a Soxhlet apparatus. Ethyl acetate fraction was prepared by partitioning methanol extract with ethyl acetate using standard procedure ...
... of Abies webbiana aerial parts and its ethyl acetate fraction. Properly identified aerial parts were defatted with petroleum ether and then extracted with methanol in a Soxhlet apparatus. Ethyl acetate fraction was prepared by partitioning methanol extract with ethyl acetate using standard procedure ...
PH.1. The hospital has a pharmacy service department and headed
... formulary drugs for un-approved indications. PH.21.1 Written multidisciplinary IPP for using a formulary drug for an un-approved indication and/or investigation. PH.21.2 Request form for using formulary drug for an un-approved indication is available. PH.21.3 Clear evidence of proper adherence to th ...
... formulary drugs for un-approved indications. PH.21.1 Written multidisciplinary IPP for using a formulary drug for an un-approved indication and/or investigation. PH.21.2 Request form for using formulary drug for an un-approved indication is available. PH.21.3 Clear evidence of proper adherence to th ...
Hydrogels: Introduction, Preparation, Characterization and
... medicine, Diagnostics, Cellular immobilization, separation of biomolecules or cells, and barrier materials to regulate biological adhesions. Hydrogels are also relatively deformable and can conform to the shape of the surface to which they are applied. In the latter context, the mucoadhesive or bioa ...
... medicine, Diagnostics, Cellular immobilization, separation of biomolecules or cells, and barrier materials to regulate biological adhesions. Hydrogels are also relatively deformable and can conform to the shape of the surface to which they are applied. In the latter context, the mucoadhesive or bioa ...
VCE Chemistry Study Design
... Chemistry is a key science in explaining the workings of our universe through an understanding of the properties and interaction of substances that make up matter. Most processes, from the formation of molecules in outer space to the complex biological interactions occurring in cells, can be describ ...
... Chemistry is a key science in explaining the workings of our universe through an understanding of the properties and interaction of substances that make up matter. Most processes, from the formation of molecules in outer space to the complex biological interactions occurring in cells, can be describ ...
DiphenhydrAMINE Hydrochloride Injection, USP
... is effective in adults and pediatric patients, other than premature infants and neonates, for the following conditions when diphenhydramine hydrochloride in the oral form is impractical. Antihistaminic: For amelioration of allergic reactions to blood or plasma, in anaphylaxis as an adjunct to epinep ...
... is effective in adults and pediatric patients, other than premature infants and neonates, for the following conditions when diphenhydramine hydrochloride in the oral form is impractical. Antihistaminic: For amelioration of allergic reactions to blood or plasma, in anaphylaxis as an adjunct to epinep ...
DRUG CALCULATIONS
... Intermittent infusions usually involve administering a certain dose over a short time period, e.g. clarithromycin 500mg in 250ml glucose 5% over 60 minutes. This can be given in drops per minute via a standard giving set, or via a volumatic device. Using a volumatic device Number of ml per hour ...
... Intermittent infusions usually involve administering a certain dose over a short time period, e.g. clarithromycin 500mg in 250ml glucose 5% over 60 minutes. This can be given in drops per minute via a standard giving set, or via a volumatic device. Using a volumatic device Number of ml per hour ...
Cortisol Calm - Pure Encapsulations
... Vitamin D3 is derived from lanolin. Sensoril® ashwagandha extract is derived from Withania somnifera root and leaf. Rhodiola rosea extract is derived from the root and standardized to contain 3% total rosavins and min. 1% salidrosides. Magnolia officinalis extract is derived from the bark and standa ...
... Vitamin D3 is derived from lanolin. Sensoril® ashwagandha extract is derived from Withania somnifera root and leaf. Rhodiola rosea extract is derived from the root and standardized to contain 3% total rosavins and min. 1% salidrosides. Magnolia officinalis extract is derived from the bark and standa ...
Cyclodextrins in peptide and protein delivery
... T. Irie, K. Uekama / Advanced Drug Delivery Reviews 36 (1999) 101 – 123 ...
... T. Irie, K. Uekama / Advanced Drug Delivery Reviews 36 (1999) 101 – 123 ...
EA_QA66.6_warfarin+ppis
... Warfarin is the anticoagulant of choice in the UK for a number of conditions including prophylaxis of deep vein thrombosis (DVT), treatment of DVT and pulmonary embolism, atrial fibrillation, cardioversion and dilated cardiomyopathy (1). Patients taking warfarin are monitored regularly to check prot ...
... Warfarin is the anticoagulant of choice in the UK for a number of conditions including prophylaxis of deep vein thrombosis (DVT), treatment of DVT and pulmonary embolism, atrial fibrillation, cardioversion and dilated cardiomyopathy (1). Patients taking warfarin are monitored regularly to check prot ...
Annexure – II
... Nephrotoxicity is caused by several xenobiotic substances damaging renal proximal tubule, the portion of nephron with greater sensitivity to nephrotoxic effects. Alcohol is the commonly consumed xenobiotic. Some of the agents which cause damage to the proximal tubule are anti-bacterial agents such a ...
... Nephrotoxicity is caused by several xenobiotic substances damaging renal proximal tubule, the portion of nephron with greater sensitivity to nephrotoxic effects. Alcohol is the commonly consumed xenobiotic. Some of the agents which cause damage to the proximal tubule are anti-bacterial agents such a ...
Ocular Delivery of peptides and proteins
... PLGA microspheres for the ocular delivery of a peptide drug, vancomycin using emulsification/spray-drying as the preparation method: in vitro/in vivo studies, Gavini E, Chetoni P, Cossu M, Alvarez MG, Saettone MF, Giunchedi P, Eur J Pharm Biopharm. 2004 Mar;57(2):207-12 ...
... PLGA microspheres for the ocular delivery of a peptide drug, vancomycin using emulsification/spray-drying as the preparation method: in vitro/in vivo studies, Gavini E, Chetoni P, Cossu M, Alvarez MG, Saettone MF, Giunchedi P, Eur J Pharm Biopharm. 2004 Mar;57(2):207-12 ...
Full Report
... activate neurons (excitatory neurotransmitters), while others decrease neuron activity (inhibitory neurotransmitters). Sometimes a receptor for one neurotransmitter can affect a receptor for another neurotransmitter. In such cases, the receptors are biochemically coupled: the activation of one modul ...
... activate neurons (excitatory neurotransmitters), while others decrease neuron activity (inhibitory neurotransmitters). Sometimes a receptor for one neurotransmitter can affect a receptor for another neurotransmitter. In such cases, the receptors are biochemically coupled: the activation of one modul ...
ajinomoto acquires althea
... Angel has been facing financial difficulties, as it has had problems reaching a viable level of revenues. In its most recent financial statement (six months to September 2012), the company recorded a loss of £2.9 million ($4.3 million) on revenues of only £1 million ($1.5 million). For the financial ...
... Angel has been facing financial difficulties, as it has had problems reaching a viable level of revenues. In its most recent financial statement (six months to September 2012), the company recorded a loss of £2.9 million ($4.3 million) on revenues of only £1 million ($1.5 million). For the financial ...
hydromorphone hcl prolonged release
... pain medication. Reduction in pain and adverse events were also identified a priori and were reviewed. The use of breakthrough medication increased in all groups, with no significant difference between groups. There were no statistically significant differences between groups for any other efficacy ...
... pain medication. Reduction in pain and adverse events were also identified a priori and were reviewed. The use of breakthrough medication increased in all groups, with no significant difference between groups. There were no statistically significant differences between groups for any other efficacy ...
ARISE Curriculum Guide Chemistry: Topic 21—Organic Chemistry ChemMatters
... Order a CD with 25 years of ChemMatters, $30 Articles for Student Use The Absorbing Story of the Thirsty Polymer: Oct. 1999, pp. 4-5. Alcohol: Feb. 1985, pp. 8-11. Antifreeze Antidote: Oct. 1996, pp. 4-6. Artificial Sweeteners: Feb. 1988, pp. 4-8. Aspirin: Feb. 1993, pp. 4-7. A calorie-free fat? Apr ...
... Order a CD with 25 years of ChemMatters, $30 Articles for Student Use The Absorbing Story of the Thirsty Polymer: Oct. 1999, pp. 4-5. Alcohol: Feb. 1985, pp. 8-11. Antifreeze Antidote: Oct. 1996, pp. 4-6. Artificial Sweeteners: Feb. 1988, pp. 4-8. Aspirin: Feb. 1993, pp. 4-7. A calorie-free fat? Apr ...
Context-induced relapse to drug seeking: a review
... throughout the period of self-administration; a different stimulus, termed the SK (or SD), is presented when the drug is not available on alternate days or sessions. Investigators have used discrimination procedures to study the role of discriminative drug cues on reinstatement of drug seeking (McFa ...
... throughout the period of self-administration; a different stimulus, termed the SK (or SD), is presented when the drug is not available on alternate days or sessions. Investigators have used discrimination procedures to study the role of discriminative drug cues on reinstatement of drug seeking (McFa ...
Bioisosterism: A Rational Approach in Drug Design
... a Concentration of compound that decreased specific binding of 1.5 nM [3H]diazepam to rat brain receptors by 50%. ...
... a Concentration of compound that decreased specific binding of 1.5 nM [3H]diazepam to rat brain receptors by 50%. ...
Speaker`s Notes
... For example, your pig may be extremely sick and you think that Q. T/F: One benefit of a VCPR is that your you need to give it a little more veterinarian will be able to assist you with medication than the medication withdrawal times and recordkeeping. label instructs you to give to A. TRUE make sure ...
... For example, your pig may be extremely sick and you think that Q. T/F: One benefit of a VCPR is that your you need to give it a little more veterinarian will be able to assist you with medication than the medication withdrawal times and recordkeeping. label instructs you to give to A. TRUE make sure ...
Potassium Sparing Diuretics
... Aldosterone enhance K+ secretion by increasing Na+/K+ ATPase and the same for H+ . Therefore, Spironolactone binds to mineralocorticoid receptors “Lippincott: Spironolactone is asynthetic steroid that antagonizes aldosterone at intracellular cytoplasmic receptor sites. The spironolactone-receptor co ...
... Aldosterone enhance K+ secretion by increasing Na+/K+ ATPase and the same for H+ . Therefore, Spironolactone binds to mineralocorticoid receptors “Lippincott: Spironolactone is asynthetic steroid that antagonizes aldosterone at intracellular cytoplasmic receptor sites. The spironolactone-receptor co ...
ROBERT E. GOLDSTEIN and STEPHEN E. EPSTEIN 1973;48:917-920 doi: 10.1161/01.CIR.48.5.917
... -care must be observed in choice of drug dosage-particularly when comparing two or more agents. Amplitude and duration of drug response are, in general, intimately related to the particular drug dose administered. Thus, a larger dose of a given drug may appear relatively "long-acting" simply because ...
... -care must be observed in choice of drug dosage-particularly when comparing two or more agents. Amplitude and duration of drug response are, in general, intimately related to the particular drug dose administered. Thus, a larger dose of a given drug may appear relatively "long-acting" simply because ...
Is there an interaction between warfarin and proton pump inhibitors?
... Warfarin is the anticoagulant of choice in the UK for a number of conditions including prophylaxis of deep vein thrombosis (DVT), treatment of DVT and pulmonary embolism, atrial fibrillation, cardioversion and dilated cardiomyopathy (1). Patients taking warfarin are monitored regularly to check prot ...
... Warfarin is the anticoagulant of choice in the UK for a number of conditions including prophylaxis of deep vein thrombosis (DVT), treatment of DVT and pulmonary embolism, atrial fibrillation, cardioversion and dilated cardiomyopathy (1). Patients taking warfarin are monitored regularly to check prot ...
annexure – ii - Rajiv Gandhi University of Health Sciences
... COURSE OF THE STUDY & Master of Pharmacy ...
... COURSE OF THE STUDY & Master of Pharmacy ...
Ocular Drug Delivery
... physiological barriers obstruct drug entry into posterior ocular tissues such as retina and choroid. After topical instillation, a large fraction (about 90%) of the applied dose is lost due to nasolacrimal drainage, tear dilution, and tear turnover, leading to poor ocular bioavailability. Less than ...
... physiological barriers obstruct drug entry into posterior ocular tissues such as retina and choroid. After topical instillation, a large fraction (about 90%) of the applied dose is lost due to nasolacrimal drainage, tear dilution, and tear turnover, leading to poor ocular bioavailability. Less than ...
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.