Drug use in renal and hepatic disorders.
... ECF ( ascites, edema) & ↓↓ muscle mass. •↓↓ plasma protein binding due to impaired albumin production or drug displacement from accumulated substance normally cleared by the liver •↑ Bio avail through ↓↓ first pass metabolism •↓↓ Bioavailability due to malabsorption of fats in cholestatic liver dise ...
... ECF ( ascites, edema) & ↓↓ muscle mass. •↓↓ plasma protein binding due to impaired albumin production or drug displacement from accumulated substance normally cleared by the liver •↑ Bio avail through ↓↓ first pass metabolism •↓↓ Bioavailability due to malabsorption of fats in cholestatic liver dise ...
More Dosage calculations 2
... 4. Pediatric Dosage: Dosage calculations in pediatrics is based on age, body surface area (BSA) and body weight. BSA and body weight are the methods most frequently used to calculate pediatric dosage. Following are the formulas used for these calculations. Clark’s rule: Weight of child divided by 15 ...
... 4. Pediatric Dosage: Dosage calculations in pediatrics is based on age, body surface area (BSA) and body weight. BSA and body weight are the methods most frequently used to calculate pediatric dosage. Following are the formulas used for these calculations. Clark’s rule: Weight of child divided by 15 ...
Animal Use Protocol – Hazardous Agent Addendum (Chemicals
... recommended choices (eg. Recommendation of lab coat, gloves, and use of a fumehood/BSCII for a particular material). Once you have completed all areas of this form for your specific usage, taking into account the [red] recommendations, please change all text to [black]. Please remove these instructi ...
... recommended choices (eg. Recommendation of lab coat, gloves, and use of a fumehood/BSCII for a particular material). Once you have completed all areas of this form for your specific usage, taking into account the [red] recommendations, please change all text to [black]. Please remove these instructi ...
Ayurveda and Traditional Chinese Medicine: A Comparative
... Increased side effects, lack of curative treatment for several chronic diseases, high cost of new drugs, microbial resistance and emerging diseases are some reasons for renewed public interest in complementary and alternative medicines (1). It has been postulated that by 2010 at least two-thirds of ...
... Increased side effects, lack of curative treatment for several chronic diseases, high cost of new drugs, microbial resistance and emerging diseases are some reasons for renewed public interest in complementary and alternative medicines (1). It has been postulated that by 2010 at least two-thirds of ...
งานนำเสนอ PowerPoint
... any unwanted change from an organism’s normal state dependent upon the concentration of active compound at the target site (receptor)for a sufficient time. ...
... any unwanted change from an organism’s normal state dependent upon the concentration of active compound at the target site (receptor)for a sufficient time. ...
A-level Chemistry
... To develop a candidate’s knowledge and understanding of chemistry and provide a pathway to further education and/or work ...
... To develop a candidate’s knowledge and understanding of chemistry and provide a pathway to further education and/or work ...
On-Label and Off-Label Usage of Prescription Medicines and
... tested, has been tested or will be tested to assess the efficacy for a particular condition, and to include scientific evidence to suggest that the off-label usage of the product (prescription medicine) offers a viable alternative or clinical advantage over currently available options. 2) To prescri ...
... tested, has been tested or will be tested to assess the efficacy for a particular condition, and to include scientific evidence to suggest that the off-label usage of the product (prescription medicine) offers a viable alternative or clinical advantage over currently available options. 2) To prescri ...
IN SITU FOR LEVOFLOXACIN HYDROCHLORIDE Research Article
... Ophthalmic drug delivery is one of the most interesting and challenging areas facing the pharmaceutical scientist. The unique anatomy and physiology of the eye make it difficult to achieve an effective drug concentration at the target site. The challenge remains to ci ...
... Ophthalmic drug delivery is one of the most interesting and challenging areas facing the pharmaceutical scientist. The unique anatomy and physiology of the eye make it difficult to achieve an effective drug concentration at the target site. The challenge remains to ci ...
Organic alcohols and Ethers by Dr. Alaa J.Mahrath
... Ethanol, we know, is made when fruit sugars ferment. Ethanol (and methanol) can become an addictive material. Prolonged intake can damage tissues, particularly the liver. It has been found that people with alcohol dependency can be treated using a drug called ‘antabuse’ or disulfiran, which has no e ...
... Ethanol, we know, is made when fruit sugars ferment. Ethanol (and methanol) can become an addictive material. Prolonged intake can damage tissues, particularly the liver. It has been found that people with alcohol dependency can be treated using a drug called ‘antabuse’ or disulfiran, which has no e ...
orodispersible_dosage_forms
... -Rate of absorption from the saliva solution; and -Overall bioavailability. a.Zydis Technology Using concept of Gregory et al.51 Scherer has patented the Zydis technology. Zydis, the best known of the fast-dissolving/disintegrating tablet preparations, was the first marketed new technology tablet. T ...
... -Rate of absorption from the saliva solution; and -Overall bioavailability. a.Zydis Technology Using concept of Gregory et al.51 Scherer has patented the Zydis technology. Zydis, the best known of the fast-dissolving/disintegrating tablet preparations, was the first marketed new technology tablet. T ...
Chapter 11 Chemical Reactions
... only C, H, (and maybe O) is reacted with oxygen – usually called “burning” If the combustion is complete, the products will be CO2 and H2O. If the combustion is incomplete, the products will be CO (or possibly just C) and H2O. ...
... only C, H, (and maybe O) is reacted with oxygen – usually called “burning” If the combustion is complete, the products will be CO2 and H2O. If the combustion is incomplete, the products will be CO (or possibly just C) and H2O. ...
Dissolution testing and in vitro in vivo correlation of conventional
... subjects to characterize adequately the performance of the drug product under study. ! Any in vitro dissolution method may be used to obtain the dissolution characteristics of the dosage form. The same system should be used for all formulations tested. ! The preferred dissolution apparatus is USP ap ...
... subjects to characterize adequately the performance of the drug product under study. ! Any in vitro dissolution method may be used to obtain the dissolution characteristics of the dosage form. The same system should be used for all formulations tested. ! The preferred dissolution apparatus is USP ap ...
An Identification Guide - Sunshine Coast Health Centre
... cal uses, effect duration, or methods of ingestion (oral, injected, smoked, or snorted). However, drugs within a particular class typically share similar effects, overdose risk, and withdrawal symptoms. Although considered a hallucinogen, the prevalence and unique features of cannabis warrant a sepa ...
... cal uses, effect duration, or methods of ingestion (oral, injected, smoked, or snorted). However, drugs within a particular class typically share similar effects, overdose risk, and withdrawal symptoms. Although considered a hallucinogen, the prevalence and unique features of cannabis warrant a sepa ...
New Initiatives and Building on Lessons Learned Presentation
... • MRI • Vision Screening • Skin Biopsy and Fibroblast Cell Culture ...
... • MRI • Vision Screening • Skin Biopsy and Fibroblast Cell Culture ...
ANTIMICROBIAL DRUGS
... Note: In concomitant use with Amphotericin b, Aminoglycosides, Colistimethate sodium – increased risk of development and severity of nephrotoxicity, ototoxicity. The use with furosemide - increased risk of ototoxicity ( for all – OTO - and nephro-toxicity). ...
... Note: In concomitant use with Amphotericin b, Aminoglycosides, Colistimethate sodium – increased risk of development and severity of nephrotoxicity, ototoxicity. The use with furosemide - increased risk of ototoxicity ( for all – OTO - and nephro-toxicity). ...
Effect & Sites of Action of Different Agonist Drugs on The Isolated
... analgesic, effect on blood pressure ...
... analgesic, effect on blood pressure ...
2016 MLI Biennial Drug Alch Policy Review
... legs, nodding, lack of sex drive and appetite, sweating, cramps and nausea when withdrawing from the drug. Treatment: Medication and behavioral therapy, alone or in combination, are aspects of an overall therapeutic process that often begins with detoxification, followed by treatment and relapse pre ...
... legs, nodding, lack of sex drive and appetite, sweating, cramps and nausea when withdrawing from the drug. Treatment: Medication and behavioral therapy, alone or in combination, are aspects of an overall therapeutic process that often begins with detoxification, followed by treatment and relapse pre ...
An overview of the evidence and mechanisms of herb–drug
... structured assessment procedure, the evidence of HDI presents with varying degree of clinical significance. While the potential for HDI for a number of herbal products is inferred from non-human studies, certain HDIs are well established through human studies and documented case reports. Various mech ...
... structured assessment procedure, the evidence of HDI presents with varying degree of clinical significance. While the potential for HDI for a number of herbal products is inferred from non-human studies, certain HDIs are well established through human studies and documented case reports. Various mech ...
Biomarkers and surrogate endpoints: How and when might they
... search. There is significant value in measuring appropriately selected biomarkers in early phase development of the NME to ensure that it alters the pharmacology/physiology/pathology as desired. A NME that does not demonstrate a change in the pathway it is supposed to affect, may have a lower likeli ...
... search. There is significant value in measuring appropriately selected biomarkers in early phase development of the NME to ensure that it alters the pharmacology/physiology/pathology as desired. A NME that does not demonstrate a change in the pathway it is supposed to affect, may have a lower likeli ...
Pharmacokinetic Considerations
... Monitor drug levels—free phenytoin level with low albumin • Ex: warfarin, phenytoin, naproxen ...
... Monitor drug levels—free phenytoin level with low albumin • Ex: warfarin, phenytoin, naproxen ...
Slide 1
... • Identify the signs of addiction and discuss types of addictions, including compulsive behaviors such as gambling and shopping. • Identify the six categories of drugs and distinguish between drug misuse and drug abuse. • Discuss the issues of over-the-counter and prescription drug misuse and abuse, ...
... • Identify the signs of addiction and discuss types of addictions, including compulsive behaviors such as gambling and shopping. • Identify the six categories of drugs and distinguish between drug misuse and drug abuse. • Discuss the issues of over-the-counter and prescription drug misuse and abuse, ...
L04 Cannabinoids Part 1 Medicinal Plants
... We will continue today with the nicest topic in medicinal chemistry, phytochemistry or even in pharmacology, which is discussed in the different disciplines of PHARMACY♥, the Cannabinoids, we headline it as the chemistry of the metabolism of cannabinoids because it’s such a big topic not a lecture ...
... We will continue today with the nicest topic in medicinal chemistry, phytochemistry or even in pharmacology, which is discussed in the different disciplines of PHARMACY♥, the Cannabinoids, we headline it as the chemistry of the metabolism of cannabinoids because it’s such a big topic not a lecture ...
Mechanism of action
... Large doses of tetracycline and chloramphenicol are toxic as they interact with mitochondrial ribosomes (which are nearly similar in human and bacteria). ...
... Large doses of tetracycline and chloramphenicol are toxic as they interact with mitochondrial ribosomes (which are nearly similar in human and bacteria). ...
Chemistry Syllabus
... b. Relate the information to the concepts you are studying. Discuss the patterns of the graphs how they relate to the concept. If there is no graph, use the data to help explain the concept. Error Analysis (Sources of Error): This is the last section where you explain what errors were committed duri ...
... b. Relate the information to the concepts you are studying. Discuss the patterns of the graphs how they relate to the concept. If there is no graph, use the data to help explain the concept. Error Analysis (Sources of Error): This is the last section where you explain what errors were committed duri ...
Surface Contamination on Packages and Vials of Hazardous Drugs
... medication-use safety, (2) quality, (3) outcomes, and (4) the value of drug therapy; further, To encourage pharmacy department leaders to develop and maintain patientcentered practice models that integrate into a team all pharmacy professionals engaged in the medication-use process, including genera ...
... medication-use safety, (2) quality, (3) outcomes, and (4) the value of drug therapy; further, To encourage pharmacy department leaders to develop and maintain patientcentered practice models that integrate into a team all pharmacy professionals engaged in the medication-use process, including genera ...
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.