Pharmaceutical Medicinal Chemistry-3
... Course module description: The first part of the subject deals with drugs used in cancer with main emphasis on alkylating agents, platinum based drugs, antimetabolites, antibiotics, mitotic inhibitors and combination therapy. The second part of the course will concentrate on studying diuretics and r ...
... Course module description: The first part of the subject deals with drugs used in cancer with main emphasis on alkylating agents, platinum based drugs, antimetabolites, antibiotics, mitotic inhibitors and combination therapy. The second part of the course will concentrate on studying diuretics and r ...
Tip sheet for cutting down alcohol consumption
... Usually, it is of little use to try and get patients off a number of drugs simultaneously; negotiate with them about their priorities and the most significant risks to their health and well being. Generally, try approaching polydrug use sequentially, acknowledging the need to minimise harm as effect ...
... Usually, it is of little use to try and get patients off a number of drugs simultaneously; negotiate with them about their priorities and the most significant risks to their health and well being. Generally, try approaching polydrug use sequentially, acknowledging the need to minimise harm as effect ...
Core Concepts in Pharmacology
... • What other organs are involved in excretion? • What effect will liver or kidney impairment have on the pharmacokinetics of medication. • What are the implications for the prescriber? ...
... • What other organs are involved in excretion? • What effect will liver or kidney impairment have on the pharmacokinetics of medication. • What are the implications for the prescriber? ...
Substance abuse
... • May be pharmacokinetic or pharmacodynamic tolerance • pharmacokinetic : induction of hepatic metabolic enzymes e.g. barbiturates; • pharmacodynamic: alteration at receptor levels e.g. decrease of GABA receptors followed by increase of barbiturate administration; morphine and its receptor. • Tolera ...
... • May be pharmacokinetic or pharmacodynamic tolerance • pharmacokinetic : induction of hepatic metabolic enzymes e.g. barbiturates; • pharmacodynamic: alteration at receptor levels e.g. decrease of GABA receptors followed by increase of barbiturate administration; morphine and its receptor. • Tolera ...
Airgas template
... • A prolonged time may be required for an adverse reaction to become apparent. • Adverse reactions can be demonstrated after a drug has been discontinued. • Adverse reactions can develop to drugs that have been used for a long period without problems. ...
... • A prolonged time may be required for an adverse reaction to become apparent. • Adverse reactions can be demonstrated after a drug has been discontinued. • Adverse reactions can develop to drugs that have been used for a long period without problems. ...
Regulatory Authority Mission
... “ … as the absence of a significant difference in the rate and extent to which the active ingredient or active moiety in the pharmaceutical equivalents or pharmaceutical alternatives becomes available at the site of drug action when administered at the same molar dose under similar conditions ...
... “ … as the absence of a significant difference in the rate and extent to which the active ingredient or active moiety in the pharmaceutical equivalents or pharmaceutical alternatives becomes available at the site of drug action when administered at the same molar dose under similar conditions ...
Chapter 1 An Introduction To Pharmacology
... procedures such as surgery, are also important, of course, but none is so widely applied as drug-based therapeutics. The Main Branches of Pharmacology Clinical pharmacology Biochemical pharmacology Molecular pharmacology Immunopharmacology Cardiovascular pharmacology Neuropharmacology Pharmacogeneti ...
... procedures such as surgery, are also important, of course, but none is so widely applied as drug-based therapeutics. The Main Branches of Pharmacology Clinical pharmacology Biochemical pharmacology Molecular pharmacology Immunopharmacology Cardiovascular pharmacology Neuropharmacology Pharmacogeneti ...
Program Status
... marketed therapeutics, they provide opportunities for producing first-of-class drugs. A benefit of the program diversity is thsat it provides a hedges against drug development risks. Tularik has identified lead compounds for 27 of company-validated targets. Thirteen of these lead compounds are being ...
... marketed therapeutics, they provide opportunities for producing first-of-class drugs. A benefit of the program diversity is thsat it provides a hedges against drug development risks. Tularik has identified lead compounds for 27 of company-validated targets. Thirteen of these lead compounds are being ...
Chapter 1 - Drugs and Agents - Factors Affecting their Action
... chemical properties of drugs Also looks at the ways in which drugs affect living systems Various subdivisions of pharmacology have evolved ...
... chemical properties of drugs Also looks at the ways in which drugs affect living systems Various subdivisions of pharmacology have evolved ...
Pharmacology Basics
... Absorption may be further influenced by gut motility, prior surgery to the intestines, simultaneous intake of food, other drugs, and many other factors. ...
... Absorption may be further influenced by gut motility, prior surgery to the intestines, simultaneous intake of food, other drugs, and many other factors. ...
Pharmacokinetics for the Non-Specialist
... rate. At the point of Cmax, these two rates are equal and after this the elimination rate is greater than the absorption rate. Eventually the concentration of the drug decreases and the effect diminishes. ...
... rate. At the point of Cmax, these two rates are equal and after this the elimination rate is greater than the absorption rate. Eventually the concentration of the drug decreases and the effect diminishes. ...
Document
... Drugs may bind to both their desired target and to other molecules in an organism. If interactions with other targets are negligible then a drug is said to be specific. In most cases drugs will show a non-exclusive preference for their target - selective. The interaction with both their inte ...
... Drugs may bind to both their desired target and to other molecules in an organism. If interactions with other targets are negligible then a drug is said to be specific. In most cases drugs will show a non-exclusive preference for their target - selective. The interaction with both their inte ...
Pharmacology
... • Essential Medicines (drugs) - those that satisfy the priority healthcare needs of the population. • They are selected with due regard to public health relevance, evidence on efficacy and safety, and comparative cost effectiveness. • Essential medicines are intended to be available within the cont ...
... • Essential Medicines (drugs) - those that satisfy the priority healthcare needs of the population. • They are selected with due regard to public health relevance, evidence on efficacy and safety, and comparative cost effectiveness. • Essential medicines are intended to be available within the cont ...
PHARMACOLOGY AND PRINCIPLES OF DRUG ACTION
... What is pharmacology? • Medical pharmacology is the science of chemicals (drugs) that interact with the human body. ...
... What is pharmacology? • Medical pharmacology is the science of chemicals (drugs) that interact with the human body. ...
Lecture 3 - personal.kent.edu
... A. Drug administration and absorption 1. Ingestion 2. Injection 3. Inhalation 4. Absorption B. Drug metabolism VI. Tolerance A. Cross tolerance B. Tolerance develops to some chars (effects) but not others C. Types of tolerance 1. decreased drug binding (sequestering) 2. binding has less effect 3. me ...
... A. Drug administration and absorption 1. Ingestion 2. Injection 3. Inhalation 4. Absorption B. Drug metabolism VI. Tolerance A. Cross tolerance B. Tolerance develops to some chars (effects) but not others C. Types of tolerance 1. decreased drug binding (sequestering) 2. binding has less effect 3. me ...
Drugs - Images
... on an individual. Intensity of dependence depends on the nature of the drug. Drugs resulting in high degree of ...
... on an individual. Intensity of dependence depends on the nature of the drug. Drugs resulting in high degree of ...
A Primer on Pharmacological Processes
... curves. ED, or Effective Dose, refers to the amount of a drug needed to have a desired effect. LD, or Lethal Dose, the amount of a drug needed to cause death. Together, these form the therapeutic index. Pharmacodynamics refers to the changes to the brain and body as a result of taking a pharmacologi ...
... curves. ED, or Effective Dose, refers to the amount of a drug needed to have a desired effect. LD, or Lethal Dose, the amount of a drug needed to cause death. Together, these form the therapeutic index. Pharmacodynamics refers to the changes to the brain and body as a result of taking a pharmacologi ...
Student Lesson Guide
... 4. Why does an atom make an ionic bond only with certain other atoms? 5. Compare the possession of electrons in ionic and covalent bonds. 6. What types of particles are formed by covalent bonds? 7. What is the difference in polar and non-polar molecules? Chapter 19 – Section 3 1. What is a binary co ...
... 4. Why does an atom make an ionic bond only with certain other atoms? 5. Compare the possession of electrons in ionic and covalent bonds. 6. What types of particles are formed by covalent bonds? 7. What is the difference in polar and non-polar molecules? Chapter 19 – Section 3 1. What is a binary co ...
Medicines additional questions LT Scotland
... Drug discovery in the first half of the twentieth century owe d much to good fortune and good observation. For example, sulphonamides were discovered when it was found that certain dyes had antibacterial activity. Penicillin was discovered when Alexander Fleming returned from holiday and noticed a f ...
... Drug discovery in the first half of the twentieth century owe d much to good fortune and good observation. For example, sulphonamides were discovered when it was found that certain dyes had antibacterial activity. Penicillin was discovered when Alexander Fleming returned from holiday and noticed a f ...
General and Physical Chemistry
... Grades: Final exam 70%, Home tasks 15%, Midterm exam 10%, level exam ...
... Grades: Final exam 70%, Home tasks 15%, Midterm exam 10%, level exam ...
BDS Ist YEAR EXAMINATION 2008-09
... Describe various mechanism of drug action with suitable example. ...
... Describe various mechanism of drug action with suitable example. ...
RATIONAL DRUG THERAPY
... 3) Routes of administration : 1) Oral route : Easiest, least expensive and most convenient. Its not appropriate in very young infants and in short bowel syndrome. 2) Rectal route : Its reserved for those who cannot take oral medications. However drug distribution with it is not uniform. 3) Parenter ...
... 3) Routes of administration : 1) Oral route : Easiest, least expensive and most convenient. Its not appropriate in very young infants and in short bowel syndrome. 2) Rectal route : Its reserved for those who cannot take oral medications. However drug distribution with it is not uniform. 3) Parenter ...
REGULATORY REQUIREMENTS FOR PREFORMULATION STUDIES
... the timing of anti microbial tests for preservatives E.g.: Japan does not accept phenol, where it is commonly used in US. The ...
... the timing of anti microbial tests for preservatives E.g.: Japan does not accept phenol, where it is commonly used in US. The ...
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.