Acta okl1-2014.cdr - Polskie Towarzystwo Farmaceutyczne
... AGNIESZKA MICHALAK* and GRAØYNA BIA£A Chair and Department of Pharmacology and Pharmacodynamics, Medical University of Lublin, Chodüki 4A, 20-093 Lublin, Poland Abstract: The consequences of alcohol dependence concern serious health care, social and economic problems. The scope of many studies is to ...
... AGNIESZKA MICHALAK* and GRAØYNA BIA£A Chair and Department of Pharmacology and Pharmacodynamics, Medical University of Lublin, Chodüki 4A, 20-093 Lublin, Poland Abstract: The consequences of alcohol dependence concern serious health care, social and economic problems. The scope of many studies is to ...
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... ● Medicinal chemistry is a chemistry-based discipline, also involving aspects of biological, medical and pharmaceutical sciences. It is concerned with the invention, discovery, design, identification and preparation of biologically active compounds, the study of their metabolism, the interpretation ...
... ● Medicinal chemistry is a chemistry-based discipline, also involving aspects of biological, medical and pharmaceutical sciences. It is concerned with the invention, discovery, design, identification and preparation of biologically active compounds, the study of their metabolism, the interpretation ...
Mechanism of Action
... The onset of action of loratadine 1-3 hours Peak effects in 8-12 hours Duration of action greater than 24 hours The normal mean elimination half-lives of loratadine and its metabolite 8.4 hours (range 3-20 hours) and 28 hours, respectively. Elimination occurs through the fecal and rena ...
... The onset of action of loratadine 1-3 hours Peak effects in 8-12 hours Duration of action greater than 24 hours The normal mean elimination half-lives of loratadine and its metabolite 8.4 hours (range 3-20 hours) and 28 hours, respectively. Elimination occurs through the fecal and rena ...
Chapter-1 Introduction 1.1 INTRODUCTION
... Convenience of administration and patient compliance are gaining significant importance in the design of dosage forms. Recently, more stress is laid down on the development of organoleptically elegant and patient friendly drug delivery system for paediatric and geriatric patients (Bhusan SY,2000, Wa ...
... Convenience of administration and patient compliance are gaining significant importance in the design of dosage forms. Recently, more stress is laid down on the development of organoleptically elegant and patient friendly drug delivery system for paediatric and geriatric patients (Bhusan SY,2000, Wa ...
New Mexico EMS - New Mexico Department of Health
... 1. Activated charcoal is used in the treatment of certain cases of poisoning and over-doses in the alert patient. Most commonly given in the hospital after gastric lavage, but it is appropriate to give in the pre-hospital setting before lavage if a long transport time is anticipated. CONTRAINDICATIO ...
... 1. Activated charcoal is used in the treatment of certain cases of poisoning and over-doses in the alert patient. Most commonly given in the hospital after gastric lavage, but it is appropriate to give in the pre-hospital setting before lavage if a long transport time is anticipated. CONTRAINDICATIO ...
European Credit Transfer and Accumulation System
... CONTENTS: Nomenclature of organic compounds; structure of substances from the quantum-mechanical point of view; basics of stereochemistry; relationship between structure and reactivity; mechanisms of organic reactions; spectral methods of analysis (infrared spectroscopy, nuclear magnetic resonance, ...
... CONTENTS: Nomenclature of organic compounds; structure of substances from the quantum-mechanical point of view; basics of stereochemistry; relationship between structure and reactivity; mechanisms of organic reactions; spectral methods of analysis (infrared spectroscopy, nuclear magnetic resonance, ...
Drug Metabolism Phcy 172 - University of North Carolina at
... • Aryl hydrocarbon receptor (AHR) is a basic helixloop-helix (bHLH) protein belonging to the PerArnt-Sim (PAS) family of transcription factors • It transcriptionally induces expression of hepatic CYP1A1, CYP1A2, and CYP1B1 , as well as several other genes, including some phase II metabolizing enzyme ...
... • Aryl hydrocarbon receptor (AHR) is a basic helixloop-helix (bHLH) protein belonging to the PerArnt-Sim (PAS) family of transcription factors • It transcriptionally induces expression of hepatic CYP1A1, CYP1A2, and CYP1B1 , as well as several other genes, including some phase II metabolizing enzyme ...
Drug-related morbidity and mortality: Pharmacoepidemiological aspects Anna K. Jönsson
... the patient as well as for society. Suspected ADRs have been reported to occur in about 214% of hospitalised patients. In about 5% of deceased hospitalised patients suspected ADRs may have caused or contributed to the fatal outcome. When a pharmaceutical drug is approved for marketing, the drug has ...
... the patient as well as for society. Suspected ADRs have been reported to occur in about 214% of hospitalised patients. In about 5% of deceased hospitalised patients suspected ADRs may have caused or contributed to the fatal outcome. When a pharmaceutical drug is approved for marketing, the drug has ...
Digoxin
... Toxicity is difficult to diagnose as anorexia, nausea and vomiting, mental confusion and cardiac arrhythmias may all be signs of both cardiac failure and digoxin toxicity. Specific signs of toxicity include bradycardia, bigeminy, reverse tick on ECG and visual disturbances. Digibind administration m ...
... Toxicity is difficult to diagnose as anorexia, nausea and vomiting, mental confusion and cardiac arrhythmias may all be signs of both cardiac failure and digoxin toxicity. Specific signs of toxicity include bradycardia, bigeminy, reverse tick on ECG and visual disturbances. Digibind administration m ...
Size: 841 kB 25th Aug 2014 Pharmacology Basics
... • Once the drug has been absorbed from the stomach and/or intestines (GI tract) into the blood, it is circulated to some degree to all areas of the body to which there is blood flow…this process is distribution (the choo-choo so to speak) • Organs with high blood flow (brain, heart, liver, etc.) ar ...
... • Once the drug has been absorbed from the stomach and/or intestines (GI tract) into the blood, it is circulated to some degree to all areas of the body to which there is blood flow…this process is distribution (the choo-choo so to speak) • Organs with high blood flow (brain, heart, liver, etc.) ar ...
nephr%gy
... may occur [BIanco et al. 1997]. Clinical remission is not common in patients with HSP and, as Pillebout observed, it was achieved in only 20% out of250 adult patients [Pillehout et al. 2002]. Factors associated with a poor prognosis, like high degree of proteinuria, renal failure, high percentage of ...
... may occur [BIanco et al. 1997]. Clinical remission is not common in patients with HSP and, as Pillebout observed, it was achieved in only 20% out of250 adult patients [Pillehout et al. 2002]. Factors associated with a poor prognosis, like high degree of proteinuria, renal failure, high percentage of ...
Psychopharmacology for the Clinician
... study raised concerns about long-term symptom control and suggested that generic substitution be considered a potential indication for therapeutic drug monitoring.12,13 For pharmacokinetic bioequivalence, the generic and brand-name medication must have maximum plasma concentration (Cmax) and the are ...
... study raised concerns about long-term symptom control and suggested that generic substitution be considered a potential indication for therapeutic drug monitoring.12,13 For pharmacokinetic bioequivalence, the generic and brand-name medication must have maximum plasma concentration (Cmax) and the are ...
Guidelines for Registration of Fixed
... The World Health Organization has published a series of guidelines relating to marketing authorization of finished pharmaceutical products (FPPs) (see Table 1). Currently there are no specific international guidelines for FDCs. Some national authorities have developed their own guidelines, some for ...
... The World Health Organization has published a series of guidelines relating to marketing authorization of finished pharmaceutical products (FPPs) (see Table 1). Currently there are no specific international guidelines for FDCs. Some national authorities have developed their own guidelines, some for ...
Molecular Pharmacology of Nucleoside and Nucleotide HIV
... antiviral drug to be approved for clinical use. Zidovudine is a thymidine analog in which the 3’-OH group has been replaced with an azido (-N3) group (Figure 1). Zidovudine permeates the cell membrane by passive transport and not via a nucleoside carrier transporter (Zimmerman et al., 1987). It has ...
... antiviral drug to be approved for clinical use. Zidovudine is a thymidine analog in which the 3’-OH group has been replaced with an azido (-N3) group (Figure 1). Zidovudine permeates the cell membrane by passive transport and not via a nucleoside carrier transporter (Zimmerman et al., 1987). It has ...
A Rare Case of Domperidone Induced Oculogyric Crisis in Young
... chances of symptoms occurring again are high. ...
... chances of symptoms occurring again are high. ...
Overdose Emergency Procedures and Narcan
... Using prescription drugs prescribed to someone else Users who snorts or inject drugs for greater effects Former users who are recently released from prison or who entering and exiting from drug treatment programs Only 17 % of opiate related deaths are among new users As many as 1 in 4 people who rec ...
... Using prescription drugs prescribed to someone else Users who snorts or inject drugs for greater effects Former users who are recently released from prison or who entering and exiting from drug treatment programs Only 17 % of opiate related deaths are among new users As many as 1 in 4 people who rec ...
formulation and evalution of medicated chewing gum of
... Medicated Chewing Gums are solid, single dose preparations with a base consisting mainly of gum that is intended to be chewed but not swallowed. They contain one or more active substance which released by chewing and are to be used for local treatment diseases of oral cavity as well as treatment of ...
... Medicated Chewing Gums are solid, single dose preparations with a base consisting mainly of gum that is intended to be chewed but not swallowed. They contain one or more active substance which released by chewing and are to be used for local treatment diseases of oral cavity as well as treatment of ...
Drug treatment of paediatric epilepsy RICHARD E. APPLETON and J. HELEN CROSS
... appear to have the broadest spectrum of action, being effective against many generalised and focal seizure types, and relatively free of serious side effects, other than lamotrigine producing an allergic or idiosyncratic rash, that rarely develops into Stevens-Johnson syndrome6,7. Lamotrigine can be ...
... appear to have the broadest spectrum of action, being effective against many generalised and focal seizure types, and relatively free of serious side effects, other than lamotrigine producing an allergic or idiosyncratic rash, that rarely develops into Stevens-Johnson syndrome6,7. Lamotrigine can be ...
ICH, WHO AND SUPAC GUIDELINES ICH GUIDELINES
... product registration in order to reduce or obviate the need to duplicate the testing carried out during the research and development of new medicines. The objective of such harmonisation is a more economical use of human, animal and material resources, and the elimination of unnecessary delay in the ...
... product registration in order to reduce or obviate the need to duplicate the testing carried out during the research and development of new medicines. The objective of such harmonisation is a more economical use of human, animal and material resources, and the elimination of unnecessary delay in the ...
Solid dosage forms
... drug will dissolve at different rates. They are designed to produce drug effects over an extended time. SR tablets are administered less frequently (usually once daily). e.g. Isoptin SR, Ravel SR ...
... drug will dissolve at different rates. They are designed to produce drug effects over an extended time. SR tablets are administered less frequently (usually once daily). e.g. Isoptin SR, Ravel SR ...
Final Program - American College of Clinical Pharmacology
... worked to develop a program focused on prominent global issues where clinical pharmacology can have an impact, resulting in a series of Workshops and Symposia that are timely and will critically challenge current and future practice and professional activity paradigms, while encouraging audience int ...
... worked to develop a program focused on prominent global issues where clinical pharmacology can have an impact, resulting in a series of Workshops and Symposia that are timely and will critically challenge current and future practice and professional activity paradigms, while encouraging audience int ...
The use of animals for research in the
... also important for the identification of disease mechanisms and for understanding how a person’s genes can affect both disease processes and their responses to medicines.14 Stage 2: identification of possible medicines 8.9 In the next stage, compounds that might interact with the selected targets ar ...
... also important for the identification of disease mechanisms and for understanding how a person’s genes can affect both disease processes and their responses to medicines.14 Stage 2: identification of possible medicines 8.9 In the next stage, compounds that might interact with the selected targets ar ...
... Drug resistance is a global public health problem particularly for the treatment of infectious diseases [1,2] and cancer [3]. It has become increasingly possible for cross country transmission of drug-resistant organisms. There is an urgent need to develop resistance-evading drugs. Several mechanism ...
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.