IMPORTANT PHARMACY SITES

>> Monday, January 18, 2010

SITES FOR PHARMACY

Click Into The title


Sites FOR Pharmacy Examination Board Of CANADA

1-Pharmacy Examination Board Of CANADA


2-PHARMALearn

3-RXBriefCase

4-Pharmacy Gateway

5-
Canadian Pharmacy Skills

6-International Pharmacy Bridging Program

7-Institute for Safe Medication Practices

8-Dalhousie University (Halifax, Nova Scotia)

9-
College of Pharmacists



10-College of Pharmacists of British Columbia
11-Canadian Pharmacists Association (CPhA)
12-National Association of Provincial Regulatory Authorities

13-
Health CANADA





GENERAL PHARMACY SITES

RxList Drug Info







EgyDocs Drug List






Drug Reference On line






Drugs.Com



















EgyPharmaZone







Sayadla.Com








Pharmacists World








PharmaGates











Clinical Pharmacology merck







U.S. Pharmacopeia




British National Formulary










































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And also TRY:
Adverse Drug Reaction DatabaseOpen
Medical CalculatorsOpen
All Refer Health.Open
Medlineplus.Open
NIST Chemistry Web BookOpen
HolisticOnLIne - Herbal medicine.Open
National Center of Biotechnology InformationOpen
Drug Bank.Open
Family Practice Notebook.Open
Healthopedia.Open
WebMD.Open
Medicine EncyclopediaOpen
Altdrug.Open
Drug digest.Open
Drug Information ResourcesOpen
Phramweb.Open
InterpharmaOpen
DrugInfonetOpen
Ebling LibraryOpen
PubMed CentralOpen
Online-medical-dictionaryOpen
Pharma lexiconOpen
BaloghOpen
National Electronic Library for MedicineOpen
keeps kid healthyOpen
All ExpertsOpen
All ExpertsOpen
Medication AdvisorOpen
Drugs News WireOpen
Medication SenseOpen
Health LinkOpen
MedicationWizardOpen
E-MedicomOpen
Pharmacy & Health InformationOpen
InPharmOpen

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MEDICINAL CHEMISTRY

Burger's Medicinal Chemistry and Drug Discovery, 6 Volume Set, 6th Edition



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Here >> Volumes from 1 to 5 only .. trying to find 6

This new sixth edition of Burger's Medicinal Chemistry and Drug Discovery offers several new and unique features. For the first time, an online version of this major reference work will offer updated content from the print edition and easy access. For the first time, all volumes are structured entirely according to content and published simultaneously to provide broad coverage of medicinal chemistry and drug discovery for new or experienced medicinal chemists, biologists, pharmacologists and molecular biologists. This includes a current and global perspective of drug design, and drug development.With expanded content from 69 chapters to over 100 chapters, this sixth edition of Burger's Medicinal Chemistry and Drug Discovery includes more than 50% new material. An entire section has been dedicated to cancer research. Areas included are those at the foreground of life science including:* Proteomics* Genomics* Bioinformatics* Combinatorial Chemistry* High-Throughput Screening* Blood Substitutes* Allosteric Effectors as Potential Drugs* COX Inhibitors* Statins* High-Throughput Pharmacology* and More.The new sixth edition of Burger's Medicinal Chemistry and Drug Discovery is a Memorial Edition to Professor Alfred Burger who published this major reference work in the first edition as "Medicinal Chemistry" in two volumes in 1951. Dr. Burger's research focused on analgesics, antidepressants and chemotherapeutic agents. He is one of the few academicians to have a drug, designed and synthesized in his laboratories and brought to market. Dr. Burger's contribution to the fields of medicinal chemistry and drug discovery are well renowned and documented. He received the Louis Pasteur Medal of the Pasteur Institute and the American Chemical Society Smissman Award.


Content



VOLUME 1
Structure Based Drug-Design
History of Quantitative Structure Activity Relationships
Recent and Developing Trends in QSAR: From Data Analysis and Model Validation to Drug Design and Discovery
Molecular Modeling in Drug Design
Drug-Target Binding Forces: Advances in Force Field Approaches
Combinatorial Library Design, Molecular Similarity and Diversity Applications
Virtual Screening
Docking and Scoring Functions/Virtual Screening
Bioinformatics
Chemical Information Computing Systems in Drug Discovery
X-ray Crystallography Drug Discovery
Electron Microscopy of Biological Macromolecules
Design of Peptidomimetics
Approaches to the Rational Design of Enzyme Inhibitors
Chirality and Biological Activity
Structural Concepts in the Prediction of the Toxicity of Therapeutical Agents
Natural Products as Leads for New Pharmaceuticals
Analog Design
NMR and Drug Discovery
Mass Spectrometry and Drug Design
VOLUME 2
Combinatorial Chemistry and Multiple Parallel Synthesis
Highthroughput Screening for Lead Discovery
High Throughput Pharmacology
The Application of Recombinant DNA Technology in Medicinal Chemistry and Drug Discovery
Oligonucleotide Therapeutics
Therapeutic Agents Acting on RNA
Carbohydrate Based Therapeutics
Membrane Transport Proteins and Drug Transport
Allosteric Proteins and Drug Discovery
Receptor Targets in Drug Discovery and Development
Large Scale Synthesis
Principles of Drug Metabolism
Metabolic Considerations in Prodrug Design
Retrometabolism-Based Drug Design and Targeting
Drug Discovery: The Role of Toxicology
Drug Absorption, Distribution, and Elimination
The FDA and Regulatory Issues
Intellectual Property in Drug Discovery and Biotechnology
Nicotinic Acetylcholine Receptors
Physicochemical Characterization and Principles of Oral Dosage Form Selection
VOLUME 3
Cardiac Drugs: Antianginal, Vosodilators, Antiarrhythmic
Diuretics and Uricosuric Agents
Myocardial Infarction Agents
Endogenous Vasoactive Peptides
Hematopoietic Agents
Anticoagulatns, Antithrombotics and Hemostatics
Antihyperlipedemic Agents
Oxygen Delivery via Allosteric Effectors of Hemoglobin, Blood Substitutes, and Plasma Expanders
Sickle Cell Anemia
Iron Chelators and Therapeutic Uses
Thyroid Hormones and Thyromimetics
Male Sex Hormones, Analogs, and Antogonists
Anti-inflammatory Steroids
Female Sex Hormones, Contraceptives & Fertility Drugs
Fundamentals of Steroid Chemistry and Biochemistry
VOLUME 4
Peptide and Protein Hormones, Peptide Neurotransmitters, and Therapeutic Agents
Inhibitors of Gastric Acid Secretion
Chemokines and Cytokine Modulators
COX Inhibitors and Leukotriene Modulators
Agents Acting on Prostanoid Receptors
Retinoids
Vitamins
Life Style and Over-the-Counter Agents
Radiopaques
Microarrays and Gene Expression Profiling Applied to Drug Research
SNPs: Single Nucleotide Polymorphisms and Pharmacogenomics
Gene Therapy with Plasmid DNA
Insulin and Hypoglycemic Agents
VOLUME 5
Molecular Biology of Cancer
Synthetic DNA-targeted Chemotherapeutic Agents and Related Tumor-Activated Prodrugs
Antitumor Natural Products
Radiosensitizers and Radioprotective Agents
Synthetic Anti-angiogenic Agents
Future Strategies in Immunotherapy
Selective Toxicities
Drug Resistance in Cancer Chemotherapy
Antiviral Agents, DNA
Antiviral Agents, RNA (Viruses other than HIV), Orthopoxviruses
Rationale of Design of Anti-HIV Drugs
Organ Transplantation Drugs
Synthetic Antibacterial Agents
Lactam Antibiotics
Tetracyclines, Aminolycoside, Macrolide, and Miscellaneous Antibiotics
Antimycobacterial Agents
Antifungal Agents
Antimalarial Agents
Antiprotozoal Agents
Anthelmintic Agents
VOLUME 6
Andrenergics and Andrenergic Blocking Agents
Cholinergics
Anticholinergic Drugs
CNS Stimulants
Sedatives and Hypnotics
Anticonvulsants
Analgesics
Antidepressants
Antianxiety Agents
Antipsychotic Agents
Investigative Agents for use in Neurodegenerative Conditions
Therapeutic and Diagnostic Agents for Parkinson's Disease
Alzheimer's Disease: Search for Therapeutics
Cognition Enhancers
Drugs to Treat Eating and Body Weight Disorders


Download

Vol 1 burgers medicinal chemistry.pdf
http://mihd.net/x2v7fc
Vol 2 burger textbook of medicinal chemistry.pdf
http://mihd.net/3qzpaf
Vol 3-burger medicinal chemistry.pdf
http://mihd.net/akzwnl
Vol 4-burger medicinal chemistry.pdf
http://mihd.net/xnugqw
Vol 5-burger medicinal chemistry.pdf
http://mihd.net/wy2s50
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Remington The Science and Practice of Pharmacy Twenty First Edition

Remington
The Science and Practice
of Pharmacy
Twenty First Edition




For over 100 years, Remington has been the definitive textbook and reference on the science and practice of pharmacy. This Twenty-First Edition keeps pace with recent changes in the pharmacy curriculum and professional pharmacy practice.
More than 95 new contributors and 5 new section editors provide fresh perspectives on the field. New chapters include pharmacogenomics, application of ethical principles to practice dilemmas, technology and automation, professional communication, medication errors, re-engineering pharmacy practice, management of special risk medicines, specialization in pharmacy practice, disease state management, emergency patient care, and wound care.
Purchasers of this textbook are entitled to a new, fully indexed Bonus CD-ROM, affording instant access to the full content of Remington in a convenient and portable format.
A must-have resource for all in the pharmaceutical industry!
Contents
I. Orientation
  1. Scope of Pharmacy
  2. Evolution of Pharmacy
  3. Ethics and Professionalism
  4. The Practice of Community Pharmacy
  5. Pharmacists in Industry
  6. Pharmacists in Government
  7. Pharmacists and Public Health
  8. Information Resources in Pharmacy and the Pharmaceutical Sciences
  9. Clinical Drug Literature
  10. Research
II. Pharmaceutics
  1. Metrology and Pharmaceutical Calculations
  2. Statistics
  3. Molecular Structure, Properties, and States of Matter
  4. Complex Formation
  5. Thermodynamics
  6. Solutions and Phase Equilibria
  7. Ionic Solutions and Electrolytic Equilibria
  8. Tonicity, Osmoticity, Osmolality, and Osmolarity
  9. Chemical Kinetics
  10. Interfacial Phenomena
  11. Colloidal Dispersions
  12. Coarse Dispersions
  13. Rheology
III. Pharmaceutical Chemistry
  1. Inorganic Pharmaceutical Chemistry
  2. Organic Pharmaceutical Chemistry
  3. Natural Products
  4. Drug Nomenclature—United States Adopted Names
  5. Structure-Activity Relationship and Drug Design
  6. Fundamentals of Medical Radionuclides
IV. Pharmaceutical Testing, Analysis and Control
  1. Analysis of Medicinals
  2. Biological Testing
  3. Clinical Analysis
  4. Chromatography
  5. Instrumental Methods of Analysis
  6. Dissolution
V. Pharmaceutical Manufacturing
  1. Separation
  2. Powders
  3. Property-Based Drug Design and Preformulation
  4. Solutions, Emulsions, Suspensions and Extracts
  5. Sterilization
  6. Parenteral Preparations
  7. Intravenous Admixtures
  8. Ophthalmic Preparations
  9. Medicated Topicals
  10. Oral Solid Dosage Forms
  11. Coating of Pharmaceutical Dosage Forms
  12. Extended-Release and Targeted Drug-Delivery Systems
  13. The New Drug Approval Process and Clinical Trial Design
  14. Biotechnology and Drugs
  15. Aerosols
  16. Quality Assurance and Control
  17. Stability of Pharmaceutical Products
  18. Bioavailability and Bioequivalency Testing
  19. Plastic Packaging Materials
  20. Pharmaceutical Necessities
VI. Pharmacodynamics
  1. Diseases: Manifestations and Pathophysiology
  2. Drug Absorption, Action and Disposition
  3. Basic Pharmacokinetics and Pharmacodynamics
  4. Clinical Pharmacokinetics and Pharmacodynamics
  5. Principles of Immunology
  6. Adverse Drug Reactions and Clinical Toxicology
  7. Pharmacogenomics
  8. Pharmacokinetics/Pharmacodynamics in Drug Development
VII. Pharmaceutical and Medicinal Agents
  1. Diagnostic Drugs and Reagents
  2. Topical Drugs
  3. Gastrointestinal and Liver Drugs
  4. Blood, Fluids, Electrolytes and Hematological Drugs
  5. Cardiovascular Drugs
  6. Respiratory Drugs
  7. Sympathomimetic Drugs
  8. Cholinomimetic Drugs
  9. Adrenergic Antagonists and Adrenergic Neuron Blocking Drugs
  10. Antimuscarinic and Antispasmodic Drugs
  11. Skeletal Muscle Relaxants
  12. Diuretic Drugs
  13. Uterine and Antimigraine Drugs
  14. Hormones and Hormone Antagonists
  15. General Anesthetics
  16. Local Anesthetics
  17. Antianxiety Agents and Hypnotic Drugs
  18. Antiepileptic Drugs
  19. Psychopharmacologic Agents
  20. Analgesic, Antipyretic, and Anti-inflammatory Drugs
  21. Histamine and Antihistaminic Drugs
  22. Central Nervous System Stimulants
  23. Antineoplastic Drugs
  24. Immunoactive Drugs
  25. Parasiticides
  26. Immunizing Agents and Allergenic Extracts
  27. Anti-Infectives
  28. Enzymes
  29. Nutrients and Associated Substances
  30. Pesticides
VIII. Pharmacy Practice
Fundamentals of Pharmacy Administration
  1. Applications of Ethical Principles to Practice Dilemmas
  2. Technology and Automation
  3. The Patient: Behavioral Determinants
  4. Patient Communication
  5. Patient Compliance
  6. Drug Education
  7. Professional Communications
  8. The Prescription
  9. Providing a Framework for Ensuring Medication Use Safety
  10. Poison Control
  11. Drug Interactions
  12. Extemporaneous Prescription Compounding
  13. Nuclear Pharmacy Practice
  14. Nutrition in Pharmacy Practice
  15. Pharmacoepidemiology
  16. Surgical Supplies
  17. Health Accessories
Social, Behavioral, andEconomic, and Administrative Sciences
  1. Laws Governing Pharmacy
  2. Re-engineering Pharmacy Practice
  3. Pharmacoeconomics
  4. Community Pharmacy Economics and Management
  5. Product Recalls and Withdrawals
  6. Marketing Pharmaceutical Care Services
  7. Documenting, Billing, and Reimbursement for Pharmaceutical Care Services
  8. Pharmaceutical Risk Management
  9. Integrated Health Care Delivery Systems
Patient Care
  1. Specialization in Pharmacy Practice
  2. Pharmacists and Disease State Management
  3. Development of a Pharmacy Care Plan and Patient Problem-Solving
  4. Ambulatory Patient Care
  5. Self-Care
  6. Diagnostic Self-Care
  7. Preventive Care
  8. Hospital Pharmacy Practice
  9. Emergency Medicine Pharmacy Practice
  10. Long-Term Care
  11. Aseptic Processing for Home Infusion Pharmaceuticals
  12. The Pharmacist's Role in Substance Use Disorders
  13. Complementary and Alternative Medical Health Care
  14. Chronic Wound Care
Index
DOWNLOAD FROM

http://rapidshare.com/files/45552201/Remington.part1.rar

http://rapidshare.com/files/45685773/Remington.part2.rar

IMPORTANT
YOU Need The Program Diamon tool to make it work , and only this program not other mounting program
download daemon from here:
http://www.disc-tools.com/request?p=73b4c3cb2620037f6e27954683b856bd/daemon408-139-x86.exe

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1-set daemon up
2- Put Regminton on CD
3-do not set up the program regminton from cd but
4-click:"run from cd"
do not INSTALL the regminton program from CD just put regminton cd in it and it will make an autoplay itself giving you a green window with 2 choices . choose:
"run from cd"





OTHER LINKS FOR REGMiNTON:
part 1 100MB
http://rapidshare.de/files/25208340/REM05PER.part1.rar.html
Part2 40MB
http://rapidshare.de/files/25208001/REM05PER.part2.rar.html
password : AboJim
OR
part1
http://www.badongo.com/file/1070295
part2
http://www.badongo.com/file/1072021

password : AboJim



Or:
Part - I: http://rapidshare.com/files/45552201/Remington.part1.rar
Part - II: http://rapidshare.com/files/45685773/Remington.part2.rar

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Q.C. & ANALYTICAL PROFILES

Analytical Profiles of Drug Substances and Excipients , vol 28




Analytical Profiles of Drug Substances and Excipients
Academic Press ISBN: 0122608267 1999-10-05 PDF 508 pages 12 Mb


Although the official compendia define a drug substance as to identity, purity, strength, and quality, they normally do not provide other physical or chemical data, nor do they list methods of synthesis or pathways of physical or biological degradation and metabolism. Such information is scattered throughout the scientific literature and the files of pharmaceutical laboratories. Edited by the Associate Director of Analytical Research and Development for the American Association of Pharmaceutical Scientists, Analytical Profiles of Drug Substances and Excipients brings this information together into one source. The scope of the series has recently been expanded to include profiles of excipient materials.

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Analysis of Drug Impurities







Analysis of Drug Impurities (Sheffield Analytical Chemistry Series)
By Richard J. Smith, Michael L. Webb

Publisher: Wiley-Blackwell
Number Of Pages: 288
Publication Date: 2007-05-04
ISBN-10 / ASIN: 1405133589
ISBN-13 / EAN: 9781405133586
Binding: Hardcover

The presence of impurities, even in small amounts, may affect the efficacy and safety of pharmaceuticals. The methods for detecting and controlling them are subject to continuous review and improvement. Characterisation of impurities is a crucial aspect of drug development and approval, and is central to quality control.

This book provides a source of reference on the techniques available for accurate identification and quantification of drug impurities, and it brings together all the relevant disciplines within one volume for the first time.






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Drug Safety Evaluation


Drug Safety Evaluation presents an all-inclusive, practical guide for those who are responsible for ensuring the safety of drugs and biologics for patients, for health care providers, for those involved in the manufacture of medicinal products, and for all those who need to understand how the safety of these products is evaluated.
Individual chapters address specific approaches to evaluating hazards, including problems that are encountered and their solutions. Author Shayne Gad draws upon over twenty years of experience in toxicology, drug development, and risk assessment, explaining the scientific and philosophical bases for evaluating specific concerns (carcinogenicity, development toxicity, etc.) to provide both understanding and guidance for approaching new problems. Containing information specifically relevant to the pharmaceutical and biotechnology industries, Drug Safety Evaluation covers a wide variety of topics, including:
  • Acute toxicity testing in pharmaceutical safety evaluation
  • Genotoxicity
  • Safety assessment of inhalant drugs
  • Immunotoxicology in pharmaceutical development
  • Large animal studies
  • Evaluation of human tolerance and safety in clinical trials
Drug Safety Evaluation provides a road map for safety assessment as an integral part of the development of new drugs and therapeutics.

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http://rapidshare.com/files/51526582/Drug_Safety_Evaluation.zip

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Quality Assurance of Pharmaceuticals, Volume 2 Update



The second volume of the Compendium on quality assurance of pharmaceuticals has been updated to include all new and revised texts published by WHO through the end of 2003 in the area of good manufacturing practices (GMP), inspection and the use of risk analysis in production of pharmaceuticals. All together it includes 15 different guidance texts which were all adopted by the WHO Expert Committee on Specifications for Pharmaceutical Preparations. The texts have been developed, revised and reviewed in a consultative process through participation of members of WHO expert panels, specialists, international professional associations , institutions, international organizations, NGOs and other third parties recognized as being competent in this field.
The texts cover good manufacturing practices and inspection of production sites and distribution channels, as well as the quality system requirements of national GMP inspectorates. The good manufacturing practices include main principles as well as supplementary texts for a number of specific types of products. There are in total six new guidance texts ; two guidelines have been updated.
Download This Book:

http://rapidshare.com/files/42080113/quality_assurance_of_pharmaceuticals_vol2.zip
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Handbook of Bioequivalence Testing (Drugs and the Pharmaceutical Sciences)




Handbook of Bioequivalence Testing (Drugs and the Pharmaceutical Sciences)
Publisher: Informa Healthcare 2007-08-22 ISBN 0849303958 Pages: 550 PDF 17 MB

As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct efficient and successful bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence, and advances in the analytical technology used to detect drug and metabolite levels have made bioequivalence testing more difficult to conduct and summarize. The Handbook of Bioequivalence Testing offers a complete and timely description of every aspect of bioequivalence testing, including worldwide regulatory requirements for filing for approval of generic drugs, applying for a waiver, securing regulatory approval of reports, and obtaining regulatory certification of facilities conducting bioequivalence studies.

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Quality Control Methods For Medicinal Plant Materials
WHO ISBN: 9241545100 1998 PDF 123 pages 1.61 Mb RS

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High Content Screening: Science, Techniques and Applications




Steven A. Haney “High Content Screening: Science, Techniques and Applications"
Wiley-Interscience 2008-01-18 ISBN: 047003999X 424 pages PDF 11,3 Mb

This book provides comprehensive coverage of high content screening (HCS) and serves as an important reference for researchers in academics, biotechnology, and pharmaceutical companies. It covers varied and important subjects like: assay development, applications for drug discovery and development, cell culture, image processing, database architecture and management, and model systems for analysis.



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Handbook of Modern Pharmaceutical Analysis (Separation Science and Technology)




Handbook of Modern Pharmaceutical Analysis (Separation Science and Technology)
Academic Press 2001-07-27 ISBN: 0120455552 600 pages PDF 9,2 Mb

This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability studies, international regulatory aspects and documentation, and future technologies that are likely to impact the field. Emphasis is placed on current, easy-to-follow methods that readers can apply in their laboratories.

No book has effectively replaced the very popular text, Pharmaceutical Analysis, that was edited in the 1960s by Tak Higuchi. This book will fill that gap with an up-to-date treatment that is both handy and authoritative.


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Enzyme Assays: High-throughput Screening, Genetic Selection and Fingerprinting


Enzyme Assays: High-throughput Screening, Genetic Selection and FingerprintingPublisher: Wiley-VCH
Language: english
ISBN: 3527310959
Paperback: 386 pages
Data: March 10, 2006
Format: PDF
Description: Edited by one of the leading experts in the field, this book fills the need for a book presenting the most important methods for high-throughput screenings and functional characterization of enzymes. It adopts an interdisciplinary approach, making it indispensable for all those involved in this expanding field, and reflects the major advances made over the past few years.
For biochemists, analytical, organic and catalytic chemists, and biotechnologists.





РЎРєР°Ð¡‡Ð °Ð¡‚СЊ Download - (3 Mb)
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Raman and SERS Investigations of Pharmaceuticals




Raman and SERS Investigations of Pharmaceuticals
Springer 2008 ISBN: 3540782826 214 pages PDF 2 MB

Over the last several years it has become apparent to most researchers that interdisciplinary research is the key to success in the sciences’ future. The present book exemplifies such interdisciplinary work. Thus, some new derivatives have been prepared by chemists and consecutively analyzed by physicists in order to better understand their physical-chemical properties for future tests to be performed by pharmacists. The book consists of an introductory section and other eight chapters. First, the fundamentals of infrared, Raman and surface-enhanced Raman spectroscopy and those of the theoretical methods employed for the vibrational prediction modes are highlighted. The SERS investigations illustrated in the following chapters are focused on different kinds of drugs: tranquilizers and sedatives, anti-inflammatory drugs, vitamins, drugs with anti-bacterial properties, etc. Since there is an increased interest in designing highly effective and controllable SERS-active substrates, a few newly developed substrates that could contribute to a deeper understanding and knowledge of the adsorption behavior of various types of molecules of pharmaceutical and medical interest are also presented.

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Quality Assurance in Analytical Chemistry: Applications in Environmental, Food and Materials Analysis, Biotechnology, and Medical Engineering




Quality Assurance in Analytical Chemistry: Applications in Environmental, Food and Materials Analysis, Biotechnology, and Medical Engineering

Paperback: 300 pages
Data: January 9, 2007
Format: PDF
Description: This best-selling title both in German and English is now enhanced by a new chapter on the important topical subject of measurement uncertainty, plus a CD-ROM with interactive examples in the form of Excel-spreadsheets. These allow readers to gain an even better comprehension of the statistical procedures for quality assurance while also incorporating their own data.

Following an introduction, the text goes on to elucidate the 4-phase model of analytical quality assurance: establishing a new analytical process, preparative quality assurance, routine quality assurance and external analytical quality assurance.

Besides updating the relevant references, the authors took great care to incorporate the latest international standards in the field.

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Method Validation in Pharmaceutical Analysis: A Guide to Best Practice



Hardcover: 418 pages
Publisher: Wiley-VCH (May 6, 2005) English ISBN-10: 3527312552 ISBN-13: 978-3527312559
File type : PDFFile
size : 2.9 MB
Book Description
Adopting a practical approach, the authors provide a detailed interpretation of the existing regulations (GMP, ICH), while also discussing the appropriate calculations, parameters and tests. The book thus allows readers to validate the analysis of pharmaceutical compounds while complying with both the regulations as well as the industry demands for robustness and cost effectiveness. Following an introduction to the basic parameters and tests in pharmaceutical validation, including specificity, linearity, range, precision, accuracy, detection and quantitation limits, the text focuses on a life-cycle approach to validation and the integration of validation into the whole analytical quality assurance system. The whole is rounded off with a look at future trends. With its first-hand knowledge of the industry as well as regulating bodies, this is an invaluable reference for analytical chemists, the pharmaceutical industry, pharmaceutists, QA officers, and public authorities.
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Pharmaceutical Stress Testing







(Drugs and the Pharmaceutical Sciences)


Pharmaceutical Stress Testing (Drugs and the Pharmaceutical Sciences)
Author: Steven W. Baertschi (Editor)
Publisher: Informa Healthcare
PDF 504 pages 7,7mb English language ISBN 0824740211The first book devoted to the topic, this reference discusses the predictive power and limitations of current stress testing strategies and emphasizes the critical role of stress testing in the determination of the stability characteristics of pharmaceuticals-offering an extensive compilation of drug degradation studies from real-world examples in the literature.

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http://rapidshare.com/files/5013454/pharmastress.rar
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DRUG INTERACTIONS

Antiepileptic Drugs: Combination Therapy and Interactions




Antiepileptic Drugs: Combination Therapy and Interactions
Pages: 514 Date: 2005 ISBN:052182219X Rared PDF File Rapidshare & Depositfiles 2 MB


This book reviews the use of antiepileptic drugs focusing on the interactions between these drugs and between antiepileptics and other drugs. These interactions can be beneficial or can cause harm. The aim of this book is to increase awareness of the possible impact of combination pharmacotherapies. Pharmacokinetic and pharmacodynamic interactions are discussed supported by clinical and experimental data. The book consists of five sections covering the general concepts and advantages of combination therapies, the principles of drug interactions, the mechanisms of interactions, drug interactions in specific populations or in patients with co-morbid health conditions, and concludes with a look at the future directions for this field of research. The book will be of interest to all who prescribe antiepileptics to epileptic and non-epileptic patients, including epileptologists, neurologists, neuro-pediatricians , psychiatrists and general practitioners.


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pass: giga

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Drug-Induced Liver Disease .. 2 editions














Book Description:

Epidemiological studies have found that drugs are now the most common cause of liver failure in the United States, and the past decade has seen an explosion of new information concerning the immunology, toxicology, and pharmacology of drug-induced liver disease. This expertly written Second Edition supplies an in-depth discussion of the recent developments in drug-induced hepatotoxicity, covering mechanisms, histopathology, management, risk factors, and patterns of drug and toxin-induced liver disease.

# Publisher: Informa Healthcare
# Number Of Pages: 808
# Publication Date: 2007-07-10
# ISBN / ASIN: 0849398967
# EAN: 9780849398964


http://mihd.net/pgiotx



------------------------------------



Drug-Induced Liver Disease
By Neil Kaplowitz, Laurie D. DeLeve
Publisher: Informa Healthcare
Number Of Pages: 784
Publication Date: 2002-10-16
ISBN-10 / ASIN: 0824708113
ISBN-13 / EAN: 9780824708115
Binding: Hardcover

Featuring more than 4100 references, Drug-Induced Liver Disease will be an invaluable reference for gastroenterologists, hepatologists, family physicians, internists, pathologists, pharmacists, pharmacologists, and clinical toxicologists, and graduate and medical school students in these disciplines.

http://www.filefactory.com/fil e/724b0b/
or
http://rapidshare.com/files/11 407176...43709.zip.html




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Herbal Supplements-Drug Interactions: Scientific and Regulatory Perspectives








The international popularity of herbal remedies has recently outpaced quality information on the utilization and dosing of these compounds. This book fills a void in the literature by offering an authoritative overview of the mechanisms of herbal remedies and their impact on standard medications. It offers a practical approach that focuses not only on specific drug interactions, but the mechanisms behind those interactions and their clinical significance. With contributions from leading experts on the subject, this text examines the overall use of herbs, includes sections on individual herbs, and considers pertinent regulatory issues and concerns in industry.

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Stockley's Drug Interactions, Other eddition




Karen Baxter, "Stockley's Drug Interactions, 7th Edition"
Not Avail; 7 Har/Cdr edition ISBN: 0853696640 1208 pages CHM 11,4 Mb

Univ. of Nottingham Medical School, UK. Reference includes more than 13,000 references for more than 2,500 monographs. Provides international, British, and American drug names and extensive bibliographies. Covers clinical evidence, mechanism, importance, and over-the-counter and prescribed drugs. For clinicians.

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Overcoming Steroid Insensitivity in Respiratory Disease




Overcoming Steroid Insensitivity in Respiratory Disease
Publisher:Wiley Pages:304 2008-05-19 ISBN:0470058080 PDF 3.5 MB

Written by well-known experts in field, this is the first book dedicated to dealing with the single most challenging management issue in long-term steroid therapy.

Overcoming Steroid Insensitivity in Respiratory Disease reviews important new advances in therapeutics and provides the clinician with the most up to date information on one of the most significant therapeutic challenges to effective management of these diseases. This unique book is an invaluable resource for all postgraduate students and specialist physicians in pulmonology allergy and asthma. It is also of interest for workers in biomedical and pharmaceutical research.

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Litt's Drug Eruption Reference Manual Including Drug Interactions




Litt's Drug Eruption Reference Manual Including Drug Interactions, 14th Edition
Publisher:Informa HealthCare Pages:657 2008-01-31 ISBN:0415458854 PDF 3.1 MB

Litt's Drug Eruption Reference Manual, 14th edition, has been updated and improved and incorporates dermatological drug eruptions plus reactions affecting the nails, hair, nails, eyes and mucosal.. This valuable resource also includes herbal and supplements reactions, in addition to hazardous drug-drug interactions. This book is a must have for all dermatologists, general practitioners and those working in emergency medicine.



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Drugs Compromising Male Sexual Health by Walter Krause
Publisher: Springer 2008-01 | 702 Pages | ISBN: 3540698590 | PDF | 2.8 MB

This concise drug guide lists 500 substances, such as pharmaceutical drugs, lifestyle drugs, and environmental toxicants, that show documented untoward effects on the male sexual organs and their functions. All substances are listed in user-friendly alphabetical order with a uniform structure throughout the book. Each listing includes evidence-based information with up-to-date references and all studies mentioned are evaluated and categorized according to study and sample types.

This unique compendium provides more detailed information on each drug than any other standard pharmacology title. Knowledge of the relevance of undesirable drug effects will enable the physician working in the fields of andrology and reproductive medicine to decide whether there is a relationship between a disturbance of male sexual function and a drugs adverse side effects. An electronic CD-ROM accompanies the book.


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Drug-Drug Interactions, Second Edition




A. David Rodrigues “Drug-Drug Interactions, Second Edition"
Informa Healthcare 2008-02-08 ISBN: 0849375932 768 pages PDF 6,3 Mb

Helping researchers predict drug interactions in a more accurate and effective manner, this comprehensive volume covers every critical aspect of metabolism-based drug-drug interactions, including preclinical, clinical, toxicological, regulatory, and marketing perspectives by renowned thought leaders in their respective fields. Thoroughly updated, the Second Edition reflects key developments in the field, including an improved understanding of the relationship between transporters and enzymes in drug metabolism and drug interactions. Formatted to benefit the reader, this source provides helpful case examples, representative enzyme systems, and computer-aided modeling, as well as 200 valuable tables, equations, drawings, and photographs to clarify key concepts.





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Drugs and Human Lactation




Drugs and Human Lactation
Elsevier Science ISBN: 0444819819 1996-11-01 PDF 722 pages 23.6 MB

Now in its second edition, Drugs and Human Lactation is a comprehensive guide to the content and consequences of xenobiotics and micronutrients in human milk, and remains by far the most thorough and extensive work available on this subject. The excellent methodology used for the compilation of the 1st edition has been retained.

It begins with an outline of the processes by which substances enter milk during its formation, the effects of drugs on the milk production process, the main determinants of drug excretion into milk and their disposition in the child. There follows an analysis of current data on 234 individual drugs, describing the extent of their passage into human milk, and assessing the risk to the suckling infant. Vitamins and essential trace elements, and radiopharmaceuticals are similarly reviewed. Also included is an account of the factors that influence the passage of environmental and occupational chemicals into milk. The result is a complete overview of what is known and proven, with clear pointers to matters which require further study, and brings the various subject areas up to date. Risks, uncertainties and false alarms which exist have been defined in such a way that they can be avoided.
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Drug Hypersensitivity




W. j. Pichler “Drug Hypersensitivity"
Not Avail 2007-05-31 ISBN: 3805582692 438 pages PDF 6,4 Mb


Drug hypersensitivities are immune-mediated reactions characterized by exanthems, fever and internal organ involvement. They represent a challenging field of research: many different drugs can induce a variety of clinical symptoms through multiple mechanisms of drug-host interaction, many of which are poorly understood. This is the first book to approach the phenomenon of drug hypersensitivity in a comprehensive manner. Besides epidemiological aspects, it addresses the immunological mechanisms underlying these complicated reactions which go far beyond the IgE-mediated drug allergies also considered in the book. Furthermore, the book covers clinical manifestations and new diagnostic methods, and introduces some recently established animal models. Well-accepted and also completely new concepts are presented and discussed in detail. Many topics are treated from multiple perspectives, and the 33 chapters are thoroughly cross-referenced. This publication will be of immense value not only to allergologists, dermatologists and anyone prescribing medication, but also to scientists in a pharmaceutical industry challenged by the economic effects of failures in drug development or drug removal from the market. Elucidating the mechanisms of drug hypersensitivity will not only help to identify patients at risk but will also provide novel insights into the pathophysiology of numerous immune-mediated diseases.



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Stockley's Drug Interactions, 7th Edition






Title: Stockley's Drug Interactions, 7th Edition (Drug Interactions (Stockley))
Author: Ivan H Stockley
Publisher: Not Avail
Publication Date: 2005-10-30
Number Of Pages: 1208
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Drug-Drug Interaction Primer: A Compendium of Case Vignettes for the Practicing Clinician




Drug-Drug Interaction Primer: A Compendium of Case Vignettes for the Practicing Clinician
American Psychiatric Publishing 2007-06-05 ISBN: 1585623059 408 pages PDF 13,5 MB

This user-friendly resource offers complete and comprehensive coverage of the difficult challenges posed by drug-drug interactions. Over 170 case vignettes illustrate a variety of interactions (DDIs) to provide an unintimidating even entertaining approach to understanding these issues. Drug-Drug Interaction Primer builds on the author's earlier work, Drug Interactions Casebook: The Cytochrome P450 System and Beyond, and features updated references throughout and 29 new cases that provide such clinical examples as: a patient diagnosed with schizoaffective disorder transitions from haloperidol to aripiprazole with disastrous results; an AIDS patient's trimethoprim-sulfamethoxazole is replaced with warfarin following atrial fibrillation, resulting in ischemic stroke; and a delusional patient on risperidone is placed on phenytoin following seizures, and delusions return.

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Drug-Induced Mitochondrial Dysfunction




Drug-Induced Mitochondrial Dysfunction (US$145)
Stationary Office Pages: 616 2008-09-22 ISBN:0470111313 9 MB Rapidshare and Megaupload

Drug-Induced Mitochondrial Dysfunction
By James A. Dykens, Yvonne Will

* Publisher: Wiley-Interscience
* Number Of Pages: 616
* Publication Date: 2008-09-22
* ISBN-10 / ASIN: 0470111313
* ISBN-13 / EAN: 9780470111314
* Binding: Hardcover

Product Description:

This is the definitive, one-stop resource on preclinical drug evaluation for potential mitochondrial toxicity, addressing the issue upfront in the drug development process. It discusses mitochondrial impairment to organs, skeletal muscle, and nervous systems and details methodologies used to assess mitochondria function. It covers both in vitro and in vivo methods for analysis and includes the latest models. This is the authoritative reference on drug-induced mitochondrial dysfunction for safety assessment professionals in the pharmaceutical industry and for pharmacologists and toxicologists in both drug and environmental health sciences.


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Drug-DNA Interactions: Structures and Spectra (2008)



Drug-DNA Interactions: Structures and SpectraPublisher: Wiley English ISBN: 0471786268 370 pages 2008 PDF 16 Mb
Description:
Learn vital information about drug-DNA interactions from Drug-DNA Interactions: Structures and Spectra, the only comprehensive book written about this topic. Understand the types of structural and bonding information that can be obtained using specific physico-chemical methods and discover how to design new drugs that are more effective than current treatments and have fewer side effects. Find detailed information about X-ray crystallography, NMR spectroscopy, molecular modeling, and optical spectroscopy such as UV-Visible absorption, fluorescence, circular dichroism (CD), flow linear dichroism (FLD), infrared (IR) and Raman spectroscopy.
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Drugs and the Liver: A Guide to Drug Handling in Liver Dysfunction



Publisher:Pharmaceutical Press Pages:324 2008-01-31 ISBN:0853697108 PDF 1 MB
Liver disease is a widespread and increasing problem throughout the world, however little is published on how different types and degrees of liver dysfunction affect the body's ability to handle medicines."Drugs and the Liver" is designed to assist practitioners in making pragmatic choices for their patients. It aims to: enable the practitioner to assess liver function using biochemical markers, other tests, signs, symptoms and disease knowledge; identify which pharmacokinetic and pharmacodynamic parameters of a drug are likely to be affected by different types of liver disease; and consider the impact of a drug's side effects on a patient with liver disease.This practical guide covers background information on liver function, the principles of drug use in liver disease and includes a section of worked examples of commonly asked questions. It will be invaluable to clinical pharmacists and anyone making medicine choices in patients with liver impairment.

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Handbook of Food-Drug Interactions





Beverly J. McCabe “Handbook of Food-Drug Interactions" CRC 2003 ISBN: 084931531X 567 pages PDF 3,5 MB
While pharmacists may know that a particular drug is inactive in a given pH environment, they may not know the pH of common foods. For dietitians the situation is reverse. With contributions from pharmacy, dietetics, and medicine, this book serves as a guide to the interdisciplinary prevention or correction of negative food-drug interactions. While other books simply list potential food-drug interactions, this book gives specific recommendations based on frequency and severity of reactions. It provides special dietary modifications necessary for prevention of adverse side effects. It also identifies new foods, supplements, and ethnic dishes that may contribute significantly to food-drug interactions.

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Drug Benefits and Risks: International Textbook of Clinical Pharmacology




Publisher:IOS Press Pages:821 2008-07-31 ISBN:158603880X PDF 4.8 MBThis is an inclusive reference exploring the scientific basis and practice of drug therapy. The key concept is to look at the balance between the benefits and risks of drugs but in this context also the social impact which drugs have in modern societies is highlighted. Taking an evidence-based approach to the problem, the practice of clinical pharmacology and pharmacotherapy in the developing as well as the developed world is examined. For this purpose the book* Covers general clinical pharmacology, pharmacology of various drug groups and the treatments specific to various diseases* Gives guidance on how doctors should act so that drugs can be used effectively and safely* Encourages the rational use of drugs in societyThis book brings together a large amount of excellent content that will be invaluable for anyone working within, or associated with, the field of clinical pharmacology and pharmacotherapy - undergraduates, postgraduates, regulatory authorities and the pharmaceutical industry.

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