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  • Pharmacovigilance: A Practical Approach

    Pharmacovigilance: A Practical Approach by Doan, Thao; Scarazzini, Linda; Renz, Cheryl;

      • GET 13% OFF

      • The discount is only available for 'Alert of Favourite Topics' newsletter recipients.
      • Publisher's listprice EUR 90.99
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        37 738 Ft (35 941 Ft + 5% VAT)
      • Discount 13% (cc. 4 906 Ft off)
      • Discounted price 32 832 Ft (31 269 Ft + 5% VAT)

    37 738 Ft

    Availability

    Out of print

    Why don't you give exact delivery time?

    Delivery time is estimated on our previous experiences. We give estimations only, because we order from outside Hungary, and the delivery time mainly depends on how quickly the publisher supplies the book. Faster or slower deliveries both happen, but we do our best to supply as quickly as possible.

    Product details:

    • Publisher Elsevier
    • Date of Publication 2 August 2018

    • ISBN 9780323581165
    • Binding Paperback
    • No. of pages228 pages
    • Size 234x190 mm
    • Weight 480 g
    • Language English
    • Illustrations 100 illustrations (100 in full color)
    • 0

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    Long description:

    Written by experts in the field of pharmacovigilance and patient safety, this concise resource provides a succinct, easy-to-digest overview of an increasingly critical area of medical safety. Drs. Thao Doan, Cheryl Renz, Fabio Lievano, Mondira Bhattacharya, and Linda Scarazzini provide essential information for health care professionals, clinical researchers, and regulators who need a comprehensive, up-to-date source of information on the principles and practice of pharmacovigilance.

    • Covers the evolving regulatory landscape, as well as current and future use of digital technologies.
    • Uses case studies to ensure content is relevant to everyday practice.
    • Discusses behavioral science and patient perspectives, risk communication, and new frontiers in pharmacovigilance.
    • Consolidates today's available information on this timely topic into one convenient resource.

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    Table of Contents:

    Introduction

    1. Does Regulation Drive Science or Does Science Drive Regulation?

    2. Role of Epidemiology in Pharmaceutical Industry

    3. Real World Epidemiologic Studies and Patient Registries

    Section III. Benefit-Risk in the Drug Development Life Cycle

    4. Signal Management and Methods of Signal Detection

    5. Causality Assessment and Examples of Adverse Drug Reactions (Drug Induced Liver Injury, Skin, Major Adverse Cardiac Events and Renal)

    6. Product Safety Monitoring in Clinical Trials

    7. Benefit-Risk Assessments

    8. Communicating benefit risk

    9. Pharmacovigilance and Medical Devices

    10. Vaccine Safety Surveillance

    11. Pharmacovigilance in Special Populations (Pediatrics and Elderly)

    12. Pharmacovigilance in Pregnancy

    13. Impact and Implications of Technology on Pharmacovigilance

    14. The Future of Pharmacovigilance

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