Pharmacovigilance / / editors, Ronald D. Mann, Elizabeth B. Andrews |
Edizione | [2nd ed.] |
Pubbl/distr/stampa | Chichester, West Sussex, England : , : Wiley, , 2007 |
Descrizione fisica | 1 online resource (708 p.) |
Disciplina |
363.19/463
615.1901 615.7 |
Soggetto topico | Pharmacoepidemiology |
Soggetto genere / forma | Electronic books. |
ISBN |
1-280-83869-8
9786610838691 0-470-05921-4 0-470-05922-2 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Pharmacovigilance; Contents; Contributors; Preface; Foreword; Part I. The Basis of Pharmacovigilance; 1. Introduction; 2. Legal Basis - EU; 3. Legal Basis - United States; 4. Ethical Oversight, Consent and Confidentiality; 5. Pharmacovigilance-Related Topics at the Level of the International Conference on Harmonisation; 6. Periodic Safety Update Reports; 7. Non-Clinical Safety Evaluation and Adverse Events in Phase I Trials; 8. Mechanisms of Adverse Drug Reactions; 9. Micturin and Torsades de Pointes; 10. Withdrawal of Terodiline: A Tale of Two Toxicities
11. Nomifensine and Haemolytic AnaemiaPart II. Signal Generation; 12. WHO Programme - Global Monitoring; 13. Medical Dictionary for Regulatory Activities (MedDRA®); 14. Regulatory Pharmacovigilance in the EU; 15. Spontaneous Reporting - UK; 16. Spontaneous Reporting - France; 17. Spontaneous Reporting in Germany; 18. Spontaneous Reporting - United States; 19. Statistical Methods of Signal Detection; 20. Statistical Methods of Evaluating Pharmacovigilance Data; 21. Data Mining in Pharmacovigilance: A View from the Uppsala Monitoring Centre; 22. Pharmacovigilance in the Netherlands 23. CIOMS Working Groups and their Contribution to Pharmacovigilance24. PEM in the UK; 25. PEM in New Zealand; 26. MEMO in the United Kingdom; 27. The General Practice Research Database: Now and the Future; 28. Overview of North American Databases; 29. Other Databases in Europe for the Analytic Evaluation of Drug Effects; 30. Surveillance for Medical Devices - USA; 31. Pharmacovigilance and Risk Management in Japan; Part III. Pharmacovigilance and Selected System Organ Classes; 32. Dermatological ADRs; 33. Gastrointestinal ADRs; 34. Haematological ADRs; 35. Hepatic ADRs 36. Ocular Side Effects of Prescription Medications37. Drug Safety in Pregnancy; 38. Renal Adverse Drug Reactions; 39. Anaesthetic Adverse Drug Reactions; 40. Pharmacovigilance in Pediatrics; 41. The Cardiovascular Spectrum of Adverse Drug Reactions; 42. Drugs and the Elderly; Part IV. Key Current Topics; 43. US Activities in Risk Management of Pharmaceutical Products; 44. Risk Management - a European Regulatory View; 45. The Efficacy and Safety of Selective Serotonin Reuptake Inhibitors for the Treatment of Depression in Children and Adolescents 46. Pharmacoepidemiology of Hormone Therapy: An Evolving Picture47. NSAIDs - COX-2 Inhibitors - Risks and Benefits; 48. Introduction to Pharmionics: The Vagaries in Ambulatory Patients' Adherence to Prescribed Drug Dosing Regimens, and Some of Their Clinical and Economic Consequences; Part V. Lessons and Directions; 49. Teaching and Learning Pharmacovigilance; 49b. Practical Experience in Teaching Pharmacovigilance; 50. Fatal Medication Errors and Adverse Drug Reactions - Coroners' Inquests and Other Sources; 51. Pharmacogenetics and the Genetic Basis of ADRs 52. Keynote Clinical Lessons from Pharmacovigilance |
Record Nr. | UNINA-9910143731603321 |
Chichester, West Sussex, England : , : Wiley, , 2007 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Pharmacovigilance / / editors, Ronald D. Mann, Elizabeth B. Andrews |
Edizione | [2nd ed.] |
Pubbl/distr/stampa | Chichester, West Sussex, England : , : Wiley, , 2007 |
Descrizione fisica | 1 online resource (708 p.) |
Disciplina |
363.19/463
615.1901 615.7 |
Soggetto topico | Pharmacoepidemiology |
ISBN |
1-280-83869-8
9786610838691 0-470-05921-4 0-470-05922-2 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Pharmacovigilance; Contents; Contributors; Preface; Foreword; Part I. The Basis of Pharmacovigilance; 1. Introduction; 2. Legal Basis - EU; 3. Legal Basis - United States; 4. Ethical Oversight, Consent and Confidentiality; 5. Pharmacovigilance-Related Topics at the Level of the International Conference on Harmonisation; 6. Periodic Safety Update Reports; 7. Non-Clinical Safety Evaluation and Adverse Events in Phase I Trials; 8. Mechanisms of Adverse Drug Reactions; 9. Micturin and Torsades de Pointes; 10. Withdrawal of Terodiline: A Tale of Two Toxicities
11. Nomifensine and Haemolytic AnaemiaPart II. Signal Generation; 12. WHO Programme - Global Monitoring; 13. Medical Dictionary for Regulatory Activities (MedDRA®); 14. Regulatory Pharmacovigilance in the EU; 15. Spontaneous Reporting - UK; 16. Spontaneous Reporting - France; 17. Spontaneous Reporting in Germany; 18. Spontaneous Reporting - United States; 19. Statistical Methods of Signal Detection; 20. Statistical Methods of Evaluating Pharmacovigilance Data; 21. Data Mining in Pharmacovigilance: A View from the Uppsala Monitoring Centre; 22. Pharmacovigilance in the Netherlands 23. CIOMS Working Groups and their Contribution to Pharmacovigilance24. PEM in the UK; 25. PEM in New Zealand; 26. MEMO in the United Kingdom; 27. The General Practice Research Database: Now and the Future; 28. Overview of North American Databases; 29. Other Databases in Europe for the Analytic Evaluation of Drug Effects; 30. Surveillance for Medical Devices - USA; 31. Pharmacovigilance and Risk Management in Japan; Part III. Pharmacovigilance and Selected System Organ Classes; 32. Dermatological ADRs; 33. Gastrointestinal ADRs; 34. Haematological ADRs; 35. Hepatic ADRs 36. Ocular Side Effects of Prescription Medications37. Drug Safety in Pregnancy; 38. Renal Adverse Drug Reactions; 39. Anaesthetic Adverse Drug Reactions; 40. Pharmacovigilance in Pediatrics; 41. The Cardiovascular Spectrum of Adverse Drug Reactions; 42. Drugs and the Elderly; Part IV. Key Current Topics; 43. US Activities in Risk Management of Pharmaceutical Products; 44. Risk Management - a European Regulatory View; 45. The Efficacy and Safety of Selective Serotonin Reuptake Inhibitors for the Treatment of Depression in Children and Adolescents 46. Pharmacoepidemiology of Hormone Therapy: An Evolving Picture47. NSAIDs - COX-2 Inhibitors - Risks and Benefits; 48. Introduction to Pharmionics: The Vagaries in Ambulatory Patients' Adherence to Prescribed Drug Dosing Regimens, and Some of Their Clinical and Economic Consequences; Part V. Lessons and Directions; 49. Teaching and Learning Pharmacovigilance; 49b. Practical Experience in Teaching Pharmacovigilance; 50. Fatal Medication Errors and Adverse Drug Reactions - Coroners' Inquests and Other Sources; 51. Pharmacogenetics and the Genetic Basis of ADRs 52. Keynote Clinical Lessons from Pharmacovigilance |
Record Nr. | UNINA-9910830084503321 |
Chichester, West Sussex, England : , : Wiley, , 2007 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|