Literature DB >> 9643613

Pharmacovigilance in the pharmaceutical industry.

J C Talbot1, B S Nilsson.   

Abstract

Mesh:

Year:  1998        PMID: 9643613      PMCID: PMC1873545          DOI: 10.1046/j.1365-2125.1998.00713.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


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  11 in total

1.  Review of company postmarketing surveillance studies.

Authors:  P C Waller; S M Wood; M J Langman; A M Breckenridge; M D Rawlins
Journal:  BMJ       Date:  1992-06-06

2.  Study of United Kingdom product licence applications containing new active substances, 1987-9.

Authors:  M D Rawlins; D B Jefferys
Journal:  BMJ       Date:  1991-01-26

3.  Concepts in risk-benefit assessment. A simple merit analysis of a medicine?

Authors:  R Edwards; B E Wiholm; C Martinez
Journal:  Drug Saf       Date:  1996-07       Impact factor: 5.606

4.  End of the line for "third-generation-pill" controversy?

Authors:  J P Vandenbroucke; F R Rosendaal
Journal:  Lancet       Date:  1997-04-19       Impact factor: 79.321

5.  The case for recording events in clinical trials.

Authors:  D C Skegg; R Doll
Journal:  Br Med J       Date:  1977-12-10

Review 6.  The way towards adverse event monitoring in clinical trials.

Authors:  M A Wallander
Journal:  Drug Saf       Date:  1993-03       Impact factor: 5.606

7.  Computer-assisted evaluation of adverse events using a Bayesian approach.

Authors:  K L Lanctôt; C A Naranjo
Journal:  J Clin Pharmacol       Date:  1994-02       Impact factor: 3.126

8.  Guidelines for company-sponsored Safety Assessment of Marketed Medicines (SAMM) guidelines. Medicines Control Agency, Committee on Safety of Medicines, Royal College of General Practitioners, British Medical Association and Association of the British Pharmaceutical Industry (November 1993)

Authors: 
Journal:  Br J Clin Pharmacol       Date:  1994-08       Impact factor: 4.335

9.  Variability in risk of gastrointestinal complications with individual non-steroidal anti-inflammatory drugs: results of a collaborative meta-analysis.

Authors:  D Henry; L L Lim; L A Garcia Rodriguez; S Perez Gutthann; J L Carson; M Griffin; R Savage; R Logan; Y Moride; C Hawkey; S Hill; J T Fries
Journal:  BMJ       Date:  1996-06-22

10.  The increased risk of venous thromboembolism and the use of third generation progestagens: role of bias in observational research. The Transnational Research Group on Oral Contraceptives and the Health of Young Women.

Authors:  M A Lewis; L A Heinemann; K D MacRae; R Bruppacher; W O Spitzer
Journal:  Contraception       Date:  1996-07       Impact factor: 3.375

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  8 in total

1.  Pharmacy student perceptions of adverse event reporting.

Authors:  Sirisha Kalari; Matthew Dormarunno; Oleg Zvenigorodsky; Aparna Mohan
Journal:  Am J Pharm Educ       Date:  2011-09-10       Impact factor: 2.047

2.  Risk management policy and black-box warnings: a qualitative analysis of US FDA proceedings.

Authors:  Daniel M Cook; Rama K Gurugubelli; Lisa A Bero
Journal:  Drug Saf       Date:  2009       Impact factor: 5.606

3.  Adverse Drug Reaction Case Safety Practices in Large Biopharmaceutical Organizations from 2007 to 2017: An Industry Survey.

Authors:  Stella Stergiopoulos; Mortiz Fehrle; Patrick Caubel; Louise Tan; Louise Jebson
Journal:  Pharmaceut Med       Date:  2019-12

Review 4.  Evolution of adverse drug reactions reporting systems: paper based to software based.

Authors:  M T Madhushika; T P Weerarathna; P L G C Liyanage; S S Jayasinghe
Journal:  Eur J Clin Pharmacol       Date:  2022-07-05       Impact factor: 3.064

5.  Pharmacovigilance: a worldwide master key for drug safety monitoring.

Authors:  G Jeetu; G Anusha
Journal:  J Young Pharm       Date:  2010-07

6.  Impact of a Policy Change on Pharmacists' Reporting of Adverse Drug Reactions.

Authors:  Renaud Roy; Janice Ma
Journal:  Can J Hosp Pharm       Date:  2018-08-28

7.  Identification of Adverse Drug Event-Related Japanese Articles: Natural Language Processing Analysis.

Authors:  Shogo Ujiie; Shuntaro Yada; Shoko Wakamiya; Eiji Aramaki
Journal:  JMIR Med Inform       Date:  2020-11-27

Review 8.  Adverse event reporting tools and regulatory measures in India through outcome of Pharmacovigilance Programme of India.

Authors:  Jai Prakash; Raghav Sachdeva; Tarani Prakash Shrivastava; C V Jayachandran; Aseem Sahu
Journal:  Indian J Pharmacol       Date:  2021 Mar-Apr       Impact factor: 1.200

  8 in total

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