Web-based intensive monitoring of adverse events following influenza vaccination in general practice.
暂无分享,去创建一个
[1] L. Härmark,et al. Non‐response in a pharmacy and patient‐based intensive monitoring system: a quantitative study on non‐response bias and reasons for non‐response , 2012, The International journal of pharmacy practice.
[2] Rumke Hc,et al. Reported adverse events following influenza vaccination , 2014 .
[3] M. Watson,et al. Patient versus Healthcare Professional Spontaneous Adverse Drug Reaction Reporting , 2012, Drug Safety.
[4] L. Härmark,et al. Web-based intensive monitoring: from passive to active drug surveillance , 2012, Expert opinion on drug safety.
[5] E. Hak,et al. Monitoring the safety of influenza A (H1N1) vaccine using web-based intensive monitoring. , 2011, Vaccine.
[6] I. Cook. Sex differences in injection site reactions with human vaccines , 2009, Human vaccines.
[7] T. Egberts. Signal Detection , 2007, Drug safety.
[8] D. Burwen,et al. Extensive limb swelling after immunization: reports to the Vaccine Adverse Event Reporting System. , 2003, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[9] Robert T. Chen,et al. The Brighton Collaboration: addressing the need for standardized case definitions of adverse events following immunization (AEFI). , 2002, Vaccine.
[10] D. Scheifele,et al. Evaluation of adverse events after influenza vaccination in hospital personnel. , 1990, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.