Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 234,150,457 papers from all fields of science
Search
Sign In
Create Free Account
Report Adverse Events
The healthcare provider or setting must report adverse events of interest to the Manufacturer, MedWatch, and/or a REMS Program.
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
Adverse Drug Experience Report
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A Study of Natural products Adverse Reactions (SONAR) in adult HIV-infected patients- a cross sectional study
Emma Sparks
2019
Corpus ID: 213232915
Background: As a result of advances in treatment, human immunodeficiency virus (HIV) is a chronic manageable infection. Many…
Expand
2017
2017
ORAL PRESENTATIONS
J. McEwen
,
I. Boyd
Indian Journal of Nephrology
2017
Corpus ID: 71680229
2017
2017
Bayesian methods in health technology assessment: application to overactive bladder syndrome
R. Owen
2017
Corpus ID: 80010402
i
Review
2016
Review
2016
Committee Opinion No. 681 Summary: Disclosure and Discussion of Adverse Events.
Obstetrics and Gynecology
2016
Corpus ID: 3873918
Adverse outcomes, preventable or otherwise, are a reality of medical care. Most importantly, adverse events affect patients, but…
Expand
2015
2015
Challenges and Opportunities Recommendations in Brief Conclusion Recommended Actions Recommendation 1 : Leverage the Addis Declaration on Immunization ( ADI ) commitments Recommendation 2 :
J. Mphahlele
2015
Corpus ID: 52834717
TARGETS Objective 1: To improve immunization coverage beyond the current levels • DTP3 vaccine coverage to reach 90% region-wide…
Expand
2013
2013
Doctors in the private sector should report adverse events after immunisation to complete dataset
S. Bhaumik
British medical journal
2013
Corpus ID: 2947938
The Indian Academy of Pediatrics has called for doctors working in the private sector to report adverse events after…
Expand
2012
2012
Universities will have to report adverse events in research to higher education funding body, consultation proposes
N. Hawkes
British medical journal
2012
Corpus ID: 20802874
Measures to ensure that research in UK universities complies with high standards of integrity have been put out for consultation…
Expand
2005
2005
TRAIL: a model to promote active learning from adverse events
C. Armitage
2005
Corpus ID: 79807800
This article describes TRAIL, a model developed within Leicestershire Partnership NHS Trust’s City Adult Mental Health Services…
Expand
2001
2001
Implementing a stronger patient safety program using the Internet takes step-by-step planning.
T. Atherton
The Quality Letter for Healthcare Leaders
2001
Corpus ID: 45156635
Just over a year ago at the 104-bed Baylor Medical Center at Grapevine in Texas, supporting patient safety meant mostly relying…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE