Examples of 'reaction reports' in a sentence
Meaning of "reaction reports"
Reaction reports: Documentation or summaries of responses or feedback received in response to a particular stimulus or event
How to use "reaction reports" in a sentence
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reaction reports
Adverse reaction reports were not submitted electronically.
Records of adverse transfusion reaction reports must be maintained.
Adverse reaction reports were not submitted to all the relevant parties.
Inadequate evaluation of adverse reaction reports.
Adverse drug reaction reports worldwide.
Inexplicable reclassification of adverse reaction reports.
Adverse reaction reports.
Health Canada will continue to monitor international and Canadian adverse drug reaction reports for Ketek.
The majority of the adverse reaction reports described skin and subcutaneous disorders.
European Medicines Agency releases adverse reaction reports.
Conduct analysis of adverse reaction reports and periodic safety update reports in a timely manner.
Health professionals and consumers can submit adverse reaction reports on a voluntary basis.
Individual adverse reaction reports held on the Eudravigilance database may be requested by the public.
EudraVigilance electronic reporting for adverse drug reaction reports for centrally authorised products.
Adverse reaction reports related to anti-acne medication.
See also
Ombudsman welcomes release of adverse reaction reports by European Medicines Agency.
Strong interest in Drug Analysis Prints with data from Danish adverse reaction reports.
Access to adverse reaction reports on anti-bacterial medicine.
Follow-up information on adverse reaction reports.
Ensure that adverse reaction reports contain the highest quality information possible ;.
Post-market assessments rely on information received through adverse reaction reports.
Quality adverse drug reaction reports also provide useful information, especially about rare adverse.
Marketing authorisation holders shall establish mechanisms enabling the traceability and follow-up of adverse reaction reports.
EMA discloses adverse reaction reports on anti-acne drug.
EMEA refused access, arguing that EU transparency rules do not apply to adverse reaction reports.
European database of suspected adverse drug reaction reports - Understanding a web report.
Serious adverse reaction reports should be submitted directly to BGTD at the following address,.
EU and non-EU adverse drug reaction reports.
No follow-up on adverse reaction reports or follow-up made at a very late stage.
European database of suspected adverse drug reaction reports - Disclaimer.
Adverse reaction reports are not processed and submitted on time (all levels).
European database of suspected adverse drug reaction reports - Background.
Adverse Drug Reaction reports ( international sources first, followed by Canadian sources ).
European database of suspected adverse drug reaction reports - Copyright.
Summary of adverse drug reaction reports in Sweden with Pandemrix ( received up to November 10 ).
European database of suspected adverse drug reaction reports - Search.
The Agency received some 43 000 adverse drug reaction reports ( ADRs ) concerning centrally authorised products during.
Similarly, the publicly accessible European database of suspected adverse drug reaction reports will remain live.
European database of suspected adverse drug reaction reports - How to report a side effect.
EMA eventually followed the Ombudsman 's recommendation to release the adverse reaction reports.
European database of suspected adverse drug reaction reports - Frequently asked questions.
This Working Group has adopted one guideline GL 24 regarding the managment of adverse reaction reports.
European database of suspected adverse drug reaction reports - Browser compatibility.
Article 47 guidance on the collection, verification and presentation of adverse reaction reports.
European database of suspected adverse drug reaction reports - Patient safety warnings.
In Canada, Health Canada has had a system to gather information on adverse reaction reports since 1965.
Key data elements for adverse reaction reports appendix 2,.
European database of suspected adverse drug reaction reports - Glossary.
Handling of adverse reaction reports (ICSRs).
European database of suspected adverse drug reaction reports - News.
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