Results 21 to 30 of about 3,194,674 (312)

Incorporating adverse event relatedness into dose-finding clinical trial designs [PDF]

open access: yes, 2014
Dose-finding designs estimate the dose level of a drug based on observed adverse events. Relatedness of the adverse event to the drug has been generally ignored in all proposed design methodologies.
Thompson, Mery H.   +3 more
core   +1 more source

Safety profile following mRNA-1273 COVID-19 primary vaccination in healthy adults in Indonesia

open access: yesGlobal Epidemiology
Objectives: To evaluate the safety and benefit-risk profile of mRNA-1273 following the vaccine's authorization and the administration of over one million doses in Indonesia.
Bernie Endyarni Medise   +11 more
doaj   +1 more source

Ethics of safety reporting of a clinical trial

open access: yesIndian Journal of Dermatology, 2017
Clinical trial related injury and serious adverse events (SAE) are a major area of concern. In all such scenarios the investigator is responsible for medical care of the trial participant and also ethically bound to report the event to all the ...
Amrita Sil, Nilay Kanti Das
doaj   +1 more source

Adverse event.

open access: yes, 2019
Adverse event.
Ki Chul Sung (6569525)   +5 more
core   +1 more source

Adverse events

open access: yesBritish Journal of Surgery, 2004
No room for ...
openaire   +2 more sources

Revaccination and Adverse Event Recurrence in Patients with Adverse Events following Immunization

open access: yesThe Journal of Pediatrics, 2022
To estimate the risk of recurrence of adverse events following immunization (AEFIs) upon revaccination and to determine among patients with suspected vaccine allergy whether allergy skin test positivity was associated with AEFI recurrence.This prospective observational study included patients assessed in the Canadian Special Immunization Clinic Network
Caroline E. Muñoz   +21 more
openaire   +2 more sources

Final values Adverse Event Unit (AEU).

open access: yes, 2022
Final values Adverse Event Unit (AEU).
Katherine Ruzhansky (12102301)   +9 more
core   +1 more source

Adverse event frequencies.

open access: yes, 2018
Adverse event frequencies.
Raymond Bergan (3847795)   +14 more
core   +1 more source

Thromboembolic adverse event study of combined estrogen-progestin preparations using Japanese Adverse Drug Event Report database.

open access: yesPLoS ONE, 2017
Combined estrogen-progestin preparations (CEPs) are associated with thromboembolic (TE) side effects. The aim of this study was to evaluate the incidence of TE using the Japanese Adverse Drug Event Report (JADER) database.
Shiori Hasegawa   +12 more
doaj   +1 more source

A clinical grid infrastructure supporting adverse hypotensive event prediction [PDF]

open access: yes, 2009
The condition of hypotension - where a person's arterial blood pressure drops to an abnormally low level - is a common and potentially fatal occurrence in patients under intensive care. As medical interventions to treat such events are typically reactive
Jiang, J.   +5 more
core   +1 more source

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