Monitoring vaccine safety by studying temporal variation of adverse events using vaccine adverse event reporting system
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Publication:2233166
Recommendations
- Signal detection of adverse events with imperfect confirmation rates in vaccine safety studies using self-controlled case series design
- A statistical signalling model for use in surveillance of adverse drug reaction data
- Case‐base methods for studying vaccination safety
- Active postmarketing drug surveillance for multiple adverse events
- A positive event dependence model for self-controlled case series with applications in postmarketing surveillance
Cites work
- scientific article; zbMATH DE number 5849508 (Why is no real title available?)
- scientific article; zbMATH DE number 4100431 (Why is no real title available?)
- scientific article; zbMATH DE number 890348 (Why is no real title available?)
- A likelihood ratio test based method for signal detection with application to FDA's drug safety data
- A note on pseudolikelihood constructed from marginal densities
- An Optimum Property of Regular Maximum Likelihood Estimation
- Composite likelihood inference under boundary conditions
- On pseudolikelihood inference for semiparametric models with boundary problems
- On the asymptotic behaviour of the pseudolikelihood ratio test statistic with boundary problems
Cited in
(3)- Case‐base methods for studying vaccination safety
- Mining adverse events in large frequency tables with ontology, with an application to the vaccine adverse event reporting system
- Signal detection of adverse events with imperfect confirmation rates in vaccine safety studies using self-controlled case series design
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