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A review of methods used in assessing non-serious adverse drug events in observational studies among type 2 diabetes mellitus patients
Clinical drug trials are often conducted in selective patient populations, with relatively small numbers of patients, and a short duration of follow-up. Observational studies are therefore important for collecting additional information on adverse drug events (ADEs). Currently, there is no guidance...
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| Hoofdauteurs: | , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3198877/ https://ncbi.nlm.nih.gov/pubmed/21958008 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1477-7525-9-83 |
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