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An Evaluation of “Drug Ineffective” Postmarketing Reports in Drug Safety Surveillance
INTRODUCTION: The most commonly reported adverse event, based on frequency of Medical Dictionary for Regulatory Activities (MedDRA) preferred terms (PTs), in the US FDA Adverse Event Reporting System (FAERS) database is “drug ineffective” (DI). This study aimed to describe the DI reports and provide...
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| Pubblicato in: | Drugs Real World Outcomes |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer International Publishing
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5984607/ https://ncbi.nlm.nih.gov/pubmed/29476420 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40801-018-0131-3 |
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