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Dose modification and dose intensity during treatment with pirfenidone: analysis of pooled data from three multinational phase III trials
INTRODUCTION: Temporary dose modifications, such as reductions or interruptions, may allow patients to better manage adverse events (AEs) associated with pirfenidone use and continue treatment for idiopathic pulmonary fibrosis (IPF). However, the impact of such dosing adjustments on efficacy and saf...
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| Vydáno v: | BMJ Open Respir Res |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6089326/ https://ncbi.nlm.nih.gov/pubmed/30116539 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjresp-2018-000323 |
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