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10.7326/M20-6703

http://scihub22266oqcxt.onion/10.7326/M20-6703
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33136427!7643168!33136427
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suck abstract from ncbi


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pmid33136427      Ann+Intern+Med 2021 ; 174 (2): 256-257
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  • Emergency Approvals for COVID-19: Evolving Impact on Obligations to Patients in Clinical Care and Research #MMPMID33136427
  • Lynch HF; Bateman-House A; Joffe S
  • Ann Intern Med 2021[Feb]; 174 (2): 256-257 PMID33136427show ga
  • There currently is debate regarding whether U.S. institutions and clinicians may or should restrict patient access to COVID-19 drugs and vaccines that have been granted emergency use authorization by the U.S. Food and Drug Administration. The authors provide their views on the legal, ethical, and clinical ramifications of such restriction.
  • |*Emergencies[MESH]
  • |COVID-19 Serotherapy[MESH]
  • |COVID-19/epidemiology/*immunology/*therapy[MESH]
  • |Clinical Trials as Topic[MESH]
  • |Health Services Accessibility[MESH]
  • |Humans[MESH]
  • |Immunization, Passive[MESH]
  • |National Institutes of Health (U.S.)[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/epidemiology/*immunology[MESH]
  • |SARS-CoV-2[MESH]
  • |United States[MESH]


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