Update on REMS-Required Testing During COVID-19 Pandemic - MPR
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“The completion of some REMS-required laboratory testing or imaging studies may be difficult because patients suspected of having COVID-19 may be self-isolating and/or subject to quarantine,” said FDA Principal Deputy Commissioner Amy Abernethy, MD, PhD.
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The FDA's Convoluted Stance on Abortion Pills Doesn't Protect Patients — It Endangers Them
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Safety and Efficacy of a Third Dose of BNT162b2 Covid-19 Vaccine
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Medication Abortion and Telemedicine: Innovations and Barriers During the COVID-19 Emergency
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CA Covid-19 School Readiness Hub
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Clozapine During COVID-19: How Best to Ensure Patient Safety
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REMS Program & Liver Function JYNARQUE® (tolvaptan) tablets
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Risk Evaluation and Mitigation Strategy programs: How they can be improved
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Lift Unnecessary Restrictions: Access to Medication Abortion During the COVID-19 Pandemic
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The utility of the Rapid Emergency Medicine Score (REMS) compared with three other early warning scores in predicting in-hospital mortality among COVID-19 patients in the emergency department: a multicenter validation study
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FDA Relaxes Certain Lab and Imaging Test Requirements for REMS Programs During the COVID-19 Pandemic
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COVID-19: Federal Efforts Could Be Strengthened by Timely and Concerted Actions
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FDA Emergency Use Authorizations
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BNT162b2 Protection against the Omicron Variant in Children and Adolescents