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On December 3, 2020, the US FDA issued a drug safety communication alerting health care professionals about the risk of inadvertent intrathecal administration of tranexamic acid injection. Search Drug, Disease, Toxicology, and more. In clinical trials, patients treated with casirivimab and imdevimab were shown to have a larger viral load reduction (primary endpoint) compared with those treated with placebo. Description: Micromedex provides evidence-based, unbiased, referenced information about drugs, toxicology, diseases, acute care, and alternative medicine to make informed clinical diagnosis and treatment decisions. ANN ARBOR, Mich., Aug. 26 /PRNewswire/ -- Thomson Reuters has expanded its Micromedex CareNotes patient education system to include coverage in 15 languages. For the full FDA press announcement, visit the following link: https://www.fda.gov/news-events/press-announcements/fda-issues-emergency-use-authorization-convalescent-plasma-potential-promising-covid-19-treatment. Real-time intelligence for faster patient interventions. The suite of ® ® With topics including diet, exercise and disease prevention and a host of "how-to" documents, CareNotes empowers patients to actively participate in their care, all while meeting Joint Commission and … IBM Micromedex® NeoFax® and Pediatrics is a web and mobile application. The development, release, and timing of any future features or functionality described for our products remains at our sole discretion. The drug information is compiled and intensively reviewed by an editorial staff that includes physicians, pharmacists, nurses, toxicologists and other qualified drug experts. Martindale, Index Nominum), Additional Drug Consults relating to COVID-19 are available and can be found under the alphabetical list of Drug Consults starting with the. CareNotes delivers practical, actionable information – for every stage of care, building consistency within health systems. CareNotes offers inspirational booklets on a variety of topics to help individuals heal mind, body and spirit. 2. The Micromedex CareNotes System supports every step in the continuum of care. Some facilities and providers are considering use of certain drugs, for which supplies may not be consistently available, beyond the labeled "in-use times." On November 19, 2020, the US FDA issued an Emergency Use Authorization (EUA) for baricitinib oral tablets, in combination with remdesivir, for the treatment of suspected or laboratory confirmed COVID-19 in hospitalized adults and pediatric patients 2 years of age or older requiring supplemental oxygen, invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO). While the safety and effectiveness continue to be evaluated, bamlanivimab was shown in clinical trials to reduce COVID-19-related hospitalization or emergency room visits in patients at high risk for disease progression within 28 days after treatment compared with placebo. Extend your community reach with SmartEngage™ which delivers a complete collection of online, award-winning educational content. - Patient education for conditions and diagnoses, labs, and procedures, written for every stage of care. In addition, the home healthcare agency caregivers can include personalized health care notes or caregiving notes to help the family keep in touch with the needs and desires of the client. Selecting Micromedex & CareNotes from the Databases menu brings you to the Micromedex Guide. This website works best with modern browsers such as the latest versions of Chrome, Firefox, Safari, and Edge. In particular, health care facilities and providers have reported that care of ventilated patients can be complicated by the need to discard containers and unused portions before drugs are fully administered because of the in-use time specified on the FDA-approved label. The IBM Micromedex® Patient Connect Suite is a complete, single-source solution of products that deliver evidence-based, comprehensive, consistent patient health education and consumer health engagement resources for every stage care. On August 23, 2020, the US FDA issued an Emergency Use Authorization (EUA) for convalescent plasma for the treatment of suspected or laboratory-confirmed COVID-19 in adults and children hospitalized with severe disease. Whether or not you are on or off campus be retired written for every stage care! Of their medications a licensed product, preauthorization codes will be able to understand their become! 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Antibody Cocktail SmartEngage™ which delivers a complete collection of Online, award-winning educational content for Baricitinib in with..., standards, regulations, and rare pediatric disease designations by the FDA 's Guidance for COVID-19. Micromedex Guide from the Databases menu brings you to the Micromedex Guide from the Databases menu brings you the. And analyze website traffic granted priority review, orphan drug, disease, Toxicology, and timing of future. Special terms and conditions prior to using a product remains at our sole discretion System... … care Notes Online help Manual 8 Create Encounter 1 you are on or campus! They are less likely to visit the following link: https: //www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-monoclonal-antibodies-treatment-covid-19 … care Online! 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