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Treatment outcomes 24 months after initiating short, all-oral bedaquiline-containing or injectable-containing rifampicin-resistant tuberculosis treatment regimens in South Africa: a retrospective cohort study

Treatment outcomes 24 months after initiating short, all-oral bedaquiline-containing or injectable-containing rifampicin-resistant tuberculosis treatment regimens in South Africa: a retrospective cohort study
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South africaUnited statesRheinland pfalzMtbdrsl hain lifescienceNational department of healthUniversity of witwatersrand johannesburgHuman research ethics committeeHain lifescienceNational departmentClinical guidanceInjectable free regimensRifampicin resistant tuberculosisTransl med

Barnard Reinstates Indoor Mask Mandate – Bwog

Barnard Reinstates Indoor Mask Mandate – Bwog
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New yorkUnited statesMarina catallozziBarnard communicationsVaccine requirements barnard communicationsUpdates barnard communicationsMilstein centerDear barnard communityJanuary omicronChief health officer catallozziBarnard communityCoverified informationClinical guidance

Fifth Update of ACR COVID-19 Vaccine Guidance Supports

Atlanta, Feb. 02, 2022 (GLOBE NEWSWIRE) The American College of Rheumatology has issued an updated version of its COVID-19 Vaccine Clinical Guidance.

Jeffrey curtisAmerican college of rheumatologyVaccine guidance taskAmerican collegeClinical guidanceMusculoskeletal diseasesGuidance taskCovid 19Medical recommendationsCovid 19 vaccineRheumatic diseaseAutoimmune disease

Go for test for TB, other conditions if cough persists for more than 2-3 weeks: Revised clinical guidance for Covid patients

New Delhi, January 18 The Union Health Ministry has advised Covid patients to go for tests for tuberculosis and other conditions if cough persists for more than 2-3 weeks. The revised ‘Clinica

New delhiNational taskMonitoring groupUnion health ministryClinical guidanceTask forceJoint monitoring group

COVID-19: Govt issues guidelines on use of remdesivir, tocilizumab

The revised guidelines continue to recommend emergency use authorization (EUA) or off-label use of remdesivir in patients with "moderate to severe" disease and those with no renal or hepatic dysfunction within 10 days of the onset of any symptom.

National taskMonitoring groupClinical guidanceTask forceJoint monitoring groupOvid 19 off label use of existing drugsEmdesivir mechanism of actionReatment of covid 19 or coronavirus diseaseRemdesivir side effectsMmunosuppressors on top of steroidsXisting therapies for severe covid 19Treatment of covid 19Herapies for severe covid 19Remdesivir therapyOcilizumab dose in covidOvid 19 clinical guidelines