Malaysian Ivermectin Study Inconclusive

2 years ago
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Malaysian Ivermectin Study Inconclusive

A study from Malaysia for Ivermectin vs. standard of care shows in significant efficacy in any of its primary or secondary outcomes. Let's review the data.

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URL list from Friday, Feb. 18 2022

Efficacy of Ivermectin Treatment on Disease Progression Among Adults With Mild to Moderate COVID-19 and Comorbidities: The I-TECH Randomized Clinical Trial | Critical Care Medicine | JAMA Internal Medicine | JAMA Network
https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/2789362

ioi220006va_1644957302.1595.png (3011×1698)
https://cdn.jamanetwork.com/ama/content_public/journal/intemed/0/ioi220006va_1644957302.1595.png?Expires=1648255758&Signature=N8G8Cff1bwPM~-vD2bpfeAOmT~-olY2v1TOEShUchIKWfuFKZ-v3vQ~jv0GwXTCWr0MzO5CyKgVPiuqVmtqUc-xokAXWDKm~zmtnu8cVAg2wR2FwNMlyCb5ewjzrm1doTKGoy3Vt5zmOCWpd-M0VphlhdBvAMg1f91obZ76eVsUFbHoD6MdBf0HJt2ksfHotkMVsj4yp~WyTMJi4ywU1tcpd77p~QpcgYNz5pakXFlpVhddxWnqgR3pptjdXB9bvmCmf9uKLXiFZm4KuJk1gnNDd9UGgdP~CIU0aTHefTJlre0h5BqRsb5iEUYkEH51mREPZAFPNgV0F-m9ED0rLRw__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA

Coronavirus (COVID-19) Update: FDA Authorizes New Monoclonal Antibody for Treatment of COVID-19 that Retains Activity Against Omicron Variant | FDA
https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-new-monoclonal-antibody-treatment-covid-19-retains

Effectiveness of Remdesivir, Lopinavir/Ritonavir, and Favipiravir for COVID-19 Treatment: A Systematic Review - PMC
https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC8627269/

The FDA delays considering the Pfizer COVID vaccine for kids under age 5 : NPR
https://www.npr.org/2022/02/11/1080204817/the-fda-delays-considering-the-pfizer-covid-vaccine-for-kids-under-age-5

Pfizer and BioNTech Provide Update on Ongoing Studies of COVID-19 Vaccine | Pfizer
https://www.pfizer.com/news/press-release/press-release-detail/pfizer-and-biontech-provide-update-ongoing-studies-covid-19

Pfizer and BioNTech Initiate Rolling Submission for Emergency Use Authorization of Their COVID-19 Vaccine in Children 6 Months Through 4 Years of Age Following Request From U.S. FDA | Pfizer
https://www.pfizer.com/news/press-release/press-release-detail/pfizer-and-biontech-initiate-rolling-submission-emergency

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