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Michael Felberbaum
@FDASpox
Asst. Commissioner for Media Affairs at . Tripawd dog dad. Extremely amateur hockey player.
Silver Spring, MDfda.govJoined January 2022

Michael Felberbaum’s Tweets

Today’s action to limit the use of Evusheld prevents exposing patients to possible side effects such as allergic reactions, which can be potentially serious, at a time when fewer than 10% of circulating variants in the U.S. causing infection are susceptible to the product.
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Based on today’s revision to the Emergency Use Authorization (EUA) for Evusheld (tixagevimab co-packaged with cilgavimab), it is not currently authorized for emergency use in the U.S. fda.gov/drugs/drug-saf
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Coronavirus molecule on a black background with the text “COVID-19 Announcement”. FDA logo in corner.
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WATCH LIVE: Today’s VRBPAC meeting is underway where the committee will discuss whether and how the composition for primary doses of the currently available COVID-19 vaccines should be modified and whether booster doses should be adjusted moving forward.
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For more than 30 years, the FDA has been working to reduce exposure to lead, and other environmental contaminants, from foods. This work has resulted in a dramatic decline in lead exposure from foods since the mid-1980s.
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Today we announced draft guidance for industry on action levels for lead in processed foods that are intended for babies and children under 2 years of age, to help reduce potential health effects in this vulnerable population from dietary exposure to lead. fda.gov/news-events/pr
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Complete your week with the latest “FDA Roundup”, our at-a-glance summary of agency updates.
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Today’s “FDA Roundup” has info on a draft guidance related to mpox, a final rule on radiological health regulations & an immediately-in-effect guidance on compounding certain ibuprofen products in an effort to bolster the supply of pediatric ibuprofen. fda.gov/news-events/pr
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From cosmetics, to medical devices, to tobacco, the FDA exists to protect and promote the public health. This short informational video briefly covers the creation of the FDA, its expansion, and some of what it regulates today.
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The bivalent COVID-19 vaccines have been associated with a significant reduction in hospitalization and death in all populations examined, which is clinically meaningful. See this page on COVID-19 hospitalizations from . gis.cdc.gov/grasp/covidnet
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The Covid bivalent vaccine booster works better than expected. I've reviewed the cumulative data erictopol.substack.com/p/the-bivalent That's in contrast to a @NEJM essay today and 2 lab studies that used a pseudovirus assay without assessing the XBB variants
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It was great to speak on a panel today with Dr. Renee Wegrzyn. is building a great team – on the cutting edge – to support transformative research driving biomedical and health breakthroughs.
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Our @ARPA_HDirector, Dr. Renee Wegrzyn, is LIVE on the @US_FDA & ARPA-H: Life Sciences, Biopharma & MedTech Priorities in a New Year panel with Commissioner @DrCaliff_FDA at the 41st Annual @jpmorgan Healthcare Conference. #JPM23 #JPM2023 jpmorgan.com/solutions/cib/
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Significant progress has been made in the collaborative work to ensure nutritious, safe infant formulas are on store shelves.
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@US_FDA continues to support a diversified and stable infant formula supply by providing a pathway for certain manufacturers to continue marketing their products in the U.S. fda.gov/food/cfsan-con
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Today, we approved a new medication for the treatment of Alzheimer’s disease, the second of a new category of medications approved for Alzheimer's that target the fundamental pathophysiology of the disease. fda.gov/news-events/pr
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#ICYMI over the holidays, Director Dr. Brian King and I wrote this article for on the need for a smoking cessation “care package.”
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FDA leaders propose the creation of a comprehensive “care package” framework of resources to help maximize cessation of tobacco use, including components focused on strategies at the individual, health system, and population levels. ja.ma/3vv2RpH
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It’s a new year, but misinformation/disinformation is still prevalent. After reading this editorial, I think we should talk about XBB and the COVID-19 vaccines. Thread… 🧵
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Some New Year’s vaccine disinformation from the WSJ. wsj.com/articles/are-v
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This afternoon, sent the following message to staff regarding the passage of the end-of year spending bill and the numerous FDA-related provisions included that will help strengthen the agency’s authority and ability to fulfill our public health mandate.
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It’s been exactly two years since the first COVID-19 vaccine was delivered outside of clinical trials. We’ve made so much progress in combating COVID, but we all need to do our part. We continue to strongly encourage you to consider getting vaccinated.
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