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Problem: Unapproved stem-cell therapies are being marketed to people with long COVID

New research has identified 38 direct-to-consumer businesses marketing stem-cell treatments and exosome therapies for COVID-19 infections and, especially, long COVID, despite lacking approval by US Food and Drug Administration and other regulatory body in the United States. Descriptions of the businesses and an analysis of their marketing strategies are published in Stem Cell Reports.

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Beyfortus drug to protect infants from RSV is in short supply--CDC warns

 

... The agency told doctors to prioritize getting those doses to infants at the highest risk of severe RSV, including infants younger than 6 months and those with underlying conditions. The CDC also advised doctors to preserve 50 mg doses for infants who weigh less than 11 pounds.

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Growing anti-vax movement perplexes Biden administration, medical community

Biden world at a loss over how to stop the growing anti-vax movement - POLITICO

A Biden administration that vowed to restore Americans’ faith in public health has grown increasingly paralyzed over how to combat the resurgence in vaccine skepticism. ...

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Moderna combination Covid, flu vaccine moves to final stage trial after positive data

Moderna combination Covid, flu vaccine shows positive data (cnbc.com)

 

  • Moderna on Wednesday said its combination vaccine targeting Covid and the flu will move to a final stage trial after showing positive results in an earlier study.
  • The biotech company is hoping its shot, mRNA-1083, can win approval from regulators in 2025. 

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