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FDA proposes to exclude semaglutide, tirzepatide, and liraglutide on the 503B bulks list. After careful review, we did not identify sufficient clinical need for outsourcing facilities to compound these drugs from bulk substances. Public comment period now open. Learn more:

FDA proposes to exclude semaglutide, tirzepatide, and liraglutide on the 503B bulks list. After careful review, we did not identify sufficient clinical need for outsourcing facilities to compound these drugs from bulk substances. Public comment period now open. Learn more:

105,392 Aufrufe

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"We have the safest food supply in the world." – Acting Commissioner Deputy Commissioner Kyle Diamantas on CNBC. "Americans should feel confident in eating fresh produce including leafy greens at this point. FDA remains confident that all iceberg lettuce related to the cyclospora outbreak has been effectively removed from the market."

"We have the safest food supply in the world." – Acting Commissioner Deputy Commissioner Kyle Diamantas on CNBC. "Americans should feel confident in eating fresh produce including leafy greens at this point. FDA remains confident that all iceberg lettuce related to the cyclospora outbreak has been effectively removed from the market."

47,241 Aufrufe • vor 6 Tagen

Today, FDA provided important updates on the risk of myocarditis after receiving an mRNA COVID-19 vaccine, noting the risk is higher in young men.

Today, FDA provided important updates on the risk of myocarditis after receiving an mRNA COVID-19 vaccine, noting the risk is higher in young men.

1,898,803 Aufrufe • vor 1 Jahr

FDA approved two new drugs for rare diseases this week! Learn more about these approvals and other good news:

FDA approved two new drugs for rare diseases this week! Learn more about these approvals and other good news:

30,360 Aufrufe • vor 4 Monaten

For patients with severe Leukocyte Adhesion Deficiency Type I (LAD-I), treatment options have been limited. A new gene therapy may offer hope through the FDA’s accelerated approval pathway.

For patients with severe Leukocyte Adhesion Deficiency Type I (LAD-I), treatment options have been limited. A new gene therapy may offer hope through the FDA’s accelerated approval pathway.

10,387 Aufrufe • vor 4 Monaten

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