Sydney Lupkin
speaker
1,087 appearances
111 recordings
3 series
first heard Dec 2024
last heard 4d ago
Sydney Lupkin’s voice in public audio — every appearance, attributed to the second.
Trend
recordings per month · last 12 monthsRecordings per month over the last 12 months — 96 in all, peaking in Sep 2026 with 23.
Appearances
She says patients can use vaccine finders, which Pfizer and Moderna both have up and running, to find pharmacies with COVID shots in their area.
Sidney Lupkin, NPR News.
The President signed a memo Tuesday to ramp up Food and Drug Administration enforcement and curb some direct to consumer drug ads.
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Senior officials speaking to reporters on condition of anonymity say they will be looking beyond TV and print ads and focusing on social media and influencer drug advertising.
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Still, experts like Dr.
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Caleb Alexander at the Johns Hopkins Bloomberg School of Public Health questioned how much the administration can do.
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According to a statement from the Department of Health and Human Services, the administration wants to close a loophole that allowed ads to include abbreviated safety information and then direct patients elsewhere for full disclosures.
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Sidney Lefkin, NPR News.
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Serepta therapeutics says it is stopping all shipments of Alevitus, a gene therapy for patients with Duchenne muscular dystrophy.
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The company is working with the FDA to update the gene therapy's safety label.
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The FDA announced last week that it asked Zerepta to pause shipments after three patients died of acute liver failure.
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Serepta had already paused shipments of Elevitus for patients unable to walk following the deaths.
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It initially resisted doing so for patients still able to walk, saying there was no new applicable safety data.
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Serepta's CEO said the decision to pause all shipments was painful but necessary to ensure a good relationship with the agency.
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Sidney Lupkin, NPR News.
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Theraputics says it is stopping all shipments of Alevitus, a gene therapy for patients with Duchenne muscular dystrophy.
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The company is working with the FDA to update the gene therapy's safety label.
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The FDA announced last week that it asked Zerepta to pause shipments after three patients died of acute liver failure.
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Serepta had already paused shipments of Elevitus for patients unable to walk following the deaths.
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It initially resisted doing so for patients still able to walk, saying there was no new applicable safety data.
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Showing 1041–1060 of 1,087 · page 53 of 55
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