FDA Authorizes Pfizer Covid Booster For Kids As Young As 6 Months
The shot is for children who were previously vaccinated with three doses of the original vaccine. In other covid-related news, operators of an upscale Los Angeles care facility for dementia patients were charged Tuesday with felony elder abuse.
CNBC:
FDA Authorizes Pfizer's Covid Omicron Booster As Fourth Shot For Kids Under 5
The U.S. Food and Drug Administration on Tuesday authorized Pfizer’s omicron booster shot for kids under five years old who were previously vaccinated with three doses of the company’s original vaccine. Children six months through four years old who completed their three-dose primary series with Pfizer and BioNTech’s original monovalent shots more than two months ago are now eligible to receive a single booster dose of the updated shot. The new shot is bivalent, meaning it targets the original Covid strain as well as omicron BA.4 and BA.5. (Constantino, 3/14)
In other Pfizer news —
Reuters:
Pfizer's COVID Drug Data Supports Use In High-Risk Patients - FDA Staff
The U.S. health regulator's staff reviewers said on Tuesday data from Pfizer Inc's COVID-19 drug trials support its use in adults at high risk of progressing to severe disease, bringing the pill closer to a full approval. The Food and Drug Administration made its assessment in briefing documents ahead of a meeting of the agency's external advisers on Thursday to discuss full approval to use Pfizer's oral pill for high-risk COVID-19 patients exhibiting mild to moderate symptoms. (Mandowara and Leo, 3/14)
CNBC:
FDA Staff: Pfizer's Covid Treatment Paxlovid Appears Effective To Use In High-Risk Adults
U.S. Food and Drug Administration staff on Tuesday said Pfizer’s clinical trial results on its Covid antiviral pill Paxlovid support the drug’s use in adults at high risk of progressing to severe disease. The FDA staff made the conclusion in briefing documents ahead of a meeting on Thursday, when external advisors on the agency’s Antimicrobial Drugs Advisory Committee will discuss whether to recommend full approval of Paxlovid for the treatment of mild to moderate Covid in high-risk adults. (Constantino, 3/14)
Axios:
FDA: Paxlovid Not Associated With COVID Rebound
Paxlovid isn't associated with COVID rebound, in which patients test positive or have symptoms days after a course of the drug is completed, Food and Drug Administration staff said in briefing documents released Tuesday. (Moreno, 3/14)
In other covid news —
Los Angeles Times:
L.A. Care Facility Operators Charged In 14 COVID Deaths
The operators of an upscale Los Angeles care facility for dementia patients were charged Tuesday with felony elder abuse and other criminal counts related to the deaths of an employee and thirteen residents during the early days of the pandemic. Silverado Beverly Place, near the Fairfax district, specializes in caring for elderly residents with Alzheimer’s and dementia, and was the site of a COVID-19 outbreak in March 2020. (Solis, 3/14)
WMFE:
Exploring Long COVID, Part 1: Why Don't We Know More About It?
More than 1 million Americans have died from COVID-19 since President Donald Trump declared it a national emergency three years ago. That includes 87,000 Floridians. Among the survivors, are those with long-haul COVID, or long COVID, a phenomenon still not fully understood. But what is long COVID? (Pedersen, 3/14)
WMFE:
Exploring Long COVID Part 2: What's It Like To Have It?
One year after first testing positive for COVID-19, Mount Dora resident Tanya Balyeat still has weakened lungs and the short-term memory loss phenomenon known as brain fog. They are the lingering symptoms of long COVID, experienced by about 29% of those who test positive for COVID-19, according to the Centers for Disease Control and Prevention. (Pedersen, 3/15)
