NewsBreak Original

According to a source involved with the conversations who wanted to remain anonymous because they were not authorized to disclose specifics of ongoing negotiations, US officials are debating whether to offer those who are at a high risk of developing severe COVID-19 the opportunity to receive another bivalent booster.

The recalled buns were distributed in retail stores in Michigan, Ohio, Indiana, and Illinois. Perfection Bakeries D/B/A Aunt Millie’s of Fort Wayne, IN. is recalling 8 ct. packages of Our Family® White Hot Dog Buns because they may contain undeclared sesame. People who have an allergy or severe sensitivity to sesame run the risk of serious or life- threatening allergic reaction if they consume these products." States the FDA website.

On Wednesday, AbbVie Inc. (ABBV.N) announced that the United States Food and Drug Administration (FDA) had denied the approval of its medication for Parkinson's disease in adults and had asked for additional information on the device that is used to deliver the medicine.

A new study unveils a startling revelation: 60% of US food purchases comprise colorful and flavorful delights packed with, you guessed it, additives. From preservatives to sweeteners, it seems Americans' palates are dancing to an artificial tune.

In the 2018 farm bill, hemp and its derivatives were broadly legalized, though it seemed to be a side effect of the legislation and not an intended purpose. The Farm Bill also accidentally legalized what is known as Delta 8 and Delta 10 cannabinoids derivatives, these are low potent THC derivatives like the well known Delta 9 THC, which gives marijuana users the signature high.

A hepatitis A outbreak may be linked to certain brands of frozen organic strawberries that are sold nationwide at retailers including Trader Joe's and Costco, according to the U.S. Federal Drug Administration, which announced a recall of the products this week.

Pennsylvania State Senator, Elder A. Vogel Jr. will soon propose legislation to “clearly define” milk in Pennsylvania. Vogel plans to introduce the bill in response to a recent decision by the federal Food and Drug Administration (FDA) to allow plant-based milk alternatives, such as soy, almond, and coconut milk, to continue using the term “milk.” The senator claims that this contradicts the FDA's own definition and harms the dairy industry.

Quickly as possible, mammography facilities will have to abide by new regulations. Earlier this week, the U.S. Food and Drug Administration (FDA) updated the rules requiring mammogram providers to inform patients of the density of their breast tissue.

EzriCare Artificial Tears Linked to Infections - Did you use EzriCare or Delsam Pharma artificial tears to treat dry or irritated eyes? Did you get an eye infection?. The FDA and CDC are reporting that EzriCare Artificial Tears Lubricant Eye Drops, as well as Delsam Pharma Eye Ointment has been causing eye infections in people who used these ey drops. Delsam Pharma and EzriCare are sold over the counter to relieve dry and irritated eyes. Recently, there have been a significant number of cases where people developed antibiotic-resistant eye infections following use of artificial tears. Some infections became so severe they led to permanent vision loss, hospitalization and even death when an infection got into the bloodstream.

On January 6th, 2023, Leqembi (previously known as BAN2401) was granted FDA approval, as it is the first disease-modifying treatment that has demonstrated effectiveness for individuals with mild cognitive impairment (MCI) and mild Alzheimer's disease (AD). Leqembi, its brand name, was developed under the name Lecanemab. In this article we will discuss the drug, dementia, and its potential for treating Alzheimer's disease, as well as costs. Helpdementia spends a lot of time researching and writing about Dementia and Alzheimer's.

Despite the widespread and well-grounded belief that food additives are a big threat to our general health, there are 2 common additives that can actually help the body when consumed in moderation. These 2 components are Guar Gum and Xanthan Gum.

Walgreens, one of the largest drugstore chains in the US, recently announced that it will not sell the abortion pill, mifepristone, in 20 states where it had been warned of legal consequences if it did so. This decision has implications for women’s reproductive rights in the US, and has sparked controversy and debate across the country. In this article, we take a closer look at the issue of abortion pills and what Walgreens’ decision means for women’s access to this medication.

Photo by(Sarah Silbiger/Getty Images) (PORTLAND, Ore.) Hello Portlanders! It's Friday, March 3 - Here's your daily round up of all the news happening in the City of Roses.

The US Food and Drug Administration has urged Pfizer to conduct a safety study if the shot is approved following the diagnosis of Guillain-Barre syndrome in two people who received Pfizer's respiratory syncytial virus (RSV) vaccine during a clinical trial. Agency documents were made public on Friday.

The US Food and Drug Administration (FDA) has issued a warning to consumers and healthcare practitioners to avoid using EzriCare Artificial Tears or Delsam Pharma’s Artificial Tears due to the potential risk of bacterial contamination. Both products are over-the-counter and are manufactured by Global Pharma Healthcare Private Limited with the intention of being sterile.

TRENTON, NJ. - The New Jersey Senate and General Assembly are considering a new bill requiring health insurance carriers to cover prescribed anti-obesity medication approved by the U.S. Food and Drug Administration. If passed, this bill would expand access to obesity medication and improve prevention efforts for the disease.

In response to a request from the Alzheimer's Association, the U.S. government health plan for individuals over 65 stated on Wednesday that it would not change the stringent coverage restrictions that were put in place last year for new Alzheimer's medicines.

FDA's Rejection of Soligenix Inc's Cancer Treatment Application Leads to a Steep Drop in Stock Value. The drug manufacturer Soligenix Inc. (SNGX.O) announced on Tuesday that the U.S. Food and Drug Administration (FDA) had decided not to review its request for approval of its cancer treatment. This news caused a more than 30% downturn in the stock price in opening trade.

Following early data examined by U.S. health authorities, a safety monitoring system warned that the revised COVID-19 shot from American pharmaceutical company Pfizer Inc. (PFE.N) and German partner BioNTech might be connected to a specific type of cerebral stroke in older persons.