logo
Capricor treatment of Becker muscular dystrophy granted orphan designation

Capricor treatment of Becker muscular dystrophy granted orphan designation

Business Insider13 hours ago

The FDA granted orphan designation to a treatment of Becker muscular dystrophy being developed by Capricor, according to a post to the agency's website.
Confident Investing Starts Here:
Easily unpack a company's performance with TipRanks' new KPI Data for smart investment decisions
Receive undervalued, market resilient stocks right to your inbox with TipRanks' Smart Value Newsletter
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Dr Pepper Has Recalled Thousands of Cases of Soda
Dr Pepper Has Recalled Thousands of Cases of Soda

Yahoo

time2 hours ago

  • Yahoo

Dr Pepper Has Recalled Thousands of Cases of Soda

In perhaps the funniest mislabeling blunder ever, Pepsi Beverages Company is recalling over 19,000 cases of Dr Pepper Zero Sugar products because they actually do, in fact, contain sugar. Whoops! The Class II recall has a low risk of serious health consequences, but temporary or reversible effects may occur, according to the FDA. To date, no illnesses or adverse reactions have been reported. While the recall pertains to a large amount of product, the sodas in question were only distributed to retail locations in three states—Florida, South Carolina, and Georgia. The affected products were packaged in 12 fl oz. aluminum cans in both 12-pack and 24-pack cartons and have a "best by" date of February 16, 2026 and product code XXXXRS05165. While the average consumer might not have issues with accidentally consuming these mislabeled products, the error could indeed pose health risks for people with diabetes or anyone with conditions instructed to monitor their sugar intake. A can of regular Dr Pepper contains 39 grams of sugar, while Dr Pepper Zero Sugar, obviously is meant to contain zero. The latter does, however, contain artificial sweeteners and additional ingredients like aspartame, acesulfame potassium, and sodium phosphate. Good thing we have a doctor in the house. All recalled products should either be thrown away or returned to your place of purchase. You Might Also Like Can Apple Cider Vinegar Lead to Weight Loss? Bobbi Brown Shares Her Top Face-Transforming Makeup Tips for Women Over 50

Dark chocolate almonds recalled over potentially fatal allergen contamination
Dark chocolate almonds recalled over potentially fatal allergen contamination

Yahoo

time2 hours ago

  • Yahoo

Dark chocolate almonds recalled over potentially fatal allergen contamination

Grocery chain Meijer has announced the recall of certain packages of dark chocolate almonds due to contamination with an undeclared allergen. The company announced the recall June 13, stating that packages of Frederik's Dark Chocolate Almonds may also contain dark chocolate cashews, according to a press release. Those with a cashew allergy run the risk of experiencing a life-threatening reaction if they consume the product, as the nuts were not declared on the packaging. Two different packages of Frederik's Dark Chocolate Almonds were affected by the recall: The black stand-up pouches sold at Meijer stores in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin with a sell-by date of 05/07/2026 or 05/28/2026, and the 8-count, 1.5-ounce multi-pack boxes with a sell-by date of 05/05/2026. No illnesses have been reported. Customers who have purchased the product are urged to return it to Meijer to claim a full refund. Meijer's statement is the latest in a slew of recalls impacting various foods and chains. Turkana Food Inc issued a recall on 352 cases of its Floria Dried Apricots, according to a press release shared by the U.S. Food and Drug Administration on Thursday. The product was recalled because it contains an undeclared allergen, sulfites, or 'chemicals used as preservatives' added to foods, beverages, and medications to prevent them from spoiling, according to the Cleveland Clinic. Floria Dried Apricots impacted by the recall were sold at stores in 19 states: Alabama, California, Florida, Illinois, Indiana, Kentucky, Massachusetts, Maryland, Michigan, Missouri, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Rhode Island, Tennessee, Texas, and Virginia. The product has the LOT number 440090478-15-333 on the bottom portion of the packaging. The UPC Label 2539560010 is marked by a sticker on the side of the packaging. The expiration date of November 2026 is also on the bottom of the packaging. Then, ice cream company Breyers recalled one of its flavors following customer concerns that there was a mislabeling error. On Tuesday, the United States Food and Drug Administration (FDA) confirmed in a report that 6,668 cases of Breyers Chocolate Truffle Ice Cream were voluntarily recalled by Unilever Manufacturing on June 2 after it was found that the tubs actually contained Rocky Road ice cream. The Chocolate Truffle flavor has an allergen label that reads, 'may contain tree nuts,' while the Rocky Road flavor declares almonds as one of the ingredients. In a statement made to People, a representative for Breyers said, 'People with an almond allergy should not consume the product due to risk of serious or life-threatening allergic reaction. The safety and quality of our products are our top priority. For more information, consumers can visit or call 1-800-931-2826.'

‘Gas station heroin' is technically illegal and widely available. Here are the facts
‘Gas station heroin' is technically illegal and widely available. Here are the facts

The Hill

time3 hours ago

  • The Hill

‘Gas station heroin' is technically illegal and widely available. Here are the facts

WASHINGTON (AP) — Health officials want you to think twice before buying one of those brightly colored little bottles often sold at gas stations, convenience stores and smoke shops. Sometimes called 'gas station heroin,' the products are usually marketed as energy shots or cognitive supplements but actually contain tianeptine, an unapproved drug that can be addictive and carries risks of serious side effects. U.S. poison control centers have reported a steady rise in calls linked to the drug for more than a decade. And last month the Food and Drug Administration sent a warning to health professionals about 'the magnitude of the underlying danger or these products.' Here's what to know about gas station heroin. Tianeptine is approved in a number foreign countries as an antidepressant, usually as a low-dose pill taken three times a day. But it has never been approved by the FDA for any medical condition in the U.S. Additionally, the drug cannot legally be added to foods and beverages or sold as a dietary supplement — something the FDA has repeatedly warned U.S. companies about. Still, under-the-radar firms sell tianeptine in various formulas, often with brand names like Zaza, Tianaa, Pegasus and TD Red. Although that is technically illegal, the FDA does not preapprove ingredients added to supplements and beverages. 'It's kind of this grey area of consumer products, or supplements, where the contents are not regulated or tested the way they would be with a medication,' said Dr. Diane Calello of the New Jersey Poison Information and Education System. Last year, Calello and her colleagues published a study documenting a cluster of emergency calls in New Jersey tied to a flavored elixir called Neptune's Fix. People experienced distress, rapid heartbeat, low blood pressure and seizures after drinking it. More than a dozen of the 20 patients had to be admitted for intensive care. Many tianeptine products claim— without evidence or FDA approval— to help users treat medical conditions, including addiction, pain and depression. In 2018, the FDA issued a warning letter to the maker of a product called Tianna, which claimed to provide 'an unparalleled solution to cravings for opiates.' While tianeptine is not an opioid, the drug binds to some of the same receptors in the brain, which can temporarily produce effects akin to oxycodone and other opioids. Tianeptine also carries some of the same physiological risks of opioids, including the potential to dangerously depress breathing. 'That's what tends to get people into trouble,' said Dr. Hannah Hays of Nationwide Children's Hospital in Columbus, Ohio. 'They use it for opioid-like effects or to self-treat opioid withdrawal and that can lead to slow breathing and problems like that.' People dealing with opioid addiction, pain, depression, anxiety and other conditions should see a health professional to get a prescription for FDA-approved treatments, Hays said. Experts aren't sure but national figures show a big rise in emergency calls involving the drug. Calls to poison control centers increased 525% between 2018 and 2023, according to a data analysis published earlier this year. In about 40% of cases, the person had to seek medical care, with more than half of them needing critical care. One explanation for the rise in calls is simply that more Americans are using the products. But experts also say that the products are triggering more emergencies as they become more potent and dangerous. And the researchers in New Jersey who analyzed Neptune's Fix found that the liquid also contained synthetic cannabis and other drugs. 'You never quite know what's in that bottle,' Calello said. 'It's important for people to know that even if they have used a product before, they could get a bottle that contains something very different from what they're looking for.' Tianeptine is not included in the federal Controlled Substances Act, which bans or restricts drugs that have no medical use or have a high potential for abuse, such as heroin, LSD and PCP. But about a dozen states have passed laws prohibiting or restricting tianeptine, including Alabama, Georgia, Michigan, Minnesota, Ohio and Tennessee. In some cases, those laws have led to more cases of withdrawal among users of tianeptine, which can be chemically addictive. But state data also shows some success in reducing harm tied to the drug. Until recently, Alabama had the highest rate of tianeptine-related calls in the southern U.S., which increased more than 1,400% between 2018 to 2021. But after the state restricted tianeptine in 2021 calls began modestly decreasing while calls across other southern states continued to climb. ___ The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute's Science and Educational Media Group and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store