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- ByHeart sued over recalled formula by parents of infants sickened with botulism15.11.2025Two families have filed lawsuits against ByHeart Inc. after their infants contracted botulism from allegedly consuming the company's formula.
- Volcanic eruption led to the Black Death, new research suggests04.12.2025New data suggests an eruption cooled Europe, disrupted harvests and pushed Italian states into grain trades that may have begun one of history’s deadliest pandemics.
- Improving as a Pioneer: Examples from My Vocation25.09.2023Initiative isn't only a title; it's a guarantee to nonstop development and improvement. All through my vocation, I've had the
- BioMarin to acquire Amicus Therapeutics for $4.8 billion in rare disease bet19.12.2025Dec 19 () - BioMarin Pharmaceutical said on Friday it would acquire Amicus Therapeutics for about $4.8 billion, expanding its presence in rare metabolic diseases.
- San Francisco sues 10 companies that make ultraprocessed food02.12.2025San Francisco on Tuesday sued 10 major food companies, alleging that they marketed and sold ultraprocessed foods that they knew were harmful to human health.
- Figure out How to Use Your Nursing Abilities for Better Compensation17.10.2023Exploring the scene of nursing remuneration can be complicated, yet with the right methodology, utilizing your skills is conceivable
- Comet C/2025 K1 (ATLAS) breaks apart in incredible telescope photos19.11.2025Astronomer Gianluca Masi captured breathtaking imagery of solar system comet C/2025 K1 (ATLAS) breaking into multiple pieces after being warmed by the sun.
- FDA adds strongest warning to Sarepta gene therapy linked to 2 patient deaths14.11.2025The Food and Drug Administration said Friday it will add a new warning and other limitations to a gene therapy for Duchenne’s muscular dystrophy that's been linked to two patient deaths. The infused therapy from Sarepta Therapeutics will carry a boxed warning — the most serious type — alerting doctors and patients to the risk of potentially fatal liver failure with the treatment, the FDA said in a release. The one-time therapy, Elevidys, has been under FDA scrutiny since the company reported t
