Cơ quan Quản lý Thực phẩm và Dược phẩm Mỹ (FDA) yêu cầu Nara Organics tự nguyện thu hồi 16 lô sữa bột công thức hữu cơ trên toàn quốc sau khi 3 trẻ sơ sinh nhập viện vì nhiễm độc tố botulinum.
The FDA has approved bemotrizinol, a new chemical UV filter for sunscreens, for the first time in nearly 30 years. Dermatologists are cheering the ingredient's broad-spectrum UVA/UVB protection, photo stability, and safety profile, which could lead to better, more aesthetically pleasing sunscreens.
The US FDA has issued an import alert for Dabur India's factory in Dadra and Nagar Haveli, India, due to significant data integrity and maintenance lapses, including falsified manufacturing records and unsanitary conditions.
US regulators are warning consumers about potential kidney problems linked to GSK's Alli weight loss pill. The FDA identified 12 cases of kidney complications and advises those with kidney history to consult a doctor.
The FDA's investigation into a botulism outbreak linked to ByHeart's infant formula, which sickened 48 infants across 17 states, failed to determine the source or root cause of contamination despite tracing the bacteria to ingredients. Three companies involved (ByHeart, Organic West, Dairy Farmers of America) deny responsibility.
Um teste de sangue para rastrear múltiplos tumores, o NHS-Galleri, não reduziu casos avançados de câncer no Reino Unido, mas detectou mais tumores em estágio inicial e menos em estágio 4, indicando potencial para detecção precoce.
Taiwan's FDA is planning new regulations to restrict functional claims for 17 health food ingredients, requiring product registration and adherence to approved wording to combat misleading marketing and enhance transparency.
Pune FDA seized 16 tonnes of jaggery, 20 tonnes of sugar, and 68 kg of artificially colored fried green peas during raids. Adulterated flour, hoarded areca nuts, and banned gutka products were also confiscated. Three establishments received stop-work notices.
Taiwan's FDA is proposing amendments to the Pharmaceutical Affairs Act to combat illegal online drug sales. The changes would empower authorities to use technology for online patrols and require internet providers to block or remove illegal content within 24 hours, retaining data for 180 days. Non-compliance could result in fines of NT$200,000 to NT$5 million.
Um novo medicamento, daraxonrasib, dobrou a sobrevida mediana de pacientes com câncer de pâncreas metastático em estudo de fase 3, reduzindo o risco de morte em 60% e apresentando baixa toxicidade. Os resultados foram apresentados na ASCO e devem levar à aprovação regulatória nos EUA.
Wockhardt's novel antibiotic Zaynich (cefepime and zidebactam) has received US FDA approval for treating complicated urinary tract infections (UTIs), including pyelonephritis, caused by resistant microorganisms. It also gained approval in India for UTIs and concurrent Gram-negative bacteremia, addressing the growing antimicrobial resistance threat.
新藥公司北極星藥業-KY宣布撤回向美國FDA提出Pegargiminase（ADI-PEG 20）用於治療惡性胸膜間皮瘤之上市許可證申請案，導致股價跳空跌停，創下掛牌來新低價。
醫材廠晉弘科技的電子式關節鏡EJA100已通過台灣TFDA第二類醫療器材審查，繼美國FDA核准後，取得台灣上市許可證。此產品為硬式拋棄式內視鏡，可降低交叉感染風險並提升效率，完善公司在軟硬式內視鏡的布局。
ABD'nin araştırma kuruluşu DARPA ve biyoteknoloji şirketi KaloCyte, toz halindeki sentetik kanı başarıyla üretti. ErythroMer adlı ürün, savaş alanlarında kan kaybı ölümlerini azaltmayı hedefliyor ve soğutma gerektirmeden taşınabiliyor.
The FDA has identified a new Salmonella outbreak with an unknown source, raising concerns about wider spread. No products have been recalled yet, and investigations are ongoing. Symptoms include diarrhea and fever, with severe cases potentially leading to life-threatening complications.
The FDA has classified the recall of over 4,000 bottles of 'Neveronix' multivitamin, produced by Lorenz Pharmaceuticals International, as Class II. The product, containing B vitamins, C, and folic acid, was sold between February and May 2026 in several US states and Puerto Rico.
Taiwan's TFDA issued guidelines clarifying that influencer marketing, unboxing videos, and testimonials can be considered advertisements for food products if they aim to drive consumption. Such content, if implying medical efficacy, faces fines up to NT$5 million.
Nova droga oral, daraxonrasib, dobra sobrevida de pacientes com câncer de pâncreas em estágio avançado. Em ensaio clínico, reduziu risco de morte em 60% e oferece esperança onde antes havia poucas opções.
工研院舉辦全球藥品韌性高峰會，邀集國內外產官學研代表，探討全球藥物供應鏈重組趨勢。經濟部推動國家藥物韌性整備計畫，聚焦關鍵藥品自主製造，並透過科專資源協助產業提升技術與國際競爭力。
Maggot therapy, FDA-approved in 2004, uses maggots to dissolve dead infected tissue in serious wounds, offering an alternative to surgery. Experts call them 'nature's microsurgeons,' though it's often a last resort.
Eine internationale Studie mit über 500.000 Teilnehmern hat die ideale Schlafdauer ermittelt. Zu wenig oder zu viel Schlaf lässt nahezu jedes Organ schneller altern und erhöht das Sterberisiko. Die optimale Schlafdauer liegt zwischen 6,5 und 7,8 Stunden.
Maggot therapy, approved by the FDA in 2004, uses maggots to dissolve dead infected tissue in serious wounds, acting as "nature's microsurgeons." Doctors often turn to this treatment when other methods fail, as it can be less invasive than surgery and avoids the need for anesthesia.
Yeni antiviral ilaç ensitrelvir, Covid-19 bulaşmasını önlemede başarılı oldu. FDA onayı bekleniyor. İlaç, virüsün çoğalmasını engelleyerek enfeksiyon oranını önemli ölçüde düşürüyor.
Dr. Tracy Beth Hoeg, an FDA official who led investigations into antidepressants, vaccines, and other therapies, has been removed from her role as acting director of the agency's drug program. Her departure follows a series of leadership changes at the FDA amid criticism from various groups.
