The Hong Kong Department of Health (HKDH) found Xiaokeshuping Jiangtangning Jiaonang capsules to contain the undeclared pharmaceutical drugs phenformin, rosiglitazone, and glibenclamide, which may be used in diabetes to lower blood sugar. The HKDH conducted the analysis following receipt of a report that one woman in China had been hospitalized due to a serious hypoglycaemic attack (very low blood sugar) after using Xiaokeshuping Jiangtangning Jiaonang.

حذر خبراء في الصيدلة من الادعاءات التي يسوق لها أصحاب محلات العطارة لمنتجات عشبية (سامة)، ومستحضرات ضارة بالصحة.

وأكدوا ل"الرياض": أن حجر السعادة(حجر جهنم) والذي يؤكد المسوقون له بأنه علاج فعال ومضمون ولا يوجد له محاذير طبية، هو عبارة عن مجموعة من المواد الصمغية والتي تحتوي على مواد سامة لها آثار جانبية ضارة تؤدي إلى تليف الكبد، ومواد مهلوسة محظورة دوليا.

ويأتي هذا التحذير في الوقت الذي تسوق محلات العطارة لأعشاب وأدوية لمعالجة جميع الأمراض، في ظل غياب الجهات الرقابية.

The Centers for Disease Control and Prevention (CDC), collaborating with the Food and Drug Administration, state and other partners, has identified an outbreak of a serious but rare eye infection called Acanthamoeba keratitis (AK). This infection is caused by a free-living ameba (Acanthamoeba) a microscopic organism found everywhere in nature. Infections can result in permanent visual impairment or blindness. AK primarily affects otherwise healthy people, most of whom wear contact lenses.

أصدرت صحة كندا تحذيراً للمستهلكين بعدم استخدام مستحضر HS Joy of Love وذلك لاحتمالية حدوث آثار سلبية بالغة. وذلك بعد تلقيها بلاغاً من إدارة الغذاء والدواء الأمريكية يقضي بعدم استخدام هذا المنتج الأمريكي المصدر، والذي يسوق لغرض علاج حالات الضعف الجنسي. وهو موجود على هيئة علب كرتونية يحتوي كل منها على 12 كبسولة وتسوق على صيغة مكملات غذائية.

Novartis and FDA notified healthcare professionals of changes to the WARNINGS and ADVERSE REACTIONS sections of the product labeling for Exjade, a drug used to treat chronic iron overload due to blood transfusions (transfusional hemosiderosis) in patients 2 years of age and older. Cases of acute renal failure, some with a fatal outcome, have been reported following the post marketing use of Exjade. Most of the fatalities occurred in patients with multiple co-morbidities and who were in advanced stages of their hematological disorders.

The Food and Drug Administration (FDA) is advising consumers not to purchase or use "True Man" or "Energy Max" products promoted and sold as dietary supplements throughout the United States. Both products -- touted as sexual enhancement products and as treatments for erectile dysfunction (ED) -- are illegal drug products that contain potentially harmful, undeclared ingredients.The products contain substances called analogs that have similar structures to active ingredients in approved prescription drugs.

Consumers are urged not to buy or use four health products and two proprietary Chinese medicines that contain potentially hazardous ingredients which can cause side effects, the Department of Health says.

The health products are Power 58 Extra, Platinum Power 58 Extra, E nhanix New Extra Men's Formula and Valentino. The two proprietary Chinese medicines are King Power Oral Solution and Stretch Up Capsules.

 Power 58 Extra

FDA warned consumers to avoid using tubes of toothpaste labeled as "Made in China". The warning and an import alert were issued to prevent toothpaste containing a poisonous chemical, diethylene glycol (DEG) from entering the United States from China. The substance is used in antifreeze and as a solvent. Although FDA is not aware of any U.S. reports of poisonings from toothpaste containing DEG, FDA is concerned about chronic exposure to DEG and exposure to the product in certain populations, such as children and individuals with kidney or liver disease.

OTTAWA - Health Canada is warning consumers not to use the product Encore Tabs for Men, because it contains an undeclared pharmaceutical ingredient similar to the approved drug tadalafil. Tadalafil is a prescription medication indicated for the treatment of erectile dysfunction and should only be used under the supervision of a health professional.

FDA notified healthcare professionals and cystic fibrosis patients in U.S that the Agency is investigating the possible connection between the use of a liquid solution of Colistimethate that was premixed for inhalation with a nebulizer and the death of a patient with cystic fibrosis (CF).