1. Retiros Masivos de Medicamentos para la Presión Arterial por Riesgo de Cáncer.
Múltiples lotes de medicamentos para la presión arterial, específicamente Prazosin Hydrochloride, fueron retirados del mercado debido a la preocupación de que contienen niveles elevados de químicos cancerígenos (nitrosaminas).
- Fda recalls blood pressure medication due to cancer risk, affecting 500,00 bottles tnnd the u.s. Food and drug administration fda has recalled nearly 500,00 bottles of the blood pressure medication prazosin hydrochloride due to concerns about the chemical causing cancer. The 580,00.
- Drugmakers recalled blood pressure med tainted with cancer-causing chemical the u.s. Food and drug administration says drugmakers have recalled more than a half-million bottles of the blood.
- Rxrecall two pharmaceutical companies have issued voluntary nationwide recalls of prazosin hydrochloride capsules because the pills contain an impurity in amounts that exceed the acceptable safety limit, according to the food and drug administration fda.
2. Retiro de Medicamentos para el Colesterol por Problemas de Disolución.
Cientos de miles de botellas de Atorvastatin Calcium (versión genérica de Lipitor), el medicamento más recetado en EE. UU. para el colesterol, fueron retiradas porque las píldoras podrían no disolverse correctamente, afectando su eficacia.
- Massive recall of atorvastatin what you need to know if you take cholesterol drugs a major recall of generic atorvastatin, the most prescribed cholesterol-lowering drug in the us, has raised concerns over.
- Cholesterol medication recalled because it may not dissolve properly when taken the u.s. Food and drug administration and a drug company have recalled at least 140,00 bottles of the.
- Also note the issue with the recall is failed dissolution specifications, meaning the drug did not dissolve as expected in laboratory settings, which could make it less effective. Reported side effects are temporary and reversible.
3. Retiros de Medicamentos por Contaminación Cruzada.
Se emitieron alertas de retiro para medicamentos para la presión arterial como Ziac debido a la posible contaminación cruzada con otros fármacos, en este caso, un medicamento para reducir el colesterol.
- Blood pressure medication recalled may be contaminated with wrong drug wsb-tv channel 2 the food and drug administration has recalled a popular treatment for high blood pressure. The agency said that.
- Glenmark pharmaceuticals has recalled over 11,100 bottles of ziac tablets, a common blood pressure medication, after the drug may have been cross-contaminated with a cholesterol medication.
- Recall ziac blood pressure pills read fda recalls blood pressure medication over cholesterol drug contamination on smartnews l.smartnews.comp-6jt70xawo.
4. Alertas de Seguridad en Suplementos Dietéticos y Alimentos.
Varios suplementos dietéticos fueron retirados por contaminación con salmonela o por contener niveles peligrosos de plomo. Además, hubo retiros significativos de queso rallado por fragmentos metálicos y leche por contaminación.
- Dietary supplement sold nationwide recalled over salmonella concerns the food and drug administration and the centers for disease control and prevention are investigating salmonella reports in.
- Recall alert a consumer-level joint pain supplement has been recalled due to high levels of lead, the u.s. Food drug administration announced monday.
- The u.s. Food and drug administration announced a recall affecting more than 1.5 million bags of shredded cheese made by great lakes cheese co. Inc., based in ohio, citing possible contamination with metal fragments originating from supplier raw materials.
5. Retiros de Fórmulas Infantiles por Riesgo de Botulismo.
La fórmula infantil ByHeart Whole Nutrition fue objeto de un retiro voluntario debido a la posible contaminación con Clostridium botulinum, vinculada a múltiples casos de botulismo infantil en varios estados.
- Byheart baby formula recalled amid 10-state outbreak of infant botulism a maker of organic baby formula is recalling some of the product after federal officials linked it to a 10-state infant botulism outbreak. The u.s. Food and drug administration said 13 children have been hospitalized since.
- The food and drug administration said that botulism illnesses have been reported in multiple states.
- The leader of the association of food and drug officials told healthbeat that the fda has been slow to share distribution lists for recalled byheart formula. Im not sure they recognize the sense of urgency, he said.
6. Advertencias sobre Dispositivos Médicos y Cosméticos.
Se emitieron alertas urgentes sobre monitores de glucosa Abbott Freestyle Libre vinculados a muertes y lesiones graves. Además, la FDA retiró una regla propuesta que habría requerido pruebas de asbesto en cosméticos a base de talco.
- Abbott glucose sensors linked to 700 injuries and 7 deaths, fda issues urgent alert the food and drug administration has issued an urgent alert after malfunctioning abbott continuous glucose sensors were linked to more than 700 injuries and seven deaths. Abbott has warned patients to.
- The food and drug administration today initiated the process for revised cooking instructions to reflect evidence suggesting that the consumption of chicken cooked to 165 by pregnant women may be associated with an increased risk of neurological conditions such as autism and adhd in children.
- The food and drug administration has withdrawn a proposed rule that would have required makeup manuf.