Recall of Marcaine (Bupivacaine HCI Injection, USP)

Marcaine (Bupivacaine HCI Injection, USP), 0.5 percent, 30 ML, Single-Dose, Preservative-Free Vial: Recall - Visible ParticulatesISSUE: Hospira announced a voluntary nationwide recall to the user level for one lot of 0.5% Marcaine (Bupivacaine HCl Injection, USP), 30 mL, Single-dose Vial – Preservative Free (NDC 0409-1560-29), Lot 33-545-DD. ...

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Instituto de Salud Pública de Chile detectó nueva droga sintética

Departamento de Salud Ambiental. Hallazgo es un derivado clorado de la feniletilaminas, y es incluso más potente que el LSD.  El Instituto de Salud Pública,  informa que se ha detectado un nuevo hallazgo de droga psicodélica sintética en nuestro país, DOC derivado clorado de las feniletilaminas, cuyo nom...

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FDA Takes Final Step on Infant Formula Protections

The Food and Drug Administration (FDA) oversees manufacturers of infant formulas and helps ensure that these products are safe and support healthy growth in infants who consume them.In keeping with that mission, FDA announced on June 9, 2014 that it is finalizing a rule—first published as an interim final rule on February 10, 2014—that ...

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La Jiao Shou Shen Contains Hidden Drug Ingredient

FDA laboratory analysis confirmed that La Jiao Shou Shencontains sibutramine. Sibutramine is a controlled substance that was removed from the market in October 2010 for safety reasons. The product poses a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may pr...

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Recomendaciones a los profesionales sanitarios ante una ola de calor

Algunos medicamentos pueden agravar el síndrome de agotamiento–deshidratación o de golpe de calor.Recomendaciones generales de la AEMPS a los profesionales sanitarios ante una ola de calor:Revisar la lista de los medica mentos de prescripción médica o de automedicación, utilizados por el pacie...

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FDA Proposes First Regulations for E-Cigarettes‏

WASHINGTON (AP) — The federal government wants to ban sales of electronic cigarettes to minors and require approval for new products and health warning labels under regulations being proposed by the Food and Drug Administration.While the proposal being issued Thursday won't immediately mean changes for the popular devices, the move is aimed a...

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Recall of Super Arthgold Due to Undeclared Ingredients

http://www.fda.gov/Safety/Recalls/ucm394631.htmFOR IMMEDIATE RELEASE - April 21, 2014 - La Mirada, CA, Nano Well-being Health Inc. is voluntarily recalling lot L1P1-6100/Expiration date June 25, 2016 and lot L1P2-6000/Expiration date September 16, 2016 of Super Arthgold, 500 mg capsules to the consumer level. FDA laboratory analysis has found the p...

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