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EU Selenium Supplement Users Risk Exceeding EFSA’s Proposed Intake Limit For Mineral

 
• By Tom Gallen

The European Food Safety Authority is recommending lowering the tolerable upper intake level for selenium from 300 μg/day to 255 μg/day. Regular users of high-dose selenium supplements could potentially breach this new limit, which has been set to reduce the risk of adverse health effects.

EFSA (European Food Standards Agency) word cloud graphic
• Source: Shutterstock

The European Food Safety Authority has lowered its recommended maximum safe daily intake from foods for the mineral selenium to protect consumers from potential adverse effects. The move could lead regular users of high-dose selenium supplements to exceed the new intake limit.

In a draft scientific opinion – which is open for consultation until 18 October – EFSA Panel on Nutrition,...

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• By David Ridley

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AESGP Annual Meeting: Wastewater Directive Impact Assessment ‘Fundamentally Flawed’

 
• By David Ridley

AESGP president Jonathan Workman opens the 61st Annual Meeting with calls for industry unity in the face of the problematic revised EU Urban Wastewater Treatment Directive.

Over The Counter: Driving Innovation In France’s Self-Care Market, With NèreS’ Luc Besançon

 
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‘We Must Have The Truth’ – Calls For UWWTD Review Intensify As Evidence Looks ‘Shaky’

 
• By David Ridley

The evidence underpinning the “polluter pays” principle of the revised Urban Wastewater Treatment Directive - which calls on Europe's pharmaceutical industry to cough up at least 80% of the cost of updating wastewater treatment facilities - is looking increasingly shaky, according to a new report.

More from Geography

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• By David Ridley

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Self-Care Must Be Central To NHS Reform, Says UK Industry And Pharmacy Alliance

 
• By David Ridley

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• By Natasha Barrow

“It’s quite likely [consumer wearable manufacturers] are changing the sensitivity and specificity based on consumer feedback, but not for medical reasons,” said Dipak Kotecha, a University of Birmingham professor of cardiology. Often, self-reported performance evidence from manufacturers is “low quality and biased.”