Connect with us

Supplements

Supplements warning: Certain types could increase chances of cancer, new study says – WLS-TV

Published

on


Many people take vitamin supplements to add years to their life, but a new study says some supplements could actually increase your chances of cancer.

Researchers from Tufts University compared the intake of a range of nutrients with rates of death from all causes.

They found people could be putting themselves at risk from taking calcium supplement doses higher than one-thousand milligrams a day.

Researchers also say people who take unnecessary supplements of vitamin D may also have deadly consequences.

Let’s block ads! (Why?)



Source link

Supplements

"You're Just Peeing Out a Lot of Money." This Is the Real Way You're Flushing Your Retirement Savings Down the Drain – MONEY

Published

on

By


| Money

this link is to an external site that may or may not meet accessibility guidelines.

Let’s block ads! (Why?)



Source link

Continue Reading

Supplements

FDA Sends Warning Letters on Dietary Supplements – Wall Street Journal

Published

on

By


The FDA has sent warning letters to companies marketing dietary supplements.


Photo:

Jacquelyn Martin/Associated Press

The U.S. Food and Drug Administration said it sent warning letters to 11 companies for marketing dietary supplements that don’t meet its guidelines.

The agency issued warnings to three companies for marketing dietary supplements containing phenibut, which is sometimes sold as a sleep aid or to treat anxiety. It said that phenibut doesn’t meet the statutory definition of a dietary ingredient, which is generally a vitamin, herb or other natural substance used to supplement the diet. 

A Wall Street Journal article last week on the $40 billion supplement industry said that phenibut, developed as a drug in the former Soviet Union, was being marketed as a “nootropic,” or brain supplement, in the U.S. A spokeswoman for the FDA said that the agency was already investigating phenibut.

The FDA also issued warnings to eight companies for marketing dietary supplements containing DMHA, a stimulant sometimes found in exercise and weight-loss supplements. The companies have 15 business days to inform the FDA of steps they will take to bring their products into compliance. That could include a decision to recall, reformulate or discontinue sales.

Supplements aren’t tightly regulated by the FDA like prescription drugs. Dietary-supplement manufacturers don’t need approval from the FDA before introducing their products to the market. The FDA has oversight for taking action against any misbranded supplement after it reaches the market.

The FDA said it is launching a new online tool to help warn consumers of ingredients that appear to be unlawfully marketed in supplements. The agency said the Dietary Supplement Ingredient Advisory List will help get cautionary information to the public more quickly before it issues any final determination. It is on the FDA website, and consumers can also sign up to receive updates and changes to the list.

Write to Anne Marie Chaker at anne-marie.chaker@wsj.com

Let’s block ads! (Why?)



Source link

Continue Reading

Supplements

New Tool Alerts Public to Unlawfully Marketed Dietary Supplement Ingredients – The Cardiology Advisor

Published

on

By


In an effort to better alert the public of unlawful ingredients in dietary supplements, the Food and Drug Administration (FDA) has created the Dietary Supplement Ingredient Advisory List, a new reference tool for consumers and manufacturers.

Available on the FDA website, the list includes ingredients that may not lawfully be included in dietary supplements. Consumers may wish to avoid supplements that include these ingredients as they may not fit the definition of a dietary ingredient or may require pre-market notification that was not submitted; inclusion in this list does not necessarily mean the ingredient poses a safety concern.

“It is important to note that the List is not exhaustive; it will always be a work in progress,” said Frank Yiannas, the FDA’s Deputy Commissioner for Food Policy and Response. “We expect the List will evolve as new ingredients are identified and others are removed.” In addition, the FDA will continue to communicate with the public regarding any safety concerns identified with new dietary supplement ingredients.

In a press statement, Yiannas also noted that the agency recently sent out warning letters to 8 companies that were marketing dietary supplements containing DMHA and 3 companies marketing supplements with phenibut; neither one of these currently meets the FDA’s definition of a lawful dietary ingredient. “We take these violations very seriously and stand ready to take enforcement action without further notice if the companies do not immediately cease distribution of the products,” said Yiannas. In February 2019, the FDA went after 17 companies selling unapproved and/or misbranded products (most sold as dietary supplements) claiming to prevent, treat, or cure Alzheimer disease and other serious disease and health conditions.

Consumers who wish to receive alerts related to updates to the Dietary Supplement Ingredient Advisory List can sign up here.

For more information visit FDA.gov.

Related Articles

This article originally appeared on MPR

Let’s block ads! (Why?)



Source link

Continue Reading

Trending