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Dietary Supplementation News (Page 16)
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Substituting Meat Could Reduce Ammoniagenesis in Cirrhosis
FRIDAY, May 10, 2024 – When substituting meat for a nonmeat alternative, lower ammoniagenesis and altered serum metabolomics are seen for patients with cirrhosis, regardless of hepatic...
More Data Suggests 'Ultraprocessed' Foods Can Shorten Your Life
THURSDAY, May 9, 2024 – People who eat large amounts of ultra-processed foods have a slightly higher risk of premature death than those who mostly shun the industrially produced eats, a new 30-year...
Mortality Slightly Increased With Consumption of Ultraprocessed Foods
THURSDAY, May 9, 2024 – Mortality is slightly higher in association with a higher intake of ultraprocessed foods, according to a study published online May 8 in The BMJ. Zhe Fang, M.B.B.S., from the...
FDA Medwatch Alert: Stop Clopez Corp. Issues Voluntary Worldwide Recall of Schwinnng Capsules Due to the Presence of Undeclared Nortadalafil
April 22, 2024– Hollywood, FL, US, Stop Clopez Corp. is voluntarily recalling one lot of Schwinnng capsules to the consumer level. FDA analysis has found the Schwinnng products to contain N...
FDA Medwatch Alert: Today The World Issues Voluntary Nationwide Recall of All Lots of Sustain and Schwinnng brand Dietary Supplement Capsules Due to the Presence of Undeclared Tadalafil and Nortadalafil
February 2, 2024 - VANCOUVER, WA, "Today The World" is voluntarily recalling two lots of Sustain herbal dietary supplement capsules and one lot of Schwinnng capsules to the consumer level. FDA...
FDA Medwatch Alert: Today The World Issues Voluntary Nationwide Recall of All Lots of Arize Herbal Dietary Supplement Capsules Due to the Presence of Undeclared Nortadalafil
Feb 2, 2024 - VANCOUVER, WA, “Today The World” is voluntarily recalling one lot of Arize Herbal Dietary Supplement capsules to the consumer level. FDA analysis has found the products to contain und...
FDA Medwatch Alert: Neptune Resources, LLC Issues Voluntary Nationwide Recall of Neptune’s Fix
KANSAS CITY, Mo., Jan. 28, 2024 /PRNewswire-PRWeb/ – Neptune Resources, LLC is voluntarily recalling All lots of Neptune's Fix Elixir, Neptune's Fix Extra Strength Elixir, and Neptune's Fix Tablets...
FDA Medwatch Alert: Update: FDA Warns Consumers Not to Purchase or Use Neptune’s Fix or Any Tianeptine Product Due to Serious Risks
January 23, 2024 -- FDA continues to receive severe adverse event reports after use of Neptune‘s Fix products, including seizures, loss of consciousness and death. These products may interact, in li...
FDA Medwatch Alert: WS Global Issues Nationwide Recall of Himalayan Pain Relief Tea Due to the Presence of Hidden Drug Ingredients, Diclofenac and Dexamethasone
December 13, 2023 –WS Global, INC Brooklyn, NY is voluntarily recalling all lots of Himalayan Pain Relief Tea, tea packets to the consumer level. The products have been found to contain undeclared d...
FDA Medwatch Alert: 8th Avenue Pharmacy Issues Voluntary Nationwide Recall of Notoginseng Formula Special Gout Granule Due to the Presence of Hidden Drug Ingredients, Diclofenac and Dexamethasone
December 14, 2023 – Brooklyn, NY, 8th Avenue Pharmacy is voluntarily recalling all lots within expiry of Notoginseng Formula Special Gout Granule, distributed by 8th Avenue Pharmacy, to the consumer...
FDA Medwatch Alert: Noah’s Wholesale, LLC Issues Voluntary Nationwide Recall of the Rock Due to Presence of Undeclared Sildenafil
October 18, 2023 – Miami Gardens, Florida, Noah’s Wholesale, LLC is voluntarily recalling one lot of the rock# 03032021,exp:12/2027,1200 mg/capsule, to the consumer level. FDA analysis has found the p...
FDA Medwatch Alert: FDA Warns Consumers Not To Purchase or Use Neptune’s Fix or Any Tianeptine Product Due To Serious Risks
November 21, 2023 – FDA is warning consumers to not purchase or use any Neptune’s Fix products, or any other product with tianeptine – a potentially dangerous substance that is not FDA-approved for ...
FDA Medwatch Alert: FDA Raises Concerns About Probiotic Products Sold for Use in Hospitalized Preterm Infants
October 26, 2023 – As part of the U.S. Food and Drug Administration’s commitment to protecting public health, the agency is advising the public, including healthcare providers, of the possible risks ...
FDA Medwatch Alert: Botanical-Be Issues Voluntary Nationwide Recall of Kuka Flex Forte, Artri King, and Reumo Flex (Capsules) Due to Presence of Undeclared Diclofenac
October 22, 2023 – El Paso, TX. Botanical-Be is voluntarily recalling of all lots of Kuka Flex Forte, Capsules, Artri King, Capsules, and Reumo Flex, Capsules to the consumer level. FDA analysis has f...
FDA Medwatch Alert: Warning Regarding Use of Probiotics in Preterm Infants
September 29, 2023 – The U.S. Food and Drug Administration (FDA) is providing important safety information to healthcare providers on the use of products containing live bacteria or yeast (commonly...
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