Product Reviews and Information for Adrenal Fatigue / Adrenal Insufficiency
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Adrenal Fatigue and Adrenal Support Supplements: Do they work and are they safe?
Find out what's really in supplements for adrenal support and adrenal fatigue, including herbal adrenal support supplements and bovine derived adrenal support supplements. Find out if they really work and if they are safe. ConsumerLab.com's answer explains.
Product Review
DHEA Supplements Review
Choose the Best DHEA Supplement. Beware of Big Differences in Dose and Price.
CL Answer
Rhodiola and ashwagandha are both promoted to help with stress and anxiety. Is it safe to take them at the same time?
Find out if it is safe to take ashwagandha and rhodiola together. Both herbs are promoted to help with stress and anxiety, but may also lower blood pressure and have other side effects. ConsumerLab.com's answer explains.
CL Answer
Desiccated Beef Liver and Beef Organ Supplements: Nutrition & Safety
Description of desiccated beef liver, including what it is used for, its nutrient content, and safety concerns.
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Do any supplements help for varicose veins or chronic venous insufficiency?
Find out which supplements help for varicose veins and chronic venous insufficiency, including citrus bioflavonoids and grape seed extract.
CL Answer
Is there evidence that d-limonene can help fight cancer?
Find out if d-limonene can help fight cancer or help for GERD (gastroesophageal reflux disorder), including evidence from clinical studies.
CL Answer
Which supplements help to improve energy and decrease fatigue?
Energy supplements and vitamins - Some can help increase energy and reduce fatigue, including CoQ10, curcumin/turmeric, cocoa, and B vitamins.
Recalls & Warnings
December 19, 2024
Force Forever Joint Pain Supplement Recalled
On December 12, 2024, GNMart INC recalled all lots of Force Forever, a supplement promoted for joint pain, because FDA tests found it to contain undeclared diclofenac and dexamethasone.
Recalls & Warnings
April 23, 2025
FDA Warns Consumers Not to Use ADVANCED KING Joint Supplement
On February 10, 2025, the FDA warned consumers not to purchase or use the joint pain supplement ADVANCED KING (Naturista Store LLC), because FDA analysis confirmed the product contains dexamethasone, diclofenac, and methocarbamol.
Recalls & Warnings
September 24, 2024
Supplement for Eczema Recalled
On September 18, 2024, 123Herbals LLC issued a recall for all lots of Vail-Bon Jie Yang Wan capsules, which are promoted to treat eczema and other skin conditions, because they contain undeclared dexamethasone and chlorpheniramine.
Recalls & Warnings
October 08, 2024
AK Forte Joint Pain Supplement Recalled
On October 8, 2024, C&A Naturistics voluntarily recalled all lots of AK Forte, 400 mg tablets because FDA laboratory analysis found products to contain undeclared diclofenac, dexamethasone, and methocarbamol.
Recalls & Warnings
December 05, 2024
Liquid Multivitamin Recalled
On November 6, 2024, Armonia Natural Store LLC issued a recall of 64 bottles of OneMultivitaminic GAF-PLUS Advance 300 ml because they contain undeclared acetaminophen and dexamethasone phosphate (which are not permitted in dietary supplements) and the undeclared sweetener aspartame.
Recalls & Warnings
December 19, 2024
Gout and Arthritis Supplement Recalled Due to Undeclared Drugs
On December 12, 2024, Buy-herbal recalled all lots of Nhan Sam Tuyet Lien Truy Phong Hoan capsules within expiry after FDA testing found them to contain undeclared furosemide, dexamethasone and chlorpheniramine. These drugs are not permitted in dietary supplements.
Recalls & Warnings
September 25, 2023
FDA Warns Consumers Not to Use Tapee Tea
On August 31, 2023, the FDA warned consumers not to purchase or use Tapee Tea products after FDA laboratory analysis found them to contain dexamethasone and piroxicam, drugs that are not listed on the product's label.
Recalls & Warnings
December 14, 2023
Pain Relief Tea Recalled, Found to Contain Prescription Drugs
On December 13, 2023, WS Global issued a recall of all lots of the company’s Himalayan Pain Relief Tea after products were found to contain diclofenac and dexamethasone, prescription drugs that are not listed on the product’s label.
Recalls & Warnings
May 29, 2025
Umary Joint Pain Supplements Recalled
On May 21, 2025, UMARY USA recalled all lots of Unavy Ácido HIALURÓNICO (30 caplets/850 mg) and Umovy Ácido HIALURÓNICO (30 caplets/850 mg).
Recalls & Warnings
June 16, 2022
Omega 3 Supplements Recalled Due to Undeclared Drug Ingredients
On May 28, 2022, Latin Foods Market issued a voluntary recall of one lot of Artri King Reforzado con Ortiga y Omega 3 tablets after FDA laboratory analysis found the presence of undeclared diclofenac and dexamethasone.
News Release
December 10, 2002
Lupus patients cautioned about hormone supplement — ConsumerLab.com releases DHEA testing results online today
WHITE PLAINS, NY — December 10, 2002 — In its latest Product Review, ConsumerLab.com found that 3 of the 17 DHEA (dehydroepiandrosterone) supplement products it tested contained less than their claimed amounts of this hormone — one having less than one-fifth of what it claimed.
Recalls & Warnings
February 06, 2023
FDA Warns Companies Promoting Products to Treat Monkeypox, COVID-19, & Other Viruses
On January 30, 2023, the FDA issued a warning letter to four companies following review of the company websites, which found statements about company products to be drug claims because they were promoted to mitigate, prevent, treat, diagnose, or cure viruses such as monkeypox.
News Release
March 13, 2001
ConsumerLab.com review of vitamin E supplements finds some insufficiencies and need for clearer labeling; test results released online today
WHITE PLAINS, NY — March 13, 2001 — ConsumerLab.com today released results of its Product Review of vitamin E products. Vitamin E is one of the most popular dietary supplements in the U.S.
Recalls & Warnings
September 20, 2010
Many Supplements Recalled for Hormone-Affecting Compounds
On September 20, 2010, the U.S. FDA posted a Safety Notice regarding the recalls of several products marketed as dietary supplements that contain aromatase inhibitors, commonly known as "ATD.
Recalls & Warnings
September 15, 2010
Recall of Testosterone-Boosting Supplement
On September 14, 2010, the FDA posted a notice that KiloSports is recalling Clomed (60 count bottles), a supplement with claims to "release gonadatropin," "elevate testosterone" and "promote spermatogenesis."
Recalls & Warnings
October 13, 2018
Pharmaceutical Drugs Found In Dietary Supplements Pose Danger to Consumers
Almost 800 dietary supplements sold between 2007 and 2016 contained unapproved pharmaceutical ingredients, according to a study published today in the Journal of the American Medical Association (JAMA).
Recalls & Warnings
July 15, 2011
FDA Inspection Finds Manufacturing Problems with Several Supplements Including Women's Multivitamin
The U.S. FDA recently posted a Warning Letter sent to BioSan Laboratories of Derry, New Hampshire on June 17, 2011 concerning multiple violations of Good Manufacturing Practice regulations and labeling rules.
Recalls & Warnings
June 04, 2012
FDA Warning on Supplement for Pain Relief
On June 1, 2012, the U.S. FDA warned consumers that Reumofan Plus, marketed as a “natural” dietary supplement for pain relief and other serious conditions, contains several active pharmaceutical ingredients not listed on the label that could be harmful.
Recalls & Warnings
December 21, 2012
Dangerous Supplement Being Sold Under New Name
On December 21, 2012, the FDA warned consumers that Reumofan Plus, a dietary supplement promoted for arthritis and muscle pain that has been linked to serious and sometimes fatal side effects, is now being sold under the name WOW.
Recalls & Warnings
May 29, 2018
FDA Warns Seller of "Aromatase Inhibitor" Supplement
On May 18, 2018, the FDA issued a warning letter to Performance Nutrition Formulators LLC d.b.a. VMI Sports because its product Arimistane contains Androsta-3,5-Diene-7,17-Dione, an ingredient that the FDA considers to be a new drug and not a dietary supplement ingredient.
Recalls & Warnings
February 20, 2013
Recall: Arthritis and Muscle Pain Supplement Contains Prescription Drugs
On February 15, 2013, Reumofan Plus USA, LLC and Reumofan USA, LLC announced a recall of Reumofan Plus, a dietary supplement promoted for arthritis and muscle pain, because it was found to contain the active pharmaceutical ingredients methocarbamol, dexamethasone, and diclofenac.
Recalls & Warnings
January 17, 2018
Joint and Pain Relief Product Contains Undeclared Drug
On January 17, 2018 Health Canada warned consumers that Linsen Double Caulis Plus, a supplement for joint pain, was found to contain the undeclared drug dexamethasone.
Recalls & Warnings
November 14, 2014
FDA Warns Consumers Not to Buy or Use Muscle Enhancement Supplement
On November 13, 2014, the FDA advised consumers not to buy or use the muscle enhancement supplement Mayhem (Chaotic-Labz) because it was found to contain the undeclared drugs cyproheptadine and dexamethasone. These drugs can cause serious side effects and can interact with other medications.
Recalls & Warnings
August 22, 2012
FDA Warns of Life-Threatening Side Effects and Withdrawal Symptoms from Two Arthritis, Muscle Pain Supplements
On August 21, 2012, the FDA issued a warning to consumers about the dangers of taking Reumofan Plus and Reumofan Plus Premium, two dietary supplements marketed for arthritis, osteoporosis and muscle pain.
Recalls & Warnings
October 18, 2017
FDA Warns Seller of Arthritis, Blood Pressure, Diabetes Supplements For Making Drug Claims
On August 15, 2017, the FDA issued a warning letter to Years to Your Health, Inc., following an inspection of the company's website which found a number of their products to be misbranded, as they contained drug claims.
Recalls & Warnings
October 18, 2017
Total Body Nutrition Warned for Banned Stimulant in Supplements
On September 28, 2017, the FDA issued a warning letter to Total Body Nutrition following a facility inspection which found some of the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...
Recalls & Warnings
October 21, 2014
Seller of Weight Loss, Saw Palmetto Supplements and More Warned for Drug Claims
On October 9, 2014, the FDA issued a warning letter to Bethel Nutritional Consulting, Inc., following a review of the company's website which found statements made about 15 Day Detox Diet, Alpha Lipoic Acid. 300 mg.
Recalls & Warnings
May 06, 2015
Joint Pain Supplements Found to Contain Diuretics, Antihistamines and Other Undeclared Drugs
On May 4, 2015, the FDA warned consumers not to buy or use the following supplements promoted for joint or back pain because they were found to contain undeclared drugs. Each was identified during an examination of international mail shipments.
