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Kiriko, LLC. Ban h ành Quyết định Thu hồi Tự nguyện Toàn Quốc đối với sản phẩm A1 Slim Do có chứa các chất Sibutramine, Phenolphthalein và N-Desmethyl sibutramine Không được Khai báo
Ng ày 5 Tháng Mười, 2017-Manvel, TX, Kiriko, LLC. xin thu hồi tự nguyện tất cả các lô hàng A1 Slim dạng lọ chứa 30 viên con nhộng ở cấp độ người tiêu dùng. Phân tích trong phòng thí nghiệm của FDA đã phát hiện rằng sản phẩm A1 Slim có lẫn cá c chất sibutramine, phenolphthalein và N-Desmethyl sibutramine. (Source: Food and Drug Administration)
Source: Food and Drug Administration - October 19, 2017 Category: Food Science Source Type: news

Kiriko, LLC. Ban h à nh Quy ế t đ ị nh Thu h ồ i T ự nguy ệ n To à n Qu ố c đ ố i v ớ i s ả n ph ẩ m A1 Slim Do c ó ch ứ a c á c ch ấ t Sibutramine, Phenolphthalein v à N-Desmethyl sibutramine Kh ô ng đ ư ợ c Khai b á o
Ng à y 5 Th á ng M ư ờ i, 2017-Manvel, TX, Kiriko, LLC. xin thu h ồ i t ự nguy ệ n t ấ t c ả c á c l ô h à ng A1 Slim d ạ ng l ọ ch ứ a 30 vi ê n con nh ộ ng ở c ấ p đ ộ ng ư ờ i ti ê u d ù ng. Ph â n t í ch trong ph ò ng th í nghi ệ m c ủ a FDA đ ã ph á t hi ệ n r ằ ng s ả n ph ẩ m A1 Slim c ó l ẫ n c á c ch ấ t sibutramine, phenolphthalein v à N-Desmethyl sibutramine. (Source: Food and Drug Administration)
Source: Food and Drug Administration - October 19, 2017 Category: Food Science Source Type: news

Meridia (Sibutramine Hydrochloride Monohydrate) - updated on RxList
(Source: RxList - New and Updated Drug Monographs)
Source: RxList - New and Updated Drug Monographs - October 12, 2017 Category: Drugs & Pharmacology Source Type: news

EZ Weight Loss TX LLC Issues Voluntary Nationwide Recall of Atomic and Xplode Capsules Due to the Presence of Undeclared Sibutramine
Corpus Christi, TX, EZ Weight Loss TX is voluntarily recalling all lots of La Bri ’s Body Health Atomic and Xplode capsules to the consumer level. FDA analysis has found the products to be tainted with sibutramine.Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010 for safety reasons. The presence of sibutramine in these products renders it an unapproved drug for which safety and efficacy have not been established and, therefore subject to  recall. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - August 8, 2017 Category: Complementary Medicine Authors: NCCIH Source Type: news

FDA Drug Safety Communication: FDA Recommends Against the Continued Use of Meridia (sibutramine)
(Source: FDA Center for Drug Evaluation and Research - What's New)
Source: FDA Center for Drug Evaluation and Research - What's New - August 3, 2017 Category: Drugs & Pharmacology Source Type: news

La Bri's Body Health Atomic and Xplode Capsules by EZ Weight Loss TX: Recall - Undeclared Drug Ingredient
EZ Weight Loss TX voluntarily recalls La Bri’s Body Health Atomic and Xplode capsules due to contamination with sibutramine. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - July 26, 2017 Category: Complementary Medicine Authors: NCCIH Source Type: news

EZ Weight Loss TX LLC Issues Voluntary Nationwide Recall of Atomic and Xplode Capsules Due to the Presence of Undeclared Sibutramine
Corpus Christi, TX, EZ Weight Loss TX is voluntarily recalling all lots of La Bri's Body Health Atomic and Xplode capsules to the consumer level. FDA analysis has found the products to be tainted with sibutramine. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010 for safety reasons. The presence of sibutramine in these products renders it an unapproved drug for which safety and efficacy have not been established and, therefore subject to recall. (Source: Food and Drug Administration)
Source: Food and Drug Administration - July 25, 2017 Category: Food Science Source Type: news

URGENT: Envy Me Is Recalling LaBri ’s Body Health Atomic 60 Capsules Due To Undeclared Sibutramine
Envy Me is recalling LaBri ’s Body Health Atomic, dietary supplement marketed for weight loss, sold in 60 capsule, plastic bottles. The recall includes all lot codes, manufacturing codes and expiration dates. The United States Food and Drug Administration has analyzed samples of La Bri’s Body Health Atomic and found it to contain the undeclared ingredient sibutramine. (Source: Food and Drug Administration)
Source: Food and Drug Administration - March 29, 2017 Category: Food Science Source Type: news

URGENT: Envy Me Is Recalling LaBri ’ s Body Health Atomic 60 Capsules Due To Undeclared Sibutramine
Envy Me is recalling LaBri ’ s Body Health Atomic, dietary supplement marketed for weight loss, sold in 60 capsule, plastic bottles. The recall includes all lot codes, manufacturing codes and expiration dates. The United States Food and Drug Administration has analyzed samples of La Bri ’ s Body Health Atomic and found it to contain the undeclared ingredient sibutramine. (Source: Food and Drug Administration)
Source: Food and Drug Administration - March 29, 2017 Category: Food Science Source Type: news

Ultimate Body Tox PRO: Recall - Undeclared Drug Ingredient
Ultimate Body –Tox voluntarily recalls Ultimate Body Tox PRO capsules due to undeclared sibutramine, which can increase blood pressure. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - December 2, 2016 Category: Complementary Medicine Authors: NCCIH Source Type: news

Ultimate Body-Tox Issues a Nationwide Voluntary Recall of Ultimate Body Tox PRO Found to Contain Undeclared Sibutramine
High Point, NC, Ultimate Body-Tox is voluntarily recalling all lots of Ultimate Body Tox PRO capsules to the consumer level. FDA analyses of this product found it to contain undeclared sibutramine. Sibutramine is a controlled substance that was removed from the U.S. market in October 2010 for safety reasons. (Source: Food and Drug Administration)
Source: Food and Drug Administration - November 30, 2016 Category: Food Science Source Type: news

FDA Warns ABX Weight Loss Has Hidden Danger
ABX Weight Loss contains sibutramine, a controlled substance that was removed from the market in October 2010, and could lead to heart attack and stroke (Source: PharmaManufacturing.com)
Source: PharmaManufacturing.com - November 16, 2016 Category: Pharmaceuticals Source Type: news

Love My Tru Body Issues Voluntary Nationwide Recall of Skinny Bee Diet Due To Presence of Undeclared Sibutramine, Desmethylsibutramine and/Phenolphthalein
McDonough, Georgia, Love My Tru Body McDonough, GA is voluntarily recalling all of Skinny Bee Diet 500 mg MFD: 03.07.2106 EXP: 03.06.2018 distributed March 23 - April 28, 2016 to the consumer level after FDA laboratory testing found Skinny Bee Diet to contain sibutramine, desmethylsibutramine, and/phenolphthalein. (Source: Food and Drug Administration)
Source: Food and Drug Administration - November 8, 2016 Category: Food Science Source Type: news

Can social media data lead to earlier detection of drug-related adverse events? - Duh MS, Cremieux P, Audenrode MV, Vekeman F, Karner P, Zhang H, Greenberg P.
PURPOSE: To compare the patient characteristics and the inter-temporal reporting patterns of adverse events (AEs) for atorvastatin (Lipitor( ®) ) and sibutramine (Meridia(®) ) in social media (AskaPatient.com) versus the FDA Adverse Event Reporting System... (Source: SafetyLit)
Source: SafetyLit - September 9, 2016 Category: Global & Universal Tags: Alcohol and Other Drugs Source Type: news

Weight Loss Pills And Products Don't Work And Aren't Safe
Our ancestors lived in a feast or famine world. When you don't know where your next meal is coming from, or when it will arrive, the smart play is to pig out every time food is available. Our genes are programmed to extract as much energy as possible from what we eat and to store any extra energy in fat reservoirs, available in reserve for future famines. These deeply ingrained genetic tendencies worked great in the austere world of our ancestors, but are a disaster in our current world of refrigerators, ubiquitous fast food joints and milk shakes. Only one third of Americans are now able to maintain a normal weight; one ...
Source: Science - The Huffington Post - September 5, 2016 Category: Science Source Type: news

Dream Body Weight Loss Issues Voluntary Nationwide Recall of Dream Body 450mg, Dream Body Extreme Gold 800mg, Dream Body Advanced 400mg Due to Undeclared Sibutramine
Dream Body Weight Loss issues voluntary product recall. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - July 12, 2016 Category: Complementary Medicine Authors: NCCIH Source Type: news

Dream Body Weight Loss Issues Voluntary Nationwide Recall of Dream Body 450mg, Dream Body Extreme Gold 800mg, Dream Body Advanced 400mg Due to Undeclared Sibutramine
Grand Prairie, TX, Dream Body Weight Loss is voluntarily recalling all lots of Dream Body Extreme Gold 800mg 30 gold capsules, Dream Body 450mg 30 white capsules, and Dream Body Advanced 400mg 30 purple capsules to the consumer level. The Dream Body Extreme 800mg Gold, Dream Body 450mg and Dream Body Advanced 400mg have been found to contain sibutramine after FDA sampling and testing. (Source: Food and Drug Administration)
Source: Food and Drug Administration - July 1, 2016 Category: Food Science Source Type: news

The Body Shot Bar Issues Voluntary Nationwide Recall of Step 2 Due to Undeclared Sibutramine
Body Shot Bar voluntarily recalls lots of Step 2 60 because they contain the drug subutramine. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - June 13, 2016 Category: Complementary Medicine Authors: NCCIH Source Type: news

The Body Shot Bar Issues Voluntary Nationwide Recall of Step 2 Due to Undeclared Sibutramine
The Body Shot Bar is voluntarily recalling all lots distributed March 1- May 6 2016 of Step 2 60 gold capsule (350MG per) capsules to the consumer level. Step 2 has been found positive for Sibutramine after FDA sampling and testing. (Source: Food and Drug Administration)
Source: Food and Drug Administration - June 7, 2016 Category: Food Science Source Type: news

Making It A Lifestyle, L.L.C. Issues a Voluntary Nationwide Recall of 3rd Degree, Black Gold X Advanced, and Black Label X Due to the Presence of Undeclared Sibutramine and Sildenafil
Making It A Lifestyle, L.L.C. is voluntarily recalling all lots of 3rd Degree, Black Gold X Advanced and Black Label X capsule form supplements to the consumer level. The products have been found to contain undeclared sibutramine and sildenafil. These undeclared ingredients make these products an unapproved new drug for which safety and efficacy have not been established. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - May 2, 2016 Category: Complementary Medicine Authors: NCCIH Source Type: news

Super Herbs Issues Voluntary Nationwide Recall Of SUPER HERBS Due To Presence Of Undeclared Sibutramine, Desmethylsibutramine and/or Phenolphthalein
Super Herbs is voluntarily recalling all bottles of SUPER HERBS, light green and dark green capsules to the consumer level after FDA laboratory testing found SUPER HERBS to contain sibutramine, desmethylsibutramine, and/or phenolphthalein. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - April 20, 2016 Category: Complementary Medicine Authors: NCCIH Source Type: news

Herbal weight loss pill overdose: sibutramine hidden in pepper pill - Pamukcu Gunaydin G, Dogan NO, Levent S, Kurtoglu Celik G.
We report a case of a female patient who presented to the emergency departmen... (Source: SafetyLit)
Source: SafetyLit - April 13, 2016 Category: Global & Universal Tags: Alcohol and Other Drugs Source Type: news

FDA Drug Safety Communication: FDA Recommends Against the Continued Use of Meridia (sibutramine)
(Source: FDA Center for Drug Evaluation and Research - What's New)
Source: FDA Center for Drug Evaluation and Research - What's New - March 11, 2016 Category: Drugs & Pharmacology Source Type: news

Urgent: Drug Recall - Weight Loss Dietary Supplements with Undeclared Sibutramine and Phenolphthalein
Under the brands: La' Trim Plus, Jenesis and Oasis, all lots and expiration dates.Recent Analysis by the Food and Drug Administration has found undeclared Sibutramine and Phenolphthalein in the Dietary Supplement "La'Trim Plus", "Oasis", and "Jenesis". (Source: Food and Drug Administration)
Source: Food and Drug Administration - December 23, 2015 Category: Food Science Source Type: news

Bee Extremely Amazed LLC Issues Voluntary Nationwide Recall of Various Products Distributed For Weight Loss Due to Undeclared Drug Ingredients
Bee Extremely Amazed LLC, Jewett, OH is voluntarily recalling various products marketed for weight loss to the consumer level due to findings of undeclared drug ingredients including sibutramine and/or phenolphthalein. (Source: Food and Drug Administration)
Source: Food and Drug Administration - December 23, 2015 Category: Food Science Source Type: news

SmartLipo365 Issues Voluntary Nationwide Recall of Smart Lipo Due to Undeclared Sibutramine, Desmethylsibutramine and Phenolphthalein
SmartLipo365 is voluntarily recalling all lots of Smart Lipo (800, 900, 950 mg) capsules, to the consumer level. FDA's analysis found the Smart Lipo products to contain undeclared sibutramine, desmethylsibutramine, and phenolphthalein. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010. (Source: Food and Drug Administration)
Source: Food and Drug Administration - December 18, 2015 Category: Food Science Source Type: news

Fit Firm and Fabulous Issues Voluntary Nationwide Recall of Ultimate Herbal Slimcaps Due to the Presence of Undeclared Sibutramine
Company recalls Ultimate Herbal Slimcap capsules. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - December 11, 2015 Category: Complementary Medicine Authors: NCCAM Source Type: news

Lipo Escultura Corp. Issues Nationwide Recall of Lipo Escultura Due to Undeclared Sibutramine and Diclofenac
Lipo Escultura Corp. of Brooklyn, NY dba JAT Productos Naturales Corp., and JAT Natural Products Corp. are voluntarily recalling all Lipo Escultura within expiry to the consumer level. The Lipo Escultura capsules were tested by the U.S. Food and Drug Administration and have been found to contain two potentially harmful ingredients--sibutramine and diclofenac. (Source: Food and Drug Administration)
Source: Food and Drug Administration - December 4, 2015 Category: Food Science Source Type: news

Fit Firm and Fabulous Issues Voluntary Nationwide Recall of Ultimate Herbal Slimcaps Due to the Presence of Undeclared Sibutramine
Fit Firm and Fabulous is voluntarily recalling lots 05/02/2015 to 05/01/2017 of Ultimate Herbal Slimcap capsules, to the consumer level. FDA analysis has found the product to contain undeclared sibutramine. Sibutramine was a previously approved controlled substance that was removed from the U.S. market in October 2010 for safety reasons. (Source: Food and Drug Administration)
Source: Food and Drug Administration - November 19, 2015 Category: Food Science Source Type: news

Inaffit, LLC Issues Voluntary Nationwide Recall of Natureal Due to Undeclared Sibutramine
Inaffit, LLC is voluntarily recalling all lots of Natureal light green and dark green capsules to the consumer level after FDA laboratory testing found Natureal to contain sibutramine. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010. (Source: Food and Drug Administration)
Source: Food and Drug Administration - November 9, 2015 Category: Food Science Source Type: news

Lucy's Weight Loss System Issues Voluntary Nationwide Recall of Pink Bikini and Shorts on The Beach Due to Undeclared Sibutramine and Phenolphthalein
Lucy's Weight Loss System is voluntarily recalling all lots distributed May 25 - June 23 2015 of Pink Bikini and Shorts on the Beach Blue and Gold Edition, 30 blue capsules (750MG per) capsules and 30 gold capsule (800MG per) capsules to the consumer level. The Pink Bikini and Shorts on the Beach have been found positive for Sibutramine and Phenolphthalein after FDA sampling and testing. (Source: Food and Drug Administration)
Source: Food and Drug Administration - September 23, 2015 Category: Food Science Source Type: news

Near infrared spectroscopy detection and quantification of herbal medicines adulterated with sibutramine - da Silva NC, Honorato RS, Pimentel MF, Garrigues S, Cervera ML, de la Guardia M.
In this study, two strategies using near infrared (NIR) spectroscopy ... (Source: SafetyLit: All (Unduplicated))
Source: SafetyLit: All (Unduplicated) - August 16, 2015 Category: Global & Universal Tags: Alcohol and Other Drugs Source Type: news

Blue Square Market Issues Voluntary Nationwide Recall of Kaboom Action Strips and Lida Daidaihua Due to the Presence Of Undeclared Sulfoaildenafil, Sibutramine And Phenolphthalein
Blue Square Market Inc. of North Huntingdon, PA, is recalling "Kaboom Actions Strip 12 Pack" and LiDa DaiDaiHua to the user level after FDA analysis revealed the products contain undeclared active pharmaceutical ingredients. Kaboom was found to contain sulfoaildenafil and LiDa DaiDaiHua was found to contain sibutramine and phenolphthalein. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010 due to increased risk of heart attacks and strokes. Phenolphthalein is an ingredient previously used in over-the-counter laxatives, but because of concerns of carcinogenicity, it is n...
Source: Food and Drug Administration - August 7, 2015 Category: Food Science Source Type: news

Blue Square Market Issues Update to Voluntary Nationwide Recall of Kaboom Action Strips and Lida Daidaihua Due to the Presence of Undeclared Sulfoaildenafil, Sibutramine and Phenolphthalein
Blue Square Market Inc. of North Huntingdon, PA, is recalling "Kaboom Actions Strip 12 Pack" and LiDa DaiDaiHua to the user level after FDA analysis revealed the products contain undeclared active pharmaceutical ingredients. Kaboom was found to contain sulfoaildenafil and LiDa DaiDaiHua was found to contain sibutramine and phenolphthalein. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010 due to increased risk of heart attacks and strokes. (Source: Food and Drug Administration)
Source: Food and Drug Administration - August 7, 2015 Category: Food Science Source Type: news

Life & More, L.L.C. Issues Nationwide Voluntary Recall of Akttive High Performance Fat Burner Gold Capsules Due to Undeclared Drug Ingredients
Life & More, L.L.C. is voluntarily recalling 783 Bottles from Lot #000185004400 Akttive High Performance Fat Burner Gold capsules weight loss supplements. The firm was informed by the US Food and Drug Administration (FDA) that a sample of Akttive High Performance Fat Burner Gold capsules was found to contain Sibutramine, desmethylsibutramine, and Phenolphthalein. (Source: Food and Drug Administration)
Source: Food and Drug Administration - July 23, 2015 Category: Food Science Source Type: news

FDA cracks down on 1,000 illegal online medicine sellers
(Reuters) — The FDA said yesterday it had sent warning letters and seized potentially dangerous, unapproved medicines and medical devices from more than 1,050 websites globally. Inspectors from the FDA and other federal agencies screened and seized illegal drugs and medical devices received through international mail facilities in Chicago, Miami and New York, the FDA said in a statement. The health regulator said it sent warning letters to operators of nearly 400 websites and to 9 firms distributing unapproved medical devices online. The prescription drugs targeted included some purported to be the generic ...
Source: Mass Device - June 19, 2015 Category: Medical Equipment Authors: Brad Perriello Tags: Business/Financial News Food & Drug Administration (FDA) Regulatory/Compliance Source Type: news

SmartLipo365 Issues Voluntary Nationwide Recall of Smart Lipo Due to Undeclared Sibutramine, Desmethylsibutramine, and Phenolphthalein
SmartLipo365 is voluntarily recalling 122 lots of Smart Lipo (800, 900, 950 mg) capsules, to the consumer level. FDA received samples of 800 and 900mg capsules of Smart Lipo and the lab results found the Smart Lipo products to contain undeclared sibutramine, desmethylsibutramine, and phenolphthalein. (Source: Food and Drug Administration)
Source: Food and Drug Administration - June 4, 2015 Category: Food Science Source Type: news

Ultra ZX LABS, L.L.C. Issues Voluntary Nationwide Recall of Ultra ZX Since It Contains Undeclared Sibutramine and Phenolphthalein
Recall - Firm Press Release — UltraZx, Labs, L.L.C. is voluntarily recalling UltraZx weight loss supplements. This product has been found to contain undeclared Sibutramine and phenolphthalein. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - March 11, 2015 Category: Complementary Medicine Authors: NCCAM Source Type: news

Slim-Vie: Public Notification - Undeclared Drug Ingredient
Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. (Source: FDA MedWatch)
Source: FDA MedWatch - November 26, 2014 Category: American Health Source Type: news

Bee Thin: Public Notification - Undeclared Drug Ingredient
Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. (Source: FDA MedWatch)
Source: FDA MedWatch - November 24, 2014 Category: American Health Source Type: news

Super Extreme Accelerator: Public Notification - Undeclared Drug Ingredient
Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. (Source: FDA MedWatch)
Source: FDA MedWatch - November 24, 2014 Category: American Health Source Type: news

Bee Slim: Public Notification - Undeclared Drug Ingredient
Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. (Source: FDA MedWatch)
Source: FDA MedWatch - November 24, 2014 Category: American Health Source Type: news

REFA Enterprises, LLC Issues Voluntary Nationwide Recall of Forever Beautiful Bee Pollen Due to Undeclared Sibutramine and Phenolphthalein
REFA Enterprises, LLC is voluntarily recalling one lot of each: Forever Beautiful Bee Pollen (UPC # 6333090804632), Forever Beautiful Infinity UPC # 633090804649), to the consumer level. The products have been found to contain undeclared Sibutramine or a combination of both Sibutramine and Phenolphthalein through FDA laboratory analyses. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010 (due to increased risk of seizures, heart attacks, arrhythmia and strokes). (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - November 20, 2014 Category: Complementary Medicine Authors: NCCAM Source Type: news

V26 Slimming Coffee: Public Notification - Undeclared Drug Ingredient
Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. (Source: FDA MedWatch)
Source: FDA MedWatch - November 5, 2014 Category: American Health Source Type: news

Sit and Slim II: Public Notification - Hidden Drug Ingredients
FDA analysis found these products to contain undeclared Sibutramine, which may increase blood pressure and/or pulse rate, and may also interact in life-threatening ways with other medications. (Source: FDA MedWatch)
Source: FDA MedWatch - October 10, 2014 Category: American Health Source Type: news

Anti-obesity drugs 'may still work in middle-age'
Conclusion This animal study has found that anti-obesity medications that increase serotonin signalling reduce food intake in “middle-aged, obese” mice to a similar extent as in young mice. There had been concern as both obesity and ageing are associated with rewiring of the main brain pathway involved in energy homeostasis. The “rewiring” leads to reduced activity of POMC neurons, found in the hypothalamus and these POMC neurons make hormones that are important in regulating appetite and body weight. A number of anti-obesity drugs (lorcaserin, d-fenfluramine and sibutramine) work by increasing the...
Source: NHS News Feed - August 13, 2014 Category: Consumer Health News Tags: Obesity Medication Source Type: news

FDA Advises Not to Use La Jiao Shou Shen: AttorneyOne Monitor and Keep...
On June 11, the FDA advised consumers and health professionals not to use La Jiao Shou Shen because it contains undeclared sibutramine and phenolphthalein. In light of this news, AttorneyOne, a...(PRWeb June 12, 2014)Read the full story at http://www.prweb.com/releases/2014/06/prweb11938006.htm (Source: PRWeb: Medical Pharmaceuticals)
Source: PRWeb: Medical Pharmaceuticals - June 12, 2014 Category: Pharmaceuticals Source Type: news

Asset Bee Pollen: Public Notification - Undeclared Drug Ingredient
Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients. (Source: FDA MedWatch)
Source: FDA MedWatch - May 12, 2014 Category: American Health Source Type: news

FDA Advises Not to Purchase Slim Trim U: AttorneyOne Monitor and Keep...
On May 6, the FDA notified consumers not to purchase or use Slim Trim U because it was found to contain undeclared sibutramine. In light of this news, AttorneyOne, a recognized authority on law,...(PRWeb May 12, 2014)Read the full story at http://www.prweb.com/releases/2014/05/prweb11843276.htm (Source: PRWeb: Medical Pharmaceuticals)
Source: PRWeb: Medical Pharmaceuticals - May 12, 2014 Category: Pharmaceuticals Source Type: news

Public Notification: Lite Fit USA Contains Hidden Drug Ingredient
This FDA warning advises consumers against purchasing the product Lite Fit USA promoted for weight loss. It contains sibutramine, a controlled substance removed from the market in October 2010 for safety reasons. Sibutramine substantially increases blood pressure and/or pulse rate in some patients and may be a risk for people with a history of heart problems or stroke. (Source: NCCAM Featured Content)
Source: NCCAM Featured Content - April 28, 2014 Category: Complementary Medicine Authors: NCCAM Source Type: news