Showing posts with label . Supplements. Show all posts
Showing posts with label . Supplements. Show all posts

Thursday, November 19, 2015

Health News: Alarming New ‘Superbug’ Gene found in animals and people ♦ DOJ: Consumers must remain on guard about supplement risks ♦ Electronic cigarettes need restrictions

Alarming New ‘Superbug’ Gene found in animals and people in China A new gene that makes bacteria highly resistant to a last-resort class of antibiotics has been found in people and pigs in China - including in samples of bacteria with epidemic potential, researchers said on Wednesday.The discovery was described as "alarming" by scientists, who called for urgent restrictions on the use of polymyxins - a class of antibiotics
DOJ: Consumers must remain on guard about supplement risks Putting out too much information is rarely a problem for the government, but most reports about Tuesday’s announcement by federal agencies of their new and ongoing “sweep” against unlawful dietary supplements overlooked some important consumer information. In addition to the criminal and civil actions made public Nov. 17, 2015, by the U.S. Department of Justice
New microscopy technology may help surgeons save more lives Biomedical engineers and neurosurgeons have developed an augmented microscopy technology to help surgeons operate with greater precision and reduced risk of harming patients.
Teens and parents agree: Electronic cigarettes need restrictions More than three fourths of both teens and adults say e-cigarettes should be restricted in public spaces, come with health warnings and be taxed like conventional cigarettes.

Tuesday, January 6, 2015

Beware of Products Promising Miracle Weight Loss

Avoid Weight-loss Fraud on Bathroom Scale Graphic (350 x 205)

“This year, I’m going to lose some weight.”
If you find yourself making this common New Year’s resolution, know this: many so-called “miracle” weight loss supplements and foods (including teas and coffees) don’t live up to their claims. Worse, they can cause serious harm, say FDA regulators. The agency has found hundreds of products that are marketed as dietary supplements but actually contain hidden active ingredients (components that make a medicine effective against a specific illness) contained in prescription drugs, unsafe ingredients that were in drugs that have been removed from the market, or compounds that have not been adequately studied in humans.
“When the product contains a drug or other ingredient which is not listed as an ingredient we become especially concerned about the safety of the product,” says James P. Smith, M.D., an acting deputy director in FDA’s Office of Drug Evaluation.
Tainted Products
For example, FDA has found weight-loss products tainted with the prescription drug ingredient sibutramine. This ingredient was in an FDA-approved drug called Meridia, which was removed from the market in October 2010 because it caused heart problems and strokes.
“We’ve also found weight-loss products marketed as supplements that contain dangerous concoctions of hidden ingredients including active ingredients contained in approved seizure medications, blood pressure medications, and antidepressants,” says Jason Humbert, a senior regulatory manager at FDA. Most recently, FDA has found a number of products marketed as dietary supplements containing fluoxetine, the active ingredient found in Prozac, a prescription drug marketed for the treatment of depression and other conditions. Another product contained triamterene, a powerful diuretic (sometimes known as “water pills”) that can have serious side-effects and should only be used under the supervision of a health care professional.
Many of these tainted products are imported, sold online, and heavily promoted on social media sites. Some can also be found on store shelves.
And if you’re about to take what you think of as “natural” dietary supplements, such as bee pollen or Garcinia cambogia, you should be aware that FDA has found some of these products also contain hidden active ingredients contained in prescription drugs.
“The only natural way to lose weight is to burn more calories than you take in,” says James P. Smith, M.D. That means a combination of healthful eating and physical activity.
Dietary Supplements are not FDA-Approved
Under the Federal Food, Drug and Cosmetics Act (as amended by the Dietary Supplement Health and Education Act of 1994), dietary supplement firms do not need FDA approval prior to marketing their products. It is the company’s responsibility to make sure its products are safe and that any claims made about such products are true.
But just because you see a supplement product on a store shelf does not mean it is safe, Humbert says. FDA has received numerous reports of harm associated with the use of weight loss products, including increased blood pressure, heart palpitations (a pounding or racing heart), stroke, seizure and death. When safety issues are suspected, FDA must investigate and, when warranted, take steps to have these products removed from the market.
FDA has issued over 30 public notifications and recalled 7 tainted weight loss products in 2014. The agency also has issued warning letters, seized products, and criminally prosecuted people responsible for marketing these illegal diet products. In addition, FDA maintains an online list of tainted weight-loss products.
To help people with long-term weight management, FDA has approved prescription drugs such as Belviq, Qysmia, and Contrave, but these products are intended for people at least 18 years of age who:
  • have a body mass index (BMI, a standard measure of body fat) of 30 or greater (considered obese); or
  • have a BMI of 27 or greater (considered overweight) and have at least one other weight-related health condition.
Moreover, if you are going to embark on any type of weight control campaign, you should talk to your healthcare professional about it first, Smith says.
Know the Warning Signs
Look for potential warning signs of tainted products, such as:
  • promises of a quick fix, for example, “lose 10 pounds in one week.”
  • use of the words “guaranteed” or “scientific breakthrough.”
  • products marketed in a foreign language.
  • products marketed through mass e-mails.
  • products marketed as herbal alternatives to an FDA-approved drug or as having effects similar to prescription drugs.
Advice for Consumers
Generally, if you are using or considering using any product marketed as a dietary supplement, FDA suggests that you:
  • check with your health care professional or a registered dietitian about any nutrients you may need in addition to your regular diet.
  • ask yourself if it sounds too good to be true.
  • be cautious if the claims for the product seem exaggerated or unrealistic.
  • watch out for extreme claims such as “quick and effective” or “totally safe.”
  • be skeptical about anecdotal information from personal “testimonials” about incredible benefits or results from using a product.
If you suspect a product marketed as a dietary supplement sold online may be tainted, FDA urges you to report that information online. You or your healthcare professional can also report an illness or injury you believe to be related to the use of a dietary supplement by calling 1-800-FDA-1088 or visiting FDA online.

Friday, January 10, 2014

Supplements for Sexual Enhancement Recalled

Midwest Wholesale is voluntarily recalling the following products and Lot numbers.
List of Products included in this Recall:
Boost Ultra
12 pill bottle, Lot# B 70130, Exp 03/15
3 pill bottle, Lot# B 70130, Exp 3/2015
1 pill pack, Lot# 06012011, Exp 6/2014

XZone Gold
1 pill pack, Lot#130710 GL, Exp 7/31/18
Sexy Monkey
1 pill pack, Exp 12/31/14

Triple MiracleZen Platinum
1 pill pack, Lot# OAWF 1027, Exp 1/31/15 and Lot# OAWF1003, Exp 1/31/15

Magic for Men
12 pill bottle, Lot# GP 808, Exp 10/16
1 pill pack, Lot#BN 030613, Exp 2/6/15

"New" Extenze
30 pill box, Lot# 0512058, Exp 05/16

New XZen Platinum
1 pill pack, Lot#130520 PL, Exp 5/31/17
This recall is being conducted to the consumer level. FDA analysis found these products to contain undeclared Sildenafil and/or Tadalafil, the active ingredients in FDA-approved prescription drugs used to treat erectile dysfunction (ED). These undeclared ingredients may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. Men with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates.
Consumers should stop using this product immediately and throw it away. Consumers who have experienced any negative side effects should consult a health care professional as soon as possible.
These products are labeled and intended to be used as dietary supplements for sexual enhancement. The products are packaged in 1 capsule blister packs, 3 pill bottles, 6 pill bottles, 12 pill bottles and 30 tablet boxes. These products were distributed to 20 selected retail locations in several states by Midwest Wholesale from August 1, 2013 to October 22, 2013.
Midwest Wholesale is notifying its retailers and customers by telephone and recall letter and is arranging for return of all recalled products. Consumers and retailers that have these products which are being recalled should stop consumption or further distribution and return to place of purchase or directly to Midwest Wholesale, 617 N Althea Ave, Nixa, MO 65714.
Consumers are requested to have their order number or proof of purchase.
Consumers with questions regarding this recall can contact Midwest Wholesale by phone (888-514-7110), Monday to Friday, 09:00am-5:00pm, Central Time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch-Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report online: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm, or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.


   
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