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The heavily marketed diet product line Hydroxycut has been blamed in the death of at least one person and for nearly two dozen serious ailments, prompting the U.S. Food and Drug Administration to ...
Following the reformulation, case reports in the medical literature have continued to link Hydroxycut to serious side effects. An article published in 2010 reported on a case of atrial fibrillation that the author suspected was due to epigallocatechin gallate [36] in Hydroxycut Green Tea, a product that as of 2012 is no longer marketed. [37]
Anaphylaxis, possibly due to carrier oil (Cremophor EL). [3] Amineptine (Survector) 1999 France, US Hepatotoxicity, dermatological side effects, and abuse potential. [7] Aminopyrine: 1999 France, Thailand Risk of agranulocytosis and severe acne. [3] Amobarbital: 1980 Norway Risk of barbiturate toxicity. [3] Amoproxan: 1970 France
If it's "too easy" to pull up independent, reliable sources detailing Hydroxycut lawsuits/recalls/side effects, then one possible conclusion is that these are the things that are actually notable about the supplement, and thus the things we should be covering. MastCell Talk 05:47, 8 December 2010 (UTC) I couldn't have said it better, MastCell.
Think before you drink. The FDA has recalled 28 beverages so far in 2024, The Daily Mail reported. All but four of the drinks were recalled because they had drugs, bacteria or harmful chemicals in ...
Lighter Side. Politics. Science & Tech. Sports. ... Ford Motor is recalling over 200,000 vehicles in the United States due to concerns over battery failure, reports said. ... The recall affects ...
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]
The FDA said the recall of the device BioZorb Marker, initiated by Hologic in March, was not a product removal, but a correction. The agency also urged patients to report any side effects they ...