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The pressure on the FDA to quickly approve medications may be resulting in poor standards and a lack of complete and thorough testing of potentially harmful medications. Recent drug recalls prompted by numerous consumer deaths have raised suspicion of FDA practices and their lumbering mechanism to protect consumers once a drug has been approved. In some cases, years have gone by before the FDA takes action after studies prove that a medication is actually harmful to consumers.
There is also increasing concern that doctors are not being given enough documentation by the FDA and drug companies describing the dangers of these medications before prescribing them to patients.
About the author: Mike Adams is an award-winning journalist and holistic nutritionist with a passion for sharing empowering information to help improve personal and planetary health He has authored more than 1,800 articles and dozens of reports, guides and interviews on natural health topics, impacting the lives of millions of readers around the world who are experiencing phenomenal health benefits from reading his articles. Adams is an independent journalist with strong ethics who does not get paid to write articles about any product or company. In 2010, Adams co-founded NaturalNews.TV, a natural health video sharing site that has now grown in popularity. He also founded an environmentally-friendly online retailer called BetterLifeGoods.com that uses retail profits to help support consumer advocacy programs. He's also the founder of a well known HTML email software company whose 'Email Marketing Director' software currently runs the NaturalNews subscription database. Adams also serves as the executive director of the Consumer Wellness Center, a non-profit consumer protection group, and practices nature photography, Capoeira, martial arts and organic gardening. Known as the 'Health Ranger,' Adams' personal health statistics and mission statements are located at www.HealthRanger.org Related CounterThink Cartoons:
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Friday, November 26, 2004
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