Paper Details 
Original Abstract of the Article :
<b>Background</b>: The Food and Drug Administration (FDA) originated from the passage of the 1906 Pure Food and Drugs act aimed to rein in the long-standing abuse in the consumer product marketplace. The act was passed to prohibit interstate commerce of misbranded and adulterated foods, drinks, dru...See full text at original site
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ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
難解な医学論文を、専門知識のない方にも理解しやすいように、噛み砕いて説明することを目指しています。

* ラクダ博士による解説は、あくまで論文の要点をまとめたものであり、原論文の完全な代替となるものではありません。詳細な内容については、必ず原論文をご参照ください。
* ラクダ博士は架空のキャラクターであり、実際の医学研究者や医療従事者とは一切関係がありません。
* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。


引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686678/

データ提供:米国国立医学図書館(NLM)

The FDA's Perfunctory Approach: A Cause for Concern

This narrative review explores the Food and Drug Administration's (FDA) regulatory approach to dietary supplements, highlighting its shortcomings and the resulting rise in adverse event reports. The authors argue that the FDA's perfunctory approach has failed to adequately protect consumers from the potential dangers of dietary supplements, leading to a significant number of adverse events.

Dietary Supplements: A Regulatory Gap

The review examines the FDA's regulatory framework for dietary supplements, highlighting the lack of stringent requirements for efficacy and safety testing. The authors present a series of case studies involving adverse events associated with dietary supplements, including products marketed for weight loss, muscle building, and other health claims. They argue that the FDA's current approach is insufficient to protect consumers from potential risks associated with these products.

Navigating the Dietary Supplement Landscape: A Call for Action

Dietary supplements are widely available and marketed as safe and effective alternatives to conventional medicine. However, this review underscores the importance of understanding the potential risks associated with these products. It highlights the need for more stringent regulatory oversight, robust safety testing, and transparent labeling to protect consumers and ensure the safe use of dietary supplements. It's like a camel crossing a desert with shifting sand dunes – navigating this landscape requires caution and a clear understanding of the potential dangers.

Dr.Camel's Conclusion

This review raises serious concerns about the FDA's approach to regulating dietary supplements. The lack of stringent safety and efficacy requirements has led to a significant number of adverse events, highlighting the need for a more robust regulatory framework. It's a reminder that we must be vigilant about the products we consume and prioritize our health and safety.

Date :
  1. Date Completed n.d.
  2. Date Revised 2023-12-02
Further Info :

Pubmed ID

38035313

DOI: Digital Object Identifier

PMC10686678

Related Literature

SNS
PICO Info
in preparation
Languages

English

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