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FDA Investigates Kratom Supplement Linked to ICU Admissions

The FDA is investigating kratom, a natural supplement marketed for over a decade, due to its potential to cause serious health issues. Kratom contains compounds that interact with opioid receptors, leading to concerns about its safety and potential for misuse. The agency is collecting data to assess the risks associated with its consumption. AI

IMPACT This investigation highlights the challenges in regulating natural supplements and the potential health risks associated with products interacting with opioid receptors.

RANK_REASON The FDA is investigating a supplement based on reported adverse events, which falls under regulatory and safety research. [lever_c_demoted from research: ic=1 ai=0.4]

Read on Forbes — Innovation →

AI-generated summary · Google Gemini · from 1 sources. How we write summaries →

FDA Investigates Kratom Supplement Linked to ICU Admissions

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The FDA is investigating a supplement based on reported adverse events, which falls under regulatory and safety research. [lever_c_demoted from research: ic=1 ai=0.4]
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COVERAGE [1]

  1. Forbes — Innovation TIER_1 English(EN) · Robert Glatter, MD, Contributor ·

    The ‘Natural’ Supplement Sending People To The ICU

    Marketed for over a decade as a natural wellness product, kratom contains mitragynine and its derivative 7-hydroxymitragynine, which both interact with opioid receptors.