The Risks of Glutathione: FDA Issues Warning
The pursuit of longevity through supplements has taken a concerning turn with the FDA recently issuing a warning about glutathione, dubbed the “master detoxifier.” Reports indicate that at least 30 patients have experienced severe side effects, resembling symptoms of sepsis, after receiving dietary-grade glutathione via IV. These side effects included fever, chills, and signs of shock, necessitating hospitalization for some individuals.
This caution comes on the heels of a previous warning in 2019 regarding the use of dietary glutathione in compounding injectables. According to the FDA, compounded drugs, which are customized by pharmacists or doctors, should not use dietary supplement-grade ingredients, as they may contain harmful impurities unsuitable for injection.
What is Glutathione?
Glutathione is a naturally occurring antioxidant critical for protecting cells from damage. Its levels can drop due to factors like aging, stress, and poor nutrition. While many believe that supplementing glutathione can combat age-related changes and promote cell repair, experts caution against its use, particularly in injectable forms.
The Dangers of IV Glutathione
The FDA reiterated that all ingredients used in injectable drugs must be appropriate, and dietary-grade glutathione presents a risk due to potential contaminants. Reports of adverse effects from IV glutathione have been concerning, leading to recalls from pharmacies.
Despite its trendiness, evidence supporting glutathione’s benefits is limited. Some studies even suggest that glutathione supplementation could potentially shorten lifespan in certain organisms, prompting experts to recommend caution in its use.
The FDA plans to investigate further and continue monitoring reports related to glutathione injections.
