FDA's Recent Announcement on At-Home Ketamine Treatments

I consistently strive to stay informed on the latest ketamine-related news. On October 10th, 2023, the FDA released an intriguing letter and warning which focused on both patients and healthcare providers, highlighting the risks associated with oral compounded at-home ketamine use. Notably, there's a growing trend: an upsurge of telehealth companies delivering large amounts of ketamine directly to patients' homes, resulting in bypassing medical supervision and with minimal assessment of the risks.

We believe that continuous monitoring during treatments is crucial when it comes to ketamine use.

Why Is Medical Supervision Important During Ketamine Use?

The FDA's letter cited reports from patients who experienced adverse effects, including severe medical complications such as hypoxia. It's because of these reasons that we and many other clinics administer IV ketamine under constant medical supervision. We diligently monitor patients' oxygen levels, cardiac rhythm, blood pressure, and respiratory rate—collectively known as vital signs. Why the term "vital signs"? Because they are crucial to the functioning and physiology of human life. We believe that continuous monitoring during ketamine treatments not only embodies utmost integrity but also ensures the safest experience for our patients.

It’s best to stay informed about the possible risks of ketamine before undergoing the treatment.

Key Takeaways from the FDA's Advisory on At-Home Ketamine

To sum up, the FDA's recent advisory underscores the inherent risks of at-home ketamine use. This is crucial information for anyone considering such treatments. Another point worth noting is that ketamine for the treatment of mood disorders in its oral or even intravenous form is off-label. Which means the FDA hasn't approved them for certain indications. Being fully informed and aware before undergoing any treatment, especially ketamine infusions, is key for your safety and well being.

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