Female Depression Patient Treated by Brainsway Deep TMS Technology

Why this resource is helpful:

Brainsway Deep TMS is indicated by the FDA for the treatment of depressive
episodes in adult patients suffering from Major Depressive Disorder, who failed to achieve satisfactory improvement from previous anti-depressant medication treatment in the current episode. FDA 510(k) No. K122288.
Safety Information:
Patients should consult with their doctor before undergoing Deep TMS. The most common side effects include headaches and application site pain or discomfort. There is also a very rare risk of seizure associated with the treatment. Patients with metal in or around the head, such as in metal plates, implants and stents, should not undergo Deep TMS treatment.

Indication:Brainsway Deep TMS is indicated by the FDA for the treatment of depressiveepisodes in adult patients suffering from Major Depressive Disorder, who...
Quoted From: https://www.youtube.com/watch?v=omeBGRtFwHI

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