NeuroStar® TMS Therapy
FDA-cleared, non-medication depression treatment
(855) 940-4867
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Regional Medical Director Greater St. Louis
Several medications can help people with depression find relief from their symptoms. Sometimes, however, first-line treatments don’t work, and patients may need to seek out additional strategies to help reduce symptoms. This scenario—where adults who have tried at least two medications don’t find any relief from their symptoms—is called treatment-resistant depression (TRD). One option for those with TRD is esketamine nasal spray for depression. Here’s what you should know about the benefits of this ketamine-based depression treatment.
Esketamine is a form of ketamine, a medication that has been around for decades. Ketamine is given as an anesthetic and pain reliever, but it’s been used as an off-label treatment for depression for years. Unlike traditional antidepressants, ketamine works within hours or days, making it a promising short-term treatment for patients who find no relief from other forms of antidepressants. In March of 2019, the FDA approved SPRAVATO® as the first esketamine nasal spray for resistant depression.
While esketamine nasal spray works similarly to ketamine, there’s a key difference between the two medications. Ketamine is a racemic mixture of “S” and “R” mirror-image molecules, whereas esketamine consists only of the “S” molecule. This difference means that esketamine is more potent than ketamine but with fewer side effects. In addition, esketamine for depression is thought to work more quickly than ketamine to relieve symptoms of depression.
Because it is a Schedule III Controlled Substance, esketamine nasal spray can only be given to patients at certified clinics under the supervision of a medical professional. The provider will tell patients how much esketamine to use and instruct them on how to spray it up their own nostrils. After self-administering the prescribed number of sprays, patients will remain under observation for two hours.
Esketamine for depression works by initiating activity in the glutamatergic system of the brain. This activity then helps to quickly restore neural pathways that had previously been lost as a result of treatment-resistant depression.
The results of depression treatment nasal spray typically become apparent within hours. Patients may notice a renewed sense of hopefulness, along with a decrease in anxiety and depressive symptoms. The results can last from one to two weeks, depending on the patient and the situation. The provider will know how much esketamine nasal spray to prescribe and how often it should be administered.
Patients return to the clinic twice per week for their treatment during the first four weeks. After that, they typically continue treatment once per week for a while, and then, depending on how they’re doing, less often after that.
It’s important to note that esketamine for depression should be taken along with an antidepressant. Side effects typically last less than two hours after the dose of esketamine is given and may include drowsiness, dissociation, dizziness, nausea, and lightheadedness.
Depression treatment nasal spray is meant for people who struggle with treatment-resistant depression. In order to qualify for SPRAVATO®, patients with TMD must have tried two previous oral antidepressants with unsatisfactory results.
Esketamine nasal spray is also approved to treat people who have major depressive disorder with acute harmful behaviors. One of the major benefits of using esketamine nasal spray is that it works rapidly to treat symptoms. Many patients feel substantial relief within hours.
Ketamine IV treatment can also provide rapid relief, but in many patients, it takes at least three separate IV infusions before symptoms begin to improve. Unlike SPRAVATO® nasal spray, ketamine IV treatment is not approved by the FDA for treatment of depression. Because of this, insurance does not cover the cost of ketamine IV treatment.
Esketamine is FDA approved for two indications: treatment-resistant depression and major depressive disorder with acute harmful behaviors. SPRAVATO® is monitored as a Schedule III drug. This means that in order to receive treatment, you will need to visit a certified clinic and administer the medication to yourself under the supervision of a medical provider. Because it is FDA approved, esketamine is covered by insurance.
If you have TRD or MDD with acute harmful behaviors, schedule your no-cost consult with Greenbrook TMS NeuroHealth Centers. We are a certified SPRAVATO® treatment center, and we are also FDA-cleared to provide transcranial magnetic stimulation (TMS) therapy. Our care team can help you discover which treatment is right for your situation.
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NeuroStar Adult Indications for Use
The NeuroStar Advanced Therapy System is indicated for the treatment of depressive episodes and for decreasing anxiety symptoms for those who may exhibit comorbid anxiety symptoms in adult patients suffering from Major Depressive Disorder (MDD) and who failed to achieve satisfactory improvement from previous antidepressant medication treatment in the current episode.
The NeuroStar Advanced Therapy System is intended to be used as an adjunct for the treatment of adult patients suffering from Obsessive-Compulsive Disorder (OCD).
NeuroStar Adolescent Indications for Use
NeuroStar Advanced Therapy is indicated as an adjunct for the treatment of Major Depressive Disorder (MDD) in adolescent patients (15-21).
Important Safety Information
NeuroStar Advanced Therapy is only available by prescription. A doctor can help decide if NeuroStar Advanced Therapy is right for you. Patients’ results may vary.
The most common side effect is pain or discomfort at or near the treatment site. These events are transient; they occur during the TMS treatment course and do not occur for most patients after the first week of treatment. There is a rare risk of seizure associated with the use of TMS therapy (<0.1% per patient).
Visit neurostar.com for full safety and prescribing information.
Important Safety Information
What is the most important information I should know about SPRAVATO®?
SPRAVATO® can cause serious side effects, including:
Do not take SPRAVATO® if you:
If you are not sure if you have any of the above conditions, talk to your healthcare provider before taking SPRAVATO®.
Before you take SPRAVATO®, tell your healthcare provider about all of your medical conditions, including if you:
Tell your healthcare provider about all the medicines that you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. Taking SPRAVATO® with certain medicine may cause side effects.
Especially tell your healthcare provider if you take central nervous system (CNS) depressants, psychostimulants, or monoamine oxidase inhibitors (MAOIs) medicine. Keep a list of them to show to your healthcare provider and pharmacist when you get a new medicine.
How will I take SPRAVATO®?
What should I avoid while taking SPRAVATO®?
Do not drive, operate machinery, or do anything where you need to be completely alert after taking SPRAVATO®. Do not take part in these activities until the next day following a restful sleep. See “What is the most important information I should know about SPRAVATO®?”
What are the possible side effects of SPRAVATO®?
SPRAVATO® may cause serious side effects including:
See “What is the most important information I should know about SPRAVATO®?”
Increased blood pressure. SPRAVATO® can cause a temporary increase in your blood pressure that may last for about 4 hours after taking a dose. Your healthcare provider will check your blood pressure before taking SPRAVATO® and for at least 2 hours after you take SPRAVATO®. Tell your healthcare provider right away if you get chest pain, shortness of breath, sudden severe headache, change in vision, or seizures after taking SPRAVATO®.
Problems with thinking clearly. Tell your healthcare provider if you have problems thinking or remembering.
Bladder problems. Tell your healthcare provider if you develop trouble urinating, such as a frequent or urgent need to urinate, pain when urinating, or urinating frequently at night.
The most common side effects of SPRAVATO® include:
If these common side effects occur, they usually happen right after taking SPRAVATO® and go away the same day.
These are not all the possible side effects of SPRAVATO®.
Call your doctor for medical advice about side effects. You may report side effects to Johnson & Johnson at 1-800-526-7736, or to the FDA at 1-800-FDA-1088.
What is SPRAVATO® (esketamine) CIII nasal spray?
SPRAVATO® is a prescription medicine used:
SPRAVATO® is not for use as a medicine to prevent or relieve pain (anesthetic). It is not known if SPRAVATO® is safe or effective as an anesthetic medicine.
It is not known if SPRAVATO® is safe and effective for use in preventing suicide or in reducing suicidal thoughts or actions. SPRAVATO® is not for use in place of hospitalization if your healthcare provider determines that hospitalization is needed, even if improvement is experienced after the first dose of SPRAVATO®.
It is not known if SPRAVATO® is safe and effective in children.
Please see full Prescribing Information, including Boxed WARNINGS, and Medication Guide for SPRAVATO® and discuss any questions you may have with your healthcare provider.
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