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Spravato (Esketamine) in Fordyce, Arkansas

Compare 2 Spravato (Esketamine) clinics in Fordyce, Arkansas that offer care for treatment-resistant depression and major depressive disorder. Review services, ratings, and contact details to find the right provider near you.
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Clinics

2 clinics shown

  • Dallas County Medical Center

    Dallas County Medical Center operates as a general hospital in Fordyce, serving the rural Arkansas community with inpatient and outpatient medical services. The facility does not advertise specialized psychiatric treatment programs such as TMS therapy, esketamine, or ketamine infusions in available listings. Patients seeking treatment-resistant depression care or procedural mental health interventions should contact the hospital directly to confirm whether psychiatric services or referrals to regional specialists are available through their system.

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  • Millcreek Behavioral Health

    Millcreek Behavioral Health operates a psychiatric hospital on Industrial Drive in Fordyce, providing inpatient and outpatient mental health services for adults and adolescents. The facility treats acute psychiatric conditions including depression, anxiety, bipolar disorder, and psychotic disorders through stabilization programs and medication management. Specific procedural treatments such as TMS or esketamine are not detailed in available listings; patients should contact the facility directly to confirm current treatment modalities and admission criteria.

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About Spravato (Esketamine)

Spravato is the brand name for esketamine, an FDA-approved nasal spray for treatment-resistant depression and major depressive disorder with suicidal ideation. It's derived from ketamine and works on the brain's glutamate system — a different mechanism than traditional antidepressants like SSRIs.

Treatment is administered only at REMS-certified clinics under direct medical supervision. Patients self-administer the spray under a clinician's guidance, then remain at the clinic for at least two hours of monitoring after each dose. The induction phase typically involves twice-weekly sessions for four weeks, followed by weekly or biweekly maintenance dosing depending on response.

Many patients report meaningful symptom improvement within the first one to two weeks — substantially faster than the 4 to 8 weeks typical of oral antidepressants. Spravato is taken alongside an oral antidepressant, not as a replacement.

The most common side effects are dissociation, dizziness, sedation, and elevated blood pressure during and shortly after dosing. These typically resolve within the two-hour monitoring window. Patients cannot drive on the day of treatment.

Most commercial insurance and Medicare cover Spravato for treatment-resistant depression with prior authorization. Clinics offering Spravato in our directory hold active REMS certification and are staffed to provide the required in-clinic monitoring period.