Brintexa 5 is an antidepressant medication. It acts by increasing the levels of certain chemical messengers (such as serotonin) in the brain that can stabilize mood and mental health. As a result, it improves your mood and energy and reduces the signs of depression.
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Brintexa 5 contains Vortioxetine which belongs to the group of medicines called Antidepressants. It is used to manage depression (major depressive episodes) in adults. Depression is a mood disorder characterized by persistent feelings of sadness, loss of interest, feeling guilty or worthless, attention impairment, lack of energy, suicidal thoughts,s and slow or abnormal physical movements.
Before taking Brintexa 5. Inform your doctor if you have any liver or kidney problems. You must also inform your doctor if you currently have or have a previous history of fits (epilepsy), glaucoma, suicidal thoughts, mania, or bleeding problems as a precaution.
Brintexa 5 is not recommended for use in pregnant or breastfeeding women unless considered necessary by the physician. It is also not suitable for use in children aged below 18 years.
The most common side effects of taking Brintexa 5 are nausea, vomiting, diarrhoea, constipation, dizziness, itching of the whole body, abnormal dreams (nightmares), and increased sweating. These side effects are usually temporary and will resolve on their own within 2 weeks of therapy. However, consult your doctor if they worsen.
Recommended Dose:
The usual starting dose of Vortioxetine is 10 mg taken orally once daily, with or without food. Based on patient tolerance and clinical response, the dose may be increased to a maximum of 20 mg per day. The safety and effectiveness of doses exceeding 20 mg daily have not been established in controlled clinical studies.
For patients who experience intolerance at higher doses, a dose reduction to 5 mg once daily may be considered. In elderly patients (≥65 years), treatment should always be initiated at the lowest effective dose of 5 mg once daily.
Maintenance Therapy:
In patients with major depressive disorder (MDD), Vortioxetine may be continued for several months or longer as maintenance therapy. For long-term use, patients should be periodically reassessed to determine the ongoing need and benefit of treatment.
Discontinuation of Treatment:
Although Vortioxetine can be stopped abruptly, clinical trials have reported temporary adverse effects such as headache and muscle tension, particularly following sudden discontinuation of 15 mg or 20 mg daily doses. To minimize these effects, it is recommended to taper the dose to 10 mg once daily for one week before complete discontinuation when stopping higher doses.
Switching To or From Monoamine Oxidase Inhibitors (MAOIs):
To reduce the risk of serotonin syndrome, a minimum of 14 days should elapse between stopping an MAOI intended for psychiatric disorders and initiating Vortioxetine therapy. Conversely, at least 21 days should pass after discontinuing Vortioxetine before starting treatment with an MAOI.
⚠️Disclaimer:
At ePharma, we’re committed to providing accurate and accessible health information. However, all content is intended for informational purposes only and should not replace medical advice from a qualified physician. Please consult your healthcare provider for personalized guidance. We aim to support, not substitute, the doctor-patient relationship.