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BRINTELLIX PACKAGE INSERT PDF

This leaflet answers some common questions about Brintellix. Do not take Brintellix if the packaging is torn or shows signs of having been tampered with. Product details on treatment with TRINTELLIX (vortioxetine), including available savings if eligible, and support sign-up. Watch videos of actual patients. See full. Attachment 1: Product information for AusPAR vortioxetine hydrobromide Brintellix Lundbeck Australia Pty Ltd PM Final 8 July.

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Individual results may vary. You are now leaving lundbeck.

You can also report side effects directly via:. Do not give Brintellix to a child or adolescent. Symptoms may include agitation, hallucinations, coma or other changes in mental status; problems controlling movements or muscle twitching, apckage or tightness; fast heartbeat, high or low blood pressure; sweating or fever; nausea, vomiting or diarrhea.

National Center for Biotechnology InformationU. There is an increased risk of serotonin syndrome when vortioxetine is used in combination with other serotonergic agents. Call your healthcare provider right away if symptoms such as anxiety, irritability, impulsivity, trouble sleeping, aggressive behavior or suicidal thoughts are new, worse or worry you.

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Taking Brintellix with MAOIs may cause a serious reaction including sudden changes in mental state, twitching, rapid heartbeat, high blood pressure, fever and diarrhoea. Brintellix vortioxetine package insert.

AUST R 10 mg tablet: You might ask them to tell you if they think your depression is getting worse, or if they are worried about changes in your behaviour. Depression is diagnosed using the Diagnostic and Statistical Manual of Mental Health Disorders, 5th Edition DSM-5 criteria of having five or more of the following symptoms present for at least two weeks.

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The pack sizes of 56 x 1, 98 x 1 and film-coated tablets are presented in unit dose brrintellix. Brintellix tablets 5, 10 and 20mg Package leaflet: The concomitant use of NSAIDs, aspirin, warfarin, and anticoagulants may increase the risk of abnormal bleeding.

Vortioxetine has a linear and dose-proportional pharmacokinetic profile with single daily dosing of 2.

Brintellix® (vortioxetine hydrobromide)

Nausea, diarrhea, dry mouth, and headaches were the most commonly reported adverse effects. It does not contain all the available information. If you take the tablets out of the box or blister pack they may not keep well. There is no experience with the use of Brintellix in children or adolescents less than 18 years of age. After taking Brintellix Storage Keep Brintellix in the blister pack until it is time to take them.

Patients were excluded if they had any current psychiatric disorder other than MDD; a current or past history of manic or hypomanic episodes, schizophrenia, or any other psychotic disorder, including MDD with psychotic features; mental retardation, organic mental disorders, or mental inesrt due to a general medical condition; or substance abuse.

There was a statistically significant reduction in HDRS total score at week 8 for the vortioxetine mg group compared with placebo 4.

The half-life of vortioxetine is approximately 66 hours. Patients and care givers should pay attention for any of the following warning signs of suicide-related behaviour while taking Brintellix: American Psychiatric Association; Tell your doctor or pharmacist as soon as possible if packaage do not feel well while you are taking Brintellix.

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Additional comparative studies are need to better compare efficacy and safety with traditional agents and determine the best place in practice to use vortioxetine.

Brintellix tablets 5, 10 and 20mg

If you take too much overdose Immediately telephone your doctor or Poisons Information Centre Telephone 13 11 26 for advice, or go to the Accident and Emergency department at your nearest hospital if you think that you or anyone else may have taken too much Brintellix.

The links to third-party websites contained on this website are provided solely for your convenience. Do not take Brintellix after the expiry date EXP printed on the pack. Method of administration Inswrt one tablet with a glass of water. It may have no effect at all or, an entirely unexpected effect if you indert it after the expiry date.

Brintellix tablets 5, 10 and 20mg – Patient Information Leaflet (PIL) – (eMC)

Back to top Lundbeck Limited contact details. Once an MAOI is stopped, vortioxetine cannot be initiated within the following 14 days. How to take it Swallow the tablets whole with a full glass of water. Continue to take Brintellix even if it takes some time before you feel any improvement in your condition.

The study did not show as much sexual dysfunction and weight gain as found with typical SSRIs, but it found a statistically significant risk of nausea and nasopharyngitis compared with placebo.