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Latuda® (lurasidone): Home Page

Report an Adverse Reaction. European Marketing Authorisation for Latuda. Now held by Sunovion Pharmaceuticals Europe Ltd. The licence for the joint development and exclusive commercialisation of all pharmaceutical products containing lurasidone (LATUDA. An atypical antipsychotic agent indicated for the treatment of schizophrenia in adults of 18 years and over, has been transferred back to Sumitomo Dainippon Pharma Co., Ltd. (Sumitomo Dainippon Pharma) effective 31 January 2016. From 16 May 2016 Sunovion ...

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Latuda® (lurasidone): Home Page | latuda.eu Reviews

https://latuda.eu

Report an Adverse Reaction. European Marketing Authorisation for Latuda. Now held by Sunovion Pharmaceuticals Europe Ltd. The licence for the joint development and exclusive commercialisation of all pharmaceutical products containing lurasidone (LATUDA. An atypical antipsychotic agent indicated for the treatment of schizophrenia in adults of 18 years and over, has been transferred back to Sumitomo Dainippon Pharma Co., Ltd. (Sumitomo Dainippon Pharma) effective 31 January 2016. From 16 May 2016 Sunovion ...

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latuda.eu latuda.eu
1

Latuda® (lurasidone): Prescribing Information

http://www.latuda.eu/prescribing-information.html

Report an Adverse Reaction. PRESCRIBING INFORMATION-SCHIZOPHRENIA FILM-COATED TABLETS. Please refer to the full Summary of Product Characteristics (SmPC) before prescribing, particularly in relation to adverse reactions, precautions and contraindications. Latuda film-coated tablets, containing lurasidone hydrochloride equivalent to 18.6mg, 37.2mg and 74.5mg lurasidone. Latuda is indicated for the treatment of schizophrenia in adults ( 18 years). For oral administration. Adults. Caution is advised when co...

2

Latuda® (lurasidone): Site Map

http://www.latuda.eu/sitemap.html

Report an Adverse Reaction. Report an Adverse Reaction. And LATUDA are registered trademarks of Sumitomo Dainippon Pharma Co., Ltd. THIS SITE IS INTENDED FOR EU AND EEA HEALTHCARE PROFESSIONALS ONLY. Privacy Policy and Cookie Notice.

3

Latuda® (lurasidone): Summary of Product Characteristics (SmPC)

http://www.latuda.eu/smpc.html

Report an Adverse Reaction. Summary of Product Characteristics. To access the Latuda Summary of Product Characteristics in your chosen language please click on the link below, open the. Ldquo;PRODUCT INFORMATION”. Tab and select your language from the drop-down box “. LATUDA EPAR Product Information”. Http:/ www.ema.europa.eu/ema/index.jsp? Curl=pages/medicines/human/medicines/002713/human med 001737.jsp&mid=WC0b01ac058001d124. And LATUDA are registered trademarks of Sumitomo Dainippon Pharma Co., Ltd.

4

Latuda® (lurasidone): Report an Adverse Reaction

http://www.latuda.eu/report-an-adverse-reaction.html

Report an Adverse Reaction. Report an Adverse Reaction. If you need to report an adverse reaction please phone 44207 821 2899. You will be given several language options to enable you to select your preferred language. Adverse reactions should be reported to the Competent Authority in your country. And LATUDA are registered trademarks of Sumitomo Dainippon Pharma Co., Ltd. THIS SITE IS INTENDED FOR EU AND EEA HEALTHCARE PROFESSIONALS ONLY. Privacy Policy and Cookie Notice.

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Official Website - Innovation today, healthier tomorrows : Sunovion Pharmaceuticals Europe Ltd.

http://www.sunovion.eu/index.html

Sunovion Europe specialises in improving people’s health and wellbeing:. At Sunovion Pharmaceuticals Europe Ltd. (Sunovion Europe) we focus on the development and introduction of innovative medicines that improve people’s health and wellbeing. We currently specialise in Psychiatry and Neurology - including mental health - and other areas of unmet medical need that require highly specialised drug development. For more information click here. About Sunovion Pharmaceuticals Europe Ltd. Sunovion Celebrates F...

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This site is for healthcare professionals only. Members of the UK Public. Enter Healthcare Professionals Site. This site is intended for UK Healthcare Professionals. By clicking to enter this site, you are confirming that you are. A UK Healthcare Professional. Job code: LAT642-15 August 2015. Click here to find out more about Sunovion. Privacy Policy and Cookie Notice. Job code: UK/LUR/14/0072 September 2014. And LATUDA are registered trademarks of Sumitomo Dainippon Pharma Co., Ltd.

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Latuda® (lurasidone): Home Page

Report an Adverse Reaction. European Marketing Authorisation for Latuda. Now held by Sunovion Pharmaceuticals Europe Ltd. The licence for the joint development and exclusive commercialisation of all pharmaceutical products containing lurasidone (LATUDA. An atypical antipsychotic agent indicated for the treatment of schizophrenia in adults of 18 years and over, has been transferred back to Sumitomo Dainippon Pharma Co., Ltd. (Sumitomo Dainippon Pharma) effective 31 January 2016. From 16 May 2016 Sunovion ...

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