Insuman European Medicines Agency

Insuman is used in patients with diabetes type 1 and 2 who need treatment with insulin. Insuman Rapid can also be used for the treatment of hyperglycaemic coma coma caused by too much blood glucose [sugar] and ketoacidosis high levels of ketones [acids] in the blood, and to control blood glucose before, during or after an operation. The full EPAR for Insuman can be found on the Agency’s website: ema.europa.eu/Find medicine/Human medicines/European public assessment reports. For more information about treatment with Insuman, read the package leaflet also part of the EPAR or con tact your doctor or pharmacist. Other information about Insuman. The European Commission granted a marketing authorisation valid throughout the European Union for Insuman on 21 February 1997. The full EPAR for Insuman can be found on the Agency's website: ema.europa.eu/Find medicine/Human medicines/European public assessment reports. o. EUROPEAN MEDICINES AGENCY. SCIENCE MEDICINES HEALTH. EMA/477741/2013. EMEA/H/C/000201. Sammanfattning av EPAR för allmänheten. Insuman humaninsulin. Detta är en sammanfattning av det offentliga europeiska utredningsprotokollet EPAR för Insuman. 13/07/2016 · Insuman Basal is an intermediate-acting insulin suspension containing isophane insulin, and Insuman Comb is available in various combinations of fast- and intermediate-acting insulins. Reason for shortage In November 2015,. European Medicines Agency Keywords.

Results for insuman comb European Medicines Agency - EMA 1 - 1 of 1 sorted by relevance / date. Click export CSV or RIS to download the entire page or use the checkboxes to. Insuman X-91 Assessment report EMA/565846/2013 Page 6/79 1. Background information on the procedure 1.1. Submission of the dossier The applicant Sanofi-Aventis Deutschland GmbH submitted on 25 July 2012 an application for Marketing Authorisation to the European Medicines Agency EMA for Insuman Implantable, through. Insuman ® Comb 50 100 IU/ml suspension for injection in a cartridge insulin human Read all of this leaflet carefully before you start using this medicine because it contains important information for you. 22/09/2017 · The European Commission granted a marketing authorisation valid throughout the European Union for Insulin lispro Sanofi on 19 July 2017. For more information about treatment with Insulin lispro Sanofi, read the package leaflet also part of.

Insuman Comb 50 100 IU/ml in a cartridge. Each ml contains 100 IU insulin human equivalent to 3.5 mg. Each cartridge contains 3 ml of suspension for injection, equivalent to 300 IU insulin. Insuman Comb 25 100 IU/ml suspension for injection in a cartridge - Summary of Product Characteristics SmPC - eMC Source: electronic Medicines Compendium - eMC This is just the first eMC Summary of Product Characteristics from your search.

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