Evarrest

RSS

Withdrawn

This medicine's authorisation has been withdrawn

human fibrinogen / human thrombin
MedicineHumanWithdrawn

Irish is available via eTranslation, the European Commission's machine translation service.

Translate to Irish | Important information about machine translation

  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

On 15 November 2017, the European Commission withdrew the marketing authorisation for Evarrest (human fibrinogen / human thrombin) in the European Union (EU). The withdrawal was at the request of the marketing authorisation holder, Omrix Biopharmaceuticals N. V., which notified the European Commission of its decision to permanently discontinue the marketing of the product in the EU for commercial reasons. 

Evarrest was granted marketing authorisation in the EU on 25 September 2013 for the treatment of haemostasis and as an adjunct to haemostasis in bleeding.

The European Public Assessment Report (EPAR) for Evarrest is updated accordingly to reflect the fact that the marketing authorisation is no longer valid.

български (BG) (597.14 KB - PDF)

Amharc

español (ES) (515.07 KB - PDF)

Amharc

čeština (CS) (578.52 KB - PDF)

Amharc

dansk (DA) (518.89 KB - PDF)

Amharc

Deutsch (DE) (516.28 KB - PDF)

Amharc

eesti (ET) (518.26 KB - PDF)

Amharc

ελληνικά (EL) (600.8 KB - PDF)

Amharc

français (FR) (518 KB - PDF)

Amharc

hrvatski (HR) (535.13 KB - PDF)

Amharc

italiano (IT) (514.66 KB - PDF)

Amharc

latviešu (LV) (593.61 KB - PDF)

Amharc

lietuvių (LT) (538.4 KB - PDF)

Amharc

magyar (HU) (571.9 KB - PDF)

Amharc

Malti (MT) (577.35 KB - PDF)

Amharc

Nederlands (NL) (514.67 KB - PDF)

Amharc

polski (PL) (576.8 KB - PDF)

Amharc

português (PT) (536.9 KB - PDF)

Amharc

română (RO) (1020.06 KB - PDF)

Amharc

slovenčina (SK) (100.5 KB - PDF)

Amharc

slovenščina (SL) (567.85 KB - PDF)

Amharc

suomi (FI) (513.9 KB - PDF)

Amharc

svenska (SV) (514.56 KB - PDF)

Amharc

Product information

български (BG) (1.55 MB - PDF)

Amharc

español (ES) (896.44 KB - PDF)

Amharc

čeština (CS) (1.51 MB - PDF)

Amharc

dansk (DA) (813.54 KB - PDF)

Amharc

Deutsch (DE) (845.01 KB - PDF)

Amharc

eesti (ET) (787.41 KB - PDF)

Amharc

ελληνικά (EL) (1.55 MB - PDF)

Amharc

français (FR) (818.58 KB - PDF)

Amharc

hrvatski (HR) (898.08 KB - PDF)

Amharc

italiano (IT) (816.34 KB - PDF)

Amharc

latviešu (LV) (1.31 MB - PDF)

Amharc

lietuvių (LT) (910.1 KB - PDF)

Amharc

magyar (HU) (1.15 MB - PDF)

Amharc

Malti (MT) (1.31 MB - PDF)

Amharc

Nederlands (NL) (827.81 KB - PDF)

Amharc

polski (PL) (1.32 MB - PDF)

Amharc

português (PT) (818.67 KB - PDF)

Amharc

română (RO) (934.43 KB - PDF)

Amharc

slovenčina (SK) (1.32 MB - PDF)

Amharc

slovenščina (SL) (1.25 MB - PDF)

Amharc

suomi (FI) (923.42 KB - PDF)

Amharc

svenska (SV) (864.7 KB - PDF)

Amharc

Íslenska (IS) (877.78 KB - PDF)

Amharc

norsk (NO) (860 KB - PDF)

Amharc
Latest procedure affecting product information:II/0027/G
15/11/2017
icon globe

This medicine’s product information is available in all official EU languages.
Select 'available languages' to access the language you need.

 

Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

български (BG) (496.48 KB - PDF)

Amharc

español (ES) (460.12 KB - PDF)

Amharc

čeština (CS) (486.03 KB - PDF)

Amharc

dansk (DA) (460.06 KB - PDF)

Amharc

Deutsch (DE) (459.93 KB - PDF)

Amharc

eesti (ET) (459.94 KB - PDF)

Amharc

ελληνικά (EL) (496.65 KB - PDF)

Amharc

français (FR) (459.86 KB - PDF)

Amharc

hrvatski (HR) (472.28 KB - PDF)

Amharc

italiano (IT) (459.91 KB - PDF)

Amharc

latviešu (LV) (489.48 KB - PDF)

Amharc

lietuvių (LT) (474.86 KB - PDF)

Amharc

magyar (HU) (484.42 KB - PDF)

Amharc

Malti (MT) (490.05 KB - PDF)

Amharc

Nederlands (NL) (459.69 KB - PDF)

Amharc

polski (PL) (489.07 KB - PDF)

Amharc

português (PT) (459.81 KB - PDF)

Amharc

română (RO) (930.92 KB - PDF)

Amharc

slovenčina (SK) (29.59 KB - PDF)

Amharc

slovenščina (SL) (483.95 KB - PDF)

Amharc

suomi (FI) (460.2 KB - PDF)

Amharc

svenska (SV) (459.88 KB - PDF)

Amharc

Íslenska (IS) (460 KB - PDF)

Amharc

norsk (NO) (459.61 KB - PDF)

Amharc

Product details

Name of medicine
Evarrest
Active substance
  • human fibrinogen
  • human thrombin
International non-proprietary name (INN) or common name
  • human fibrinogen
  • human thrombin
Therapeutic area (MeSH)
Hemostasis
Anatomical therapeutic chemical (ATC) code
B02BC30

Pharmacotherapeutic group

Local hemostatics

Therapeutic indication

Supportive treatment in adult surgery where standard surgical techniques are insufficient (see section 5.1):

- for improvement of haemostasis.

Authorisation details

EMA product number
EMEA/H/C/002515
Marketing authorisation holder
Omrix Biopharmaceuticals N. V.

Leonardo Da Vinci Laan 15
1831 Diegem
Belgium

Marketing authorisation issued
25/09/2013
Withdrawal of marketing authorisation
15/11/2017
Revision
4

Assessment history

This page was last updated on

Share this page