Medicine guide

Xigris

·

  • Prescription status not stated
  • Blood, clotting and anaemia
Made by
Eli Lilly Nederland B.V.

Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.

What it is for

  • Xigris is indicated for the treatment of adult patients with severe sepsis with multiple organ failure when added to best standard care. The use of Xigris should be considered mainly in situations when therapy can be started within 24 hours after the onset of organ failure (for further information see section 5.1).

From the official label · 2026-09-30 · European Medicines Agency

Details

Made byEli Lilly Nederland B.V.
Active substanceDrotrecogin alfa (activated)
Used inBlood, clotting and anaemia
ClassificationB01AD10 · Blood, clotting and anaemia
Authorised on2002-08-22
Last updated by the regulator2012-02-21
EMA product numberEMEA/H/C/000396

Source: European Medicines Agency — medicine data · 2026-09-30 · not reviewed by a clinician

Source: European Medicines Agency (EMA). Product information as published by EMA. Reuse terms: EMA legal notice (reproduction authorised).