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  • Trisenox® (arsenic trioxide) Teva


    (arsenic trioxide)

Prescribing Trisenox®

Trisenox® (arsenic trioxide) 1mg/mL, concentrate for solution for infusion

Therapeutic Indications

Trisenox® (arsenic trioxide) is indicated for induction of remission and consolidation in adult patients with relapsed/refractory acute promyelocytic leukaemia (APL), characterised by the presence of the t(15;17) translocation and/or the presence of the Pro-Myelocytic Leukaemia/Retinoic-Acid-Receptoralpha (PML/RAR-alpha) gene. Previous treatment should have included a retinoid and chemotherapy.1

The response rate of other acute myelogenous leukaemia subtypes to Trisenox® has not been examined.1

About Trisenox®

1mL of Trisenox® contains 1mg of arsenic trioxide

For a full list of excipients, see Section 6.1 of the Summary of Product Characteristics.1

  • Trisenox® is a concentrate for solution for infusion
  • It is a sterile, clear, colourless, aqueous solution
Trisenox® must be administered under the supervision of a physician who is experienced in the management of acute leukaemias, and the special monitoring procedures described in Section 4.4 of the Summary of Product Charateristics must be followed.1

Marketing Authorisation

Teva B.V.
Swensweg 5
2031 GA Haarlem

Marketing Authorisation Number(s)

  • EU/1/02/204/001

Resources for Trisenox®

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Medicine supporting documentation for Trisenox®

1 Trisenox® (arsenic trioxide) Summary of Product Characteristics.

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