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Kanakinumab

Fara - P - B - T - Risk Undantagen

Information

Assessment report

Assessment report för Ilaris (kanakinumab), 15 December 2016 EMA/26517/2017.

"As a protein, canakinumab is not expected to pose a risk to the environment.

According to Directive 2001/83/EC and Guideline EMEA/CHMP/SWP/4447/00 corr2, medicinal products consisting of substances occurring naturally in the environment, such as electrolytes, vitamins, proteins etc. do not need to be accompanied by an environmental risk assessment because they are unlikely to result in significant risk to the environment."

Fass miljöinformation

Fass miljöinformation för Ilaris från Novartis (hämtad 2019-07-10).

Användning av aminosyror, proteiner och peptider bedöms inte medföra någon miljöpåverkan.

"In the case of products containing vitamins, electrolytes, amino acids, peptides, proteins, carbohydrates and lipids as active pharmaceutical ingredient(s), an ERA should be provided. This ERA may consist of a justification for not submitting ERA studies, e.g. due to their nature they are unlikely to result in a significant risk to the environment. The same applies to vaccines and herbal medicinal products (European Medicines Agency guideline on Doc. Ref. EMEA/CHMP/SWP/4447/00 corr 2). It can be expected that any medicinal absorbed monoclonal antibody is completely metabolized and adsorbed in the body. Any medicinal product that reaches water streams via eventual spills during application or after disposal of unused drug is expected to be very rapidly degraded and mineralized to CO2 by microbial activity."

Författad vid avdelningen Strategiska vårdgivarfrågor, Region Stockholm

Reviderat datum

2019-07-10

[Helena Ramström 2019-07-10] 2019-07-10. Finns Fass-info från Novartis och finns assessment report också för Ilaris. Inget i några mätrapporter. Ändrat revideratdatum från 2016-04-05 till 2019-07-10.[Siv Martini 2015-08-25] Kollat