Acute Porphyria Drug Database

Monograph

L04AC03 - Anakinra
Propably not porphyrinogenic
PNP

Important Information
Patients on immunosuppressive therapy have an increased risk of infections. Since infections have a potential to trigger acute porphyric attacks vigilance is motivated regarding signs or symptoms of infection and/or possible symptoms of a porphyric attack.
Side effects
Infections are common in patients using immunosuppressants and since infections might trigger an acute porphyric attack, vigilance regarding signs and symptoms of an infection and/ or a porphyric attack is recommended.
Rationale
Antibody preparation with no CYP metabolism. Based on the pharmacokinetics, Anakinra is not expected to have any porphyrinogenic effects.
Chemical description
Human interleukin 1 receptor antagonist produced in Escherichia coli cells by recombinant DNA technology.
Therapeutic characteristics
Anakinra is used in the treatment of rheumatoid arthritis as monotherapy or in combination with methotrexate in patients with an inadequate response to methotrexate alone. It is administered as a subcutaneous injection.
Metabolism and pharmacokinetics
Anakinra is not metabolised by the liver via phase 1 mechanisms and is not known to inhibit cytochrome P450 enzymes. The metabolism of anakinra is expected to be similar as for endogenous antibodies, which are metabolised to peptides and amino acids in various body tissues and in plasma by circulating phagocytic cells or by their target antigen-containing cells.

References

# Citation details PMID
*Drug reference publications
1. Sweetman SC, editor. Martindale: The complete drug reference. Anakinra. Pharmaceutical Press 2009.
*Government bodies
2. European Public Assessment Report, Kineret (Scientific discussion).European Medicines Agency (EMEA). Accessible from: emea.europa.eu
*Summary of Product Characteristics
3. The electronic Medicines Compendium (emc). Summary of Product Characteristics (SPC). Kineret. (Last edition: November 2013).

Similar drugs
Explore alternative drugs in similar therapeutic classes L04A / L04AC or go back.

Tradenames and packages
From some sources, we get a list of packages (United Kingdom, Ireland, Estonia). Other sources contain more or less "clean" versions of the trade name (Denmark, Finland, Iceland, Lithuania, Norway). What you see here is the raw data we get from each country, so there will appear to be duplicates. The bold names are the searchable terms. The gray names that follow are all mapped to the bolded term.
Note: The cleaning is done automatically by a proprietary algorithm, and it may produce errors. We strive to improve it continuously.
Netherlands
Kineret · Kineret 100 mg/0,67 ml/ (150 mg/ml), oplossing voor injectie
Belgium
Kineret · Kineret 100 mg/0.67 ml sol. inj. s.c. ser. préremplie
United Kingdom
Kineret · Kineret 100mg/0.67ml solution for injection pre-filled syringes
Denmark
Kineret
Norway
Kineret
Poland
Kineret
Luxembourg
Kineret
Iceland
Kineret
Finland
Kineret
Latvia
Kineret
 
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