Acute Porphyria Drug Database

Monograph

L04AG04 - Belimumab
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 like nausea and vomiting may potentially be porphyrinogenic through reduction in carbohydrate intake.
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. Common adverse reactions of belimumab that can be confused with an acute porphyric attack are nausea and vomiting. These side effects may potentially be porphyrinogenic if leading to a decrease in carbohydrate intake.
Rationale
Belimumab is not metabolized by cytochrome P450 enzymes. No pharmacokinetic porphyrinogenic effects are suspected.
Chemical description
Belimumab is a human IgG1-lambda monoclonal antibody specific for soluble human B Lymphocyte Stimulator protein.
Therapeutic characteristics
Belimumab is used in the treatment of active, autoantibody-positive systemic lupus erythematosus in adults as an addition to standard therapy. It is administered as an intravenous infusion.
Metabolism and pharmacokinetics
Belimumab is a protein for which the expected metabolic pathway is degradation to small peptides and individual amino acids by widely distributed proteolytic enzymes. Classical biotransformation studies have not been conducted (SPC, Keizer 2010).

References

# Citation details PMID
*Scientific articles
1. Clinical pharmacokinetics of therapeutic monoclonal antibodies.
Keizer RJ, Huitema AD et al. Clin Pharmacokinet. 2010 Aug; 49 (8):493-507.
*Drug reference publications
2. Micromedex® 2.0 (online). Belimumab (Drugdex System).
*Summary of Product Characteristics
3. The electronic Medicines Compendium (emc). Summary of Product Characteristics (SPC). Benlysta.

Similar drugs
Explore alternative drugs in similar therapeutic classes L04A / L04AG 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
Benlysta · Benlysta 120 mg, Poeder voor oplossing voor infusie · Benlysta 200 mg oplossing voor injectie in voorgevulde pen · Benlysta 200 mg oplossing voor injectie in voorgevulde spuit · Benlysta 400 mg, Poeder voor oplossing voor infusie
Belgium
Benlysta · Benlysta 120 mg sol. perf. (pdr., à diluer) i.v. flac. · Benlysta 200 mg sol. inj. s.c. ser. préremplie · Benlysta 200 mg sol. inj. s.c. stylo prérempli · Benlysta 400 mg sol. perf. (pdr., à diluer) i.v. flac.
United Kingdom
Benlysta · Benlysta 120mg powder for concentrate for solution for infusion vials · Benlysta 200mg/1ml solution for injection pre-filled pens · Benlysta 400mg powder for concentrate for solution for infusion vials
Denmark
Benlysta
Norway
Benlysta
Iceland
Benlysta
Finland
Benlysta
Latvia
Benlysta
 
© NAPOS 2024
An unhandled error has occurred. Reload 🗙