Acute Porphyria Drug Database

Monograph

L04AG05 - Vedolizumab
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 immunosuppressant drugs. 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 vedolizumab 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
Vedolizumab is not metabolized by cytochrome P450 enzymes. No pharmacokinetic porphyrinogenic effects are suspected.
Chemical description
Vedolizumab is a humanised IgG1 monoclonal antibody that binds to the human alpha4 beta7 integrin.
Therapeutic characteristics
Vedolizumab is used in the treatment of adult patients with moderately to severely active ulcerative colitis or Crohns disease. It is administered as an intravenous injection.
Metabolism and pharmacokinetics
The exact elimination route of vedolizumab is not known. Mechanisms for elimination of monoclonal antibodies are not well documented but are reported to include proteolysis by the liver and the reticuloendothelial system, target-mediated elimination and nonspecific endocytosis (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.
*Summary of Product Characteristics
2. The electronic Medicines Compendium (emc). Summary of Product Characteristics (SPC). Entyvio.

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
Entyvio · Entyvio 108 mg, oplossing voor injectie in voorgevulde pen · Entyvio 108 mg, oplossing voor injectie in voorgevulde spuit · Entyvio 300 mg, poeder voor concentraat voor oplossing voor infusie
Belgium
Entyvio · Entyvio 108 mg sol. inj. s.c. ser. préremplie · Entyvio 108 mg sol. inj. s.c. stylo prérempli · Entyvio 300 mg sol. perf. (pdr., à diluer) i.v. flac.
United Kingdom
Entyvio · Entyvio 108mg/0.68ml solution for injection pre-filled pens · Entyvio 108mg/0.68ml solution for injection pre-filled syringes · Entyvio 300mg powder for concentrate for solution for infusion vials
Denmark
Entyvio
Norway
Entyvio
Iceland
Entyvio
Finland
Entyvio
Latvia
Entyvio
 
© NAPOS 2024
An unhandled error has occurred. Reload 🗙