Acute Porphyria Drug Database

Monograph

L04AA24 - Abatacept
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 abatacept 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
Abatacept is not metabolized by cytochrome P450 enzymes. No pharmacokinetic porphyrinogenic effects are suspected.
Chemical description
Abatacept, a recombinant fusion protein, consists of the extracellular domain of human cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) linked to a modified Fc portion of human immunoglobulin G1 (IgG1).
Therapeutic characteristics
Abatacept is used in the treatment of moderate to severe active rheumatoid arthritis, and is given by intravenous infusion.
Metabolism and pharmacokinetics
Protein, not metabolized by CYP enzymes. No formal drug-drug-interaction studies have been conducted, but are nor expected considering the nature of the product.

References

# Citation details PMID
*Drug reference publications
1. McEvoy GK, editor. Abatacept. The AHFS Drug Information 2008. Bethesda, MD: American Society of Health-System Pharmacists; 2009. Electronic version (31.08.10).
2. Sweetman SC, editor. Martindale: The complete drug reference. Abatacept. Pharmaceutical Press 2009.
*Government bodies
3. European Public Assessment Report, Orencia (Scientific discussion).European Medicines Agency (EMEA). Accessible from: emea.europa.eu
*Summary of Product Characteristics
4. The electronic Medicines Compendium (emc). Summary of Product Characteristics (SPC). Orencia.

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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
ORENCIA · ORENCIA 125 mg oplossing voor injectie in een voorgevulde spuit · ORENCIA 250 mg poeder voor concentraat voor oplossing voor infusie. · ORENCIA 50 mg oplossing voor injectie in een voorgevulde spuit · ORENCIA 87,5 mg oplossing voor injectie in een voorgevulde spuit
Belgium
Orencia · Orencia 125 mg sol. inj. s.c. ser. préremplie · Orencia 125 mg sol. inj. s.c. stylo prérempli · Orencia 250 mg sol. perf. (pdr., à diluer) i.v. flac. · Orencia 50 mg sol. inj. s.c. ser. préremplie · Orencia 87.5 mg sol. inj. s.c. ser. préremplie
United Kingdom
Orencia · Orencia 125mg/1ml solution for injection pre-filled syringes · Orencia 250mg powder for concentrate for solution for infusion vials · Orencia 50mg/0.4ml solution for injection pre-filled syringes · Orencia 87.5mg/0.7ml solution for injection pre-filled syringes · Orencia ClickJect 125mg/1ml solution for injection pre-filled pens
Denmark
Orencia
Norway
Orencia
Poland
Orencia
Luxembourg
Orencia · ORENCIA-250
Iceland
Orencia
Finland
Orencia
Latvia
Orencia
 
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