Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Certolizumab pegol
Drug ID BADD_D00416
Description Certolizumab pegol is a pegylated monoclonal antibody against the tumor necrosis factor-alpha (TNF-alpha).[A176585] It is formed with a humanized Fab fragment of 50 kDa, from an IgG 1 isotype, fused to a 40 kDa polyethylene glycol moiety replacing the Fc antibody region. The absence of the Fc region was ideated to prevent complement fixation and antibody-mediated cytotoxicity as well as to markedly increase its half-life.[A176606] Certolizumab does not require glycosylation for active function and hence, its production is significantly more affordable when compared to other existing TNF-alpha therapies as it can be done directly in bacterial hosts such as _E. coli_.[A176606] It was developed and manufactured by UCB Pharma, first FDA approved in 2008[L4894] and updated for a new indication on March 28, 2019.[L5819]
Indications and Usage Certolizumab pegol has been approved for several different conditions listed below: - Symptomatic management of Chron's disease patients and for the maintenance of clinical response in patients with moderate to severe disease with inadequate response to conventional therapy. - Treatment of adult patients with moderate to severely active rheumatoid arthritis. - Treatment of adult patients with active psoriatic arthritis. - Treatment of adult patients with active ankylosing spondylitis. - Treatment of adult patients with moderate-to-severe plaque psoriasis that are candidates for systemic therapy or phototherapy.[FDA label] - Treatment of adult patients with active non-radiographic axial spondyloarthritis with objective signs of inflammation.[L5819] In Canada, certolizumab pegol is additionally approved in combination with [methotrexate] for the symptomatic treatment, including major clinical response, and for the reduction of joint damage in adult patients with moderately to severely active rheumatoid arthritis and psoriatic arthritis.[L5825] Inflammation is a biological response against a potential threat. This response can be normal but in certain conditions, the immune system can attack the body's normal cells or tissues which causes an abnormal inflammation.[L5840] TNF-alpha has been identified as a key regulator of the inflammatory response. The signaling cascades of this inflammatory mediator can produce a wide range of reactions including cell death, survival, differentiation, proliferation and migration.[A176660]
Marketing Status approved
ATC Code L04AB05
DrugBank ID DB08904
KEGG ID D03441
MeSH ID D000068582
PubChem ID Not Available
TTD Drug ID Not Available
NDC Product Code 50474-700; 49187-0228; 28877-7100; 68225-045; 28877-7300; 50474-710
UNII UMD07X179E
Synonyms Certolizumab Pegol | Cimzia | CDP870 | CDP 870
Chemical Information
Molecular Formula Not Available
CAS Registry Number 428863-50-7
SMILES Not Available
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Alopecia totalis23.02.02.006--Not Available
Anaemia01.03.02.001--
Angina pectoris24.04.04.002; 02.02.02.002--
Anxiety19.06.02.002--
Arrhythmia02.03.02.001--Not Available
Atrial fibrillation02.03.03.002--
Back pain15.03.04.005--
Blastomycosis11.03.02.001--Not Available
Bronchitis22.07.01.001; 11.01.09.001--
Cardiac failure02.05.01.001--
Cerebrovascular accident24.03.05.001; 17.08.01.007--
Coccidioidomycosis22.07.08.004; 11.03.09.001--Not Available
Dermatitis23.03.04.002--Not Available
Erythema multiforme10.01.03.015; 23.03.01.003--
Erythema nodosum23.07.02.001; 10.02.01.020--Not Available
Fatigue08.01.01.002--
Headache17.14.01.001--
Hepatitis09.01.07.004--Not Available
Histoplasmosis11.03.06.001--Not Available
Hypercoagulation01.01.02.007--Not Available
Hypertension24.08.02.001--
Hypertensive heart disease02.11.02.001; 24.08.05.002--Not Available
Injection site haemorrhage24.07.01.010; 12.07.03.005; 08.02.03.005--Not Available
Leukopenia01.02.02.001--Not Available
Listeriosis11.02.11.001--Not Available
Lymphadenopathy01.09.01.002--Not Available
Menstrual disorder21.01.01.004--Not Available
Myocardial infarction24.04.04.009; 02.02.02.007--
Myocardial ischaemia24.04.04.010; 02.02.02.008--Not Available
Nasopharyngitis22.07.03.002; 11.01.13.002--Not Available
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