Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Ustekinumab
Drug ID BADD_D02322
Description Ustekinumab is a human immunoglobulin (Ig) G1 kappa monoclonal antibody directed against interleukin(IL)-12 and IL-23, which are cytokines that are involved in immune and inflammatory responses.[A187349] It was generated via recombinant human IL-12 immunization of human Ig (hu-Ig) transgenic mice.[A187349] It is a targeted biologic disease-modifying anti-rheumatic drug (bDMARDs) that is used in the management of various inflammatory conditions that involve the activation of IL-12 and IL-23 signalling pathways.[A187346] The therapeutic use of the drug started in Canada, the US, and Europe since 2009 when it was first approved for the treatment of adult patients with moderate to severe plaque psoriasis and active psoriatic arthritis, alone or in combination with [methotrexate]. In September 2016, ustekinumab was additionally approved for the management of moderate to severe Crohn's disease in selected adult patients. In October 2019, it was also approved by the FDA for use to manage moderately to severely active ulcerative colitis in adults. Ustekinumab is currently the first and only approved biologic therapy for ulcerative colitis that targets the interleukin (IL)-12 and IL-23 cytokines.[L9392] The dosing regimen for ustekinumab is based on the patient's weight and there are intravenous and subcutaneous formulations of the drug based on the dosing schedule and condition being treated. Ustekinumab is commonly marketed under the trade name STELARA.
Indications and Usage Ustekinumab is indicated for the management of moderate to severe plaque psoriasis in children aged 6 and above, adolescents, and adults who are candidates for phototherapy or systemic therapy.[L9383,L9386] It is indicated for the management of active psoriatic arthritis in adults, alone or in combination with methotrexate.[L9383] It is indicated for the management of moderately to severely active Crohn’s disease in adults who were clinically unresponsive or intolerant to immunomodulator or corticosteroid therapy (but never failed a tutor necrosis factor (TNF) blocker) or treatment with one or more TNF blockers.[L9383] It is indicated for the management of moderately to severely active ulcerative colitis in adults.[L9386]
Marketing Status approved; investigational
ATC Code L04AC05
DrugBank ID DB05679
KEGG ID D09214
MeSH ID D000069549
PubChem ID Not Available
TTD Drug ID D0A2UV
NDC Product Code 65267-896; 57894-060; 57894-061; 57894-054
UNII FU77B4U5Z0
Synonyms Ustekinumab | Stelara | CNTO 1275 | CNTO-1275
Chemical Information
Molecular Formula Not Available
CAS Registry Number 815610-63-0
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)
Urinary tract infection20.08.02.001; 11.01.14.004--
Urticaria23.04.02.001; 10.01.06.001--
Viral infection11.05.04.001--Not Available
Viral upper respiratory tract infection22.07.02.004; 11.05.04.007--Not Available
Tooth infection11.01.04.004; 07.09.01.004--
Contusion24.07.06.001; 23.03.11.002; 12.01.06.001; 15.03.05.007--
Acute coronary syndrome02.02.02.015; 24.04.04.011--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Injection site swelling12.07.03.018; 08.02.03.017--Not Available
Haemorrhage24.07.01.002--Not Available
Induration08.01.03.020--Not Available
Connective tissue disorder10.04.04.026; 15.06.01.006--Not Available
Infestation23.11.01.002; 11.09.01.001--Not Available
Mediastinal disorder22.09.03.001--Not Available
Mental disorder19.07.01.002--Not Available
Oropharyngeal pain22.12.03.016; 07.05.05.004--
Posterior reversible encephalopathy syndrome17.13.02.007--
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