Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Tofacitinib
Drug ID BADD_D02236
Description Tofacitinib is an inhibitor of Janus kinases, a group of intracellular enzymes involved in signalling pathways that affect hematopoiesis and immune cell function. It is approved by the FDA for treatment of moderate to severe rheumatoid arthritis that responds inadequately to methotrexate or in those who are intolerant to methotrexate. Besides rheumatoid arthritis, tofacitinib has also been studied in clinical trials for the prevention of organ transplant rejection, and is currently under investigation for the treatment of psoriasis. Known adverse effects include nausea and headache as well as more serious immunologic and hematological adverse effects. Tofacitinib is marketed under the brand name Xeljanz by Pfizer.
Indications and Usage It is not to be initiated in patients with a history of chronic or recurrent infections, or in the presence of active infection, even if localized, due to reports of serious and sometimes fatal infections (commonly pneumonia, herpes zoster and urinary tract infections). Use of tofacitinib is also discouraged in those who have been, or are likely to be, exposed to TB. An increased likelihood of exposure may be encountered by traveling to certain areas. In addition, tofacitinib is not to be used in patients with severe hepatic impairment, or low hemoglobin (less than 9g/dL). Cautioned is advised when using tofacitinib in patients at risk of gastrointestinal perforation, and in the elderly who are more susceptible to infection.
Marketing Status Prescription
ATC Code L04AA29
DrugBank ID DB08895
KEGG ID D09970
MeSH ID C479163
PubChem ID 9926791
TTD Drug ID D0EG1I
NDC Product Code 63539-012; 63539-016; 63539-502; 63539-501; 0069-1029; 0069-1002; 0069-1001; 0069-0502; 0069-0501
Synonyms tofacitinib | tasocitinib | tofacitinib citrate | Xeljanz | CP 690,550 | CP690550 | CP-690550 | CP 690550 | CP-690,550
Chemical Information
Molecular Formula C16H20N6O
CAS Registry Number 477600-75-2
SMILES CC1CCN(CC1N(C)C2=NC=NC3=C2C=CN3)C(=O)CC#N
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Decreased immune responsiveness10.02.01.0410.006948%Not Available
Decreased interest19.15.02.0040.002316%Not Available
Decubitus ulcer23.03.11.006--Not Available
Defaecation urgency07.02.04.0010.004053%Not Available
Dehydration14.05.05.001--
Delirium19.13.02.001--
Dementia19.20.02.001; 17.03.01.001--Not Available
Dementia Alzheimer's type19.20.03.001; 17.03.06.001--Not Available
Demyelination17.16.02.0010.004632%Not Available
Dental caries07.09.01.001--
Depressed level of consciousness17.02.04.002--
Depressed mood19.15.02.0010.034739%Not Available
Depression19.15.01.0010.134326%
Dermal cyst23.10.02.001; 16.26.02.0010.001737%Not Available
Dermatitis23.03.04.0020.007527%Not Available
Dermatitis acneiform23.02.01.0040.004053%
Dermatitis allergic10.01.03.014; 23.03.04.003--Not Available
Dermatitis bullous23.03.01.002--
Dermatitis contact23.03.04.004; 12.03.01.040; 10.01.01.003--Not Available
Dermatomyositis23.03.02.001; 15.05.01.002; 10.04.02.0010.002316%Not Available
Diabetes mellitus05.06.01.001; 14.06.01.001--Not Available
Diabetes mellitus inadequate control14.06.01.004; 05.06.01.004--Not Available
Diarrhoea07.02.01.0010.436560%
Diarrhoea haemorrhagic24.07.02.004; 07.02.01.0020.005211%Not Available
Diplopia06.02.06.002; 17.17.01.005--Not Available
Discomfort08.01.08.0030.027792%Not Available
Disorientation19.13.01.002; 17.02.05.015--Not Available
Disseminated intravascular coagulation01.01.02.002; 24.01.01.010--
Disseminated tuberculosis11.04.01.001--Not Available
Disturbance in attention19.21.02.002; 17.03.03.001--
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