Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Nintedanib
Drug ID BADD_D02470
Description Nintedanib is a small molecule kinase inhibitor used in the treatment of pulmonary fibrosis, systemic sclerosis-associated interstitial lung disease, and non-small cell lung cancer (NSCLC).[L8453,L8459] It was first approved for use in the United States in 2014.[L8453] Within the spectrum of idiopathic pulmonary fibrosis treatment options, nintedanib is currently one of only two disease-modifying therapies available and indicated for the condition (the other being [Pirfenidone]) and as such is used as a first-line treatment following diagnosis to slow down the progressive loss of lung function.[A185237] As a chemotherapeutic agent for NSCLC, nintedanib, in combination with [Docetaxel], is reserved for patients who have tried and failed first-line chemotherapeutic options.[L8459]
Indications and Usage In the US, nintedanib is indicated for the treatment of idiopathic pulmonary fibrosis (IPF)[L8453] and to slow declining pulmonary function in patients with systemic sclerosis-associated interstitial lung disease.[L8462] In the EU, nintedanib is indicated in combination with docetaxel for the treatment of adult patients with metastatic, locally advanced, or locally recurrent non-small cell lung cancer of adenocarcinoma histology who have already tried first-line therapy.[L8459]
Marketing Status approved
ATC Code L01EX09
DrugBank ID DB09079
KEGG ID D10481
MeSH ID C530716
PubChem ID 135423438
TTD Drug ID D09HNV
NDC Product Code 55361-0020; 66499-0061; 0597-0143; 0597-0145; 51869-0040; 55361-0021
UNII G6HRD2P839
Synonyms nintedanib | Nintedanib esylate | Ofev | Vargatef | BIBF 1120 | BIBF1120 | BIBF-1120
Chemical Information
Molecular Formula C31H33N5O4
CAS Registry Number 656247-17-5
SMILES CN1CCN(CC1)CC(=O)N(C)C2=CC=C(C=C2)N=C(C3=CC=CC=C3)C4=C(NC5=C4C=CC(=C5)C(=O)OC)O
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)
Cerebral haematoma17.08.01.014; 24.07.04.0060.000168%-
Haemorrhoidal haemorrhage07.15.03.002; 24.10.02.0010.000168%
Haemorrhage24.07.01.002---
Faecaloma07.01.03.004---
Pulmonary mass22.02.07.0040.000414%-
Colitis microscopic07.08.01.0110.000112%-
Pneumatosis intestinalis07.11.01.0430.000224%-
Urine odour abnormal20.02.01.0200.000246%-
Paraesthesia oral07.05.05.035; 17.02.06.0080.000112%-
Cancer pain16.32.03.0040.000112%-
Pulseless electrical activity02.03.04.0200.000112%-
Lung neoplasm malignant16.19.02.001; 22.08.01.0010.001847%-
Intestinal haemorrhage07.12.03.005; 24.07.02.0310.000336%-
Prostate cancer16.25.01.001; 21.04.02.002---
Abdominal symptom07.01.06.0070.000246%-
Appetite disorder14.03.01.004; 19.09.01.002---
Cardiac disorder02.11.01.0030.001545%-
Feeding disorder14.03.02.003; 19.09.01.0030.000280%-
Embolism24.01.01.0090.000437%
Gastrointestinal motility disorder07.02.03.0010.000358%-
Infarction24.04.02.0170.000112%-
Inflammation08.01.05.007; 10.02.01.0890.000336%-
Jaw disorder15.02.04.009---
Malnutrition14.03.02.0040.000224%-
Decreased appetite08.01.09.028; 14.03.01.0050.018737%
Ill-defined disorder08.01.03.0490.000504%-
Lip and/or oral cavity cancer07.21.07.001; 16.13.07.0010.000168%-
Ulcer haemorrhage08.03.06.003; 24.07.01.0400.000168%-
Blood disorder01.05.01.0040.000112%-
Adverse drug reaction08.06.01.009---
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