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)
Arthritis15.01.01.0010.001007%
Ascites09.01.05.003; 07.07.01.001; 02.05.04.002--
Aspiration22.02.07.0070.000280%
Asthenia08.01.01.0010.007634%Not Available
Atrial fibrillation02.03.03.0020.002026%
Atrioventricular block02.03.01.0020.000246%Not Available
Back disorder15.03.05.003--Not Available
Back pain15.03.04.005--
Bladder cancer20.03.04.001; 16.08.01.001--Not Available
Blindness17.17.01.003; 06.02.10.003--Not Available
Blindness transient06.02.10.006; 17.17.01.0040.000112%Not Available
Blood pressure fluctuation24.06.01.0020.000302%Not Available
Bone pain15.02.01.001--
Bronchiectasis22.03.02.0050.000112%Not Available
Bronchitis chronic22.03.01.0190.000302%Not Available
Burning sensation17.02.06.001; 08.01.09.029--Not Available
Cachexia16.32.03.011; 14.03.02.001; 08.01.01.0090.000168%Not Available
Cardiac arrest02.03.04.0010.001175%
Cardiac failure02.05.01.0010.002239%
Cardiac failure congestive02.05.01.0020.001231%Not Available
Cardio-respiratory arrest02.03.04.002; 22.02.06.0070.000839%Not Available
Cardiogenic shock24.06.02.006; 02.05.01.0030.000224%Not Available
Cardiomegaly02.04.02.0010.000112%Not Available
Cardiomyopathy02.04.01.0010.000560%Not Available
Cardiovascular disorder02.11.01.010; 24.03.02.0090.000224%Not Available
Carotid artery stenosis17.08.02.001; 24.04.06.0010.000112%Not Available
Cataract06.06.01.001--
Cerebral haemorrhage24.07.04.001; 17.08.01.0030.001007%Not Available
Cerebral infarction24.04.06.002; 17.08.01.0040.001063%Not Available
Cerebrovascular accident17.08.01.007; 24.03.05.0010.003358%
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