Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Etravirine
Drug ID BADD_D00857
Description Etravirine is an antiretroviral agent more specifically classified as a Non-Nucleoside Reverse Transcriptase Inhibitor(NNRTI). Etraverine is used clinically for the treatment of human immunodeficiency virus type 1 (HIV-1) infection. On January 18, 2007, the FDA granted accelerated approved for the use of etravirine 100mg tablets in the treatment of adult HIV-1 infection documented to be resistant to therapy with other NNRTIs and antiretroviral agents. On March 26, 2012, approval was extended for use in treatment-experienced pediatric patients 6 to 18 years of age, weighing at least 16 kg. Etravarine must always be used in combination with other antiretroviral drugs. Etravirine exerts its effects via direct inhibition of the reverse transcriptase enzyme of human immunodeficiency virus type 1 (HIV-1), and consequently blocks DNA-dependent and RNA-dependent polymerase activity. Etravirine does not inhibit human DNA polymerase alpha, beta or gamma. Common side effects of use include mild to moderate rash within the first 6 weeks of therapy, nausea, diarrhea and peripheral neuropathy. Patients are advised to immediately contact their healthcare provider if a rash develops. In 2009, postmarketing case reports of Stevens-Johnson Syndrome, toxic epidermal necrolysis, erythema multiforme, and other hypersensitivity reactions lead to a revision of etravirine's "Warnings and Precautions," as well as notification of health care providers. In 2013, reports of Autoimmune disorders (such as Graves’ disease, polymyositis, and Guillain-Barré syndrome) in the setting of immune reconstitution, as well as more in depth information about the development of rashes in patients taking etravirine, lead to a modification of etravirine's monograph.
Indications and Usage Indicated as an adjunct therapy in the treatment of adult HIV-1 infections resistant to therapy with other NNRTIs and antiretroviral agents.
Marketing Status approved
ATC Code J05AG04
DrugBank ID DB06414
KEGG ID D04112
MeSH ID C451734
PubChem ID 193962
TTD Drug ID D0BP9C
NDC Product Code 68554-0137; 69766-001; 42291-474; 60219-1720; 65015-856; 52493-200; 68554-0056; 60219-1721; 69238-1722; 80005-113; 59676-572; 59676-570; 59676-571; 60219-1722; 69315-285; 69315-286; 69238-1721; 42291-473; 69238-1720; 80005-112
UNII 0C50HW4FO1
Synonyms etravirine | benzonitrile, 4-((6-amino-5-bromo-2-((4-cyanophenyl)amino)-4-pyrimidinyl)oxy)-3,5-dimethyl- | 4-((6-amino-5-bromo-2-((4-cyanophenyl)amino)-4-pyrimidinyl)oxy)-3,5-dimethyl-benzonitrile | Intelence | R165335 | TMC 125 | TMC125 cpd | TMC-125
Chemical Information
Molecular Formula C20H15BrN6O
CAS Registry Number 269055-15-4
SMILES CC1=CC(=CC(=C1OC2=NC(=NC(=C2Br)N)NC3=CC=C(C=C3)C#N)C)C#N
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)
Haemoglobin decreased13.01.05.003--Not Available
Haemolytic anaemia01.06.03.002--Not Available
Haemorrhagic stroke17.08.01.011; 24.07.04.014--Not Available
Headache17.14.01.0010.119928%
Hemiparesis17.01.04.0010.019660%
Hepatic failure09.01.03.002--
Hepatic steatosis14.08.04.005; 09.01.07.003--Not Available
Hepatitis09.01.07.004--Not Available
Hepatitis B09.01.09.003; 11.05.28.003--
Hepatitis C11.05.28.004; 09.01.09.005--Not Available
Hepatomegaly09.01.05.001--Not Available
Hypercholesterolaemia14.08.01.001--Not Available
Hyperglycaemia14.06.02.002; 05.06.02.002--
Hyperhidrosis08.01.03.028; 23.02.03.004--
Hypersensitivity10.01.03.003--
Hypersomnia19.02.05.001; 17.15.01.001--
Hypertension24.08.02.0010.029490%
Hypertriglyceridaemia14.08.02.001--
Hypoaesthesia17.02.06.023; 23.03.03.081--Not Available
Immune system disorder10.02.01.001--Not Available
Infection11.01.08.002--Not Available
Insomnia19.02.01.002; 17.15.03.0020.066845%
Lipase increased13.05.01.003--
Loss of consciousness17.02.04.004--Not Available
Low density lipoprotein13.12.01.011--Not Available
Malaise08.01.01.003--
Myalgia15.05.02.0010.019660%
Myocardial infarction24.04.04.009; 02.02.02.0070.019660%
Nausea07.01.07.0010.086505%
Neoplasm malignant16.16.01.0010.019660%Not Available
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