Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Efavirenz
Drug ID BADD_D00749
Description Efavirenz (brand names Sustiva® and Stocrin®) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) and is used as part of highly active antiretroviral therapy (HAART) for the treatment of a human immunodeficiency virus (HIV) type 1. For HIV infection that has not previously been treated, efavirenz and lamivudine in combination with zidovudine or tenofovir is the preferred NNRTI-based regimen. Efavirenz is also used in combination with other antiretroviral agents as part of an expanded postexposure prophylaxis regimen to prevent HIV transmission for those exposed to materials associated with a high risk for HIV transmission.
Indications and Usage For use in combination treatment of HIV infection (AIDS)
Marketing Status approved; investigational
ATC Code J05AG03
DrugBank ID DB00625
KEGG ID D00896
MeSH ID C098320
PubChem ID 64139
TTD Drug ID D07HVY
NDC Product Code 48087-0127; 65862-105; 68554-0018; 65862-049; 69097-301; 72865-172; 70966-0025; 31722-504; 48087-0131; 65015-641; 67835-0001; 12783-0510; 65862-324; 65862-106; 65862-267; 69988-0008; 0056-0474; 53104-7544; 65675-1584; 68554-0042; 42543-889; 64380-889; 65862-104; 70518-3258; 64980-406; 48087-0062; 65015-868; 76302-021; 51407-382; 64980-407; 70518-2962; 48087-0128; 64220-195; 65015-859; 70366-002; 0056-0470; 65015-836
UNII JE6H2O27P8
Synonyms efavirenz | (s)-6-chloro-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one | efavirenz, (S)-isomer | efavirenz, (R)-isomer | Stocrin | Sustiva | DMP 266 | DMP-266 | L 743726 | L-743726 | L 743,726 | L-743,726
Chemical Information
Molecular Formula C14H9ClF3NO2
CAS Registry Number 154598-52-4
SMILES C1CC1C#CC2(C3=C(C=CC(=C3)Cl)NC(=O)O2)C(F)(F)F
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)
Blindness06.02.10.003; 17.17.01.0030.005505%-
Blister12.01.06.002; 23.03.01.001---
Blood bilirubin increased13.03.04.018--
Blood cholesterol13.12.01.014---
Blood cholesterol increased13.12.01.002--
Blood creatinine increased13.13.01.004--
Blood glucose increased13.02.02.002---
Blood triglycerides increased13.12.03.001---
Body temperature increased13.15.01.001---
Bone pain15.02.01.001--
Breast enlargement21.05.04.001---
Cachexia08.01.01.009; 14.03.02.001; 16.32.03.011---
Cardiac failure congestive02.05.01.002---
Cardiovascular disorder02.11.01.010; 24.03.02.0090.003670%-
Cerebellar syndrome17.02.02.0020.003670%-
Chest pain02.02.02.011; 08.01.08.002; 22.12.02.003---
Cholestasis09.01.01.0010.003670%-
Chronic hepatitis09.01.07.021; 11.07.01.0090.003670%-
Chronic lymphocytic leukaemia01.10.06.001; 16.01.06.0010.003670%-
Cleft palate03.04.02.001; 07.05.08.001---
Completed suicide08.04.01.010; 19.12.01.001---
Confusional state17.02.03.005; 19.13.01.001--
Constipation07.02.02.001--
Coordination abnormal17.02.02.004---
Coronary artery disease02.02.01.001; 24.04.04.0060.009175%-
Cough22.02.03.001--
Death08.04.01.0010.163321%
Death neonatal08.04.01.002; 18.04.01.0020.003670%
Delirium19.13.02.001--
Delusion19.10.01.001--
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ADReCS-Target
Drug Name ADR Term Target
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