Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Maraviroc
Drug ID BADD_D01352
Description Maraviroc (brand-named Selzentry, or Celsentri outside the U.S.) is a chemokine receptor antagonist drug developed by the drug company Pfizer that is designed to act against HIV by interfering with the interaction between HIV and CCR5. It was originally labelled as UK-427857 during development but was assigned the Maraviroc name as it entered trials. It was approved for use by the FDA in August, 2007.
Indications and Usage For treatment-experienced adult patients infected with only CCR5-tropic HIV-1 detectable, who have evidence of viral replication and HIV-1 strains resistant to multiple antiretroviral agents.
Marketing Status approved; investigational
ATC Code J05AX09
DrugBank ID DB04835
KEGG ID D06670
MeSH ID D000077592
PubChem ID 3002977
TTD Drug ID D0NR6S
NDC Product Code 49702-260; 69037-0061; 76072-1019; 49702-235; 50090-6238; 68554-0040; 49702-233; 69037-0062; 49702-237; 50923-0414; 31722-579; 31722-580; 49702-223; 49702-224; 72865-232; 12828-0091; 72865-231
UNII MD6P741W8A
Synonyms Maraviroc | 4,4-Difluoro-N-((1S)-3-(exo-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo(3.2.1)oct-8-yl)-1-phenylpropyl)cyclohexanecarboxamide | Selzentry | UK-427,857 | UK 427,857 | UK427,857 | UK-427857 | UK 427857 | UK427857
Chemical Information
Molecular Formula C29H41F2N5O
CAS Registry Number 376348-65-1
SMILES CC1=NN=C(N1C2CC3CCC(C2)N3CCC(C4=CC=CC=C4)NC(=O)C5CCC(CC5)(F)F)C(C)C
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)
Lipoma16.18.01.001; 15.09.01.001--Not Available
Loss of consciousness17.02.04.004--Not Available
Lower respiratory tract infection22.07.01.002; 11.01.09.002--Not Available
Lymphadenopathy01.09.01.002--Not Available
Lymphoma16.20.01.001; 01.12.01.0010.000282%Not Available
Malaise08.01.01.0030.000282%
Meningitis17.06.03.001; 11.01.03.001--
Meningitis viral17.06.08.001; 11.05.04.009--Not Available
Metastases to liver16.22.02.001; 09.04.02.004--Not Available
Mucormycosis22.07.07.005; 17.06.09.003; 11.03.05.011; 07.05.07.011--Not Available
Muscle atrophy17.05.03.004; 15.05.03.003--Not Available
Myalgia15.05.02.001--
Myocardial infarction24.04.04.009; 02.02.02.0070.000282%
Myocardial ischaemia24.04.04.010; 02.02.02.008--Not Available
Myositis15.05.01.001--
Nasal congestion22.04.04.001--
Nasal inflammation22.04.04.002--Not Available
Nasopharyngitis22.07.03.002; 11.01.13.002--Not Available
Nausea07.01.07.001--
Neoplasm16.16.02.001--Not Available
Neoplasm malignant16.16.01.001--Not Available
Nervous system disorder17.02.10.001--Not Available
Neuritis17.09.03.001--Not Available
Neuropathy peripheral17.09.03.003--Not Available
Neutropenia01.02.03.004--Not Available
Neutrophil count13.01.06.046--Not Available
Non-Hodgkin's lymphoma16.35.01.001; 01.17.01.001--Not Available
Oedema14.05.06.010; 08.01.07.006--Not Available
Oesophageal candidiasis11.03.03.008; 07.19.06.001--Not Available
Oesophageal carcinoma16.13.06.001; 07.21.06.001--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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