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)
Vasculitis10.02.02.006; 24.12.04.027--
Venous thrombosis24.01.01.008---
Viral infection11.05.04.001---
Visual field defect06.02.07.003; 17.17.01.001---
Vomiting07.01.07.003--
Sinobronchitis11.01.13.022; 22.07.03.025---
Lipodystrophy acquired14.08.04.008; 23.07.01.003---
Lipase13.05.01.011---
Deep vein thrombosis24.01.02.0030.000621%-
Cardiopulmonary failure02.05.01.004; 22.02.06.0040.000565%-
Acute coronary syndrome02.02.02.015; 24.04.04.011---
Metastases to peritoneum07.21.03.003; 16.22.02.008---
Gastrointestinal hypomotility07.02.02.005---
Lymphatic disorder01.09.01.003---
Paranasal sinus discomfort22.12.03.018---
Protein urine present13.13.02.006---
Musculoskeletal discomfort15.03.04.001---
Type IV hypersensitivity reaction10.01.03.022---
Transaminases increased13.03.04.036---
Bone cancer metastatic15.09.03.004; 16.29.02.001---
Hepatic cancer metastatic09.04.02.006; 16.07.02.002---
Varices oesophageal07.15.05.001; 09.01.06.009; 24.10.02.004---
Angiopathy24.03.02.007---
Anogenital warts07.19.04.002; 11.05.07.002; 16.26.01.003; 21.10.03.004; 23.10.01.003---
Blood alkaline phosphatase increased13.04.02.004--
Drug resistance08.06.01.0050.001694%-
Urine output increased13.13.03.002---
Tinea infection11.03.08.002; 23.11.03.011---
Abdominal neoplasm07.21.04.001; 16.16.02.002---
Adverse event08.06.01.0100.000565%-
The 8th Page    First    Pre   8 9 10    Next   Last    Total 10 Pages
ADReCS-Target
Drug Name ADR Term Target
Tip:  Drug Name  ADR Term  Protein  Variation  Gene