Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Vancomycin
Drug ID BADD_D02332
Description Antibacterial obtained from Streptomyces orientalis. It is a glycopeptide related to ristocetin that inhibits bacterial cell wall assembly and is toxic to kidneys and the inner ear. As of January 29 2018, CutisPharma's Firvanq is the only FDA approved vancomycin oral liquid treatment option available for the the treatment of _Clostridium difficile_ associated diarrhea and enterocolitis caused by _Staphylococcus aureus_, including methicillin-resistant strains [LP1196]. Such an oral liquid formulation is expected to make _Clostridium difficile_ associated diarrhea therapy more accessible in comparison to previously available specialty compounding products [LP1196].
Indications and Usage Additionally, a unique FDA approved oral liquid treatment is also available and indicated for the treatment of Clostridium difficile associated diarrhea and enterocolitis caused by _Staphylococcus aureus_, including methicillin-resistant strains [L1196].
Marketing Status Prescription; Discontinued
ATC Code A07AA09; J01XA01; S01AA28
DrugBank ID DB00512
KEGG ID D00212
MeSH ID D014640
PubChem ID 14969
TTD Drug ID D0B1IV
NDC Product Code 45932-0050; 65628-200; 65628-201; 70594-043; 68001-338; 70594-058; 52946-0836; 70594-056; 70594-040; 68001-339; 70594-057; 70594-041; 70594-044; 70594-042
Synonyms Vancomycin | Vancomycin Hydrochloride | Hydrochloride, Vancomycin | Vancomycin Sulfate | Sulfate, Vancomycin | Vancomycin-ratiopharm | Vancomycin Hexal | Vancomycine Dakota | AB-Vancomycin | Vanco Azupharma | Diatracin | VANCO-cell | Vanco-saar | Vancocin | Vancocin HCl | Vancomycin Lilly | Vancocine | Vancomicina Abbott | Vancomicina Chiesi | Vancomicina Combino Phar | Vancomicina Norman | Vancomycin Phosphate (1:2) | Vancomycin Phosphate (1:2), Decahydrate
Chemical Information
Molecular Formula C66H75Cl2N9O24
CAS Registry Number 1404-90-6
SMILES CC1C(C(CC(O1)OC2C(C(C(OC2OC3=C4C=C5C=C3OC6=C(C=C(C=C6)C(C(C(=O)NC(C(=O)NC5C(=O)N C7C8=CC(=C(C=C8)O)C9=C(C=C(C=C9O)O)C(NC(=O)C(C(C1=CC(=C(O4)C=C1)Cl)O)NC7=O)C(=O) O)CC(=O)N)NC(=O)C(CC(C)C)NC)O)Cl)CO)O)O)(C)N)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Flushing08.01.03.025; 24.03.01.002; 23.06.05.003--
Fungal infection11.03.05.001--Not Available
Gastrointestinal disorder07.11.01.001--Not Available
Gastrointestinal pain07.01.05.005--
Headache17.14.01.001--
Hypersensitivity10.01.03.003--
Hypokalaemia14.05.03.002--
Hypotension24.06.03.002--
Infection11.01.08.002--Not Available
Injection site inflammation12.07.03.009; 08.02.03.008--Not Available
Insomnia19.02.01.002; 17.15.03.002--
Linear IgA disease23.03.01.015; 10.04.02.006--Not Available
Muscle spasms15.05.03.004--
Nausea07.01.07.001--
Necrosis24.04.02.006; 08.03.03.001--Not Available
Nephropathy toxic20.05.03.002; 12.03.01.010--Not Available
Nervous system disorder17.02.10.001--Not Available
Neutropenia01.02.03.004--Not Available
Oedema peripheral08.01.07.007; 02.05.04.007; 14.05.06.011--
Ototoxicity12.03.01.012; 04.03.01.004--Not Available
Pain08.01.08.004--
Palpitations02.01.02.003--
Phlebitis24.05.03.001; 12.02.01.002--
Pregnancy18.08.02.004--Not Available
Pruritus23.03.12.001--
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Rash macular23.03.13.003--Not Available
Red man syndrome23.03.06.011; 10.01.01.013--Not Available
Renal failure20.01.03.005--Not Available
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