Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Cefoxitin
Drug ID BADD_D00393
Description Cefoxitin is a semi-synthetic, broad-spectrum cepha antibiotic for intravenous administration. It is derived from cephamycin C, which is produced by Streptomyces lactamdurans.
Indications and Usage For the treatment of serious infections caused by susceptible strains microorganisms.
Marketing Status approved
ATC Code J01DC01
DrugBank ID DB01331
KEGG ID D02345
MeSH ID D002440
PubChem ID 441199
TTD Drug ID D02VFC
NDC Product Code 25021-111; 25021-110; 0143-9876; 44567-245; 66288-4100; 0143-9877; 44567-246; 44567-247; 0143-9878; 25021-109
UNII 6OEV9DX57Y
Synonyms Cefoxitin | MK-306 | MK 306 | MK306 | Cefoxitin Sodium | Sodium, Cefoxitin | Mefoxin | Méfoxin | Mefoxitin
Chemical Information
Molecular Formula C16H17N3O7S2
CAS Registry Number 35607-66-0
SMILES COC1(C2N(C1=O)C(=C(CS2)COC(=O)N)C(=O)O)NC(=O)CC3=CC=CS3
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)
Abdominal pain07.01.05.002--
Agranulocytosis01.02.03.001--Not Available
Alanine aminotransferase increased13.03.04.005--
Anaemia01.03.02.001--
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Anaphylactic shock24.06.02.004; 10.01.07.002--Not Available
Anaphylactoid reaction24.06.03.007; 10.01.07.003--Not Available
Angioedema22.04.02.008; 23.04.01.001; 10.01.05.009--Not Available
Aplastic anaemia01.03.03.002--Not Available
Aspartate aminotransferase increased13.03.04.011--
Azotaemia20.01.01.001--Not Available
Blood bilirubin increased13.03.04.018--
Blood creatinine increased13.13.01.004--
Blood lactate dehydrogenase increased13.04.02.002--
Body temperature increased13.15.01.001--Not Available
Cholestasis09.01.01.001--Not Available
Colitis07.08.01.001--
Dermatitis23.03.04.002--Not Available
Dermatitis exfoliative23.03.07.001; 10.01.01.004--
Diarrhoea07.02.01.001--
Dyspnoea22.02.01.004; 02.11.05.003--
Eosinophilia01.02.04.001--
Erythema23.03.06.001--Not Available
Erythema multiforme23.03.01.003; 10.01.03.015--
Flushing24.03.01.002; 23.06.05.003; 08.01.03.025--
Gastrointestinal pain07.01.05.005--
Glucose urine13.13.02.016--Not Available
Granulocytopenia01.02.03.003--Not Available
Gravitational oedema08.01.07.005; 02.05.04.014--Not Available
Haemoglobin13.01.05.018--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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