Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Cefpodoxime proxetil
Drug ID BADD_D00396
Description Cefpodoxime is an oral third generation cephalosporin antibiotic with effectiveness against most Gram positive and Gram negative bacteria. Commonly used to treat acute otitis media, pharyngitis, and sinusitis, cefpodoxime proxetil is a prodrug which is absorbed and de-esterified by the intestinal mucosa to Cefpodoxime.
Indications and Usage For the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms.
Marketing Status Prescription; Discontinued
ATC Code J01DD13
DrugBank ID DB01416
KEGG ID D00920
MeSH ID C053267
PubChem ID 6321414
TTD Drug ID Not Available
NDC Product Code 61788-5000; 65862-095; 16714-403; 16714-394; 69043-006; 65862-381; 16714-402; 65862-140; 69043-007; 65862-096; 0781-5439; 64980-403; 16714-395; 65862-141; 55289-393; 0781-5438; 63785-112; 64980-402; 57297-100
Synonyms cefpodoxime proxetil | 1-(isopropoxycarbonyloxy)ethyl-7-(2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetamido)-3-methoxymethyl-8-oxo-5-thia-1-azabicyclo(4,2,0)-oct-2-ene-2-carboxylate | Vantin | U 76252 | U-76,252 | cephalosporin 807 | CS 807 | CS-807 | Doxef
Chemical Information
Molecular Formula C21H27N5O9S2
CAS Registry Number 87239-81-4
SMILES CC(C)OC(=O)OC(C)OC(=O)C1=C(CSC2N1C(=O)C2NC(=O)C(=NOC)C3=CSC(=N3)N)COC
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)
Abdominal pain07.01.05.002--
Abortion spontaneous18.01.04.001--Not Available
Acne23.02.01.001--Not Available
Activated partial thromboplastin time prolonged13.01.02.001--
Agranulocytosis01.02.03.001--Not Available
Alanine aminotransferase increased13.03.01.003--
Anaphylactic shock10.01.07.002; 24.06.02.004--Not Available
Aplastic anaemia01.03.03.002--Not Available
Asthenia08.01.01.001--Not Available
Basophilia01.02.01.009--Not Available
Blepharitis23.03.04.012; 06.04.04.001--Not Available
Blood bilirubin increased13.03.01.008--
Blood creatine increased13.13.01.001--Not Available
Blood lactate dehydrogenase increased13.04.02.002--
Blood urea increased13.13.01.006--Not Available
Cholestasis09.01.01.001--Not Available
Colitis ulcerative10.02.01.004; 07.08.01.005--Not Available
Coombs direct test positive13.01.01.001--Not Available
Dermatitis diaper23.03.04.005--Not Available
Dermatitis exfoliative10.01.01.004; 23.03.07.001--
Diarrhoea07.02.01.001--
Diarrhoea haemorrhagic24.07.02.004; 07.02.01.002--Not Available
Dry mouth07.06.01.002--
Dysgeusia17.02.07.003; 07.14.03.001--
Eosinophilia01.02.04.001--
Epistaxis24.07.01.005; 22.04.03.001--
Erythema multiforme23.03.01.003; 10.01.03.015--
Fungal infection11.03.05.001--Not Available
Fungal skin infection23.09.02.001; 11.03.05.002--Not Available
Gamma-glutamyltransferase increased13.03.01.011--
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