Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Cephalexin
Drug ID BADD_D00412
Description Cephalexin is the first of the first generation cephalosporins.[A179071,A179074] This antibiotic contains a beta lactam and a dihydrothiazide.[A179071] Cephalexin is used to treat a number of susceptible bacterial infections through inhibition of cell wall synthesis.[A179083,Label] Cephalexin was approved by the FDA on 4 January 1971.[L6547]
Indications and Usage Cephalexin is indicated for the treatment of certain infections caused by susceptible bacteria.[Label,L6550,L6553] These infections include respiratory tract infections, otitis media, skin and skin structure infections, bone infections, and genitourinary tract infections.[Label,L6550,L6553]
Marketing Status approved; investigational; vet_approved
ATC Code J01DB01
DrugBank ID DB00567
KEGG ID D00263; D00906
MeSH ID D002506
PubChem ID 27447
TTD Drug ID D0Z5EM
NDC Product Code 80425-0006; 43063-536; 43063-678; 50268-152; 53002-2182; 53002-2260; 55289-057; 62250-801; 63629-9206; 67877-545; 68071-2249; 68071-4429; 70518-3066; 70934-040; 72789-251; 80425-0005; 0093-2238; 0093-3145; 0093-3147; 50090-0219; 53002-2181; 63629-8184; 63629-8858; 63629-9207; 68071-2889; 68071-4434; 68071-4516; 68788-7796; 70518-3362; 70518-3378; 72789-252; 76420-034; 42708-017; 42708-145; 50090-3199; 62135-480; 62250-802; 63187-046; 63629-7742; 63629-8854; 63629-9436; 65862-018; 67877-254; 69043-008; 70518-3059; 63629-4222; 67877-255; 68071-4355; 68788-9713; 70518-3448; 80425-0121; 65862-338; 43063-497; 53002-2540; 62135-481; 63629-8855; 63629-8857; 63629-9198; 63629-9199; 63629-9201; 68180-440; 68180-441; 68788-7761; 68788-9539; 71205-553; 76420-287; 76420-288; 80425-0004; 0093-2240; 0093-4177; 0143-9769; 0143-9770; 50268-151; 60687-152; 63187-205; 63629-8856; 63629-9435; 67877-219; 67877-220; 68071-2246; 68788-7938; 70518-2273; 82982-024; 24979-155; 42291-209; 42582-211; 42582-212; 43063-634; 50090-3427; 62135-711; 63629-7927; 63629-9202; 63629-9205; 67877-544; 68071-4465; 72162-1833; 42708-070; 50090-0220; 53002-2180; 60687-163; 61919-606; 62135-710; 63629-7739; 63629-9203; 65862-019; 68071-4406; 68071-5038; 68071-5241; 68180-121; 68788-7529; 68788-9326; 69043-009; 42708-100; 50090-2749; 55289-058; 63629-7743; 63629-9200; 67296-0246; 68180-122; 70518-3595; 76420-035; 59651-230; 0093-4175; 24979-154; 42291-208; 50090-3202; 50090-3252; 50090-6445; 63629-7740; 63629-9204; 68071-2726; 68071-2940; 68788-9538; 69778-930; 69778-931; 71205-591; 71205-672; 72287-310; 76420-052; 45865-428; 50090-4795
UNII OBN7UDS42Y
Synonyms Cephalexin | Cefalexin | Cephalexin Hydrochloride | Cephalexin Monohydrochloride, Monohydrate | Cephalexin, (6R-(6alpha,7alpha(R*)))-Isomer | Cephalexin, (6R-(6alpha,7beta(S*)))-Isomer | Cephalexin, (6R-(6alpha,7beta))-Isomer | Cephalexin, Monosodium Salt | Cephalexin Monohydrochloride | Ceporexine | Palitrex | Cephalexin Monohydrate | Cephalexin Dihydride | Cephalexin Hemihydrate | 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-((aminophenylacetyl)amino)-3-methyl-8-oxo-, (6R-(6alpha,7beta(R*)))- | Cephalexin, Monosodium Salt, (6R-(6alpha,7beta))-Isomer
Chemical Information
Molecular Formula C16H17N3O4S
CAS Registry Number 15686-71-2
SMILES CC1=C(N2C(C(C2=O)NC(=O)C(C3=CC=CC=C3)N)SC1)C(=O)O
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)
Chills08.01.09.001; 15.05.03.0160.000089%
Cholecystitis acute09.03.01.0030.000017%Not Available
Cholestasis09.01.01.0010.000026%Not Available
Colitis07.08.01.0010.000026%
Confusional state19.13.01.001; 17.02.03.005--
Crying19.04.02.002; 17.02.05.013; 12.02.11.001; 08.01.03.005--Not Available
Deafness04.02.01.001--Not Available
Dehydration14.05.05.0010.000046%
Depressed level of consciousness17.02.04.0020.000017%
Dermatitis23.03.04.002--Not Available
Dermatitis bullous23.03.01.0020.000017%
Diarrhoea07.02.01.0010.000359%
Dizziness02.11.04.006; 24.06.02.007; 17.02.05.003--
Drug eruption23.03.05.001; 10.01.01.005; 08.01.06.0150.000072%Not Available
Drug hypersensitivity10.01.01.0010.000676%Not Available
Dysarthria19.19.03.001; 17.02.08.0010.000017%
Dyspepsia07.01.02.001--
Dysphagia07.01.06.0030.000105%
Dyspnoea02.11.05.003; 22.02.01.0040.000203%
Ear pain04.03.01.003--
Eczema23.03.04.0060.000017%
Encephalopathy17.13.02.0010.000017%
Eosinophilia01.02.04.0010.000017%
Erythema23.03.06.0010.000316%Not Available
Erythema multiforme23.03.01.003; 10.01.03.0150.000093%
Face oedema23.04.01.004; 10.01.05.002; 08.01.07.0030.000046%
Faeces discoloured07.01.03.002--Not Available
Fatigue08.01.01.002--
Febrile neutropenia08.05.02.004; 01.02.03.0020.000017%
Feeling abnormal08.01.09.014--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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