Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Tetracycline hydrochloride
Drug ID BADD_D02181
Description Tetracycline is a broad spectrum polyketide antibiotic produced by the Streptomyces genus of Actinobacteria. It exerts a bacteriostatic effect on bacteria by binding reversible to the bacterial 30S ribosomal subunit and blocking incoming aminoacyl tRNA from binding to the ribosome acceptor site. It also binds to some extent to the bacterial 50S ribosomal subunit and may alter the cytoplasmic membrane causing intracellular components to leak from bacterial cells.
Indications and Usage Used to treat bacterial infections such as Rocky Mountain spotted fever, typhus fever, tick fevers, Q fever, rickettsialpox and Brill-Zinsser disease. May be used to treat infections caused by Chlamydiae spp., B. burgdorferi (Lyme disease), and upper respiratory infections caused by typical (S. pneumoniae, H. influenzae, and M. catarrhalis) and atypical organisms (C. pneumoniae, M. pneumoniae, L. pneumophila). May also be used to treat acne. Tetracycline may be an alternative drug for people who are allergic to penicillin.
Marketing Status Discontinued; Prescription
ATC Code A01AB13; D06AA04; J01AA07; S01AA09; S02AA08; S03AA02
DrugBank ID DB00759
KEGG ID D02122
MeSH ID D013752
PubChem ID 54704426
TTD Drug ID D08NQZ
NDC Product Code 79218-002; 17158-0100; 49884-732; 0395-8128; 72053-002; 69006-012; 67630-0007; 51552-0463; 38779-0053; 23155-767; 71262-002; 71491-100; 69238-1523; 81489-002; 0591-2475; 51991-906; 59566-0350; 69006-002; 69006-005; 64380-890; 79790-000; 79790-001; 69006-011; 62135-225; 72053-000; 51991-907; 62135-266; 49884-733; 23155-017; 0591-2474; 64380-891; 62991-2941; 42291-799; 81489-001; 23155-766; 23155-018; 71262-003; 42291-798; 72891-0430; 69238-1522; 79218-000
Synonyms Tetracycline | Tetrabid | 4-Epitetracycline | 4 Epitetracycline | Topicycline | Achromycin V | Hostacyclin | Tetracycline Hydrochloride | Tetracycline Monohydrochloride | Sustamycin | Achromycin
Chemical Information
Molecular Formula C22H24N2O8.HCl
CAS Registry Number 64-75-5
SMILES CC1(C2CC3C(C(=O)C(=C(C3(C(=O)C2=C(C4=C1C=CC=C4O)O)O)O)C(=O)N)N(C)C)O.Cl
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)
Rash erythematous23.03.06.003--Not Available
Rash maculo-papular23.03.13.004--
Serum sickness-like reaction10.01.03.005; 08.01.03.003--Not Available
Systemic lupus erythematosus23.03.02.006; 15.06.02.003; 10.04.03.004--Not Available
Thrombocytopenia01.08.01.002--Not Available
Thrombocytopenic purpura23.06.01.007; 01.08.01.003--Not Available
Tongue discolouration07.14.02.006--Not Available
Tooth discolouration07.09.02.001--
Tooth hypoplasia07.09.08.003; 03.04.01.002--Not Available
Urticaria23.04.02.001; 10.01.06.001--
Vomiting07.01.07.003--
Necrotising colitis07.08.01.013--Not Available
Epigastric discomfort07.01.02.004--Not Available
Inflammation08.01.05.007--Not Available
Decreased appetite14.03.01.005; 08.01.09.028--
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