Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Tigecycline
Drug ID BADD_D02217
Description Tigecycline is a glycylcycline antibiotic developed and marketed by Wyeth under the brand name Tygacil. It was developed in response to the growing prevalence of antibiotic resistance in bacteria such as Staphylococcus aureus. It was granted fast-track approval by the U.S. Food and Drug Administration (FDA) on June 17, 2005.
Indications and Usage For the treatment of infections caused by susceptible strains of the designated microorganisms in the following conditions: Complicated skin and skin structure infections caused by Escherichia coli, Enterococcus faecalis (vancomycin-susceptible isolates only), Staphylococcus aureus (methicillin-susceptible and -resistant isolates), Streptococcus agalactiae, Streptococcus anginosus grp. (includes S. anginosus, S. intermedius, and S. constellatus), Streptococcus pyogenes and Bacteroides fragilis. Complicated intra-abdominal infections caused by Citrobacter freundii, Enterobacter cloacae, Escherichia coli, Klebsiella oxytoca, Klebsiella pneumoniae, Enterococcus faecalis (vancomycin-susceptible isolates only), Staphylococcus aureus (methicillin-susceptible isolates only), Streptococcus anginosus grp. (includes S. anginosus, S. intermedius, and S. constellatus), Bacteroides fragilis, Bacteroides thetaiotaomicron, Bacteroides uniformis, Bacteroides vulgatus, Clostridium perfringens, and Peptostreptococcus micros.
Marketing Status approved
ATC Code J01AA12
DrugBank ID DB00560
KEGG ID D01079
MeSH ID D000078304
PubChem ID 54686904
TTD Drug ID D0G4OD
NDC Product Code 67680-002; 63323-960; 70121-1647; 71288-019; 55150-228; 0781-3481; 0008-4990; 58623-0048; 63415-0134; 68225-013; 60505-6098; 60715-1001; 16729-364; 0008-4994; 70600-002; 44657-0055
UNII 70JE2N95KR
Synonyms Tigecycline | TBG-MINO | 9-(tert-Butylglycylamido)minocycline | Tygacil | GAR 936 | GAR-936 | GAR936
Chemical Information
Molecular Formula C29H39N5O8
CAS Registry Number 220620-09-7
SMILES CC(C)(C)NCC(=O)NC1=CC(=C2CC3CC4C(C(=O)C(=C(C4(C(=O)C3=C(C2=C1O)O)O)O)C(=O)N)N(C) C)N(C)C
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)
Ill-defined disorder08.01.03.049---
Blood disorder01.05.01.004---
Disease progression08.01.03.0380.000194%
Disease recurrence08.01.03.0500.000049%-
Drug intolerance08.06.01.0130.000437%-
Hepatobiliary disease09.01.08.003---
Renal impairment20.01.03.0100.000267%-
Increased bronchial secretion22.12.01.002---
Haemorrhagic diathesis01.01.03.003; 24.07.01.0200.000049%-
Device malfunction27.01.02.002---
Vulvovaginal mycotic infection11.03.05.004; 21.14.02.004---
Bone marrow failure01.03.03.0050.000122%
Treatment failure08.06.01.0170.000292%-
Liver injury09.01.07.022; 12.01.17.0120.000608%-
Adverse reaction08.06.01.0180.000049%-
Traumatic liver injury09.01.08.010; 12.01.17.027---
Acute kidney injury20.01.03.0160.000292%
Drug-induced liver injury09.01.07.023; 12.03.01.0440.000122%-
Candida infection11.03.03.021--
Multiple organ dysfunction syndrome08.01.03.0570.000146%
Anal incontinence07.01.06.029; 17.05.01.021--
Haemorrhagic necrotic pancreatitis07.18.01.010; 24.07.02.0470.000049%-
Drug ineffective for unapproved indication08.06.01.038; 12.09.02.0020.000146%-
Dysbiosis07.11.01.034; 12.02.05.0530.000049%-
Idiopathic intracranial hypertension17.07.02.011---
Myelosuppression01.03.03.0150.000049%-
Vulvovaginal inflammation21.14.02.014---
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ADReCS-Target
Drug Name ADR Term Target
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