Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Gemifloxacin mesylate
Drug ID BADD_D01014
Description Gemifloxacin is a quinolone antibacterial agent with a broad-spectrum activity that is used in the treatment of acute bacterial exacerbation of chronic bronchitis and mild-to-moderate pneumonia. It is available in oral formulations. Gemifloxacin acts by inhibiting DNA synthesis through the inhibition of both DNA gyrase and topoisomerase IV, which are essential for bacterial growth.
Indications and Usage For the treatment of bacterial infection caused by susceptible strains such as S. pneumoniae, H. influenzae, H. parainfluenzae, or M. catarrhalis, S. pneumoniae (including multi-drug resistant strains [MDRSP]), M. pneumoniae, C. pneumoniae, or K. pneumoniae.
Marketing Status approved; investigational
ATC Code J01MA15
DrugBank ID DB01155
KEGG ID D02471
MeSH ID D000077735
PubChem ID 9588170
TTD Drug ID D0VR7W
NDC Product Code 68801-320; 50370-0021
UNII X4S9F8RL01
Synonyms Gemifloxacin | 7-(3-aminomethyl-4-methoxyimino-pyrrolidine-1-yl)-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-(1,8)-naphthyridine-3-carboxylic acid | Factive | Gemifloxacin Mesylate | SB-265805 | SB265805 | SB 265805 | LB 20304 | LB-20304 | LB20304
Chemical Information
Molecular Formula C19H24FN5O7S
CAS Registry Number 210353-53-0
SMILES CON=C1CN(CC1CN)C2=C(C=C3C(=O)C(=CN(C3=N2)C4CC4)C(=O)O)F.CS(=O)(=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)
Neutrophil count increased13.01.06.011--Not Available
Oedema peripheral14.05.06.011; 08.01.07.007; 02.05.04.007--
Pain08.01.08.004--
Pharyngitis22.07.03.004; 11.01.13.003; 07.05.07.004--
Photosensitivity reaction23.03.09.003--
Platelet count decreased13.01.04.001--
Pneumonia11.01.09.003; 22.07.01.003--Not Available
Protein total decreased13.09.01.004--Not Available
Pruritus23.03.12.001--
Pruritus genital23.03.12.008; 21.10.01.002--Not Available
Rash23.03.13.001--Not Available
Red blood cell count decreased13.01.05.007--Not Available
Red blood cell count increased13.01.05.008--Not Available
Renal failure20.01.03.005--Not Available
Retinal haemorrhage24.07.05.003; 06.10.01.001--Not Available
Skin exfoliation23.03.07.003--Not Available
Somnolence19.02.05.003; 17.02.04.006--
Supraventricular tachycardia02.03.03.012--
Swelling face10.01.05.018; 08.01.03.100; 23.04.01.018--Not Available
Syncope02.11.04.015; 17.02.04.008; 24.06.02.012--
Tendon rupture15.07.01.008; 12.01.07.003--Not Available
Thrombocytopenia01.08.01.002--Not Available
Thrombocytosis01.08.02.001--Not Available
Transient ischaemic attack17.08.04.001; 24.04.06.005--
Tremor17.01.06.002--
Urticaria23.04.02.001; 10.01.06.001--
Vaginal infection21.14.02.002; 11.01.10.002--
Vertigo04.04.01.003; 17.02.12.002--
Visual impairment06.02.10.013--Not Available
Vomiting07.01.07.003--
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