Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Lodoxamide
Drug ID BADD_D01307
Description Lodoxamide is a mast-cell stabilizer for topical administration into the eye. Mast-cell stabilizers, first one approved being cromolyn sodium, are used in treatment of ocular hypersensitivity reactions such as vernal conjunctivitis. These conditions often require treatment with anti-inflammatory medications such as ophthalmic NSAIDs or topical steroids which may cause systemic or toxic effects long-term. Although less effective than topical steroids at decreasing inflammation, mast-cell stabilizers offer another treatment option and exhibit minimal adverse effects. Lodoxamide is marketed under the brand name Alomide by Alcon.
Indications and Usage Indicated in the treatment of the ocular disorders referred to by the terms vernal keratoconjunctivitis, vernal conjunctivitis, and vernal keratitis.
Marketing Status approved
ATC Code S01GX05
DrugBank ID DB06794
KEGG ID D08139
MeSH ID C021702
PubChem ID 44564
TTD Drug ID D0OG3K
NDC Product Code 58567-102
UNII SPU695OD73
Synonyms lodoxamide ethyl | diethyl N,N'-(2-chloro-5-cyano-m-phenylene)dioxamate | U-42,718 | lodoxamide
Chemical Information
Molecular Formula C11H6ClN3O6
CAS Registry Number 53882-12-5
SMILES C1=C(C=C(C(=C1NC(=O)C(=O)O)Cl)NC(=O)C(=O)O)C#N
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)
Abdominal discomfort07.01.06.001--Not Available
Asthenia08.01.01.001--Not Available
Blepharitis23.03.04.012; 06.04.04.001--Not Available
Conjunctival oedema06.04.01.001--Not Available
Corneal abrasion12.01.04.001; 06.11.03.001--Not Available
Corneal erosion06.06.03.003--Not Available
Dermatitis23.03.04.002--Not Available
Discomfort08.01.08.003--Not Available
Dizziness02.11.04.006; 24.06.02.007; 17.02.05.003--
Dry eye06.08.02.001--
Eye pain06.08.03.002--
Fatigue08.01.01.002--
Feeling hot08.01.09.009--Not Available
Headache17.14.01.001--
Hyperaemia24.03.02.002--Not Available
Hypersensitivity10.01.03.003--
Keratopathy06.06.03.007--Not Available
Lacrimation increased06.08.02.004--
Nasal dryness22.04.03.002--Not Available
Nausea07.01.07.001--
Oedema14.05.06.010; 08.01.07.006--Not Available
Pain08.01.08.004--
Pruritus23.03.12.001--
Rash23.03.13.001--Not Available
Sneezing22.12.03.024--
Somnolence19.02.05.003; 17.02.04.006--
Swelling08.01.03.015--Not Available
Ulcer08.03.06.001--Not Available
Vision blurred17.17.01.010; 06.02.06.007--
Eye pruritus06.04.05.006--Not Available
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