Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Olopatadine
Drug ID BADD_D01605
Description Olopatadine is a selective histamine H1 antagonist and mast cell stabilizer that works by attenuating inflammatory and allergic reactions. It is a structural analog of [doxepin], which has a minimal anti-allergic activity.[L6790] Olopatadine works by blocking the effects of histamine, which is a primary inflammatory mediator that causes inflammatory and allergic reactions. An ophthalmic solution of olopatadine was approved by the FDA and European Union for the treatment of seasonal and perennial allergic conjunctivitis in 1996 and 2002, respectively.[A1172] In comparison to other anti-allergenic ophthalmic medications, olopatadine displays a good comfort and tolerability profile since it does not cause perturbation of cell membranes.[A179809] Olopatadine is used for the symptomatic treatment of ocular itching associated with allergic conjunctivitis in ophthalmic formulations and seasonal allergic rhinitis in intranasal formulations. It is currently marketed under several brand names, including Pazeo, Patanase, and Opatanol.
Indications and Usage For the treatment of ocular itching associated with allergic conjunctivitis.
Marketing Status Prescription; Discontinued
ATC Code R01AC08; S01GX09
DrugBank ID DB00768
KEGG ID D08293
MeSH ID D000069605
PubChem ID 5281071
TTD Drug ID D05GPO
NDC Product Code Not Available
Synonyms Olopatadine Hydrochloride | Hydrochloride, Olopatadine | KW-4943A | KW 4943A | KW4943A | Olopatadine | 11-(3-(dimethylamino)propylidene)-6,11-dihydrodibenz(b,e)oxepin-2-acetic acid | KW 4679 | 4679, KW | KW-4679 | Patanol
Chemical Information
Molecular Formula C21H23NO3
CAS Registry Number 113806-05-6
SMILES CN(C)CCC=C1C2=CC=CC=C2COC3=C1C=C(C=C3)CC(=O)O
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)
Abdominal discomfort07.01.06.0010.001122%Not Available
Abdominal pain07.01.05.002--
Abnormal sensation in eye06.01.01.0010.001870%Not Available
Anaphylactic reaction24.06.03.006; 10.01.07.0010.000748%
Anosmia22.04.03.006; 17.04.04.001--
Asthenia08.01.01.001--Not Available
Back pain15.03.04.005--
Blepharospasm17.17.02.001; 06.05.01.001--Not Available
Blindness17.17.01.003; 06.02.02.0010.000748%Not Available
Body temperature increased13.15.01.001--Not Available
Cataract06.06.01.0010.000748%
Conjunctival follicles06.06.02.002--Not Available
Conjunctivitis11.01.06.012; 06.04.01.0020.000748%
Corneal abrasion12.01.04.001; 06.11.03.0010.000748%Not Available
Corneal deposits06.06.03.002--Not Available
Corneal epithelium defect06.06.03.012--Not Available
Corneal erosion06.06.03.0030.000748%Not Available
Corneal oedema06.04.02.001--Not Available
Cough22.02.03.0010.001870%
Depression19.15.01.001--
Dermatitis23.03.04.002--Not Available
Dermatitis contact10.01.01.003; 23.03.04.004; 12.03.01.040--Not Available
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Dizziness24.06.02.007; 17.02.05.003; 02.01.02.004--
Drug hypersensitivity10.01.01.001--Not Available
Dry eye06.08.02.0010.004487%
Dry mouth07.06.01.002--
Dry skin23.03.03.001--
Dysgeusia17.02.07.003; 07.14.03.0010.002991%
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