Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Citalopram
Drug ID BADD_D00475
Description Citalopram belongs to a class of antidepressant agents known as selective _serotonin-reuptake inhibitors_ (SSRIs) and is widely used to treat the symptoms of depression. Its chemical structure is unrelated to that of other SSRIs or of tricyclic, tetracyclic, or other prescribed antidepressants [FDA label]. Citalopram is also known as _Celexa_, and available in tablet and solution forms [FDA label]. This drug was initially approved by the FDA in 1998 [L5230].
Indications and Usage For the treatment of depression, as indicated by the FDA label [FDA label]. Off-label indications include but are not limited to: treatment of sexual dysfunction, post-stroke behavioural changes, ethanol abuse, obsessive-compulsive disorder (OCD) in children, and diabetic neuropathy [FDA label], [A321], [A322], [A323], [A324], [A174406], [A174409], [A174412].
Marketing Status approved
ATC Code N06AB04
DrugBank ID DB00215
KEGG ID D07704
MeSH ID D015283
PubChem ID 2771
TTD Drug ID D0Y5DO
NDC Product Code 42806-020; 71335-0541; 76282-206; 80425-0093; 37662-0340; 43353-091; 54458-980; 0054-0062; 70518-2601; 63850-3616; 0456-4040; 68071-3034; 68788-7899; 70518-2228; 76282-207; 76282-629; 43353-112; 43353-208; 50090-5172; 50090-5175; 61919-390; 0378-6231; 69097-822; 69097-824; 71610-092; 37662-0341; 37662-0342; 52427-691; 65162-053; 0378-6233; 69097-823; 60429-175; 62135-540; 65162-052; 0378-6232; 70518-2553; 70518-2617; 70518-2671; 37662-0339; 37662-0343; 50090-5170; 51655-137; 60429-173; 60429-174; 61919-389; 0456-4020; 42806-021; 54458-889; 54458-981; 65162-054; 0456-4010; 76282-628; 37662-0337; 37662-0338; 42806-019; 51655-938; 71610-412; 71610-422; 76282-208; 37662-0336; 43063-063; 51655-209
UNII 0DHU5B8D6V
Synonyms Citalopram | Cytalopram | Citalopram Hydrobromide | Lu-10-171 | Lu10171 | Seropram | Celexa
Chemical Information
Molecular Formula C20H21FN2O
CAS Registry Number 59729-33-8
SMILES CN(C)CCCC1(C2=C(CO1)C=C(C=C2)C#N)C3=CC=C(C=C3)F
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)
Sinus arrest02.03.03.0070.000019%Not Available
Sinus congestion22.04.06.001--Not Available
Sinus tachycardia02.03.03.010--
Sinusitis11.01.13.005; 22.07.03.007--
Skin discolouration23.03.03.005--Not Available
Skin fissures23.03.03.008--Not Available
Sleep disorder19.02.04.0010.000048%Not Available
Somnolence19.02.05.003; 17.02.04.0060.000150%
Speech disorder22.12.03.027; 19.19.02.002; 17.02.08.0030.000019%Not Available
Sputum increased22.02.03.007--Not Available
Stomatitis07.05.06.005--
Stupor19.02.05.004; 17.02.04.007--Not Available
Sudden death08.04.01.003; 02.03.04.013--
Suicidal ideation19.12.01.0030.000207%
Suicide attempt19.12.01.0040.000095%
Supraventricular extrasystoles02.03.03.011--Not Available
Swelling08.01.03.0150.000074%Not Available
Swelling face10.01.05.018; 08.01.03.100; 23.04.01.0180.000042%Not Available
Swollen tongue23.04.01.014; 07.14.02.003; 10.01.05.0150.000065%Not Available
Syncope02.11.04.015; 24.06.02.012; 17.02.04.0080.000156%
Tachycardia02.03.02.0070.000076%Not Available
Tachypnoea22.02.01.014--Not Available
Tendon disorder12.01.07.019; 15.07.01.002--Not Available
Tension19.06.02.0050.000042%Not Available
Testicular disorder21.13.01.002--
Therapeutic response decreased08.06.01.0160.000042%Not Available
Therapeutic response unexpected08.06.01.0010.000019%Not Available
Thinking abnormal19.10.03.001; 17.02.05.0230.000019%Not Available
Thirst14.03.02.007; 08.01.09.021--Not Available
Throat irritation22.12.03.029; 07.05.05.037--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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