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. Off-label indications include: treatment of mild dementia-associated agitation in nonpsychotic patients, smoking cessation, ethanol abuse, obsessive-compulsive disorder (OCD) in children, and diabetic neuropathy [FDA label].
Marketing Status Prescription
ATC Code N06AB04
DrugBank ID DB00215
KEGG ID D07704
MeSH ID D015283
PubChem ID 2771
TTD Drug ID D0Y5DO
NDC Product Code 69097-823; 42806-020; 70518-0561; 43063-385; 43353-112; 70518-2228; 65162-054; 67046-102; 71610-092; 0456-4020; 50090-5170; 69097-824; 68788-7899; 70518-2617; 43063-063; 70934-539; 65162-052; 54458-980; 69097-822; 70518-2553; 0054-0062; 52427-691; 60429-174; 67046-106; 76282-629; 61919-390; 76282-628; 50090-5172; 54458-889; 70518-2601; 70518-2671; 54458-981; 0378-6233; 71335-0541; 60429-173; 71610-412; 63850-3616; 65162-053; 0378-6231; 0456-4010; 42806-021; 76282-206; 68071-3034; 67046-101; 70518-0449; 60429-175; 70934-397; 43353-208; 50090-5175; 63629-6761; 0456-4040; 61919-389; 76282-208; 71610-422; 80425-0093; 76282-207; 0378-6232; 43353-091; 42806-019
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
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Poisoning and toxicityCytochrome P450 2D6P10635T57392Not Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Blood pressure decreased13.14.03.0020.000542%Not Available
Blood pressure diastolic13.14.03.021--Not Available
Blood pressure increased13.14.03.005--Not Available
Blood pressure systolic13.14.03.012--Not Available
Blood prolactin increased13.10.03.0020.000167%Not Available
Blood sodium decreased13.11.01.012--Not Available
Blunted affect19.04.01.0030.000208%Not Available
Body temperature increased13.15.01.001--Not Available
Bone disorder15.02.04.004--Not Available
Bone pain15.02.01.001--
Bradycardia02.03.02.0020.001916%Not Available
Bradycardia foetal18.03.02.006; 02.03.02.0180.000250%Not Available
Bradykinesia17.01.02.0040.000458%Not Available
Bradypnoea22.02.01.0020.000083%Not Available
Brain abscess17.06.07.001; 11.01.03.0030.000022%Not Available
Breast enlargement21.05.04.001--Not Available
Breast mass21.05.04.0020.000292%Not Available
Breast pain21.05.05.0030.000167%
Breast swelling21.05.05.0080.000292%Not Available
Breast tenderness21.05.05.0040.000083%Not Available
Bronchitis22.07.01.001; 11.01.09.001--
Bronchospasm22.03.01.004; 10.01.03.0120.000167%
Bruxism19.11.03.001; 07.01.06.0080.001291%Not Available
Bundle branch block02.03.01.009--Not Available
Bundle branch block left02.03.01.0070.000076%Not Available
Bundle branch block right02.03.01.0110.000167%Not Available
Burning sensation17.02.06.001; 08.01.09.0290.000500%Not Available
Bursitis15.04.01.001--Not Available
Cardiac arrest02.03.04.0010.000565%
Cardiac failure02.05.01.001--
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