Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Cimetidine
Drug ID BADD_D00467
Description A histamine congener, it competitively inhibits histamine binding to histamine H2 receptors. Cimetidine has a range of pharmacological actions. It inhibits gastric acid secretion, as well as pepsin and gastrins output. It also blocks the activity of cytochrome P-450 which might explain proposals for use in neoadjuvant therapy.
Indications and Usage Cimetidine is indicated to reduce gastric acid secretion and to treat the following disease states: duodenal ulcers, non-malignant gastric ulcers, gastroesophageal reflux disease, and pathological hypersecretion associated with Zollinger-Ellison Syndrome, systemic mastocytosis, and multiple endocrine adenomas.[L30280] It is indicated for prophylaxis of recurrent gastric or duodenal ulcers, as adjunctive therapy in the management of cystic fibrosis in children, and to treat NSAID induced lesions and gastrointestinal symptoms.[L30280]
Marketing Status approved; investigational
ATC Code Not Available
DrugBank ID DB00501
KEGG ID D00295
MeSH ID D002927
PubChem ID 2756
TTD Drug ID D02DPA
NDC Product Code 49964-0006; 0113-0022; 63029-222; 63187-333; 69256-022; 50090-0500; 0378-0372; 38779-0325; 0093-8192; 50090-3574; 59640-022; 0378-0053; 70934-931; 72288-022; 51927-0190; 24385-111; 0363-0022; 0378-0317; 0378-0541; 59779-022; 63029-223; 0093-8204; 51552-0531; 71052-456; 0093-8305; 49452-2063; 49711-0095; 62991-1456; 49035-820; 49348-246; 51655-697; 52183-223; 53002-3280; 70518-2809; 55289-581
UNII 80061L1WGD
Synonyms Cimetidine | N-Cyano-N'-methyl-N''-(2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)guanidine | Biomet | Biomet400 | Cimetidine Hydrochloride | Hydrochloride, Cimetidine | Cimetidine HCl | HCl, Cimetidine | Histodil | SK&F-92334 | SK&F 92334 | SK&F92334 | SKF-92334 | SKF 92334 | SKF92334 | Tagamet | Altramet | Eureceptor
Chemical Information
Molecular Formula C10H16N6S
CAS Registry Number 51481-61-9
SMILES CC1=C(N=CN1)CSCCNC(=NC)NC#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)
White blood cell count decreased13.01.06.012--
Tubulointerstitial nephritis20.05.02.002--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Skin burning sensation23.03.03.021; 17.02.06.009--Not Available
Transaminases increased13.03.04.036--Not Available
Mental disorder due to a general medical condition19.07.03.005--Not Available
Decreased appetite14.03.01.005; 08.01.09.028--
Erectile dysfunction21.03.01.007; 19.08.04.001--
Immunodeficiency10.03.02.002--Not Available
Psychotic disorder19.03.01.002--
Renal impairment20.01.03.010--Not Available
Bone marrow failure01.03.03.005--
Mixed liver injury09.01.07.015--Not Available
Liver injury12.01.17.012; 09.01.07.022--Not Available
Cholestatic liver injury09.01.07.016--Not Available
Traumatic liver injury12.01.17.027; 09.01.08.010--Not Available
Autoimmune haemolytic anaemia10.04.01.005; 01.06.01.004--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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