Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Esomeprazole sodium
Drug ID BADD_D00817
Description Esomeprazole, sold under the brand name Nexium, is a proton pump inhibitor (PPI) medication used for the management of gastroesophageal reflux disease (GERD), for gastric protection to prevent recurrence of stomach ulcers or gastric damage from chronic use of NSAIDs, and for the treatment of pathological hypersecretory conditions including Zollinger-Ellison (ZE) Syndrome. It can also be found in quadruple regimens for the treatment of _H. pylori_ infections along with other antibiotics including [DB01060], [DB01211], and [DB00916], for example.[A177271, F4498] Its efficacy is considered similar to other medications within the PPI class including [DB00338], [DB00213], [DB00448], [DB05351], and [DB01129]. Esomeprazole is the s-isomer of [DB00338], which is a racemate of the S- and R-enantiomer. Esomeprazole has been shown to inhibit acid secretion to a similar extent as [DB00338], without any significant differences between the two compounds _in vitro_. Esomeprazole exerts its stomach acid-suppressing effects by preventing the final step in gastric acid production by covalently binding to sulfhydryl groups of cysteines found on the (H+, K+)-ATPase enzyme at the secretory surface of gastric parietal cells. This effect leads to inhibition of both basal and stimulated gastric acid secretion, irrespective of the stimulus. As the binding of esomeprazole to the (H+, K+)-ATPase enzyme is irreversible and new enzyme needs to be expressed in order to resume acid secretion, esomeprazole's duration of antisecretory effect persists longer than 24 hours.[FDA Label] PPIs such as esomeprazole have also been shown to inhibit the activity of dimethylarginine dimethylaminohydrolase (DDAH), an enzyme necessary for cardiovascular health. DDAH inhibition causes a consequent accumulation of the nitric oxide synthase inhibitor asymmetric dimethylarginie (ADMA), which is thought to cause the association of PPIs with increased risk of cardiovascular events in patients with unstable coronary syndromes.[A177577, A177580] Due to their good safety profile and as several PPIs are available over the counter without a prescription, their current use in North America is widespread. Long term use of PPIs such as esomeprazole has been associated with possible adverse effects, however, including increased susceptibility to bacterial infections (including gastrointestinal _C. difficile_), reduced absorption of micronutrients such as iron and B12, and an increased risk of developing hypomagnesemia and hypocalcemia which may contribute to osteoporosis and bone fractures later in life.[A177571] Rapid discontinuation of PPIs such as esomeprazole may cause a rebound effect and a short term increase in hypersecretion.[A177574] Esomeprazole doses should be slowly lowered, or tapered, before discontinuing to prevent this rebound effect.
Indications and Usage For the treatment of acid-reflux disorders (GERD), peptic ulcer disease, H. pylori eradication, and prevention of gastroinetestinal bleeds with NSAID use.
Marketing Status Prescription; OTC; Discontinued
ATC Code A02BC05
DrugBank ID DB00736
KEGG ID D04056
MeSH ID D064098
PubChem ID 10959536
TTD Drug ID D0C6DT
NDC Product Code 70436-190; 0186-6040; 65862-723; 69766-004; 51838-900; 68083-451; 14335-060; 14335-140; 51014-7111; 68083-452; 17478-850; 62756-843; 55150-185; 49711-0119; 65372-1139; 16729-252
Synonyms Esomeprazole | Esomeprazole Sodium | Esomeprazole Strontium | Strontium, Esomeprazole | Esomeprazole Magnesium | Nexium | Esomeprazole Potassium | Esomeprazole Strontium Anhydrous
Chemical Information
Molecular Formula C17H18N3NaO3S
CAS Registry Number 95510-70-6
SMILES CC1=CN=C(C(=C1OC)C)CS(=O)C2=NC3=C([N-]2)C=CC(=C3)OC.[Na+]
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)
Vision blurred17.17.01.010; 06.02.06.007--
Visual field defect17.17.01.001; 06.02.07.003--Not Available
Visual impairment06.02.06.008--Not Available
Vitamin B12 deficiency14.12.02.004--Not Available
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
Weight increased13.15.01.006--
White blood cell count13.01.06.027--Not Available
Tubulointerstitial nephritis20.05.02.002--Not Available
Fibromyalgia15.05.02.002--Not Available
Lymphadenectomy25.06.03.002--Not Available
Mouth injury12.01.09.005; 07.05.01.003--Not Available
Blood gastrin13.10.02.007--Not Available
Epigastric discomfort07.01.02.004--Not Available
Mucosal discolouration08.01.06.008--Not Available
Varices oesophageal24.10.02.004; 07.15.05.001; 09.01.06.009--Not Available
Colitis microscopic07.08.01.011--Not Available
Dysplasia08.03.04.007--Not Available
Epidermal necrosis23.03.03.035--Not Available
Blood alkaline phosphatase increased13.04.02.004--
Hot flush24.03.01.005; 21.02.02.001; 08.01.03.027--
Oesophageal disorder07.11.02.001--Not Available
Decreased appetite14.03.01.005; 08.01.09.028--
Erectile dysfunction19.08.04.001; 21.03.01.007--
Bowel movement irregularity07.02.03.003--Not Available
Regurgitation07.01.07.004--Not Available
Anal pruritus07.03.03.002--Not Available
Oropharyngeal discomfort22.02.05.027; 07.05.05.008--Not Available
Candida infection11.03.03.021--
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