Esomeprazole

Esomeprazole, sold under the brand names Nexium among others,[2] is a medication which reduces stomach acid.[4] It is used to treat gastroesophageal reflux disease, peptic ulcer disease, and Zollinger–Ellison syndrome.[4][5] Effectiveness is similar to other proton pump inhibitors (PPIs).[6] It is taken by mouth or injection into a vein.[4]

"Nexium" redirects here. It is not to be confused with NXIVM.

Esomeprazole
Clinical data
Pronunciation/ˌɛsoʊˈmɛprəˌzoʊl, -ˈmiː-, -ˌzɒl/[1]
Trade namesNexium, others[2]
AHFS/Drugs.comMonograph
MedlinePlusa699054
License data
Pregnancy
category
  • AU: B3
  • US: C (Risk not ruled out)
    Routes of
    administration    		By mouth, IV
    Drug classproton pump inhibitor
    ATC code
    Legal status
    Legal status
    • AU: S2 (Pharmacy medicine) /  S4 (Prescription Only Medicine)[3]
    • UK: General sales list (GSL, OTC)
    • US: OTC / Rx-only
    Pharmacokinetic data
    Bioavailability50 to 90%
    MetabolismLiver (CYP2C19, CYP3A4)
    Elimination half-life1–1.5 hours
    Excretion80% Kidney
    20% Faecal
    Identifiers
    CAS Number
    PubChem CID
    DrugBank
    ChemSpider
    UNII
    KEGG
    ChEBI
    ChEMBL
    CompTox Dashboard (EPA)
    ECHA InfoCard100.149.048
    Chemical and physical data
    FormulaC17H19N3O3S
    Molar mass345.42 g·mol−1
    3D model (JSmol)
     NY (what is this?)  (verify)

    Common side effects include headache, constipation, dry mouth, and abdominal pain.[4] Serious side effects may include angioedema, Clostridium difficile infection, and pneumonia.[4] Use in pregnancy appears to be safe, while safety during breastfeeding is unclear.[7] Esomeprazole is the (S)-(−)-isomer of omeprazole.[4] It works by blocking H+/K+-ATPase in the parietal cells of the stomach.[4]

    It was patented in 1993 and approved for medical use in 2000.[8] It is available as a generic medication and sold over the counter in a number of countries.[9][5] In 2017, it was the 88th most commonly prescribed medication in the United States, with more than nine million prescriptions.[10][11] It is also available without a prescription in the United States.[12]

    Medical use

    The primary uses of esomeprazole are gastroesophageal reflux disease, treatment and maintenance of erosive esophagitis, treatment of duodenal ulcers caused by H. pylori, prevention of gastric ulcers in those on chronic NSAID therapy, and treatment of gastrointestinal ulcers associated with Crohn's disease.[13][14]

    Gastroesophageal reflux disease

    Gastroesophageal reflux disease (GERD) is a condition in which the digestive acid in the stomach comes in contact with the esophagus. The irritation caused by this disorder is known as heartburn. Long-term contact between gastric acids and the esophagus can cause permanent damage to the esophagus. Esomeprazole reduces the production of digestive acids, thus reducing their effect on the esophagus.

    Duodenal ulcers

    Esomeprazole is combined with the antibiotics clarithromycin and amoxicillin (or metronidazole instead of amoxicillin in penicillin-hypersensitive patients) in a 10-day eradication triple therapy for Helicobacter pylori. Infection by H. pylori is a causative factor in the majority of peptic and duodenal ulcers.

    Efficacy

    A 2006 meta analysis concluded that compared to other proton pump inhibitors, esomeprazole confers a modest overall benefit in esophageal healing and symptom relief. When broken down by disease severity, the benefit of esomeprazole relative to other proton pump inhibitors was negligible in people with mild disease (number needed to treat 50), but appeared more in those with severe disease (number needed to treat 8).[15] A second meta analysis also found increases in erosive esophageal healing (>95% healing rate) when compared to standardized doses in broadly selected patient populations.[16] A 2017 study found esomeprazole to be among a number of effective doses of PPIs.[17]

    Adverse effects

    Common side effects include headache, diarrhea, nausea, flatulence, decreased appetite, constipation, dry mouth, and abdominal pain. More severe side effects are severe allergic reactions, chest pain, dark urine, fast heartbeat, fever, paresthesia, persistent sore throat, severe stomach pain, unusual bruising or bleeding, unusual tiredness, and yellowing of the eyes or skin.[18]

    Proton pump inhibitors may be associated with a greater risk of hip fractures[19] and Clostridium difficile-associated diarrhoea.[20] Patients are frequently administered the drugs in intensive care as a protective measure against ulcers, but this use is also associated with a 30% increase in occurrence of pneumonia.[21]

    Long-term use of PPIs in patients treated for Helicobacter pylori has been shown to dramatically increase the risk of gastric cancer.[22]

    Interactions

    Esomeprazole is a competitive inhibitor of the enzyme CYP2C19, and may therefore interact with drugs that depend on it for metabolism, such as diazepam and warfarin; the concentrations of these drugs may increase if they are used concomitantly with esomeprazole.[23] Conversely, clopidogrel (Plavix) is an inactive prodrug that partially depends on CYP2C19 for conversion to its active form; inhibition of CYP2C19 blocks the activation of clopidogrel, thus reducing its effects.[24][25]

    Drugs that depend on stomach pH for absorption may interact with omeprazole; drugs that depend on an acidic environment (such as ketoconazole or atazanavir) will be poorly absorbed, whereas drugs that are broken down in acidic environments (such as erythromycin) will be absorbed to a greater extent than normal.[23]

    Pharmacokinetics

    Single 20 to 40 mg oral doses generally give rise to peak plasma esomeprazole concentrations of 0.5-1.0 mg/l within 1–4 hours, but after several days of once-daily administration, these levels may increase by about 50%. A 30-minute intravenous infusion of a similar dose usually produces peak plasma levels on the order of 1–3 mg/l. The drug is rapidly cleared from the body, largely by urinary excretion of pharmacologically inactive metabolites such as 5-hydroxymethylesomeprazole and 5-carboxyesomeprazole. Esomeprazole and its metabolites are analytically indistinguishable from omeprazole and the corresponding omeprazole metabolites unless chiral techniques are employed.[26]

    Dosage forms
    Esomeprazole strontium delayed-release capsules, 49.3 mg
    40 mg Nexium (esomeprazole magnesium) capsules

    Esomeprazole is available as delayed-release capsules in the United States or as delayed-release tablets in Australia, the United Kingdom, and Canada (containing esomeprazole magnesium) in strengths of 20 and 40 mg, as delayed-release capsules in the United States (containing esomeprazole strontium) in a 49.3 mg strength (delivering the equivalent of 40 mg of esomeprazole,[27] and as esomeprazole sodium for intravenous injection/infusion. Oral esomeprazole preparations are enteric-coated, due to the rapid degradation of the drug in the acidic conditions of the stomach. This is achieved by formulating capsules using the multiple-unit pellet system.

    The combination naproxen/esomeprazole magnesium (brand name Vimovo) is used for the prevention of gastric ulcers associated with chronic NSAID therapy. Vimovo is available in two dosage strengths: 500/20 mg and 375/20 mg. Clinical trials of naproxen/esomeprazole demonstrated an incidence of GI ulcer in 24% of patients on naproxen (alone) versus 7% on naproxen/esomeprazole.[28] The FDA has added warnings to the label for Vimovo concerning acute interstitial nephritis and risk of kidney problems in some patients.[29]

    Multiple-unit pellet system

    Esomeprazole capsules, as well as Losec/Prilosec tablets, are formulated as a "multiple-unit pellet system" (MUPS). Essentially, the capsule consists of extremely small enteric-coated granules (pellets) of the esomeprazole formulation inside an outer shell. When the capsule is immersed in an aqueous solution, as happens when the capsule reaches the stomach, water enters the capsule by osmosis. The contents swell from water absorption, causing the shell to burst, and releasing the enteric-coated granules. For most patients, the multiple-unit pellet system is of no advantage over conventional enteric-coated preparations. Patients for whom the formulation is of benefit include those requiring nasogastric tube feeding and those with difficulty swallowing (dysphagia).

    Society and culture

    Global distribution

    In 2010, AstraZeneca announced a co-promotion agreement with Daiichi Sankyo to distribute Nexium in Japan.[30] In September 2011, Nexium was approved for sale and was launched by Daiichi Sankyo in Japan.[31] Esomeprazole was approved for use in the United States in February 2001.[32][33]

    Economics

    Between the launch of esomeprazole in 2001 and 2005, the drug netted AstraZeneca about $14.4 billion.[34]

    Controversy
    Main article: AstraZeneca's marketing of Nexium

    There has been some controversy about AstraZeneca's behaviour in creating, patenting, and marketing of the drug. Esomeprazole's successful predecessor, omeprazole, is a mixture of two mirror-imaged molecules (esomeprazole which is the S-enantiomer, and R-omeprazole); critics said the company was trying to "evergreen" its omeprazole patent by patenting the pure esomeprazole and aggressively marketing to doctors that it is more effective than the mixture.[35]

    Thomas A. Scully, head of the Centers for Medicare and Medicaid Services (CMS), also criticized AstraZeneca for their aggressive marketing of Nexium. At a conference of the American Medical Association (AMA), he said that Astra was using the new drug to overcharge consumers and insurance companies.

    Brand names

    Generic versions of esomeprazole magnesium are available worldwide.[2] It is available over-the-counter under the brand name Nexium in the United States[12][36] and the UK.[37]

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    References
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    2. Esomeprazole brand names
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    4. "Esomeprazole Magnesium Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. Retrieved 3 March 2019.
    5. British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 78. ISBN 9780857113382.
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    22. Cheung, Ka Shing; Chan, Esther W.; Wong, Angel Y. S.; Chen, Lijia; Wong, Ian C. K.; Leung, Wai Keung (18 September 2017). "Long-term proton pump inhibitors and risk of gastric cancer development after treatment for Helicobacter pylori: a population-based study". Gut. 67 (1): gutjnl–2017–314605. doi:10.1136/gutjnl-2017-314605. ISSN 0017-5749. PMID 29089382.
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    34. Financial impact information: 2005, $4.6 billion; 2004, $3.9 billion Archived 2007-02-02 at the Wayback Machine; 2003, $3.3 billion Archived 2004-07-28 at the Wayback Machine; 2002, $2 billion Archived 2003-06-08 at the Wayback Machine; 2001, launch and $580 million.
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    Further reading
    • "Esomeprazole". Drug Information Portal. U.S. National Library of Medicine.
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