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Rabeprazole

A02B - Drugs for peptic ulcer and GORD ATC A02BC04 Small molecule approved 1999 Oral Natural product

JFDA label: Ulcerbrex 20mg Tab

Mechanism of Action

Potent proton pump inhibitor; suppresses gastric acid secretion by inhibiting the parietal cell H+/K+ ATP pump

Indications

Approved

  • Canadian labeling
  • Duodenal ulcers (tablets only)
  • Erosive or ulcerative (tablets only)
  • Gastroesophageal reflux disease
  • Helicobacter pylori eradication (tablets only)
  • Pathological hypersecretory conditions (tablets only)
  • Symptomatic

Off-label

  • Duodenal ulcer (maintenance of healing/prevention of relapse)
  • NSAID-induced ulcer (treatment/prevention)
  • Stress ulcer prophylaxis in critically-ill patients

Contraindications

Source: Lexicomp

  • Hypersensitivity (eg, anaphylaxis, anaphylactic shock, angioedema, bronchospasm, acute interstitial nephritis, urticaria) to rabeprazole, other substituted benzimidazoles, or any component of the formulation Absolute
  • concomitant use with rilpivirine-containing products Absolute

Adverse Reactions

Very Common >10%Common 1–10%Uncommon 0.1–1% Rare 0.01–0.1%Very Rare <0.01%Not Known

Cardiac disorders (1)

Very Common Peripheral edema, flatulence, constipation, xerostomia

Musculoskeletal and connective tissue disorders (1)

Very Common Arthralgia

Other (1)

Very Common Gastrointestinal: Diarrhea (children and adolescents: 5% to 21%; adults: 1% to 10%:

Dosing

Source: Lexicomp

Duodenal ulcer: Tablets: Oral: 20 mg once daily for ≤4 weeks; additional therapy to achieve healing may be required for some patients. Gastric ulcers: Canadian labeling: Tablets: Oral: 20 mg once daily up to 6 weeks; additional therapy to achieve healing may be required for some patients. Gastroesophageal reflux disease (GERD): Tablets: Oral: Erosive or ulcerative GERD: Treatment: 20 mg once daily for 4 to 8 weeks; if inadequate response, may repeat up to an additional 8 weeks; maintenance: 20 mg once daily Symptomatic GERD: Treatment: 20 mg once daily for ≤4 weeks; if inadequate response, may repeat for an additional 4 weeks. Helicobacter pylori eradication: Tablets: Oral: Manufacturer labeling: 20 mg twice daily administered with amoxicillin 1,000 mg and clarithromycin 500 mg twice daily for 7 days American College of Gastroenterology guidelines (ACG [Chey 2007; Chey 2017]): Clarithromycin triple regimen: 20 to 40 mg twice daily in combination with clarithromycin 500 mg twice daily and either amoxicillin 1 g twice daily or metronidazole 500 mg 3 times per day; continue regimen for 14 days. Note: Avoid use of clarithromycin triple therapy in patients with risk factors for macrolide resistance (eg, prior macrolide exposure, local clarithromycin resistance rates ≥15%, eradication rates with clarithromycin-based regimens ≤85%) (ACG [Chey 2017]; Fallone 2016). Bismuth quadruple regimen: 20 mg twice daily in combination with tetracycline 500 mg 4 times per day, metronidazole 250 mg 4 times per day or 500 mg 3 or 4 times per day, and either bismuth subcitrate 120 to 300 mg 4 times per day or bismuth subsalicylate 300 mg 4 times per day; continue regimen for 10 to 14 days. Concomitant regimen: 20 mg twice daily in combination with amoxicillin 1 g twice daily, clarithromycin 500 mg twice daily, and either metronidazole or tinidazole 500 mg twice daily; continue regimen for 10 to 14 days. Sequential regimen: 20 mg twice daily plus amoxicillin 1 g twice daily for 5 to 7 days; then continue rabeprazole along with clarithromycin 500 mg twice daily, and either metronidazole or tinidazole 500 mg twice daily for 5 to 7 days. Hybrid regimen: 20 mg twice daily plus amoxicillin 1 g twice daily for 7 days; then continue rabeprazole and amoxicillin along with clarithromycin 500 mg twice daily, and either metronidazole or tinidazole 500 mg twice daily for 7 days. Levofloxacin triple regimen: 20 mg twice daily in combination with amoxicillin 1 g twice daily and levofloxacin 500 mg once daily; continue regimen for 10 to 14 days. Hypersecretory conditions (including Zollinger-Ellison Syndrome): Tablets: Oral: Initial: 60 mg once daily; adjust dose to patient needs (some may require divided doses). Doses as high as 100 mg once daily and 60 mg twice daily have been used; continue as long as clinically indicated. Nonerosive reflux disease (NERD): Canadian labeling: Tablets: Oral: Treatment: 10 mg (maximum: 20 mg once daily) for 4 weeks; lack of symptom control after 4 wee
(For additional information see "Rabeprazole: Pediatric drug information") Gastroesophageal reflux disease (GERD), symptomatic: Children 1 to 11 years: Capsules: Oral: ≥15 kg: 10 mg once daily for ≤12 weeks. Children ≥12 years and Adolescents: Oral: Tablets: 20 mg once daily for ≤8 weeks.
Refer to adult dosing.
No dosage adjustment necessary.
Mild-to-moderate impairment (Child-Pugh class A or B): No dosage adjustment necessary. Severe impairment (Child-Pugh class C): Avoid use; if treatment is necessary, monitor for adverse reactions.

Warnings & Precautions

Source: Lexicomp

Atrophic gastritis

Long-term omeprazole therapy has caused atrophic gastritis (by biopsy); this may also occur with rabeprazole.

Carcinoma

No reports of adenomatoid, dysplastic or neoplastic changes of enterochromaffin-like (ECL) cells in the gastric mucosa have occurred.

Clostridium difficile-associated diarrhea (CDAD)

Use of proton pump inhibitors (PPIs) may increase risk of CDAD, especially in hospitalized patients; consider CDAD diagnosis in patients with persistent diarrhea that does not improve. Use the lowest dose and shortest duration of PPI therapy appropriate for the condition being treated.

Cutaneous and systemic lupus erythematosus

Has been reported as new onset or exacerbation of existing autoimmune disease; most cases were cutaneous lupus erythematosus (CLE), most commonly, subacute CLE (occurring within weeks to years after continuous therapy). Systemic lupus erythematosus (SLE) is less common (typically occurs within days to years after initiating treatment) and occurred primarily in young adults up to the elderly. Discontinue therapy if signs or symptoms of CLE or SLE occur and refer to specialist for evaluation; most patients improve 4 to 12 weeks after discontinuation of rabeprazole.

Fractures

Increased incidence of osteoporosis-related bone fractures of the hip, spine, or wrist may occur with proton pump inhibitor (PPI) therapy. Patients on high-dose (multiple daily doses) or long-term therapy (≥1 year) should be monitored. Use the lowest effective dose for the shortest duration of time, use vitamin D and calcium supplementation, and follow appropriate guidelines to reduce risk of fractures in patients at risk.

Gastrointestinal infection (eg, Salmonella, Campylobacter)

Use of proton pump inhibitors may increase risk of these infections.

Hypomagnesemia

Reported rarely, usually with prolonged PPI use of ≥3 months (most cases >1 year of therapy). May be symptomatic or asymptomatic; severe cases may cause tetany, seizures, and cardiac arrhythmias. Consider obtaining serum magnesium concentrations prior to beginning long-term therapy, especially if taking concomitant digoxin, diuretics, or other drugs known to cause hypomagnesemia; and periodically thereafter. Hypomagnesemia may be corrected by magnesium supplementation, although discontinuation of rabeprazole may be necessary; magnesium levels typically return to normal within 1 week of stopping.

Interstitial nephritis

Acute interstitial nephritis has been observed in patients taking PPIs; may occur at any time during therapy and is generally due to an idiopathic hypersensitivity reaction. Discontinue if acute interstitial nephritis develops.

Vitamin B12 deficiency

Prolonged treatment (>3 years) may lead to vitamin B12 malabsorption and subsequent vitamin B12 deficiency. The magnitude of the deficiency is dose-related and the association is stronger in females and those younger in age ( Disease-related concerns:

Gastric malignancy

Relief of symptoms does not preclude the presence of a gastric malignancy.

Hepatic impairment

Avoid use in patients with severe hepatic impairment; if treatment is necessary monitor for adverse reactions. Concurrent drug therapy issues:

Clopidogrel

Proton pump inhibitors (PPIs) may diminish the therapeutic effect of clopidogrel, thought to be due to reduced formation of the active metabolite of clopidogrel. The manufacturer of clopidogrel recommends either avoidance of both omeprazole (even when scheduled 12 hours apart) and esomeprazole or use of a PPI with comparatively less effect on the active metabolite of clopidogrel. Avoidance of rabeprazole appears prudent due to potent in vitro CYP2C19 inhibition (Li 2004) and lack of sufficient comparative in vivo studies with other PPIs. In contrast to these warnings, others have recommended the continued use of PPIs, regardless of the degree of inhibition, in patients with a history of GI bleeding or multiple risk factors for GI bleeding who are also receiving clopidogrel since no evidence has established clinically meaningful differences in outcome; however, a clinically-significant interaction cannot be excluded in those who are poor metabolizers of clopidogrel (Abraham 2010; Levine 2011).

Drug-drug interactions

Potentially significant interactions may exist, requiring dose or frequency adjustment, additional monitoring, and/or selection of alternative therapy. Consult drug interactions database for more detailed information. Other warnings/precautions:

Appropriate use

Helicobacter pylori eradication: Short-term combination therapy (≤7 days) has been associated with a higher incidence of treatment failure. The American College of Gastroenterology recommends 10 to 14 days of therapy (triple or quadruple) for eradication of H. pylori (Chey 2017).

Pregnancy & Lactation

Pregnancy

Available studies have not shown an increased risk of major birth defects following maternal use of proton pump inhibitors during pregnancy; however, information specific to rabeprazole is limited (Pasternak 2010); most information available for omeprazole. When treating GERD in pregnancy, PPIs may be used when clinically indicated (Katz 2013).

Lactation

It is not known if rabeprazole is present in breast milk. According to the manufacturer, the decision to continue or discontinue breastfeeding during therapy should take into account the risk of infant exposure, the benefits of breastfeeding to the infant, and benefits of treatment to the mother.

Monitoring

Clinical pearlMagnesium levels (prior to initiation of therapy and periodically thereafter) in patients on long-term treatment or those taking digoxin, diuretics, or other drugs that cause hypomagnesemia; susceptibility testing recommended in patients who fail H. pylori eradication regimen.

Chemistry & Properties

2D structure
FormulaC18H21N3O3S
Molecular weight359.45 g/mol
IUPAC name2-[[4-(3-methoxypropoxy)-3-methyl-2-pyridinyl]methylsulfinyl]-1H-benzimidazole
CAS117976-89-3
PubChem CID5029
InChIKeyYREYEVIYCVEVJK-UHFFFAOYSA-N
logP2.99 (XLogP 1.9)
Polar surface area83.09 Ų
H-bond acceptors / donors5 / 1
Drug-likeness (QED)0.49
Lipinski violations0
SMILESCOCCCOc1ccnc(C[S+]([O-])c2nc3ccccc3[nH]2)c1C

Biology & Pharmacokinetics

Pharmacokinetics predicted

Bioavailability10.0%
Half-life0.651 h
Volume of distribution0.273 L/kg
Protein binding95.0%
BBB penetrantNo

Enzyme interactions

EnzymeRoleDetail
CYP1A2Inhibitor
CYP1A2Substrate
CYP2C19Inhibitor
CYP2C19Substrate
CYP2C8Inhibitor
CYP3A4Inhibitor
CYP3A4Substrate

Transporters

BCRP (Inhibitor)BCRP (Inhibitor)BSEP (Inhibitor)BSEP (Inhibitor)MDR1 (Inhibitor)MRP1 (Inhibitor)MRP2 (Inhibitor)MRP3 (Inhibitor)MRP4 (Inhibitor)OAT3 (Inhibitor)OATP1B1 (Inhibitor)OATP1B3 (Inhibitor)OCT1 (Inhibitor)OCT2 (Inhibitor)OCT3 (Inhibitor)P-gp (Inhibitor)Transporter(unspecified) (Inhibitor)P-gp (Substrate)

Drug–drug interactions (100+, DDInter)

Interacting drugSeverityManagement
Acalabrutinib major
Atazanavir major
Clopidogrel major
Dacomitinib major
Dasatinib major
Erlotinib major
Methotrexate major
Nelfinavir major
Neratinib major
Pazopanib major
Pexidartinib major
Rilpivirine major
Selpercatinib major
Velpatasvir major
Abametapir (topical) moderate
Amikacin moderate
Amikacin (liposome) moderate
Amphetamine moderate
Amphotericin B moderate
Amphotericin B (cholesteryl sulfate) moderate
Amphotericin B (lipid complex) moderate
Amphotericin B (liposomal) moderate
Anisindione moderate
Apalutamide moderate
Aprepitant moderate
Armodafinil moderate
Bacampicillin moderate
Bendroflumethiazide moderate
Benzthiazide moderate
Bosutinib moderate
Brigatinib moderate
Bumetanide moderate
Capreomycin moderate
Carboplatin moderate
Cefditoren moderate
Cefpodoxime moderate
Cefuroxime moderate
Ceritinib moderate
Cetuximab moderate
Chlorothiazide moderate

Showing 40 of 100+.

Registered Products (2)

BrandForm / strengthPackAgentCitizen (JOD)
Ulcerbrex Tablet 20 mg 14 tab Ibn Rushd Drug Store 5.690
Rabex Tablet 20 mg 28 tab Alshefra Dru Store company 11.060