• Approval by: DTC Approval Date: TBA
  • Action Omeprazole is a proton pump inhibitor (PPI). Drug Type
  • Presentation
  • Maximum daily dose 1.5 mg/kg/dose Route
  • Administration
  • Original version Date: 2014




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    Original version Date: 2014

    Author: AK, JD

    Current Version number: 2.0

    Current Version Date: 24/12/2020

    Risk Rating: Medium

    Due for Review: 24/12/2025

    Approval by: DTC

    Approval Date: TBA

    Omeprazole


    Revision Date :19/07/2018

    Approved: TC, KOH




    Alert

    Short- and long-term safety data in infants are limited. There have been several safety concerns with long-term usage in adults.

    The bioavailability of the in-house pharmacy suspension made from the contents of the capsule may be less (up to 50% less) than that of the capsule itself. Dose may need to be adjusted if no clinical response.



    Indication


    Treatment of gastroesophageal reflux disease (GORD).

    Prophylaxis in congenital tracheoesophageal fistula and oesophageal atresia (role unclear).



    Action

    Omeprazole is a proton pump inhibitor (PPI).

    Drug Type

    Proton Pump Inhibitor.

    Trade Name

    APO-Omeprazole Capsules (Apotex) 20 mg

    Omeprazole Sandoz IV Powder for injection (Sandoz]) 40 mg.



    Presentation

    20 mg/capsule; 10 mg tablets; 20 mg tablets.

    Oral suspension of 2 mg/mL prepared in pharmacy.

    Omeprazole Sandoz IV Powder for injection 40 mg.


    Dosage / Interval

    PO: 0.5–1.5 mg/kg/dose daily

    IV: 0.5 mg/kg/dose daily



    Maximum daily dose

    1.5 mg/kg/dose

    Route

    PO, IV

    Preparation/Dilution

    PO: In-house pharmacy can prepare a 2 mg/mL suspension using these capsules as follows: Disperse 100 mg omeprazole in 50 mL of 8.4% sodium bicarbonate solution.

    1 mL of omeprazole suspension contains 2 mg omeprazole, 1 mmol sodium and 1 mmol bicarbonate.


    IV: Add 10 mL of sodium chloride 0.9% to 40 mg powder for reconstitution to make a concentration of 4 mg/mL. Draw up 1 mL (4 mg) and add 9 mL of sodium chloride 0.9% to make a final volume of 10 mL with a concentration of 0.4 mg/mL.

    Administration

    PO: Administer prior to meals.

    IV: Infuse over 30 minutes.



    Monitoring

    Serum magnesium in patients on prolonged therapy or who use digoxin or drugs that may cause hypomagnesaemia (e.g. diuretics) concomitantly.20-21

    Serum vitamin B12 — every 1 to 2 years in patients on prolonged therapy.20-21




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