Pantoprazole Dosage Guide + Max Dose, Adjustments - Drugs.com (2024)

Medically reviewed by Drugs.com. Last updated on Dec 13, 2023.

Applies to the following strengths: 40 mg; 20 mg; 0.4 mg/mL-NaCl 0.9%; 0.8 mg/mL-NaCl 0.9%; 4 mg/mL

Usual Adult Dose for:

  • Erosive Esophagitis
  • Gastroesophageal Reflux Disease
  • Zollinger-Ellison Syndrome
  • Pathological Hypersecretory Conditions

Usual Pediatric Dose for:

  • Erosive Esophagitis
  • Gastroesophageal Reflux Disease

Additional dosage information:

  • Renal Dose Adjustments
  • Liver Dose Adjustments
  • Dose Adjustments
  • Precautions
  • Dialysis
  • Other Comments

Usual Adult Dose for Erosive Esophagitis

Treatment: 40 mg orally once a day

  • Duration of therapy: 8 weeks

Maintenance: 40 mg orally once daily

Comments:

  • If patients are not healed after 8 weeks or erosive esophagitis (EE) recurs with the oral formulation, treatment for another 8 weeks may be considered.
  • Controlled studies using the oral formulation for maintenance did not extend beyond 12 months.

Uses:

  • Short-term treatment in the healing and symptomatic relief of EE
  • Maintenance of healing of EE

Usual Adult Dose for Gastroesophageal Reflux Disease

Oral: 40 mg orally once a day

  • Duration of therapy: 8 weeks

Parenteral: 40 mg via IV infusion once a day, given over at least 2 minutes OR over 15 minutes

  • Duration of therapy: 7 to 10 days

Comments:

  • IV treatment should be discontinued once the patient is able to take an oral formulation.
  • Use of the IV formulation has not been studied for longer than 10 days.
  • Safety and efficacy for uses otherwise described (e.g., life-threatening gastrointestinal bleeds) are not available; however, use of this drug at 40 mg/day doses did not raise gastric pH to sufficient levels to contribute to the treatment of life-threatening conditions.
  • If patients are not healed after 8 weeks with the oral formulation, treatment for another 8 weeks may be considered.

Uses:

  • Short-term treatment of gastroesophageal reflux disease (GERD) in patients with a history of erosive esophagitis
  • Reduction of relapse rates of daytime and nighttime heartburn symptoms in adult patients with GERD

Usual Adult Dose for Zollinger-Ellison Syndrome

Oral: 40 mg orally 2 times a day

  • Maximum dose: 240 mg/day

Parenteral:

  • Initial dose: 80 mg via IV infusion every 12 hours, given over at least 2 minutes OR over 15 minutes
  • Maintenance dose: 80 mg via IV infusion every 8 to 12 hours, given over at least 2 minutes OR over 15 minutes
  • Maximum dose: 240 mg/day
  • Maximum duration of therapy: 6 days

Comments:

  • IV treatment should be discontinued once the patient is able to take an oral formulation.
  • Use of the IV formulation for longer than 6 days and/or with doses higher than 240 mg has not been adequately studied.
  • Patients may be vulnerable to increased acid production despite a short period of loss of effective inhibition.
  • Patients given the oral formulation should be continued on therapy for as long as clinically necessary.

Uses:

  • Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome
  • Pathological hypersecretion conditions, including Zollinger-Ellison syndrome

Usual Adult Dose for Pathological Hypersecretory Conditions

Oral: 40 mg orally 2 times a day

  • Maximum dose: 240 mg/day

Parenteral:

  • Initial dose: 80 mg via IV infusion every 12 hours, given over at least 2 minutes OR over 15 minutes
  • Maintenance dose: 80 mg via IV infusion every 8 to 12 hours, given over at least 2 minutes OR over 15 minutes
  • Maximum dose: 240 mg/day
  • Maximum duration of therapy: 6 days

Comments:

  • IV treatment should be discontinued once the patient is able to take an oral formulation.
  • Use of the IV formulation for longer than 6 days and/or with doses higher than 240 mg has not been adequately studied.
  • Patients may be vulnerable to increased acid production despite a short period of loss of effective inhibition.
  • Patients given the oral formulation should be continued on therapy for as long as clinically necessary.

Uses:

  • Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome
  • Pathological hypersecretion conditions, including Zollinger-Ellison syndrome

Usual Pediatric Dose for Erosive Esophagitis

5 years and older:
15 to less than 40 kg: 20 mg orally once a day
40 kg and greater: 40 mg orally once a day
Duration of therapy: Up to 8 weeks

Comment: Safety has not been established in treatment beyond 8 weeks.

Uses:

  • Short-term treatment in the healing and symptomatic relief of EE
  • Short-term treatment of GERD in patients with a history of EE

Usual Pediatric Dose for Gastroesophageal Reflux Disease

5 years and older:
15 to less than 40 kg: 20 mg orally once a day
40 kg and greater: 40 mg orally once a day
Duration of therapy: Up to 8 weeks

Comment: Safety has not been established in treatment beyond 8 weeks.

Uses:

  • Short-term treatment in the healing and symptomatic relief of EE
  • Short-term treatment of GERD in patients with a history of EE

Renal Dose Adjustments

Data not available

Liver Dose Adjustments

IV: Data not available

Oral: Doses over 40 mg/day have not been studied in patients with liver impairment. No adjustment recommended.

Dose Adjustments

CYP450 2C19 Poor Metabolizers:
Adults: No adjustment recommended.
Pediatric patients: Oral dose reductions should be considered.

Pathological Hypersecretion (including Zollinger-Ellison syndrome):

  • Acid output target range: Less than 10 mEq/h

Precautions

CONTRAINDICATIONS:

  • Hypersensitivity to the active component, substituted benzimidazoles, or any of the ingredients
  • Patients receiving rilpivirine-containing products

Safety and efficacy of oral formulations have not been established in patients younger than 5 years. The IV formulation is not recommended for use in children.

Consult WARNINGS section for additional precautions.

Dialysis

Data not available

Other Comments

Administration advice:

  • Tablet formulations should be swallowed whole, without crushing/chewing; tablets may be taken with or without food.
  • For patients unable to swallow a 40 mg tablet, two 20 mg tablets may be taken; however, the 40 mg oral suspension packet formulation should not be divided to create two-20 mg dosages.
  • Oral suspension/granule formulations should be taken on an empty stomach, preferably 30 to 60 minutes before a meal.
  • The granule formulation may be sprinkled into applesauce or mixed into a small volume of either apple juice or orange juice and swallowed immediately. This drug may be mixed with apple juice and administered via nasogastric tube.

Storage requirements: The manufacturer product information should be consulted.

Reconstitution/preparation techniques: The manufacturer product information should be consulted.

IV compatibility: The manufacturer product information should be consulted.

General:

  • This drug may be used concomitantly with antacids without affecting the absorption.
  • Reflux symptoms may take 2 to 3 days to improve after initiation.
  • Rapid acid control may be achieved within an hour at an IV dose of 160 mg.

Monitoring:

  • HEPATIC: Liver function tests, especially in patients with impaired liver function
  • METABOLIC: Magnesium levels, especially in patients taking other drugs that could result in hypomagnesemia or those on long-term therapy; Vitamin B12 levels, especially in patients on long-term therapy
  • MUSCULOSKELETAL: Bone fractures, especially in patients at high-risk for osteoporosis-related events
  • RENAL: Renal function tests

Patient advice:

  • Advise patients to avoid taking concomitant proton pump inhibitors and/or H2 antagonists during treatment.
  • If using this drug to treat H pylori, tell patients that it is important to complete the full regimen.
  • Instruct patients to seek medical attention if signs/symptoms of hypersensitivity, Clostridium difficile, or systemic cutaneous lupus erythematosus occur.
  • Patients should be told that treatment may not provide immediate relief and that they should not take this drug for prophylaxis. Symptomatic relief may occur after 1 day of treatment, but patients should continue treatment for the full duration to achieve complete symptom control.
  • Inform patients that this drug may cause dizziness or blurred vision, and they should avoid driving or operating machinery if these side effects occur.
  • Advise patients to speak to their healthcare provider if they become pregnant, intend to become pregnant, or are breastfeeding.

Frequently asked questions

  • Pantoprazole vs. omeprazole: What's the difference between them?
  • Can you take pantoprazole 40 mg twice a day?
  • How long can I take pantoprazole?
  • Does pantoprazole cause bloating?

More about pantoprazole

  • Check interactions
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  • Patient tips
  • During pregnancy
  • Support group
  • Drug class: proton pump inhibitors
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Patient resources

  • Pantoprazole drug information
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  • Pantoprazole Injection

Other brands

Protonix, Protonix IV

Professional resources

  • Pantoprazole monograph
  • Pantoprazole (FDA)
  • Pantoprazole Granules (FDA)
  • Pantoprazole Injection (FDA)
  • Pantoprazole Oral Suspension (FDA)

Other brands

Protonix

Related treatment guides

  • Barrett's Esophagus
  • Dumping Syndrome
  • Erosive Esophagitis
  • Duodenal Ulcer

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circ*mstances.

Medical Disclaimer

Pantoprazole Dosage Guide + Max Dose, Adjustments - Drugs.com (2024)
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