Protonix Dosage
Generic name: PANTOPRAZOLE SODIUM 40mg in 10mL
Dosage form: injection, powder, for solution
Drug class: Proton pump inhibitors
Medically reviewed by Drugs.com. Last updated on Sep 4, 2024.
Recommended Dosage for GERD Associated with a History of EE
Adult Patients
The recommended adult dosage of PROTONIX I.V. is 40 mg once daily by intravenous injection (over at least 2 minutes) or intravenous infusion (for 15 minutes) for up to 10 days. Discontinue PROTONIX I.V. as soon as the patient is able to tolerate oral treatment. Switch to an appropriate oral medication within 10 days of starting PROTONIX I.V.
Pediatric Patients
- •
- The recommended dosage for pediatric patients 3 months of age and older is based on age and actual body weight as shown in Table 1 below.
- •
- Administer as an intravenous infusion over 15 minutes once daily.
Age and Body Weight |
Recommended Dosage Regimen (up to 7 days) |
|
3 months to less than 1 year of age |
Less than 12.5 kg |
0.8 mg/kg once daily |
12.5 kg and above |
10 mg once daily |
|
1 year to 17 years of age |
Up to 15 kg |
10 mg once daily |
Greater than 15 kg up to 40 kg |
20 mg once daily |
|
Greater than 40 kg |
40 mg once daily |
- •
- Discontinue PROTONIX I.V. as soon as the patient is able to tolerate oral treatment. Switch to an appropriate oral medication within 7 days of starting PROTONIX I.V.
Recommended Dosage for Pathological Hypersecretion Including Zollinger-Ellison Syndrome
- •
- The recommended adult dosage of PROTONIX I.V. is 80 mg every 12 hours by intravenous injection (over at least 2 minutes) or intravenous infusion (for 15 minutes).
- •
- Adjust the frequency of dosing to individual patient needs based on acid output measurements. In those patients who need a higher dosage, 80 mg intravenously every 8 hours is expected to maintain acid output below 10 mEq/h.
- •
- When switching between intravenous to oral formulations of gastric acid inhibitors, consider the pharmacodynamic action of the drugs to ensure continuity of acid suppression.
Preparation and Administration Instructions for GERD Associated with a History of EE
15-Minute Intravenous Infusion for Pediatric or Adult Patients
1. Reconstitute each vial of PROTONIX I.V. with 10 mL of 0.9% Sodium Chloride Injection.
2. Dilute the resulting solution to a final concentration as described below:
- •
- Pediatric patients 3 months to less than 1 year of age: Dilute with 21 mL 0.9% Sodium Chloride Injection to a final concentration of approximately 1.3 mg/mL.
- •
- Pediatric patients 1 year to 17 years old and adult patients: Further dilute with 100 mL 5% Dextrose Injection or 0.9% Sodium Chloride Injection to a final concentration of approximately 0.4 mg/mL.
3. Inspect the diluted PROTONIX I.V. solution visually for particulate matter and discoloration prior to and during administration.
4. Withdraw the desired dose of the diluted PROTONIX I.V. solution for a pediatric or adult dose.
5. Discard any unused portion of the remaining PROTONIX I.V. solution.
6. Infuse intravenously over a period of approximately 15 minutes through a dedicated line or through a Y-site.
7. Flush the intravenous line before and after administration of PROTONIX I.V. with either 5% Dextrose Injection or 0.9% Sodium Chloride Injection.
Storage
- •
- Store the reconstituted solution may be up to 6 hours at room temperature up to 30°C (86°F) prior to further dilution.
- •
- Store the diluted solution at room temperature up to 30°C (86°F) and must be used within 24 hours from the time of initial reconstitution.
- •
- Do not freeze the reconstituted or diluted solution.
2-Minute Intravenous Injection for Adult Patients
1. Reconstitute each vial of PROTONIX I.V. with 10 mL of 0.9% Sodium Chloride Injection, to a final concentration of approximately 4 mg/mL.
2. Withdraw the dose of 40 mg of reconstituted PROTONIX I.V. solution.
3. Inspect the diluted PROTONIX I.V. solution visually for particulate matter and discoloration prior to and during administration.
4. Administer intravenously over a period of at least 2 minutes.
5. Flush the intravenous line before and after administration of PROTONIX I.V. with either 5% Dextrose Injection or 0.9% Sodium Chloride Injection.
Preparation and Administration Instructions for Pathological Hypersecretion Including Zollinger-Ellison Syndrome
15-Minute Intravenous Infusion
1. Reconstitute each vial of PROTONIX I.V. with 10 mL of 0.9% Sodium Chloride Injection.
2. Combine the contents of the two vials and dilute with 80 mL of 5% Dextrose Injection or Sodium Chloride Injection to a total volume of 100 mL with a final concentration of approximately 0.8 mg/mL.
3. Inspect the diluted PROTONIX I.V. solution visually for particulate matter and discoloration prior to and during administration.
4. Administer intravenously over a period of approximately 15 minutes at a rate of approximately 7 mL/min.
5. Flush the intravenous line before and after administration of PROTONIX I.V. with either 5% Dextrose Injection or 0.9% Sodium Chloride Injection.
Storage
- •
- The reconstituted solution can be stored at room temperature up to 30°C (86°F) for up to 6 hours prior to further dilution.
- •
- Once further diluted, the diluted solution can be stored at room temperature up to 30°C (86°F) for up to 24 hours from the time of initial reconstitution.
- •
- Do not freeze the reconstituted or diluted solution.
2-Minute Intravenous Injection
1. Reconstitute each vial of PROTONIX I.V. with 10 mL of 0.9% Sodium Chloride Injection per vial to a final concentration of approximately 4 mg/mL.
2. Inspect the diluted PROTONIX I.V. solution visually for particulate matter and discoloration prior to and during administration.
3. Administer the total volume from both vials intravenously over a period of at least 2 minutes.
4. Flush the intravenous line before and after administration of PROTONIX I.V. with either 5% Dextrose Injection or 0.9% Sodium Chloride Injection.
Compatibility Information
- •
- Administer PROTONIX I.V. intravenously through a dedicated line or through a Y-site.
- •
- When administering through a Y-site, PROTONIX I.V. is compatible with the following solutions:
- o
- 5% Dextrose Injection
- o
- 0.9% Sodium Chloride Injection
- •
- Midazolam hydrochloride is incompatible with Y-site administration of PROTONIX I.V.
- •
- PROTONIX I.V. may not be compatible with products containing zinc.
- •
- Stop administering PROTONIX I.V. immediately through a Y-site if precipitation or discoloration occurs.
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