Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride
An intravenous electrolyte and buffer solution used during continuous renal replacement therapy (CRRT) to restore fluid, electrolyte, and acid-base balance — available as PRISMASOL and PHOXILLUM.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 1 clinical label set within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
How we combine label and product data →
Patient information guide — a plain-language walkthrough of Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride, written from its FDA label.
What Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride is used for
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PRISMASOL and PHOXILLUM are intravenous electrolyte and buffer replacement solutions used exclusively during continuous renal replacement therapy (CRRT) in intensive care settings.
- PRISMASOL is indicated in adult and pediatric patients as a replacement solution during CRRT to replace plasma volume removed by ultrafiltration and to correct electrolyte and acid-base imbalances.
- PHOXILLUM is indicated in adult and pediatric patients as a replacement solution during CRRT for the same purposes.
- Both PRISMASOL and PHOXILLUM may be used when CRRT is employed to help remove a dialyzable substance in cases of drug poisoning.
How Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride works
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PRISMASOL and PHOXILLUM are pharmacologically inactive — they don't act on receptors or block enzymes. Instead, they work by replenishing the specific electrolytes (such as sodium, potassium, magnesium, and calcium) that are filtered out of the blood during CRRT. The electrolyte concentrations in each formulation are designed to bring plasma levels back to a clinically safe range.
Each solution also contains a buffer — either bicarbonate directly, or lactate (a precursor that the body converts to bicarbonate) — to help correct metabolic acidosis, meaning too much acid in the blood. PHOXILLUM formulations also include phosphate to help address low phosphate levels during CRRT.
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride dosage
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PRISMASOL and PHOXILLUM are given intravenously through specialized CRRT equipment — never by mouth. The right formulation, flow rate, and duration are determined entirely by the treating physician based on the patient's clinical status, electrolyte levels, acid-base balance, and glucose levels.
- PRISMASOL is available in 7 different formulations with varying electrolyte and buffer concentrations.
- PHOXILLUM is available in 2 different formulations, both containing phosphate.
- Both are supplied in a two-compartment bag that must be mixed immediately before use.
- Follow your care team's instructions exactly — therapy is individualized for each patient.
Dosing details from the FDA-approved label
From the Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- PRISMASOL and PHOXILLUM replacement solutions in CRRT (general, individualized therapy)
- Therapy must be individualized based on the patient's clinical condition, fluid, electrolyte, acid-base and glucose balance
- The mode of therapy, solute formulation, flow rates, and length of replacement therapy should be established by a physician based on the patient's clinical condition, blood concentration of phosphate and other electrolytes, acid-base a
- Solution must be mixed immediately prior to use; after removal of the overwrap the solution is stable for 24 hours including the duration of the treatment
- Adding phosphate to PRISMASOL solutions
- Up to 1.2 mmol/L of phosphate can be added to the bag as potassium phosphate or sodium phosphate
- Use sodium phosphate if the total potassium concentration in PRISMASOL solution is 4 mEq/L
- Maximum: Total potassium concentration of PRISMASOL solution should not exceed 4 mEq/L
- Adding phosphate to PHOXILLUM solutions
- Phosphate up to 0.2 mmol/L may be added to the solution
- Use sodium phosphate if adding phosphate to bag
- Maximum: Total phosphate concentration should not exceed 1.2 mmol/L
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION • Therapy must be individualized based on the patient's clinical condition, fluid, electrolyte, acid-base and glucose balance ( 2.2 ) • Solution must be mixed prior to use ( 2.2 ) • Use only with extracorporeal dialysis equipment appropriate for CRRT ( 2.3 ) 2.1 Administration Instructions Visually inspect PRISMASOL and PHOXILLUM for particulate matter and discoloration prior to administration. Administration should only be under the direction of a physician competent in intensive care treatment including CRRT. Use only with extracorporeal dialysis equipment appropriate for CRRT. The prepared solution is for single patient use only. Aseptic technique should be used throughout administration to the patient. Discard any unused solution. 2.2 Dosing Considerations PRISMASOL replacement solutions contain 4 different combinations of active ingredients (7 different products with varying ingredient amounts). PHOXILLUM replacement solutions contain 2 different combinations of active ingredients (2 different products with varying ingredient amounts). PRISMASOL and PHOXILLUM are supplied in a two-compartment bag that must be mixed immediately prior to use [see Dosage and Administration (2.3) ]: • Small compartment A (250 mL) containing an electrolyte solution, and • Large compartment B (4750 mL) containing the buffer solution. See Table 1 for the concentrations of the active ingredients (after mixing) in these 9 different replacement solutions (total volume is 5 Liters).
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride side effects
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Common side effects
- Electrolyte imbalances (such as high potassium or phosphate levels)
- Fluid imbalance
- Acid-base disorders
- Metabolic acidosis (too much acid in the blood)
- Low blood pressure (hypotension)
- High or low blood sugar (with PRISMASOL or PHOXILLUM solutions containing dextrose)
- Elevated ionized calcium levels (reported with PRISMASOL solutions containing calcium)
- Low phosphate levels (hypophosphatemia)
When to get medical help
- Call your care team right away if you develop signs of severe electrolyte imbalance — such as muscle weakness, irregular heartbeat, or confusion.
- Alert your team if blood sugar becomes too high or too low during treatment.
- Watch for signs of too much acid in the blood (metabolic acidosis) — such as rapid breathing, fatigue, or confusion — especially with PHOXILLUM, which contains phosphate that may increase this risk.
- Tell your care team if you have a known allergy or sensitivity to any component of PRISMASOL or PHOXILLUM.
The following side effects have been reported with PRISMASOL and PHOXILLUM or similar CRRT replacement solutions:
- Metabolic acidosis (excess acid in the blood)
- Low blood pressure (hypotension)
- Acid-base disorders
- Electrolyte imbalances — including high potassium (hyperkalemia), high phosphate (hyperphosphatemia), or low phosphate (hypophosphatemia)
- Elevated ionized calcium levels (reported with PRISMASOL solutions containing calcium)
- Fluid imbalance
- High or low blood sugar — depending on the dextrose content of the solution used
Alert your care team immediately if you notice signs of serious electrolyte shifts — such as muscle weakness, an irregular heartbeat, difficulty breathing, or confusion — as these require prompt evaluation.
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride warnings and precautions
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- Electrolyte and fluid changes: PRISMASOL and PHOXILLUM can cause electrolyte levels — especially potassium and phosphate — to go too high or too low. Your care team will monitor blood chemistry throughout the procedure and may adjust the formulation or flow rate.
- Metabolic acidosis risk with PHOXILLUM: PHOXILLUM contains hydrogen phosphate, a weak acid that may increase the risk of metabolic acidosis (too much acid accumulating in the blood). Acid-base balance must be monitored closely.
- Blood sugar changes: Treatment can cause blood glucose to rise or fall depending on which formulation is used. Regular glucose monitoring is required, and antidiabetic therapy or other corrective steps may be needed.
- Drug removal during CRRT: The hemofilter can remove other medications from the blood, reducing their effectiveness. Blood levels of affected drugs may need to be checked and doses adjusted.
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride interactions
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Because CRRT physically filters the blood, it can affect how other drugs behave in the body:
- Dialyzable drugs: Any drug that can be removed by the hemofilter may have lower blood levels during CRRT — potentially reducing effectiveness. Your care team may need to monitor levels and adjust doses of affected medications.
- Citrate (used as an anticoagulant): When citrate is used to prevent clotting in the CRRT circuit, it adds to the overall buffer load and can lower plasma calcium levels. The choice of PRISMASOL or PHOXILLUM formulation should take this into account.
Interactions listed in the FDA-approved label
From the Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Dialyzable drugs: Blood concentrations of dialyzable drugs may be reduced by CRRT due to their removal by the hemofilter or hemodiafilter. The blood concentrations of certain drugs may need to be monitored and appropriate therapy implemented to correct for removal during treatment.
- Citrate (used as an anticoagulant): Citrate contributes to the overall buffer load and can reduce plasma calcium levels. Select the PRISMASOL/PHOXILLUM formulation(s) accordingly.
Read the label’s full interactions text
7 DRUG INTERACTIONS As with the use of other replacement solutions, blood concentrations of dialyzable drugs may be reduced by CRRT due to their removal by the hemofilter or hemodiafilter. The blood concentrations of certain drugs may need to be monitored and appropriate therapy implemented to correct for removal during treatment. 7.1 Citrate When used as an anticoagulant, citrate contributes to the overall buffer load and can reduce plasma calcium levels. Select the PRISMASOL/PHOXILLUM formulation(s) accordingly.
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride
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- Allergy to any ingredient: PRISMASOL and PHOXILLUM are contraindicated if you have a known hypersensitivity to any component.
- Pregnancy: Appropriate use with proper monitoring is not expected to harm the baby. Maintaining normal acid-base balance is especially important for fetal health during CRRT.
- Breastfeeding: Components pass into breast milk, but appropriate use is not expected to harm a nursing infant.
- Children (including newborns): Safety and effectiveness are established for pediatric patients, including newborns through age 17, based on clinical studies.
- Older adults: No novel safety concerns have been identified in geriatric patients, though careful monitoring still applies as with all patients.
How your body processes Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride
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How these solutions behave in the body depends heavily on each patient's own situation. The distribution of electrolytes, bicarbonate, and dextrose is shaped by the patient's clinical condition, metabolic status, and any remaining kidney function. How quickly water, electrolytes, and buffer are removed or retained depends on the patient's electrolyte and acid-base balance, metabolism, residual kidney function, and ongoing losses through the intestines, breathing, and skin.
How to store Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride
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Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15ºC to 30ºC (59ºF to 86ºF). Do not freeze or expose to excessive heat.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly are PRISMASOL and PHOXILLUM, and why am I receiving them?
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Will this affect my blood sugar?
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What side effects should I or my family watch for during treatment?
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I take other medications. Will CRRT wash them out of my system?
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Is it safe to use if I'm pregnant or breastfeeding?
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Can children receive PRISMASOL or PHOXILLUM?
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Is Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride available over the counter?
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When was Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride first available?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride on HelloPharmacist
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride forms and strengths (how it comes)
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Injection
How this form is used
- PRISMASOL is used as a replacement solution during CRRT to replace fluid and electrolytes removed by ultrafiltration and to correct electrolyte and acid-base imbalances.
- PHOXILLUM is used as a replacement solution during CRRT to replace fluid and electrolytes removed by ultrafiltration and to correct electrolyte and acid-base imbalances.
- Both PRISMASOL and PHOXILLUM may be used when CRRT is being performed to help remove a dialyzable substance in cases of drug poisoning.
- PRISMASOL and PHOXILLUM come in a two-compartment bag — both compartments must be mixed together immediately before use by squeezing the bag until the peel seal opens, then shaking gently.
- After mixing, PRISMASOL and PHOXILLUM solutions should be used right away; once the overwrap is removed, the mixed solution is stable for 24 hours including treatment time.
- PRISMASOL and PHOXILLUM are administered through extracorporeal CRRT equipment — either before (pre-dilution) or after (post-dilution) the hemofilter or hemodiafilter, or both.
- Additional medications (including phosphate) may be added to the bag via the injection connector using aseptic technique — do not use if color change or particles appear after addition.
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride on the U.S. market: products, makers and brands
How Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
1 company lists 6 Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride product records with the FDA, mostly as injection; the earliest marketing or approval year on record is 2006. Brand names on the directory include Prismasol Bgk4/0/1.2, Prismasol Bgk2/0, Prismasol B22gk4/0 and 6 more; the rest are generics.
Compare Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride products
A representative set of FDA-listed product records for Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Injection | ||||
| MAGNESIUM CHLORIDE 2.03 g/L; ANHYDROUS DEXTROSE 20 g/L; LACTIC ACID 5.4 g/L; SODIUM CHLORIDE 6.46 g/L; SODIUM BICARBONATE 3.09 g/L; POTASSIUM CHLORIDE 0.157 g/L | Intravenous | Vantive US Healthcare LLC | NDA | View NDC → |
| MAGNESIUM CHLORIDE 2.44 g/L; ANHYDROUS DEXTROSE 20 g/L; LACTIC ACID 5.4 g/L; SODIUM CHLORIDE 6.46 g/L; SODIUM BICARBONATE 3.09 g/L; POTASSIUM CHLORIDE 0.314 g/L | Intravenous | Vantive US Healthcare LLC | NDA | View NDC → |
| MAGNESIUM CHLORIDE 3.05 g/L; ANHYDROUS DEXTROSE 20 g/L; LACTIC ACID 5.4 g/L; SODIUM CHLORIDE 7.07 g/L; SODIUM BICARBONATE 2.21 g/L; POTASSIUM CHLORIDE 0.314 g/L | Intravenous | Vantive US Healthcare LLC | NDA | View NDC → |
| ANHYDROUS DEXTROSE 20 g/L; LACTIC ACID 5.4 g/L; MAGNESIUM CHLORIDE 2.03 g/L; POTASSIUM CHLORIDE 0.157 g/L; SODIUM BICARBONATE 3.09 g/L; SODIUM CHLORIDE 6.46 g/L | Intravenous | Vantive US Healthcare LLC | NDA | View NDC → |
| ANHYDROUS DEXTROSE 20 g/L; LACTIC ACID 5.4 g/L; MAGNESIUM CHLORIDE 2.44 g/L; POTASSIUM CHLORIDE 0.314 g/L; SODIUM BICARBONATE 3.09 g/L; SODIUM CHLORIDE 6.46 g/L | Intravenous | Vantive US Healthcare LLC | NDA | View NDC → |
| ANHYDROUS DEXTROSE 20 g/L; LACTIC ACID 5.4 g/L; MAGNESIUM CHLORIDE 3.05 g/L; POTASSIUM CHLORIDE 0.314 g/L; SODIUM BICARBONATE 2.21 g/L; SODIUM CHLORIDE 7.07 g/L | Intravenous | Vantive US Healthcare LLC | NDA | View NDC → |
Showing 6 of 6 products — FDA National Drug Code Directory.
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride FDA approval history
How Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list no Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride recalls since July 2021.
✅No Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride supply and shortage status
Whether Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride brand names
Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride is sold under 9 brand names in the FDA directory — Prismasol Bgk4/0/1.2, Prismasol Bgk2/0, Prismasol B22gk4/0, Prismasol Bgk2/3.5 and others. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride: manufacturers and labelers
One company lists Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride products with the FDA. By number of product records, the largest are Vantive US Healthcare LLC. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Sources for this Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Baxter Healthcare Corporation is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →