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 →
📖 Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride: Patient Information Guide
A plain-language walkthrough of Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride — what it treats, how it works, how it’s taken, side effects, warnings and interactions. Tap any section to expand it.
🎯What it's used for▾
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 it works▾
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.
💊How it's taken▾
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.
🤒Side effects — in detail▾
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.
⚠️Warnings & precautions▾
- 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.
🔀What it interacts with▾
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.
This is not a complete list of interactions. Always talk with your doctor or pharmacist before starting, stopping, or changing any medication.
📋Before taking it▾
- 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.
🔬Pharmacokinetics — how your body processes it▾
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 it▾
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 Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Every point is grounded in that labeling — nothing is invented. How we use AI →
🩺 Pharmacist Counseling Corner
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? ▾
Will this affect my blood sugar? ▾
What side effects should I or my family watch for during treatment? ▾
I take other medications. Will CRRT wash them out of my system? ▾
Is it safe to use if I'm pregnant or breastfeeding? ▾
Can children receive PRISMASOL or PHOXILLUM? ▾
Is Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride available over the counter? ▾
When was Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride first available? ▾
💬 Answers drafted from Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Grounded in that labeling — nothing is made up. How we use AI →
🧰 Keep exploring
💊 How Dextrose Anhydrous / Lactic Acid / Magnesium Chloride / Potassium Chloride / Sodium Bicarbonate / Sodium Chloride 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 across the U.S. market
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.
🔍 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.
📈 What people report — real-world data (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.
🏛️ The road to your pharmacy
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.
🚨 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.
Source: openFDA drug enforcement (recall) reports.
📦 Supply & 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.
🏷️ Sold under these brand names
🏭 Manufacturers & labelers
🔬 Where this comes from
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 we combine label and product data
HelloPharmacist combines public FDA and NLM records; we don’t author the underlying clinical facts. We identified 1 FDA-filed SPL label set within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. The representative label is the starting point for the displayed reference monograph; the 12 largest stored in-scope SPL records, which may include that representative, are compared section by section, and the longest available version of each section is retained. Forms, routes, brands, labelers, product-listed strengths, and product-record counts are aggregated separately from ingredient-matched FDA NDC Directory records; package records listed above are associated with the linked SPL; and the normalized concept hierarchy comes from NLM RxNorm.
For canonical ingredient pages, bounded product-attributed indication and administration excerpts may be added to the AI evidence, and the generator is instructed to preserve available product, brand, route, and form qualifiers instead of treating one label as universal. Where a section is identified as AI-written, its plain-language text is generated from bounded label evidence. New draft drug pages remain in the admin review queue before first publication. Baxter Healthcare Corporation is the representative DailyMed label linked for verification and dates; it is not the sole source used for the page.
This is general education, not medical advice — always consult your doctor or pharmacist about your medications and any medical condition. For the exact wording of the linked representative label, view that label on DailyMed; some displayed composite sections may come from other in-scope SPL labels. Learn how we use AI and our data sources & update cadence.