Dextrose / Heparin
Heparin Sodium in Dextrose is an intravenous blood thinner used to treat and prevent dangerous blood clots, including deep vein thrombosis, pulmonary embolism, and clotting complications during surgery and dialysis.
🧬 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 / Heparin: Patient Information Guide
A plain-language walkthrough of Dextrose / Heparin — 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▾
Heparin Sodium in 5% Dextrose Injection is an intravenous anticoagulant (blood thinner) used to prevent and treat dangerous blood clots and related complications. All uses below apply to the IV formulation.
- Prevention and treatment of venous thrombosis (clots in the veins)
- Prevention and treatment of pulmonary embolism (clots in the lungs)
- Prevention and treatment of thromboembolic complications associated with atrial fibrillation
- Treatment of acute and chronic disseminated intravascular coagulation (DIC) — a dangerous condition where abnormal clotting and bleeding occur simultaneously
- Prevention of clotting during arterial and cardiac surgery
- Prevention and treatment of peripheral arterial embolism (clots blocking arteries in the limbs)
- Anticoagulant use during blood transfusions, extracorporeal (heart-lung bypass) circulation, and dialysis procedures
⚙️How it works▾
Heparin works by activating a natural blood protein called Antithrombin III. Once activated, Antithrombin III dramatically speeds up the shutdown of key clotting factors — especially Factor Xa and Factor IIa (thrombin). Heparin also blocks the final step of clot formation, preventing a stable fibrin mesh from being built. The result: new clots are stopped from forming, and existing ones can't grow. Heparin does not dissolve clots that already exist.
In some patients — including those with fever, active infection, cancer, heart attack, or a deficiency of Antithrombin III — heparin may be less effective (a phenomenon called heparin resistance). In those cases, more frequent blood monitoring and dose adjustments are needed.
💊How it's taken▾
Heparin Sodium in 5% Dextrose Injection is given by continuous intravenous infusion or intermittent IV injection in a hospital or clinical setting — it cannot be taken by mouth. Dosing is highly individualized and adjusted based on regular blood clotting tests (such as APTT). Your care team will monitor these results and adjust the rate of infusion accordingly.
- For continuous IV infusion, the infusion runs around the clock; clotting time is checked approximately every 4 hours early in treatment
- For intermittent IV injection, clotting tests are done before each injection in the early stages
- During cardiovascular surgery and dialysis, dosing follows specific protocols based on body weight and the equipment being used
- Platelet counts and blood counts (hematocrits) should also be checked regularly throughout therapy
🤒Side effects — in detail▾
The most common side effects of heparin include:
- Bleeding — the most frequent and potentially serious complication
- Low platelet count (thrombocytopenia)
- Heparin-induced thrombocytopenia and thrombosis (HIT/HITT) — a serious immune reaction
- High potassium levels (hyperkalemia)
- Elevated liver enzymes (AST and ALT)
- Allergic reactions: chills, fever, hives, and rarely severe anaphylactic shock
- Redness, pain, or ulceration at the infusion site
- With long-term high-dose use: bone thinning (osteoporosis) and temporary hair loss
Bleeding is the most important side effect to watch for. Any unusual bruising, blood in urine or stool, or unexpected drop in blood pressure should be reported to your care team immediately.
⚠️Warnings & precautions▾
- Fatal medication errors: Heparin comes in multiple concentrations. Confirming the correct strength before administration is critical — errors have caused fatal bleeding.
- Serious bleeding risk: Bleeding can occur anywhere in the body, including rare but life-threatening sites like the adrenal glands or behind the abdomen. People over 60 (especially women) face a higher risk. Blood pressure drops or falling blood counts should prompt immediate evaluation.
- HIT and HITT: Heparin can trigger an immune reaction that dangerously lowers platelet counts and, paradoxically, causes new blood clots. This can occur 5–10 days into treatment or within 24 hours in recently exposed patients. If suspected, heparin must be stopped immediately.
- Hyperkalemia (high potassium): Heparin can suppress the hormone aldosterone, raising potassium levels — especially in people with diabetes, kidney disease, or those on potassium-sparing medications. Potassium should be monitored during extended therapy.
- Hypersensitivity: This product contains sodium metabisulfite, which can cause severe allergic reactions in susceptible individuals, particularly those with asthma.
- Heparin resistance: Fever, active infection, cancer, and certain other conditions can make heparin less effective. More frequent monitoring may be needed.
🔀What it interacts with▾
Several medications can interfere with heparin's blood-thinning effect — either increasing your bleeding risk or reducing how well heparin works:
- Warfarin and other oral anticoagulants — combined use increases bleeding risk; timing of lab tests must be carefully coordinated
- NSAIDs (aspirin, ibuprofen, naproxen, indomethacin, celecoxib) — impair platelet function and raise bleeding risk with heparin
- Antiplatelet drugs (clopidogrel, dipyridamole, abciximab, eptifibatide, tirofiban) — significantly increase bleeding risk
- Hydroxychloroquine and dextran — interfere with platelet aggregation; use with caution
- Intravenous nitroglycerin — can reduce heparin's effect; a rebound increase in clotting may occur when nitroglycerin is stopped
- Digitalis, tetracyclines, nicotine, antihistamines — may partially counteract heparin's anticoagulant effect
- Antithrombin III (human) — dramatically amplifies heparin's effect in certain patients; heparin dose reduction is required to avoid excessive bleeding
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▾
- Do not use if you have a history of HIT (heparin-induced thrombocytopenia) or HITT — this is an absolute contraindication
- Do not use if you are allergic to heparin or pork products — heparin is derived from animal tissue
- Do not use if you have uncontrolled active bleeding (unless caused by DIC)
- Do not use if adequate blood clotting tests cannot be performed and monitored regularly (for full-dose heparin)
- Use with caution if you have liver or kidney disease — these conditions slow heparin clearance and can raise drug levels in the blood
- Use with caution if you are over 60, especially if female — higher bleeding risk has been reported in this group
- Tell your doctor if you are pregnant — published data do not show increased birth defect risk, but animal studies showed increased pregnancy loss at high doses; discuss the risks and benefits with your provider
- Breastfeeding: heparin is unlikely to pass into breast milk, and would not be absorbed by a nursing infant if it did — discuss with your doctor
- Children: pediatric dosing is based on clinical experience, not controlled studies; close monitoring is essential
- Tell your care team if you have asthma or a known sulfite allergy — this product contains sodium metabisulfite
- Tell your doctor if you have diabetes, chronic kidney failure, or take potassium-sparing medications — higher risk of high potassium (hyperkalemia)
🚑If you take too much▾
Too much heparin causes excessive bleeding. Early warning signs include easy bruising, tiny red spots on the skin (petechiae), nosebleeds, blood in the urine, or dark/tarry stools. If overdose is suspected, the heparin infusion should be stopped immediately. The antidote is protamine sulfate, a medication given slowly by IV that directly neutralizes heparin — but it carries its own risk of severe allergic reactions and must be given in a setting where emergency care is available.
📡Pharmacodynamics — effects in the body▾
Full therapeutic doses of heparin measurably prolong several blood clotting tests, including activated partial thromboplastin time (APTT) and whole blood clotting time — these tests are used to guide dosing. Low doses of heparin may not noticeably affect these tests. Heparin does not typically affect bleeding time. Patients over 60 may show longer APTTs compared to younger patients at the same dose, reflecting higher heparin levels in the blood.
🔬Pharmacokinetics — how your body processes it▾
Heparin cannot be absorbed through the digestive tract, so it must be given intravenously. When given by IV, it acts immediately. It binds extensively to proteins in the blood and has a small volume of distribution. Heparin is cleared mainly by the liver and certain immune cells; it is not broken down by enzymes. The half-life — how long it takes the body to clear half the drug — ranges from about 30 minutes to 2 hours, depending on the dose. People with kidney or liver disease, and adults over 60, may clear heparin more slowly and reach higher blood levels than others.
📦How to store it▾
Avoid excessive heat. Protect from freezing. Store at 20°C to 25°C (68°F to 77°F).
📄 Written from Dextrose / Heparin’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 / Heparin — the kind of thing our pharmacy team would talk through with you at the counter.
Why am I getting heparin through an IV instead of a pill? ▾
What's the biggest side effect I should watch out for? ▾
I heard heparin can actually cause clots. Is that true? ▾
Can I take my usual pain relievers like ibuprofen or aspirin while I'm on this? ▾
I'm pregnant — is heparin safe for my baby? ▾
Why do I need so many blood tests while I'm on heparin? ▾
Is Dextrose / Heparin available over the counter? ▾
When was Dextrose / Heparin first available? ▾
Who makes Dextrose / Heparin? ▾
💬 Answers drafted from Dextrose / Heparin’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 / Heparin comes
Dextrose / Heparin 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
- Heparin Sodium in Dextrose is used to prevent and treat venous thrombosis and pulmonary embolism
- Heparin Sodium in Dextrose is used to treat clotting complications associated with atrial fibrillation and disseminated intravascular coagulation (DIC)
- Heparin Sodium in Dextrose is used to prevent clotting during arterial and cardiac surgery and extracorporeal dialysis
- Heparin Sodium in Dextrose is used as an anticoagulant during blood transfusions and heart-lung bypass procedures
- Heparin Sodium in Dextrose is administered by intravenous infusion only — it must not be used as a catheter lock flush
- Heparin Sodium in Dextrose must not be mixed with other drugs in the same container
- Heparin Sodium in Dextrose should only be used if the solution is clear and the container and seals are intact — discard any unused portion
- Heparin Sodium in Dextrose infusion should not be run under pressure, and plastic containers should not be connected in series
📊 Dextrose / Heparin across the U.S. market
How Dextrose / Heparin 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.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
📈 How widely Dextrose / Heparin is used
A general measure of how commonly Dextrose / Heparin is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1 2025 – Q1 2026, summed across every form and brand of the drug.
Think of this as a proxy for how widely Dextrose / Heparin is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Dextrose / Heparin prescribed? Of the 1,596 medications we measure, Dextrose / Heparin ranks #1,200 by Medicaid prescriptions — more than 25% of them.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Dextrose / Heparin, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 3 of 3 listed Dextrose / Heparin NDCs with Medicaid activity.
🔍 Compare Dextrose / Heparin products
A representative set of FDA-listed product records for Dextrose / Heparin — 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 | ||||
| 5; 5000 g/100 mL; [USP'U]/100 mL | Intravenous | A-S Medication Solutions | NDA | Find on DailyMed ↗ |
| 5; 4000 g/100 mL; [USP'U]/100 mL | Intravenous | B. Braun Medical Inc. × 2 listings | NDA | View NDC → |
| 5; 5000 g/100 mL; [USP'U]/100 mL | Intravenous | B. Braun Medical Inc. × 2 listings | NDA | View NDC → |
| 5; 10000 g/100 mL; [USP'U]/100 mL | Intravenous | B. Braun Medical Inc. × 2 listings | NDA | View NDC → |
| HEPARIN SODIUM 4000 [USP'U]/100 mL; DEXTROSE MONOHYDRATE 5 g/100 mL | Intravenous | B. Braun Medical Inc. | NDA | View NDC → |
| HEPARIN SODIUM 5000 [USP'U]/100 mL; DEXTROSE MONOHYDRATE 5 g/100 mL | Intravenous | B. Braun Medical Inc. | NDA | View NDC → |
| HEPARIN SODIUM 10000 [USP'U]/100 mL; DEXTROSE MONOHYDRATE 5 g/100 mL | Intravenous | B. Braun Medical Inc. | NDA | View NDC → |
Showing 10 of 10 products — FDA National Drug Code Directory. See every product, package size and price: browse all 10 Dextrose / Heparin NDCs →
📈 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 / Heparin — 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 / Heparin 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 / Heparin 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 / Heparin 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.
🏭 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. B. Braun Medical Inc. 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.