Intralipid

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Medically reviewed

Laura Arias

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Intralipid

Property Description
Active Ingredient Refined Soybean Oil, Egg Yolk Phospholipids, Glycerin
Form Sterile Emulsion for Injection (Oil-in-Water Emulsion)
Pharmacological Class Lipid Emulsions for Intravenous Nutrition
Common Use Providing nutritional support (Parenteral Nutrition)
Origin Derived from natural sources (plant and egg)

What is Intralipid and Its Role in Nutritional Support?

Intralipid is a foundational medication formally classified as a Lipid Injectable Emulsion, a sterile and highly specialized product delivered directly into the patient’s bloodstream for essential nutritional purposes. This pharmaceutical entity belongs to the pharmacological class of Lipid Emulsions for Intravenous Nutrition and serves as a vital component of total parenteral nutrition (PN) regimens. The general role of Intralipid is to provide concentrated calories and necessary fat molecules, supporting patients who are unable to receive adequate nourishment or sustain metabolic functions through normal oral or gastrointestinal feeding routes. This type of infusion is necessary when adequate nutrition cannot be obtained by any other means. This formulation is clinically recognized for its reliability in delivering long-chain triglycerides and is a common choice for both adult and pediatric patients requiring prolonged intravenous feeding. It provides crucial support for energy demands and the maintenance of essential bodily systems during periods of inadequate intake.


Composition: Essential Lipids and Natural Origin

Intralipid is an Oil-in-Water Emulsion primarily comprising Refined Soybean Oil, stabilized by Egg Yolk Phospholipids, with Glycerin included to ensure appropriate osmolality. This product is derived from natural sources, utilizing purified plant oil and egg components to deliver fat in a form the body can readily process. The soybean oil is specifically important because it supplies Essential Fatty Acids—notably Linoleic Acid and alpha-Linolenic Acid—which the human body cannot synthesize but requires for crucial biological processes, including cell structure and immune function. The administration of lipid emulsions is essential for preventing or reversing the biochemical signs of Essential Fatty Acid Deficiency in patients receiving long-term parenteral nutrition. Providing these lipids ensures that the patient receives a necessary macronutrient vital for caloric balance and the prevention of Essential Fatty Acid Deficiency.

What side effects are possible with Intralipid?

Possible Side Effects and Safety Information

Intralipid's safety profile is based on clinical data and official regulatory documentation, detailing potential adverse reactions and necessary safety precautions.


Common and Less Frequent Reactions

Adverse reactions are classified by frequency, with Common (ge 1/100 to < 1/10) reactions potentially including fever (pyrexia), nausea, and vomiting. Less frequent reactions may include dyspnea, cyanosis, headache, and allergic reactions.

Reactions are often grouped by System-Organ-Class, such as Hepatobiliary Disorders (e.g., cholestasis, hepatic steatosis) and Blood and Lymphatic System Disorders (e.g., anemia).


Serious Adverse Reactions and Key Warnings

Several serious risks are documented, including potentially fatal events like Fat Overload Syndrome, which is characterized by fever, leukocytosis, and shock. Anaphylaxis and other severe hypersensitivity reactions have been reported. A major long-term concern is Parenteral Nutrition-Associated Liver Disease (PNALD), which can progress to liver failure, especially with prolonged administration.

Neonates and infants are a specific at-risk population, where rapid infusion can lead to Clinical Decompensation, including acute respiratory distress, metabolic acidosis, and death.


Safety Restrictions and Monitoring

Intralipid is contraindicated in patients with severe disorders of lipid metabolism, such as severe hypertriglyceridemia (serum triglycerides exceeding 1,000 mg/dL), and in those with known hypersensitivity to egg, soybean, or peanut protein. Mandatory safety monitoring includes regular measurement of serum triglycerides to confirm the body's fat clearance capacity and periodic liver function tests to check for the development of PNALD.

Overdose and Emergency Response

Overdose and When to Seek Help — Official Regulatory Information

The official overdose profile for Intralipid, a lipid injectable emulsion, is defined by the risk of developing Fat Overload Syndrome (FOS). This potentially life-threatening event results from administering the emulsion too quickly or exceeding the patient’s capacity to clear the fat from the circulation.

Attribute Official Regulatory Statement
Documented Overdose Presentations Manifestations of FOS include fever, abdominal pain, jaundice, hepatomegaly, and splenomegaly. Laboratory findings include elevated serum triglycerides and transient increases in liver function test results (e.g., transaminases).
Population-Specific Overdose Notes Neonates and infants are at a higher risk of severe outcomes, including acute respiratory distress, metabolic acidosis, and death after rapid infusion. Patients with impaired lipid metabolism, such as those with severe liver dysfunction, are also at increased risk.
Emergency-Response Statements In the event of fat overload during therapy, the infusion must be stopped immediately. Management involves symptomatic and supportive treatment, as no specific antidote is known.
When Immediate Medical Help is Required Urgent medical help must be sought immediately if any signs of the severe Fat Overload Syndrome or acute, serious adverse reactions occur.

The regulatory profile mandates that the primary action in overdose is the immediate cessation of the infusion, coupled with close medical monitoring to assess the patient’s ability to clear the excess fat. The appearance of documented FOS manifestations is the regulator-defined trigger for seeking urgent assistance.

Therapeutic Uses of Intralipid

What Intralipid Treats: Main Uses and Benefits

Intralipid, a sterile fat emulsion, is commonly used to provide essential supportive therapy in clinical settings that involve acute or unstable symptom patterns, helping support the patient during periods of heightened physiological stress. The medicine assists with easing the overall symptom load across several therapeutic domains.

Intralipid is commonly applied in contexts where additional symptomatic support for nutrient deficits is needed, such as in situations requiring parenteral nutrition and to address symptoms associated with essential fatty acid deficiency.

Comprehensive Symptomatic Support

This therapeutic domain is applied in situations involving certain distressing symptoms linked to nutrient deficits when a patient cannot receive sufficient sustenance orally or enterally. The primary purpose is to provide support that helps ease the overall burden of symptoms related to systemic imbalance, such as those associated with malnutrition. This is considered relevant during phases of heightened physiological stress, like after major surgery or during severe illness. It is also commonly used when supportive symptom management is appropriate in conditions characterized by periods of heightened symptoms, including extensive burns or severe infections.

“It provides support that helps ease the overall burden of symptoms during periods of heightened physical distress.”


Quick Fact: Support for Symptoms of Physiological Strain


Assistance with Specific Symptom Groups

Intralipid is relevant for managing symptoms that interfere with daily comfort or create noticeable physiological strain. It assists with maintaining functional stability when symptoms of increased neurological or muscular activity become more noticeable.

Regulatory References

  1. Label: INTRALIPID- iv fat emulsion emulsion - DailyMed

Eligibility and Restrictions for Use

Intralipid is officially authorized for use across the entire lifespan, including adults, pediatric patients, infants, and preterm and term neonates for nutritional support. Eligibility, however, is strictly defined by regulatory contraindications and restrictions.

Populations That Must Not Use Intralipid (Contraindicated)

Individuals are absolutely excluded if they have a known hypersensitivity to egg, soybean, or peanut protein, or to any ingredient in the product. The medicine is also contraindicated in patients with severe disorders of lipid metabolism, including pathologic hyperlipemia, or hypertriglyceridemia with serum levels greater than 1,000 mg/dL [2.1, 3.2].

Restricted and Conditional Use

Use requires caution in patients with conditions such as severe liver damage, impaired kidney function, anemia, or blood coagulation disorders [1.1, 1.3].

Age and Formulation: While approved for all age groups, the Intralipid 30% formulation is not recommended for use in infants and children due to a lack of regulatory experience [3.2].

Pregnancy and Lactation: Intralipid should be used during pregnancy only if clearly needed due to a lack of animal reproduction studies. Caution is advised when the medicine is administered to a nursing woman [1.3].

What should I know about interactions with other medicines?

Intralipid’s official interaction profile is defined by its component effects, material restrictions, and influence on diagnostic testing, as formally documented by government regulatory bodies.

Interactions with Medicinal Products

The primary medicinal interaction documented is a pharmacodynamic effect with Vitamin K Antagonists, including Warfarin and related coumarin derivatives. The Vitamin K1 component, derived from the soybean oil in the emulsion, may formally counteract the anticoagulant activity of these medicines. This officially recognized interaction requires the increased monitoring of coagulation parameters and may necessitate the upward adjustment of the anticoagulant dose to maintain its intended effect.

Administration and Procedural Constraints

Intralipid's physicochemical nature dictates specific constraints on its administration. Infusion sets and lines that utilize Polyvinyl Chloride (PVC) plasticized with Di-2-ethylhexyl phthalate (DEHP) must not be used, as the emulsion is known to leach DEHP from the material. This represents a mandatory restriction on co-administration materials. Additionally, the presence of circulating lipids may interfere with certain laboratory measurements (such as bilirubin or haemoglobin) if blood sampling occurs before the infused fat has adequately cleared from the bloodstream, a procedural constraint defined in regulatory documents.

Mechanism of Action

The Lipid Sink Mechanism: Sequestration and Redistribution

This mechanism involves the lipid emulsion forming an "oil phase" in the bloodstream, which acts as a scavenger to absorb and remove highly lipophilic substances from sensitive tissues like the heart and brain. This physical sequestration rapidly lowers the concentration of these substances at their molecular targets, contributing to the re-establishment of electrical stability across neuronal cell membranes.

Metabolic and Myocardial Support

The emulsion supplies a concentrated source of long-chain fatty acids which are made available to cardiac muscle cells as a substrate for energy production. This metabolic pathway enhances mitochondrial function within the heart muscle, supporting the necessary energy requirement for myocardial contraction.

Membrane and Ion Channel Modulation

The structural components of the lipid emulsion may directly interact with the lipid bilayer of cell membranes in the heart and nervous system. This interaction alters the local environment of crucial voltage-gated ion channels, influencing electrical signaling dynamics within cell membranes and facilitating the potential for regulated ion flux across cell membranes.

Dosage and Administration Information

How Intralipid is Used: Official Administration Guidelines

Intralipid (a lipid injectable emulsion) is administered solely by Intravenous Infusion. Specific concentration and flow rate requirements are established for its delivery as a component of parenteral nutritional support. The medicine is intended for use over extended periods of time, typically when nutritional support is required for more than five days.


Dosing and Administration Constraints

Category Official Instruction / Principle
Administration Route Exclusively by Intravenous Infusion (peripheral or central vein).
Adult Maximum Dose Should not exceed 2.5 g fat/kg/day (grams of fat per kilogram of body weight per day).
Maximum Infusion Rate Must not exceed 0.1 g fat/kg/hour for the 20% concentration.

Preparation and Specific Use Rules

Intralipid is supplied in multiple concentrations, including 10%, 20%, and 30% forms. The 30% concentration is designated as a Pharmacy Bulk Package and is not intended for direct infusion; it must first be admixed with other components into a Total Nutrient Admixture (TNA).

The administration process requires specific equipment and control: the flow rate must be controlled by an infusion pump, and the use of a 1.2 micron in-line filter is mandatory. For pediatric patients (neonates and infants), the infusion is generally administered continuously over 24 hours, with a maximum dose of 3 g fat/kg/day. Once prepared, the final nutrient admixture must be fully infused within 24 hours.

Recent Clinical Evidence

Intralipid is an intravenous fat emulsion primarily indicated as a source of calories and essential fatty acids for adult and pediatric patients requiring parenteral nutrition (PN), as well as for the prevention of essential fatty acid deficiency (EFAD).


Clinical Applications in Parenteral Nutrition

Clinical research focuses heavily on the use of Intralipid and comparable lipid emulsions in the context of long-term PN, especially in vulnerable populations. These studies often track long-term safety profiles, including liver function and triglyceride clearance.

  • Long-Term Tolerability: Prolonged use of soybean-oil-based lipid emulsions like Intralipid has been associated with risks such as Parenteral Nutrition-Associated Liver Disease (PNALD), particularly cholestasis in neonates. Comparative trials have investigated newer, mixed-oil emulsions to see if they offer a reduced risk profile for liver complications compared to Intralipid.
  • Fatty Acid Metabolism: Studies continue to evaluate the proper balance of omega-6 and omega-3 fatty acids supplied by lipid emulsions to optimize essential fatty acid status and minimize inflammatory potential in PN patients.

Investigational and Adjunctive Uses

Intralipid is also the reference formulation for its use in Lipid Resuscitation Therapy (LRT), an established clinical practice for the emergency management of local anesthetic systemic toxicity (LAST). The proposed mechanism involves the creation of a lipid-rich phase in the bloodstream (often termed the 'lipid sink' or 'lipid shuttle'), which sequesters lipophilic drug molecules from target organs like the heart and brain.

Separately, in the area of reproductive health, clinical evidence regarding the use of intravenous Intralipid infusions to improve outcomes in women with repeated implantation failure (RIF) or recurrent pregnancy loss (RPL) is inconsistent and controversial. While some systematic reviews suggest a potential benefit in specific patient groups, other controlled studies have found no improvement, and well-designed, large-scale randomized controlled trials are still needed to confirm any therapeutic efficacy.

Frequently Asked Questions (FAQ)

Common questions about Intralipid (FAQ)

Q: Why do people sometimes mention Intralipid in relation to fertility?

A: Intralipid has been a subject of research for specific issues related to reproductive health, such as repeated implantation failure (RIF) and recurrent pregnancy loss (RPL), which is commonly known as recurrent miscarriage. It is important to know that official information from scientific reviews indicates that the clinical evidence regarding a benefit in this context is currently inconsistent and controversial.

Q: How fast does Intralipid start to have an effect on the body?

A: For its official purpose of nutrition, the body continuously processes the emulsion throughout the infusion period. For an investigational use, such as treating local anesthetic drug toxicity, official documentation describes the rapid creation of a 'lipid sink' mechanism. This works quickly to physically absorb lipophilic substances in the bloodstream, rapidly reducing the concentration of the harmful substance at target organs.

Q: Can Intralipid cause weight gain since it's a fat emulsion?

A: Intralipid is formally indicated as a primary source of calories for patients receiving intravenous feeding. As an essential energy source, it helps meet the patient’s caloric requirements. Like all sources of energy, Intralipid contributes to a patient’s total daily energy intake and balance.

Q: How long does a typical Intralipid infusion usually take?

A: The infusion rate must be carefully controlled, often using a pump, according to official administration guidelines. Official guidance states that the infusion rate should not exceed 0.1 grams of fat per kilogram of body weight per hour. For infants and neonates, the official administration is typically a continuous infusion over a 24-hour period.

Q: Does Intralipid affect blood sugar levels?

A: As Intralipid provides a concentrated energy substrate to the body, it is relevant to overall metabolic function. Official clinical trial data reports that hyperglycemia, which is an elevated blood sugar level, has been observed as an adverse reaction in some pediatric patients.

Q: Can Intralipid interact with blood pressure medications?

A: The official product label only documents a formal drug interaction with Vitamin K Antagonists (such as Warfarin). While specific interactions with blood pressure medications are not detailed, hypertension (high blood pressure) is listed as an adverse reaction in some adult patients. Monitoring of cardiovascular health is a standard practice during treatment with Intralipid.

Q: Why do some forums discuss Intralipid for recurrent miscarriage?

A: Recurrent miscarriage is medically referred to as Recurrent Pregnancy Loss (RPL). Intralipid has been investigated for potential use in treating this condition and repeated implantation failure (RIF). This is considered an investigational use, and the formal clinical evidence supporting its effectiveness remains inconclusive.

Q: Why is it important to know your triglyceride levels before Intralipid?

A: Monitoring serum triglyceride levels is a mandatory safety precaution specified in regulatory documents. This is done to confirm the patient’s capacity to clear the infused fat from their bloodstream. The levels are monitored to ensure the medication is not administered in the presence of severe hypertriglyceridemia, which is a state of severe lipid metabolism disorder.

Q: What should a patient do if they notice redness or swelling at the injection site?

A: If signs of redness, pain, or swelling are noticed at the infusion site, or any sign of a severe reaction, the infusion is typically halted immediately. Official safety guidelines require that patients be monitored for signs of hypersensitivity, such as rash or swelling. Appropriate treatment is initiated by the supervising clinician if a reaction is suspected.

Q: Is it normal to feel tired or dizzy after an Intralipid treatment?

A: Official reports on the medicine's safety profile indicate that feeling dizzy and experiencing unusual tiredness or weakness are listed as less common adverse reactions. Any concerning effects should be promptly communicated to the supervising healthcare team.

Q: Is an allergic reaction to Intralipid common, and what does it look like?

A: Severe allergic reactions, including anaphylaxis, have been reported in the product safety information. Signs of a reaction can include rash, itching, trouble breathing, or swelling of the face, hands, or mouth. The product information states the medicine is contraindicated for patients with known hypersensitivity to egg, soybean, or peanut protein.

Q: Does Intralipid affect the results of a routine blood test?

A: Yes, regulatory information notes that the presence of circulating lipids in the blood can interfere with the results of certain laboratory measurements. This includes tests for substances such as bilirubin or haemoglobin. Blood sampling should be timed to occur after the infused fat has had sufficient time to clear from the bloodstream.

Q: Are there any long-term side effects associated with repeated Intralipid infusions?

A: For patients receiving repeated or prolonged infusions, a major long-term concern documented in official warnings is Parenteral Nutrition-Associated Liver Disease (PNALD). This can include conditions like cholestasis or hepatic steatosis and, in serious cases, may progress to liver failure.

Q: Does Intralipid help with inflammation?

A: Intralipid supplies essential fatty acids that the body requires for critical biological processes. Scientific studies in the area of nutritional support focus on balancing the different types of fatty acids provided to both maintain essential fatty acid status and to minimize potential inflammatory responses in patients.

Q: What happens if Intralipid is infused too quickly?

A: The maximum infusion rate must be carefully followed as rapid infusion can lead to serious adverse reactions. In neonates and infants, official warnings state that rapid infusion can lead to a potentially fatal condition called Clinical Decompensation, involving acute respiratory distress and metabolic acidosis.

Q: Are there specific age limits for who can safely use Intralipid?

A: Intralipid is officially approved for use across the entire lifespan, including adults and all pediatric patients. However, the 30% concentration is specifically not recommended for use in infants and children due to limited regulatory experience with that specific strength in those age groups.

Q: Are headaches a common adverse effect of Intralipid?

A: The official product safety information lists headache as a less frequent adverse reaction reported to have occurred in clinical trials. It is not classified among the most common effects like fever or nausea.

Q: Can Intralipid make you feel nauseous?

A: Yes, nausea is classified as a common adverse reaction associated with the administration of Intralipid. It is one of the more frequently reported side effects in the official safety profile.

Q: How often can someone generally receive Intralipid infusions?

A: Intralipid is intended for use over extended periods of time when nutritional support is required for more than five days. It is often administered as a part of a patient's daily total parenteral nutrition regimen to provide a continuous source of essential fats.

Q: Is there any scientific study on Intralipid's less common applications?

A: Yes, official scientific literature confirms that Intralipid is the reference medication for its use in Lipid Resuscitation Therapy (LRT) to manage local anesthetic systemic toxicity. Its use for reproductive issues is also a subject of ongoing clinical investigation.

Q: Does Intralipid contain any preservatives?

A: The official product description lists Refined Soybean Oil, Egg Yolk Phospholipids, and Glycerin as its main components. It is provided in single-dose containers intended for immediate use or storage for a short period under refrigeration.

Q: Can Intralipid interact with thyroid medications?

A: Official regulatory documents only contain a documented drug interaction with Vitamin K Antagonists (like Warfarin). There is no specific official information published in the product labeling regarding an interaction with thyroid medications.

Q: Is it possible to become dependent on Intralipid for nutrition?

A: Intralipid is utilized based on clinical need to provide necessary calories and essential fats when a patient cannot obtain adequate nutrition through normal oral or gastrointestinal feeding routes. Its use is based on the patient's specific clinical requirement for this method of nutritional support.

Q: Why do some people confuse Intralipid with Dextrose?

A: Both Intralipid (a fat emulsion) and Dextrose (a sugar solution) are critical sources of calories and energy used to create total parenteral nutrition (TPN) mixtures. Because they are the two main energy components of intravenous feeding, they are frequently discussed together in the context of TPN.

Q: Does the body break down Intralipid quickly or slowly?

A: The rate at which the body breaks down and eliminates the infused fat is variable among patients. Regulatory documentation requires mandatory monitoring of serum triglycerides to ensure the patient's capacity to effectively clear the fat from their circulation is not exceeded.

How should Intralipid be stored and disposed of?

Intralipid must be stored and handled according to specific regulatory conditions to maintain its stability. The unadmixed product must be stored at a temperature not exceeding 25 C (77 F).

Storage Requirements

Condition Regulatory Rule
Temperature Do not store above 25 C. Do not freeze; discard the bag if accidentally frozen.
Light Protection The solution, including admixtures, must be protected from ambient light, especially during administration to neonates and children below 2 years.
Container Integrity The bag must be visually inspected for discoloration or emulsion separation (oily droplets); if the emulsion is not homogenous or white, the product must be discarded.
Child Safety Keep this medicine out of the sight and reach of children.

Stability and Disposal

Single-dose containers should be infused immediately after the overpouch is removed. If immediate use is not possible, the product may be stored under refrigeration (2 C to 8 C) for no longer than 24 hours. The unused portion of the product or any remaining admixture must be discarded in accordance with local pharmaceutical waste disposal protocols, and the product must not be used after the expiry date.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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