Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
The electronic medicines compendium (emc) no longer publishes a Summary of Product Characteristics for this product, which usually means it is no longer marketed in the UK. The patient leaflet below is kept for reference, but the product may not be available.
If you were prescribed this medicine, other products containing Soya bean oil, refined, Medium-chain triglycerides may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.
for
Lipofundin MCT/LCT 20% is a milky white, sterile emulsion. Lipofundin MCT/LCT 20% is used to provide fat, including essential fatty acids to patients needing to be fed intravenously (through a small tube placed into a vein) because they are unable to eat food normally or the normal intake is not enough. The oils contained in Lipofundin MCT/LCT 20% are foodstuffs and they act as sources of energy and provide an essential nutrient, the essential fatty acids.
2.
e Lipofundin MCT/LCT 20%
Do not use Lipofundin MCT/LCT 20%
Children In infants at risk of jaundice the blood fat (serum triglyceride) and bilirubin levels should be monitored by your doctor. It may become necessary for your doctor to adjust the daily fat doses.
Other medicines and Lipofundin MCT/LCT 20% Tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. Lipofundin MCT/LCT 20% can interact with some other medicines. Tell your doctor if you are taking or receiving certain medicines to control your blood clotting, namely: ● heparin ● coumarin products, for example warfarin. Pregnancy and breast-feeding If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. There are no adequate data from the use of Lipofundin MCT/LCT 20% in pregnant women. If you are pregnant you will receive this medicine only if the doctor considers it absolutely necessary for your recovery. Breast-feeding is not recommended for mothers on parenteral nutrition. Driving and using machines Lipofundin MCT/LCT 20% is normally given to immobile patients in a controlled setting (a hospital or clinic). This will exclude driving and using machines. Lipofundin MCT/LCT 20% contains sodium This medicine contains less than 1 mmol sodium (23 mg) per litre, i.e. it is essentially 'sodium-free'.
3.
Lipofundin MCT/LCT 20%
This medicine is administered by intravenous infusion (drip), that is, through a small tube directly into a vein. The following doses are recommendations for guidance. Your doctor will decide how much of this medicine you need and for how long you will require treatment with this medicine. Adults The usual dose is 0.7 – 1.5 g lipids/kg body weight per day. A maximum dose of 2.0 g lipids/kg body weight/day, for instance when your energy requirements are high or your fat utilisation is increased (e.g. cancer patients), should not be exceeded by your doctor. In the following patient groups the provision of intravenous lipids should not exceed 1.0 g/kg body weight/day: ● Patients on long-term home parenteral nutrition treatment (> 6 months) ● Patients with short bowel syndrome For a patient weighing 70 kg a daily dose of 2.0 g/kg body weight/day corresponds to a maximum daily dose of 700 ml Lipofundin MCT/LCT 20%. Paediatric population A successive increase of the lipid dose in steps of 0.5 – 1.0 g/kg body weight/day may be beneficial. It can help the doctor to monitor the increase of the plasma triglyceride level and to prevent too high blood fat levels (hyperlipidaemia).
Infants (0-2 years of age) It is recommended not to exceed a daily lipid dose of 3.0 (max. 4.0) g/kg body weight/day. In this age group the daily dose of lipids should be infused continuously over about 24 hours. Children and adolescents (>2 years of age) It is recommended not to exceed a daily lipid dose of 2.0 – 3.0 g/kg body weight/day. Infusion rate The infusion should be administered at the lowest possible infusion rate. During the first 15 minutes the infusion rate should only be 50% of the maximum infusion rate to be used. The doctor should monitor the patient closely for the occurrence of side effects. Maximum infusion rate Adults Up to 0.15 g lipids/kg body weight/hour. For a patient weighing 70 kg this corresponds to a maximum infusion rate of 52.5 ml per hour Lipofundin MCT/LCT 20%. The amount of lipids administered then is 10.5 g per hour. Infants (0-2 years of age) Up to 0.17 g lipids/kg body weight/hour. Children and adolescents (>2 years of age) Up to 0.13 g lipids/kg body weight/hour. If you use more Lipofundin MCT/LCT 20% than you should If you have received too much Lipofundin MCT/LCT 20%, you may get abnormally high blood fat levels (hyperlipidaemia), your blood may become too acidic (metabolic acidosis) or you may suffer from a so-called 'fat overload syndrome'. For symptoms of the fat overload syndrome please see section 4 "Possible side effects". If you have received too much Lipofundin MCT/LCT 20%, the infusion will be stopped. The infusion will not be started again until you have recovered. It may be necessary for your doctor to adjust the daily fat doses. Your doctor will decide on any additional treatment.
4.
Like all medicines, Lipofundin MCT/LCT 20% can cause side effects, although not everybody gets them.
The following side effects may be serious. If any of the following side effects occur, tell your doctor immediately, he will stop giving you this medicine: Very rare (may affect up to 1 in 10,000 people) ● allergic reactions, for example skin reactions, shortness of breath, swelling of the lips, mouth and throat, difficulty breathing ● breathing problems (dyspnoea) ● bluish skin (cyanosis) Other side effects: Very rare (may affect up to 1 in 10,000 people)
● ● ● ● ● ● ● ● ● ● ● ● ● ● ●
fat overload syndrome (see "Fat overload syndrome" below) increased tendency of your blood to clot (hypercoagulability) abnormally high blood fat levels (hyperlipidaemia) abnormally high blood sugar levels (hyperglycaemia) metabolic conditions where your blood becomes acidic (metabolic acidosis, ketoacidosis) decrease or increase in blood pressure drowsiness feeling sick, vomiting, loss of appetite headache flush reddening of the skin (erythema) high body temperature sweating feeling cold, chills pain in the back, bones, chest and lumbar region
Not known (frequency cannot be estimated from the available data) ● impaired bile flow (cholestasis) ● reduction of white blood cell count (leukopenia) ● reduction of blood platelet count (thrombocytopenia) Fat overload syndrome: You might suffer from a "fat overload syndrome" if you have received too much Lipofundin MCT/LCT 20% or when your body has problems using fat. Your body's ability to use fat might be influenced by a sudden change in your condition (due to renal problems or an infection). The symptoms are usually reversible if the infusion is stopped. A fat overload syndrome is characterised by the following symptoms: ● ● ● ● ● ● ● ● ● ● ● ● ●
high blood fat levels (hyperlipidaemia) fever deposition of fat in the liver or other organs (fat infiltration) enlargement of the liver (hepatomegaly), which may sometimes be accompanied by jaundice (icterus) enlargement of the spleen (splenomegaly) reduction of red blood cell count (anaemia) reduction of white blood cell count (leukopenia) reduction of blood platelet count (thrombocytopenia) disorder of blood clotting rupture of blood cells (haemolysis) increase in immature red blood cells (reticulocytosis) abnormal liver function tests loss of consciousness
Reporting of side effects If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can also report side effects directly via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.
5.
Lipofundin MCT/LCT 20%
Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date that is stated on the label. The expiry date refers to the last day of that month. Do not store above 25°C. Store bottles in the outer carton, in order to protect from light. Do not freeze. Emulsions that have been frozen must be discarded. Do not use if Lipofundin MCT/LCT 20% if you notice:
6.
What Lipofundin MCT/LCT 20% contains Lipofundin MCT/LCT 20% is an emulsion of oils in water. It contains 20 percent (weight per volume) of a mixture of oils.
8095 kJ/l ≙ 1935 kcal/l 380 mOsm/l < 0.5 mmol/l 6.0 – 8.5
What Lipofundin MCT/LCT 20% looks like and contents of the pack Lipofundin MCT/LCT 20 % is a milky white, sterile emulsion for infusion (i.e., for administration directly into a vein.), contained in glass bottles of 100 ml, 250 ml or 500 ml size. It is available in packs of: 10 x 100 ml, 10 x 250 ml, 10 x 500 ml Not all pack sizes may be marketed. Marketing Authorisation Holder and Manufacturer: B. Braun Melsungen AG, Carl-Braun-Straße 1, 34212 Melsungen,
Germany; Telephone.: +49-5661-71-0 Fax: +49-5661-71-4567 Postal address 34209 Melsungen, Germany.
This leaflet was last revised in December 2021 The following information is intended for healthcare professionals only: Additional special warnings and precautions for use Mixing with incompatible substances might lead to breaking of the emulsion or to precipitation of particles, both resulting in a high risk of embolism. In solutions with higher lipid concentration (e.g. Lipofundin MCT/LCT 20%), the ratio of emulsifier (phospholipid) to oil is lower than in lower concentrated lipid emulsions. This ensures a favourable lower plasma concentration of triglycerides, phospholipids, free fatty acids as well as the pathological lipoprotein X in the patient`s blood. Therefore higher concentrated lipid emulsions like Lipofundin MCT/LCT 20% should be preferred over lower concentrated lipid emulsions. Interference with laboratory tests Lipids may interfere with certain laboratory tests (such as bilirubin, lactate dehydrogenase, oxygen saturation) when the blood sample is taken before the lipids have been eliminated from the bloodstream; this may take 4 to 6 hours. Incompatibilities Lipofundin MCT/LCT 20% must not be used as carrier solution for electrolyte concentrates or other pharmaceuticals nor must the emulsion be mixed with other infusion solutions, since adequate stability of the emulsion would no longer be guaranteed. Special precautions for disposal and other handling Shake gently prior to use. The emulsion has to be brought to room temperature unaided prior to infusion, i.e., the product should not be put in a heating device (such as oven or microwave). If filters are used they must be permeable to lipids. Before infusing a lipid emulsion together with other solutions via a Y connector or bypass set, the compatibility of these fluids should be checked, especially when co-administering carrier solutions to which medicinal products have been added. Particular caution should be exercised when co-infusing solutions that contain divalent electrolytes (such as calcium or magnesium). Method of administration Lipid emulsions are suitable for peripheral venous administration and can also be administered separately via peripheral veins as part of total parenteral nutrition. The Y- or the bypass connector should be placed as close to the patient as possible, if lipid emulsions are co-administered with amino acid and carbohydrate solutions. The duration of administration of Lipofundin MCT/LCT 20% is usually 1 – 2 weeks. If parenteral nutrition with lipid emulsions is further indicated, Lipofundin MCT/LCT 20% can be administered over longer periods provided appropriate monitoring is employed.
Lipofundin MCT/LCT 20 %, emulsion for infusion comes as infusion. Always follow the dose your doctor or pharmacist has given you, and read the leaflet that comes with the medicine.
The active substance in Lipofundin MCT/LCT 20 %, emulsion for infusion is soya bean oil, refined, medium-chain triglycerides.
This leaflet reproduces the patient information leaflet approved for Lipofundin MCT/LCT 20 %, emulsion for infusion, as published on the electronic medicines compendium (emc). The version printed inside your medicine’s packaging is the one that applies to you.
Whether a medicine is available over the counter or on prescription only depends on its licence. Check the leaflet, or ask your pharmacist — they can tell you straight away.
The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.
Lipofundin MCT/LCT is indicated as a source of calories and essential fatty acids for patients requiring parenteral nutrition.
Posology
Maximum daily doses should only be administered after stepwise increase with careful monitoring of the tolerance of the infusions.
The utilisation of intravenous lipids depends on e.g. the severity of underlying disease, body weight, gestational and postnatal age and specific body functions.
Depending on energy requirements, the following daily doses are recommended:
Adults
The usual dose is 0.7 to 1.5 g lipids/kg body weight (b.w.) per day. A maximum dose of 2.0 g lipids/kg b.w./d, for instance when energy requirements are high or fat utilisation is increased (e.g. oncology patients), should not be exceeded. For long-term home parenteral nutrition treatment (> 6 months) and in patients with short bowel syndrome the provision of intravenous lipids should not exceed 1.0 g/kg b.w./d.
For a patient weighing 70 kg a daily dose of 2.0 g/kg b.w./d corresponds to a maximum daily dose of 700 ml Lipofundin MCT/LCT 20%.
Paediatric population
A gradual increase of lipid intake in increments of 0.5 – 1.0 g/kg b.w./d may be beneficial regarding the possibility to monitor the increase of the plasma triglyceride level and prevent hyperlipidaemia.
Preterm newborn infants, term newborn infants, infants and toddlers
It is recommended not to exceed a daily dose of 3.0 (max. 4.0) g/kg b.w./d of lipids.
In preterm newborn infants, term newborn infants, infants and toddlers, the daily dose of lipids should be infused continuously over about 24 hours.
Children and adolescents
It is recommended not to exceed a daily lipid dose of 2.0 – 3.0 g/kg b.w./d.
Infusion rate
The infusion should be administered at the lowest possible infusion rate. During the first 15 minutes the infusion rate should only be 50% of the maximum infusion rate to be used.
The patient should be monitored closely for the occurrence of adverse reactions.
Maximum infusion rate
Adults
Up to 0.15 g/kg b.w./h lipids.
For a patient weighing 70 kg this corresponds to a maximum infusion rate of 52.5 ml per hour Lipofundin MCT/LCT 20%. The amount of lipids administered then is 10.5 g per hour.
Preterm newborn infants, term newborn infants, infants and toddlers
Up to 0.17 g/kg b.w./h lipids.
Children and adolescents
Up to 0.13 g/kg b.w./h lipids.
Method of administration
Intravenous use.
Lipid emulsions are suitable for peripheral venous administration and can also be administered separately via peripheral veins as part of total parenteral nutrition.
The Y- or the bypass connector should be placed as close to the patient as possible, if lipid emulsions are co-administered with amino acid and carbohydrate solutions.
The duration of administration of Lipofundin MCT/LCT 20% is usually 1 - 2 weeks. If parenteral nutrition with lipid emulsions is further indicated, Lipofundin MCT/LCT 20% can be administered over longer periods provided appropriate monitoring is employed.
When used in infants aged from preterm to 2 years old, the emulsion (including administration sets) should be protected from light exposure after preparation for infusion until administration is completed (see sections 4.4, 6.3 and 6.6).
● Hypersensitivity to egg or soya-bean protein, soya-bean or peanut products or to any of the active substances or the excipients listed in section 6.1.
● Severe hyperlipidaemia
● Severe coagulopathy
● Severe hepatic insufficiency
● Intrahepatic cholestasis
● Severe renal insufficiency in absence of renal replacement therapy
● Acute thromboembolic events
● Fat embolism
● Aggravating haemorrhagic diatheses
● Metabolic acidosis
General contraindications to parenteral nutrition include:
● Unstable circulatory status with vital threat (states of collapse and shock)
● Unstable metabolic conditions (e.g. severe post-aggression syndrome, severe sepsis, coma of un-known origin)
● Acute phase of myocardial infarction or stroke
● Uncorrected disorders of fluid and electrolyte balance, such as hypokalaemia and hypotonic dehy-dration (see also section 4.4)
● Decompensated cardiac insufficiency
● Acute pulmonary oedema
The serum triglyceride concentration should be regularly monitored during the infusion of Lipofundin MCT/LCT 20%.
Depending on the patient's metabolic condition, occasional hypertriglyceridaemia may occur. If the plasma triglyceride concentration exceeds 4.6 mmol/l during administration of the lipid emulsion, it is recommended to reduce the infusion rate. The infusion must be interrupted if the plasma triglyceride concentration exceeds 11.4 mmol/l.
Disorders of the fluid, electrolyte or acid-base balance must be corrected before the start of infusion.
Controls of serum electrolytes, fluid balance, acid-base balance, cardiovascular function and – during long-term administration – of blood cell counts, coagulation status, and hepatic function are necessary.
Hypersensitivity reactions to an ingredient of Lipofundin MCT/LCT 20% (e.g. due to traces of protein in soya-bean oil or egg phospholipids for injection) are extremely rare, but cannot be totally excluded for sensitised patients. Infusion of Lipofundin MCT/LCT should immediately be discontinued in case of appearance of any sign of allergic reaction, e.g. fever, shivering, rash, dyspnoea.
Energy supply with lipid emulsions alone could cause metabolic acidosis. It is therefore recommended to infuse an adequate quantity of intravenous carbohydrates and amino acids along with the fat emulsion.
For patients requiring complete parenteral nutrition, complementary carbohydrate, amino acid, electrolyte, vitamin, and trace element supplements are required. Also, an adequate total fluid intake has to be ensured.
Mixing with incompatible substances might lead to breaking of the emulsion or to precipitation of particles (see sections 6.2 and 6.6), both resulting in a high risk of embolism.
In solutions with higher lipid concentration (e.g. Lipofundin MCT/LCT 20%), the ratio of emulsifier (phospholipid) to oil is lower than in lower concentrated lipid emulsions. This ensures a favourable lower plasma concentration of triglycerides, phospholipids, free fatty acids as well as the pathological lipoprotein-X in the patient`s blood. Therefore higher concentrated lipid emulsions like Lipofundin MCT/LCT 20% should be preferred over lower concentrated lipid emulsions.
Elderly patients
Caution should be exercised in patients suffering from further diseases like cardiac insufficiency or renal insufficiency that may frequently be associated with advanced age.
Patients with impaired lipid metabolism
Lipofundin MCT/LCT 20% should be administered cautiously to patients with disturbances of lipid metabolism, e.g. renal insufficiency, diabetes mellitus, pancreatitis, impaired hepatic function, hypothyroidism (with hypertriglyceridaemia), and sepsis. If Lipofundin MCT/LCT 20% is administered to patients with these conditions, close monitoring of serum triglycerides is necessary. The dose should be adjusted to the metabolic tolerance. The presence of hypertriglyceridaemia 12 hours after lipid administration also indicates a disturbance of lipid metabolism.
Paediatric population
Free fatty acids (FFA) compete with bilirubin for albumin binding sites. Especially very premature infants may be at increased risk of hyperbilirubinaemia due to high levels of FFA released from triglycerides resulting in a high FFA/albumin ratio. In parenterally fed infants at risk of hyperbilirubinaemia, serum triglyceride and bilirubin levels should be monitored and lipid infusion rate be adjusted if deemed necessary. During infusion Lipofundin MCT/LCT 20% should be protected from phototherapy light to decrease the formation of potentially harmful triglyceride hydroperoxides.
The serum triglyceride concentration should be regularly monitored during the infusion of Lipofundin MCT/LCT 20%, especially if there is an increased risk of hyperlipidaemia. A stepwise increase of the daily dose may be advisable.
Depending on the patient's metabolic condition, occasional hypertriglyceridaemia may occur. In infants dose reduction should be considered if the plasma triglyceride concentration during infusion exceeds 2.8 mmol/l. In older children dose reduction should be considered if the plasma triglyceride concentration during infusion exceeds 4.5 mmol/l.
Light exposure of mixtures for intravenous parenteral nutrition, especially after admixture with trace elements and/or vitamins, may have adverse effects on clinical outcome in neonates, due to generation of peroxides and other degradation products. When used in infants aged from preterm to 2 years old, Lipofundin MCT/LCT 20% should be protected from light exposure after preparation for infusion until administration is completed (see sections 4.2, 6.3 and 6.6).
Interference with laboratory tests
Lipids may interfere with certain laboratory tests (such as bilirubin, lactate dehydrogenase, oxygen saturation) when the blood sample is taken before the lipids have been eliminated from the bloodstream; this may take 4 to 6 hours.
● Heparin
Heparin given in clinical doses causes a transient release of lipoprotein lipase into the circulation. This may result initially in increased plasma lipolysis, followed by a transient decrease in triglyceride clearance.
● Coumarin derivatives
Soya-bean oil has a natural content of vitamin K1. The content is however so low in Lipofundin MCT/LCT 20% that it is not expected to influence the coagulation process significantly in patients treated with coumarin derivatives. Nevertheless, the coagulation status should be monitored in patients treated concomitantly with coumarins.
Pregnancy
There are no or limited amount of data from the use of Lipofundin MCT/LCT 20% in pregnant women. Animal data are insufficient with respect to reproductive toxicity (see section 5.3).
Parenteral nutrition may become necessary during pregnancy. Lipofundin MCT/LCT 20% should only be administered to pregnant women after careful benefit-risk consideration.
Breastfeeding
Components / metabolites of Lipofundin MCT/LCT 20% are excreted in human milk, but at therapeutic doses no effects on the breastfed newborns / infants are anticipated. In general, breastfeeding is not recommended to mothers receiving parenteral nutrition.
Fertility
No human data available. Animal studies have indicated no evidence of an effect on fertility.
Not applicable.
The following listing includes a number of systemic adverse reactions that may be associated with the use of Lipofundin MCT/LCT 20%. Under the conditions of correct use, in terms of dosing, monitoring, observation of safety restrictions and instructions, most of them are very rare (< 1/10,000).
Listing of undesirable effects
Undesirable effects are listed according to their frequencies as follows:
Very common
(≥ 1/10)
Common
(≥ 1/100 to < 1/10)
Uncommon
(≥ 1/1,000 to < 1/100)
Rare
(≥ 1/10,000 to < 1/1,000)
Very rare
(< 1/10,000)
Not known
(frequency cannot be estimated from the available data)
Blood and lymphatic system disorders
Very rare:
Hypercoagulability
Not known:
Leucopenia, thrombocytopenia
Immune system disorders
Very rare:
Allergic reactions (e.g. anaphylactic reactions, dermal eruptions, laryngeal, oral and facial oedema)
Metabolism and nutrition disorders
Very rare:
Hyperlipidaemia, hyperglycaemia, metabolic acidosis, ketoacidosisThe frequency of these adverse reactions is dose-dependent and may be higher under conditions of absolute or relative overdose.
Nervous system disorders
Very rare:
Headache, drowsiness
Vascular disorders
Very rare:
Hypertension or hypotension, flush
Respiratory, thoracic and mediastinal disorders
Very rare:
Dyspnoea, cyanosis
Gastrointestinal disorders
Very rare:
Nausea, vomiting, loss of appetite
Hepatobiliary disorders
Not known:
Cholestasis
Skin and subcutaneous tissue disorders
Very rare:
Erythema, sweating
Musculoskeletal and connective tissue disorders
Very rare:
Pain in the back, bones, chest and lumbar region
General disorders and administration site conditions
Very rare:
Elevated body temperature, feeling cold, chills, fat overload syndrome (see below).
If adverse reactions occur, the infusion of Lipofundin MCT/LCT 20% must be stopped or, if necessary, continued at a reduced dosage.
If the infusion is restarted, the patient must be carefully monitored, especially at the beginning, and serum triglycerides should be determined at short intervals.
Information on particular undesirable effects
Nausea, vomiting, lack of appetite and hyperglycaemia are symptoms related to conditions constituting an indication for parenteral nutrition and may sometimes be associated with parenteral nutrition.
Fat overload syndrome
Overdose of lipid emulsion or impaired capacity to eliminate triglycerides can lead to “fat overload syn-drome”. Possible signs of metabolic overload must be observed.
The cause may be genetic (individually different metabolism) or the fat metabolism may be affected by ongoing or previous diseases.
This syndrome may also appear during severe hypertriglyceridaemia, even at the recommended infusion rate, and in association with a sudden change in the patient's clinical condition, such as renal function impairment or infection.
The fat overload syndrome is characterised by hyperlipidaemia, fever, fat infiltration, hepatomegaly with or without icterus, splenomegaly, anaemia, leukopenia, thrombocytopenia, coagulation disorder, haemolysis and reticulocytosis, abnormal liver function tests and coma.
The symptoms are usually reversible if the infusion of the fat emulsion is discontinued.
Should signs of a fat overload syndrome occur, the infusion of Lipofundin MCT/LCT 20% must be discon-tinued immediately.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Symptoms
Hyperlipidaemia, metabolic acidosis.
Also, a fat overload syndrome may occur. See section 4.8.
Treatment
Immediate cessation of infusion is indicated for overdose. Other therapeutic measures will depend on the particular symptoms and their severity.
When the infusion is recommenced after symptoms have declined, it is recommended that the infusion rate be raised gradually with monitoring at frequent intervals.
Ask anything about Lipofundin MCT/LCT 20 %, emulsion for infusion. The assistant answers only from this leaflet — if the leaflet does not cover it, it will say so. It does not give medical advice.
Answers come from the patient leaflet published on the electronic medicines compendium (emc). They are not medical advice. Ask a pharmacist or your GP if you are unsure. For urgent help call NHS 111, or 999 in an emergency.
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