Vitalipid N Adult Emulsion for infusion
Vitalipid N Adult Emulsion for infusion is a brand of medicine containing the active ingredients retinyl palmitate - ergocalciferol - alpha tocopherol - phytomenadione.
Find out more about active ingredients.
Consumer medicine information (CMI) leaflet
Developed by the pharmaceutical company responsible for this medicine in Australia, according to TGA regulations.
Vitalipid N® Infant and Adult
Retinyl Palmitate, Ergocalciferol, dl-α-Tocopherol and Phytomenadione
Consumer Medicine Information
What is in this leaflet
This leaflet answers some common questions about VITALIPID N. It does not contain all the available information. It does not take the place of talking to your doctor or pharmacist. All medicines have risks and benefits. Your doctor has weighed the risks of you or your child given VITALIPID N against any benefits they expect it will have for you or your child.
Please read this leaflet carefully before you are given VITALIPID N. If you have any questions or are unsure about anything, please ask the doctor or pharmacist. Keep this leaflet with the medicine. You may need to read it again.
What is VITALIPID N used for and how does it work
VITALIPID N is a sterile emulsion which provides the body with fat-soluble multivitamins by the intravenous route. When the intake of nutrients or food into the mouth or directly into the gut is not possible, or it is not enough to supply the body’s needs, then intravenous nutrients or foods can be given. This is especially important for people whose bodies are under physical stress from illness or recent surgery. During illness or after surgery the body requires nutrition or food.
Before you are given VITALIPID N
You or your child should not be given VITALIPID N if:
- You have an allergy to soya oil, eggs, peanuts or any of the ingredients listed at the end of this leaflet.
- You have very high levels of vitamins in your system.
- You have a sudden, dangerous drop in your blood pressure.
- You have an inability to break down fats.
If you are not sure whether any of these apply to you, check with your doctor.
You should tell your doctor BEFORE given VITALIPID N if the answer to any of the following questions is YES.
- Are you pregnant or trying to become pregnant?
- Are you breastfeeding?
- Are you allergic to soya-, egg- or peanut protein?
- Do you have liver or kidney disease?
- Are you taking anticoagulants (medicines for preventing blood clotting)?
- Are you taking any other medicines including any that you buy without a prescription from your pharmacy, supermarket or health food shop. These medicines may affect the action of VITALIPID N or may affect how well VITALIPID N works.
If you have not told your doctors about any of the above, tell them before you are given VITALIPID N.
How is VITALIPID N given
The dose of VITALIPID N will be determined by the doctor or pharmacist. The doctor will supervise your treatment or your child’s treatment with VITALIPID N.
VITALIPID N is usually mixed in a bottle or a bag of amino acids, glucose and/or fats, fat-soluble vitamins and given as a continuous infusion into a central vein. An electronic pump may be used to control the speed of the infusion of drip.
Since VITALIPID N has to be diluted with other nutrient solutions, it may cause unwanted effects in some people. All the unwanted effects associated with VITALIPID N may not yet been detected.
If you or your child have/has any unwanted effects during treatment, tell your doctor or pharmacist.
If you are given too much (overdose)
This rarely happens as VITALIPID N is administered under the care of a trained professional in a hospital or clinic setting. However if you or your child is given too much of VITALIPID N, you or your child may experience a condition of high levels of vitamins in your system.
Your doctor has information on how to recognise and treat an overdose. Ask your doctor if you have any concerns.
Otherwise, immediately telephone your doctor or contact the Poisons Information Centre in your country.
Australia: 13 11 26
New Zealand: 0800 764 766.
The expiry date of VITALIPID N is on the label of the ampoule and pack. VITALIPID N should not be used if the expiry date has passed. VITALIPID N should be stored at room temperature below 25ºC. It should be protected from light and not frozen. The contents of each ampoule of VITALIPID N should be dissolved first and then diluted for single infusion only. Any unused VITALIPID N should be discarded.
What it looks like
VITALIPID N is a sterile, white emulsion in an ampoule. It comes in a carton pack of 10 ampoules.
VITALIPID N can be identified by the following:
- Vitalipid N Adult - AUST R 40252
- Vitalipid N Infant - AUST R 40253
VITALIPID N ADULT
One mL contains Vitamin A (as retinyl palmitate) 99 mg, Ergocalciferol 0.5 mg, dl-a -Tocopherol 0.91 mg, Phytomenadione 15 mg, Soya oil 100 mg, Egg lecithin 12 mg, Glycerol 22.0 mg, Sodium hydroxide to pH 8 and Water for Injections to 1 mL.
VITALIPID N INFANT
One mL contains Vitamin A (as retinyl palmitate) 69 mg, Ergocalciferol 1.0 mg, dl-a -Tocopherol 0.64 mg, Phytomenadione 20 mg, Soya oil 100 mg, Egg lecithin 12 mg, Glycerol 22.0 mg, Sodium hydroxide to pH 8 and Water for Injections to 1 mL.
VITALIPID N does not contain gluten, lactose, sucrose, tartrazine or any other azo dyes. VITALIPID N does not contain any preservative.
More detailed information is available from your doctor or pharmacist. Therefore, if you have any concerns about the information or about VITALIPID N ask your doctor or pharmacist.
Fresenius Kabi Australia Pty Limited
964 Pacific Highway
Pymble, NSW 2073
Telephone: (02) 9391 5555
Fresenius Kabi New Zealand Limited
60 Pavilion Drive
Airport Oaks, Auckland 2022
Freecall: 0800 144 892
® = Registered Trademark
Date of Information
This leaflet was prepared in March, 2010
CMI provided by MIMS Australia, June 2013