This leaflet is about the use of pancreatin for children who do not produce enough digestive enzymes, a condition called pancreatic insufficiency. This happens most commonly in cystic fibrosis but it may have other causes.
This leaflet has been written specifically for parents and carers about the use of this medicine in children. The information may differ from that provided by the manufacturer. Please read this leaflet carefully. Keep it somewhere safe so that you can read it again.
Pancreatin
Brand names: Creon®, Nutrizym®, Pancrex®, Pancrease HL®
The pancreas produces enzymes that help to digest food. In pancreatic insufficiency, the pancreas does not make enough of these enzymes. Pancreatin contains three types of enzyme (protease, lipase, amylase), which digest the food your child eats so their body can use it to stay healthy.
There are many different types of pancreatin. The different medicines contain different amounts of the enzymes. Your doctor will prescribe the right one for your child. Pancreatin comes as tablets, capsules, granules and powder.
You will need to give pancreatin with every meal and large snack. This is at least three times a day. Give the medicine just before your child starts eating, or straight after they have finished. Your dietician will provide you with more information about the types of snacks that you need to give with the medicine.
It is important that you follow your doctor’s instructions about how much to give.

Tablets should be swallowed with a glass of water, milk or juice. Your child should not chew the tablet.
Capsules should be swallowed with a glass of water, milk or juice. Your child should not chew the tablet. You can open the capsule and mix the contents with a small amount of soft food such as yogurt, honey or jam. Make sure your child swallows it straight away without chewing.
Granules or powder: You will be given a measure to allow you to measure the correct amount of granules/powder. It is important that you use this every time, to make sure you give the correct dose. Mix the correct amount with a small amount of soft food or a small drink of milk or water. Your child should swallow the food or drink straight away without chewing. Make sure that they take it all.
Do not mix pancreatin with hot food or drink because it will not work.
It may take a few weeks for pancreatin to work properly and you may not see any difference in your child. It is important that you continue to give pancreatin with every meal during this time. If you are worried about whether it is working, talk to your doctor but continue to give the medicine.
Do not give the missed dose.
Never give a double dose of pancreatin.
It may be dangerous to give too much pancreatin.
If you think you may have given your child too much pancreatin, get them to drink a large cup of water and contact your doctor or NHS Direct (0845 4647) straight away.
Have the medicine or packaging with you if you telephone for advice.
We use medicines to make our children better, but sometimes they have other effects that we don’t want (side-effects).
Side-effects you must do something about
If your child gets stomach cramps or bad stomach pain that will not go away, contact your doctor or take your child to hospital straight away, as there may be a problem with your child’s intestines.
If your child is short of breath or is wheezing, or their face, lips or tongue start to swell, or they develop a rash, they may be allergic to pancreatin. Take your child to hospital or call an ambulance straight away.
Other side-effects you need to know about
If you think someone else may have taken the medicine by accident, contact your doctor straight away.
Pancrex V must be kept in the fridge.
Your doctor, pharmacist or nurse will be able to give you more information about pancreatin and about other medicines used to treat pancreatic insufficiency.
7/12/2011
Version 1.2, September 2011 (November 2011). © NPPG, RCPCH and WellChild 2011, all rights reserved. Reviewed by: September 2013.
The primary source for the information in this leaflet is the British National Formulary for Children. For details on any other sources used for this leaflet, please contact us through our website, www.medicinesforchildren.org.uk
We take great care to make sure that the information in this leaflet is correct and up-to-date. However, medicines can be used in different ways for different patients. It is important that you ask the advice of your doctor or pharmacist if you are not sure about something. This leaflet is about the use of these medicines in the UK, and may not apply to other countries. The Royal College of Paediatrics and Child Health (RCPCH), the Neonatal and Paediatric Pharmacists Group (NPPG), WellChild and the contributors and editors cannot be held responsible for the accuracy of information, omissions of information, or any actions that may be taken as a consequence of reading this leaflet.