Creon Micro Pancreatin 60.12 Mg Gastro-Resistant Granules
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Creon® Micro Pancreatin 60.12 mg Gastro-resistant Granules
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each 100 mg of gastro-resistant granules (equivalent to one measuring spoonful) contains 60.12mg of pancreatin, containing the following pancreatic enzymes:
Lipase 5,000 PhEur units
Amylase 3,600 PhEur units
Protease 200 PhEur units
For excipients, see 6.1.
3. PHARMACEUTICAL FORM
Gastro-resistant granules.
Round, light brown gastro-resistant granules.
4. CLINICAL PARTICULARS
4.1 Therapeutic indications
For the treatment of pancreatic exocrine insufficiency.
4.2. Posology and method of administration
Initially 100 mg (5000 lipase units) of gastro-resistant granules (one measure) should be taken with each feed or meal. Dose increases, if required, should be added slowly, with careful monitoring of response and symptomatology. The maximum daily dosage should not exceed 10,000 units lipase/kg/day. The required quantity of gastro-resistant granules should be dispensed using the measuring scoop contained in the pack which holds 100 mg.
In young infants, Creon Micro granules should be mixed with a small amount of apple juice and given from a spoon directly before the feed. In weaned infants, granules should be taken with acidic liquids or soft foods (e.g. mixed with apple juice or apple puree), but without chewing, directly before the meal. When giving Creon Micro to young or weaned infants the apple juice should not be diluted.
If the granules are mixed with fluid or food it is important that they are taken immediately and the mixture not stored, otherwise dissolution of the enteric coating may result. In order to protect the enteric coating, it is important that the granules are not crushed or chewed.
Crushing and chewing of the minimicrospheres or mixing with food or fluid with a pH greater than 5.5 can disrupt the protective enteric coating. This can result in early release of enzymes in the oral cavity and may lead to reduced efficacy and irritation of the mucous membranes.
Care should be taken to ensure that no product is retained in the mouth.
It is important to ensure adequate hydration of patients at all times whilst dosing with Creon.
Fibrosing colonopathy has been reported in patients with cystic fibrosis taking in excess of 10000 units of lipase/kg/day (see section 4.4).
4.3 Contraindications
Hypersensitivity to pancreatin of porcine origin or to any of the excipients.
4.4. Special warnings and precautions for use
Strictures of the ileo-caecum and large bowel (fibrosing colonopathy) have been reported in patients with cystic fibrosis taking high doses of pancreatin preparations. As a precaution, unusual abdominal symptoms or changes in abdominal symptoms should be medically assessed to exclude the possibility of fibrosing colonopathy, especially if the patient is taking in excess of 10 000 units of lipase/kg/day.
As with all currently marketed porcine pancreatin products, Creon Micro is sourced from pancreatic tissue from swine used for food consumption. Although the risk that Creon Micro will transmit an infectious agent to humans has been reduced by the testing and inactivation of certain viruses during manufacturing, there is a theoretical risk for transmission of viral disease, including diseases caused by novel or unidentified viruses. The presence of porcine viruses that might infect humans cannot be definitely excluded. However, no cases of transmission of an infectious illness associated with the use of porcine pancreatic extracts have been reported, whereas they have been used for a long time.
4.5 Interaction with other medicinal products and other forms of interaction
No interaction studies have been performed.
4.6 Pregnancy and lactation
Pregnancy
For pancreatic enzymes no clinical data on exposed pregnancies are available. Animal studies show no evidence for any absorption of porcine pancreatic enzymes. Therefore, no reproductive or developmental toxicity is to be expected.
Caution should be exercised when prescribing to pregnant women.
Lactation
No effects on the suckling child are anticipated since animal studies suggest no systemic exposure of the breastfeeding woman to pancreatic enzymes. Pancreatic enzymes can be used during breastfeeding.
If required during pregnancy or lactation Creon should be used in doses sufficient to provide adequate nutritional status.
4.7 Effects on ability to drive and use machines
Creon has no or negligible influence on the ability to drive or use machines.
4.8 Undesirable effects
In clinical trials, more than 900 patients with were exposed to Creon. The most commonly reported adverse reactions were gastrointestinal disorders and were primarily mild or moderate in severity.
The following adverse reactions have been observed during clinical trials with the below indicated frequencies
|
Organ system |
Very common > 1/10 |
Common > 1/100 to < 1/10 |
Uncommon > 1/1000 to < 1/100 |
Frequency not known |
|
Gastrointestinal disorders |
abdominal pain* |
nausea, vomiting, constipation, abdominal distention, diarrhoea* |
strictures of the ileo-caecum and large bowel (fibrosing colonopathy) | |
|
Skin and subcutaneous tissue disorders |
rash |
pruritus, urticaria |
|
Immune system disorders |
hypersensitivity (anaphylactic reactions). | |||
|
*Gastrointestinal d |
isorders are mainly associated with the underlying disease. | |||
Similar or lower incidences compared to placebo were reported for abdominal pain and diarrhoea.
Strictures of the ileo-caecum and large bowel (fibrosing colonopathy) have been reported in patients with cystic fibrosis taking high doses of pancreatin preparations, see section 4.4 Special warnings and precautions for use.
Allergic reactions mainly but not exclusively limited to the skin have been observed and identified as adverse reactions during post-approval use. Because these reactions were reported spontaneously from a population of uncertain size, it is not possible to reliably estimate their frequency.
Paediatric population
No specific adverse reactions were identified in the paediatric population. Frequency, type and severity of adverse reactions were similar in children with cystic fibrosis as compared to adults.
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 directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.
4.9 Overdose
Extremely high doses of pancreatin have been reported to be associated with hyperuricosuria and hyperuricaemia.
Supportive measures including stopping enzyme therapy and ensuring adequate rehydration are recommended.
5. PHARMACOLOGICAL PROPERTIES
5.1. Pharmacodynamic properties
Multienzymes (amylase, lipase, protease), ATC code: A09A A02
Creon Micro contains porcine pancreatin formulated as enteric-coated (acid-resistant) minimicrospheres, a multi-dose principle which is designed to achieve good mixing with the chyme, emptying from the stomach together with the chyme and after release, good distribution of enzymes within the chyme.
When the minimicrospheres reach the small intestine the coating rapidly disintegrates (at pH > 5.5) to release enzymes with lipolytic, amylolytic and proteolytic activity to ensure the digestion of fats, starches and proteins. The products of pancreatic digestion are then either absorbed directly, or following further hydrolysis by intestinal enzymes.
Clinical efficacy:
Overall 30 studies investigating the efficacy of Creon (Creon capsules with 10000, 25000 or 40000 Ph. Eur units of lipase and Creon 5000) in patients with pancreatic exocrine insufficiency have been conducted. Ten of these were placebo controlled studies performed in patients with cystic fibrosis, chronic pancreatitis or post surgical conditions.
In all randomized, placebo-controlled, efficacy studies, the pre-defined primary objective was to show superiority of Creon over placebo on the primary efficacy parameter, the coefficient of fat absorption (CFA).
The coefficient of fat absorption determines the percentage of fat that is absorbed into the body taking into account fat intake and faecal fat excretion. In the placebo-controlled PEI studies, the mean CFA (%, mean ± SD) was higher with Creon treatment (83.0 ± 12.6%) as compared to placebo (62.6 ± 21.8%). The median treatment duration was 7 days on both treatments. In all studies, irrespective of the design, the mean CFA (%) at the end of the treatment period with Creon was similar to the mean CFA values for Creon in the placebo controlled studies.
In all performed studies, irrespective of etiology, an improvement was also shown in disease specific symptomatology (stool frequency, stool consistency, flatulence).
Paediatric population
In cystic fibrosis (CF) the efficacy of Creon was demonstrated in 288 paediatric patients covering an age range from newborns to adolescents. In all studies, the mean end-of treatment CFA values exceeded 80% on Creon comparably in all paediatric age groups.
Additional data in paediatric population for Creon Micro:
Creon Micro has been specifically developed to offer a dosage form for infants and children.
One baseline-adjusted specific study performed over 8 weeks in infants demonstrated that Creon Micro was effective regarding the improvement of CFA and stool fat excretion as well as faecal energy loss after two weeks of treatment.
This study was designed mainly to evaluate the efficacy of Creon Micro in 12 infants, aged 1-23 months. The analysis of the results showed that the primary efficacy parameter, CFA, significantly increased from a baseline mean of 58.0% to a mean of 84.7% (mean increase 26.7%, 95% CI [12.9; 40.4], p = 0.0013, paired t-test). Height and weight increased, but the weight for height percentile remained nearly constant and close to 100%.
5.2 Pharmacokinetic properties
Pharmacokinetic data are not available as the enzymes act locally in the gastro-intestinal tract.
After exerting their action, the enzymes are digested themselves in the intestine.
5.3 Preclinical safety data
None stated.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Hypromellose phthalate Macrogol 4000 Dimeticone Cetyl alcohol Triethyl citrate
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
2 years. 12 weeks after first opening.
6.4 Special precautions for storage
Do not store above 30°C.
Keep the container tightly closed in order to protect from moisture.
6.5 Nature and contents of container
Glass bottle with LDPE stopper. Containers hold 20 g of gastro-resistant granules.
6.6 Instruction for use and handling
No special requirements.
7 MARKETING AUTHORISATION HOLDER
Abbott Healthcare Products Limited
Abbott House
Vanwall Business Park
Vanwall Road
Maidenhead
SL6 4XE
UK
8. MARKETING AUTHORISATION NUMBER
PL 00512/0179
9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
3 August 2004
10 DATE OF REVISION OF THE TEXT
11/09/2014