Label: Information for the User
Peyona 20mg/mL infusion solution and oral solution
caffeine citrate
Read this label carefully before starting to use this medication, as it contains important information for your child.
1.What Peyona is and for what it is used
2.What you need to know before starting your child's treatment with Peyona
3.How to use Peyona
4.Possible adverse effects
5.Storage of Peyona
6.Contents of the package and additional information
Peyona contains citrate of caffeine as its active ingredient, which is a central nervous system stimulant belonging to a group of medications called methylxanthines.
Peyona is used in the treatment of breathing interruption in premature babies (primary apnea of premature newborns).
These brief periods during which premature babies stop breathing are due to the fact that the child's respiratory center is not fully developed.
It has been observed that this medication reduces the number of episodes of breathing interruption in premature newborns.
No use Peyona
Warnings and Precautions
Consult your child's doctor before starting treatment with Peyona.
Before starting treatment for premature apnea with Peyona, your child's doctor must have ruled out or adequately treated other causes of apnea.
Peyona should be used with caution. Inform your child's doctor:
Other Medications and Peyona
Inform your child's doctor if your child is taking, has recently taken, or may need to take any other medication.
Inform your child's doctor if your child has been previously treated with theophylline.
Do not use the following medications during treatment with Peyona without first speaking with your child's doctor. The doctor may need to adjust the dose or replace one of the medications with a different one:
- theophylline (used to treat respiratory difficulties)
- doxapram (used to treat respiratory difficulties)
- cimetidine (used to treat stomach diseases)
- ketoconazole (used to treat fungal infections)
- phenobarbital (used to treat epilepsy)
- phenytoin (used to treat epilepsy)
This medication may increase the risk of severe intestinal disease that includes bloody stools (necrotizing enterocolitis) when administered with certain medications used to treat stomach diseases (such as H2 receptor antagonists or proton pump inhibitors that reduce gastric acid secretion).
Pregnancy and Breastfeeding
If you (the mother) are breastfeeding while your child receives treatment with Peyona, you should not drink coffee or consume other products with high caffeine content, as caffeine passes into breast milk.
Peyona contains sodium
This medication contains less than 1 mmol (23 mg) of sodium per dose; it is essentially “sodium-free”.
Peyona should only be used in a neonatal intensive care unit that has the necessary facilities for patient observation and monitoring. Treatment should be initiated under the supervision of a doctor with experience in neonatal intensive care.
Dose
Your child's doctor will prescribe the correct amount of Peyona based on your child's weight.
The initial dose is 20mg per kg of body weight (equivalent to 1mL per kg of body weight).
The maintenance dose is 5mg per kg of body weight (equivalent to 0.25mL per kg of body weight) every 24hours.
Route and form of administration
Peyona should be administered through controlled intravenous infusion, using a syringe pump or other volumetric infusion device. This method is also known as "drip" administration.
Some of the doses (maintenance doses) may be administered orally.
Your child's doctor may need to monitor the caffeine concentration through periodic blood tests throughout the treatment to avoid toxicity.
Duration of treatment
Your child's doctor will decide exactly how long the treatment with Peyona should last. If your child remains without apnea crises for5 to7 days, the doctor will stop the treatment.
If your child receives more Peyona than they should
Your child may experience fever, rapid breathing (tachypnea), nervousness, muscle tremors, vomiting, elevated blood sugar (hyperglycemia), decreased potassium levels (hypokalemia), elevated blood concentrations of certain chemicals (urea), elevated white blood cell counts (leukocytosis), and seizures if they receive more caffeine citrate than they should.
In these cases, treatment with Peyona should be stopped immediately and your child's doctor will need to treat the overdose.
If you have any other questions about the use of this medication, ask your child's doctor.
Like all medicines, this medicine can cause side effects, although not everyone will experience them. However, it is difficult to distinguish them from the frequent complications that occur in premature babies and from the complications inherent in the disease.
Your child may experience some of the following reactions during treatment with Peyona:
Severe side effects
Side effectswhose frequency cannot be calculated from the available data.
- severe intestinal disease with bloody stools (necrotizing enterocolitis).
The following other side effects may also be considered severe by your child's doctor in the context of the overall clinical evaluation.
Other side effects
Side effects observed at afrequentfrequency (may affect up to 1 in 10 people)
- local inflammatory reactions at the site of infusion
- cardiac disorders such as rapid heartbeat (tachycardia)
- alterations in blood sugar concentration or serum glucose (hyperglycemia)
Side effects observed at ainfrequentfrequency (may affect up to 1 in 100 people)
- stimulation of the central nervous system, for example, convulsions
- cardiac disorders such as irregular heartbeat (arrhythmia)
Side effects observed at ararefrequency (may affect up to 1 in 1000 people)
- allergic reactions
Side effectswhose frequency cannot be calculated from the available data:
- blood infection (sepsis)
- alterations in blood sugar or serum glucose (hypoglycemia), growth delay, feeding intolerance
- stimulation of the central nervous system, such as irritability, nervousness, and restlessness; brain injury
- hearing loss
- regurgitation, increased aspiration of stomach contents
- increased urine volume, increased levels of certain components of urine (sodium and calcium)
- alterations in blood tests (reduction of hemoglobin after prolonged treatment and decrease in thyroid hormone at the beginning of treatment)
Reporting side effects
If your newborn baby experiences any type of side effect, consult your doctor, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Usehttps://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date shown on the label. The expiration date is the last day of the month indicated.
This medication does not require special storage conditions.
All parenteral solution ampoules must be visually inspected before administration to detect the presence of particles. Once the ampoule is opened, the medication must be used immediately.
Composition of Peyona
The active principle is citrate of caffeine.
Each mL contains 20mg of citrate of caffeine (equivalent to 10mg/mL of caffeine base).
Each ampoule of 1mL contains 20mg of citrate of caffeine (equivalent to 10 mg of caffeine base).
Each ampoule of 3mL contains 60mg of citrate of caffeine (equivalent to 30mg of caffeine base).
The other components are citric acid, sodium citrate, and water for injectable preparations.
Appearance of the product and content of the container
Peyona is a perfusion solution and an oral solution.
Peyona is a clear and colorless solution presented in glass ampoules. Each box contains 10ampoules.
Marketing Authorization Holder
Chiesi Farmaceutici S.p.A.
Via Palermo 26/A
43122Parma
Italy
Responsible for manufacturing (batch approval)
Alfasigma S.p.A.
Via Enrico Fermi 1
Alanno (PE)
Italy
Chiesi Pharmaceuticals GmbH,
Gonzagagasse 16/16,
A-1010 Wien
Austria
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
Spain Chiesi España, S.A.U. Tel: + 34 93 494 8000 |
Last review date of this leaflet: December 2021
Detailed information about this medication is available on the European Medicines Agency website:http://www.ema.europa.eu.
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This information is intended solely for doctors or healthcare professionals:
For detailed information, please consult the Peyona technical datasheet attached.
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