Patient info Open main menu

Caffeine Citrate 20 mg/ml solution for infusion – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
20 mg/ml
Contains active substance:
ATC code:
Similar medicines:

Patient leaflet - Caffeine Citrate 20 mg/ml solution for infusion

1. What Caffeine Citrate is and what it is used for

Caffeine Citrate contains the active substance caffeine citrate, which is a stimulant of the central nervous system, belonging to a group of medicines called methylxanthines. Caffeine Citrate is used in the treatment of interrupted breathing in premature babies (primary apnoea of premature newborns). These short periods when premature babies stop breathing are due to the baby’s breathing centres not being fully developed. This medicine has been shown to reduce the number of episodes of interrupted breathing in premature newborns.

2. What you need to know before your baby is given Caffeine Citrate

Do not use Caffeine Citrate:

  • If your newborn is allergic to caffeine citrate or any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Talk to your baby’s doctor before your newborn is given Caffeine Citrate.

Prior to starting treatment for apnoea of prematurity with Caffeine Citrate other causes of apnoea should have been excluded or properly treated by your baby’s doctor.

Caffeine Citrate should be used with caution. Please inform your baby’s doctor:

  • If your newborn suffers from seizures
  • If your newborn suffers from any heart disease
  • If your newborn has kidney or liver problems
  • If your newborn has frequent regurgitation
  • If your newborn produces more urine than usual
  • If your newborn has a reduced weight gain or food intake
  • If you (the mother) consumed caffeine prior to delivery

Other medicines and Caffeine Citrate

Tell your baby’s doctor if your newborn is using, has recently used or might take use any other medicines.

Please inform your baby’s doctor if

your newborn has been previously treated with theophylline.

Do not use the following medicines during the treatment with Caffeine Citrate without talking to your baby’s doctor. The doctor may need to adjust the dose or change one of the medicines to something else:

  • theophylline (used to treat breathing difficulties)
  • doxapram (used to treat breathing difficulties)
  • cimetidine (used to treat gastric disease)
  • ketoconazole (used to treat fungine infections)
  • phenobarbital (used to treat epilepsy)
  • phenytoin (used to treat epilepsy) This medicine may increase the risk for serious intestinal disease with bloody stools (necrotising enterocolitis) when administered with medicines used to treat gastric disease (such as antihistamine H2 receptor blockers or proton-pump inhibitors that reduces gastric acid secretion).

Pregnancy and breast-feeding

If you (the mother) are breast-feeding while your infant is treated with Caffeine Citrate, you should not drink coffee or take any other high caffeine product as caffeine passes into breast milk.

Caffeine Citrate contains sodium

This medicinal product contains less than 1 mmol sodium (23 mg) per 1 ml, that is to say essentially “sodium-free”.

3. How to use Caffeine Citrate

Caffeine Citrate should only be used in a neonatal intensive care unit in which adequate facilities are available for patient surveillance and monitoring. Treatment should be initiated under supervision of a physician experienced in neonatal intensive care.

Dose

Your baby’s doctor will prescribe the right amount of Caffeine Citrate based on your baby’s weight. The starting dose is 20 mg per kg body weight (equivalent to 1 mL per kg body weight).

The maintenance dose is 5 mg per kg body weight (equivalent to 0.25 mL per kg body weight) every 24 hours.

Route and method of administration

Caffeine Citrate will be infused by controlled intravenous infusion, using a syringe infusion pump or other metered infusion device. This method is also known as “a drip”. Some of the doses (maintenance doses) may be given by mouth. It may be needed that your baby’s doctor decides to check the levels of caffeine in a blood test periodically throughout treatment to avoid toxicity.

Duration of treatment

Your baby’s doctor will decide exactly how long your newborn must continue therapy with Caffeine Citrate.

Package leaflet: Information for the user Caffeine Citrate 20 mg/ml Solution for Infusion

If your baby has 5 to 7 days without apnoea attacks, the doctor will stop the treatment.

If your newborn receives more Caffeine Citrate than he/she should

Your newborn may experience fever, rapid breathing (tachypnoea), jitteriness, muscular tremor vomiting, high blood levels of sugar (hyperglycemia), low blood levels of potassium (hypokalaemia), high blood levels of certain chemicals (urea), elevated number of certain cells (leukocyte) in blood and seizures if he/she receives more caffeine citrate than he/she should. In the event of this happening treatment with Caffeine Citrate should be stopped immediately and your baby’s doctor should treat the overdose.

If you have any further questions on the use of this medicinal product, ask your baby’s doctor.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them. However, it is difficult to distinguish them from frequent complications occurring in premature babies and complications due to the disease. While under treatment with Caffeine Citrate, your newborn may experience some of the following reactions:

Serious side effects

Side effects where the frequency cannot be estimated from the available data

  • serious intestinal disease with bloody stools (necrotising enterocolitis)

The following other side effects may also be considered serious by your baby’s doctor in the context of the global clinical evaluation. Other side effects

Common reported side effects (may affect up to 1 in 10 people)

  • local inflammatory reactions at the infusion site
  • cardiac disorders such as fast heart beat (tachycardia)
  • changes of sugar in blood or serum (hyperglycaemia)

Uncommon reported side effects (may affect up to 1 in 100 people)

  • stimulation of central nervous system such as convulsion
  • cardiac disorders such as irregular heart beat (arrhythmia) Rare reported side effects (may affect up to 1 in 1,000 people)
  • allergic reactions

Side effects where the frequency cannot be estimated from the available data

  • bloodstream infection (sepsis)
  • changes of sugar in blood or serum (hypoglycaemia ), failure to grow, feeding intolerance
  • stimulation of central nervous system such as irritability, nervousness and restlessness; brain injury
  • deafness
  • regurgitation, increase in stomach aspirate
  • increase of urine flow, increase of certain urine components (sodium and calcium)
  • changes in blood tests (reduced levels of haemoglobin after prolonged treatment and reduced

    thyroid hormone at the start of treatment)

    Reporting of side effects

    If your newborn gets any side effects, talk to your baby’s doctor. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme, Website: 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. How to store Caffeine Citrate

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the carton and ampoule label after ‘EXP’. The expiry date refers to the last day of that month.

The medicinal product does not require any special storage conditions.

Ampoules of all parenteral solutions must be inspected visually for particulate matter prior to administration.

After opening the ampoules, the medicinal product should be used immediately.

6. What Caffeine Citrate contains

The active substance is caffeine citrate.

Each 1 mL ampoule contains 20 mg caffeine citrate (equivalent to 10 mg of caffeine base). The other ingredients are citric acid monohydrate, sodium citrate dihydrate and water for injections.

What Caffeine Citrate looks like and contents of the pack

Caffeine Citrate is a clear, colourless solution, supplied in a type I clear glass 1 mL ampoule. Each carton contains 5 ampoules.

Marketing Authorisation Holder and Manufacturer

Marketing Authorization Holder Galvany Pharma Limited

Business & Technology Centre Bessemer Drive

Stevenage

SG1 2DX

United Kingdom

Manufacturer

S.A.L.F. S.p.A. Laboratorio Farmacologico

Via G. Mazzini, 9

24069 Cenate Sotto (Bergamo) Italy

This leaflet was last revised in February 2026.

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 56809/0002

Last revision stated in the text: February 2026 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Caffeine Citrate 20 mg/ml solution for infusion

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Caffeine citrate
Strength 20 mg/ml
Pharmaceutical form Solution for infusion
Clear, colourless solution at pH between 4.2 and 5.2
How is it taken Oral, Intravenous
Excipients Citric acid monohydrate, Sodium citrate dihyrate, Water for injections
Pack sizes 10 vial
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 36 months.
Storage This medicinal product does not require any special storage condition. For storage conditions after dilution of the medicinal product, see section 6.3.
Drug group (ATC) Psychoanaleptics, xanthine derivatives
  1. N Nervous system drugs
    1. N06 Psychoanaleptics
      1. N06B Psychostimulants, agents used for ADHD and nootropics
        1. N06BC Xanthine derivatives, psychostimulants, agents used for ADHD and nootropics
          1. N06BC01 caffeine
Marketing authorisation PL 56809/0002 (first authorised 16 May 2023)
Marketing authorisation holder Galvany Pharma Limited
Codes GTIN 5060124643052 · BNF 04040000

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.