


Ask a doctor about a prescription for GLUTAFERRO 170 mg/ml ORAL SOLUTION DROPS
Package Leaflet: Information for the User
GLUTAFERRO170 mg/ml oral drops in solution
(Ferroglycine sulfate)
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
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Contents of the package leaflet:
Glutaferro is presented as oral drops in solution.
This medicinal product belongs to the group of medicinal products called iron supplements.
Glutaferro is used for the treatment of iron deficiency conditions.
Do not take Glutaferro
Warnings and precautions
Consult your doctor, pharmacist, or nurse before taking this medicinal product.
Iron preparations can cause poisoning, especially in children.
This medicinal product should be administered with caution.
Other medicines and Glutaferro
Use of Glutaferro with other medicines. Inform your doctor or pharmacist if you are using, have recently used, or might use any other medicines.
The effect of treatment may be affected if Glutaferro is administered simultaneously with other medicines.
Intravenous administration of iron salts and doxycycline should be avoided.
Glutaferro should not be administered until at least two to four hours after the administration of any of the following therapeutic agents:
Use of Glutaferro with food, beverages, and alcohol
It is advisable to take the medicine at least 2 hours away from meals, as absorption may be reduced. Do not take the medicine with food, vegetable foods, milk or derivatives, coffee, tea, or beverages containing calcium. Iron absorption is decreased with calcium and with other agents present in certain foods that form complexes with iron.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking any medicine.
No known risks have been described with iron intake during pregnancy and breastfeeding.
Driving and using machines
No effects of this medicine on the ability to drive or use machines have been observed.
Glutaferro contains sorbitol.
This medicinal product contains 300 mg of sorbitol per ml.
Sorbitol is a source of fructose. If your doctor has told you that you (or your child) have an intolerance to some sugars, or have been diagnosed with hereditary fructose intolerance (HFI), a rare genetic disease in which the patient cannot break down fructose, consult your doctor before taking this medicine.
Glutaferro contains sodium
This medicinal product contains less than 23 mg of sodium (1 mmol) per daily dose, which is essentially "sodium-free".
Follow exactly the administration instructions of this medicinal product given by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.
Iron salts should be taken between meals for maximum absorption. If gastrointestinal side effects are observed, they should be administered during or after meals. In the case of children, Glutaferro can be administered mixed with water, juices, and even milk.
The recommended dose in adults is 1.5-2.5 ml three times a day.
Use in children and adolescents:
Up to 1 year and premature: ………….. 0.3-0.5 ml per day distributed with food.
From 1 to 6 years: …………………………. 0.2-0.7 ml three times a day.
Over 6 years: ………………….. 0.7 ml three times a day.
Treatment should continue until normal iron values are reached in the blood or until body iron reserves are restored.
If you experience side effects, consult your doctor. If you think the action of Glutaferro is too strong or too weak, tell your doctor or pharmacist.
If you take more Glutaferro than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist or call the Toxicology Information Service. Telephone 91 562.04.20 indicating the medicine and the amount ingested. Bring the package leaflet with you.
If you forget to take Glutaferro
Do not take a double dose to make up for forgotten doses.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
During the administration of Glutaferro, the following adverse reactions may occur:
Abdominal discomfort, heartburn, vomiting, diarrhea, constipation, dark stools, and exanthema (temporary skin rash).
These adverse reactions appear very rarely (affect less than 1 in 10,000 people).
Reporting of side effects
If you experience side effects, consult your doctor, pharmacist, or nurse, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the Spanish Medicines and Healthcare Products Agency (AEMPS) https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicinal product out of the sight and reach of children.
This medicinal product does not require any special storage temperature.
Expiry date:
Do not use this medicinal product after the expiry date stated on the packaging after - EXP. The expiry date is the last day of the month indicated.
Do not use this medicinal product if you notice that the packaging or closure is damaged.
Medicines should not be disposed of via wastewater or household waste. Place the packaging and medicines you no longer need in the pharmacy's SIGRE point. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. This will help protect the environment.
Composition of Glutaferro
The active substance of this medicinal product is ferroglycine sulfate 170 mg equivalent to 30 mg of Iron(II).
The other ingredients (excipients) are: sorbitol (E-420), sodium saccharin, orange essence, caramel. See section 2.
Appearance of the product and pack contents
Glutaferro is presented as oral drops in solution in packs containing 25 ml of solution and a dosing dropper.
Marketing authorization holder
MEDIX, S.A.
Calle del Plástico, nº 5 nave 9
Polígono Industrial Miralcampo
19200 Azuqueca de Henares (Guadalajara)
Manufacturer
INDUSTRIA QUIMICA Y FARMACEUTICA VIR, S.A.
C/La Laguna 66-68-70, Polígono Industrial Urtinsa II Alcorcón, 28923 (Madrid)
This leaflet was last revised in 07/2021
Detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Healthcare Products (AEMPS) http://www.aemps.es/
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