RUPAFIN 1 MG/ML ORAL SOLUTION
Active substance(s): RUPATADINE FUMARATE
Rupafin 1 mg/ml oral solution
Read all of this leaflet carefully before you start taking this medicine.
Keep this leaflet. You may need to read it again.
If you have further questions, ask your doctor or pharmacist.
This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even
if their symptoms are the same as yours.
If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet,
please tell your doctor or pharmacist (see section 4).
In this leaflet
1. What Rupafin is and what it is used for
2. Before you take Rupafin
3. How to take Rupafin
4. Possible side effects
5. How to store Rupafin
6. Further information
WHAT RUPAFIN IS AND WHAT IT IS USED FOR
Rupafin contains the active substance rupatadine which is an antihistamine.
Rupafin oral solution relieves the symptoms of allergic rhinitis such as sneezing, runny nose, nasal
congestion, itching in the eyes and nose in children aged 2 to 11 years.
Rupafin is also used to relieve the symptoms associated with urticaria (an allergic skin rash) such as
itching and hives (localised skin redness and swelling) in children aged 2 to 11 years.
BEFORE YOU TAKE RUPAFIN
Do not take Rupafin
- If you are allergic (hypersensitive) to rupatadine or any of the other ingredients of Rupafin.
Take special care with Rupafin
If you suffer from kidney or liver insufficiency, ask your doctor for advice. The use of Rupafin is at
present not recommended in patients with impaired kidney or liver functions.
If you have low blood levels of potassium and/or if you have a certain abnormal pattern to your heart
beat (known prolongation of the QTc interval on the ECG) which can occur in some forms of heart
disease, ask your doctor for advice.
This medicine is not for use in children under 2 years of age or weighing less than 10 kg.
Using other medicines
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines,
including medicines obtained without a prescription.
If you are taking Rupafin do not take medicines containing ketoconazole or erythromycin.
If you are taking central nervous system depressant medicines or statin medicines, ask your doctor for
advice before taking Rupafin.
Taking Rupafin with food and drink
Rupafin may be taken with or without food.
Rupafin should not be taken in combination with grapefruit juice, as this may increase the level of
Rupafin in your body.
Rupafin, at dose of 10 mg, does not increase the drowsiness produced by alcohol.
Pregnancy and breastfeeding
Do not take Rupafin during pregnancy and breastfeeding, unless clearly indicated by your doctor.
Ask your doctor or pharmacist for advice before taking any medicine.
Driving and using machines
At the recommended dosage, Rupafin is not expected to influence your ability to drive or use
machinery. However, when you first start taking Rupafin you should take care to see how the
treatment affects you before driving or using machines.
Important information about some of the ingredients of Rupafin
This medicinal product contains sucrose, so it may be harmful to the teeth.If you have been told by
your doctor that you have an intolerance to some sugars, contact your doctor before taking this
This medicinal product contains methyl parahydroxybenzoate, may cause allergic reactions (possibly
HOW TO TAKE RUPAFIN
Always take Rupafin exactly as your doctor has told you. You should check with your doctor or
pharmacist if you are not sure.
Rupafin oral solution is for oral use.
Dosage in children weighing 25 kg or more: 5 ml (5 mg of rupatadine) of oral solution once a day,
with or without food.
Dosage in children weighing equal or more than 10 kg to less than 25 kg: 2.5 ml (2.5 mg of
rupatadine) of oral solution once a day, with or without food.
Your doctor will tell you how long your treatment with Rupafin will last.
Instructions of use:
To open the bottle press the cap and turn it anticlockwise.
Take the syringe and put it in the perforated stopper and turn the bottle upside down.
Fill the syringe with the prescribed dose.
Administer directly from the dosing syringe.
Wash the syringe after use.
If you take more Rupafin than you should
If you have accidentally taken a high dose of your medicine, talk to your doctor or pharmacist
If you forget to take Rupafin
Do not take a double dose to make up for forgotten individual doses.
POSSIBLE SIDE EFFECTS
Like all medicines, Rupafin can cause side effects, although not everybody gets them.
Common side effects (may affect up to 1 in 10 people) is headache and sleepiness. Uncommon side
effects (may affect up to 1 in 100 people) are influenza, nasopharyngitis, upper respiratory tract
infection, eosinophilia, neutropenia, dizziness, nausea, eczema, night sweats and fatigue.
If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please
tell your doctor or pharmacist.
Reporting of side effects
If you get any side effects, talk to your doctor orpharmacist.This includes any possible side effects not
listed in this leaflet.You can also report side effects directly via the national reporting system listed in
Appendix V*. By reporting side effects you can help provide more information on the safety of this
HOW TO STORE RUPAFIN
This medicinal product does not require any special storage conditions.
Keep out of the reach and sight of children.
Do not use Rupafin after the expiry date which is stated on the bottle and box after EXP. The expiry
date refers to the last day of that month. The shelf life after first opening is the same as the expiry date
placed on the box and the bottle.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to
dispose of medicines no longer required. These measures will help to protect the environment.
What Rupafin contains
The active substance is rupatadine. Each ml contains 1 mg of rupatadine (as fumarate).
The other ingredients are propylene glycol, citric acid anhydrous, disodium phosphate
anhydrous, saccharin sodium, sucrose, methyl parahydroxybenzoate (E-218), quinoline yellow (E104), banana flavour, purified water.
What Rupafin looks like and contents of the pack
Rupafinis a clear yellow oral solution.
Rupafin is packaged in an amber plastic bottle with a perforated stopper and a child-resistant cap. Each
bottle contains 120 ml Rupafin solution. A 5 ml oral syringe graduated at 0.25 ml intervals is provided in
Marketing Authorisation Holder:
J. Uriach & Cía., S.A.
Av. Camí Reial, 51-57
E-08184 Palau-solità i Plegamans (Barcelona - Spain)
San Rafael, 3
Pol. Ind. Alcobendas
E-28108 Alcobendas (Spain)
Recipharm Parets S.L.
Ramón y Cajal, 2
08150 Parets del Vallés (Spain)
This medicinal product is authorised in the Member States of the EEA under the following
Rupatall 1mg/ml oral solution
Rinialer 1mg/ml oral solution
Rupafin 1mg/ml oral solution
Wystamm 1mg/mloral solution
Tamalis 1mg/mloral solution
Pafinur 1 mg/ml oral solution
Austria, Bulgaria, Croatia, Cyprus, Denmark, Estonia,
Germany, Greece, Iceland, Italy, Ireland, Latvia,
Liechtenstein, Lithuania, Netherlands, Norway, Poland,
Slovenia, Slovak Republic, Spain, United Kingdom
Hungary, Czech Republic, Romania
This leaflet was last approved in February 2015