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The product code(s) for this leaflet is: PL 08553/0718.
Fexofenadine Hydrochloride 120 mg Film-Coated Tablets
Boots Fexofenadine Hydrochloride 120mg Film-Coated Tablets
fexofenadine hydrochloride
Fexofenadine Hydrochloride 120mg Film-Coated Tablets will also be referred to in this leaflet as Fexofenadine Tablets.
Always take this medicine exactly as described in this leaflet or as your doctor or pharmacist have told you.
1. What Fexofenadine Tablets are and what they are used for
2. What you need to know before you take Fexofenadine Tablets
3. How to take Fexofenadine Tablets
4. Possible side effects
5. How to store Fexofenadine Tablets
6. Contents of the pack and other information
Fexofenadine Tablets contain fexofenadine hydrochloride, which is a non-drowsy antihistamine.
Fexofenadine Tablets are used in adults and adolescents over 12 years of age to relieve the symptoms of allergic rhinitis (for example hayfever) such as sneezing, itchy, runny or blocked nose and itchy, red and watery eyes.
Talk to your doctor or pharmacist before taking Fexofenadine Tablets if you:
If any of these apply to you, or if you are not sure, tell your doctor before taking Fexofenadine Tablets.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
It is recommended that you leave about 2 hours between the time that you take Fexofenadine Tablets and your indigestion remedy.
Fexofenadine Tablets should not be taken during pregnancy and whilst breast-feeding unless advised by a doctor.
Fexofenadine Tablets are unlikely to affect your ability to drive or operate machinery. However, you should check that these tablets do not make you feel sleepy or dizzy before driving or operating machinery.
Fexofenadine Tablets also contain Allura Red AC Lake, which may cause allergic reactions.
For a full list of ingredients, please see 'Contents of the pack and other information'.
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
The recommended dose is one tablet (120mg) daily. Take your tablet with water before a meal. This medicine starts to relieve your symptoms within 1 hour and lasts for 24 hours. Fexofenadine Tablets are not recommended for children under 12 years of age.
If you take too many tablets, contact your doctor or the nearest hospital emergency department immediately. Symptoms of an overdose in adults are dizziness, drowsiness, fatigue and dry mouth.
Do not take a double dose to make up for a forgotten tablet. Take the next dose at the usual time.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following undesirable effects have been reported in clinical trials, with an incidence similar to those observed in patients who did not receive the drug (placebo).
Common side effects (may affect up to 1 in 10 people):
Uncommon side effects (may affect up to 1 in 100 people):
Additional side effects (frequency not known: cannot be estimated from the available data) which may occur are:
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: 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.
Keep this medicine out of the sight and reach of children.
The active substance is fexofenadine hydrochloride. Each film-coated tablet contains 120mg of fexofenadine hydrochloride; equivalent to 112mg of fexofenadine.
The other ingredients (excipients) are:
Fexofenadine Tablets are pink coloured, oval, tablets marked with “FXF” on one side and “120” on the other side.
Fexofenadine Tablets are packed in blister strips packaged in cartons.
The cartons contain 7, 10, 15, 20, 30 Tablets.
Not all pack sizes may be marketed.
This leaflet was last revised in July 2024.
Reference number: PL 08553/0718
If you would like any further information about this medicine, please contact
9047670-9047689