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Fexofenadine Hydrochloride 120 mg Film-Coated Tablets

Active Ingredient:
ATC code: 
R06AX26
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About Medicine
The Patient Information Leaflet (PIL) is the leaflet included in the pack with a medicine.
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Last updated on emc: 06 Mar 2025

Below is a text only representation of the Patient Information Leaflet (ePIL).

The text only version may be available in large print, Braille or audio CD. For further information call emc accessibility on {phone} 0800 198 5000. The product code(s) for this leaflet is: PL 08553/0718.

Fexofenadine Hydrochloride 120 mg Film-Coated Tablets

PACKAGE LEAFLET: INFORMATION FOR THE USER

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.

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

Always take this medicine exactly as described in this leaflet or as your doctor or pharmacist have told you.

  • Keep this leaflet. You may need to read it again.
  • Ask your pharmacist if you need more information or advice.
  • This medicine is for your use only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
  • If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.
  • You must talk to a doctor if you do not feel better or if you feel worse after taking Fexofenadine Tablets.

What is in this leaflet

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

1. What Fexofenadine Tablets are and what they are used for

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.

2. What you need to know before you take Fexofenadine Tablets
Do not take Fexofenadine Tablets:
  • If you are allergic to fexofenadine or any of the other ingredients of this medicine (listed in Section 6).

Warnings and precautions

Talk to your doctor or pharmacist before taking Fexofenadine Tablets if you:

  • have problems with your liver or kidneys.
  • have or ever had heart disease, since this kind of medicine may lead to a fast or irregular heartbeat.
  • are elderly.

If any of these apply to you, or if you are not sure, tell your doctor before taking Fexofenadine Tablets.

Other medicines and Fexofenadine Tablets

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

  • If you are taking apalutamide (a medicine to treat prostate cancer), as the effect of fexofenadine may be decreased.
  • Indigestion remedies containing aluminium and magnesium may affect the action of Fexofenadine Tablets, by lowering the amount of medicinal product absorbed.

It is recommended that you leave about 2 hours between the time that you take Fexofenadine Tablets and your indigestion remedy.

Pregnancy and breast-feeding

Fexofenadine Tablets should not be taken during pregnancy and whilst breast-feeding unless advised by a doctor.

Driving and using machines

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'.

3. How to take Fexofenadine Tablets

Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.

For adults and children aged 12 years and over

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 more Fexofenadine Tablets than you should

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.

If you forget to take Fexofenadine Tablets

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.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Tell your doctor immediately and stop taking Fexofenadine Tablets if you experience:
  • swelling of the face, lips, tongue or throat and difficulty breathing, as these may be signs of a serious allergic reaction.

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):

  • headache
  • drowsiness
  • feeling sick (nausea)
  • dizziness.

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

  • tiredness
  • sleepiness.

Additional side effects (frequency not known: cannot be estimated from the available data) which may occur are:

  • difficulty sleeping (insomnia)
  • sleeping disorders
  • bad dreams
  • nervousness
  • blurred vision
  • fast or irregular heartbeat
  • diarrhoea
  • skin rash and itching
  • hives
  • serious allergic reactions which can cause swelling of the face, lips, tongue or throat, flushing, chest tightness, and difficulty breathing.

Reporting of side effects

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.

5. How to store Fexofenadine Tablets

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 after ‘EXP’. The expiry date refers to the last day of that month.
  • This medicine does not require any special storage condition.
  • Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. Contents of the pack and other information
What Fexofenadine Tablets contain

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:

  • Tablet core: powdered cellulose, mannitol (E421), maize starch, croscarmellose sodium, colloidal anhydrous silica, magnesium stearate.
  • Tablet coating: opadry pink film-coating mixture containing hypromellose (E464), titanium dioxide (E171), macrogol 400, allura red AC lake (FD&C Red #40) (E129), and iron oxide, black (E172)

What Fexofenadine Tablets look like and contents of the pack

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.

Marketing Authorisation Holder and Manufacturer
Dr. Reddy’s Laboratories (UK) Ltd
410 Cambridge Science Park
Milton Road
Cambridge
CB4 0PE
UK

Distributed by
The Boots Company PLC
Nottingham
NG2 3AA

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

The Boots Company PLC
Nottingham
NG2 3AA

9047670-9047689

THE BOOTS COMPANY PLC
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Address
1 Thane Road West, Beeston, Nottingham, NG2 3AA
Telephone
+44 (0)1159 595 165
Fax
+44 (0)1159 592 565