Patient Leaflet Updated 14-Jun-2023 | Dr. Reddy's Laboratories (UK) Ltd
Fexofenadine hydrochloride 180mg Film-coated Tablets
Fexofenadine hydrochloride 180 mg Film-Coated Tablets
Fexofenadine hydrochloride
1. What Fexofenadine hydrochloride 180 mg Film-Coated Tablets are and what they are used for
2. What you need to know before you take Fexofenadine hydrochloride 180 mg Film-Coated Tablets
3. How to take Fexofenadine hydrochloride 180 mg Film-Coated Tablets
4. Possible side effects
5. How to store Fexofenadine hydrochloride 180 mg Film-Coated Tablets
6. Contents of the pack and other information
Fexofenadine hydrochloride 180 mg Film-Coated Tablets contain fexofenadine hydrochloride, which is an antihistamine.
Fexofenadine hydrochloride 180 mg Film-Coated Tablets are used in adults and adolescents of 12 years and older to relieve the symptoms that occur with long term allergic skin reactions (chronic idiopathic urticaria) such as itching, swelling and rashes.
Fexofenadine Hydrochloride 180 mg Film-Coated Tablets will also be referred to in this leaflet as Fexofenadine Tablets.
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.
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.
If you are pregnant or breastfeeding, think you may be pregnant or planning to have a baby, ask your doctor or pharmacist for advice before taking any medicine.
Do not take Fexofenadine hydrochloride 180 mg Film-Coated Tablets if you are pregnant, unless necessary. Fexofenadine Tablets are not recommended during breastfeeding.
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 (180 mg) daily. Take your tablet with water before a meal. This medicine starts to relieve your symptoms within 1 hour and lasts for 24 hours.
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 as prescribed by your doctor.
Tell your doctor if you want to stop taking Fexofenadine Tablets before you have finished your course of treatment. If you stop taking Fexofenadine Tablets earlier than planned, your symptoms may return.
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.
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 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.
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.
The active substance is fexofenadine hydrochloride. Each Film-Coated Tablet contains 180 mg of fexofenadine hydrochloride; equivalent to 168 mg 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)
Fexofenadine hydrochloride 180 mg Film-Coated Tablets are pink coloured, oval, tablets marked with “FXF” on one side and “180” on the other side.
Fexofenadine Tablets are packed in blister strips packaged in cartons.
The cartons contain 20 or 30 Tablets. Not all packs may be marketed.
Fexofenadine hydrochloride 180 mg Film-Coated Tablets: PL08553/0274
This leaflet was last revised in 02/2023
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