AERIUS 5 mg FILM-COATED TABLETS

2. What you need to know before you take Aerius

Do not take Aerius

• if you are allergic to desloratadine or any of the other ingredients of this medicine (listed in section 6) or to loratadine.

Warnings and precautions

Consult your doctor, pharmacist, or nurse before taking Aerius:

• if you have impaired kidney function.
• if you have a history of seizures.

Children and adolescents

Do not give this medicine to children under 12 years of age.

Other medicines and Aerius

There are no known interactions between Aerius and other medicines.

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

Taking Aerius with food, drinks, and alcohol

Aerius can be taken with or without food.

Be careful when taking Aerius with alcohol.

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 this medicine.

Aerius is not recommended if you are pregnant or breastfeeding.

No data are available on male and female fertility.

Driving and using machines

At the recommended dose, this medicine is not expected to affect your ability to drive or use machines. Although most people do not experience drowsiness, it is recommended not to engage in activities that require a state of alertness, such as driving a car or using machinery, until you have determined your own response to the medicine.

Aerius tablets contain lactose

If your doctor has told you that you have an intolerance to some sugars, contact them before taking this medicine.

3. How to take Aerius

Follow exactly the instructions given to you by your doctor or pharmacist. If you are not sure, ask your doctor or pharmacist again.

Use in adults and adolescents aged 12 and over

The recommended dose is one tablet once daily with water, with or without food.

This medicine is for oral use.

Swallow the tablet whole.

Regarding the duration of treatment, your doctor will determine the type of allergic rhinitis you have and for how long you should take Aerius.

If your allergic rhinitis is intermittent (symptoms present for less than 4 days a week or for less than 4 weeks), your doctor will recommend a treatment schedule based on the evaluation of your disease history.

If your allergic rhinitis is persistent (symptoms present for 4 or more days a week and for more than 4 weeks), your doctor may recommend long-term treatment.

For urticaria, the duration of treatment may vary from one patient to another, and you should follow your doctor's instructions.

If you take more Aerius than you should

Take Aerius only as directed by your doctor. An accidental overdose is not expected to cause serious problems. However, if you take more Aerius than you should, tell your doctor, pharmacist, or nurse immediately.

If you forget to take Aerius

If you forget to take your dose at the scheduled time, take it as soon as possible and then continue with your regular dosing schedule. Do not take a double dose to make up for forgotten doses.

If you stop taking Aerius

If you have any further questions on the use of this medicine, ask your doctor, pharmacist, or nurse.

4. Possible side effects

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

During the marketing of Aerius, very rare cases of severe allergic reactions (difficulty breathing, wheezing, itching, rash, and swelling) have been reported. If you experience any of these serious side effects, stop taking this medicine and seek medical attention immediately.

In clinical trials in adults, side effects were approximately the same as with a placebo. However, fatigue, dry mouth, and headache were reported more frequently than with a placebo. In adolescents, headache was the most commonly reported adverse reaction.

In clinical trials with Aerius, the following side effects were reported:

Frequent: may affect up to 1 in 10 people

• fatigue
• dry mouth
• headache

Very rare: may affect up to 1 in 10,000 people

• severe allergic reactions
• skin rash
• strong or irregular heartbeat
• fast heartbeat
• stomach pain
• nausea
• vomiting
• upset stomach
• diarrhea
• dizziness
• drowsiness
• difficulty sleeping
• muscle pain
• hallucinations
• seizures
• agitation with increased body movement
• liver inflammation
• abnormal liver function tests

Frequency not known: cannot be estimated from the available data

• unusual weakness
• yellowing of the skin and/or eyes
• increased sensitivity of the skin to the sun, even on cloudy days, and to ultraviolet light, such as from a sunlamp
• changes in heart rhythm
• abnormal behavior
• aggression
• weight gain, increased appetite
• depressed mood
• dry eyes

Children

Frequency not known: cannot be estimated from the available data

• slow heartbeat

• aggression
• changes in heart rhythm
• abnormal behavior

Reporting of side effects

If you experience 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 national reporting system listed in the website: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of Aerius

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 and blister after EXP. The expiry date refers to the last day of the month.

Do not store above 30°C. Store in the original package.

Do not use this medicine if you notice any change in the appearance of the tablets.

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 protect the environment.

6. Contents of the pack and other information

Composition of Aerius

• The active substance is desloratadine 5 mg
• The other ingredients of the tablet are: calcium hydrogen phosphate dihydrate, microcrystalline cellulose, maize starch, talc. The tablet coating contains a film coating (containing lactose monohydrate (see section 2 "Aerius tablets contain lactose"), hypromellose, titanium dioxide, macrogol 400, indigo carmine (E-132)), a clear coating (containing hypromellose, macrogol 400), carnauba wax, white wax.

Appearance and packaging

Aerius 5 mg film-coated tablets are light blue, round, and engraved with "C5" on one side and are smooth on the other.

Aerius 5 mg film-coated tablets are available in blisters in packs of 1, 2, 3, 5, 7, 10, 14, 15, 20, 21, 30, 50, 90, or 100 tablets.

Not all pack sizes may be marketed.

Marketing authorisation holder and manufacturer

Marketing authorisation holder:

N.V. Organon

Kloosterstraat 6

5349 AB Oss

Netherlands

Manufacturer:

Organon Heist bv, Industriepark 30, 2220 Heist-op-den-Berg, Belgium.

For further information on this medicine, contact the local representative of the marketing authorisation holder:

Date of last revision of this leaflet:02/2025.

Detailed information on this medicine is available on the European Medicines Agency website: https://www.ema.europa.eu.