Basic Information
R06AX27
desloratadine
Antihistamines for systemic use
Therapeutic indication
Aerius is indicated for the relief of symptoms associated with:
- allergic rhinitis;
- urticaria.
Overview Summary
This is a summary of the European public assessment report (EPAR) for Aerius. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Aerius.
Active Substances (1)
desloratadine
Documents (19)
Aerius : EPAR - Summary for the public
June 18, 2008
OVERVIEW_DOCUMENT
Aerius-H-C-313-P46-0064 : EPAR - Assessment Report
March 30, 2015
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius : EPAR - All Authorised presentations
August 30, 2007
AUTHORISED_PRESENTATIONS
Aerius-H-C-313-X-0033 : EPAR - Assessment Report - Extension
July 22, 2014
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius-H-C-313-X-0032 : EPAR - Assessment Report - Extension
July 22, 2014
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius-H-C-313-P46-0060 : EPAR - Assessment Report
February 28, 2013
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP post-authorisation summary of positive opinion for Aerius on 21 February 2008
February 20, 2008
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius : EPAR - Steps taken after authorisation when a cutoff date has been used
April 2, 2006
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius-H-C-PSUSA-00000962-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
June 9, 2022
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius : EPAR - Scientific Discussion
April 2, 2006
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Aerius : EPAR - Procedural steps taken before authorisation
April 2, 2006
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius : EPAR - Scientific Discussion
April 2, 2006
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius : EPAR - Risk-management-plan summary
June 21, 2021
RISK_MANAGEMENT_PLAN_SUMMARY
Aerius-H-C-PSUSA-00000962-201607 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
June 6, 2017
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius : EPAR - Procedural steps taken before authorisation
April 2, 2006
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Aerius-H-C-313-P46-0063 : EPAR - Assessment Report
November 12, 2014
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius : EPAR - Procedural steps taken and scientific information after authorisation
March 31, 2009
CHANGES_SINCE_INITIAL_AUTHORISATION
Aerius : EPAR - Product information
June 25, 2009
DRUG_PRODUCT_INFORMATION
Aerius-H-C-313-P45-0057: EPAR - Assessment Report
September 25, 2012
CHANGES_SINCE_INITIAL_AUTHORISATION
Overview Q&A (9)
Question
What is Aerius?
Answer
Aerius is a medicine containing the active substance desloratadine. It is available as a 5 mg tablet, 2.5 mg and 5 mg orodispersible tablets (tablets that dissolve in the mouth), a 0.5 mg/ml syrup and a 0.5 mg/ml oral solution.
Question
What is Aerius used for?
Answer
Aerius is used to relieve the symptoms of allergic rhinitis (inflammation of the nasal passages caused by an allergy, for example, hay fever or allergy to dust mites) or urticaria (a skin condition caused by an allergy, with symptoms including itching and hives).
The medicine can only be obtained with a prescription.
Question
How is Aerius used?
Answer
The recommended dose for adults and adolescents (12 years of age and over) is 5 mg once a day. The dose in children depends on their age. For children from one to five years of age, the dose is 1.25 mg once a day, taken as 2.5 ml syrup or oral solution. For children from six to 11 years of age, the dose is 2.5 mg once a day, taken either as 5 ml of the syrup or oral solution, or as one 2.5-mg orodispersible tablet. Adults and adolescents can use any form of the medicine.
Question
How does Aerius work?
Answer
The active substance in Aerius, desloratadine, is an antihistamine. It works by blocking the receptors to which histamine, a substance in the body that causes allergic symptoms, normally attaches itself. When the receptors are blocked, histamine cannot have its effect, and this leads to a decrease in the symptoms of allergy.
Question
Other information about Aerius
Answer
The European Commission granted a marketing authorisation valid throughout the European Union for Aerius on 15 January 2001.
For more information about treatment with Aerius, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.
Question
How has Aerius been studied?
Answer
Aerius has been studied in a total of eight studies involving about 4,800 adult and adolescent patients with allergic rhinitis (including four studies in seasonal allergic rhinitis, and two studies in patients who also had asthma). The effectiveness of Aerius was measured by looking at the change in the symptoms (nasal discharge, itching, sneezing and congestion) before and after two or four weeks of treatment.
Aerius has also been studied in 416 patients with urticaria. The effectiveness was measured by looking at the change in the symptoms (itching, number and size of hives, interference with sleep and daytime function) before and after six weeks of treatment.
In all studies, the effectiveness of Aerius was compared with that of placebo (a dummy treatment).
Additional studies were presented to show that the syrup, oral solution and orodispersible tablets are treated by the body in the same way as the tablets, and to show that they can be used safely in children.
Question
What benefit has Aerius shown during the studies?
Answer
In allergic rhinitis, looking at the results of all studies taken together, two weeks of treatment with 5 mg Aerius led to an average decrease in symptom score of 25 to 32%, compared with a decrease of 12 to 26% in the patients receiving placebo. In the two studies in urticaria, the decrease in symptom score after six weeks of treatment with Aerius was 58 and 67%, compared with 40 and 33% in placebo-treated patients.
Question
Why has Aerius been approved?
Answer
The CHMP decided that Aerius’s benefits are greater than its risks for the relief of symptoms associated with allergic rhinitis or urticaria and recommended that it be given marketing authorisation.
Question
What is the risk associated with Aerius?
Answer
In adults and adolescents, the most common side effects are fatigue (tiredness; 1.2%), dry mouth (0.8%) and headache (0.6%). The side effects seen in children are similar. In children less than two years of age, the most common side effects are diarrhoea (3.7%), fever (2.3%) and insomnia (difficulty sleeping; 2.3%). For the full list of all side effects reported with Aerius, see the package leaflet.
Aerius must not be used in people who are hypersensitive (allergic) to desloratadine, loratadine or any of the other ingredients.