Basic Information
S01GX09
olopatadine
Ophthalmologicals
Therapeutic indication
Treatment of ocular signs and symptoms of seasonal allergic conjunctivitis.
Overview Summary
This is a summary of the European public assessment report (EPAR) for Opatanol. 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 Opatanol.
Active Substances (2)
olopatadine hydrochloride
olopatadine hydrochloride
Documents (14)
Opatanol : EPAR - All Authorised presentations
October 20, 2005
AUTHORISED_PRESENTATIONS
Opatanol : EPAR - Product Information
February 12, 2009
DRUG_PRODUCT_INFORMATION
Opatanol : EPAR - Procedural steps taken before authorisation
October 20, 2005
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Opatanol-H-C-407-P45-0013: EPAR - Assessment Report
November 13, 2012
CHANGES_SINCE_INITIAL_AUTHORISATION
Opatanol : EPAR - Procedural steps taken and scientific information after authorisation
February 12, 2009
CHANGES_SINCE_INITIAL_AUTHORISATION
Opatanol-H-C-407-P46-027 : EPAR - Assessment Report
January 9, 2019
CHANGES_SINCE_INITIAL_AUTHORISATION
Opatanol-H-C-407-P46-0016 : EPAR - Assessment Report
July 23, 2018
CHANGES_SINCE_INITIAL_AUTHORISATION
Opatanol : EPAR - Scientific Discussion
October 20, 2005
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Opatanol-H-C-407-P46-026 : EPAR - Assessment Report
January 9, 2019
CHANGES_SINCE_INITIAL_AUTHORISATION
Opatanol-H-C-407-P46-0019 : EPAR - Assessment Report
August 15, 2018
CHANGES_SINCE_INITIAL_AUTHORISATION
Opatanol-H-C-407-P46-0017 : EPAR - Assessment Report
July 23, 2018
CHANGES_SINCE_INITIAL_AUTHORISATION
Opatanol : EPAR - Summary for the public
February 12, 2009
OVERVIEW_DOCUMENT
Opatanol : EPAR - Procedural steps taken before authorisation
October 20, 2005
CHANGES_SINCE_INITIAL_AUTHORISATION
Opatanol : EPAR - Scientific Discussion
October 20, 2005
CHANGES_SINCE_INITIAL_AUTHORISATION
Overview Q&A (9)
Question
Other information about Opatanol
Answer
The European Commission granted a marketing authorisation valid throughout the European Union for Opatanol on 17 May 2002.
For more information about treatment with Opatanol, read the package leaflet (also part of the EPAR) or contact your doctor of pharmacist.
Question
What is Opatanol?
Answer
Opatanol is a clear eye drop solution, which contains the active substance olopatadine.
Question
What is Opatanol used for?
Answer
Opatanol is used to treat the eye symptoms of seasonal allergic conjunctivitis (inflammation of the eyes caused by pollen in patients with hayfever). These include itching, redness and swelling.
The medicine can only be obtained with a prescription.
Question
How is Opatanol used?
Answer
Opatanol is used in adults and children aged three years and older. It is given as one drop into the affected eye(s) twice a day, given eight hours apart. If another eye treatment is also being used, there should be a gap of five minutes between treatments; eye ointments should be administered last. Opatanol can be used for up to four months, if needed.
Question
How does Opatanol work?
Answer
The active substance in Opatanol, olopatadine, is an antihistamine. Olopatadine works by blocking the receptors on 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
Why has Opatanol been approved?
Answer
The CHMP decided that Opatanol’s benefits are greater than its risks for the treatment of ocular signs and symptoms of seasonal allergic conjunctivitis and recommended that it be given marketing authorisation.
Question
How has Opatanol been studied?
Answer
Opatanol has been studied in 688 patients in four main studies lasting between six and 14 weeks. Two of these studies included children. Opatanol was compared with cromolyn sodium (another anti-allergy medicine), with levocabastine (another antihistamine) and, in two studies, with placebo (a dummy treatment). In all of the studies, the main measure of effectiveness was based on the degree of itching and redness in the eye. One of the placebo studies also looked at these symptoms in relation to pollen counts.
Question
What benefit has Opatanol shown during the studies?
Answer
Opatanol was as effective as cromolyn sodium and as levocabastine. When compared with placebo, Opatanol was more effective only when pollen counts were taken into account, showing that the higher the level of pollen in the air, the greater the difference between the effects of Opatanol and those of placebo. At lower pollen counts, there were no differences between the two treatments.
Question
What is the risk associated with Opatanol?
Answer
The most common side effects with Opatanol (seen in between 1 and 10 patients in 100) are headache, dysgeusia (taste disturbances), eye pain, eye irritation, dry eyes, abnormal sensations in the eye, dry nose and fatigue (tiredness).
For the full list of all side effects reported with Opatanol, see the Package Leaflet.
Opatanol contains benzalkonium chloride, which is known to discolour soft contact lenses. Therefore care should be taken by people who wear soft contact lenses.