MedPath
EMA Approval

Opatanol

S01GX09

olopatadine

Ophthalmologicals

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.

Authorisations (1)

EMEA/H/C/000407

Novartis Europharm Limited,Vista Building,Elm Park,Merrion Road,Dublin 4,Ireland

Authorised

May 16, 2002

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.

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