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Latest Drugs
Eye Health and Disorders Drug Data - A-Z (English)
Drug Class Description
Anti-inflammatories, non-steroid.Generic Name
Sodium Cromoglicate [cromoglycate]Drug Description
Aqueous drops.Presentation
Eye drops, sodium cromoglicate 2%.Indications
Allergic conjunctivitis.Adult Dosage
1 or 2 drops in each affected eye up to four times daily. Therapy should be continuous.Contra Indications
Soft contact lenses.Adverse Reactions
Transient burning or stinging.Manufacturer
Baker NortonDrug Availability
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Related News
MedImmune and Pfizer collaborate on anti cancer tremelimumab Eye Health and Disorders Page
Pfizer and MedImmune ( a subsidiary of AstraZeneca) will collaborate to develop tremelimumab. The drug was unsuccessful in a Phase III trial for Melanoma but discovery of a biomarker has spurred development and DebioPharm are running a Phase III trial for treatment of Melanoma.The agreement will give MedImmune global rights for cancer indications and Pfizer will retain rights to certain undisclosed combinations.
Luveniq is withdrawn from EMA for chronic non-infectious Uveitis Eye Health and Disorders Page
Lux Biosciences has withdrawn Luveniq (voclosporin oral) from the EMA as a treatment for chronic non-infectious Uveitis following a negative opinion from the CHMP which considered that the benefits of the drug did mnot outweight its risks.
Ocriplasmin for Vitromacular Adhesion is filed at EMA Eye Health and Disorders Page
The European Medicines Agency has accepted for review ocriplasmin (2.5 mg/ml, solution for injection) from Thrombogenics ,for the treatment of symptomatic Vitreomacular Adhesion (VMA) including macular hole. Ocriplasmin's MAA will be evaluated through the EMA's centralised procedure with an official start date of 19 October 2011 and, if approved, the product will gain marketing authorisation for all EU Member States simultaneously. Successful approval will make it the first pharmacological treatment for this indication. The company has kept to its stated time frames for the European filing and in announcing the EMA's acceptance of the MAA, the company once more reiterated its plans for the treatment to be filed with the US FDA by the end of the year
