Valsts: Lielbritānija
Valoda: angļu
Klimata pārmaiņas: MHRA (Medicines & Healthcare Products Regulatory Agency)
Ketorolac trometamol
Necessity Supplies Ltd
S01BC05
Ketorolac trometamol
5mg/1ml
Eye drops
Ocular
No Controlled Drug Status
Valid as a prescribable product
BNF: 11080200
UNCOMMON may affect up to 1 in 100 people. Inflammation or damage to the front clear layer of the eye, eye dryness and/or wa- tery eyes. NOT KNOWN frequency cannot be estimated from the available data. Damage on the surface of the eye such as thinning, erosion, degradation of cell(s), difficulty in breathing or wheezing, aggravation of asthma, ulcer-damage to the surface of the eye. REPORTING OF SIDE EFFECTS If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the GOOGLE PLAY or APPLE APP STORE. By reporting side effects you can help provide more information on the safety of this medicine. KEEP OUT OF THE SIGHT AND REACH OF CHILDREN. Do not use Acular if you notice the tamper-proof seal is broken. Do not use Acular after the expiry date which is stated on the bottle label and the bottom of the carton after EXP. The expiry date refers to the last day of that month. Do not store above 25°C. DISCARD THE BOTTLE 15 DAYS AFTER OPENING, EVEN IF THERE IS SOLUTION REMAINING. 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 to protect the environment. WHAT ACULAR CONTAINS It contains 0.5% ketorolac trometamol as the active ingredient. It also contains the following ingredients: benzalkonium chloride, disodium edetate, octoxynol 40, sodium chloride, sodium hydroxide or hydrochloric acid (to adjust pH) and purified water. WHAT ACULAR LOOKS LIKE AND CONTENTS OF THE PACK Acular are supplied as a clear, colourless to slightly yellow solution in a plastic bottle containing 5ml of the solution. MANUFACTURER This product is manufactured by: ALLERGAN PHARMACEUTICALS, (IRELAND) LTD, CASTLEBAR ROAD, WESTPORT, COUNTY MAYO, IRELAND. It is procured from within the EU. Product Licence holder: G-PHARMA LTD, SALFORD Izlasiet visu dokumentu