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Cystocalm 4g Granules For Oral Solution

Document: leaflet GALPHARM_PL 12063-0045 change

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Lystocalm 4g Granules for Oral Solution

1 Sodium Citrate

PATIENT INFORMATION LEAFLET

Read all of this leaflet carefully before • have a history of kidney disease you take this medicine because it • are on a low sodium (salt) diet. c^rnsirnpcji-tarrt informationu Talk to your doctor if you have: need to know. * symptoms which carry on for more than 4 This medicine is available without days after you ^ start taking this medicine. prescription, however, you still need to use * symptoms which keep recurring.

this product carefully to get the best results Talk to your doctor or pharmacist if you

from it. Keep this leaflet as you may need to are taking:

read it again. Ask your pharmacist if you * lithium for manic depression

need more information or advice. * methenamine for urinary infections

* other medicines as these may be

1.    What is this medicine and affected by taking this medicine.

what is it used for? Please see your doctor or pharmacist This medicine contains: before taking this medicine if you:

*    sodium citrate, which is used to relieve * have an intolerance to some sugars. discom.fort in urinary tratf hfecfo^ such other important information:

as cystitis by making the urine less acidic. Pregnancy and breast feeding:

These sachets are used for the relief of the This medicine is not recommended if you symptoms of cystitis in women. Cystitis is are pregnant or breastfeeding. please see an inflammation of the bladder, which your doctor or pharmacist before taking causes painful irritation and an unpleasant this medicineburning sensation when passing water. Information about some of the

ingredients in this medicine:

2.    Is this medicine suitable Contains sucrose. If you have been told for you? by your doctor that you have an intolerance

Do not take this medicine if you: t^Te sugar®., contactyoutr doctor before

*    are allergic to sodium citrate* or any of taking this medicinal product

the other ingredients Each sachet contains 939 mg of sodium.

*    suffer from heart disease To be taken into consideration by patients

*    have high blood pressure on a controlled sodium diet.

*    have diabetes Please turn over ^

3.    How to take this medicine 5. How to store your medicine

Mix the contents of the sachet with a (200 ml) Keep out of the sight and reach of glass of water and drink immediately. children.

This is a 2-day course of treatment. Do not use this medicine after the expiry

date printed on the pack.

Adult women: r r

1 sachet 3 times a day for 2 days, as Store below 25°C, in a dry place. required.

This medicine is not to be used by men 6 What is in this medicine?

Ior children. Each 5.6 g sachet of granules contains the

active ingredient: sodium citrate dihydrate

Do not exceed the stated dose. 4.0 g. ___

If symptoms persist or worsen after the

2-day course is completed, consult your The other ingredients are: sucrose (sugar) doctor or pharmacist. Do not repeat the colloidial anhydrous si|ica, saccharin treatment without medical advice. sodium and cranberry flavouring.

If you take too many sachets by mistake, This product is available in a pack size of 6 contact your doctor or pharmacist straight sachets.

away' 7. Who makes this medicine?

4.    Possible side effects The Marketing Authorisation holder and Most people do not have any side effects while manufacturer is Wrafton Laboratories taking this medicine. However, if you experience Limited, Braunton, Devon, IEX33 2DU any side effects, or anything unusual happens, United Kingdom.

stop taking the medicine immediately, and see

your doctor or pharmacist. Text revised: December 2015.

* Passing water more frequently.

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. 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.

By reporting side effects you can help provide more information on the safety of

this medicine. PL 12063/0045 2753324

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