Diamox 250mg Tablets
PACKAGE LEAFLET: INFORMATION FOR THE USER
Diamox® 250mg Tablets
(acetazolamide)
Read all of this leaflet carefully before you start taking this med icine.
Keep this leaflet. You may need to read it again.
If you have any further questions, ask your doctor or pharmacist.
This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours. If any of the side effects become serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist. The name of your medicine is Diamox 250mg Tablets but will be referred to as Diamox Tablets throughout this leaflet.
I n this leaflet:
1. What Diamox Tablets are and what they are used for
2. Before you take Diamox Tablets
3. How to take Diamox Tablets
4. Possible side effects
5. How to store Diamox Tablets
6. Further information
1. WHAT DIAMOX TABLETS ARE AND WHAT THEY ARE USED FOR
Diamox Tablets contain the active substance acetazolamide. This belongs to a group of medicines known as carbonic anhydrase inhibitors.
Diamox Tablets are used to treat:
• glaucoma (a condition of the eye), by reducing the pressure within the eye
• abnormal retention of fluids (Diamox Tablets act as a diuretic)
• epilepsy (fits or convulsions)
2. BEFORE YOU TAKE DIAMOX TABLETS
DO NOT take Diamox Tablets if:
• you know you are allergic to sulphonamides, sulphonamide derivatives including acetazolamide or to any of the ingredients in the medicine (listed in Section 6 at the end of this leaflet)
• you have severe liver problems
• you have or have ever had severe kidney problems
• you have a particular type of glaucoma known as chronic non congestive angle closure glaucoma (your doctor will be able to advise you)
• you have reduced function of the adrenal glands - glands above the kidneys - (also known as Addison’s disease)
• you have low blood levels of sodium and/or potassium or high blood levels of chlorine (your doctor will advise you)
Speak to your doctor if any of the above applies to you
Take special care and speak to your doctor before taking Diamox Tablets if:
• you have or have ever had kidney problems such as kidney stones
• you have lung problems such as chronic bronchitis or emphysema, which cause difficulty in breathing
• you are over the age of 65
• a small number of people being treated with anti-epileptics such as acetazolamide have had thoughts of harming or killing themselves, if at any time you have these thoughts, immediately contact your doctor
Diamox Tablets may affect some medical tests. If you visit a hospital or clinic for any medical tests, you should tell the doctor concerned that you are taking Diamox Tablets.
Taking other medicines:
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. The effects of any of these medicines may change, particularly if you are taking, or using, any of the following:
• medicines for your heart such as cardiac glycosides (e.g. digoxin)
• medicines to reduce blood pressure
• medicines to thin your blood (e.g. warfarin)
• medicines to lower the sugar in your blood (e.g. metformin, gliclazide)
• medicines for epilepsy or fits (in particular, phenytoin, primidone or carbamazepine or topiramate)
• drugs which interfere with folic acid, e.g. methotrexate, pyrimethamine, or trimethoprim
• steroids such as prednisolone
• aspirin and related medicines, e.g. salicylic acid or choline salicylate for mouth ulcers
• other drugs in the group of medicines called carbonic anhydrase inhibitors (e.g. dorzolamide or brinzolamide which are also used to treat glaucoma)
• amphetamines (a stimulant), quinidine (treats an irregular heart beat), methenamine (prevents urine infections) or lithium (treats severe mental problems)
• sodium bicarbonate therapy (used to treat high states of acid in your body)
• ciclosporin (used to suppress the immune system)
Pregnancy and breast-feeding:
Ask your doctor or pharmacist for advice before taking any medicines.
Diamox Tablets SHOULD NOT be taken if you are pregnant, think you are pregnant or are planning to become pregnant.
It may be taken when breast-feeding but only on the advice of the doctor.
Driving and using machines:
If Diamox Tablets make you feel drowsy or confused you should not drive or operate machines. Diamox Tablets can occasionally cause short-sightedness; if this happens and you feel that you can no longer drive safely, you should stop driving and contact your doctor.
3. HOW TO TAKE DIAMOX TABLETS
• Always take the number of tablets your doctor has told you to take. This information will also be on the label.
• Diamox Tablets should be swallowed whole with a drink of water, just before or just after a meal. Do not chew or crush the tablets.
• The dose varies from person to person depending on their condition. Your doctor will decide on the most appropriate dose. If you are not sure how many tablets to take or when to take them, ask your doctor or pharmacist.
USUAL DOSES:
Glaucoma:
Adults: 250mg-1000mg (1-4 tablets) every 24 hours, in divided doses.
Retention of fluid:
Adults: starting dose is 250-375mg (1-1.5 tablets) once daily in the morning. Your doctor will adjust the dose and tell you how often to take your dose.
Epilepsy:
Adults: 250-1000mg daily in divided doses.
Children: the dose will depend on the bodyweight of the child, to be taken in divided doses. Dose should not be more than 750mg (3 tablets) per day.
• Before starting and during treatment your doctor may monitor your blood to check that treatment with Diamox Tablets is suitable for you.
If you take more Diamox Tablets than you should:
Get medical help immediately, either by calling your doctor or going to the nearest hospital casualty department. Take any remaining tablets and this leaflet with you so that the medical staff know exactly what you have taken.
If you forget to take your Diamox Tablets:
You should take it as soon as you remember. However, if this is within two hours of your next dose you should skip the missed tablet and carry on taking the rest of your tablets as usual.
DO NOT take a double dose of tablets to make up the missed dose.
If you have any further questions about these tablets, ask your doctor or pharmacist.
POSSIBLE SIDE EFFECTS
Like all medicines, Diamox Tablets can cause side effects, although not everybody gets them.
ll medicines can cause allergic reactions although serious allergic reactions are very rare. Any sudden wheeziness, difficulty in breathing, swelling of the eyelids, face or lips, rash or itching (especially affecting your whole body) should be reported to a doctor immediately.
Extremely rarely, Diamox Tablets can affect the cells in your blood. This could mean that you are more likely to catch infections and that your blood may not clot properly. If you have a sore throat or fever or you notice bruises or tiny red or purple spots on your skin you should contact your doctor immediately. If your muscles feel weak or you have fits, you should see your doctor immediately.
Very rarely, Diamox Tablets can affect the liver and kidneys. If you experience pain in your lower back, pain or burning when you pass urine, have difficulty in passing urine, or you stop passing urine, have blood in your urine, pale stools, or if your skin or eyes look slightly yellow, you should contact your doctor. You should also contact your doctor if your stools are black or tarry, or if you notice blood in your stools.
Common side effects are:
• headache
• diarrhoea
• feeling or being sick, loss of appetite, thirst, or a metallic taste in the mouth
• dizziness, loss of full control of arms or legs
• looking flushed
• a need to pass urine more often than normal
• tiredness or irritability
• feeling over-excited
• a tingling or numbness in the fingers or toes, or coldness in the extremities
Uncommon side effects are:
• depression
• drowsiness or confusion
• a loss of interest in sex
• ringing in the ears or difficulty in hearing
• temporary short-sightedness which subsides when the dosage is reduced or treatment is stopped
Rare cases of skin rashes including an increased sensitivity to sunlight have been reported. If you experience any unusual skin rashes, inform your doctor.
If you take Diamox Tablets for a long time it can occasionally affect the amount of potassium, or sodium in your blood. Your doctor will probably take blood tests to check that this does not happen. You might also experience bone thinning or the risk of kidney stones with long-term therapy. High or low blood sugar levels may occasionally occur.
If any of the side effects becomes serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
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.
5. HOW TO STORE DIAMOX TABLETS
KEEP OUT OF THE SIGHT AND REACH OF CHILDREN.
o not take your tablets after the expiry date which is stated on the carton/blister label after ‘Exp’. The expiry date refers to the last day of that month.
Do not store above 25°C.
If your tablets become discoloured or show any signs of deterioration, you should seek the advice of your pharmacist.
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.
REMEMBER: This medicine is for you. Only a doctor can prescribe it for you. Never give this medicine to someone else; it could harm them, even if their symptoms seem the same as yours.
6. FURTHER INFORMATION
What Diamox Tablets contain
he active ingredient is acetazolamide.
Each tablet contains 250mg acetazolamide. The other ingredients are sodium starch glycolate, povidone K29-32, calcium phosphate dihydrate, maize starch and magnesium stearate.
What Diamox Tablets look like and contents of pack
Diamox tablets are round, white tablets engraved with “DIAMOX 250” on one side and scored in quarters on the other.
Diamox Tablets are available in blister packs containing 12 tablets.
Manufactured by: TEOFARMA S.r.l. - Viale Certosa, 8/A -27100 PAVIA, Italy.
Procured from within EU and repackaged by the Product Licence holder: B&S Healthcare, Unit 4, Bradfield Road, Ruislip, Middlesex, HA4 0NU, UK.
Diamox® 250mg Tablets, PL No: 18799/2327 |POM|
Leaflet date: 06.07.2015
_Acetazolamide Mercury Pharma 250mg Tablets_
Read all of this leaflet carefully before you start taking this med icine.
Keep this leaflet. You may need to read it again.
If you have any further questions, ask your doctor or pharmacist.
This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.
If any of the side effects become serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
The name of your medicine is Acetazolamide Mercury Pharma 250mg Tablets but will be referred to as Acetazolamide Tablets throughout this leaflet.
I n this leaflet:
1. What Acetazolamide Tablets are and what they are used for
2. Before you take Acetazolamide Tablets
3. How to take Acetazolamide Tablets
4. Possible side effects
5. How to store Acetazolamide Tablets
6. Further information
1. WHAT ACETAZOLAMIDE TABLETS ARE AND WHAT THEY ARE USED FOR
Acetazolamide Tablets contain the active substance acetazolamide. This belongs to a group of medicines known as carbonic anhydrase inhibitors.
Acetazolamide Tablets are used to treat:
• glaucoma (a condition of the eye), by reducing the pressure within the eye
• abnormal retention of fluids (Acetazolamide Tablets act as a diuretic)
• epilepsy (fits or convulsions)
2. BEFORE YOU TAKE ACETAZOLAMIDE TABLETS
DO NOT take Acetazolamide Tablets if:
• you know you are allergic to sulphonamides, sulphonamide derivatives including acetazolamide or to any of the ingredients in the medicine (listed in Section 6 at the end of this leaflet)
• you have severe liver problems
• you have or have ever had severe kidney problems
• you have a particular type of glaucoma known as chronic non congestive angle closure glaucoma (your doctor will be able to advise you)
• you have reduced function of the adrenal glands - glands above the kidneys - (also known as Addison’s disease)
• you have low blood levels of sodium and/or potassium or high blood levels of chlorine (your doctor will advise you)
Speak to your doctor if any of the above applies to you
Take special care and speak to your doctor before taking Acetazolamide Tablets if:
• you have or have ever had kidney problems such as kidney stones
• you have lung problems such as chronic bronchitis or emphysema, which cause difficulty in breathing
• you are over the age of 65
• a small number of people being treated with anti-epileptics such as acetazolamide have had thoughts of harming or killing themselves, if at any time you have these thoughts, immediately contact your doctor
Acetazolamide Tablets may affect some medical tests. If you visit a hospital or clinic for any medical tests, you should tell the doctor concerned that you are taking Acetazolamide Tablets.
Taking other medicines:
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. The effects of any of these medicines may change, particularly if you are taking, or using, any of the following:
• medicines for your heart such as cardiac glycosides (e.g. digoxin)
• medicines to reduce blood pressure
• medicines to thin your blood (e.g. warfarin)
• medicines to lower the sugar in your blood (e.g. metformin, gliclazide)
• medicines for epilepsy or fits (in particular, phenytoin, primidone or carbamazepine or topiramate)
• drugs which interfere with folic acid, e.g. methotrexate, pyrimethamine, or trimethoprim
• steroids such as prednisolone
• aspirin and related medicines, e.g. salicylic acid or choline salicylate for mouth ulcers
• other drugs in the group of medicines called carbonic anhydrase inhibitors (e.g. dorzolamide or brinzolamide which are also used to treat glaucoma)
• amphetamines (a stimulant), quinidine (treats an irregular heart beat), methenamine (prevents urine infections) or lithium (treats severe mental problems)
• sodium bicarbonate therapy (used to treat high states of acid in your body)
• ciclosporin (used to suppress the immune system)
Pregnancy and breast-feeding:
Ask your doctor or pharmacist for advice before taking any medicines.
Acetazolamide Tablets SHOULD NOT be taken if you are pregnant, think you are pregnant or are planning to become pregnant.
It may be taken when breast-feeding but only on the advice of the doctor.
Driving and using machines:
If Acetazolamide Tablets make you feel drowsy or confused you should not drive or operate machines. Acetazolamide Tablets can occasionally cause short-sightedness; if this happens and you feel that you can no longer drive safely, you should stop driving and contact your doctor.
3. HOW TO TAKE ACETAZOLAMIDE TABLETS
• Always take the number of tablets your doctor has told you to take. This information will also be on the label.
• Acetazolamide Tablets should be swallowed whole with a drink of water, just before or just after a meal. Do not chew or crush the tablets.
• The dose varies from person to person depending on their condition. Your doctor will decide on the most appropriate dose. If you are not sure how many tablets to take or when to take them, ask your doctor or pharmacist.
USUAL DOSES:
Glaucoma:
Adults: 250mg-1000mg (1-4 tablets) every 24 hours, in divided doses.
Retention of fluid:
Adults: starting dose is 250-375mg (1-1.5 tablets) once daily in the morning. Your doctor will adjust the dose and tell you how often to take your dose.
Epilepsy:
Adults: 250-1000mg daily in divided doses.
Children: the dose will depend on the bodyweight of the child, to be taken in divided doses. Dose should not be more than 750mg (3 tablets) per day.
• Before starting and during treatment your doctor may monitor your blood to check that treatment with Acetazolamide Tablets is suitable for you.
If you take more Acetazolamide Tablets than you should:
Get medical help immediately, either by calling your doctor or going to the nearest hospital casualty department. Take any remaining tablets and this leaflet with you so that the medical staff know exactly what you have taken.
If you forget to take your Acetazolamide Tablets:
You should take it as soon as you remember. However, if this is within two hours of your next dose you should skip the missed tablet and carry on taking the rest of your tablets as usual.
DO NOT take a double dose of tablets to make up the missed dose.
If you have any further questions about these tablets, ask your doctor or pharmacist.
POSSIBLE SIDE EFFECTS
Like all medicines, Acetazolamide Tablets can cause side effects, although not everybody gets them.
ll medicines can cause allergic reactions although serious allergic reactions are very rare. Any sudden wheeziness, difficulty in breathing, swelling of the eyelids, face or lips, rash or itching (especially affecting your whole body) should be reported to a doctor immediately.
Extremely rarely, Acetazolamide Tablets can affect the cells in your blood. This could mean that you are more likely to catch infections and that your blood may not clot properly. If you have a sore throat or fever or you notice bruises or tiny red or purple spots on your skin you should contact your doctor immediately. If your muscles feel weak or you have fits, you should see your doctor immediately.
Very rarely, Acetazolamide Tablets can affect the liver and kidneys. If you experience pain in your lower back, pain or burning when you pass urine, have difficulty in passing urine, or you stop passing urine, have blood in your urine, pale stools, or if your skin or eyes look slightly yellow, you should contact your doctor. You should also contact your doctor if your stools are black or tarry, or if you notice blood in your stools.
Common side effects are:
• headache
• diarrhoea
• feeling or being sick, loss of appetite, thirst, or a metallic taste in the mouth
• dizziness, loss of full control of arms or legs
• looking flushed
• a need to pass urine more often than normal
• tiredness or irritability
• feeling over-excited
• a tingling or numbness in the fingers or toes, or coldness in the extremities
Uncommon side effects are:
• depression
• drowsiness or confusion
• a loss of interest in sex
• ringing in the ears or difficulty in hearing
• temporary short-sightedness which subsides when the dosage is reduced or treatment is stopped
Rare cases of skin rashes including an increased sensitivity to sunlight have been reported. If you experience any unusual skin rashes, inform your doctor.
If you take Acetazolamide Tablets for a long time it can occasionally affect the amount of potassium, or sodium in your blood. Your doctor will probably take blood tests to check that this does not happen. You might also experience bone thinning or the risk of kidney stones with long-term therapy. High or low blood sugar levels may occasionally occur.
If any of the side effects becomes serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
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.
5. HOW TO STORE ACETAZOLAMIDE TABLETS
KEEP OUT OF THE SIGHT AND REACH OF CHILDREN.
o not take your tablets after the expiry date which is stated on the carton/blister label after ‘Exp'. The expiry date refers to the last day of that month.
Do not store above 25°C.
If your tablets become discoloured or show any signs of deterioration, you should seek the advice of your pharmacist.
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.
REMEMBER: This medicine is for you. Only a doctor can prescribe it for you. Never give this medicine to someone else; it could harm them, even if their symptoms seem the same as yours.
6. FURTHER INFORMATION
What Acetazolamide Tablets contain
he active ingredient is acetazolamide.
Each tablet contains 250mg acetazolamide. The other ingredients are sodium starch glycolate, povidone K29-32, calcium phosphate dihydrate, maize starch and magnesium stearate.
What Acetazolamide Tablets look like and contents of pack
Acetazolamide tablets are round, white tablets engraved with ‘DIAMOX 250' on one side and scored in quarters on the other. Acetazolamide Tablets are available in blister packs containing 12 tablets.
Manufactured by: TEOFARMA S.r.l. - Viale Certosa, 8/A -27100 PAVIA, Italy.
Procured from within EU and repackaged by the Product Licence holder: B&S Healthcare, Unit 4, Bradfield Road, Ruislip, Middlesex, HA4 0NU, UK.
Acetazolamide Mercury Pharma 250mg Tablets, PL No: 18799/2327 |POM|
Leaflet date: 06.07.2015