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DIPENTUM 500 MG TABLETS, OLSALAZINE SODIUM 500 MG TABLETS - patient leaflet, side effects, dosage

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Patient leaflet - DIPENTUM 500 MG TABLETS, OLSALAZINE SODIUM 500 MG TABLETS

3. how to take dipentum

Always use Dipentum exactly as your doctor has told you.

Important:

Your doctor will choose the dose that is right for you. Your dose will be shown clearly on the label that your pharmacist puts on your medicine. If it does not, or you are not sure, ask your doctor or pharmacist.

Remember: Your medicine should always be taken after food.

Adults, children over 12 and the elderly

Acute flare-ups

  • The usual starting dose is two tablets a day (one in the morning, one in the evening at the end of a meal).
  • Your doctor may increase your dose until your condition improves.
  • You must not take more than six tablets a day or more than two tablets at a time.
  • If a ‘flare-up’ is severe you are likely to be given additional medicines.

Maintenance treatment

  • Once the ‘flare-up’ is controlled your doctor may gradually reduce your dose to one tablet twice a day (one in the morning, one in the evening at the end of a meal).
  • This is to prevent further ‘flare-ups’
  • You may remain on this treatment, provided it remains effective, for a long period of time.

If you take more Dipentum than you should Do not take more Dipentum than you should. If you have taken too many, immediately go to the nearest hospital casualty department or your doctor. Take your tablets and this leaflet with you. Signs of taking too many Dipentum include nausea, vomiting and diarrhoea.

If you forget to take Dipentum

If you forget a dose take the next one as usual. Do not take a double dose to make up for a missed dose.

If you stop taking Dipentum

Do not stop taking Dipentum without first talking to your doctor even if your symptoms have improved.

If you have any further questions about the use of this medicine, ask your doctor or pharmacist.

4. possible side effects

Like all medicines Dipentum can cause side effects, although not everybody gets them.

Seek immediate medical help if you have any of the following symptoms (the frequency of these side effects is unknown):

  • Swelling of face, lips, tongue or throat which may cause difficulty in swallowing/bre­athing
  • Blood disorders (reduced number of blood cells) where you could have the following symptoms: bruise or bleed easily, have a persistent sore throat, mouth ulcers, dizziness and feeling tired and feverish
  • Pancreatitis where you could have the following symptoms: severe stomach pain, fever, feeling sick/being sick
  • Liver disease where you could have the following symptoms: feeling sick/being sick, loss of appetite, feeling generally unwell, itching and the whites of the eyes may become yellow.

Other possible side effects:

Common (affects less than 1 in 10 people):

  • Headache
  • Diarrhoea. It does not usually last very long,

but taking your medicine at the end of a meal helps to reduce diarrhoea.

  • Feeling sick
  • Rash
  • Joint pain

Uncommon (affects less than 1 in

100 people):

  • Fever
  • Being sick
  • Indigestion
  • Raised liver enzymes (tests your doctor may

perform will show changed liver function)

  • Itching and/or hives, a nettle-like rash
  • Unusual hair loss
  • Light sensitivity
  • Increased heart rate
  • Shortness of breath
  • Muscle pain
  • Pins and needles
  • Depression
  • Dizziness

The frequency of the following side effects is unknown:

  • Altered breakdown of blood cells in the liver which could result in jaundice (yellowing of skin/eyes)
  • Stomach pain
  • Inflammation of heart muscle
  • Awareness of your heartbeat
  • Inflammation of sac around heart muscle
  • Pain in passing urine or blood in the urine
  • Difficulty in breathing
  • Blurred vision
  • Loss of touch sensation/numbness

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:or search for MHRA Yellow Card in the Google Play or Apple App Store. Alternatively, you can call Freephone 0800 731 6789 (available from 10 a.m. to 2 p.m. Mondays to Fridays) or fill in a paper form available from your local pharmacy. By reporting side effects, you can help provide more information on the safety of this medicine.

5. how to store dipentum

Keep out of the sight and reach of children. Do not store above 25°C.

Keep the container tightly closed in order to protect from moisture.

Do not take the tablets after the expiry date which is stated on the carton and bottle labels after ‚Exp‘. The expiry date refers to the last day of that month.

If the tablet becomes discoloured or shows any signs of deterioration, 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.

  • 6. Further information

    What Dipentum contains

    The active ingredient in Dipentum is olsalazine sodium.

Each tablet contains 500mg olsalazine sodium. The other ingredients are magnesium stearate (E572), colloidal anhydrous silica, povidone (E1201) and crospovidone.

What Dipentum looks like and contents of the pack

Dipentum is yellow, capsule shaped tablet marked with ‘D500’ on one side and a score line on the other side.

Dipentum comes in plastic bottle with a tamper evident foil seal and a plastic screw cap containing 60 tablets.

Manufactured by: Waymade Plc, Sovereign House, Miles Gray Road, Basildon, Essex, SS14 3FR, UK. OR

Atnahs Pharma Denmark ApS, Orestads Blvd. 108, 2300 Kobenhavn, Denmark.

Procured from within the EU and repackaged by the Product Licence holder: B&S Healthcare, Unit 4, Bradfield Road, Ruislip, Middlesex, HA4 0NU, UK.

Dipentum ® 500mg tablets; PL 18799/2468 Leaflet date: 23.07.2020 |POM |

Dipentum is registered trademark of Atnahs Pharma UK Ltd.

Blind or partially sighted? Is this leaflet hard to see or read?

Call 0208 515 3763 to obtain the leaflet in a format suitable for you.

Patient Information Leaflet

Olsalazine sodium 500mg tablets

Read all of this leaflet carefully before you start taking this medicine.

  • 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.

The name of your medicine is Olsalazine sodium 500mg tablets but will be referred to as Olsalazine sodium throughout this leaflet.

In this leaflet:

  • 1. What Olsalazine sodium is for

  • 2. Before you take Olsalazine sodium

  • 3. How to take Olsalazine sodium

  • 4. Possible side effects

  • 5. How to store Olsalazine sodium

  • 6. Further information

  • 1. What Olsalazine sodium is for

Olsalazine sodium belongs to a group of medicines called aminosalicylates.

Olsalazine sodium works by reducing pain and swelling (inflammation) in the intestine. It reduces the actions of substances in the body that cause inflammation.

Olsalazine sodium is used to treat an inflammation of your large intestine (colon) called ulcerative colitis. It is used for short-term (acute) attacks (called ‘flare-ups’), and at a lower dose to maintain the improvement (maintenance treatment) and keep away further ‘flare-ups’.

If untreated, a severe attack of ulcerative colitis may cause death due to dehydration and bursting of the colon (peritonitis).

  • 2. Before you take Olsalazine sodium

    Do not take if:

  • You are allergic to olsalazine sodium or any of the other ingredients of Olsalazine sodium

(see section 6)

  • You have ever had an allergic reaction to any salicylates (e.g. aspirin and aspirincontaining products, including those bought over the counter)
  • You have severe kidney disease
  • You are a child under 12.

If any of the above apply to you talk to your doctor or pharmacist.

Take special care

Before you start taking Olsalazine sodium your doctor will do a blood test. This will be repeated every three months for the first year, every six months for the next four years and then once a year. This is to see how well your liver and kidneys are functioning.

You should also check for signs of worsening of allergies such as asthma.

Tell your doctor immediately if you develop unexplained bruising or bleeding accompanied with fever, dizziness, sore throat and mouth ulcers. You could have developed a blood disorder.

Tell your doctor if you are taking any of the following medicines:

  • Aspirin or any other aspirin-containing medicines or salicylates
  • Other drugs to treat ulcerative colitis
  • Blood thinning agents such as warfarin or

heparin or heparinoids

  • Drugs that treat irritable bowel syndrome and cancer such as thioguanine and 6 mercaptopurine
  • If you have recently had chickenpox vaccination (taking Olsalazine sodium may cause a greater risk of Reye's syndrome; a life threatening condition)
  • Any other medicine, including medicines obtained without a prescription.

Taking Olsalazine sodium with food and drink

Always take Olsalazine sodium with a glass of water after food.

Pregnancy and breast-feeding

If you are pregnant, or trying to become pregnant or breast-feeding, talk to your doctor before taking Olsalazine sodium.

Driving and using machines

If you experience dizziness and/or blurred vision whilst taking Olsalazine sodium do not drive or use machinery.

3. how to take olsalazine sodium

Always use Olsalazine sodium exactly as your doctor has told you.

Important:

Your doctor will choose the dose that is right for you. Your dose will be shown clearly on the label that your pharmacist puts on your medicine. If it does not, or you are not sure, ask your doctor or pharmacist.

Remember: Your medicine should always be taken after food.

Adults, children over 12 and the elderly

Acute flare-ups

  • The usual starting dose is two tablets a day (one in the morning, one in the evening at the end of a meal).
  • Your doctor may increase your dose until your condition improves.
  • You must not take more than six tablets a day or more than two tablets at a time.
  • If a ‘flare-up’ is severe you are likely to be given additional medicines.

Maintenance treatment

  • Once the ‘flare-up’ is controlled your doctor may gradually reduce your dose to one tablet twice a day (one in the morning, one in the evening at the end of a meal).
  • This is to prevent further ‘flare-ups’
  • You may remain on this treatment, provided it remains effective, for a long period of time.

If you take more Olsalazine sodium than you should

Do not take more Olsalazine sodium than you should. If you have taken too many, immediately go to the nearest hospital casualty department or your doctor. Take your tablets and this leaflet with you. Signs of taking too many Olsalazine sodium include nausea, vomiting and diarrhoea.

If you forget to take Olsalazine sodium

If you forget a dose take the next one as usual. Do not take a double dose to make up for a missed dose.

If you stop taking Olsalazine sodium

Do not stop taking Olsalazine sodium without first talking to your doctor even if your symptoms have improved.

If you have any further questions about the use of this medicine, ask your doctor or pharmacist.

4. possible side effects

Like all medicines Olsalazine sodium can cause side effects, although not everybody gets them.

Seek immediate medical help if you have any of the following symptoms (the frequency of these side effects is unknown):

  • Swelling of face, lips, tongue or throat which may cause difficulty in swallowing/bre­athing
  • Blood disorders (reduced number of blood cells) where you could have the following symptoms: bruise or bleed easily, have a persistent sore throat, mouth ulcers, dizziness and feeling tired and feverish
  • Pancreatitis where you could have the following symptoms: severe stomach pain, fever, feeling sick/being sick
  • Liver disease where you could have the following symptoms: feeling sick/being sick, loss of appetite, feeling generally unwell, itching and the whites of the eyes may become yellow.

Other possible side effects:

Common (affects less than 1 in 10 people):

  • Headache
  • Diarrhoea. It does not usually last very long,

but taking your medicine at the end of a meal helps to reduce diarrhoea.

  • Feeling sick
  • Rash
  • Joint pain

Uncommon (affects less than 1 in

100 people):

  • Fever
  • Being sick
  • Indigestion
  • Raised liver enzymes (tests your doctor may

perform will show changed liver function)

  • Itching and/or hives, a nettle-like rash
  • Unusual hair loss
  • Light sensitivity
  • Increased heart rate
  • Shortness of breath
  • Muscle pain
  • Pins and needles
  • Depression
  • Dizziness

The frequency of the following side effects is unknown:

  • Altered breakdown of blood cells in the liver which could result in jaundice (yellowing of skin/eyes)
  • Stomach pain
  • Inflammation of heart muscle
  • Awareness of your heartbeat
  • Inflammation of sac around heart muscle
  • Pain in passing urine or blood in the urine
  • Difficulty in breathing
  • Blurred vision
  • Loss of touch sensation/numbness

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:or search for MHRA Yellow Card in the Google Play or Apple App Store. Alternatively, you can call Freephone 0800 731 6789 (available from 10 a.m. to 2 p.m. Mondays to Fridays) or fill in a paper form available from your local pharmacy. By reporting side effects, you can help provide more information on the safety of this medicine.

5. how to store olsalazine sodium

Keep out of the sight and reach of children. Do not store above 25°C.

Keep the container tightly closed in order to protect from moisture.

Do not take the tablets after the expiry date which is stated on the carton and bottle label after ‚Exp‘. The expiry date refers to the last day of that month.

If the tablet becomes discoloured or shows any signs of deterioration, 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.

  • 6. Further information

    What Olsalazine sodium contains

    The active ingredient in Olsalazine sodium is olsalazine sodium.

What Olsalazine sodium looks like and contents of the pack

Olsalazine sodium is yellow, capsule shaped tablet marked with ‘D500’ on one side and a score line on the other side.

Olsalazine sodium comes in plastic bottle with a tamper evident foil seal and a plastic screw cap containing 60 tablets.

Manufactured by: Waymade Plc, Sovereign House, Miles Gray Road, Basildon, Essex, SS14 3FR, UK. OR

Atnahs Pharma Denmark ApS, Orestads Blvd. 108, 2300 Kobenhavn, Denmark.

Procured from within the EU and repackaged by the Product Licence holder: B&S Healthcare, Unit 4, Bradfield Road, Ruislip, Middlesex, HA4 0NU, UK.

Olsalazine sodium 500mg tablets; PL 18799/2468

POM Leaflet date: 23.07.2020

Blind or partially sighted? Is this leaflet hard to see or read?

Call 0208 515 3763 to obtain the leaflet in a format suitable for you.