Medine.co.uk

Videx 25 Mg Chewable Or Dispersible Tablet

10%

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Package leaflet: Information for the user

Videx 25 mg chewable/dispersible tablets

Didanosine



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BLACK

RETINO

SCREENED


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Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

■    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 only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.

■    If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.



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What is in this leaflet:

1.    What Videx is and what it is used for

2.    What you need to know before you take Videx

3.    How to take Videx

4.    Possible side effects

5.    How to store Videx

6.    Contents of the pack and other information

1.    What Videx is and what it is used for

Videx is an antiviral (or antiretroviral) medicine, used to treat Human Immunodeficiency Virus (HIV) infection. Videx belongs to a group of medicines called nucleoside reverse transcriptase inhibitors (NRTIs). It is normally used in combination with other anti-HIV medicines.

Videx is not a cure for HIV infection. You may continue to develop infections or other illnesses linked to HIV infection. You can still pass on HIV when taking this medicine, although the risk is lowered by effective antiretroviral therapy. Discuss with your doctor the precautions needed to avoid infecting other people..

2.    What you need to know before you take Videx

Videx will only be prescribed to you by a doctor with experience in medicines to treat HIV infection.

Do not take Videx

   if you are allergic to didanosine or any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Talk to your doctor or pharmacist before taking Videx.

   if you have or have had pancreatitis (inflammation of the pancreas), tell your doctor immediately. Symptoms such as stomach pain or abdominal pain might indicate the development of an inflammation of the pancreas. It can become life-threatening if left untreated.

   if you feel numbness, tingling and pain in the arms and the legs, tell your doctor. This may be a sign of toxic peripheral neuropathy.

   taking Videx can cause retinal (eye) or optic nerve changes, on rare occasions. Your doctor may decide to carry out a retinal examination yearly or if a change in vision occurs.

   Videx belongs to a class of medicines (NRTIs) that can cause a sometimes fatal condition called lactic acidosis (excess of lactic acid in your blood) and enlargement of the liver. Symptoms such as nausea, vomiting and stomach pain might indicate the development of lactic acidosis. This rare but serious side effect occurs more often in women, particularly if very overweight or in patients with liver disease. Your doctor will monitor you regularly while you are receiving Videx.

   if you have or have had problems with your kidneys, tell your doctor. This is important because Videx is eliminated from your body through the kidneys and you may need a reduced dose.

   if you have or have had a liver disease, especially chronic hepatitis B or C, tell your doctor. Some people (including pregnant women) who have taken Videx have had serious liver problems. These problems include hepatomegaly (liver enlargement), steatosis (fat in the liver), liver failure, and portal hypertension (high blood pressure in the large vein of the liver). You may be at an increased risk of severe and potentially fatal liver problems. In rare occasions, patients who have not previously had liver problems can experience liver failure. Your doctor should check your liver function while you are taking Videx. You should be especially careful if you have a history of heavy alcohol use or liver problems.

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   signs and symptoms of inflammation from previous infections may occur soon after anti-HIV treatment is started in some patients with advanced HIV infection (AIDS) and a history of opportunistic infections. It is believed that these symptoms are due to an improvement in the body’s immune response, enabling the body to fight infections that may have been present with no obvious symptoms. If you notice any symptoms of infection, tell your doctor immediately. In addition to the opportunistic infections, autoimmune disorders (a condition that occurs when the immune system attacks healthy body tissue) may also occur after you start taking medicines for the treatment of your HIV infection. Autoimmune disorders may occur many months after the start of treatment. If you notice any symptoms of infection or other symptoms such as muscle weakness, weakness beginning in the hands and feet and moving up towards the trunk of the body, palpitations, tremor or hyperactivity, please inform your doctor immediately to seek necessary treatment.

   redistribution, accumulation or loss of body fat may occur in patients receiving antiretroviral therapy. Contact your doctor if you notice changes in body fat.

some patients taking combination antiretroviral therapy may develop a bone disease called osteonecrosis (death of bone tissue caused by loss of blood supply to the bone). The length of combination antiretroviral therapy, corticosteroid use, alcohol consumption, severe immunosuppression, higher body mass index, among others, may be some of the many risk factors for developing this disease. Signs of osteonecrosis are joint stiffness, aches and pains (especially of the hip, knee and shoulder) and difficulty in movement. If you notice any of these symptoms please inform your doctor.

   infants younger than 3 months: there is limited experience with the use of Videx in this age group.

   interactions: it is not recommended to take Videx in combination with tenofovir disoproxil fumarate, hydroxyurea, xanthine oxidase inhibitors (e.g. allopurinol) or ribavirin. This may increase your risk of side effects.

   do not stop taking Videx without your doctor’s advice because your HIV infection may get worse after stopping treatment.

Other medicines and Videx

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. It is especially important that you inform your doctor if you are already being treated with ganciclovir or valganciclovir. Taking these medicines with Videx may increase the risk of side effects. Taking Videx with tenofovir disoproxil fumarate, hydroxyurea, xanthine oxidase inhibitors (e.g. allopurinol) or ribavirin is not recommended.

Taking Videx in combination with medicines that are known to cause peripheral neuropathy or pancreatitis may increase the risk of these toxicities. If you take these medicines, your health will need to be carefully monitored.

Medicines whose absorption is influenced by the stomach acid (e.g. itraconazole, ketoconazole) must be taken at least 2 hours before taking Videx tablets.

Tetracycline and quinolone antibiotics are not to be taken within 2 hours after taking Videx tablets.


Videx with food and drink

Videx is not absorbed well if there is food in the stomach. Therefore, take Videx at least 30 minutes before a meal.

Pregnancy and breast-feeding

If you are pregnant, think you may be pregnant or are planning to have a baby, tell your doctor to discuss the benefits and risks of your antiretroviral therapy to you and your child. It is not known if Videx is safe to use during pregnancy.

The combination of didanosine and stavudine in pregnant women increases the risk of lactic acidosis. Breast-feeding is not recommended while taking Videx. Tell your doctor if you are breast-feeding.

Driving and using machines

No effects on the ability to drive and use machines have been observed.

Videx tablets contain phenylalanine (from the aspartame) and sorbitol.

■    Videx tablets contain a source of phenylalanine. May be harmful for people with phenylketonuria.

■    Videx tablets contain sorbitol. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

3.    How to take Videx

Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.

Adults must thoroughly chew the tablets or mix with at least 30 ml of water before taking. To mix the tablets, stir the tablets in water until a uniform mixture forms and drink immediately. If additional flavouring is desired, 30 ml of clear apple juice may be added to the water and Videx mixture. Videx must be administered at least 30 minutes before a meal.

How much to take

Not all patients need to take the same dose of Videx. The usual dose for adults is based on your body weight and is taken once daily or divided into two doses taken approximately 12 hours apart, as follows. Each time you take a dose, you must take at least two but no more than four Videx tablets.

Your body weight

Total Daily Dose

Less than 60 kg

250 mg, either once daily, or in two 125 mg doses (taken approximately 12 hours apart).

60 kg or more

400 mg, either once daily, or in two 200 mg doses (taken approximately 12 hours apart).

Depending on the side effects you may develop and the diseases you are suffering from at the beginning

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of your treatment (e.g. pancreatitis, renal impairment), your doctor may prescribe a different dose.

Use in children

The dose for children will be based on body surface area which the doctor will calculate. The usual dose is between 120 and 360 mg a day, taken as a single dose, once daily or divided into two doses taken approximately 12 hours apart. Each dose must be taken as at least two but no more than four tablets for children older than 1 year and as only one tablet dose for children under 1 year. The Videx tablets are not recommended for infants under 3 months.

Children (1 year of age or older) must thoroughly chew the tablets or mix with at least 30 ml of water before taking. To mix the tablets, stir the tablets in water until a uniform mixture forms and drink immediately. If additional flavouring is desired, 30 ml of clear apple juice may be added to the water and Videx mixture. Children under 1 year of age, who take a one tablet dose, may chew or have the tablet mixed in 15 ml of water. Fifteen ml of clear apple juice may be added to the Videx and water mixture for flavouring. Videx must be administered at least 30 minutes before a meal.

If you take more Videx than you should

If you have taken more Videx than was prescribed by your doctor, or if someone accidentally takes Videx, contact your doctor or the nearest hospital immediately.

If you forget to take Videx

It is important that you do not miss any doses. If you miss a dose of Videx, take it as soon as possible, but at least 30 minutes before a meal, and then take your next scheduled dose at its regular time. However, if it is almost time for your next dose, do not take the missed dose, but wait and take the next dose at the regular time. Do not take a double dose to make up for a forgotten dose.

If you stop taking Videx

Do not stop taking Videx before talking with your doctor. This is very important because the amount of virus may start to increase if the medicine is stopped for even a short time. The virus may then become harder to treat.

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

4.    Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them. Contact your doctor immediately if you feel stomach pain or abdominal pain. This may be due

to inflammation of the pancreas which can become life-threatening if left untreated (see Warnings and precautions).

Tell your doctor if you notice any of the following side effects:

Very common side effects (These are likely to affect more than 1 in every 10 patients)

   Digestive problems: diarrhoea

Common side effects (These are likely to affect between 1 to 10 in every 100 patients)

   Liver problems: hepatitis (inflammation of the liver)

   Nervous system: peripheral neurologic symptoms (numbness, weakness, tingling or pain in the arms and the legs), headache

   Digestive problems: nausea, vomiting, abdominal pain, flatulence (wind), dry mouth

   Skin: rash

   General: unusual tiredness or weakness, chills and fever, pain

   Reproductive system and breast disorders: breast enlargement in males

   Metabolism and nutrition: anorexia

   Muscles and bones: muscle pain, joint pain

   Tests may show: increased levels of uric acid, increased bilirubin, increased or abnormal levels of some enzymes including liver enzymes in the blood

Uncommon side effects (These are likely to affect between 1 to 10 in every 1,000 patients)

   Digestive problems: pancreatitis

   Liver problems: excess of fat in the liver, liver failure

   Metabolism and nutrition: lactic acidosis (excess of lactic acid in the blood), diabetes (starting or getting worse), low or high blood sugar levels

   Blood: low red blood cell count, low blood platelet count, lack of white blood cells

   Muscles and bones: muscle tenderness or weakness, temporary paralysis or weakness of muscles including kidney disease and haemodialysis

   Eyes: dry eyes, changes in colour of the retina, disease of the nerves of the eyes causing blindness

   Infections: sore saliva glands

   Immune system: sudden life threatening allergic reaction

   Skin: alopecia (unusual hair loss or thinning)

Rare side effects (These are likely to affect between 1 to 10 in every 10,000 patients)

   Liver problems: portal hypertension (high blood pressure in the large vein of the liver)

   Muscles and bones: disease of the muscles

   Digestive problems: parotid gland enlargement

Changes in body fat have been seen in some patients taking antiretroviral therapy. These changes include increased amounts of fat in the upper back and neck (“buffalo hump”), breast, and around the abdomen (“belly”). Loss of fat from the legs, arms and face may also happen. The cause and long-term effects of these conditions are not known at this time.

High levels of sugar, triglycerides and resistance to insulin may also occur.

Side effects in paediatric patients are similar to those seen in adults. Higher blood cells count abnormalities have been reported with the combination with zidovudine. Retinal or optic nerve changes have been reported in a small number of paediatric patients, usually at doses above those currently recommended. Your doctor may decide to carry out a retinal (eye) examination.

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 (see details below). By reporting side effects you can help provide more information on the safety of this medicine.

Ireland

HPRA Pharmacovigilance,

Earlsfort Terrace,

IRL Dublin 2 Tel: +353 1 6764971 Fax: +353 1 6762517 Website: www.hpra.ie Email: medsafety@hpra.ie

United Kingdom

Yellow Card Scheme

Website: www.mhra.gov.uk/yellowcard

5.    How to store Videx

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the bottle or carton after EXP. The expiry date refers to the last day of that month.

Do not store Videx tablets above 30°C. Keep the bottle tightly closed in order to protect from moisture.

Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6.    Contents of the pack and other information

What Videx contains

■    The active substance is didanosine. Each tablet contains 25 mg didanosine.

■    The other ingredients are: calcium carbonate, magnesium hydroxide, aspartame, sorbitol, microcrystalline cellulose, crospovidone, mandarin orange flavour (tangerine oil, mandarin oil, gum arabic, alpha tocopherol, colloidal silica) and magnesium stearate.

What Videx looks like and contents of the pack

The chewable or dispersible tablets are white, imprinted with “25” on one side and “VIDEX” on the other side.

Videx 25 mg chewable/dispersible tablets are supplied in bottles with child resistant closure containing 60 chewable or dispersible tablets.

Marketing Authorisation Holder and Manufacturer

United Kingdom

Product Licence Holder

Bristol-Myers Squibb Pharmaceuticals Ltd.,

Uxbridge Business Park, Sanderson Road,

Uxbridge, Middlesex UB8 1DH, England.

Tel: 0800 7311736

Ireland

Product Authorisation Holder

Bristol-Myers Squibb Pharmaceuticals Ltd, Swords, County Dublin, Ireland.

Tel: 1 800 749 749

Manufacturer

Bristol-Myers Squibb, S.r.l.

Contrada Fontana del Ceraso 03012 anagni - Frosinone Italy

Aesica Queenborough Limited North Road, Queenborough,

Kent, ME11 5EL United Kingdom

This leaflet was last revised in XXXX


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