Naramig 2.5 Mg Tablets
PACKAGE LEAFLET: INFORMATION FOR THE USER
NARAMIG® 2.5MG TABLETS
_(naratriptan hydrochloride)_
Your medicine is available as Naramig 2.5mg Tablets, but will be referred to as Naramig throughout this leaflet.
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.
What is in this leaflet
1. What Naramig is and what it is used for
2. What you need to know before you take Naramig
3. How to take Naramig
4. Possible side effects
5. How to store Naramig
6. Contents of the pack and other information
1. What Naramig is and what it is used for
Naramig tablets contain naratriptan (hydrochloride), which belongs to a group of medicines called triptans (also known as 5-HTi receptor agonists).
Naramig tablets are used to treat migraine.
Migraine symptoms may be caused by the temporary widening of blood vessels in the head. Naramig tablets are believed to reduce the widening of these blood vessels. This in turn helps to take away the headache and relieve other symptoms of a migraine attack, such as feeling or being sick (nausea or vomiting) and sensitivity to light and sound.
2. What you need to know before you take Naramig
Do not take Naramig:
■ If you are allergic to naratriptan, or any of the other ingredients of this medicine (listed in section 6)
■ If you have a heart problem such as heart failure or chest pains (angina), or have already had a heart attack
■ If you have circulation problems in your legs that cause cramp-like pains when you walk (peripheral vascular disease)
■ If you have had a stroke or a mini-stroke (also called a transient ischaemic attack or TIA)
■ If you have high blood pressure. You may be able to take Naramig if your high blood pressure is mild and is being treated.
■ If you have kidney or liver disease
■ With other migraine medicines, including those which contain ergotamine, or with similar medicines such as methysergide, or with other 5-HT1 receptor agonists, such as sumatriptan.
If any of these apply to you:
* Tell your doctor, and don't take Naramig.
Warnings and precautions
Talk to your doctor or pharmacist before taking Naramig.
If you have any extra risk factors
■ If you are a heavy smoker or are using nicotine replacement therapy, and especially
■ If you are a man over 40, or
■ If you are a woman who has been through the menopause.
In very rare cases, people have developed serious heart conditions after taking Naramig, even though they had no signs of heart disease before.
If any of the points in the list applies to you, it could mean you have a greater risk of developing heart disease - so:
* Tell your doctor so that your heart function can be checked before Naramig is prescribed for you.
If you are allergic to antibiotics called sulphonamides
If so, you may also be allergic to Naramig. If you know you are allergic to an antibiotic but you are not sure whether it is a sulphonamide:
* Tell your doctor or pharmacist before taking Naramig.
If you take Naramig frequently
Taking Naramig too often may make your headaches worse.
* Tell your doctor if this applies to you. He or she may
recommend you stop taking Naramig.
If you feel pain or tightness in your chest after you take Naramig
These effects may be intense but they usually pass quickly.
If they don't pass quickly, or they become severe:
* Get medical help immediately. Section 4 of this leaflet has more information about these possible side effects.
Not for older people or children under 18 Naramig is not recommended for people aged over 65 or for children under the age of 18.
Other medicines and Naramig
Tell your doctor if you're taking, have recently taken or might take any other medicines.
Some medicines must not be taken with Naramig and others may cause adverse effects if they're taken with Naramig. You must tell your doctor if you are taking:
■ any medicines for your migraine which contain any triptan/5-HT1 agonist (such as sumatriptan or zolmitriptan). Don't take Naramig at the same time as these medicines. Stop taking these medicines at least 24 hours before taking Naramig.
■ ergotamine also used to treat migraine or similar medicines such as methysergide. Don't take Naramig at the same time as these medicines. Stop taking these medicines at least 24 hours before taking Naramig.
■ any antidepressants classed as selective serotonin reuptake inhibitors (SSRIs), such as citalopram, fluoxetine or paroxetine, or serotonin noradrenaline reuptake inhibitors (SNRIs) such as venlafaxine. If you are not sure, talk to your doctor or pharmacist.
■ St John's Wort (Hypericum perforatum). Using herbal remedies that contain St John's Wort while you are taking Naramig may make side effects more likely.
Pregnancy and breast-feeding
■ If you are pregnant, think you may be pregnant or are planning to have a baby ask your doctor for advice before taking this medicine. There is only limited information about the safety of Naramig for pregnant women, though up till now there is no evidence of any increased risk of birth defects. Your doctor may recommend that you do not take Naramig while you are pregnant.
■ Don't breast-feed your baby for 24 hours after taking Naramig. If you express any breast milk during this time, discard the milk and don't give it to your baby.
Driving and using machines
■ Either the symptoms of migraine or your medicine may make you drowsy. If you are affected, don't drive or operate machinery.
Naramig contains lactose
Naramig tablets contain a small amount of a sugar called lactose.
If you have an intolerance to lactose or any other sugars: * Ask your doctor for advice about taking Naramig.
3. How to take Naramig
Only take Naramig after your migraine headache begins. Don't take Naramig to try to prevent an attack.
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
How much to take
■ The usual dose for adults aged 18 to 65 is one
Naramig 2.5mg tablet, swallowed whole with water.
Naramig is not recommended for children under 18 and adults over 65.
When to take Naramig
■ It's best to take Naramig as soon as you feel a migraine coming on, although it can be taken at any time during an attack.
If your symptoms start to come back
■ You can take a second Naramig tablet after 4 hours, unless you have kidney or liver damage.
■ If you have kidney or liver damage don't take more than one tablet in 24 hours.
■ No one should take more than two tablets in 24 hours.
If the first tablet has no effect
■ Don't take a second tablet for the same attack.
If Naramig doesn't give you any relief:
^ Ask your doctor or pharmacist for advice.
If you take more Naramig than you should
■ Don't take more than two Naramig tablets in 24 hours.
Taking too much Naramig could make you ill. If you have taken more than two tablets in 24 hours:
^ Contact your doctor for advice.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Tell your doctor straight away if you notice any of the following serious side effects - you may need urgent medical treatment:
■ Heartbeat may go faster, slower or change rhythm (affects up to 1 in 100 people).
■ Pain in the lower left side of the stomach and
bloody diarrhoea (ischaemic colitis - affects up to 1 in 1,000 people).
■ Allergic reaction (affects up to 1 in 1,000 people). The signs of allergy include rash; hives; itching; wheezing; swollen eyelids, face or lips; complete collapse.
If you get any of these symptoms soon after taking Naramig: ^ Don't take any more. Contact a doctor straight away.
■ Heaviness, pressure, tightness or pain in the chest, throat or other parts of the body (affects up to 1 in 100 people). These effects may be intense but generally pass quickly.
If these effects continue or become severe (especially the chest pain):
* Get medical help urgently. In a very small number of people these symptoms can be caused by a heart attack.
Common: may affect up to 1 in 10 people
■ Feeling sick (nausea) or being sick (vomiting), although this may be due to the migraine itself.
■ Tiredness, drowsiness or sleepiness (somnolence), or generally feeling unwell.
■ Dizziness, tingling feelings or getting hot flushes.
If you get any of these effects:
* Tell your doctor or pharmacist.
Uncommon: may affect up to 1 in 100 people
■ Visual disturbances (although these may be due to the migraine attack itself).
■ Slight increase in blood pressure which may occur up to 12 hours after taking Naramig.
If you get any of these effects:
* Tell your doctor or pharmacist.
Very rare: may affect up to 1 in 10,000 people
■ Heart problems, including chest pains (angina) and heart attack.
■ Poor blood circulation to the arms and legs, causing pain and discomfort.
If you get these symptoms:
* 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 Naramig
■ Keep out of the sight and reach of children.
■ Do not store above 30°C.
■ Don't take Naramig after the expiry date shown on the carton. The expiry date refers to the last day of that month.
■ If your tablets appear to be discoloured or show any other signs of deterioration, please return to your pharmacist who will advise you.
■ If your doctor decides to stop your treatment, return any left over tablets to the pharmacist. Only keep them if your doctor tells you to.
■ 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. Contents of the pack and other information
What Naramig contains
Each film-coated tablet contains 2.78mg naratriptan hydrochloride equivalent to 2.5mg naratriptan.
tablet core: microcrystalline cellulose, lactose, croscarmellose sodium and magnesium stearate. coating: hypromellose, titanium dioxide (E171), triacetin, iron oxide (E172) and indigo carmine aluminium salt (E132).
What Naramig looks like and contents of the pack
Naramig are green, film-coated, D-shaped tablets, engraved 'GX CE5' on one side and plain on the reverse.
Your medicine is available in blister packs of 6 or 12 tablets.
Additional information
This leaflet does not contain all the information about your medicine. If you have any questions or are not sure about anything, ask your doctor or pharmacist who have the information you need, and will advise you.
Manufacturer
Your medicine is manufactured by: Glaxo Operations UK Ltd., Glaxo Wellcome Operations, Glaxo Wellcome House,
Berkeley Avenue, Greenford, Middlesex, UB6 0NN.
Or
GlaxoSmithKline Pharmaceuticals S.A., ul. Grunwaldzka 189, 60-322 Poznan, Poland.
Procured from within the EU and repackaged by:
Doncaster Pharmaceuticals Group Ltd., Kirk Sandall, Doncaster, DN3 1QR.
Product Licence holder: Landmark Pharma Ltd.,
7 Regents Drive, Prudhoe, Northumberland, NE42 6PX.
PL No: 21828/0407 POM
Leaflet issue and revision date (Ref): 07.04.16
Naramig® is a registered trademark of the GlaxoSmithKline group of companies.
Other formats
To request a copy of this leaflet in Braille, large print or audio please call 01302 365000 and ask for the Regulatory Department.
Please be ready to give the following information:
Product name: Naramig 2.5mg Tablets
Reference number: 21828/0407
NARATRIPTAN HYDROCHLORIDE 2.5MG TABLETS
PACKAGE LEAFLET: INFORMATION FOR THE USER
Your medicine is available as Naratriptan Hydrochloride 2.5mg Tablets, but will be referred to as Naratriptan Hydrochloride throughout this leaflet.
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.
What is in this leaflet
1. What Naratriptan Hydrochloride is and what it is used for
2. What you need to know before you take Naratriptan Hydrochloride
3. How to take Naratriptan Hydrochloride
4. Possible side effects
5. How to store Naratriptan Hydrochloride
6. Contents of the pack and other information
1. What Naratriptan Hydrochloride is and what it is used for
Naratriptan Hydrochloride tablets contain naratriptan (hydrochloride), which belongs to a group of medicines called triptans (also known as 5-HTi receptor agonists).
Naratriptan Hydrochloride tablets are used to treat migraine.
Migraine symptoms may be caused by the temporary widening of blood vessels in the head. Naratriptan Hydrochloride tablets are believed to reduce the widening of these blood vessels. This in turn helps to take away the headache and relieve other symptoms of a migraine attack, such as feeling or being sick (nausea or vomiting) and sensitivity to light and sound.
2. What you need to know before you take Naratriptan Hydrochloride
Do not take Naratriptan Hydrochloride:
■ If you are allergic to naratriptan, or any of the other ingredients of this medicine (listed in section 6)
■ If you have a heart problem such as heart failure or chest pains (angina), or have already had a heart attack
■ If you have circulation problems in your legs that cause cramp-like pains when you walk (peripheral vascular disease)
■ If you have had a stroke or a mini-stroke (also called a transient ischaemic attack or TIA)
■ If you have high blood pressure. You may be able to take Naratriptan Hydrochloride if your high blood pressure is mild and is being treated.
■ If you have kidney or liver disease
■ With other migraine medicines, including those which contain ergotamine, or with similar medicines such as methysergide, or with other 5-HT1 receptor agonists, such as sumatriptan.
If any of these apply to you:
* Tell your doctor, and don't take Naratriptan Hydrochloride.
Warnings and precautions
Talk to your doctor or pharmacist before taking Naratriptan Hydrochloride.
If you have any extra risk factors
■ If you are a heavy smoker or are using nicotine replacement therapy, and especially
■ If you are a man over 40, or
■ If you are a woman who has been through the menopause.
In very rare cases, people have developed serious heart conditions after taking Naratriptan Hydrochloride, even though they had no signs of heart disease before.
If any of the points in the list applies to you, it could mean you have a greater risk of developing heart disease - so:
* Tell your doctor so that your heart function can be checked before Naratriptan Hydrochloride is prescribed for you.
If you are allergic to antibiotics called sulphonamides
If so, you may also be allergic to Naratriptan Hydrochloride. If you know you are allergic to an antibiotic but you are not sure whether it is a sulphonamide:
* Tell your doctor or pharmacist before taking Naratriptan Hydrochloride.
If you take Naratriptan Hydrochloride frequently
Taking Naratriptan Hydrochloride too often may make your headaches worse.
* Tell your doctor if this applies to you. He or she may
recommend you stop taking Naratriptan Hydrochloride.
If you feel pain or tightness in your chest after you take Naratriptan Hydrochloride
These effects may be intense but they usually pass quickly.
If they don't pass quickly, or they become severe:
* Get medical help immediately. Section 4 of this leaflet has more information about these possible side effects.
Not for older people or children under 18 Naratriptan Hydrochloride is not recommended for
people aged over 65 or for children under the age of 18.
Other medicines and Naratriptan Hydrochloride Tell your doctor if you're taking, have recently taken or might take any other medicines.
Some medicines must not be taken with Naratriptan Hydrochloride and others may cause adverse effects if they're taken with Naratriptan Hydrochloride. You must tell your doctor if you are taking:
■ any medicines for your migraine which contain any triptan/5-HT1 agonist (such as sumatriptan or zolmitriptan). Don't take Naratriptan Hydrochloride at the same time as these medicines. Stop taking these medicines at least 24 hours before taking Naratriptan Hydrochloride.
■ ergotamine also used to treat migraine or similar medicines such as methysergide. Don't take Naratriptan Hydrochloride
at the same time as these medicines. Stop taking these medicines at least 24 hours before taking Naratriptan Hydrochloride.
■ any antidepressants classed as selective serotonin reuptake inhibitors (SSRIs), such as citalopram, fluoxetine or paroxetine, or serotonin noradrenaline reuptake inhibitors (SNRIs) such as venlafaxine. If you are not sure, talk to your doctor or pharmacist.
■ St John's Wort (Hypericum perforatum). Using herbal remedies that contain St John's Wort while you are taking Naratriptan Hydrochloride may make side effects more likely.
Pregnancy and breast-feeding
■ If you are pregnant, think you may be pregnant or are planning to have a baby ask your doctor for advice before taking this medicine. There is only limited information about the safety of Naratriptan Hydrochloride for pregnant women, though up till now there is no evidence of any increased risk of birth defects. Your doctor may recommend that you do not take Naratriptan Hydrochloride while you are pregnant.
■ Don't breast-feed your baby for 24 hours after taking Naratriptan Hydrochloride. If you express any breast milk during this time, discard the milk and don't give it to your baby.
Driving and using machines
■ Either the symptoms of migraine or your medicine may make you drowsy. If you are affected, don't drive or operate machinery.
Naratriptan Hydrochloride contains lactose
Naratriptan Hydrochloride tablets contain a small amount of a sugar called lactose.
If you have an intolerance to lactose or any other sugars: * Ask your doctor for advice about taking Naratriptan Hydrochloride.
3. How to take Naratriptan Hydrochloride
Only take Naratriptan Hydrochloride after your migraine headache begins. Don't take Naratriptan Hydrochloride to try to prevent an attack.
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
How much to take
■ The usual dose for adults aged 18 to 65 is one
Naratriptan Hydrochloride 2.5mg tablet, swallowed whole with water.
Naratriptan Hydrochloride is not recommended for children under 18 and adults over 65.
When to take Naratriptan Hydrochloride
■ It's best to take Naratriptan Hydrochloride as soon as you feel a migraine coming on, although it can be taken at any time during an attack.
If your symptoms start to come back
■ You can take a second Naratriptan Hydrochloride tablet after 4 hours, unless you have kidney or liver damage.
■ If you have kidney or liver damage don't take more than one tablet in 24 hours.
■ No one should take more than two tablets in 24 hours.
If the first tablet has no effect
■ Don't take a second tablet for the same attack.
If Naratriptan Hydrochloride doesn't give you any relief:
4 Ask your doctor or pharmacist for advice.
If you take more Naratriptan Hydrochloride than you should
■ Don't take more than two Naratriptan Hydrochloride tablets in 24 hours.
Taking too much Naratriptan Hydrochloride could make you ill. If you have taken more than two tablets in 24 hours:
4 Contact your doctor for advice.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Tell your doctor straight away if you notice any of the following serious side effects - you may need urgent medical treatment:
■ Heartbeat may go faster, slower or change rhythm (affects up to 1 in 100 people).
■ Pain in the lower left side of the stomach and
bloody diarrhoea (ischaemic colitis - affects up to 1 in 1,000 people).
■ Allergic reaction (affects up to 1 in 1,000 people). The signs of allergy include rash; hives; itching; wheezing; swollen eyelids, face or lips; complete collapse.
If you get any of these symptoms soon after taking Naratriptan Hydrochloride:
4 Don't take any more. Contact a doctor straight away.
■ Heaviness, pressure, tightness or pain in the chest, throat or other parts of the body (affects up to 1 in 100 people). These effects may be intense but generally pass quickly.
If these effects continue or become severe (especially the chest pain):
4 Get medical help urgently. In a very small number of people these symptoms can be caused by a heart attack.
Common: may affect up to 1 in 10 people
■ Feeling sick (nausea) or being sick (vomiting), although this may be due to the migraine itself.
■ Tiredness, drowsiness or sleepiness (somnolence), or generally feeling unwell.
■ Dizziness, tingling feelings or getting hot flushes.
If you get any of these effects:
4 Tell your doctor or pharmacist.
Uncommon: may affect up to 1 in 100 people
■ Visual disturbances (although these may be due to the migraine attack itself).
■ Slight increase in blood pressure which may occur up to 12 hours after taking Naratriptan Hydrochloride.
If you get any of these effects:
4 Tell your doctor or pharmacist.
Very rare: may affect up to 1 in 10,000 people
■ Heart problems, including chest pains (angina) and heart attack.
■ Poor blood circulation to the arms and legs, causing pain and discomfort.
If you get these symptoms:
4 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 Naratriptan Hydrochloride
■ Keep out of the sight and reach of children.
■ Do not store above 30°C.
■ Don't take Naratriptan Hydrochloride after the expiry date shown on the carton. The expiry date refers to the last day of that month.
■ If your tablets appear to be discoloured or show any other signs of deterioration, please return to your pharmacist who will advise you.
■ If your doctor decides to stop your treatment, return any left over tablets to the pharmacist. Only keep them if your doctor tells you to.
■ 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. Contents of the pack and other information
What Naratriptan Hydrochloride contains
Each film-coated tablet contains 2.78mg naratriptan hydrochloride equivalent to 2.5mg naratriptan.
tablet core: microcrystalline cellulose, lactose, croscarmellose sodium and magnesium stearate. coating: hypromellose, titanium dioxide (E171), triacetin, iron oxide (E172) and indigo carmine aluminium salt (E132).
What Naratriptan Hydrochloride looks like and contents of the pack
Naratriptan Hydrochloride are green, film-coated, D-shaped tablets, engraved 'GX CE5' on one side and plain on the reverse.
Your medicine is available in blister packs of 6 or 12 tablets. Additional information
This leaflet does not contain all the information about your medicine. If you have any questions or are not sure about anything, ask your doctor or pharmacist who have the information you need, and will advise you.
Manufacturer
Your medicine is manufactured by: Glaxo Operations UK Ltd., Glaxo Wellcome Operations, Glaxo Wellcome House,
Berkeley Avenue, Greenford, Middlesex, UB6 0NN.
Or
GlaxoSmithKline Pharmaceuticals S.A., ul. Grunwaldzka 189, 60-322 Poznan, Poland.
Procured from within the EU and repackaged by:
Doncaster Pharmaceuticals Group Ltd., Kirk Sandall, Doncaster, DN3 1QR.
Product Licence holder: Landmark Pharma Ltd.,
7 Regents Drive, Prudhoe, Northumberland, NE42 6PX.
PL No: 21828/0407 POM
Leaflet issue and revision date (Ref): 07.04.16
Other formats
To request a copy of this leaflet in Braille, large print or audio please call 01302 365000 and ask for the Regulatory Department.
Please be ready to give the following information:
Product name: Naratriptan Hydrochloride 2.5mg Tablets Reference number: 21828/0407
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