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Ramipril 2.5mg Tablets

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Ref:

231-30-55239-A LEA RAMIPRIL A/S TAB TUK

26 July 2013

TEVA UK LIMITED

Version:

8

Trackwise Parent: N/A

Child:

N/A

PL Number(s),

PL 00289/1714-7. TEVA UK Limited Licence, Teva Regulatory Team.

MA Holder & Packer:

MA Holder: TEVA UK Limited. Manufacturer: Merckle GmbH.

F. P. Code:

231-10-03380

231-10-03382

231-10-03384

231-10-03386

Dimensions:

L:

W:

Colours:

(PANTONE® is a registered trademark of Pantone, Inc.)

PANTONE® GREEN C BLACK


323 mm 320 mm


Pharma Code: Third party code: Fonts:

Base Font Size:


610(001100011) N/A

Univers 9.5 Pt


IMPORTANT: Artwork, text and content must not be reset, remade, amended or altered. The only exceptions to this are: bleeds, chokes, spreads or other print related adjustments required for reproduction by the supplier. We must receive a copy of any 3rd Party Supplier’s Proof before approval to print will be granted.


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PAGE 1: AFTER FOLDING FRONT FACE (INSIDE OF REEL AFTER FOLDING AND TACKING)


•    Blood tests showing less sodium than usual in your blood

•    Fingers and toes changing colour when you are cold and then tingling or feeling painful when you warm up (Raynaud's phenomenon)

•    Breast enlargement in men

•    Slowed or impaired reactions

•    Burning sensation

•    Change in the way things smell

•    Hair loss.

If you notice any side effects not listed in

this leaflet, please tell your doctor or

pharmacist.


What Ramipril Tablets look like and contents of the pack

Tablets.

1.25 mg

yellow, oblong, biplane tablets, 8.0 mm x 4.00 mm.

2.5 mg

yellow, capsule-shaped, uncoated flat tablets, 10.0 x 5.0 mm, scored on one side and side walls, marked R2.

The tablet can be divided into equal halves.


HOW TO STORE RAMIPRIL TABLETS


Keep out of the sight and reach of children.


Do not use Ramipril Tablets after the expiry date which is stated on the outer carton and blister packs after "EXP'.'

The expiry date refers to the last day of that month.


Do not store above 25°C.

Store in the original package in order to protect from moisture and light.


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.


FURTHER INFORMATION


What Ramipril Tablets contains:

The active substance is ramipril.


5 mg

pink, capsule-shaped, uncoated flat tablets, 8.8 x 4.4 mm, scored on one side and side walls, marked R3.

The tablet can be divided into equal halves.


10 mg

white to off-white, capsule-shaped, uncoated flat tablets, 11.0 x 5.5 mm, scored on one side and side walls, marked R4.

The tablet can be divided into equal halves.

Blister packs (OPA/AL/PVC - AL).

Packages with 7, 20, 21, 28, 30, 50, 56, 60, 90, 98, 100, 50x1 tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder:

Teva UK Limited, Eastbourne, BN22 9AG

Manufacturer:

Merckle GmbH, Ludwig-Merckle-StraBe 3, 89143 Blaubeuren, Germany


1.25 mg

Each tablet contains 1.25 mg ramipril. This leaflet was last revised in July 2013


2.5 mg

Each tablet contains 2.5 mg ramipril. 5 mg

Each tablet contains 5 mg ramipril. 10 mg

Each tablet contains 10 mg ramipril.


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.

PL 00289/1714, PL 00289/1715,

PL 00289/1716, PL 00289/1717


The other ingredients are 1.25 mg

Sodium hydrogen carbonate, lactose monohydrate, croscarmellose sodium, pregelatinised starch (from maize starch), sodium stearyl fumarate, iron oxide yellow (E172).


2.5 mg

Sodium hydrogen carbonate, lactose monohydrate, croscarmellose sodium, pregelatinised starch (from maize starch), sodium stearyl fumarate, iron oxide yellow (E172).


5 mg

Sodium hydrogen carbonate, lactose monohydrate, croscarmellose sodium, pregelatinised starch (from maize starch), sodium stearyl fumarate, iron oxide yellow (E172), iron oxide red (E172).


10 mg

Sodium hydrogen carbonate, lactose monohydrate, croscarmellose sodium, pregelatinised starch (from maize starch), sodium stearyl fumarate.


tnjwn

TEVA UK LIMITED    320 x 323


RAMIPRIL 1.25 mg, 2.5 mg, 5 mg AND 10 mg TABLETS


PACKAGE LEAFLET: INFORMATION FOR THE USER


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.

•    If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.


IN THIS LEAFLET:


1.    What Ramipril Tablets are and what they are used for

2.    Before you take Ramipril Tablets

3.    How to take Ramipril Tablets

4.    Possible side effects

5.    How to store Ramipril Tablets

6.    Further information

OWHAT RAMIPRIL TABLETS ARE AND WHAT THEY ARE USED FOR

Ramipril Tablets contains a medicine called ramipril.This belongs to a group of medicines called ACE inhibitors (Angiotensin Converting Enzyme Inhibitors).

Ramipril works by:

• Decreasing your body's production of substances that could raise your blood pressure

• Making your blood vessels relax and widen

• Making it easier for your heart to pump blood around your body.

Ramipril can be used:

• To treat high blood pressure (hypertension)

• To reduce the risk of you having a heart attack or stroke

• To reduce the risk or delay the worsening of kidney problems (whether or not you have diabetes)

• To treat your heart when it cannot pump enough blood to the rest of your body (heart failure)

• As treatment following heart attack (myocardial infarction) complicated with heart failure.

BEFORE YOU TAKE RAMIPRIL TABLETS

Do NOT take Ramipril Tablets:

• If you are allergic (hypersensitive) to ramipril, any other aCe inhibitor medicine or any of the ingredients of Ramipril Tablets listed in section 6.

Signs of an allergic reaction may include a rash, swallowing or breathing problems, swelling of your lips, face, throat or tongue

• If you have ever had a serious allergic reaction called "angioedema'.'The signs include itching, hives (urticaria), red marks on the hands, feet and throat, swelling of the throat and tongue, swelling around the eyes and lips, difficulty breathing and swallowing • If you are having dialysis or any other type of blood filtration. Depending on the machine that is used, Ramipril may



not be suitable for you

•    If you have kidney problems where the blood supply to your kidney is reduced (renal artery stenosis)

•    During the last 6 months of pregnancy. (see section"Pregnancy and breast-feeding")

•    If your blood pressure is abnormally low or unstable. Your doctor will need to make this assessment.

Do not take Ramipril if any of the above apply to you. If you are not sure, talk to your doctor before taking Ramipril.

Take special care with Ramipril

Check with your doctor or pharmacist before taking your medicine:

•    If you have heart, liver or kidney problems

•    If you have lost a lot of body salts or fluids (through being sick (vomiting), having diarrhoea, sweating more than usual, being on a low salt diet, taking diuretics (water tablets) for a long time or having had dialysis)

•    If you are going to have treatment to reduce your allergy to bee or wasp stings (desensitization)

•    If you are going to receive an anaesthetic. This may be given for an operation or any dental work. You may need to stop your Ramipril treatment one day beforehand; ask your doctor for advice.

•    If you have high amounts of potassium in your blood (shown in blood test results)

•    If you have collagen vascular disease such as scleroderma or systemic lupus erythematosus

•    You must tell your doctor if you think that you are (or might become) pregnant. Ramipril is not recommended in the first 3 months of pregnancy, and may cause serious harm to your baby after 3 months of pregnancy (see section "Pregnancy and breast-feeding").

Children

Ramipril is not recommended for use in children and adolescents below 18 years of age because safety and efficacy of Ramipril in children has not yet been established.

If any of the above apply to you (or you are not sure), talk to your doctor before taking Ramipril.

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 (including herbal medicines). This is because Ramipril can affect the way some other medicines work. Also some medicines can affect the way Ramipril works.

Please tell your doctor if you are taking any of the following medicines. They can make Ramipril work less well:

•    Medicines used to relieve pain and inflammation (e.g. Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) such as ibuprofen or indometacin and aspirin)

•    Medicines used for the treatment of low blood pressure, shock, cardiac failure, asthma or allergies such as ephedrine, noradrenaline or adrenaline. Your doctor will need to check your blood pressure.


Peel Here To Open


Pharma code 123 (EXAMPLE CODE)

Top of page cut-off to middle of registration mark = 44 mm    First bar is 105mm from top edge.


h r d■/11

Ref:

231-30-55239-A LEA RAMIPRIL A/S TAB TUK

26 July 2013

TEVA UK LIMITED

Version:

8

Trackwise Parent: N/A

Child:

N/A

PL Number(s),

PL 00289/1714-7. TEVA UK Limited Licence, Teva Regulatory Team.

MA Holder & Packer:

MA Holder: TEVA UK Limited. Manufacturer: Merckle GmbH.

F. P. Code:

231-10-03380

231-10-03382

231-10-03384

231-10-03386

Dimensions:

L:

W:

Colours:

(PANTONE® is a registered trademark of Pantone, Inc.)

PANTONE® GREEN C BLACK


323 mm 320 mm


Pharma Code: Third party code: Fonts:

Base Font Size:


610(001100011) N/A

Univers 9.5 Pt


IMPORTANT: Artwork, text and content must not be reset, remade, amended or altered. The only exceptions to this are: bleeds, chokes, spreads or other print related adjustments required for reproduction by the supplier. We must receive a copy of any 3rd Party Supplier’s Proof before approval to print will be granted.


PAGE 2: LEFT HAND INSIDE FACE AFTER FOLDING AND TACKING


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LINE.


PAGE 3: RIGHT HAND INSIDE FACE AFTER FOLDING AND TACKING


Please tell your doctor if you are taking

any of the following medicines. They can

increase the chance of getting side effects

if you take them with Ramipril:

•    Medicines used to relieve pain and inflammation (e.g. Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) such as ibuprofen or indometacin and aspirin)

•    Medicines for cancer (chemotherapy)

•    Medicines to stop the rejection of organs after a transplant such as ciclosporin

•    Diuretics (water tablets) such as furosemide

•    Medicines which can increase the amount of potassium in your blood such as spironolactone, triamterene, amiloride, potassium salts and heparin (for thinning blood)

•    Steroid medicines for inflammation such as prednisolone

•    Allopurinol (used to lower the uric acid in your blood)

•    Procainamide (for heart rhythm problems).


Please tell your doctor if you are taking any of the following medicines. They may be affected by Ramipril:

•    Medicines for diabetes such as oral glucose lowering medicines and insulin. Ramipril may lower your blood sugar amounts. Check your blood sugar amounts closely while taking Ramipril

•    Lithium (for mental health problems). Ramipril may increase the amount of lithium in your blood. Your lithium amount will need to be closely checked by your doctor.


If any of the above apply to you (or you are not sure), talk to your doctor before taking Ramipril.

Taking Ramipril Tablets with food and alcohol

•    Drinking alcohol with Ramipril may make you feel dizzy or light-headed. If you are concerned about how much you can drink while you are taking Ramipril, discuss this with your doctor. Medicines used to reduce blood pressure and alcohol may mutually amplify their effect, which may cause an excessive reduction of blood pressure.

•    Ramipril may be taken with or without food.

Pregnancy and breast-feeding Pregnancy

You must tell your doctor if you think you are (or might become) pregnant. You should not take Ramipril in the first 12 weeks of pregnancy, and you must not take them at all after the 13th week as their use during pregnancy may possibly be harmful to the baby.

If you become pregnant while on Ramipril, tell your doctor immediately. A switch to a suitable alternative treatment should be carried out in advance of a planned pregnancy.


Breast-feeding

You should not take Ramipril if you are breast-feeding.


Ask your doctor or pharmacist for advice before taking any medicine.


Driving and using machines

You may feel dizzy, while taking Ramipril. This is more likely to happen when you start taking Ramipril or start taking a higher dose. If this happens, do not drive or use any tools or machines.


Important information about some of the ingredients of Ramipril Tablets

This medicine contains lactose. If you have been told by your doctor that you have intolerance to some sugars, contact your doctor before taking this medicine.


HOW TO TAKE RAMIPRIL TABLETS


Always take ramipril exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.


Taking this medicine

•    Take this medicine by mouth at the same time of the day each day

•    Swallow the tablets with liquid

•    Do not crush or chew the tablets.


How much to take

Treatment of high blood pressure

•    The usual starting dose is 1.25 mg or 2.5 mg once daily

•    Your doctor will adjust the amount you take until your blood pressure is controlled

•    The maximum dose is 10 mg once daily

•    If you are already taking diuretics (water tablets), your doctor may stop or reduce the amount of the diuretic you take before beginning treatment with Ramipril.


To reduce the risk of you having a heart

attack or stroke

•    The usual starting dose is 2.5 mg once daily

•    Your doctor may then decide to increase the amount you take

•    The usual dose is 10 mg once daily.

Treatment to reduce or delay the

worsening of kidney problems

•    You may be started on a dose of 1.25 mg or 2.5 mg once daily

•    Your doctor will adjust the amount you are taking

•    The usual dose is 5 mg or 10 mg once daily.

Treatment of heart failure

•    The usual starting dose is 1.25 mg once daily

•    Your doctor will adjust the amount you take

•    The maximum dose is 10 mg daily. Two administrations per day are preferable.

Treatment after you have had a heart

attack

•    The usual starting dose is 1.25 mg once daily to 2.5 mg twice daily

•    Your doctor will adjust the amount you take

•    The usual dose is 10 mg daily. Two administrations per day are preferable.


Elderly

• Your doctor will reduce the initial dose and adjust your treatment more slowly.


If you take more Ramipril than you should

Tell a doctor or go to the nearest hospital casualty department straight away. Do not drive to the hospital, get somebody else to take you or call for an ambulance. Take the medicine pack with you. This is so the doctor knows what you have taken.

If you forget to take Ramipril

•    If you miss a dose, take your normal dose when it is next due

•    Do not take a double dose to make up for a forgotten tablet.

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

^ POSSIBLE SIDE EFFECTS

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

Stop taking Ramipril Tablets and see a doctor straight away, if you notice any of the following serious side effects - you may need urgent medical treatment:

•    Swelling of the face, lips or throat which make it difficult to swallow or breathe, as well as itching and rashes. This could be a sign of a severe allergic reaction to Ramipril.

•    Severe skin reactions including rash, ulcers in your mouth, worsening of a pre-existing skin disease, reddening, blistering or detachment of skin (such as Stevens-Johnson syndrome, toxic epidermal necrolysis or erythema multiform).

Tell your doctor immediately if you experience:

•    Faster heart rate, uneven or forceful heartbeat (palpitations), chest pain, tightness in your chest or more serious problems including heart attack and stroke

•    Shortness of breath or a cough. These could be signs of lung problems

•    Bruising more easily, bleeding for longer than normal, any sign of bleeding (e.g. bleeding from the gums), purple spots blotching on the skin or getting infections more easily than usual, sore throat and fever, feeling tired, faint, dizzy or having pale skin. These can be signs of blood or bone marrow problems

•    Severe stomach pain which may reach through to your back. This could be a sign of pancreatitis (inflammation of the pancreas).

•    Fever, chills, tiredness, loss of appetite, stomach pain, feeling sick, yellowing of your skin or eyes (jaundice). These can be signs of liver problems such as hepatitis (inflammation of the liver) or liver damage.

Other side effects include:

Please tell your doctor if any of the following gets serious or lasts longer than a few days.

Common (affects less than 1 in 10 people)

•    Headache or feeling tired

•    Feeling dizzy. This is more likely to happen when you start taking Ramipril or start taking a higher dose.

•    Fainting, hypotension (abnormally low blood pressure), especially when you stand or sit up quickly


•    Dry tickly cough, inflammation of your sinuses (sinusitis) or bronchitis, shortness of breath

•    Stomach or gut pain, diarrhoea, indigestion, feeling or being sick

•    Skin rash with or without raised area

•    Chest pain

•    Cramps or pain in your muscles

•    Blood tests showing more potassium than usual in your blood.

Uncommon (affects less than 1 in 100 people)

•    Balance problems (vertigo)

•    Itching and unusual skin sensations such as numbness, tingling, pricking, burning or creeping on your skin (paraesthesia)

•    Loss or change in the way things taste

•    Sleep problems

•    Feeling depressed, anxious, more nervous than usual or restless

•    Blocked nose, difficulty breathing or worsening of asthma

•    A swelling in your gut called "intestinal angioedema" presenting with symptoms like abdominal pain, vomiting and diarrhoea

•    Heartburn, constipation or dry mouth

•    Passing more water (urine) than usual over the day

•    Sweating more than usual

•    Loss or decrease of appetite (anorexia)

•    Increased or irregular heartbeats, swollen arms and legs. This may be a sign of your body holding onto more water than usual.

•    Flushing

•    Blurred vision

•    Pain in your joints

•    Fever

•    Sexual inability in men, reduced sexual desire in men or women

•    An increased number of certain white blood cells (eosinophilia) found during a blood test

•    Blood tests showing changes in the way your liver, pancreas or kidneys are working.

Rare (affects less than 1 in 1,000 people)

•    Feeling shaky or confused

•    Red and swollen tongue

•    Severe flaking or peeling of the skin, itchy, lumpy rash

•    Nail problem (e.g. loosening or separation of a nail from its bed)

•    Skin rash or bruising

•    Blotches on your skin and cold extremities

•    Red, itchy, swollen or watery eyes

•    Disturbed hearing and ringing in your ears

•    Feeling weak

•    Blood tests showing a decrease in the number of red blood cells, white blood cells or platelets or in the amount of haemoglobin.

Very rare (affects less than 1 in 10,000 people)

•    Being more sensitive to the sun than usual.

Other side effects reported:

Please tell your doctor if any of the following gets serious or lasts longer than a few days.

•    Difficulty concentrating

•    Swollen mouth

•    Blood tests showing too few blood cells in your blood

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