Olmetec 40 Mg Film-Coated Tablets
Out of date information, search another504054/PL1b
504054/PL1b
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. Do not pass it 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).
2) WHAT YOU NEED TO KNOW BEFORE YOU TAKE|
3) HOW TO TAKE OLMETEC®
®
Olmetec 40 mg Film Coated Tablets
(olmesartan medoxomil)
Patient Information Leaflet
The name of your medicine is Olmetec® 40 mg Film Coated Tablets. Throughout this leaflet it will be referred to as Olmetec®. Other strengths are available.
What is in this leaflet:
1) What Olmetec® is and what it is used for
®
2) What you need to know before you take Olmetec
3) How to take Olmetec®
4) Possible side effects
®
5) How to store Olmetec
6) Contents of the pack and other information
1) WHAT OLMETEC® IS AND WHAT IT IS USED FOR
Olmetec belongs to a group of medicines called angiotensin-II receptor antagonists. They lower blood pressure by relaxing the blood vessels.
Olmetec® is used for the treatment of high blood pressure (also known as 'hypertension'). High blood pressure can damage blood vessels in organs such as the heart, kidneys, brain and eyes. In some cases this may lead to a heart attack, heart or kidney failure, stroke or blindness. Usually high blood pressure has no symptoms. It is important to have your blood pressure checked to prevent damage occurring.
High blood pressure can be controlled with medicines such as Olmetec® tablets. Your doctor has probably also recommended that you make some changes in your lifestyle to help lower your blood pressure (for example losing weight, giving up smoking, reducing the amount of alcohol you drink and reducing the amount of salt in your diet). Your doctor may also have urged you to take regular exercise, such as walking or swimming. It is important to follow this advice from your doctor.
Do not take Olmetec®
• if you are allergic to olmesartan medoxomil or to any other of the ingredients of this medicine (listed in section 6).
• if you are more than 3 months pregnant. (It is also better to avoid Olmetec® tablets in early pregnancy -see pregnancy section.)
• if you suffer from yellowing of the skin and eyes (jaundice) or problems with drainage of the bile from the gallbladder (biliary obstruction e.g. gallstones).
Warnings and precautions
Talk to your doctor before taking Olmetec®. Tell your doctor if you have any of the following health problems:
• Kidney problems
• Liver disease
• Heart failure or problems with your heart valves or heart muscle
• Severe vomiting, diarrhoea, treatment with high doses of water tablets (diuretics) or if you are on a low salt diet
• Increased levels of potassium in your blood
• Problems with your adrenal glands.
As with any medicine which reduces blood pressure, an excessive drop in blood pressure in patients with blood flow disturbances of the heart or brain could lead to a heart attack or stroke. Your doctor will therefore check your blood pressure carefully.
You must tell your doctor if you think you are (or might become) pregnant. Olmetec® is not recommended in early pregnancy, and must not be taken if you are more than 3 months pregnant, as it may cause serious harm to your baby if used at that stage (see pregnancy section).
Children and adolescents
Olmetec® is not recommended for children and adolescents under the age of 18.
Other medicines and Olmetec®
Tell your doctor or pharmacist if you are taking or have recently taken or might take any of the following medicines:
• Potassium supplements, a salt substitute which contains potassium, water tablets (diuretics) or heparin (for thinning the blood). Using these medicines at the same time as Olmetec® may raise the levels of potassium in your blood.
• Lithium (a medicine used to treat mood swings and some types of depression) used at the same time as Olmetec® may increase the toxicity of lithium. If you have to take lithium, your doctor will measure your lithium blood levels.
• Non-Steroidal Anti-Inflammatory (NSAIDs) medicines (medicines used to relieve pain, swelling and other symptoms of inflammation, including arthritis) used at the same time as Olmetec® may increase the risk of kidney failure and the effect of Olmetec can be decreased by NSAIDs.
• Other blood pressure lowering medicines, as the effect of Olmetec® can be increased.
• Certain antacids (indigestion remedies), as the effect of Olmetec® can be slightly decreased.
Older people
If you are over 65 years of age and your doctor decides to increase your dose of olmesartan medoxomil to 40 mg daily, then you need to have your blood pressure regularly checked by your doctor to make sure that your blood pressure does not become too low.
Black patients
As with other similar drugs the blood pressure lowering effect of Olmetec® is somewhat less in black patients.
Olmetec® with food and drink
Olmetec® can 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. Your doctor will normally advise you to stop taking Olmetec® before you become pregnant or as soon as you know you are pregnant and will advise you to take another medicine instead of Olmetec®. Olmetec® is not recommended in early pregnancy, and must not be taken when more than 3 months pregnant, as it may cause serious harm to your baby if used after the third month of pregnancy.
Breast-feeding
Tell your doctor if you are breast-feeding or about to start breast-feeding. Olmetec® is not recommended for mothers who are breast-feeding, and your doctor may choose another treatment for you if you wish to breast-feed, especially if your baby is newborn, or was born prematurely.
Ask your doctor or pharmacist for advice before taking any medicine.
Driving and using machines
You may feel sleepy or dizzy while being treated for your high blood pressure. If this happens, do not drive or use machines until the symptoms wear off. Ask your doctor for advice.
Olmetec® contains lactose
This medicine contains lactose (a type of sugar). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
The recommended starting dose is one 10 mg tablet once a day. However, if your blood pressure is not controlled, your doctor may decide to change your dose up to 20 or 40 mg once a day, or prescribe additional medicines.
In patients with mild to moderate kidney disease, your dose will not be higher than 20 mg once a day.
The tablets can be taken with or without food. Swallow the tablets with a sufficient amount of water (e.g. one glass). If possible, take your daily dose at the same time each day, for example at breakfast time.
If you take more Olmetec® than you should
If you take more tablets than you should or if a child accidentally swallows some, go to your doctor or nearest emergency department immediately and take your medicine pack with you.
|4) POSSIBLE SIDE EFFECTS|
If you forget to take Olmetec®
If you forget a dose, take your normal dose on the following day as usual. Do not take a double dose to make up for a forgotten tablet.
If you stop taking Olmetec®
It is important to continue to take Olmetec® unless your doctor tells you to stop.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them. If they do occur, they are often mild and do not require treatment to be stopped.
Although not many people may get them, the following two side effects can be serious:
On rare occasions (may affect up to 1 in 1,000 people) the following allergic reactions that may affect the whole body have been reported:
Swelling of the face, mouth and/or larynx (voice box) together with itching and rash may occur during treatment with Olmetec®. If this happens stop taking Olmetec® and contact your doctor immediately.
Rarely (but slightly more often in older people) Olmetec® can cause the blood pressure to fall too low in susceptible individuals or as the result of an allergic reaction. This could cause severe light-headedness or fainting. If this occurs stop taking Olmetec®, contact your doctor immediately and lie down flat.
These are the other side effects known about so far with Olmetec®
Common side effects (may affect up to 1 in 10 people):
Dizziness, headache, nausea, indigestion, diarrhoea, stomach ache, gastroenteritis, tiredness, sore throat, runny or stuffy nose, bronchitis, flu-like symptoms, cough, pain, pain in the chest, back, bones or joints, infection of the urinary tract, swelling of ankles, feet, legs, hands or arms, blood in the urine.
Some changes in blood test results have also been seen and include the following:
Increased fat levels (hypertriglyceridaemia), increased uric acid levels (hyperuricaemia), rise in blood urea, increases in tests of liver and muscle function.
Uncommon side effects (may affect up to 1 in 100 people):
Quick allergic reactions that may affect the whole body and may cause breathing problems as well as a rapid fall of blood pressure that may even lead to fainting (anaphylactic reactions), vertigo, vomiting, weakness, feeling unwell, muscular pain, skin rash, allergic skin rash, itching, exanthema (skin eruption), skin lumps (wheals), angina (pain or uncomfortable feeling in the chest).
In blood tests a reduction of the numbers of a type of blood cell, known as platelets has been seen (thrombocytopenia).
Rare side effects (may affect up to 1 in 1000 people):
lack of energy, muscle cramps, impaired kidney function, kidney failure.
Some changes in blood test results have also been seen. These include increased potassium levels (hyperkalaemia) and increased levels of compounds related to kidney function.
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.
6) CONTENTS OF THE PACK AND OTHER INFORMATION
What Olmetec contains
The active substance is olmesartan medoxomil
Each film coated tablet contains 40 mg olmesartan medoxomil.
The other ingredients are microcrystalline cellulose, lactose monohydrate, hydroxypropylcellulose, magnesium stearate, titanium dioxide (E171), talc, hypromellose and low substituted hydroxypropylcellulose.
What Olmetec® looks like and contents of the pack
Olmetec® 40 mg film coated tablets are white, oval with C 15 on one side and plain on the other side.
Olmetec® 40 mg is available in packs of 30 film coated tablets.
Product Licence Holder:
Procured from within the EU. Product Licence Holder Ginova Ltd and repackager Ginova UK Ltd both at St James' House, 8 Overcliffe, Gravesend, Kent DA11 0HJ.
Manufacturer:
DAIICHI SANKYO EUROPE GmbH, Luitpoldstrasse 1, 85276, Pfaffenhofen, Germany
Olmetec® 40 mg Film Coated Tablets.
PL No: 18067/0413 |POM|
Olmetec® is a registered trademark of Sankyo Company, Limited.
Date of last revision of this leaflet: 23rd January 2014.
To request a copy of this leaflet in Braille, large print or audio please call 01622 690172.
5) HOW TO STORE OLMETEC®
Keep out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the box and on the blister strip (“EXP”). The expiry date refers to the last day of that month.
This medicinal product does not require any special storage conditions.
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 to protect the environment.
If you notice any sign of discolouration or deterioration of the tablets consult your pharmacist.
504054/PL1b
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. Do not pass it 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).
|3) HOW TO TAKE OLMESARTAN MEDOXOMIL|
500000/PL1b
Olmesartan Medoxomil 40 mg Film Coated Tablets
Patient Information Leaflet
The name of your medicine is Olmesartan Medoxomil 40 mg Film Coated Tablets. Throughout this leaflet it will be referred to as Olmesartan Medoxomil. Other strengths are available.
What is in this leaflet:
1) What Olmesartan Medoxomil is and what it is used for
2) What you need to know before you take Olmesartan Medoxomil
3) How to take Olmesartan Medoxomil
4) Possible side effects
5) How to store Olmesartan Medoxomil
6) Contents of the pack and other information
1) WHAT OLMESARTAN MEDOXOMIL IS AND WHAT IT IS| USED
Olmesartan Medoxomil belongs to a group of medicines called angiotensin-II receptor antagonists. They lower blood pressure by relaxing the blood vessels.
Olmesartan Medoxomil is used for the treatment of high blood pressure (also known as 'hypertension'). High blood pressure can damage blood vessels in organs such as the heart, kidneys, brain and eyes. In some cases this may lead to a heart attack, heart or kidney failure, stroke or blindness. Usually high blood pressure has no symptoms. It is important to have your blood pressure checked to prevent damage occurring.
High blood pressure can be controlled with medicines such as Olmesartan Medoxomil tablets. Your doctor has probably also recommended that you make some changes in your lifestyle to help lower your blood pressure (for example losing weight, giving up smoking, reducing the amount of alcohol you drink and reducing the amount of salt in your diet). Your doctor may also have urged you to take regular exercise, such as walking or swimming. It is important to follow this advice from your doctor.
|
2) WHAT YOU NEED TO |
KNOW BEFORE YOU TAKE | |
|
OLMESARTAN MEDOXOMIL |
Do not take Olmesartan Medoxomil
• if you are allergic to olmesartan medoxomil or to any other of the ingredients of this medicine (listed in section 6).
• if you are more than 3 months pregnant. (It is also better to avoid Olmesartan Medoxomil tablets in early pregnancy - see pregnancy section.)
• if you suffer from yellowing of the skin and eyes (jaundice) or problems with drainage of the bile from the gallbladder (biliary obstruction e.g. gallstones).
Warnings and precautions
Talk to your doctor before taking Olmesartan Medoxomil. Tell your doctor if you have any of the following health problems:
• Kidney problems
• Liver disease
• Heart failure or problems with your heart valves or heart muscle
• Severe vomiting, diarrhoea, treatment with high doses of water tablets (diuretics) or if you are on a low salt diet
• Increased levels of potassium in your blood
• Problems with your adrenal glands.
As with any medicine which reduces blood pressure, an excessive drop in blood pressure in patients with blood flow disturbances of the heart or brain could lead to a heart attack or stroke. Your doctor will therefore check your blood pressure carefully.
You must tell your doctor if you think you are (or might become) pregnant. Olmesartan Medoxomil is not recommended in early pregnancy, and must not be taken if you are more than 3 months pregnant, as it may cause serious harm to your baby if used at that stage (see pregnancy section).
Children and adolescents
Olmesartan Medoxomil is not recommended for children and adolescents under the age of 18.
Other medicines and Olmesartan Medoxomil
Tell your doctor or pharmacist if you are taking or have recently taken or might take any of the following medicines:
• Potassium supplements, a salt substitute which contains potassium, water tablets (diuretics) or heparin (for thinning the blood). Using these medicines at the same time as Olmesartan Medoxomil may raise the levels of potassium in your blood.
• Lithium (a medicine used to treat mood swings and some types of depression) used at the same time as Olmesartan Medoxomil may increase the toxicity of lithium. If you have to take lithium, your doctor will measure your lithium blood levels.
• Non-Steroidal Anti-Inflammatory (NSAIDs) medicines (medicines used to relieve pain, swelling and other symptoms of inflammation, including arthritis) used at the same time as Olmesartan Medoxomil may increase the risk of kidney failure and the effect of Olmesartan Medoxomil can be decreased by NSAIDs.
• Other blood pressure lowering medicines, as the effect of Olmesartan Medoxomil can be increased.
• Certain antacids (indigestion remedies), as the effect of Olmesartan Medoxomil can be slightly decreased.
Older people
If you are over 65 years of age and your doctor decides to increase your dose of olmesartan medoxomil to 40 mg daily, then you need to have your blood pressure regularly checked by your doctor to make sure that your blood pressure does not become too low.
Black patients
As with other similar drugs the blood pressure lowering effect of Olmesartan Medoxomil is somewhat less in black patients.
Olmesartan Medoxomil with food and drink
Olmesartan Medoxomil can 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. Your doctor will normally advise you to stop taking Olmesartan Medoxomil before you become pregnant or as soon as you know you are pregnant and will advise you to take another medicine instead of Olmesartan Medoxomil. Olmesartan Medoxomil is not recommended in early pregnancy, and must not be taken when more than 3 months pregnant, as it may cause serious harm to your baby if used after the third month of pregnancy.
Breast-feeding
Tell your doctor if you are breast-feeding or about to start breast-feeding. Olmesartan Medoxomil is not recommended for mothers who are breast-feeding, and your doctor may choose another treatment for you if you wish to breast-feed, especially if your baby is newborn, or was born prematurely.
Ask your doctor or pharmacist for advice before taking any medicine.
Driving and using machines
You may feel sleepy or dizzy while being treated for your high blood pressure. If this happens, do not drive or use machines until the symptoms wear off. Ask your doctor for advice.
Olmesartan Medoxomil contains lactose
This medicine contains lactose (a type of sugar). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
The recommended starting dose is one 10 mg tablet once a day. However, if your blood pressure is not controlled, your doctor may decide to change your dose up to 20 or 40 mg once a day, or prescribe additional medicines.
In patients with mild to moderate kidney disease, your dose will not be higher than 20 mg once a day.
The tablets can be taken with or without food. Swallow the tablets with a sufficient amount of water (e.g. one glass). If possible, take your daily dose at the same time each day, for example at breakfast time.
If you take more Olmesartan Medoxomil than you should
If you take more tablets than you should or if a child accidentally swallows some, go to your doctor or nearest emergency department immediately and take your medicine pack with you.
|4) POSSIBLE SIDE EFFECTS|
|6) CONTENTS OF THE PACK AND OTHER INFORMATION
If you forget to take Olmesartan Medoxomil
If you forget a dose, take your normal dose on the following day as usual. Do not take a double dose to make up for a forgotten tablet.
If you stop taking Olmesartan Medoxomil
It is important to continue to take Olmesartan Medoxomil unless your doctor tells you to stop.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them. If they do occur, they are often mild and do not require treatment to be stopped.
Although not many people may get them, the following two side effects can be serious:
On rare occasions (may affect up to 1 in 1,000 people) the following allergic reactions that may affect the whole body have been reported:
Swelling of the face, mouth and/or larynx (voice box) together with itching and rash may occur during treatment with Olmesartan Medoxomil. If this happens stop taking Olmesartan Medoxomil and contact your doctor immediately.
Rarely (but slightly more often in older people) Olmesartan Medoxomil can cause the blood pressure to fall too low in susceptible individuals or as the result of an allergic reaction. This could cause severe light-headedness or fainting. If this occurs stop taking Olmesartan Medoxomil, contact your doctor immediately and lie down flat.
These are the other side effects known about so far with Olmesartan Medoxomil
Common side effects (may affect up to 1 in 10 people):
Dizziness, headache, nausea, indigestion, diarrhoea, stomach ache, gastroenteritis, tiredness, sore throat, runny or stuffy nose, bronchitis, flu-like symptoms, cough, pain, pain in the chest, back, bones or joints, infection of the urinary tract, swelling of ankles, feet, legs, hands or arms, blood in the urine.
Some changes in blood test results have also been seen and include the following:
Increased fat levels (hypertriglyceridaemia), increased uric acid levels (hyperuricaemia), rise in blood urea, increases in tests of liver and muscle function.
Uncommon side effects (may affect up to 1 in 100 people):
Quick allergic reactions that may affect the whole body and may cause breathing problems as well as a rapid fall of blood pressure that may even lead to fainting (anaphylactic reactions), vertigo, vomiting, weakness, feeling unwell, muscular pain, skin rash, allergic skin rash, itching, exanthema (skin eruption), skin lumps (wheals), angina (pain or uncomfortable feeling in the chest).
In blood tests a reduction of the numbers of a type of blood cell, known as platelets has been seen (thrombocytopenia).
Rare side effects (may affect up to 1 in 1000 people):
lack of energy, muscle cramps, impaired kidney function, kidney failure.
Some changes in blood test results have also been seen. These include increased potassium levels (hyperkalaemia) and increased levels of compounds related to kidney function.
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.
What Olmesartan Medoxomil contains
The active substance is olmesartan medoxomil
Each film coated tablet contains 40 mg olmesartan medoxomil.
The other ingredients are microcrystalline cellulose, lactose monohydrate, hydroxypropylcellulose, magnesium stearate, titanium dioxide (E171), talc, hypromellose and low substituted hydroxypropylcellulose.
What Olmesartan Medoxomil looks like and contents of the pack
Olmesartan Medoxomil 40 mg film coated tablets are white, oval with C 15 on one side and plain on the other side.
Olmesartan Medoxomil 40 mg is available in packs of 30 film coated tablets.
Product Licence Holder:
Procured from within the EU. Product Licence Holder Ginova Ltd and repackager Ginova UK Ltd both at St James' House, 8 Overcliffe, Gravesend, Kent DA11 0HJ.
Manufacturer:
DAIICHI SANKYO EUROPE GmbH, Luitpoldstrasse 1, 85276, Pfaffenhofen, Germany
Olmesartan Medoxomil 40 mg Film Coated Tablets.
PL No: 18067/0413 |POM|
Date of last revision of this leaflet: 23rd January 2014.
To request a copy of this leaflet in Braille, large print or audio please call 01622 690172.
|5) HOW TO STORE OLMESARTAN MEDOXOMIL|
Keep out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the box and on the blister strip (“EXP”). The expiry date refers to the last day of that month.
This medicinal product does not require any special storage conditions.
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 to protect the environment.
If you notice any sign of discolouration or deterioration of the tablets consult your pharmacist.
500000/PL1b