iMeds.se

Plendil

Information för alternativet: Plendil 2,5 Mg Depottablett, Plendil 5 Mg Depottablett, Plendil 10 Mg Depottablett, visa andra alternativ
Document: Plendil prolonged-release tablet ENG PL change

Package leaflet: Information for the patient


Plendil 2.5 mg prolonged-release tablets

Plendil 5 mg prolonged-release tablets

Plendil 10 mg prolonged-release tablets

felodipine


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

- 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. This includes any possible side effects not listed in this leaflet. See section 4.


What is in this leaflet

1. What Plendil is and what it is used for

2. What you need to know before you take Plendil

3. How to take Plendil

4. Possible side effects

How to store Plendil

6. Contents of the pack and other information


What Plendil is and what it is used for


Plendil contains the active substance felodipine. This belongs to a group of medicines called calcium antagonists. It lowers blood pressure by dilating small blood vessels. It does not negatively affect the heart function.


Plendil is used in the treatment of high blood pressure (hypertension) and heart and chest pain brought on by for example exercise or stress (angina pectoris).


What you need to know before you take Plendil


Do not take Plendil


Warnings and precautions

Plendil, like other blood-pressure lowering medicinal products, may in rare cases lead to pronounced low blood pressure which in some patients may result in an inadequate supply of blood to the heart. Symptoms of excessive low blood pressure and inadequate blood supply to the heart itself, frequently include dizziness and chest pain. If you experience these symptoms, seek emergency care immediately.


Talk to your doctor before taking Plendil, especially if you have problems with your liver.


Taking Plendil may cause your gums to become swollen. Practice good oral hygiene to help avoid your gums from swelling (see section 4).


Children

The use of Plendil is not recommended in children.


Other medicines and Plendil

Tell your doctor if you are taking, have recently taken or might take any other medicines. Some medicines/herbal remedies can affect treatment with Plendil.

Examples are:

tacrolimus (medicine used in organ transplantations)


Medicines containing St John’s wort (Hypericum perforatum)(herbal product used to treat depression) may reduce the effect of Plendil and should therefore be avoided.


Plendil with food and drink

Do not drink grapefruit juice if you are treated with Plendil, as this may increase the effect of Plendil and the risk of side effects.


Pregnancy and breast-feeding

Pregnancy

Do not use Plendil if you are pregnant.


Breast-feeding

Tell your doctor if you are breast-feeding or about to start breast-feeding. Plendil is not recommended for mothers who are breast-feeding, and your doctor may choose another treatment for you if you wish to breast-feed.


Driving and using machines

Plendil can have minor or moderate influence on your ability to drive and use machines. If you experience headache, nausea, dizziness or fatigue your ability to react may be impaired. Caution is recommended especially at the start of treatment.


Plendilcontains lactose and castor oil

Plendil contains lactose that is a type of sugar. If you have been told by your doctor that you have intolerance to some sugars, contact your doctor before taking this medicine.


Plendil contains castor oil, which may cause stomach upset and diarrhoea.


How to take Plendil


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


Plendil extended release tablets should be taken in the morning and be swallowed with water. The tablet must not be divided, crushed or chewed. This medicine can be taken without food or following a light meal not high in fat or carbohydrates.


Hypertension

Treatment should be started with 5 mg once a day. If necessary, your doctor may increase the dose or add another blood-pressure lowering medicine. The usual dose when treating this disease for a long time is 5‑10 mg once a day. In elderly patients, a starting dose of 2.5 mg daily may be considered.


Stable angina pectoris

Treatment should be started with 5 mg once a day and if needed, your doctor may increase the dose to 10 mg once a day.


If you have liver problems

The level of felodipine in your blood may be increased. Your doctor may lower the dose.


Elderly people

Your doctor may initiate treatment with the lowest available dose.


If you take more Plendil than you should

If you take more than the recommended number of doses of Plendil, you may suffer from very low blood pressure and sometimes palpitations, high or, rarely, slow heart rate. Therefore, it is very important that you take the number of doses prescribed by your doctor. If you experience symptoms such as feeling faint, light-headedness or dizziness, contact your doctor immediately.


If you forget to take Plendil

If you forget to take a tablet, leave out that dose completely. Take your next dose at the right time. Do not take a double dose to make up for a forgotten dose.


If you stop taking Plendil

If you stop taking this medicine your condition may return. Please consult your doctor and seek advice before you stop taking Plendil. Your doctor will advise you how long to take your medicine.


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.


If any of the following happen to you, stop taking Plendil and tell a doctor straight away:

Hypersensitivity and allergic reactions: The signs may include raised lumps on your skin (weals) or swelling of your face, lips, mouth, tongue or throat.


The following undesirable effects have been identified. Most of these reactions appear at start of treatment or after a dose increase. Should such reactions occur, they are usually brief and diminish in intensity with time. If you experience any of the following symptoms and they persist, please tell your doctor.


Mild enlargement of the gums has been reported in patients with an inflammation in the mouth (gingivitis/periodontitis). The enlargement can be avoided or reversed by careful oral hygiene.


Very common: may affect more than 1 in 10 people

Ankle swelling


Common: may affect up to 1 in 10 people


Uncommon: may affect up to 1 in 100 people


Rare: may affect up to 1 in 1,000 people


Very rare: may affect up to 1 in 10,000 people


Other undesirable effects may occur. If you have any bothersome or unusual reaction while taking Plendil, check with your doctor right away.


Reporting of side effects

If you get any side effects, talk to your doctor.This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system listed in Appendix V. By reporting side effects you can help provide more information on the safety of this medicine.


5. How to store Plendil


This medicine does not require any special storage conditions.


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 carton, blister and bottle after ‘EXP’. The expiry date refers to the last day of that month.


Do not use this medicine if you notice the packaging is torn or damaged.


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 Plendilcontains


- The active substance is felodipine. Each tablet contains 2.5 mg (or 5 mg or 10 mg) of felodipine.


The other ingredients are:

Tablet core:

Hydroxypropylcellulose

Hypromellose 50 mPa·s

Hypromellose 10000 mPa·s

Lactose anhydrous

Macrogolglycerol hydroxystearate

Microcrystalline cellulose

Propyl gallate

Sodium aluminium silicate

Sodium stearyl fumarate


Tablet coating:

Carnauba wax

Iron oxide reddish-brown (E172) (Only used for Plendil 5 mg and 10 mg)

Iron oxide yellow (E172)

Hypromellose 6 mPa·s

Macrogol 6000

Titanium dioxide (E 171)


What Plendil looks like and contents of the pack


Plendil 2.5 mg prolonged-release tablet is yellow, circular, biconvex, engraved A/FL on one side and 2.5 on the other side, with a diameter of 8.5 mm.


Plendil 5 mg prolonged-release tablet is pink, circular, biconvex, engraved A/Fm on one side and 5 on the other side, with a diameter of 9 mm.


Plendil 10 mg prolonged-release tablet is reddish-brown, circular, biconvex, engraved A/FE on one side and 10 on the other side, with a diameter of 9.


Pack sizes prolonged-release tablets 2.5 mg

20 tablets (blister pack)

28 tablets (blister pack with days of the week printed)

30 tablets (blister pack and plastic bottle)

50 tablets (unit-dose pack)

98 tablets (blister pack with days of the week printed)
100 tablets (blister pack and plastic bottle)
500 tablets (plastic bottle for dose dispensing)


Pack sizes prolonged-release tablets 5 mg

14 tablets (blister pack with days of the week printed)
20 tablets (blister pack)

28 tablets (blister pack with days of the week printed)

30 tablets (blister pack and plastic bottle)

50 tablets (unit-dose pack)
90 tablets (blister pack)

98 tablets (blister pack with days of the week printed)
100 tablets (blister pack and plastic bottle)
500 tablets (plastic bottle for dose dispensing)


Pack sizes prolonged-release tablets 10 mg

14 tablets (blister pack with days of the week printed)
20 tablets (blister pack)

28 tablets (blister pack with days of the week printed)

30 tablets (blister pack and plastic bottle)

50 tablets (unit-dose pack)
90 tablets (blister pack)

98 tablets (blister pack with days of the week printed)
100 tablets (blister pack, plastic bottle and plastic bottle for dose dispensing)
500 tablets (plastic bottle for dose dispensing)


Not all pack sizes may be marketed.


Marketing Authorisation Holder and Manufacturer


<[To be completed nationally]>


{Name and address}

<{tel}>

<{fax}>

<{e-mail}>


This medicinal product is authorised in the Member States of the EEA under the following names:


Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Romania, Slovakia, Spain, Sweden, United Kingdom: Plendil


France: Flodil

Germany: Modip

Portugal: Preslow


This leaflet was last revised in 19 August 2016


Detailed information on this medicine is available on the website of {MS/Agency}

6