NEBIVOLOL ACTAVIS 5MG TBL N90

ATC code: C07AB12 

Active substances: Nebivololum

Vendor, principal: Actavis Hf.. 
NEBIVOLOL ACTAVIS 5MG TBL N90 is compensated medicine in Latvia. 

 Prescription drug (℞) 

NEBIVOLOL STADA 5MG N100

Package leaflet: Information for the user

Nebivolol STADA 5 mg Tablets

Nebivolol

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, please ask your doctor or your 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 Nebivolol STADA is and what it is used for
2.   What you need to know before you take Nebivolol STADA
3.   How to take Nebivolol STADA
4.   Possible side effects
5.   How to store Nebivolol STADA
6.   Contents of the pack and other information

1. What Nebivolol STADA is and what it is used for

Nebivolol STADA contains nebivolol, a cardiovascular drug belonging to the group of selective betablocking agents (i.e. with a selective action on the cardiovascular system). It prevents increased heart rate, controls heart pumping strength. It also exerts a dilating action on blood vessels, which contributes to as well lower blood pressure.
It is used to treat raised blood pressure (hypertension).
Nebivolol STADA is also used to treat stable mild and moderate chronic heart failure in patients aged 70 or over, in addition to other therapies.

2. What you need to know before you take Nebivolol STADA DO NOT take Nebivolol STADA

•   if you are allergic to nebivolol or any of the other ingredients of this medicine (listed in section 6).
•   if you have one or more of the following disorders:
-   low blood pressure
-   serious circulation problems in the arms or legs
-   very slow heartbeat (less than 60 beats per minute) or irregular heartbeat (sick sinus syndrome)
-   certain other serious heart rhythm problems (e.g. 2^nd and 3^rd degree atrioventricular block, sinoatrial block)
-   heart failure, which has just occurred or which has recently become worse, shock caused by worsening of the heart failure (cardiogenic shock) or you are receiving treatment for circulatory shock due to acute heart failure by intravenous drip feed to help your heart work
-   asthma, wheezing or a condition that affects your breathing (now or in the past)
-   untreated phaeochromocytoma, a tumour located on top of the kidneys (in the adrenal glands)
-   liver function disorder
-   a metabolic disorder (metabolic acidosis), for example, diabetic ketoacidosis.

Warnings and precautions

Talk to your doctor or pharmacist before taking Nebivolol STADA. Especially if you have
-   abnormally slow heartbeat
-   a type of chest pain due to spontaneously occurring heart cramp called Prinzmetal angina
-   untreated chronic heart failure and ischemic heart disease (restriction in blood supply)
-   1^st degree heart block (a kind of light heart conduction disorder that affects heart rhythm)
-   poor circulation in the arms or legs, e.g. Raynaud’s disease or syndrome, cramp-like pains when walking
-   diabetes: This medicine has no effect on blood sugar, but it could conceal the warning signs of a low sugar level (e.g. palpitations, fast heartbeat).
-   overactive thyroid gland: This medicine may mask the signs of an abnormally fast heart rate due to this condition.
-   allergy: This medicine may intensify your reaction to pollen or other substances you are allergic to.
-   prolonged breathing problems combined with cough (you know that you suffer from a chronic obstructive pulmonary disease [COPD])
-   psoriasis (a skin disease - scaly pink patches) or if you have ever had psoriasis
-   to have surgery, always inform your anaesthetist that you are on Nebivolol STADA before being anaesthetised.
If you have serious kidney problems do not take Nebivolol STADA for heart failure and tell your doctor.
You will be regularly monitored at the beginning of your treatment for chronic heart failure by an experienced physician (see section 3).
This treatment should not be stopped abruptly unless clearly indicated and evaluated by your doctor (see section 3).

Children and adolescents

Because of the lack of data on the use of the product in children and adolescents younger than 18 years, Nebivolol STADA is not recommended for use in them.

Other medicines and Nebivolol STADA

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Certain medicines cannot be used at the same time, while other drugs require specific changes (in the dose, for example).
Always tell your doctor if you are using or receiving any of the following medicines in addition to Nebivolol STADA:
-   Medicines for controlling the blood pressure or medicines for heart problems (such as amiodarone, amlodipine, cibenzoline, clonidine, digoxin, diltiazem, disopyramide, felodipine, flecainide, guanfacine, hydroquinidine, lacidipine, lidocaine, methyldopa, mexiletine, moxonidine, nicardipine, nifedipine, nimodipine, nitrendipine, propafenone, quinidine, rilmenidine, verapamil).
-   Sedatives and therapies for psychosis (a mental illness) e.g. barbiturates (also used for epilepsy), phenothiazines (also used for vomiting and nausea) e.g. thioridazine.
-   Medicines for depression e.g. tricyclic antidepressants, paroxetine, fluoxetine.
-   Baclofen (used for the treatment of spastic movement), amifostine (used to treat cancer)
-   Medicines used for anaesthesia during an operation.
-   Medicines for asthma, blocked nose or certain eye disorders such as glaucoma (increased pressure in the eye) or dilation (widening) of the pupil.
All these drugs as well as nebivolol may influence the blood pressure and/or heart function.
-   Medicines for treating excessive stomach acid or ulcers (antacid drug), e.g. cimetidine: you should take Nebivolol STADA during a meal and the antacid drug between meals.
-   Insulin or tablets for diabetes. Although nebivolol does not affect glucose level, concomitant use may mask certain symptoms of hypoglycaemia (increased heart beat)

Pregnancy and breast feeding

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Nebivolol STADA should not be used during pregnancy, unless clearly necessary.
Nebivolol STADA is not recommended for use while breast-feeding.

Driving and using machines

This medicine may cause dizziness or fatigue. If affected, do not drive or operate machinery.

Nebivolol STADA contains lactose

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 Nebivolol STADA

Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
Nebivolol STADA may be taken before, during or after the meal, but, alternatively, you can take it without a meal. The tablet is best taken with some water (e.g. one glass of water).

Treatment of raised blood pressure (hypertension)

-   The recommended dose is 1 tablet per day. The dose should be taken preferably at the same time of the day.
-   Elderly patients over 65 years and patients with a kidney disorder will usually start with 54 (half) tablet daily. If needed, the daily dose may be increased to 1 tablet.
-   The therapeutic effect on blood pressure becomes evident after 1 -2 weeks of treatment. Occasionally, the optimal effect is reached only after 4 weeks.

Treatment of chronic heart failure

-   Your treatment will be started and closely supervised by an experienced physician.
-   Your doctor will start your treatment with % (quarter) tablet per day. This may be increased after 12 weeks to 54 (half) tablet per day, then to 1 tablet per day and then to 2 tablets per day until the correct dose is reached for you. Your doctor will prescribe the dose that is right for you at each step and you should closely follow his/her instructions.
-   The maximum recommended dose is 2 tablets (10mg) a day.
-   You will need to be under the close supervision for at least 2 hours by an experienced physician when you start treatment and every time your dose is increased.
-   Your doctor may reduce your dose if necessary.
-   You should not stop treatment abruptly as this can make your heart failure worse.
-   Take your medicine once daily, preferably at about the same time of day.
Patients with serious kidney problems should not take Nebivolol STADA, as there is no clinical experience in these patients.
If you have been told by your doctor to take % (quarter) or 54 (half) tablet daily, you will need to break the tablet along the ‘score’ lines before taking. Nebivolol STADA tablets have a cross-score to facilitate the individual dosage. Please refer to the instructions below on how to break Nebivolol STADA tablets.
-   Place the tablet on a hard surface with the center groove facing upward.
-   Exert pressure from the top with your thumb and the tablet will break into four equal pieces.
Your doctor may decide to combine Nebivolol STADA with other medicines to treat your condition.

Use in children and adolescents

Do not use Nebivolol STADA in children or adolescents younger than 18 years.

If you take more Nebivolol STADA than you should

If you accidentally take an overdose of this medicine, tell your doctor or pharmacist immediately. The most frequent symptoms and signs of a Nebivolol STADA overdose are very slow heart beat (bradycardia), low blood pressure with possible fainting (hypotension), breathlessness such as in asthma (bronchospasm), and acute heart failure.

If you forget to take Nebivolol STADA

If you forget a dose of Nebivolol STADA, but remember a little later on that you should have taken it, take that day’s dose as usual. However, if a long delay has occurred (e.g. several hours), so that the next due dose is near, skip the forgotten dose and take the next, scheduled, normal dose at the usual time. Do not take a double dose to make up for a forgotten dose. Repeated skipping, however, should be avoided.

If you stop taking Nebivolol STADA

You should always consult with your doctor before stopping Nebivolol STADA treatment, whether you are taking it for high blood pressure or chronic heart failure.
You should not stop Nebivolol STADA treatment abruptly as this can temporarily make your heart failure worse. If it is necessary to stop Nebivolol STADA treatment for chronic heart failure, the daily dose should be decreased gradually, by halving the dose, at weekly intervals.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.
When Nebivolol STADA is used for the treatment of raised blood pressure, the possible side effects are:
Common side effects (may affect up to 1 in 10 people):
-   headache
-   dizziness
-   tiredness
-   an unusual itching or tingling feeling (paraesthesia)
-   diarrhoea
-   constipation
-   nausea
-   shortness of breath
-   accumulation of fluid in the body resulting in swelling, particularly of the legs and ankles (oedema).
Uncommon side effects (may affect up to 1 in 100 people)
-   slow heartbeat or other heart complaints
-   low blood pressure
-   cramp-like leg pains on walking (intermittent claudication)
-   abnormal vision
-   impotence
-   feelings of depression
-   digestive difficulties (dyspepsia), gas in stomach or bowel, vomiting
-   skin rash, itchiness
-   breathlessness such as in asthma, due to sudden cramps in the muscles around the airways (bron-chospasm)
-   nightmares.
Very rare side effects (may affect up to 1 in 10,000 people)
-   fainting
-   worsening of psoriasis (a skin disease - scaly pink patches).
Not known (frequency cannot be estimated from the available data)
-   swelling of the lips, eyes or tongue (angioneurotic oedema), with possible sudden difficulty breathing
-   allergic reactions
-   hives (urticaria)
Other side effects seen with drugs that are similar to nebivolol are: hallucinations, mental disorders and confusion, cold fingers and toes sometimes going pale or blue, dry eyes, and a severe disorder of the eyes and mouth.
In a clinical study for chronic heart failure, the following side effects seen were:
Very common side effects (may affect more than 1 in 10 people)
-   slow heart beat
-   dizziness
Common side effects (may affect up to 1 in 10 people)
-   worsening of heart failure
-   low blood pressure (such as feeling faint when getting up quickly)
-   inability to tolerate this medicine
-   a kind of light heart conduction disorder that affects heart rhythm (1st degree AV -block)
-   swelling of the lower limbs (such as swollen ankles).
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 via www.ravimiamet.ee. By reporting side effects, you can help provide more information on the safety of this medicine.

5. How to store Nebivolol STADA

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 and the blister (EXP). The expiry date refers to the last day of that month.
Do not store above 30 °C.
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 Nebivolol STADA contains

-   The active substance is nebivolol. Each tablet contains nebivolol hydrochloride equivalent to 5 mg nebivolol.
-   The other ingredients are Povidone K30; lactose monohydrate; maize starch, pregelatinised; croscarmellose sodium; Silica, colloidal anhydrous; magnesium stearate and crospovidone.

What Nebivolol STADA looks like and contents of the pack

There is only one strength of Nebivolol STADA. These are white, round, cross-scored tablets and are available in blister packs of 7, 10, 14, 28, 30, 50, 56, 84, 98, 100 and 500 tablets.
Not all pack sizes may be marketed.

Marketing Authorisation Holder

STADA Arzneimittel AG
Stadastrasse 2-18, D-61118 Bad Vilbel, Germany

Manufacturer

STADA Arzneimittel AG
Stadastrasse 2-18, D-61118 Bad Vilbel, Germany
Centrafarm Services B.V.
Nieuwe Donk 9, NL-4879 AC Etten-Leur, The Netherlands
For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder.
Almar Sehver Tartu mnt 16 10117 Tallinn Phone:+ 372 6605910 [email protected]

This leaflet was last revised in November 2016.

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