Patient Leaflet Updated 05-Sep-2022 | Glenmark Pharmaceuticals Europe Ltd
Nebivolol 10mg Tablets
Nebivolol 10 mg Tablets
Nebivolol (as hydrochloride)
1. What Nebivolol is and what it is used for
2. What you need to know before you take Nebivolol
3. How to take Nebivolol
4. Possible side effects
5. How to store Nebivolol
6. Contents of the pack and other information
Nebivolol contains nebivolol, a cardiovascular drug belonging to the group of selective beta-blocking 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 as well to lower blood pressure.
It is used to treat raised blood pressure (hypertension).
Nebivolol is also used to treat mild and moderate chronic heart failure in patients aged 70 or over, in addition to other therapies.
Talk to your doctor or pharmacist before taking Nebivolol.
Inform your doctor if you have or develop one of the following problems:
if you have to have surgery, always inform your anaesthetist that you are on Nebivolol before being anaesthetised.
If you have serious kidney problems do not take Nebivolol 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).
Because of the lack of data on the use of the product in children and adolescents, Nebivolol is not recommended for use in them.
Tell your doctor or pharmacist if you are using, have recently used or might use any other medicines.
Always tell your doctor if you are using or receiving any of the following medicines in addition to Nebivolol:
Please refer to section 3.
Pregnancy
Nebivolol should not be taken during pregnancy unless clearly necessary..
Breast-feeding
It is not recommended
for use while 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.
This medicine may cause dizziness or fatigue. If affected, do not drive or operate machinery.
This product 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.
This medicine contains less than 1 mmol sodium (23 mg) per tablet that is to say essentially ‘sodium-free’.
Always take Nebivolol exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
Nebivolol may be taken before, during or after the meal, but, alternatively, you can take it independently of meals. The tablet is best taken with some water.
* Nebivolol 2.5 mg and 5 mg tablets are also available on the market.
* Nebivolol 2.5 mg and 5 mg tablets are also available on the market.
Do not use in children or adolescents.
If you accidentally take an overdose of this medicine, tell your doctor of pharmacist immediately. The most frequent symptoms and signs of a Nebivolol overdose are very slow heart beat (bradycardia), low blood pressure with possible fainting (hypotension), breathlessness such as in asthma (bronchospasm), and acute heart failure.
You can take activated charcoal (which is available at your pharmacy) while you wait for the arrival of the doctor.
If you forget a dose of Nebivolol, 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 . Repeated skipping, however, should be avoided.
You should always consult with your doctor before stopping Nebivolol treatment, whether you are taking it for high blood pressure or chronic heart failure.
You should not stop Nebivolol treatment abruptly as this can temporarily make your heart failure worse.
If it is necessary to stop Nebivolol 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.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
When Nebivolol tablets are used for the treatment of raised blood pressure, the possible side effects are:
Common side effects (may affect up to 1 in 10 people):
The following side effects have been reported only in some isolated cases during nebivolol treatment (contact a doctor immediately)
Uncommon side effects (may affect up to 1 in 100 people):
Nightmares
Very rare side effects (may affect up to 1 in 10,000 people):
The following side effects have been reported only in some isolated cases during Nebivolol treatment:
In a clinical study for chronic heart failure, the following side effects were seen:
Very common side effects (may affect more than 1 in 10 people):
Common side effects (may affect up to 1 in 10 people)
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:
Ireland
United Kingdom
By reporting side effects you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use Nebivolol after the expiry date which is stated on the carton and on the blister after 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 protect the environment.
If the medicine becomes discoloured or shows any other signs of deterioration, you should seek the advice of your pharmacist who will tell you what to do.
The active substance is nebivolol.
Each tablet contains 10 mg nebivolol equivalent to 10.9 mg nebivolol hydrochloride
The other ingredients are:
lactose monohydrate; maize starch; croscarmellose sodium; hypromellose; microcrystalline cellulose; silica colloidal anhydrous; magnesium stearate.
Nebivolol 10 mg tablets: circular, white, shallow, biconvex uncoated tablets engraved with ‘G’ and ‘N’ on either side of break line on one side and plain on other side. The tablets can be divided into equal halves.
Nebivolol 10 mg tablets are available in PVC/PVdC/aluminium blisters and aluminium/ aluminium blisters of 14, 28, 30, 50, 100 tablets.
*Not all pack sizes may be marketed.
Marketing Authorization Holder
Manufacturers
This medicine is authorised in the Member States of the European Economic Area and in the United Kingdom (Northern Ireland) under the following names:
Ireland, United Kingdom (Northern Ireland): Nebivolol 10 mg Tablets
This leaflet was last revised in 07/2022.
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