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Read all of this leaflet carefully before you start using 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.
1. What Nebivolol is and what it is used for
2. Before you take Nebivolol
3. How to take Nebivolol
4. Possible side effects
5. How to store Nebivolol
6. Further information



Nebivolol contains nebivolol which is a selective beta blocker and it dilates blood vessels (vasodilator). It is
used for the treatment of raised blood pressure (hypertension).
Nebivolol is also used to treat chronic heart failure in patients aged 70 or over.



Do not take Nebivolol
• if you are allergic (hypersensitive) to nebivolol or to any of the other ingredients of Nebivolol (see section
6 of this leaflet)
• if you have low blood pressure (the systolic or “upper” pressure is less than 90 mmHg)
• if you have poor circulation in the arms or legs
• if you have a very slow heartbeat (less than 60 heart beats per minute before having started this medication)
• if you have been diagnosed with conduction disorders in your heart (such as sick sinus syndrome or
atrio-ventricular blockade) and you do not have a functioning pacemaker
• if you have acute heart failure, or you are receiving treatment into a vein (by intravenous ‘drip’) to help
your heart work
• if you have difficulty in breathing or wheezing (or a history of this)
• if you have a tumour of the adrenal gland called phaeochromocytoma
• if you have severe liver disease or liver function impairment
• if you have a metabolic acidosis (such as in diabetic patients when the blood sugar has risen too much
and blood has become too acidic)
• if you use either floctafenine or sultopride containing medications.
Take special care with Nebivolol
If you have or develop one of the following conditions:
• heart failure (inability of heart to pump enough blood for body´s needs)
• a mild (first degree) atrioventricular blockade in your heart
• chest pain caused by cramping of the coronary arteries (called Prinzmetal´s angina or variant angina)
• poor circulation in the arms or legs, e.g. Raynaud’s disease or syndrome, cramp-like pains on walking
• prolonged breathing problems
• diabetes: Nebivolol has no effect on blood sugar, but it could mask the signs of a low sugar level (e.g.
trembling, fast heartbeat)
• overactive thyroid gland, as Nebivolol may mask the signs of an abnormally fast heart rate due to this
• allergy, as the allergic reactions may become stronger and more medicines may be needed to treat them
• a skin condition known as psoriasis, as Nebivolol may aggravate the symptoms
• wear contact lenses, as Nebivolol may reduce lacrimation and make the eyes dryer.
Use in children and adolescents below 18 years old is not recommended.
In these cases, your doctor may need to adapt your treatment or check you more often.
If you need to have an operation and need an anaesthetic, it is important that you tell the surgeon or dentist
that you are taking this medicine.
If you have kidney problems, do not take this medicine for heart failure and inform your doctor.
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, herbal remedies and strong vitamins and minerals.
Always tell your doctor or pharmacist if you are using or receiving any of the following medicines in
addition to Nebivolol:
• diltiazem or verapamil (used for high blood pressure and other heart problems). During Nebivolol
treatment, verapamil should not be injected into a vein
• other medicinal products known as calcium channel blockers for high blood pressure or other heart
problems such as amlodipine, felodipine, lacidipine, nifedipine, nicardipine, nimodipine, nitrendipine
• other antihypertensive medications or organic nitrates to treat chest pain
• clonidine, guanfacin, moxonidine, methyldopa, rilmenidine used for the treatment of high blood pressure
• medicinal products for cardiac arrhythmias (irregular heartbeat) such as quinidine, hydroquinidine,
amiodarone, cibenzoline, flecainide, disopyramide, lidocaine, mexiletine, propafenone
• tricyclic antidepressants (for depression), phenothiazines (for psychoses), or barbiturates (for epilepsy)
• medicinal products for diabetes mellitus (insulins and oral preparations)
• digoxin or other so called digitalis glycosides (to treat heart failure)
• anti-inflammatory analgesics (NSAIDs) for pain and inflammation - please note that small daily
antithrombotic doses of acetylsalicylic acid (e.g., 50 or 100 mg) can be used safely with Nebivolol
• medicinal products for asthma, blocked nose or certain eye disorders such as glaucoma (increased
pressure in the eye) or dilation of the pupil
• anaesthetics: always inform your anaesthetist that you are on Nebivolol before being anaesthetized
• cimetidine (to treat excessive stomach acid) - you should take Nebivolol during a meal, and the antacid
drug between meals
• medicinal products affecting the metabolism of nebivololnamely terbinafine (for fungal or yeast
infections), bupropion (to help in cessation of smoking), chloroquine (for malaria or rheumatoid arthritis),
levomepromazine (for psychoses), paroxetine, fluoxetine, thioridiazine (for depression)
• amifostine (a protecting substance during chemo - or radiation therapy)
• baclofen (a muscle relaxant)
• mefloquine (an antimalarial).
Taking Nebivolol with food and drink
Nebivolol 5 mg tablets can be taken before, during or after a meal, but also you can take them without food.
The tablet or its parts should be swallowed with some water or another liquid.

Pharma code: 215

Pregnancy and breast-feeding
Nebivolol should not be used during pregnancy unless instructed to do so by a
Breast-feeding is not recommended during administration of Nebivolol.
Ask your doctor or pharmacist for advice before taking any medicine.
Driving and using machines
No studies on the effects on the ability to drive and use machines have been

This medicine may cause dizziness or fainting as a result to reduction in blood pressure. If these occur, DO
NOT drive or operate machinery. These effects are more likely to occur after initiation of the treatment or
after dose increases (see also section 4).
Important information about some of the ingredients of Nebivolol
This product contains lactose. If your doctor has told you that you have intolerance to some sugars, contact
your doctor before taking this medicine.



Always take Nebivolol exactly as your doctor has told you. You should check with your doctor or pharmacist
if you are not sure.
Treatment of raised blood pressure (hypertension)
• The usual dose is 1 tablet per day
• Elderly patients and patients with a kidney disorder will usually start with 1/2 tablet daily
• It may take up to 4 weeks for this medicine to have full effect.
Treatment of chronic heart failure
• Your treatment will be started and monitored by an experienced physician
• Your doctor will start your treatment with 1/4 tablet per day. This may be increased after 1-2 weeks to 1/2 tablet
per day, then to 1 tablet per day and then to 2 tablets per day until the correct dose is reached for you
• The maximum recommended dose is 10 mg (2 tablets a day)
• You will need to be monitored for 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, and you should not stop abruptly as this can worsen heart
• Patients with serious kidney problems should not take this medicine.

Take your medicine once daily, preferably at about the same time of day.
Your doctor may decide to combine your tablets with other medicine for your condition.
Nebivolol is not recommended in children and adolescents.
If you take more Nebivolol than you should
If you accidentally take too many tablets (overdose), you may experience slow heart beat, low blood
pressure or other heart problems, or difficulty in breathing or wheezing. Contact your nearest hospital
casualty department or tell your doctor or pharmacist immediately.
If you forget to take Nebivolol
If you forget to take your medicine, but remember to take it after a short time, take the next tablet normally,
when it is the time to take it. However, if a long delay has occurred (e.g. all day) skip that dose and take the
next dose the next day at the usual time and skip the forgotten dose. Do not take a double or a larger dose
to make up with a forgotten dose(s). Repeated skipping is to be avoided.
If you stop taking Nebivolol
Do not stop taking Nebivolol without consulting your doctor first. If the medication is terminated abruptly,
the patient may experience dangerous worsening of the symptoms. This concerns especially the patients
with angina pectoris.
If you have any further questions on the use of this product, ask your doctor or pharmacist.



Like all medicines, Nebivolol can cause side effects, although not everybody gets them.
When Nebivolol is used for the treatment of raised blood pressure, the possible side effects are:
Common side effects (estimated frequency is less than 1 person out of 10 but more than 1 out of 100):
• Headache
• Dizziness
• Tiredness
• An unusual itching or tingling feeling
• Diarrhoea
• Constipation
• Nausea
• Shortness of breath
• Swollen hands or feet.
Uncommon side effects (estimated frequency is less than 1 person out of 100 but more than 1 out of 1000):
• Slow heartbeat or other heart complaints
• Low blood pressure
• Cramp like pains on walking
• Abnormal vision
• Impotence (difficulty in getting an erection)
• Depressive feelings
• Indigestion, gas in stomach or bowel
• Vomiting
• Skin rash
• Itchiness
• Tightening of the chest, difficulty in breathing or wheezing
• Nightmares.
Very rare side effects (estimated frequency is less than 1 person out of 10000):
• Fainting
• Psoriasis aggravated.
The following side effects have been reported with frequency unknown:
• Whole body allergic reactions, with generalised skin eruption (hypersensitivity reactions)
• Rapid onset swelling of the skin of the face or extremities, lips, tongue, mucous membranes of
the throat and airway, resulting in shortness of breath or difficulty to swallow – contact a doctor
immediately! (Angioedema).
In a clinical study for chronic heart failure, the following side effects were seen:
Very common side effects (estimated frequency is more than 1 person out of 10):
• Slow heart beat
• Dizziness.
Common side effects (estimated frequency is less than 1 person out of 10 but more than 1 out of 100):
• 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).
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.



Keep out of the reach and sight of children.
Do not use Nebivolol after the expiry date which is stated on the carton after .
The expiry date refers to the last day of that month.
Do not store above 30°C.
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.



What Nebivolol contains
The active substance is nebivolol.
Each Tablet contains 5 mg of nebivolol equivalent to 5.45 mg of nebivolol hydrochloride.
The other ingredients are:
Lactose Monohydrate,
Crospovidone Type A,
Poloxamer 188,
Povidone K 30,
Microcrystalline Cellulose,
Magnesium Stearate.
What Nebivolol looks like and contents of the pack
Nebivolol tablets are white, round, biconvex tablets, cross-scored on one side,
with a diameter of 9 mm approximately.
Nebivolol can be divided into equal quarters.
Tablets are provided in PVC/PE/PVDC/Aluminium blisters of 7, 10 and 14.
Pack sizes: 7, 10, 14, 20, 28, 30, 50, 56, 60, 90, 100, 120 tablets
Not all pack sizes may be marketed.
Marketing Authorisation Holder
Teva UK Ltd, Hampden Park, Eastbourne, East Sussex, BN22 9AG.
Specifar S.A.
1, 28 Octovriou str., Ag. Varvara,
123 51 Athens,
This leaflet was last approved in April 2011
PL 00289/1278

P.C. 215

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Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.