LERCANIDIPINE HYDROCHLORIDE 20MG TABLETS
Active substance(s): LERCANIDIPINE HYDROCHLORIDE
ZANIDIP® 20 MG TABLETS
Your medicine is available as Zanidip® 20mg tablets but will
be referred to as Zanidip throughout the leaflet.
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
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
This includes any possible side effects not listed in this leaflet.
What is in this leaflet:
What Zanidip is and what it is used for
What you need to know before you take Zanidip
How to take Zanidip
Possible side effects
How to store Zanidip
Contents of the pack and other information
1. What Zanidip is and what it is used for
Zanidip, lercanidipine hydrochloride, belongs to a group of
medicines called Calcium Channel Blockers (dihydropyridine
derivatives) that lower blood pressure.
Zanidip is used to treat high blood pressure also known as
hypertension in adults over the age of 18 years (it is not
recommended for children under 18 years old).
2. What you need to know before you take
Do not take Zanidip:
If you are allergic (hypersensitive) to lercanidipine
hydrochloride or to any other ingredients of Zanidip
If you have had allergic reactions to drugs closely
related to Zanidip tablets (such as amlodipine,
nicardipine, felodipine, isradipine, nifedipine or
If you are suffering from certain heart diseases:
untreated heart failure
obstruction to flow of blood from the heart
unstable angina (angina at rest or progressively
within one month of heart attack
If you have severe liver or kidney problems.
If you are taking drugs that are inhibitors of CYP3A4
antifungal medicines (such as ketoconazole or
macrolide antibiotics (such as erythromycin or
antivirals (such as ritonavir)
If you are taking another drug called ciclosporin or
cyclosporin (used after transplants to prevent organ
With grapefruit or grapefruit juice.
Do not use if you are pregnant or breastfeeding (see section
Pregnancy, breast-feeding and fertility for more information).
Warning and precautions
Talk to your doctor or pharmacist before taking Zanidip:
if you have certain other heart conditions which have
not been treated by insertion of a pacemaker or have
if you have problems with your liver or kidneys or you
are on dialysis.
You must tell your doctor if you think you are (or might
become) pregnant or breast-feeding (see pregnancy, breastfeeding and fertility section).
Children and adolescents
Zanidip with food, drink and alcohol
Please do not consume alcohol during treatment with
Zanidip tablets since it may increase the effect of
Please do not take Zanidip tablets with grapefruit or
Pregnancy, breast-feeding and fertility
Zanidip should not be used if you are pregnant or breastfeeding, think you may be pregnant or are planning to have a
baby or you are not using any contraceptive method.
Ask your doctor or pharmacist for advice before taking this
Driving and using machines
Caution should be exercised because of the possibility of
dizziness, weakness, tiredness and rarely sleepiness. Do not
drive or use machines until you know how Zanidip affects
Zanidip contains lactose monohydrate
If you have been told by your doctor that you have an
intolerance to some sugars, e.g. intolerance to lactose,
galactosaemia or glucose/galactose malabsorption syndrome,
contact your doctor before taking this medicinal product, as
the tablets contain lactose monohydrate.
3. How to take Zanidip
The safety and efficacy of Zanidip in children aged up to 18
years have not been established.
No data are available.
Always take this medicine exactly as your doctor has told
Check with your doctor or pharmacist if you are not sure.
Other medicines and Zanidip
Adults: The recommended dose is 10 mg once daily at the
same time each day, preferably in the morning at least 15
minutes before breakfast, because a high fat meal
significantly increases blood levels of the drug. Your doctor
may advise you to increase the dose to one Zanidip 20 mg
daily, if needed.
The tablets should preferably be swallowed whole with some
Please tell your doctor or pharmacist if:
You are taking or have recently taken any other
medicines, including medicines obtained without a
You are taking beta-blockers e.g. metoprolol, diuretics
(water tablets) or ACE-inhibitors (medicines to treat
high blood pressure)
You are taking cimetidine (more than 800 mg, a
medicine for ulcers, indigestion, or heartburn)
You are taking digoxin (a medicine to treat a heart
You are taking midazolam (a medicine that helps you
You are taking rifampicin (a medicine to treat
You are taking astemizole or terfenadine (medicines for
You are taking amiodarone or quinidine (medicines to
treat a fast heart beat)
You are taking phenytoin or carbamazepine (medicines
for epilepsy). Your doctor will want to monitor your
blood pressure more frequently than usual.
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Use in children: This medicine should not be used in
children under 18 years of age.
Elderly patients: No adjustment of the daily dose is
required. However, special care should be exercised in
Patients with liver or kidney problems: special care is
needed in starting treatment in these patients and an
increase in daily dose to 20 mg should be approached with
If you have any further questions on the use of this medicine
ask your doctor or pharmacist.
If you take more Zanidip than you should
Do not exceed the prescribed dose.
If you take more than the prescribed dose or in the event of
overdose, seek medical advice immediately and, if possible,
take your tablets and/or the container with you.
Exceeding the correct dosage may cause blood pressure to
become too low, and the heart to beat irregularly or faster. It
may also lead to unconsciousness.
If you forget to take Zanidip
If you forget to take your tablet simply miss that dose and
then go on as before.
Do not take a double dose to make up for a forgotten dose.
Reporting of suspected adverse reactions
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 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.
5. How to store Zanidip
If you stop taking Zanidip
If you stop taking Zanidip your blood pressure may increase
again. Please consult your doctor before stopping the
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.
Some side effects can be serious:
If you experience any of these side effects tell your
doctor straight away.
Rare (affecting less than 1 out of 1,000 patients): angina
pectoris (chest pain due to lack of blood to your heart)
Store in the original package in order to protect from
Keep out of the sight and reach of children.
Do not use tablets after the expiry date, which is
marked on both the outer carton and on each blister
strip of tablets. The expiry date refers to the last day of
If your tablets appear to be discoloured or show any
other signs of deterioration, take them to your
pharmacist who will advise you.
If your doctor advises you to stop taking the tablets,
please return any which are left to your pharmacist for
safe disposal. Only keep them if your doctor tells you
to. Medicines should not be disposed of via wastewater
or household waste. These measures will help to protect
Remember: this medicine has been prescribed for you.
Do not give it to anyone else under any circumstances.
6. Contents of the pack and other
What Zanidip contains
Very rare (affecting less than 1 out of 10,000 patients): chest
pain, fall in blood pressure, fainting and allergic reactions
(symptoms include itching, rash, hives)
Each film-coated tablet contains 20 mg of lercanidipine
(as the hydrochloride), which is equivalent to 18.8 mg of
If you suffer from pre-existing angina pectoris, with the group
of medicines to which Zanidip belongs, you may experience
increased frequency, duration or severity of these attacks.
Isolated cases of heart attack may be observed.
The following inactive ingredients are also included in Zanidip
lactose monohydrate, microcrystalline cellulose, sodium
starch glycolate, povidone K30, magnesium stearate,
hypromellose, titanium dioxide (E171), macrogol 6000, and
iron oxide (E172) and talc.
Other possible side effects:
Uncommon (affecting less than 1 out of 100 patients):
headache, dizziness, faster heart beats, palpitations (heart
pounding or racing), sudden reddening of the face, neck or
upper chest, ankle swelling.
Rare (affecting less than 1 out of 1,000 patients): sleepiness,
feeling sick, vomiting, heartburn, stomach pain, diarrhoea;
skin rash, muscle pain, passage of large amounts of urine,
What Zanidip looks like and contents of the pack
Zanidip tablets are pink, circular, biconvex, film-coated
tablets, scored on one side and plain on the other side.
Zanidip is available in blister packs of 28, 50,100 tablets.
Very rare (affecting less than 1 out of 10,000 patients):
swelling of gums, changes in liver function (detected by blood
tests), increase in the usual number of times one urinates.
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RECORDATI Industria Chimica e Farmaceutica S.p.A.,
Via Matteo Civitali 1, 20148 Milan, Italy.
Procured from within the EU and repackaged by:
Doncaster Pharmaceuticals Group Ltd., Kirk Sandall,
Doncaster, DN3 1QR.
Product Licence holder: BR Lewis Pharmaceuticals Ltd.,
Kirk Sandall, Doncaster, DN3 1QR.
PL No: 08929/0556
Date of review of this leaflet: 18.07.16
Zanidip® is a registered trademark of Recordati Ireland