Consumer medicine information

ARX-Lercanidipine Tablets

Lercanidipine hydrochloride

BRAND INFORMATION

Brand name

ARX-Lercanidipine

Active ingredient

Lercanidipine hydrochloride

Schedule

S4

 

Consumer medicine information (CMI) leaflet

Please read this leaflet carefully before you start using ARX-Lercanidipine Tablets.

What is in this leaflet

Read this leaflet carefully before taking your medicine.

This leaflet answers some of the common questions about lercanidipine. It does not contain all the available information. It does not replace seeking advice from your doctor or pharmacist.

The information in this leaflet was last updated on the date listed on the last page. More recent information on this medicine may be available.

Ask your doctor or pharmacist:

  • if there is anything you do not understand in this leaflet,
  • if you are worried about taking your medicine, or
  • to obtain the most up-to-date information.

All medicines have risks and benefits. Your doctor has weighed the risks of you taking lercanidipine against the benefits this medicine is expected to have for you.

Pharmaceutical companies cannot give you medical advice or an individual diagnosis.

Keep this leaflet with the medicine. You may need to read it again.

What this medicine is used for

The name of your medicine is ARX-Lercanidipine. It contains the active ingredient lercanidipine hydrochloride.

Lercanidipine belongs to a group of medicines called dihydropyridine calcium channel blockers.

Lercanidipine helps lower high blood pressure, otherwise known as hypertension.

This medicine is available only with a doctor's prescription.

How it works

This medicine works by relaxing some of the blood vessels in the body and reducing resistance to the flow of blood through the blood vessels.

Everyone has blood pressure. This pressure helps get your blood all around your body. Your blood pressure may be different at different times of the day, depending on how busy or worried you are. If your blood pressure stays higher than is needed, even when you are calm and relaxed, you have hypertension (high blood pressure).

There are usually no symptoms of hypertension. The only way of knowing that you have hypertension is to have your blood pressure checked on a regular basis. If high blood pressure is not treated it can lead to serious health problems. Youmay feel fine and have no symptoms, but hypertension can cause stroke, heart disease and kidney failure.

There is no evidence that this medicine is addictive.

Use in children

This medicine should not be used in children.

Before you take this medicine

When you must not take it

Do not take this medicine if you have an allergy to:

  • severe liver or kidney disease.
  • taking another medicine called cyclosporin.
  • You are hypersensitive to, or have had an allergic reaction to, lercanidipine or any of the ingredients listed at the end of this leaflet.
    Symptoms of an allergic reaction may include: cough, shortness of breath, wheezing or difficulty breathing; swelling of the face, lips, tongue, throat or other parts of the body; rash, itching or hives on the skin; fainting; or hay fever-like symptoms.
    If you think you are having an allergic reaction, do not take any more of the medicine and contact your doctor immediately or go to the Accident and Emergency department at the nearest hospital.

Do not take this medicine if you are pregnant or intend to become pregnant. Like most calcium channel blockers, this medicine is not recommended for use during pregnancy.

Tell your doctor immediately if you become pregnant while you are taking this medicine.

Do not take this medicine if you are breast-feeding or plan to breastfeed. Like most calcium channel blockers this medicine is not recommended while you are breast-feeding.

Do not take this medicine if the expiry date (EXP) printed on the pack has passed.

Do not take this medicine if the packaging is torn, shows signs of tampering or it does not look quite right.

Before you start to take it

Before you start taking this medicine, tell your doctor if:

  1. You have allergies to:
  • any other medicines
  • any other substances, such as foods, preservatives or dyes.
  1. You have or have had any medical conditions, especially the following:
  • liver or kidney disease or you are on dialysis
  • other heart conditions such as: heart disease, uncontrolled heart failure, an obstruction to the flow of blood from the heart (aortic stenosis), unstable angina (chest pain or tightness at rest or progressively increasing) or you have had a heart attack (myocardial infarction) one month ago or less and/or you require a pacemaker.
  • taking other drugs for high blood pressure, such as beta-blockers, diuretics, ACE-inhibitors or angiotensin II receptor antagonists.
  1. You are planning to have surgery or on an anaesthetic.
  2. You are currently receiving or are planning to receive dental treatment.

Taking other medicines

Tell your doctor if you are taking or are planning to take any other medicines. This includes vitamins and supplements that are available from your pharmacy, supermarket or health food shop.

Some medicines may interact with lercanidipine. These include:

  • cyclosporin
  • ritonavir
  • terfenadine
  • astemizole
  • ketoconazole
  • itraconazole
  • erythromycin
  • troleandomycin
  • clarithromycin
  • fluoxetine
  • cimetidine
  • phenytoin
  • phenobarbital (phenobarbitone)
  • carbamazepine
  • rifampicin
  • amiodarone
  • quinidine
  • digoxin
  • simvastatin
  • midazolam
  • sotalol
  • metoprolol
  • propranolol

If you are taking any of these you may need a different dose or you may need to take different medicines.

Other medicines not listed above may also interact with this medicine.

How to take this medicine

Follow carefully all directions given to you by your doctor. Their instructions may be different to the information in this leaflet.

How much to take

Your doctor will tell you how much of this medicine you should take. This will depend on your condition and whether you are taking any other medicines.

The usual dose is one 10 mg tablet taken once daily, but may be increased to 20 mg once daily.

Do not stop taking your medicine or change your dosage without first checking with your doctor.

If you do not understand the instructions on the box, ask your doctor or pharmacist for help.

How to take it

Swallow the tablet whole with a glass of water.

When to take it

Take this medicine at about the same time each day, at least 15 minutes before a meal. This medicine will have the best effect if it is taken at the same time each day. This will also help you remember when to take the tablets.

How long to take it

Continue taking your medicine for as long as your doctor tells you.

This medicine helps control your condition but does not cure it therefore you must not stop taking it unless your doctor tells you to.

Make sure you have enough to last over weekends and holidays.

If you forget to take it

If you forget to take a dose but remember within 12 hours from when the dose was due, take it straight away, then continue as normal the next day. Otherwise skip that day's dose and take the next day's dose when it is due.

If you are not sure what to do, talk to your doctor or pharmacist.

Do not take a double dose to make up for missed doses. This may increase the chance of unwanted side effects.

If you have trouble remembering to take your tablets, ask your pharmacist for some hints to help you remember.

If you have missed several doses, consult your doctor.

If you use too much (overdose)

If you think that you or anyone else may have taken too much of this medicine, immediately telephone your doctor or the Poisons Information Centre (Tel: 13 11 26 in Australia) for advice. Alternatively go to the Accident and Emergency Department at your nearest hospital,

Do this even if there are no signs of discomfort or poisoning. You may need urgent medical attention. Keep telephone numbers of these places/services handy.

If you take too much of this medicine, it may cause your blood pressure to become too low and you may feel your heart beat becomes irregular and faster. It may also lead to unconsciousness.

While you are taking this medicine

Things you must do

Tell your doctor that you are taking this medicine if:

  • You are about to be started on any new medicine
  • You are pregnant or are planning to become pregnant
  • You are breast-feeding or are planning to breast-feed
  • You are about to have any blood tests
  • You are going to have surgery or are going into hospital.

Your doctor may occasionally do tests to make sure the medicine is working and to prevent side effects. Be sure to keep all of your doctor's appointments so that your progress can be checked.

Tell any other doctors, dentists and pharmacists who are treating you that you take this medicine.

Things you must not do

Do not:

  • Give this medicine to a child under the age of 18 years.
  • Give this medicine to anyone else, even if their symptoms seem similar to yours
  • Take your medicine to treat any other condition unless your doctor or pharmacist tells you to
  • Stop taking your medicine, or change the dosage, without first checking with your doctor.

Things to be careful of

Be careful driving or operating machinery until you know how this medicine affects you. This medicine generally does not affect your ability to drive a car or operate machinery. However, as with other medicines used to treat high blood pressure, some people may feel dizzy, light-headed or faint, especially when first taking this medicine or changing your dose.

Your doctor may also ask you to limit or stop your alcohol intake while taking medicines used to control your blood pressure as alcohol may increase these effects.

If you feel light-headed, dizzy or faint when getting out of bed or standing up, get up slowly.

Grapefruit juice can increase the effects of some medicines including lercanidipine. If you are taking lercanidipine speak to your doctor or pharmacist before drinking grapefruit juice or changing your intake of grapefruit juice. As with some medicines, used to treat high blood pressure (such as lercanidipine), you should avoid drinking grapefruit juice as grapefruit juice may increase the effects of these medicines.

Possible side effects

Tell your doctor as soon as possible if you do not feel well while you are taking lercanidipine or if you have any questions or concerns.

Do not be alarmed by the following lists of side effects. You may not experience any of them. All medicines can have side effects. Sometimes they are serious but most of the time they are not.

Tell your doctor if you notice any of the following:

  • flushing
  • swelling of the ankles, feet or lower legs
  • palpitations
  • headache
  • dizziness or fainting
  • gastrointestinal disturbances such as heartburn, nausea, abdominal pain or diarrhoea
  • muscle weakness
  • fatigue or sleepiness.

If you experience any of the following, stop taking your medicine and contact your doctor immediately or go to the Accident and Emergency department at your nearest hospital.

These are very serious side effects and are usually rare. You may need urgent medical attention or hospitalisation:

  • angina (chest pain or tightness)
  • increased heart beat or heart palpitations
  • difficulty breathing

Other side effects not listed above may occur in some patients.

Allergic reactions

If you think you are having an allergic reaction to lercanidipine, tell your doctor immediately or go to the Accident and Emergency department at your nearest hospital.

Symptoms of an allergic reaction may include some or all of the following:

  • cough, shortness of breath, wheezing or difficulty breathing.
  • swelling of the face, lips, tongue, or other parts of the body
  • rash, itching or hives on the skin
  • fainting
  • hayfever-like symptoms.

Storage and disposal

Storage

Keep your medicine in the original packaging until it is time to take them. If you take your medicine out of the original packaging, it may not keep well.

Keep your medicine in a cool dry place, away from sunlight, where the temperature will stay below 25°C.

Do not store your medicine, or any other medicine, in the bathroom or near a sink. Do not leave it on a window sill or in the car. Heat and dampness can destroy some medicines.

Keep this medicine where children cannot reach it. A locked cupboard at least one-and-a-half metres above the ground is a good place to store medicines.

Disposal

If your doctor tells you to stop taking this medicine or they have passed their expiry date, your pharmacist can dispose of the remaining medicine safely.

Product description

What ARX-Lercanidipine looks like

ARX-Lercanidipine is available in 10 mg or 20 mg tablets.

10 mg Tablets:
Round, biconvex, yellow, film coated tablets, scored on one side, marked “L” on the other side.

Blister pack of 28 tablets.

20 mg Tablets:
Round, biconvex, pink, film coated tablets, scored on one side, marked “L” on the other side.

Blister pack of 28 tablets.

Ingredients

Each tablet contains 10 mg or 20 mg of lercanidipine hydrochloride as the active ingredient.

It also contains the following inactive ingredients:

  • lactose monohydrate
  • microcrystalline cellulose
  • sodium starch glycollate
  • povidone
  • magnesium stearate
  • polyvinyl alcohol
  • titanium dioxide
  • macrogol 3350
  • purified talc
  • iron oxide yellow (10 mg only)
  • iron oxide red (20 mg only).

This medicine is gluten-free, sucrose-free, tartrazine-free and free of other azo dyes.

Australian Registration Numbers

ARX-Lercanidipine 10 mg tablets: AUST R 172204

ARX-Lercanidipine 20 mg tablets: AUST R 172206

Sponsor

Apotex Pty Ltd
16 Giffnock Avenue
Macquarie Park NSW 2113

This leaflet was prepared in May 2023.

Published by MIMS July 2023

BRAND INFORMATION

Brand name

ARX-Lercanidipine

Active ingredient

Lercanidipine hydrochloride

Schedule

S4

 

1 Name of Medicine

Lercanidipine hydrochloride.

2 Qualitative and Quantitative Composition

Each tablet contains 10 mg or 20 mg lercanidipine hydrochloride as the active ingredient.
Excipients with known effect. Lactose.
For the full list of excipients, see Section 6.1 List of Excipients.

3 Pharmaceutical Form

10 mg. Round biconvex yellow film coated tablets, scored on one side, marked "L" on the other side.
20 mg. Round biconvex pink film coated tablets, scored on one side, marked "L" on the other side.

4 Clinical Particulars

4.9 Overdose

In the post-marketing experience of lercanidipine, some cases of overdose have been reported ranging from 30-40 mg up to 800 mg, including reports of suicide attempt.
Symptoms. As with other dihydropyridines, overdosage might be expected to cause excessive peripheral vasodilation with marked hypotension and reflex tachycardia. However, at very high doses, the peripheral selectivity may be lost, causing bradycardia and a negative inotropic effect. In case of severe hypotension, bradycardia and unconsciousness, cardiovascular and respiratory monitoring will be required, and supportive treatment may be necessary. The most common adverse drug reactions associated to cases of overdose have been hypotension, dizziness, headache and palpitations.
Treatment. Clinically significant hypotension requires active cardiovascular support including frequent monitoring of cardiac and respiratory function, elevation of extremities and attention to circulating fluid volume and urine output. In view of the prolonged pharmacological effect of lercanidipine, it is essential that the cardiovascular status of the patient is monitored for 24 hours at least. Since the product has a high protein binding, dialysis is not likely to be effective. Patients in whom a moderate to severe intoxication is anticipated should be observed in a high-care setting.
For information on the management of overdose, contact the Poisons Information Centre on 13 11 26 (Australia).

5 Pharmacological Properties

5.3 Preclinical Safety Data

Genotoxicity. No evidence for genotoxic activity was observed with lercanidipine in in vitro assays of gene mutation (reverse mutation in S. typhimurium, forward mutation in Chinese hamster V79 fibroblasts), gene conversion (in Saccharomyces cerevisiae D4) or chromosomal damage (CHO cytogenetic assay). Negative findings were also obtained with lercanidipine in an in vivo assay of chromosomal damage (mouse micronucleus test).
Carcinogenicity. Carcinogenicity studies of lercanidipine (administered via the diet) have been performed in rats and mice (18 months), using doses up to 60 mg/kg/day for mice and 5 mg/kg/day for rats. Plasma concentrations (AUC) of lercanidipine at the highest doses used in these studies were about 2-4 times the highest AUC expected in humans during treatment with lercanidipine. Lercanidipine showed no evidence of carcinogenic activity in these studies.

6 Pharmaceutical Particulars

6.7 Physicochemical Properties

Lercanidipine hydrochloride is a microcrystalline, odourless, citrine powder, readily soluble in chloroform and methanol, practically insoluble in water. Octanol: water partition coefficient (LogP): 6.4.
Chemical structure.
https://stagingapi.mims.com/au/public/v2/images/fullchemgif/CSLERHYD.gif Lercanidipine is a dihydropyridine derivative. It is a racemate due to the presence of a chiral carbon atom at position 4 of the 1,4-dihydropyridine ring.
Chemical name: 3,5-pyridinedicarboxylic acid, 1,4- dihydro-2, 6-dimethyl-4-(3- nitrophenyl)-2- [(3,3-diphenylpropyl)methylamino]- 1,1-dimethylethyl methyl ester hydrochloride.
Molecular formula: C36H41N3O6.HCl.
Molecular weight: 648.2 (free base 611.7).
CAS number. 132866-11-6.

7 Medicine Schedule (Poisons Standard)

S4 - Prescription Only Medicine.

Summary Table of Changes

https://stagingapi.mims.com/au/public/v2/images/fulltablegif/ARXLERST.gif