Leaflet: information for the user
Lercanidipine Pensa 10 mg film-coated tablets EFG
Lercanidipine Pensa 20 mg film-coated tablets EFG
lercanidipine hydrochloride
Read the entire leaflet carefully before starting to take this medication, as it contains important information for you.
Contents of the leaflet
Lercanidipine belongs to a group of medications called calcium channel blockers (of the dihydropyridine group) that lower blood pressure.
Lercanidipine is used to treat high blood pressure, also known as arterial hypertension, in adults over 18 years of age (it is not recommended for children under 18 years of age).
Consult your doctor or pharmacist before starting to take this medication:
You should inform your doctor if you think you are pregnant (may become pregnant) or are breastfeeding (see section on pregnancy, breastfeeding, and fertility).
The safety and efficacy of lercanidipine have not been demonstrated in children under 18 years of age.
Inform your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication. This is because when lercanidipine is combined with other medications, the effect of lercanidipine or the other medication may vary, or the frequency of certain side effects may increase (see also section 2 "Do not take Lercanidipine Pensa").
In particular, inform your doctor or pharmacist if you are taking any of the following medications:
It is not recommended to take lercanidipine if you are pregnant, and it should not be taken during breastfeeding. There are no data on the use of lercanidipine in pregnant or breastfeeding women. If you are pregnant or breastfeeding, if you are not using an effective contraceptive method, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
If you experience dizziness, weakness, or numbness when taking this medication, do not drive vehicles or use machines.
This medication contains less than 1 mmol of sodium (23 mg) per tablet; it is essentially "sodium-free".
Follow the administration instructions for this medication exactly as indicated by your doctor. If in doubt, consult your doctor or pharmacist again.
Adults
The recommended usual dose is one 10 mg tablet per day, at the same time each day, preferably in the morning and at least 15 minutes before breakfast. Your doctor may increase the dose to lercanidipine 20 mg per day if necessary (see section 2 "Taking Lercanidipine Pensa with food, drinks, and alcohol").
The tablets should be swallowed whole with a little water.
The score line is only for breaking the tablet if you find it difficult to swallow it whole.
Use in children
This medication should not be used in children under 18 years of age.
Elderly population
No dose adjustment is required. However, they may require special care at the start of treatment.
Patients with kidney or liver problems
Special care is needed when starting treatment in these patients, and an increase in the dose to 20 mg per day should be done with caution.
Do not take more than the prescribed dose.
If you have taken more tablets of this medication than you should, consult your doctor or go directly to the hospital. Take the package with you.
Taking a dose higher than the correct dose may cause an excessive drop in blood pressure and irregular and faster heartbeats.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If you forget to take your tablet, do not take the missed dose, and continue the next day as your doctor indicated.
Do not take a double dose to make up for missed doses.
If you stop taking this medication, your blood pressure will increase again. Consult your doctor before stopping treatment.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication can cause side effects, although not everyone experiences them.
The following side effects may occur when taking this medication:
Rare (may affect up to 1 in 1,000 patients):angina pectoris (e.g., chest compression due to lack of blood in the heart), allergic reactions (with symptoms such as itching, rash, and hives), and fainting.
Patients with pre-existing angina pectoris may experience an increase in frequency, duration, or severity of these attacks with medications of the group to which lercanidipine belongs. Isolated cases of heart attacks have been observed.
Frequent (may affect up to 1 in 10 patients):headache, rapid heartbeat, sensation of rapid or accelerated heartbeats (palpitations), sudden reddening of the face, neck, or upper chest (flushing), swelling of the ankles.
Uncommon (may affect up to 1 in 100 patients):dizziness, low blood pressure, heartburn, discomfort, stomach pain, skin rash, itching, muscle pain, increased urine production, weakness or fatigue.
Rare (may affect up to 1 in 1,000 patients):drowsiness, vomiting, diarrhea, hives, increased urination frequency, chest pain.
Frequency not known (cannot be estimated from available data):gum swelling, changes in liver function (detected in blood tests), cloudy liquid (when performing hemodialysis through a tube into the abdomen), swelling of the face, lips, tongue, or throat that may cause difficulty breathing or swallowing.
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that is not listed in this leaflet. You can also report them directly through the national reporting system: Spanish Medicines and Healthcare Products Agency (AEMPS) http://www.aemps.gob.es/
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date, which appears on the blister pack and carton after "EXP". The expiration date is the last day of the month indicated.
Lercanidipine Pensa 10 mg film-coated tablets EFG:
Store in the original packaging to protect from light. Do not store above 25 °C.
Lercanidipine Pensa 20 mg film-coated tablets EFG:
Do not store above 25 °C.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the pharmacy's SIGRE point. Ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
Lercanidipine Pensa 10 mg film-coated tablets EFG:
Lercanidipine Pensa 20 mg film-coated tablets EFG:
Lercanidipine Pensa 10 mg film-coated tablets EFG
Round, biconvex, yellow film-coated tablets with a score line on one side and a flat surface on the other, approximately 6.5 mm in diameter.
Lercanidipine Pensa 20 mg film-coated tablets EFG
Round, biconvex, pink film-coated tablets with a score line on one side and a flat surface on the other, approximately 8.5 mm in diameter.
Lercanidipine Pensa 10 mg is available in packs of 14, 28, and 56 film-coated tablets.
Lercanidipine Pensa 20 mg is available in packs of 28 film-coated tablets.
Not all pack sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
Towa Pharmaceutical, S.A.
C/ de Sant Martí, 75-97
08107 Martorelles (Barcelona)
Spain
Manufacturer
Torrent Pharma (Malta) Limited
HHF 028 Hal Far Industrial Estate
Birzebbuga BBG 3000
Malta
Spain: Lercanidipine Pensa 10 mg film-coated tablets EFG
Lercanidipine Pensa 20 mg film-coated tablets EFG
Italy: Lercanidipine hydrochloride Pensa
Portugal: Lercanidipine toLife
Detailed information about this medication is available on the website of the Spanish Agency for Medicines and Healthcare Products (AEMPS) http://www.aemps.gob.es/