Patient Leaflet Updated 27-Mar-2024 | Zentiva
Lacidipine 2mg and 4mg film-coated tablets
Lacidipine 2 mg film-coated tablets
Lacidipine 4 mg film-coated tablets
Lacidipine
1. What Lacidipine tablets are and what they are used for
2. What you need to know before you use Lacidipine tablets
3. How to use Lacidipine tablets
4. Possible side effects
5. How to store Lacidipine tablets
6. Contents of the pack and other information
Lacidipine tablets contains a medicine called lacidipine. This belongs to a group of medicines called ‘calcium channel blockers’. Lacidipine tablets helps to relax your blood vessels so that they get wider. This helps the blood to flow more easily and lowers the blood pressure.
Lacidipine tablets taken regularly as prescribed by your doctor will help to lower your blood pressure (to treat hypertension).
Do not take Lacidipine tablets if any of the above apply to you. If you are not sure, talk to your doctor or pharmacist before taking Lacidipine tablets.
You should stop taking lacidipine if you get chest pain (angina) or a fast, weak pulse, rapid shallow breathing, low blood pressure, cold clammy skin, blue lips or feel dizzy, faint, weak or sick.
Talk to your doctor or pharmacist before using Lacidipine tablets:
Lacidipine tablets should not be administered to children and adolescents under 18 years.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. This includes herbal medicines. This is because Lacidipine tabletst can affect the way some other medicines work. Also some other medicines can affect the way Lacidipine tablets works.
In particular, tell your doctor or pharmacist if you are taking any of the following medicines:
If you are having any blood tests, tell the person giving the test that you are taking this medicine. This is because Lacidipine tablets can affect results relating to your liver.
Lacidipine tablets can be taken with or without a meal. Do not take this medicine with grapefruit juice.
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. There is no information on the safe use of Lacidipine tablets in pregnancy.
Do not take Lacidipine tablets if you are pregnant, likely to get pregnant or are breast-feeding.
The active substance and excipients of Lacidipine tablets can pass into breast milk. If you are breast-feeding, check with your doctor before starting treatment with Lacidipine tablets.
This medicine may cause dizziness. If you experience this side effect, do not drive vehicles or operate machines which require your attention.
If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.
Always use this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
It is important to take the right number of tablets at the right time of day.
If you take more of this medicine than you should, talk to a doctor or go to a hospital straight away. Take the medicine pack and the leaflet with you, even if there are no tablets left.
Medical treatment can be necessary. Effects of overdose will likely cause irregular heartbeat, rapid shallow breathing, low blood pressure, cold humid skin or feeling dizzy, fainting, weakness or nausea.
If you forget a dose in the morning, take it as soon as you remember it on the same day. However, if you remember the next day, take your normal dose on that morning.
Do not take a double dose to make up for a forgotten dose.
Take Lacidipine tablets for the period of time prescribed by your doctor. Do not stop taking Lacidipine tablets unless instructed by your doctor.
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.
The side effects have been divided according to their frequency:
Common (may affect up to 1 in10 people):
Uncommon (may affect up to 1 in 100 people):
Rare (may affect up to 1 in 1,000 people):
Very rare (may affect up to 1 in 10,000 people):
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 the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. 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 this medicine after the expiry date which is stated on the carton and blister after EXP:.
The expiry date refers to the last day of that month.
Store in the original package in order to protect from light.
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.
The active substance is lacidipine.
Lacidipine 2 mg film-coated tablets: each tablet contains lacidipine 2 mg.
Lacidipine 4 mg film-coated tablets: each tablet contains lacidipine 4 mg.
The other ingredients are:
core: lactose, povidone, magnesium stearate;
film-coat: hypromellose, talc, propylene glycol, titanium dioxide (E171).
Lacidipine 2 mg film-coated tablets:
white, round [diameter 8.1 mm], biconvex, film-coated tablets
Lacidipine 4 mg film-coated tablets:
white, oval [13 mm ×7.4 mm], biconvex, film-coated tablets with score line on one side.
The tablet can be divided into equal doses. If, in accordance with the recommended dosage, you take a half tablet of 4 mg, then the unused half should be kept out of direct light and taken within 48 hours.
Lacidipine tablets are packed into OPA/Aluminium/PVC/Aluminium blisters, placed along with the leaflet into a carton.
Pack sizes:
Lacidipine 2 mg film-coated tablets – 7, 14, 28, 56 film-coated tablets
Lacidipine 4 mg film-coated tablets – 7, 14, 28, 56 film-coated tablets
Not all pack sizes may be marketed.
Marketing Authorisation Holder:
Manufacturer:
This leaflet was last revised in January 2022
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