Patient info Open main menu

Cardura XL_4mg_8mg_28 – patient leaflet, side effects, dosage

Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
4 mg
Contains active substance:
ATC code:
Similar medicines:

Patient leaflet - Cardura XL 4 mg

1. What CARDURA XL is and what it is used for

CARDURA XL contains the active substance doxazosin mesilate and is one of a group of medicines called alpha-blockers. It is used to treat high blood pressure, or the symptoms caused by enlargement of the prostate gland in men.

CARDURA XL can be used to treat high blood pressure (hypertension), by relaxing blood vessels so that blood passes through them more easily. This helps to lower blood pressure.

In patients with an enlarged prostate gland, CARDURA XL is taken to treat poor and/or frequent passing of urine. This is common in patients with an enlarged prostate gland. CARDURA XL works by relaxing muscle around the bladder exit and prostate gland so urine is passed more easily.

2. What you need to know before you take CARDURA XL

Do not take CARDURA XL:

  • If you are allergic to doxazosin, other quinazolines

    (e.g. prazosin or terazosin), or to any of the other ingredients of this medicine (listed in section 6). This may have been itching, reddening of the skin or difficulty in breathing.

  • If you have any form of obstruction of the digestive

    tract

  • If you have an enlarged prostate gland (benign

    prostatic hyperplasia) and have low blood pressure

  • If you have a history of a condition known as

    ‘orthostatic hypotension’ which is a form of low blood pressure that causes you to feel dizzy or light-headed when you stand up from sitting or lying down

  • If you have an enlarged prostate gland with one of the

    following: any kind of congestion or blockage in your urinary tract, a longstanding infection of the urinary tract or you have bladder stones

  • If you have overflow incontinence (you do not feel the

    urge to urinate), or anuria (your body is not producing any urine) with or without kidney problems.

Warnings and precautions

Talk to your doctor or pharmacist before taking CARDURA XL as it may not be suitable for you:

  • If you are pregnant or trying to become pregnant
  • If you have liver disease
  • If you have heart disease
  • If you are also taking other medicines

If you are undergoing eye surgery because of cataract (cloudiness of the lens of the eye), please inform your eye specialist before the operation that you are using or have previously used CARDURA XL. This is because CARDURA XL may cause complications during the surgery which can be managed if your specialist is prepared in advance.

If any of these apply to you speak to your doctor before taking this medicine.

When you start to take CARDURA XL you may experience faintness or dizziness caused by low blood pressure, when getting up from sitting or lying down. If you feel faint or dizzy, you should sit or lie down until you feel better and avoid situations where you might fall or hurt yourself. Your doctor may want to measure your blood pressure regularly at the start of therapy to reduce the possibility of these effects happening.

Persistent painful erections may occur very rarely. If this happens you should contact a doctor immediately.

Before starting treatment with CARDURA XL your doctor may perform tests to rule out other conditions such as prostate cancer that may cause the same symptoms as benign prostatic hyperplasia.

Children and adolescents

CARDURA XL is not recommended for use in children or adolescents below 18 years as safety and efficacy have not yet been established. Benign prostate hyperplasia is not relevant in children.

Other medicines and CARDURA XL

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription.

There are some medicines that may interact with CARDURA XL. Ask your doctor or pharmacist before use if you are taking any of these medicines as they may change the effect of CARDURA XL:

  • Some patients who take alpha-blocker therapy for the treatment of high blood pressure or prostate enlargement may experience dizziness or light-headedness, which may be caused by low blood pressure upon sitting or standing up quickly. Certain patients have experienced these symptoms when taking medicines called PDE-5 inhibitors for the treatment of erectile dysfunction (impotence) with alpha-blockers e.g. sildenafil, tadalafil, vardenafil (please see Section "Warnings and precautions"). In order to reduce the likelihood that these symptoms occur, you should be on a regular daily dose of your alpha blocker before you start drugs for erectile dysfunction.
  • Cardura XL may lower your blood pressure even more if you are already taking other medicines to treat your high blood pressure such as terazosin and prazosin.
  • Medicines to treat bacterial or fungal infections, e.g. clarithromycin, itraconazole, ketoconazole, telithromycin, voriconazole.
  • Medicines used in the treatment of HIV e.g. indinavir, nelfinavir, ritonavir, saquinavir.
  • Nefazodone, a medicine used to treat depression.

CARDURA XL with food and drink

See section 3 How to take CARDURA XL

Pregnancy, breast-feeding and fertility

Pregnancy

The safety of using CARDURA XL during pregnancy has not been established. If you are pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

Breast-feeding

Small amounts of doxazosin, the active substance of CARDURA XL, can get into your breast milk. You should not use CARDURA XL during breast-feeding unless your doctor advises you to do so.

Driving and using machines

Take care if you drive or operate machinery. Your tablets may affect your ability to drive or operate machinery safely, particularly when you first start to take them. They may make you feel weak or dizzy. If affected, do not drive or operate machinery and contact your doctor immediately. Information about the ingredients of

CARDURA XL

This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium-free’.

3. How to take CARDURA XL

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.

CARDURA XL is a prolonged release tablet. The medicine is contained within a non-absorbable shell that has been specially designed to slowly release the medicine. Once swallowed, doxazosin is slowly released into the body from the tablet, until the tablet is empty.

Since the empty tablet is eliminated from the body in bowel movements, you may occasionally observe in the stools, something that looks like a tablet. This is to be expected and you should not be concerned.

Package leaflet: Information for the patient

CARDURA XL® 4mg and 8mg

Doxazosin mesilate Prolonged release tablets

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

    pharmacist.

  • 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.

  • You should take CARDURA XL regularly to get the

    maximum benefit, even if you are feeling well.

  • Most people do not have serious problems when

    taking CARDURA XL but side effects can occur. If you experience swelling of the face, tongue or windpipe, see your doctor immediately. If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

  • Taking other medicines may sometimes cause problems.

    Check with your doctor or pharmacist before taking this or any other medicines.

  • If you are, or are trying to become pregnant, do not take

    CARDURA XL and tell your doctor or pharmacist.

UNITED KINGDOM

YOU WILL FIND MORE ABOUT CARDURA ON THE BACK OF THIS LEAFLET

600103892

2 of 2

Date: Time:

DescriptionCardura XL_4mg_8mg_28
LeafletSite Barcode/ DataMatrixVS 6426 RS 6427No. of colours1Page Count
3986360Viatris SAP No.400568978;400568979
3770351122519706/0020
39863601
MA No.United Kingdomwith
Supplier SAP No.N/A
New Supplier Code6001038923D Render IDN/AMain FontGill Sans9.5 pt
600102943200 x 510 mm9.5 pt
Klocke Verpackungs-Service GmbH (Weingarten - DE)Keyline/Drawing No.200x510_Layout

04:58 23-NOV-2025

PL 46302/0271 and PL 46302/0272
N/A
GTIN/PCN/A

Sign-offs

Notes

N/A
N/A
V6 APR 2025

How to take your medicine

  • The recommended dose of CARDURA XL is one 4mg

    prolonged release tablet taken as a single daily dose each day.

  • Your doctor may wish to increase your dose to 8mg.

    This is the maximum dose of CARDURA XL.

  • Swallow CARDURA XL whole with water. Do not

    chew, divide or crush the tablets.

  • Take your tablets as your doctor told you or by following

    the days and arrows on the blister foil.

  • If you are still not sure, ask your doctor or pharmacist.
  • It is important to keep taking your tablets. They help to

    control your blood pressure.

  • Do not change the dose or stop taking the tablets

    without first checking with your doctor.

  • Do not wait until your tablets are finished before seeing

    your doctor.

If you take more CARDURA XL than you should:

Taking too many tablets at once may make you unwell. If several tablets are taken it may be dangerous. Tell your doctor immediately or go to your nearest hospital casualty department immediately.

If you forget to take CARDURA XL:

Do not worry. If you forget to take a tablet, leave that dose out completely. Then go on as before. Do not take a double dose to make up for a forgotten tablet.

4. Possible side effects

Like all medicines, this medicine can cause side effects although not everybody gets them.

STOP taking CARDURA XL and call an

ambulance immediately if you experience any of the following:

  • Heart attack
  • Weakness of arms, legs or problems speaking which

    may be symptoms of a stroke

  • Allergic reactions (hypersensitivity). Symptoms include

    sudden wheeziness, tightness in the chest, difficulty in breathing, swelling of the face, tongue or throat, rash or itching (especially the whole body)

Tell your doctor immediately if you experience any of the following symptoms after taking CARDURA XL:

  • Feeling your heartbeat (palpitations) (common: may

    affect up to 1 in 10 people)

  • Increased or decreased heartbeat (common: may

    affect up to 1 in 10 people)

  • Shortness of breath, difficulty breathing, wheezing

    (common: may affect up to 1 in 10 people)

  • Chest pain, angina (uncommon: may affect up to 1 in

    100 people)

  • Irregular heartbeat (very rare: may affect up to 1 in

    10,000 people)

  • Skin rash or itching (especially the whole body)

    (uncommon: may affect up to 1 in 100 people)

  • Yellowing of the skin or the eyes (jaundice) (very rare:

    may affect up to 1 in 10,000 people)

  • Low numbers of white blood cells or blood platelets,

    which may result in bruising or easy bleeding (very rare: may affect up to 1 in 10,000 people)

  • Persistent painful erection of the penis. Seek urgent

    medical advice (very rare: may affect up to 1 in 10,000 people)

The following events have been reported in patients being treated with CARDURA XL. If any of these side effects get serious, or if you notice any side effects not listed in this leaflet, please tell your doctor.

Common side effects: may affect up to 1 in

10 people

  • dizziness, feeling of spinning or rotation of

    surroundings (vertigo), headache

  • low blood pressure
  • swelling of feet, ankles or fingers
  • chest cold, coughing, respiratory tract (nose, throat,

    lungs) infection

  • nasal stuffiness, sneezing and/or runny nose caused by

    inflammation of the lining of the nose (rhinitis)

  • stomach/abdominal pains, feeling/being sick
  • urinary tract infection, urinary incontinence (inability

    to control passing urine), inflammation of the bladder (cystitis)

  • sleepiness, general weakness
  • indigestion, heartburn, dry mouth
  • back pain, painful muscles
  • flu-like symptoms

Uncommon side effects: may affect up to 1 in

100 people

  • constipation, wind, inflammation of the stomach and

    intestines (gastroenteritis) which can cause diarrhoea and vomiting

  • pain or discomfort on passing urine, needing to pass

    urine more often than usual, blood in urine

  • inflammation of the joints (gout), painful joints, general

    pain

  • swelling of the face
  • sleeplessness, anxiety, depression
  • reduced or altered sense of touch or sensation of the

    hands and feet

  • increased appetite or loss of appetite, weight gain
  • nose bleeds
  • ringing in the ears, tremor

    • failure/ inability to achieve penile erection
    • abnormal results for blood tests which show changes in the way the liver is working

Rare side effects: may affect up to 1 in

1,000 people

  • blockage of the digestive tract

Very Rare side effects: may affect up to 1 in

10,000 people

  • faintness or dizziness caused by low blood pressure when getting up from a sitting or lying position
  • hepatitis (liver inflammation) or bile disorder
  • hives, hair loss, red or purple patches on the skin, bleeding under the skin
  • tingling or numbness of the hands and feet
  • agitation, nervousness
  • tiredness, generally feeling unwell
  • aggravated wheezing
  • muscle cramps, muscle weakness
  • blurred vision
  • flushing
  • disorder in passing urine, needing to pass urine at night, increased volume of urine passed, increased production of urine causing an increase in the number of times of passing urine
  • discomfort or enlargement of the breasts in men

Not known: frequency cannot be estimated from the available data

  • little or no semen ejaculated at sexual climax, cloudy urine following sexual climax
  • eye problems may occur during eye surgery for cataract (cloudiness of the lens of the eye). See section “warnings and precautions”.

Reporting of side effects

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 report side effects directly via the Yellow Card Scheme website: 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.

5. How to store CARDURA XL

Keep this medicine out of the sight and reach of children.

Do not use CARDURA XL after the expiry date which is stated on carton and blister after EXP. The expiry date refers to the last day of that month.

Do not store above 30°C. Store in the original package.

The tablets should be whole to work effectively, if you notice any defects (such as broken tablets) consult your pharmacist immediately.

Do not throw away any medicines via wastewater or household waste. Ask you pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. Contents of the pack and other information

What CARDURA XL contains

The active substance is doxazosin. Each tablet contains either 4.85mg doxazosin mesilate equivalent to 4mg doxazosin or 9.70mg doxazosin mesilate equivalent to 8mg doxazosin within a shell that has been specially designed to slowly release the drug.

The other ingredients are: polyethylene oxide, sodium chloride (see section 2 “Information about the ingredients of CARDURA XL”), hypromellose, red ferric oxide (E172), titanium dioxide (E171), magnesium stearate, cellulose acetate, Macrogol, pharmaceutical glaze, black iron oxide (E172), ammonium hydroxide and propylene glycol.

What CARDURA XL looks like and contents of the pack

CARDURA XL tablets are white film coated, round, biconvex shaped with a hole in one side and marked CXL 4 for the 4mg and CXL 8 for the 8mg.

They are available in strengths of 4mg and 8mg prolonged release tablets and in packs of 28 or 30 tablets. Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer

Marketing Authorisation Holder

Viatris Products Limited, Station Close, Potters Bar, EN6 1TL, United Kingdom.

Manufacturer

Klocke Verpackungs-Service GmbH, Max-Becker-Strasse 6, 76356 Weingarten (Baden), Germany

This leaflet was last revised in 01/2026. MORE INFORMATION ON CARDURA XL

3986360 600103892

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 46302/0271

MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Cardura XL 4 mg

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Doxazosin
Strength 4 mg
Pharmaceutical form Modified-release tablet
White film coated, round, biconvex shaped tablets with a hole in one side, marked CXL4.
How is it taken Oral
Excipients Polyethylene oxide, Sodium chloride, Hypromellose, Red ferric oxide (E172), Titanium dioxide (E171), Magnesium stearate, Cellulose acetate, Macrogol, Pharmaceutical glaze, Black iron oxide (E172), Ammonium hydroxide, Propylene glycol.
Pack sizes 28 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life PVC/PVDC blister with aluminium foil
2 years.
Blister strips of aluminium foil/aluminium foil
3 years.
Storage Do not store above 30°C.
Store in the original package.
Drug group (ATC) Alpha-adrenoreceptor antagonists
  1. C Cardiovascular system drugs
    1. C02 Antihypertensives
      1. C02C Antiadrenergic agents, peripherally acting
        1. C02CA Alpha-adrenoreceptor antagonists, peripherally acting
          1. C02CA04 doxazosin
Marketing authorisation PL 46302/0271, PL 50622/0009 (first authorised 6 November 2006)
Marketing authorisation holder Upjohn UK Limited
Codes GTIN 1210001163454 · BNF 02050400

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.1.0 of 12 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.