Patient info

Hydralazine tablets 25 mg – patient leaflet, side effects, dosage

Updated:
Key facts
Status:
Prescription only (POM)
Medicine strength:
25 mg
Contains active substance:

Patient leaflet - Hydralazine tablets 25 mg

1. What Hydralazine is and what it is used for

Hydralazine belongs to a group of medicines called antihypertensives.

Hydralazine can be used along with other medicines:

  • to reduce high blood pressure (hypertension)
  • to treat moderate and serious heart failure.

    Anti-hypertensives work by lowering blood pressure. High blood pressure increases the workload of the heart and arteries (blood vessels) and if left untreated, can lead to damage of the blood vessels of the brain, heart and kidneys.

    • if there is a family history of the rare condition

      porphyria.

Warnings and precautions

Talk to your doctor or pharmacist before taking Hydralazine:

  • if you have liver or kidney problems.
  • if you suffer from hardened arteries (coronary artery

    disease), chest pain (angina) or are at risk of having a stroke.

    • if you are recovering from a heart attack.
    • if you need surgery.

Other medicines and Hydralazine

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines including medicines obtained without a prescription, herbal medicines or any of the following:

  • other antihypertensives including medicines used

    to widen the blood vessels such as diazoxide or nitrates,

beta-blockers (e.g. propranolol), ACE inhibitors (e.g. captopril), “water” tablets (diuretics e.g. furosemide) and medicines known as “calcium channel blockers” (e.g. verapamil)

  • medicines used to treat depression e.g. tricyclic

    antidepressants such as dosulepin, monoamine oxidase inhibitors (MAOIs) such as phenelzine or to treat a mental illness (e.g. Chlorpromazine)

    • medicines used to treat anxiety such as tranquillisers

      (e.g. diazepam)

    • anti-inflammatory painkillers (NSAIDs) e.g.

      indometacin

    • corticosteroids e.g. prednisolone
    • medicines which slow down the nervous system (CNS

      depressants)

    • carbenoxolone, used to treat stomach ulcers
    • anaesthetics
  • medicines containing oestrogens e.g. HRT, or the

    combined oral contraceptive pill.

Ask your doctor or pharmacist for advice before taking any medicine.

Hydralazine with food and drink and alcohol

Taking Hydralazine with food may decrease the amount of the medicine in your system, therefore, take it before

food. Alcohol may increase the effects of hydralazine causing side effects such as dizziness.

Pregnancy and breast-feeding

Hydralazine should only be used in the last few months of pregnancy

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.

2. What you need to know before you take Hydralazine

Do not take Hydralazine:

  • if you are allergic to hydralazine hydrochloride or

    dihydralazine, or any of the other ingredients of this medicine (listed in section 6)

  • if you suffer from the condition systemic lupus

    erythematosus (SLE) or a related disease

    • if you suffer from an unusually fast heartbeat
    • if you have heart failure, heart valve problems (aortic

      or mitral stenosis) or inflammation of the heart (constrictive pericarditis)

    • if you have an aortic aneurysm (swelling in the wall of

      the aorta which can cause sweating, a fast heartbeat, and abdominal or back pain)

    • if you have an enlarged heart often caused by lung

      disease (cor pulmonale)

3. How to take Hydralazine

Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure. If you are taking Hydralazine for a long time, your doctor may wish to test your urine and blood every six months. Your doctor will start you on a low dose of Hydralazine and gradually increase the dose depending on your condition.

The recommended dose is:

Adults

Hypertension

The recommended starting dose is 25 mg of Hydralazine twice a day, increasing to a maximum total dose of 200 mg of Hydralazine a day.

Heart failure

Treatment is started in hospital with a dose of 25 mg of Hydralazine three or four times a day; if necessary, increasing to 50-75 mg of Hydralazine four times a day. A small group of patients can break down hydralazine in their body at a different rate to the majority of patients. This can lead to unwanted effects. Your doctor will check for this possibility, and if this occurs, will change

your dose of Hydralazine as needed. You should carry on taking your medicine as long as your doctor or pharmacist tells you to, even if you feel better. Use in children and adolescents

Hydralazine should not be given to children or adolescents.

Method of administration

Swallow the tablets with a glass of water.

If you take more Hydralazine than you should

The signs and symptoms of hydralazine overdose include low blood pressure, a racing heartbeat, headache and generalised skin flushing. If you take more Hydralazine than you should contact your doctor or hospital emergency department immediately.

If you forget to take Hydralazine

If you forget to take a dose of Hydralazine, take it as soon as you remember unless it is nearly time for your

next dose. Do not take a double dose to make up for a forgotten dose.

If you stop taking Hydralazine

Do not stop taking Hydralazine without talking to your doctor, even if you feel better, because it may make your illness worse.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

Driving and using machines

Do not drive or use machines if you suffer from headaches, dizziness or have difficulty concentrating while taking this medicine. Speak to your doctor or pharmacist for advice.

Hydralazine contains sodium

Hydralazine 25 mg and 50 mg tablets contain less than 1 mmol sodium (23 mg) per tablet, that is to say they are essentially ‘sodium-free’.

Hydralazine contains lactose

The 50 mg strength tablets contain lactose. If you have been told by your doctor that you have an intolerance to some sugars, such as lactose, contact your doctor before taking this medicine.

Hydralazine contains Sunset yellow (E110)

The 50 mg tablets also contain the colouring Sunset yellow (E110) which may cause allergic reactions in some people.

  • allergic reactions such as itchy red and swollen skin,

    red skin rash on cheeks and other parts of the body, skin rashes which may be severe

  • signs of reduced numbers of different blood cells,

    which may cause unusual bruising or bleeding of the skin (reduced number of platelets), frequent infections, fever, chills, sore throat or mouth ulcers (reduced number of white blood cells)

    • liver problems, which can cause yellowing of the skin

      or whites of the eyes, dark urine and pale stools

    • blood in the urine (the urine may look red or pink) Very rare (may affect up to 1 in 10,000 people):
    • illness resulting from the destruction of red blood

      cells with signs such as looking pale, feeling tired, breathlessness, yellowing of the skin and/or eyes

  • a reduction in all types of blood cells, which may cause

    frequent infections, unusual bruising or bleeding of the skin or you to feel tired and breathless

  • changes in how much you urinate, difficulty or pain

    when passing urine, lower back pain, fever, nausea and vomiting – these may be signs of kidney problems

  • severe pain in the stomach with bloating, cramps

    constipation and vomiting

  • protruding eyes

    Other possible side effects

    Very common (may affect more than 1 in 10 people):

    • fast or irregular heartbeat
    • headache

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

  • low blood pressure
  • muscle or joint pain
  • swelling of the joints
  • feeling or being sick
  • diarrhoea, upset stomach
  • chest pain
  • flushing
  • dizziness
  • blocked nose

Rare (may affect up to 1 in 1,000 people):

  • protein in the urine which would be seen in a urine test

    • increased levels of creatinine in the blood which would

      be seen in a blood test

    • loss of appetite, weight loss
    • feeling generally unwell
    • feeling anxious or agitated
    • itchy, red, infected eyes (conjunctivitis), watery or

      swollen eyes.

    • abdominal swelling caused by enlarged liver or fluid

      retention in the body

4. Possible side effects

Like all medicines, Hydralazine can cause side effects, although not everybody gets them. If any of the following happen, stop taking this medicine and see your

doctor straight away or go to the nearest hospital immediately.

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

  • systemic lupus erythematosus (SLE) or a related disease

    with signs such as joint pain (similar to rheumatoid arthritis), fever, change in blood count and skin rash Rare (may affect up to 1 in 1,000 people):

  • swelling of the hands and lower legs, breathlessness,

    tightness of the chest, sharp chest pain, which is worse when breathing in, feeling dizzy

    • abnormal swelling of the spleen (splenomegaly). You

      may notice signs such as being unable to eat a large meal, feeling discomfort, fullness, or pain on the upper left side of the abdomen; this pain may spread to your left shoulder 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 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.

5. How to store Hydralazine

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 label or container after “EXP”. The expiry date refers to the last day of that month.

Do not store above 25°C. 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 to protect the environment.

6. Contents of the pack and other information

What Hydralazine contains

The active substance is hydralazine hydrochloride. Each 25 mg tablet contains 25 mg of hydralazine hydrochloride.

Each 50 mg tablet contains 50 mg of hydralazine hydrochloride.

The other ingredients are microcrystalline cellulose, pregelatinised maize starch, colloidal anhydrous silica, sodium starch glycolate (in 50 mg strength only), disodium edetate, talc and magnesium stearate. The coating for the 25 mg strength tablets contains diethyl phthalate, hydroxypropylcellulose, ethylcellulose, carnauba wax, red iron oxide (E172),’ hypromellose, titanium dioxide (E171) and Quinoline yellow (E104).

The coating for the 50 mg strength tablets contains titanium dioxide (E171), lactose (see section 2 “Hydralazine contains lactose”), hypromellose, macrogol, indigo carmine (E132), sunset yellow (E110) (see section 2 “Hydralazine contains sunset yellow (E110)”) iron oxide yellow (E172) and erythrosine (E127).

  • swelling of blood vessels. Signs include fever, general

    aches and pain, loss of appetite, weight loss and tiredness

  • pinkish, itchy swellings on the skin, also called hives or

    nettle rash

  • increase in some white blood cells which may be seen

    in a blood test

  • decrease in some red blood cells which may be seen in

    a blood test

    Very rare (may affect up to 1 in 10,000 people):

    • an increase in blood pressure
    • inflammation of the nerves, which may cause tingling

      or numbness especially in the hands, arms, feet or legs

    • painful swelling in the arms or legs
    • swollen (lymph) glands in the armpits, neck or groins
    • feeling depressed
    • seeing, feeling or hearing things that are not there

      (hallucinations)

      Manufacturers

      Mylan Hungary Kft., Mylan utca 1., Komárom, 2900, Hungary

      This leaflet was last revised in 06/2026.

      What Hydralazine looks like and contents of the pack

      25 mg tablets are yellow film coated tablet marked “HE 25” on one side and “G” on the

      reverse.

      50 mg tablets are pink film coated tablets marked “HE 50” on one side and “G” on the reverse.

      Hydralazine Tablets 25 mg and 50 mg are available in glass or plastic containers and blisters of 5, 7, 10, 14, 15, 20,

      21, 25, 28, 30, 50, 56, 60, 84, 90, 100, 112, 120, 168, 180, 250 and 500 tablets.

      Not all pack sizes may be marketed.

      Marketing Authorisation Holder

      Viatris,

      Station Close, Potters Bar, EN6 1TL, United Kingdom.

Hydralazine 25 mg film-coated tablets

25 mg

56 film-coated tablets

Each film-coated tablet contains: 25 mg hydralazine hydrochloride. Dosage: Oral use. Read the package leaflet before use. Keep out of the sight and reach of children. Do not store above 25°C. Store in the original package in order to protect from light

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

PL 04569/0050 UK Only

POM

Hydralazine 25 mg film-coated tablets

56 film-coated tablets

Each film-coated tablet contains: 25 mg hydralazine hydrochloride.

Dosage: Oral use. Read the package leaflet before use. Keep out of the sight and reach of children. Do not store above 25°C. Store in the original package in order to protect from light

Viatris,

Station Close, Potters Bar, EN6 1TL, United Kingdom. PL 04569/0050 UK Only

POM

25 mg

Hydralazine 25 mg film-coated tablets

56 film-coated tablets

Each film-coated tablet contains: 25 mg hydralazine hydrochloride.

Dosage: Oral use. Read the package leaflet before use. Keep out of the sight and reach of children. Do not store above 25°C. Store in the original package in order to protect from light

Viatris,

Station Close, Potters Bar, EN6 1TL, United Kingdom. PL 04569/0050 UK Only

POM

25 mg

Leaflet outside (Prima)

86 mm

Page 1 Glue

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet outside (Prima)

86 mm

Front page outside 5 mm

15 mm

Tab

Total of label / Braille placement only – CCL work area

15 mm

Tab 5 mm

For proofreading of Braille

15 mm

Tab 5 mm

Base label (Selfadhesive)

Glue

20 mm

Tab/Glue

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Page 47 (Front page inside) 5 mm 15 mm

Tab/Glue Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet inside (Sekunda)

86 mm

Leaflet outside (Prima)

86 mm

Leaflet outside (Prima)

86 mm

86 mm

86 mm

4109854 8010214

4109854 8010214

4109854 8010214

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 04569/0050

Last revision stated in the text: June 2026 · 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 Hydralazine tablets 25 mg

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Hydralazine
Strength 25 mg
Pharmaceutical form Oral tablet
Yellow film coated tablet marked “HE 25” on one side and “G” on the reverse.
How is it taken Oral
Excipients Cellulose, microcrystalline, Maize starch, pregelatinised, Silica, colloidal anhydrous, Disodium edetate, Talc, Magnesium stearate, Hypromellose, Diethyl phthalate, Titanium dioxide (E171), Quinoline yellow (E104), Hydroxypropylcellulose, Ethylcellulose, Iron oxide red (E172), Carnauba wax.
Pack sizes 56 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 3 years.
Storage Do not store above 25°C. Store in the original package in order to protect from light.
Drug group (ATC) Arteriolar smooth muscle, agents acting on; hydrazinophthalazine derivatives
  1. C Cardiovascular system drugs
    1. C02 Antihypertensives
      1. C02D Arteriolar smooth muscle, agents acting on
        1. C02DB Hydrazinophthalazine derivatives acting on arteriolar smooth muscle
          1. C02DB02 hydralazine
Marketing authorisation PL 04569/0050 (first authorised 25 February 1985)
Marketing authorisation holder Generics [UK] Limited t/a Viatris
Codes GTIN 5016695080024 · BNF 02050100

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.3.0 of 26 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.