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Angeliq 1 mg/2 mg film-coated tablets – patient leaflet, side effects, dosage

Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
1 mg/2 mg
Contains active substances:

Patient leaflet - Angeliq 1 mg/2 mg film-coated tablets

1. What Angeliq is and what it is used for

Angeliq is a Hormone Replacement Therapy (HRT). It contains two types of female hormone, an oestrogen and a progestogen. Angeliq is used in postmenopausal women with at least 12 months (1 year) since their last natural period.

What Angeliq is used for Relief of symptoms occurring after menopause

During the menopause, the amount of the oestrogen produced by a woman’s body drops. This can cause symptoms such as hot face, neck and chest (“hot flushes”). Angeliq alleviates these symptoms after menopause. You will only be prescribed Angeliq if your symptoms seriously hinder your daily life.

Prevention of osteoporosis

After the menopause, some women may develop fragile bones (osteoporosis). You should discuss all available options with your doctor.

If you are at an increased risk of fractures due to osteoporosis and other medicines are not suitable for you, you can use Angeliq to prevent osteoporosis after menopause.

2. What you need to know before you take Angeliq

Medical history and regular check-ups

The use of HRT carries risks which need to be considered when deciding whether to start taking it, or whether to carry on taking it.

The experience in treating women with a premature menopause (due to ovarian failure or surgery) is limited. If you have a premature menopause the risks of using HRT may be different. Please talk to your doctor.

Before you start (or restart) HRT, your doctor will ask about your own and your family’s medical history. Your doctor may decide to perform a physical examination. This may include an examination of your breasts and/or an internal examination, if necessary.

Once you have started on Angeliq, you should see your doctor for regular check-ups (at least once a year). At these check-ups, discuss with your doctor the benefits and risks of continuing with Angeliq.

Be sure to:

  • go for regular breast screening and cervical smear tests.
  • regularly check your breasts for any changes such as dimpling of the skin, changes in the nipple, or any lumps you can see or feel.

Do not take Angeliq

if any of the following applies to you. If you are not sure about any of the points below, talk to your doctor before taking Angeliq.

Do not take Angeliq

  • if you have or have ever had breast cancer, or if you are suspected of having it
  • if you have cancer which is sensitive to oestrogens, such as cancer of the womb lining (endometrium) or if you are suspected of having it
  • if you have any unexplained vaginal bleeding
  • if you have excessive thickening of the womb lining (endometrial hyperplasia) that is not being treated
  • if you have or have ever had a blood clot in a vein (thrombosis) such as in the legs (deep venous thrombosis) or the lungs (pulmonary embolism)
  • if you have a blood clotting disorder (such as protein C, protein S, or antithrombin deficiency)
  • If you have or recently have had a disease caused by blood clots in the arteries, such as a heart attack, stroke or angina
  • if you have or have ever had a liver disease and your liver function tests have not yet returned to normal
  • if you have a rare blood problem called “Porphyria” which is passed down in families (inherited)
  • if you have severe kidney disease or acute kidney failure
  • if you are allergic (hypersensitive) to oestrogens, progestogens or any of the other ingredients of Angeliq

    (listed in section 6)

  • if you have any reason to believe that you either are, or may be, pregnant, or if you are producing milk

    (lactating) and breast-feeding. (See also the 'Pregnancy and breast-feeding' section of this booklet)

  • If any of the above conditions appear for the first time while taking Angeliq, stop taking it at once and consult your doctor immediately.

Warnings and precautions

Talk to your doctor or pharmacist before taking Angeliq. Tell your doctor if you have ever had any of the following problems, before you start the treatment, as these may return or become worse during treatment with Angeliq. If so, you should see your doctor more often for check-ups:

  • fibroids inside your womb
  • growth of womb lining outside your womb (endometriosis) or a history of excessive growth of the womb lining (endometrial hyperplasia)
  • increased risk of developing blood clots (see "Blood clots in a vein (thrombosis)")
  • increased risk of getting an oestrogen-sensitive cancer (such as a mother, sister or grandmother who has had breast cancer)
  • high blood pressure
  • a liver disorder, such as benign liver tumour
  • diabetes
  • gallstones
  • migraine or severe headaches
  • a disease of the immune system that affects many organs of the body (systemic lupus erythematosus,

    SLE)

  • epilepsy
  • asthma
  • a disease affecting the eardrum and hearing (otosclerosis)
  • a very high level of fat in your blood (triglycerides)
  • fluid retention due to cardiac or kidney problems
  • hereditary and acquired angioedema

Stop taking Angeliq and see a doctor immediately

If you notice any of the following when taking HRT:

  • any of the conditions mentioned in the ‘DO NOT take Angeliq’ section
  • yellowing of your skin or the whites of your eyes (jaundice). These may be signs of a liver disease
  • swollen face, tongue and/or throat and/or difficulty swallowing or hives, together with difficulty breathing which are suggestive of an angioedema
  • a large rise in your blood pressure (symptoms may be headache, tiredness, dizziness)
  • migraine-like headaches which happen for the first time
  • if you become pregnant
  • if you notice signs of a blood clot, such as

    • painful swelling and redness of the legs
    • sudden chest pain
    • difficulty breathing

For more information see ‘Blood clots in a vein (thrombosis)’

Note: Angeliq is not a contraceptive. If it is less than 12 months since your last menstrual period or you are under 50 years old, you may still need to use additional contraception to prevent pregnancy. Speak to your doctor for advice.

HRT and cancer

Excessive thickening of the lining of the womb (endometrial hyperplasia) and cancer of the lining of the womb (endometrial cancer)

Taking oestrogen-only HRT will increase the risk of excessive thickening of the lining of the womb (endometrial hyperplasia) and cancer of the lining of the womb (endometrial cancer). The progestogen in Angeliq protects you from this extra risk.

Irregular bleeding

You may have irregular bleeding or drops of blood (spotting) during the first 3–6 months of taking Angeliq. However, if the irregular bleeding:

  • carries on for more than the first 6 months
  • starts after you have been taking Angeliq for more than 6 months
  • carries on after you have stopped taking Angeliq
  • See your doctor as soon as possible.

Breast cancer

Women who have breast cancer, or have had breast cancer in the past, should not take HRT.

Evidence shows that taking combined oestrogen-progestogen or oestrogen-only hormone replacement therapy (HRT) increases the risk of breast cancer. The extra risk depends on how long you use HRT. The additional risk becomes clear within 3 years of use. After stopping HRT the extra risk will decrease with time, but the risk may persist for 10 years or more if you have used HRT for more than 5 years.

Your risk of breast cancer is also higher:

  • if you have a close relative (mother, sister or grandmother) who has had breast cancer
  • if you are seriously overweight

Compare

Looking at women aged 50 to 54 who are not taking HRT, on average, 13 to 17 in 1000 will be diagnosed with breast cancer over a 5-year period.

For women aged 50 who start taking oestrogen-only HRT for 5 years, there will be 16-17 cases in 1000 users (i.e. an extra 0 to 3 cases).

For women aged 50 who start taking oestrogen-progestogen HRT for 5 years, there will be 21 cases in 1000 users (i.e. an extra 4 to 8 cases).

Women aged 50 to 59 who are not taking HRT, on average, 27 in 1000 will be diagnosed with breast cancer over a 10-year period.

For women aged 50 who start taking oestrogen-only HRT for 10 years, there will be 34 cases in 1000 users (i.e. an extra 7 cases)

For women aged 50 who start taking oestrogen-progestogen HRT for 10 years, there will be 48 cases in 1000 users (i.e. an extra 21 cases).

Regularly check your breasts. See your doctor, if you notice any changes in your breast, such as:

  • dimpling or sinking of the skin
  • changes in the nipple
  • any lumps you can see or feel

Additionally, you are advised to join mammography screening programs when offered to you. For mammogram screening, it is important that you inform the nurse/healthcare professional who is actually taking the x-ray that you use HRT, as this medication may increase the density of your breasts which may affect the outcome of the mammogram. Where the density of the breast is increased, mammography may not detect all lumps.

Ovarian cancer

Ovarian cancer (cancer of the ovaries) is rare – much rarer than breast cancer. It can be difficult to diagnose, because there are often no obvious signs of the disease. The use of oestrogen-only or combined oestrogen-progestagen HRT has been associated with a slightly increased risk of ovarian cancer.

The risk of ovarian cancer varies with age. For example, in women aged 50 to 54 who are not taking HRT, about 2 women in 2000 will be diagnosed with ovarian cancer over a 5-year period. For women who have been taking HRT for 5 years, there will be about 3 cases per 2000 users (i.e. about 1 extra case).

Effects of HRT on your heart or circulation

Blood clots in a vein (thrombosis)

The risk of blood clots in the veins (also called deep vein thrombosis, or DVT) is about 1.3 to 3–times higher in HRT users than non-users, especially during the first year of taking it.

Blood clots can be serious if one travels to the lungs it can cause chest pain, breathlessness, fainting or even death. This condition is called pulmonary embolism or PE.

DVT and PE are examples of a condition called venous thromboembolism, or VTE.

You are more likely to get a blood clot in your veins as you get older and if any of the following applies to you. Inform your doctor if any of these situations apply to you:

  • you are unable to walk for a long time because of major surgery, injury or illness (see also sections 3, If you need to have surgery)
  • you are seriously overweight (BMI >30kg/m2)
  • you have any blood clotting problem that needs long-term treatment with a medicine used to prevent blood clots such as warfarin
  • if any of your close relatives has ever had a blood clot in the leg, lung or another organ
  • you have had one or more miscarriages
  • you have systemic lupus erythematosus (SLE)
  • you have cancer

For signs of a blood clot, see “Stop taking Angeliq and see a doctor immediately”.

Compare

Looking at women in their 50s who are not taking HRT, on average, over a 5-year period, 4 to 7 in 1000 would be expected to get a blood clot in a vein.

For women in their 50s who are taking oestrogen-progestogen HRT, for over 5 years, there will be 9 – 12 cases in 1000 (i.e. an extra 5 cases).

Heart disease (heart attack)

There is no evidence that HRT will prevent a heart attack.

HRT is not recommended for women who have heart disease, or have had heart disease recently. If you have ever had heart disease, talk to your doctor to see if you should be taking HRT.

Women over the age of 60 years who use oestrogen-progestogen HRT are slightly more likely to develop heart disease than those not taking any HRT.

Studies with one type of HRT (containing conjugated oestrogen plus the progestogen MPA) have shown that women may be slightly more likely to get heart disease during the first year of taking the medication. For other types of HRT, the risk is likely to be similar, although this is not yet certain.

If you get:

  • a pain in your chest that spreads to your arm or neck
  • See a doctor as soon as possible and do not take any more HRT until your doctor says you can. This pain could be a sign of heart disease.

Stroke

The risk of getting a stroke is about 1.5–times higher in HRT users than in non–users. The number of extra cases of stroke due to HRT use will increase with age.

Other things that can increase the risk of stroke include:

  • getting older
  • high blood pressure
  • smoking
  • drinking too much alcohol
  • an irregular heartbeat

If you are worried about any of these things, or if you have had a stroke in the past, talk to your doctor to see if you should take HRT.

Compare

Looking at women in their 50s who are not taking HRT, on average, 8 in 1000 would be expected to have a stroke over a 5-year period.

For women in their 50s who are taking HRT, there will be 11 cases in 1000 users, over 5 years (i.e. an extra 3 cases).

If you get:

  • unexplained migraine-type headaches, with or without disturbed vision.
  • weakness, numbness, or paralysis of the face, arm, or leg
  • dizziness, loss of balance or coordination
  • See a doctor as soon as possible and do not take any more HRT until your doctor says you can. These headaches may be an early warning sign of a stroke.

Other conditions

  • HRT will not prevent memory loss. There is some evidence of a higher risk of memory loss in women who start using HRT after the age of 65. Speak to your doctor for advice.
  • If you have heart or kidney problems, your doctor should examine you carefully as oestrogens may cause fluid retention resulting in swelling.
  • If you have pre-existing elevated triglycerides (a type of blood fat) your doctor should monitor you closely during oestrogen replacement therapy or HRT. Rare cases of large increases of plasma triglycerides (hypertriglyceridemia) leading to inflammation of the pancreas (pancreatitis) have been reported with oestrogen replacement therapy.
  • If you have a kidney disorder and have high serum potassium levels, particularly if you are taking ACE inhibitors, angiotensin II antagonists and non-steroidal anti-inflammatory agents, your doctor may check the potassium levels in your blood during the first month of treatment.
  • If you have high blood pressure, treatment with Angeliq may decrease it. Angeliq should not be used to treat high blood pressure.
  • If you have a tendency to develop blotchy brown patches (chloasma) on the face you should avoid exposure to the sun or ultraviolet light whilst using Angeliq.

Other medicines and Angeliq

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. Some medicines may interfere with the effect of Angeliq. This might lead to irregular bleeding. This applies to the following medicines.

  • medicines for epilepsy (such as barbiturates, phenytoin, primidone, carbamazepine, oxcarbazepine, topiramate and felbamate)
  • medicines for tuberculosis (such as rifampicin, rifabutin)
  • medicines for HIV and Hepatitis C Virus infections (so-called protease inhibitors and non-nucleoside reverse transcriptase inhibitors such as nevirapine, efavirenz, nelfinavir and ritonavir)
  • medicines for inflammation or pain (such as aspirin and other non-steriodal anti-inflammatory drugs

    (NSAIDS)

  • medicines for certain types of heart disease or high blood pressure (ACE inhibitors or angiotensin II receptor antagonists, verapamil, diltiazem). If you are having treatment for high blood pressure and take Angeliq there may be an additional decrease in blood pressure.
  • Herbal remedies containing St. John’s wort (Hypericum perforatum)
  • medicines for treatment of fungal infections (such as griseofulvin, itraconazole, kenoconazole, voriconazole, fluconazole)
  • medicines for treatment of bacterial infections (such as clarithromycin, erythromycin)
  • grapefruit juice

HRT can affect the way some other medicines work:

  • a medicine for epilepsy (lamotrigine), as this could increase frequency of seizures
  • medicines for Hepatitis C virus (HCV) (such as combinations regimens ombitasvir/paritaprevir/ritonavir and dasabuvir with or without ribavirin; glecaprevir/pibrentasvir or sofosbuvir/velpatasvir/voxilaprevir) may cause increases in liver function blood test results (increase in ALT liver enzyme) in women using CHCs containing ethinylestradiol. Angeliq contains estradiol instead of ethinylestradiol. It is not known whether an increase in ALT liver enzyme can occur when using Angeliq with this HCV combination regimen. Your doctor will advise you.
  • Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines including medicines obtained without a prescription, herbal medicines or other natural products. Your doctor will advise you.

Laboratory tests

If you need a blood test, tell your doctor or the laboratory staff that you are taking Angeliq, because this medicine can affect the results of some tests.

Pregnancy and breast-feeding

Angeliq is for use in post-menopausal women.

If you become pregnant, stop taking Angeliq immediately and contact your doctor.

Driving or using machines

There is nothing to suggest that the use of Angeliq affects driving or use of machines.

Angeliq contains lactose

Angeliq contains lactose (a type of sugar). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

3. How to take Angeliq

Do not start taking Angeliq until at least 12 months after your last natural period.

About the pack

This pack is designed to help you remember to take your medicine. Each tablet is placed in a section marked with the day of the week on which it should be taken. The arrows between tablets show the order in which they must be taken. Your doctor may tell you when to start (see "when to start" for further information).

On the day you start, take your first tablet from the top row of tablets marked with the correct day. For instance, if you start on a Tuesday, press out the tablet from the blister marked 'TUE'.

Take one tablet each day, following the directions of the arrows, until you have finished all 28 tablets in the pack. When you have finished each memo strip, start the next memo strip on the following day. Do not leave a break between memo strips.

It is best to take your tablet at the same time each day. You can take Angeliq with or without food. The tablet should be swallowed whole with a glass of water or milk.

When to start

If you have been taking other HRT preparations: carry on until you have finished your current pack and have taken all the tablets for that month. Take your first Angeliq tablet the next day. Do not leave a break between your old tablets and the Angeliq tablets.

If this is your first HRT treatment: you can start your Angeliq tablets any day.

If you take more Angeliq than you should

Overdose may cause nausea and vomiting and irregular bleeding. No specific treatment is necessary but you should consult your doctor if you are concerned.

If you forget to take Angeliq

If you forget to take a tablet at your usual time and you are less than 24 hours late, take it as soon as possible. Take the next tablet at the usual time.

If you are more than 24 hours late, leave the forgotten tablet in the pack. Continue to take the rest of the tablets at the usual time every day.

If you forget to take your tablet for several days you may experience irregular bleeding.

If you stop taking Angeliq

You may begin to feel the usual symptoms of the menopause again, which may include hot flushes, trouble sleeping, nervousness, dizziness or vaginal dryness. Consult your doctor or pharmacist if you want to stop taking Angeliq tablets. If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

If you need to have surgery

If you are going to have surgery, tell the surgeon that you are taking Angeliq. You may need to stop taking Angeliq about 4 to 6 weeks before the operation to reduce the risk of a blood clot (see section 2, “Blood clots in a vein (thrombosis)”). Ask your doctor when you can start taking Angeliq again.

4. Possible side effects

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

If any of the side effects gets serious, or if you notice any side effects not listed in this booklet, please tell your doctor or pharmacist.

The following diseases are reported more often in women using HRT compared to women not using HRT:

Serious side effects

  • breast cancer
  • abnormal growth or cancer of the lining of the womb (endometrial hyperplasia or cancer)
  • ovarian cancer
  • blood clots in the veins of the leg or the lungs (venous thromboembolism)
  • heart disease
  • stroke
  • probable memory loss if HRT is started over the age of 65

For more information about these side effects see Section 2.

The following is a list of side effects that have been linked to the use of Angeliq:

Most frequent side effects (affecting more than 1 patient in every 10 patients):

These side effects occur during the first few months of treatment with Angeliq. They are usually temporary and normally disappear with continued treatment. If they do not, contact your doctor.

Common side effects (affecting between 1 and 10 in every 100 patients):

  • depression, mood changes, nervousness
  • headache
  • stomach ache, nausea, stomach enlargement
  • non-cancerous breast tumour (benign breast neoplasm), swollen breasts
  • increase in size of uterine fibroids
  • non-cancerous growth of cells at the neck of the womb (benign cervical growth)
  • irregularities in your menstrual period
  • vaginal discharge
  • loss of energy, localised swelling.

Uncommon side effects (affecting between 1 and 10 in every 1000 patients):

  • weight increase or decrease, loss or increase of appetite for food, increase blood fats
  • sleep problems, anxiety, decrease in sex drive
  • burning or pricking sensation, decreased concentration, dizziness
  • eye problems, visual disturbances (such as dry eyes or blurred vision)
  • palpitations
  • blood clot, venous thrombosis (leg pain) (also see section 2 “Blood clots in a vein (thrombosis)”), high blood pressure, migraine, inflammation of the veins, varicose veins
  • breathlessness
  • stomach disorder, diarrhoea, constipation, vomiting, dry mouth, wind, altered sense of taste
  • altered liver enzymes (will show up in blood tests)
  • skin problems, acne, hair loss, itchy skin, rash, excessive hair or hair problems
  • backache, pains in hands and feet, joint pain, muscle cramps
  • urinary tract disorders and infections
  • thickening of the lining of the womb, thrush, vaginal dryness and itchiness or burning of the vagina.
  • lumpy breast (fibrocystic breast), disorders of the ovaries, cervix and uterus, pelvic pain
  • generalised fluid retention, chest pain, feeling generally unwell, increase in sweating
  • non-cancerous tumour of the womb (benign uterine neoplasm)

Rare side effects (affecting between 1 and 10 in every 10,000 patients):

  • anaemia
  • giddiness (vertigo)
  • ringing in the ears (tinnitus)
  • gall stones (cholelithiasis)
  • muscle pain (myalgia)
  • inflammation of the fallopian tubes (salpingitis)
  • milky discharge from the nipples (galactorrhoea)
  • chills

The following side effects have occurred in clinical trials of women with high blood pressure:

  • high potassium levels (hyperkalaemia)
  • heart failure, enlargement of the heart, heart flutter, effects on heart rhythm
  • increase in blood aldosterone

The following side effects have been reported with other HRTs:

  • gall bladder disease
  • various skin disorders:

    • discoloration of the skin especially of the face or neck known as “pregnancy patches” (chloasma)
    • painful reddish skin nodules (erythema nodosum)
    • rash with target-shaped reddening or sores (erythema multiforme)

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 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 Angeliq

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

Do not use this medicine after the expiry date which is printed on the label after "EXP". The expiry date refers to the last day of that month.

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 Angeliq contains

The active substances are estradiol hemihydrate and drospirenone.

The other ingredients are lactose monohydrate, maize starch, pregelatinised maize starch, povidone and magnesium stearate. The ingredients of the tablet coating are hypromellose, macrogol 6000, talc, titanium dioxide (E171) and red ferric oxide (E172).

What Angeliq looks like and contents of the pack

Angeliq tablets are red round convex coated tablets.

One side is marked with the letters DL in a regular hexagon.

They are supplied in a blister pack (memo strip) containing 28 tablets with the days of the week printed on the blister.

Boxes containing three blister packs are available.

Marketing Authorisation Holder

Bayer plc

400 South Oak Way

Reading, RG2 6AD

Manufacturer

Bayer AG

Müllerstrasse 178

13353 Berlin

Bayer Weimar GmbH und Co. KG, Weimar

Döbereinerstraße 20

99427 Weimar

Germany

Date of the last revision of this booklet

May 2026.

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 00010/0757

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 Angeliq 1 mg/2 mg film-coated tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substances Estradiol, Drospirenone
Strength 1 mg/2 mg
Pharmaceutical form Oral tablet
Medium red, round tablet with convex faces, one side embossed with the letters DL in a regular hexagon.
How is it taken Oral
Excipients Lactose monohydrate, Maize starch, Pregelatinised maize starch, Povidone, Magnesium stearate (E470b), Hypromellose (E464), Macrogol 6000, Talc (E553b), Titanium dioxide (E171), Ferric oxide, red (E172)
Pack sizes 84 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 5 years
Storage This medicinal product does not require any special storage conditions.
Drug group (ATC) Progestogens and estrogens, combinations
  1. G Genito urinary system and sex hormones
    1. G03 Sex hormones and modulators of the genital system
      1. G03A Hormonal contraceptives for systemic use
        1. G03AA Progestogens and estrogen systemic contraceptives, fixed combinations
          1. G03AA12 drospirenone and ethinylestradiol
Marketing authorisation PL 00010/0757 (first authorised 14 July 2025)
Marketing authorisation holder Bayer plc
Codes GTIN 4057598029469 · BNF 06040101

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.