Patient info Search Menu

Noristerat 200 mg, solution for intramuscular injection – patient leaflet, side effects, dosage

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

Patient leaflet - Noristerat 200 mg, solution for intramuscular injection

1. What Noristerat is and what it is used for

  1. 2. Make sure Noristerat is OK for you
  2. 3. How to use Noristerat
  3. 4. Possible side effects
  4. 5. How to store Noristerat
  5. 6.

    What is in Noristerat and who makes it

    1. 1. What Noristerat is and what it is used for

Noristerat is an injectable (depot) contraceptive. It is intended as a short-term method of contraception, for example in women whose partners are undergoing vasectomy, until the vasectomy is effective. It is also for use in women immunised against rubella, to prevent pregnancy while the virus is active.

You use it to stop you getting pregnant.

Noristerat contains a type of female sex hormone, called a progestogen. This hormone stops you getting pregnant by working in three ways: by preventing an egg being released from your ovaries; by making the fluid (mucus) in your cervix thicker, which makes it more difficult for sperm to enter the womb; and by preventing the lining of your womb thickening enough for an egg to grow in it.

The benefits of using Noristerat include:

RR it is one of the most reliable reversible

methods of contraception if used correctly

RR you only have to remember to visit

your doctor after 8 weeks for a second injection

RR it doesn’t interrupt sex

Noristerat will not protect you against sexually transmitted infections, such as Chlamydia or HIV. Only condoms can help to do this.

  1. 2. Make sure Noristerat is OK for you

It’s important that you understand the benefits and risks of using Noristerat before you are given it, or when deciding whether to have a second injection. Although Noristerat is suitable for most healthy women it isn’t suitable for everyone.

MM Tell your doctor if you have any of

the illnesses or risk factors mentioned in this leaflet.

Before you are given Noristerat

RR Your doctor will ask about you and

your family’s medical problems, check your blood pressure and exclude the likelihood of you being pregnant. You may also need other checks, such as a breast examination, but only if these

examinations are necessary for you, or if you have any special concerns. While you’re on Noristerat

RR Check your breasts and nipples every

month for changes – tell your doctor if you can see or feel anything odd, such as lumps or dimpling of the skin. RR If you need a blood test or other

laboratory tests, tell your doctor or the laboratory staff that you are using Noristerat, because hormonal contraceptives can affect the results of some tests.

RR If you’re going to have an

operation, make sure your doctor knows about it. You may need to avoid having a second injection of Noristerat before the operation. This is to reduce the risk of a blood clot (see section 2.1).

2.1 Noristerat and blood clots Noristerat may slightly increase your risk of having a blood clot (called a thrombosis), especially in the first year of using it.

A clot in a leg vein – a deep vein thrombosis (or DVT) – is not always serious. However, if it moves up the veins and blocks an artery in the lungs, it can cause chest pain, breathlessness, collapse or even death. This is called a pulmonary embolism and is very rare.

Very rarely, blood clots can also form in the blood vessels of the heart (causing a heart attack) or the brain (causing a stroke). In healthy young women the chance of having a heart attack or stroke is extremely small.

You are more at risk of having a blood clot:

RR as you get older

RR if you smoke

RR if you are seriously overweight RR if you have some diseases of the

heart and blood vessels

RR if you suffer from migraines RR if you have recently had a baby RR if you’re off your feet for a long

time because of major surgery, injury or illness

MM Tell your doctor if any of these risk

factors apply to you. Noristerat may not be suitable for you.

Signs of a blood clot include:

RR a migraine for the first time, a

migraine that is worse than normal, or unusually frequent or severe headaches

RR any sudden changes to your

eyesight (such as loss of vision or blurred vision)

RR any sudden changes to your

hearing, speech, sense of smell, taste or touch

RR pain or swelling in your leg RR stabbing pain when you breathe RR coughing for no apparent reason RR pain and tightness in the chest RR sudden weakness or numbness in

one side or part of your body RR dizziness or fainting.

MM See a doctor as soon as possible. Do

not have a further injection until your doctor says you can. Use another method of contraception, such as condoms, in the meantime.

2.2 Noristerat and cancer

Noristerat has also been linked to liver diseases, such as jaundice and non-cancer liver tumours, but this is rare. Very rarely, Noristerat has also been linked with some forms of liver cancer in women who have used it for a long time.

MM See a doctor as soon as possible if

you get severe pain in your stomach, or yellow skin or eyes (jaundice). You may need to stop using Noristerat .

2.3 Noristerat should not be used by some women

MM Tell your doctor or family planning

nurse if you have any medical problems or illnesses.

Do not use Noristerat if you have any of the problems listed below. Using Noristerat would put your health at risk. RR If you are pregnant or might be

pregnant

RR If you have ever had a problem with

your blood circulation. This includes a blood clot (thrombosis) in the legs (deep vein thrombosis), lungs (pulmonary embolism), heart (heart attack), brain (stroke) or any other parts of the body

RR If you have or have ever had severe

liver disease, and you have been told by your doctor that your liver function test results are not yet back to normal

RR If you have or have ever had liver

tumours

RR If you have severe diabetes

affecting your blood vessels

RR If you have very high blood pressure RR If you have disorders of blood fat

(lipid) metabolism

RR If you have or suspect you have cancer

affected by sex hormones – such as some cancers of the breast or womb lining or have ever had either of these conditions

RR If you have an inherited disease called

porphyria

RR If you are allergic (hypersensitive) to

norethisterone enantate or any of the other ingredients in Noristerat (listed in section 6).

MM If you suffer from any of these, or

get them for the first time while using Noristerat, contact your doctor as soon as possible. It may not be suitable for you to have a second injection of Noristerat.

2.4 Noristerat can make some illnesses worse

Some of the conditions listed below can be made worse by using Noristerat. Or they may mean it is less suitable for you. You may still be able to be given Noristerat but you need to take special care.

RR If you have had severe depression RR If you have ever had liver problems,

e.g. jaundice (yellow skin or eyes) RR If you have any disease that tends to

get worse during pregnancy

RR If you have an irregular menstrual

pattern together with stomach pains

RR If you have abnormal vaginal

bleeding

RR If you have diabetes

RR If you have ever had an ectopic

pregnancy or fallopian tube removed.

The main ingredient of Noristerat (the progestogen, norethisterone enantate) is partly converted into the oestrogen, ethinylestradiol. The expected

concentration of ethinylestradiol in your body is relatively low compared to taking combined hormonal contraceptives containing ethinylestradiol. This means that although effects similar to those after taking combined hormonal

contraceptives containing ethinylestradiol cannot be completely ruled out, experience to date suggests that this may not be the case.

MM Tell your doctor or family planning

nurse if any apply to you. Also tell them if you get any of these for the first time after being given Noristerat, or if any get worse or come back, because it may not be suitable for you to have a second injection of Noristerat.

2.5 Psychiatric disorders

Some women using hormonal

contraceptives including Noristerat have reported depression or depressed mood. Depression can be serious and may sometimes lead to suicidal thoughts. If you experience mood changes and depressive symptoms contact your doctor for further medical advice as soon as possible.

2.6 Taking other medicines

If you ever need to take another medicine or herbal products at the same time, always tell your doctor, pharmacist or dentist that you’ve been given Noristerat. Also check the leaflets that come with all your medicines to see if they can be taken with hormonal contraceptives.

Some medicines can stop Noristerat from working properly – for example: RR certain sedatives (called

barbiturates)

RR some medicines used to treat epilepsy

RR some medicines used to treat HIV and Hepatitis C virus infections

(so-called protease inhibitors and non-nucleoside reverse transcriptase inhibitors)

RR griseofulvin (an anti-fungal

medicine)

RR phenylbutazone (an anti-

inflammatory medicine)

RR certain antibiotics

RR St John’s Wort (a herbal remedy). If you do need to take one of these medicines, you may need to use extra contraception (for example condoms) for a while. Your doctor, pharmacist or dentist can tell you if this is necessary and for how long.

Noristerat can also affect how well other medicines work. For example, if you have diabetes, you may need to take Q!

more insulin or other anti-diabetic drugs after being given Noristerat. Your doctor will tell you if this is necessary.

2.7 Using Noristerat with food and drink

There are no special instructions about food and drink while on Noristerat

2.8 Pregnancy and breast-feeding Pregnancy

You should not be given Noristerat if you are pregnant. If you think you might be pregnant, do a pregnancy test to confirm that you are and do not have your second injection.

Breast-feeding

Noristerat has not been shown to reduce the amount of milk you produce which is an advantage if you wish to breastfeed your baby. Very small amounts of the hormone are found in breast milk. There is no evidence to suggest that the small amounts of the hormone that appear in the milk are harmful to a healthy baby. However, if your baby has severe or long-lasting jaundice that requires medical treatment you should not breast-feed your baby after having your injection.

2.9 Driving and using machines

Noristerat has no known effect on the ability to drive or use machines.

2.10 Noristerat contains benzyl benzoate

This medicine contains 333.8 mg benzyl benzoate in each 1 ml ampoule. Benzyl benzoate may increase jaundice (yellowing of the skin and eyes) in newborn babies (up to 4 weeks old).

3. How to use Noristerat

3.1 How to start

Your doctor or family planning clinic will give you the first injection of Noristerat within the first five days of your period (unless you start just after a pregnancy or an abortion). The injection is given into the muscle.

By starting in this way you will have contraceptive protection at once.

3.2 Further injections of Noristerat

One injection will give you contraception for 8 weeks. After 8 weeks a second injection can be given. You must make sure that you leave no longer than 8 weeks between injections or contraceptive protection will be lost.

3.3 Starting Noristerat after having a baby

Noristerat can normally be used straight after having a baby. Your doctor will advise you on when to start.

3.4 Starting Noristerat after having a miscarriage or an abortion

You may be able to have an injection immediately. Your doctor will advise you.

3.5 Missed a period – could you be pregnant?

If, when the second injection is due, you have not had a further period since the first injection, it is unlikely that you are pregnant, but the second injection should not be given until pregnancy has been ruled out.

3.6 Being given more Noristerat than you should

Overdosage is unlikely but if it does occur no serious ill-effects are expected.

4. Possible side effects

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

MM Tell your doctor, pharmacist or

family planning nurse if you are worried about any side effects which you think may be due to Noristerat.

4.1 Serious side effects – see a doctor straight away

Signs of a blood clot:

RR a migraine for the first time, a

migraine that is worse than normal or unusually frequent or severe headaches

RR any sudden changes to your

eyesight (such as loss of vision or blurred vision)

RR any sudden changes to your

hearing, speech, sense of smell, taste or touch

RR pain or swelling in your leg RR stabbing pain when you breathe RR coughing for no apparent reason RR pain and tightness in the chest RR sudden weakness or numbness in

one side or part of your body RR dizziness or fainting.

Signs of a severe allergic reaction to Noristerat:

RR swelling of the face, lips, mouth,

tongue or throat.

Signs of severe liver problems include:

RR severe pain in your upper abdomen RR yellow skin or eyes (jaundice) RR inflammation of the liver (hepatitis) RR your whole body starts itching.

MM If you think you may have any of these, see a doctor straight away. You may need to stop using Noristerat.

4.2 Less serious side effects

RR irregular bleeding

RR bloating

RR tender breasts

RR headaches

RR depressive moods

RR dizziness

RR feeling sick

RR putting on weight

RR skin reactions (e.g. pain or itchy rash)

at the injection site

RR rarely coughing for no apparent reason, shortness of breath and disturbances of the circulatory system may develop while you are having your injection, or immediately after.

MM Tell your doctor or family planning nurse if you are worried about any side effects which you think may be due to Noristerat. Also tell them if any existing conditions get worse while you are using Noristerat. Reporting of side effects

If you get any side effects, talk to your doctor, family planning nurse 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 Noristerat

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

Noristerat should not be used after the expiry date which is stated on the packaging. The expiry date refers to the last day of that month.

Store below 25°C. Protect from light.

6. What is in Noristerat and who makes it

What is in Noristerat

The active substance is norethisterone enantate.

Each ampoule of Noristerat contains 200mg of the progestogen norethisterone enantate in 1ml of oily solution for injection into a muscle.

The other ingredients are benzyl benzoate and castor oil for injection.

What Noristerat looks like and contents of the pack

Noristerat is a solution for intramuscular injection; the injection is given into the muscle.

Noristerat is supplied in single packs of 1 ampoule.

The company that holds the product licence for Noristerat is:

Bayer plc, 400 South Oak Way, Reading, RG2 6AD

Noristerat is made by:

Bayer AG, Muellerstrasse 178, 13353 Berlin, Germany.

This leaflet was last updated in June 2019.

Noristerat®

This area must be identical on both sides!

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 00010/0548

Last revision stated in the text: June 2019 · MHRA data as of 13 October 2026

What the sections and the side effect frequencies mean: How to read a patient leaflet

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 Noristerat 200 mg, solution for intramuscular injection

What these facts mean

Prescription needed?? Yes, prescription-only medicine (POM)
Active substance? Norethisterone enantate
Strength? 200 mg
Pharmaceutical form? Solution for injection
How is it taken? Intramuscular
Excipients? Castor oil for injection, Benzyl benzoate
Pack sizes 1 ampoule
Is it available?? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life? 5 years
Storage Store below 25°C. Protect from light.
Drug group (ATC)? Progestogens
  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. G03AC Progestogen systemic hormonal contraceptives
          1. G03AC01 norethisterone
Marketing authorisation? PL 00010/0548 (first authorised 23 February 2009)
Marketing authorisation holder? Bayer plc
Codes? GTIN 5016703000617 · BNF 07030202

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 11.1.0 of 9 November 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.