Rhesonativ

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Package leaflet: Information for the user

Rhesonativ 625 IU/ml, solution for injection
Human anti-D immunoglobulin

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, pharmacist or nurse.
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.
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.

What is in this leaflet

What Rhesonativ is and what it is used for

What you need to know before you use Rhesonativ

How to use Rhesonativ

Possible side effects

How to store Rhesonativ

Contents of the pack and other information

1What Rhesonativ is and what it is used for

Rhesonativ is an immunoglobulin and contains antibodies to the Rhesus factor. If a woman who lacks the Rhesus factor in her red blood cells (=Rh-negative) is pregnant with an unborn baby which has the Rhesus factor (=Rh-positive), her immune defence system may be stimulated to form antibodies to the Rhesus factor. These antibodies may harm her unborn baby, especially in subsequent pregnancies.

Rhesonativ is used to keep the Rh-negative woman from becoming immunised in the course of pregnancy and childbirth, and in this way prevent harm to the unborn baby. Rhesonativ is used in Rh-negative woman in case of:

Anti-D prevention therapy for pregnant women who are RH- negative
Delivery of a Rh-positive baby
Abortion/threatened abortion (miscarriage/threatened miscarriage)
Pregnancy outside the uterus, certain growths inside the uterus (mole), or bleeding of blood of the unborn baby into the normally separated maternal circulation or death of the unborn baby late in pregnancy
Invasive procedures during pregnancy such as drawing of amniotic fluid with a syringe (i.e. amniocentesis), or blood sampling of the unborn baby from the umbilical vein, biopsy or obstetric manipulative procedures, e.g. procedures to manually rotate the baby to a correct position in the uterus, or belly trauma, surgical treatment of the unborn baby inside the uterus

Rhesonativ may also be used in Rh-negative individuals who have accidentally received an Rh-positive blood transfusion.

2What you need to know before you use Rhesonativ

Do not use Rhesonativ:

if you are allergic to human normal immunoglobulin or any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Talk to your doctor, pharmacist or nurse before using Rhesonativ.

Tell your doctor if you have any other illnesses.

Rhesonativ is neither intended for use in Rh(D)positive individuals nor for individuals already immunised to Rh(D) antigen.

True hypersensitivity reactions (allergic reactions) are rare, but may occur.

In case of suspected allergy or a serious allergic reaction (anaphylactic reaction), you should immediately inform your doctor or nurse. The symptoms are, for example, dizziness, palpitation of the heart, drop in blood pressure, difficulty breathing and swallowing, tightness of the chest, itching, generalised urticaria (hives), swelling of the face, tongue or throat, collapse and rash. Any of these conditions requires treatment immediately.

Children

No data are available on the use in children.

Virus safety

When medicines are made from human blood or plasma, certain measures are put in place to prevent infections being passed on to patients. These include careful selection of blood and plasma donors to make sure those at risk of carrying infections are excluded, and the testing of each donation and pools of plasma for signs of virus/infections. Manufacturers of these products also include steps in the processing of the blood or plasma that can inactivate or remove viruses. Despite these measures, when medicines prepared from human blood or plasma are administered, the possibility of passing on infection cannot be totally excluded. This also applies to any unknown or emerging viruses or other types of infections.

The measures taken are considered effective for envelopedviruses such as human immunodeficiency virus (HIV), hepatitis B virus and hepatitis C virus,and for the non-envelopedhepatitis A virus.

The measures taken may be of limited value against non-enveloped viruses such as parvovirus B19.

Immunoglobulins have not been associated with hepatitis A or parvovirus B19 infections possibly because the antibodies against these infections, which are contained in the product, are protective.

It is strongly recommended that every time you receive a dose of Rhesonativ, the name and batch number of the product are recorded in order to maintain a record of the batches used.

Other medicines and Rhesonativ

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Rhesonativ may weaken the effect of vaccines such as measles, rubella, mumps and chicken pox. Following treatment with Rhesonativ, three months should be allowed to elapse before you are vaccinated with any of these vaccines. It is therefore important that the doctor carrying out the vaccination is aware that you are having or have had treatment with Rhesonativ.
Inform your doctor that you are taking immunoglobulin when you give a blood sample, as this treatment may affect the results.

Pregnancy and breast-feeding

Rhesonativ is intended for use in pregnancy and can be used during breastfeeding.

Driving and using machines

No effects on ability to drive and use machines have been observed.

Important information about some of the ingredients of Rhesonativ

This medicinal product contains less than 1 mmol sodium (23 mg) per dose, i.e. essentially ‘sodium-free’.

3How to use Rhesonativ

Your doctor will decide if you need Rhesonativ and at what dose. Rhesonativ is administered as an intramuscular injection (in a muscle) by healthcare personnel.

4Possibleside effects

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

The following side effects may occur: headache, beating of the heart, low blood pressure, wheezing, vomiting, nausea, skin reactions, pain in a joint, fever, feelings of discomfort including chest discomfort, shivering, local reactions at the site of injection, such as swelling and pain, degradation of red blood cells and severe allergic reactions including anaphylactic shock.

If you notice any symptoms of an anaphylactic reaction like dizziness, nausea, vomiting, stomach cramps, coughing, difficulty breathing and swallowing, blueness of the skin, itching, hives, rash, beating of the heart, low blood pressure, swelling of the face, tongue or throat, collapse or pain in the chest please contact your doctor immediately because any of these conditions requires treatment immediately.

If you get any side effects, talk to your doctor. This includes any side effects not listed in this leaflet.

Reporting of suspected adverse reactions

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly (see details below). By reporting side effects you can help provide more information on the safety of this medicine.

[*to be completed nationally]

5Howto store Rhesonativ

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

Store in a refrigerator (2C – 8C). Keep the ampoule in the outer carton in order to protect from light.

Do not use this medicine after the expiry date which is stated on the label and carton 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 protect the environment.

6Contents of the pack and other information

What Rhesonativ contains

The active substance is human anti-D immunoglobulin. 1 ml contains 625 IU (125 μg) human anti-D immunoglobulin.
One ampoule of 1 ml contains 625 IU (125 g) of human anti-D immunoglobulin.
One ampoule of 2 ml contains 1250 IU (250 g) of human anti-D immunoglobulin.
The human protein content is 165 mg/ml, of which immunoglobulin G is at least 95%.
The other ingredients are glycine, sodium chloride, sodium acetate, polysorbate 80 and water for injections.

What Rhesonativ looks like and contents of the pack

Rhesonativ is a solution for injection (625 IU/ml or 1250 IU/2 ml per ampoule).

Pack sizes: 1x1 ml, 1x2 ml and 10x2 ml.

The colour of the solution can vary from colourless to pale-yellow up to light-brown.
Not all pack sizes may be marketed.

This medicinal product is authorised in the Member States of the EEA under the following names:

Name of the member state	Name of the product
Austria	Rhesonativ 625 I.E./ml Injektionslösung
Bulgaria	Rhesonativ 625 IU/ml, solution for injection
Cyprus	Rhesonativ
Czech Republic	Rhesonativ 625 IU/ml
Denmark	Rhesonativ, Octapharma AB, Injectionsvæske, opløsning, 625 IE/ml, anti-D (rh) immunoglobulin, human
Estonia	Rhesonativ süstelahus 625TÜ 1ml
Finland	Rhesonativ 625 IU/ml injektioneste, liuos
France	Rhesonativ 625 UI/ml, solution injectable
Hungary	Rhesonativ 625 NE/ml oldatos injekció
Iceland	Rhesonativ stungulyf, lausn 625 IU/ml
Ireland	Rhesonativ 625 IU/ml, solution for injection
Italy	Rhesonativ 625 IU/ml Soluzione iniettabile
Latvia	Rhesonativ 625 SV/ml šķīdums injekcijām
Lithuania	Rhesonativ 625 TV/ml injekcinis tirpalas
Luxembourg	Rhesonativ Sol. Inj. 625 UI/1 ml
Malta	Rhesonativ 625 IU/ml, solution for injection
Netherlands	Rhesonativ 625 IE/ml, oplossing voor injectie
Norway	Rhesonativ, injeksjonsvæske, oppløsning, 625 IE/ml "Octapharma"
Poland	Rhesonativ
Portugal	Rhesonativ
Romania	Rhesonativ 625 UI/ml, solutie injectabila
Slovakia	Rhesonativ
Slovenia	Rhesonativ 625 i.e./ml, raztopina za injiciranje
Sweden	Rhesonativ, 625 IE/ml injektionsvätska, lösning

Marketing Authorisation Holder and Manufacturer

Octapharma AB
SE-112 75 Stockholm
Sweden

This leaflet was last revised in 2015-02-16.

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The following information is intended for healthcare professionals only:

The product should be brought to room or body temperature before use.

Do not use solutions that are cloudy or have deposits.

The content of an opened ampoule should be used immediately. Any unused medicinal product or waste material should be disposed of in accordance with local requirements.

Injections have to be given intramuscularly and care should be taken to draw back on the plunger of the syringe before injection in order to be certain that the needle is not in a blood vessel.

If intramuscular administration is contra-indicated (bleeding disorders), the injection can be administered subcutaneously if no intravenous product is available. Careful manual pressure with a compress should be applied to the site after injection.

If a large volume (>2 ml for children or >5 ml for adults) is required, it is recommended to administer this in divided doses at different sites.

This medicinal productmust not be mixed with other medicinal products.