Prospecto: information for the user
Elonva 100micrograms injectable solution
Elonva 150micrograms injectable solution
corifolitropina alfa
Read this prospectus carefully before starting to use this medication, because it contains important information for you.
1.What is Elonva and for what it is used
2.What you need to knowbefore starting to use Elonva
3.How to use Elonva
4.Possible adverse effects
5.Storage of Elonva
6.Contents of the package andadditional information
In women
Elonva is used to help achieve pregnancy in women undergoing fertility treatment, such as in vitro fertilization (IVF). IVF includes the extraction of eggs from the ovary, fertilization of the eggs in the laboratory, and the transfer of the embryos to the uterus a few days later. Elonva causes the growth and development of several follicles at the same time through controlled stimulation of the ovaries.
In adolescent males(14years and older)
Elonva is used to induce the development and function of the testicles and to induce the development of male sexual characteristics in adolescent males with delayed puberty due to HH.
No use Elonva:
Warnings and precautions
Consult your doctor before starting to use Elonva.
Ovarian Hyperstimulation Syndrome (OHSS)
Treatment with gonadotropin hormones like Elonva can cause ovarian hyperstimulation syndrome (OHSS). This is a serious condition in which the ovaries are overstimulated and the growing follicles become larger than normal. In rare cases, severe OHSS can be potentially life-threatening. Therefore, it is very important to have close monitoring by your doctor. To check the effects of treatment, your doctor will make ultrasound scans of your ovaries. Your doctor may also check your hormone levels in the blood. (See also section 4).
OHSS causes sudden fluid accumulation in your stomach and in areas of your chest, which can cause blood clots to form. Inform your doctor immediately if you have:
You should only use Elonva once during the same treatment cycle, as the risk of OHSS may increase.
Before starting treatment with this medication, inform your doctor if you have ever had ovarian hyperstimulation syndrome (OHSS).
Ovarian Torsion
Ovarian torsion is the twisting of an ovary. The twisting of the ovary could cause a blockage of blood flow to the ovary.
Before starting to use this medication, inform your doctor if:
Blood Clots (Thrombosis)
Treatment with gonadotropin hormones like Elonva can (like pregnancy) increase the risk of blood clots (thrombosis). Thrombosis is the formation of a blood clot in a blood vessel.
Blood clots can cause serious diseases, such as:
Discuss this with your doctor before starting treatment, especially if:
Multiple Births or Birth Defects
There is an increased risk of having twins or even more babies, even when a single embryo is transferred to the uterus. Multiple pregnancies increase the risk for the health of both the mother and her babies. Multiple pregnancies and specific characteristics of infertile couples (such as the woman's age, certain semen problems, genetic backgrounds of both parents) may be associated with an increased probability of birth defects.
Complications in Pregnancy
If treatment with Elonva results in pregnancy, there is a higher risk of ectopic pregnancy. Therefore, your doctor should make an ultrasound scan at the beginning to rule out the possibility of ectopic pregnancy.
Ovarian Tumors and Other Reproductive System Tumors
Cases of ovarian tumors and other reproductive system tumors have been reported in women who have followed fertility treatment. It is not known if fertility treatment with medications increases the risk of these tumors in infertile women.
Other Diseases
Before starting to use this medication, inform your doctor if:
Use of Elonva with Other Medications
Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication.
If you have a pregnancy test during your infertility treatment with Elonva, the test may indicate incorrectly that you are pregnant. Your doctor will advise you when you can start taking pregnancy tests. If you have a positive pregnancy test, inform your doctor.
Pregnancy and Breastfeeding
You should not use Elonva if you are already pregnant, or think you may be pregnant, or if you are breastfeeding.
Consult your doctor or pharmacist before using this medication.
Driving and Operating Machines
Elonva may cause dizziness. If you feel dizzy, do not drive or operate machines.
Elonva Contains Sodium
This medication contains less than 23mg of sodium (1mmol) per injection; this is, essentially "sodium-free".
Follow exactly the administration instructions for Elonva indicated by your doctor. In case of doubt, consult your doctor or pharmacist again.
In women
Elonva is used in women who are undergoing treatment for infertility such as in vitro fertilization (IVF). During this treatment, Elonva is used in combination with a medication (called a GnRH antagonist) to prevent the ovary from releasing an egg too early. The treatment with the GnRH antagonist usually starts 5 to 6 days after the Elonva injection.
It is not recommended to use Elonva in combination with a GnRH agonist (another medication to prevent the ovary from releasing an egg too early).
In adolescent males (14 years and older)
Elonva, in combination with a medication called hCG, is used for the treatment of delayed puberty due to HH. Elonva should be administered once every two weeks, in the morning, on the same day of the week.
Dose
Women
The dose of Elonva for women in fertile age depends on weight and age.
No studies have been conducted in women over 36 years of age whose weight is less than 50 kilograms.
Body weight | ||||
Less than 50 kg | 50 – 60 kg | More than 60 kg | ||
Age | Up to 36 years inclusive | 100 micrograms | 100 micrograms | 150 micrograms |
Over 36 years | Not studied | 150 micrograms | 150 micrograms |
During the first seven days after the Elonva injection, do not use recombinant Follicle Stimulating Hormone (FSH(rec)). Seven days after the Elonva injection, your doctor may decide to continue the stimulation cycle with another gonadotropin hormone, such as FSH(rec). This can be continued for a few days until there are enough follicles of suitable size. This can be checked by ultrasound. Then the treatment with FSH(rec) is interrupted and the eggs mature by administering hCG (human chorionic gonadotropin). The eggs are extracted from the ovary 34-36 hours later.
In adolescent males (14 years and older)
The dose of Elonva depends on body weight:
For adolescent males with a body weight of 60 kg or less
For adolescent males with a body weight of more than 60 kg
Combined therapy with hCG twice a week (500 – 5000 UI) may be necessary for 52 weeks or more to achieve adult gonadal development.
How to administer Elonva
Elonva treatment should be supervised by a doctor with experience in treating fertility problems. Elonva should be injected under the skin (subcutaneously) in a skin fold (pinching with your thumb and index finger), preferably just below the navel. You may administer the injection yourself, your partner, or a healthcare professional (such as a nurse), as long as your doctor has taught you carefully.
Always use Elonva as your doctor has instructed. Consult your doctor or pharmacist if you are unsure. At the end of this leaflet, there are "instructions for use" step-by-step.
Do not inject Elonva into the muscle.
Elonva is presented in pre-filled syringes with an automatic safety system that helps to prevent needlestick injuries after use.
If you use more Elonva or FSH(rec) than you should
If you think you have used more Elonva or FSH(rec) than you should, inform your doctor immediately.
If you forgot to use Elonva
If you forgot to inject Elonva on the day you should have, inform your doctor immediately. Do not inject Elonva without consulting your doctor.
If you have any other questions about the use of this medication, ask your doctor.
Severe side effects
A possible complication of treatment with gonadotropin hormones such as Elonva is unwanted ovarian overstimulation. The likelihood of experiencing this complication can be reduced by a meticulous control of the number of mature follicles. Your doctor will perform ultrasound of your ovaries to meticulously control the number of mature follicles. Your doctor may also check hormone levels in your blood. The first symptoms of ovarian overstimulation may be noted as stomach pain (abdomen), dizziness, or diarrhea. Ovarian overstimulation may trigger a condition called ovarian hyperstimulation syndrome (OHSS), which can be a serious clinical problem. In more severe cases, it may cause an increase in the size of the ovaries, accumulation of fluid in the abdomen and/or chest (which may cause a sudden increase in weight due to fluid accumulation) or blood clots in the blood vessels.
Inform your doctor immediately if you experience stomach pain (abdomen) or any other symptoms of ovarian hyperstimulation, even if they occur a few days after the injection.
The likelihood of experiencing a side effect is classified in the following categories:
Frequent (may affect up to1in every10women)
-Ovarian hyperstimulation syndrome (OHSS)
-Pelvic pain
-Dizziness (nausea)
-Headache
-Pelvic discomfort
-Breast tenderness
-Fatigue (tiredness)
Less frequent (may affect up to1 in every100women)
-Ovarian torsion (twisting of an ovary)
-Increased liver enzymes
-Spontaneous abortion
-Pain after recovery of the oocytes
-Procedure-related pain
-Premature ovulation (ovulation too soon)
-Abdominal distension
-Vomiting
-Diarrhea
-Constipation
-Back pain
-Breast pain
-Swelling or pain at the injection site
-Irritability
-Mood changes
-Dizziness
-Hot flashes
Unknown frequency (cannot be estimated from available data)
-Allergic reactions (hypersensitivity reactions, both local and generalized, including skin rash).
Also, ectopic pregnancies (pregnancies outside the uterus) and multiple pregnancies have been reported. These side effects are not considered related to the use of Elonva, but to Assisted Reproductive Techniques (ART) or a subsequent pregnancy.
In rare cases, blood clots (thrombosis) have been associated with Elonva therapy, as well as with other gonadotropins, which form inside a blood vessel and may break and travel through the bloodstream to block another blood vessel (thromboembolism).
If you are a male adolescent
Side effects reported in male adolescents:
Frequent (may affect up to1in every10men)
Reporting of side effects
If you experienceany type of side effect, consult your doctor or pharmacist, even if it is apossibleside effect that does not appear in this leaflet.You can also report them directly through the national notification system included in theAppendix V. By reporting side effects, you can contribute to providing more information about the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after “CAD” or “EXP” (expiration date). The expiration date is the last day of the month indicated.
Conservation by the pharmacist
Store in the refrigerator (between 2°C and 8°C). Do not freeze.
Conservation by the patient
There are two options:
Store the syringe in the outer packaging to protect it from light.
Do not use Elonva
Used or unused syringes should not be thrown away through the drains or in the trash. Ask your pharmacist how to dispose of the packaging and medications that you no longer need. In this way, you will help protect the environment.
Appearance of the product and contents of the package
Elonva is a clear, colorless, and transparent injectable aqueous solution in a pre-filled syringe with an automatic safety system, which prevents needlestick injuries after use. The syringe is packaged with a sterile injection needle. Each syringe contains 0.5ml of solution.
The pre-filled syringe is presented in an individual package.
Elonva is available in two doses: 100micrograms and 150micrograms injectable solution.
Marketing authorization holder and manufacturer
N.V. Organon
Kloosterstraat 6
5349AB Oss
Netherlands
For more information about this medicine, please contact the local representative of the marketing authorization holder:
België/Belgique/Belgien Organon Belgium Tel/Tel: 0080066550123 (+32 2 2418100) | Lietuva Organon Pharma B.V.Lithuania atstovybe Tel.: +370 52041693 |
???????? ??????? (?.?.) ?.?. -???? ???????? ???.: +359 2 806 3030 | Luxembourg/Luxemburg Organon Belgium Tél/Tel: 0080066550123 (+32 2 2418100) dpoc.benelux@organon.com |
Ceská republika Organon Czech Republic s.r.o. Tel: +420 233 010 300 | Magyarország Organon Hungary Kft. Tel.:+36 1 766 1963 |
Danmark Organon Denmark ApS Tlf: +45 4484 6800 | Malta Organon Pharma B.V., Cyprus branch Tel: +356 2277 8116 |
Deutschland Organon Healthcare GmbH | Nederland N.V. Organon Tel: 0080066550123(+32 2 2418100) |
Eesti Organon Pharma B.V. Estonian RO Tel: +372 66 61 300 | Norge Organon Norway AS Tlf: +47 24 14 56 60 |
Ελλ?δα BIANEΞ Α.Ε. Τηλ: +30 210 80091 11 | Österreich Organon Healthcare GmbH Tel: +49 (0) 89 2040022 10 |
España Organon Salud, S.L. Tel: +34 91 591 12 79 | Polska Organon Polska Sp. z o.o. Tel.: +48 22 105 50 01 |
France Organon France Tél: +33 (0) 1 57 77 32 00 | Portugal Organon Portugal, Sociedade Unipessoal Lda. Tel: +351218705500 |
Hrvatska Organon Pharma d.o.o. Tel: +385 1 638 4530 | România Organon Biosciences S.R.L. Tel: +40 21 527 29 90 |
Ireland Organon Pharma (Ireland) Limited Tel: +353 15828260 | Slovenija Organon Pharma B.V., Oss, podružnica Ljubljana Tel: +386 1 300 10 80 |
Ísland Vistor hf. Sími: +354 535 7000 | Slovenská republika Organon Slovakia s. r. o. Tel: +421 2 44 88 98 88 |
Italia Organon ItaliaS.r.l. Tel:+39 06 90259059 | Suomi/Finland Organon Finland Oy Puh/Tel: +358 (0) 29 170 3520 |
Κ?προς Organon Pharma B.V., Cyprus branch Τηλ: +357 22866730 | Sverige Organon Sweden AB Tel: +46 8 502 597 00 |
Latvija Arvalsts komersanta “Organon Pharma B.V.” parstavnieciba Tel:+371 66968876 | United Kingdom (Northern Ireland) Organon Pharma (UK) Limited Tel: +44 (0) 208 159 3593 medicalinfor[email protected] |
Last update of this leaflet:MM/AAAA
Other sources of information
The detailed information about this medicine is available on the website of the European Medicines Agency:http://www.ema.europa.eu.
Instructions for use
Components of the Elonva syringe and needle
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Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.