Background pattern
ELONVA 100 micrograms injectable solution

ELONVA 100 micrograms injectable solution

This page is for general information. Consult a doctor for personal advice. Call emergency services if symptoms are severe.
About the medicine

How to use ELONVA 100 micrograms injectable solution

Introduction

Package Leaflet: Information for the User

Elonva 100micrograms solution for injection

Elonva 150micrograms solution for injection

corifollitropin alfa

Read all of this leaflet carefully before you start using 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 or pharmacist.
  • 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 experience any side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet. See section 4.

Contents of the pack

  1. What is Elonva and what is it used for
  2. What you need to know before you use Elonva
  3. How to use Elonva
  4. Possible side effects
  5. Storage of Elonva
  6. Contents of the pack and other information

1. What is Elonva and what is it used for

Elonva contains the active substance corifollitropin alfa and belongs to a group of medicines called gonadotropins. Gonadotropins play an important role in fertility and human reproduction. One of these gonadotropins is Follicle Stimulating Hormone (FSH), which is needed in women for the growth and development of follicles (small round sacs in their ovaries that contain eggs) and in adolescent males (from 14 years onwards) for the treatment of delayed puberty due to hypogonadotropic hypogonadism (HH), in combination with a medicine called human chorionic gonadotropin (hCG).

In women

Elonva is used to help achieve pregnancy in women who are undergoing infertility treatment, such as in vitro fertilization (IVF). IVF includes the removal of eggs from the ovary, fertilization of the eggs in the laboratory, and 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 (from 14 years onwards)

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.

2. What you need to know before you use Elonva

Do not use Elonva:

  • if you are allergic (hypersensitive) to corifollitropin alfa or any of the other ingredients of this medicine (listed in section 6)
  • if you have cancer of the ovary, breast, uterus, or brain (pituitary or hypothalamus)
  • if you have recently had unexpected vaginal bleeding that has not been diagnosed
  • if your ovaries do not work due to a disease called primary ovarian insufficiency
  • if you have ovarian cysts or enlargement of the ovaries
  • if you have malformations of the sex organs that make normal pregnancy impossible
  • if you have uterine fibroids that make normal pregnancy impossible
  • if you have risk factors for OHSS (OHSS is a serious clinical problem that can occur when the ovaries are overstimulated. It is explained in more detail later in this leaflet.):
  • if you have polycystic ovary syndrome (PCOS)
  • if you have had OHSS
  • if you have previously received a cycle of controlled ovarian stimulation treatment with a result of more than 30 follicles with a size of 11 mm or larger
  • if your basal antral follicle count (number of small follicles present in your ovaries at the start of the menstrual cycle) is higher than 20

Warnings and precautions

Talk to your doctor before you start using Elonva.

Ovarian Hyperstimulation Syndrome (OHSS)

Treatment with gonadotropins like Elonva may cause OHSS. This is a condition in which the ovaries are overstimulated and the growing follicles become larger than normal. In rare cases, severe OHSS can be life-threatening. Therefore, it is very important to be closely monitored by your doctor. To check the effects of treatment, your doctor will perform ultrasound scans of your ovaries. Your doctor may also check your hormone levels in blood. (See also section 4).

OHSS can cause fluid to accumulate suddenly in your stomach and chest, which can lead to the formation of blood clots. Tell your doctor immediately if you have:

  • severe abdominal swelling and pain in the stomach area (abdomen)
  • nausea
  • vomiting
  • sudden weight gain due to fluid accumulation
  • diarrhea
  • decreased urine output
  • difficulty breathing

You should only use Elonva once during the same treatment cycle, otherwise, the possibility of OHSS may increase.

Before starting treatment with this medicine, tell your doctor if you have ever had OHSS.

Ovarian Torsion

Ovarian torsion is the twisting of an ovary. The twisting of the ovary could cut off the blood flow to the ovary.

Before you start using this medicine, tell your doctor if:

  • you have ever had OHSS.
  • you are pregnant or think you may be pregnant.
  • you have had abdominal surgery.
  • you have had a twisted ovary.
  • you have cysts or have had cysts on your ovary or ovaries.

Blood Clots (Thrombosis)

Treatment with gonadotropins like Elonva may (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:

  • blockage in your lungs (pulmonary embolism)
  • stroke
  • heart attack
  • blood vessel problems (thrombophlebitis)
  • lack of blood flow (deep vein thrombosis), which can cause the loss of your arm or leg.

Talk to your doctor about this before starting treatment, especially if:

  • you already know you have an increased risk of thrombosis
  • you or a close family member have had thrombosis
  • you are significantly overweight.

Multiple Births or Birth Defects

There is an increased chance of having twins or even more than two babies, even when a single embryo is transferred to the uterus. Multiple pregnancies pose an increased risk to the health of both the mother and her babies. Multiple pregnancies and specific characteristics of couples with fertility problems (e.g., the woman's age, certain semen problems, genetic history of both parents) may be associated with an increased likelihood of birth defects.

Pregnancy Complications

If treatment with Elonva results in pregnancy, there is a higher chance of pregnancy outside the uterus (an ectopic pregnancy). Therefore, your doctor should perform an ultrasound scan at the beginning to rule out the possibility of pregnancy outside the uterus.

Ovarian Tumors and Other Reproductive System Tumors

Cases of ovarian tumors and other reproductive system tumors have been reported in women who have undergone infertility treatment. It is not known whether treatment with fertility medicines increases the risk of these tumors in infertile women.

Other Diseases

Also, before you start using this medicine, tell your doctor if:

  • you have kidney disease.
  • you have uncontrolled pituitary or hypothalamic problems.
  • you have underactive thyroid (hypothyroidism).
  • your adrenal glands do not work properly (adrenal insufficiency).
  • you have high levels of prolactin in your blood (hyperprolactinemia).
  • you have any other disease (e.g., diabetes, heart disease, or any other long-term disease).
  • your doctor has told you that pregnancy would be dangerous for you.

Using Elonva with other medicines

Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines.

If a pregnancy test is done during your infertility treatment with Elonva, the test may incorrectly indicate that you are pregnant. Your doctor will advise you when you can start doing pregnancy tests. In case of a positive pregnancy test, tell your doctor.

Pregnancy and breastfeeding

Do not use Elonva if you are already pregnant, think you may be pregnant, or are breastfeeding.

Talk to your doctor or pharmacist before using this medicine.

Driving and using machines

Elonva may cause dizziness. If you feel dizzy, do not drive or use machines.

Elonva contains sodium

This medicine contains less than 23 mg of sodium (1 mmol) per injectable; this is essentially "sodium-free".

3. How to use Elonva

Follow the instructions for administration of Elonva exactly as your doctor has told you. If you are not sure, ask your doctor or pharmacist again.

In women

Elonva is used in women who are undergoing infertility treatment, such as in vitro fertilization (IVF). During this treatment, Elonva is used in combination with a medicine (called a GnRH antagonist) to prevent your ovary from releasing an egg too early. The treatment with the GnRH antagonist usually starts 5-6 days after the injection of Elonva.

It is not recommended to use Elonva in combination with a GnRH agonist (another medicine to prevent your ovary from releasing an egg too early).

In adolescent males (from 14 years onwards)

Elonva, in combination with a medicine 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

In the treatment of women of childbearing age, the dose of Elonva depends on weight and age.

  • A single dose of 100 micrograms is recommended in women whose weight is 60 kilograms or less and whose age is up to 36 years inclusive.
  • A single dose of 150 micrograms is recommended in women:
  • whose weight is more than 60 kilograms, regardless of age.
  • from 50 kilograms of weight and older than 36 years of age.

No studies have been conducted in women over 36 years of age with a weight of 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 injection of Elonva, you should not use Follicle Stimulating Hormone (recombinant) (FSH (rec)). Seven days after the injection of Elonva, your doctor may decide to continue the stimulation cycle with another gonadotropin, such as FSH (rec). This can be continued for a few days until there are enough follicles of adequate size. This can be checked by ultrasound. Then the treatment with FSH (rec) is interrupted and the eggs mature through the administration of hCG (human Chorionic Gonadotropin). The eggs are retrieved from the ovary 34-36 hours later.

In adolescent males (from 14 years onwards)

The dose of Elonva depends on body weight:

For adolescent males with a weight of 60 kg or less

  • 100 micrograms of Elonva once every two weeks for 12 weeks, followed by the administration of Elonva (once every 2 weeks) with hCG. If during treatment your body weight increases to more than 60 kg, your doctor may increase your dose of Elonva to 150 micrograms.

For adolescent males with a weight of more than 60 kg

  • 150 micrograms of Elonva once every two weeks for 12 weeks, followed by the administration of Elonva (once every 2 weeks) with hCG.

Combination therapy with hCG twice a week (500 - 5000 IU) may be necessary for 52 weeks or more to achieve adult gonadal development.

How Elonva is administered

Treatment with Elonva should be supervised by a doctor with experience in the treatment of 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. The injection can be given by a healthcare professional (e.g., a nurse), your partner, or you yourself, as long as your doctor has carefully instructed you. Always use Elonva exactly as your doctor has told you. You should consult your doctor or pharmacist if you are not sure. At the end of this leaflet, there are step-by-step "instructions for use".

Do not inject Elonva into a muscle.

Elonva comes in pre-filled syringes that have an automatic safety system to help 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, tell your doctor immediately.

If you forget to use Elonva

If you forget to inject Elonva on the day you should, tell your doctor immediately. Do not inject Elonva without consulting your doctor.

If you have any other questions about the use of this medicine, ask your doctor.

4. Possible side effects

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

Serious side effects

A possible complication of treatment with gonadotropins like Elonva is the unwanted overstimulation of the ovaries. The chance of getting this complication can be reduced by closely monitoring the number of mature follicles. Your doctor will perform ultrasound scans of your ovaries to closely monitor the number of mature follicles. Your doctor may also check your hormone levels in blood. The first symptoms of ovarian overstimulation can be noticed as stomach pain (abdomen), nausea, or diarrhea. Ovarian overstimulation can trigger a condition called Ovarian Hyperstimulation Syndrome (OHSS), which can be a serious clinical problem. In more severe cases, it can cause enlargement of the ovaries, accumulation of fluid in the abdomen and/or chest (which can cause sudden weight gain due to fluid accumulation) or blood clots in the blood vessels.

Tell your doctor immediately if you have stomach pain (abdomen) or any other symptoms of OHSS, even if they occur a few days after the injection.

The chance of getting a side effect is classified into the following categories:

Common (may affect up to 1 in 10 women)

  • Ovarian Hyperstimulation Syndrome (OHSS)
  • Pelvic pain
  • Nausea
  • Headache
  • Pelvic discomfort
  • Breast tenderness
  • Fatigue

Uncommon (may affect up to 1 in 100 women)

  • Ovarian torsion
  • Increased liver enzymes
  • Miscarriage
  • Pain after egg retrieval
  • Pain associated with therapeutic procedure
  • Premature ovulation
  • Abdominal distension
  • Vomiting
  • Diarrhea
  • Constipation
  • Back pain
  • Breast pain
  • Bruising or pain at the injection site
  • Irritability
  • Mood swings
  • Dizziness
  • Hot flashes

Frequency not known (cannot be estimated from the available data)

  • Allergic reactions (hypersensitivity reactions, both local and generalized, including skin rash).

Ectopic pregnancies and multiple pregnancies have also been reported. These side effects are not considered to be related to the use of Elonva, but to Assisted Reproductive Technology (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 in a blood vessel and can break loose and travel in the bloodstream to block another blood vessel (thromboembolism).

If you are an adolescent male

Side effects reported in adolescent males:

Common (may affect up to 1 in 10 males)

  • Vomiting
  • Pain at the injection site
  • Hot flashes

Reporting of side effects

If you experience any side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet. You can also report side effects directly through the national reporting system listed in Appendix V. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of Elonva

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 carton after “CAD” or “EXP” (expiry date). The expiry date is the last day of the month shown.

Storage by the pharmacist

Store in a refrigerator (between 2°C and 8°C). Do not freeze.

Storage by the patient

There are two options:

  1. Store in a refrigerator (between 2°C and 8°C). Do not freeze.
  2. Store at a temperature not above 25°C for a period not exceeding one month. Note the date on which you start storing the medicine outside the refrigerator, and use it within one month from that date.

Keep the syringe in the outer packaging to protect it from light.

Do not use Elonva

  • If it has been stored outside the refrigerator for more than one month.
  • If it has been stored outside the refrigerator at a temperature above 25°C.
  • If you notice that the solution is not transparent.
  • If you realize that the syringe or needle is damaged.

Empty or unused syringes should not be disposed of in the drains or in the household waste. Ask your pharmacist how to dispose of the packaging and any unused medicines. This will help protect the environment.

6. Package contents and additional information

Composition of Elonva

  • The active substance is corifollitropin alfa. Each pre-filled syringe of Elonva 100 micrograms solution for injection contains 100 micrograms in 0.5 milliliters (ml) of solution for injection. Each pre-filled syringe of Elonva 150 micrograms solution for injection contains 150 micrograms in 0.5 milliliters (ml) of solution for injection.
  • The other ingredients are: sodium citrate, sucrose, polysorbate 20, methionine, and water for injections. The pH may have been adjusted with sodium hydroxide and/or hydrochloric acid.

Appearance and package contents of the product

Elonva is an aqueous, transparent, and colorless solution for injection in a pre-filled syringe with an automatic safety system that prevents needlestick injuries after use. The syringe is provided with a sterile needle for injection. Each syringe contains 0.5 ml of solution.

The pre-filled syringe is presented in individual packaging.

Elonva is available in two strengths: 100 micrograms and 150 micrograms solution for injection.

Marketing authorization holder and manufacturer

N.V. Organon

Kloosterstraat 6

5349 AB Oss

Netherlands

You can request more information about this medicine by contacting the local representative of the marketing authorization holder:

Belgium/Belgique/Belgien

Organon Belgium

Tel: 0080066550123 (+32 2 2418100)

dpoc.benelux@organon.com

Lithuania

Organon Pharma B.V. Lithuania atstovybe

Tel.: +370 52041693

dpoc.lithuania@organon.com

Bulgaria

Organon Bulgaria EOOD

Tel.: +359 2 806 3030

dpoc.bulgaria@organon.com

Luxembourg/Luxemburg

Organon Belgium

Tel: 0080066550123 (+32 2 2418100)

dpoc.benelux@organon.com

Czech Republic

Organon Czech Republic s.r.o.

Tel: +420 233 010 300

dpoc.czech@organon.com

Hungary

Organon Hungary Kft.

Tel.: +36 1 766 1963

dpoc.hungary@organon.com

Denmark

Organon Denmark ApS

Tlf: +45 4484 6800

info.denmark@organon.com

Malta

Organon Pharma B.V., Cyprus branch

Tel: +356 2277 8116

dpoc.cyprus@organon.com

Germany

Organon Healthcare GmbH

Tel.: 0800 3384 726 (+49 (0) 89 2040022 10)

dpoc.germany@organon.com

Netherlands

N.V. Organon

Tel: 00800 66550123 (+32 2 2418100)

dpoc.benelux@organon.com

Estonia

Organon Pharma B.V. Estonian RO

Tel: +372 66 61 300

dpoc.estonia@organon.com

Norway

Organon Norway AS

Tlf: +47 24 14 56 60

info.norway@organon.com

Greece

BIANEΞ Α.Ε.

Τηλ: +30 210 80091 11

Mailbox@vianex.gr

Austria

Organon Healthcare GmbH

Tel: +49 (0) 89 2040022 10

dpoc.austria@organon.com

Spain

Organon Salud, S.L.

Tel: +34 91 591 12 79

organon_info@organon.com

Poland

Organon Polska Sp. z o.o.

Tel.: +48 22 105 50 01

organonpolska@organon.com

France

Organon France

Tél: +33 (0) 1 57 77 32 00

Portugal

Organon Portugal, Sociedade Unipessoal Lda.

Tel: +351 218705500

geral_pt@organon.com

Croatia

Organon Pharma d.o.o.

Tel: +385 1 638 4530

dpoc.croatia@organon.com

Romania

Organon Biosciences S.R.L.

Tel: +40 21 527 29 90

dpoc.romania@organon.com

Ireland

Organon Pharma (Ireland) Limited

Tel: +353 15828260

medinfo.ROI@organon.com

Slovenia

Organon Pharma B.V., Oss, podružnica Ljubljana

Tel: +386 1 300 10 80

dpoc.slovenia@organon.com

Iceland

Vistor hf.

Sími: + 354 535 7000

Slovakia

Organon Slovakia s. r. o.

Tel: +421 2 44 88 98 88

dpoc.slovakia@organon.com

Italy

Organon Italia S.r.l.

Tel: +39 06 90259059

dpoc.italy@organon.com

Finland

Organon Finland Oy

Puh/Tel: +358 (0) 29 170 3520

dpoc.finland@organon.com

Cyprus

Organon Pharma B.V., Cyprus branch

Τηλ: +357 22866730

dpoc.cyprus@organon.com

Sweden

Organon Sweden AB

Tel: +46 8 502 597 00

dpoc.sweden@organon.com

Latvia

Arvalsts komersanta “Organon Pharma B.V.” parstavnieciba

Tel: +371 66968876

dpoc.latvia@organon.com

United Kingdom (Northern Ireland)

Organon Pharma (UK) Limited

Tel: +44 (0) 208 159 3593

medicalinformationuk@organon.com

Date of last revision of this leaflet:MM/YYYY

Other sources of information

Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu.

Instructions for use

Components of the Elonva syringe and needle

Syringe with labeled parts: plunger, solution, closure cap, nozzle, needle protector, and perforated area

Preparing the injection

Schematic representation of the abdomen with a highlighted blue circular area indicating the injection site

1.

  • Wash your hands with water and soap and dry them before using Elonva.
  • Clean the injection site (the surface just below the navel) with a disinfectant (e.g., alcohol) to remove any bacteria from the surface.
  • Clean around 5 cm around the point where you will insert the needle and let the disinfectant dry for at least one minute before proceeding.

Two hands holding a device with a yellow cylinder and a silver needle for injection

2.

  • While waiting for the disinfectant to dry, break the perforated area and remove the closure cap from the needle
  • Leave the needle protector on the needle
  • Place the needle protector (which contains the needle) on a clean and dry surface while preparing the syringe.

Auto-injector device with a green button pressed, held by a hand with a visible nail, and a dotted line indicating injection

3.

  • Hold the syringe with the gray closure cap facing upwards
  • Gently tap the syringe with your finger to help air bubbles rise to the top.

Hand holding a green auto-injector with a partially removed transparent protective cover

4.

  • Hold the syringe in a vertical position
  • Unscrew the closure cap from the syringe in a counterclockwise direction.

Needle inserted into a yellow auto-injector device with an arrow indicating rotation to secure connection

5.

  • Hold the syringe in a vertical position
  • Screw the needle protector (which contains the needle) onto the syringe in a clockwise direction.

Needle inserted into a yellow applicator device with an arrow pointing upwards and a hand holding the assembly

6.

  • Hold the syringe in position
  • Remove the needle protector upwards and discard it
  • BE CAREFULwith the needle.

Injection

Pre-filled syringe with a yellow plunger and exposed needle held by fingers with an arrow indicating pressure upwards

7.

  • Now hold the syringe between your index and middle fingers, facing upwards
  • Place your thumb on the plunger
  • Gently push the plunger upwards until a tiny drop appears at the tip of the syringe.

Applicator device with needle inserted into the skin at 90 degrees, held by a hand, and an arrow indicating direction

8.

  • Pinch a skin fold with your index and thumb
  • Insert the entire needle at a 90-degree angle into the skin fold
  • Press the plunger CAREFULLYuntil it cannot move further and hold the plunger down
  • COUNT TO FIVEto ensure the injection of the entire solution.

Hand holding an auto-injector with the plunger pressed downwards and an arrow indicating direction

9.

  • Release your thumb from the plunger
  • The needle will automatically retract into the syringe, where it will be permanently enclosed.

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