


Package Leaflet: Information for the User
MENOPUR 1200 International Units
powder and solvent for solution for injection
Highly purified menotropin
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack
Menopur contains menotropin (also known as human menopausal gonadotropin or hMG-HP). It is a highly purified extract from the urine of postmenopausal women and contains two hormones called follicle-stimulating hormone (FSH) and luteinizing hormone (LH). FSH and LH are present in both men and women and help the reproductive organs to function normally.
Menopur is indicated for the treatment of infertility in the following situations:
Before starting treatment with Menopur, you and your partner should be evaluated by a doctor to determine the causes of the infertility problem. In particular, you should be checked for the following diseases so that you can receive the most appropriate treatment:
If you know you have any of the diseases listed above, please inform your doctor before starting treatment with Menopur.
Do not use Menopur if:
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In women:
In men:
Warnings and precautions
If you have:
Consult your doctor directly, even if the symptoms develop a few days after the last injection was administered. These may be signs of high levels of activity in the ovaries that can become severe.
If these symptoms become severe, infertility treatment should be discontinued and you should receive treatment in a hospital.
By maintaining the recommended dose and careful monitoring of treatment, the likelihood of experiencing these symptoms will be reduced.
If you stop usingMenopur, you may still experience these symptoms. Please contact your doctor immediately if you experience any of these symptoms.
While you are being treated with this medicine, your doctor will normally order ultrasound scansand sometimes blood teststo monitor your response to treatment.
When being treated with hormones like Menopur, there is an increased risk of:
Some women who have been treated with several medicines for infertility have developed tumors in the ovaries and other reproductive organs. It is not yet known whether treatment with hormones like this medicine causes these problems.
It is more likely that blood clots will form in the blood vessels (veins or arteries) in pregnant women. Infertility treatment may increase the likelihood of this happening, especially if you are overweight or have a known blood coagulation disorder (thrombophilia) or if you or a family member has had blood clotting problems. Inform your doctor if you think this applies to you.
Use in children
Menopur is not indicated for use in children.
Use of Menopur with other medicines
Tell your doctor or pharmacist if you are using or have recently used or might use any other medicines.
No studies of interactions with Menopur have been performed in humans.
When treating infertile men, menotropin and human chorionic gonadotropin can be administered at the same time.
Clomifene citrate is another medicine used in the treatment of infertility. If Menopur is used at the same time as clomifene citrate, the effect on the ovaries may be increased.
Menopur can be used at the same time as Bravelle (another medicine used for the treatment of infertility). Please see section 3 “How to use Menopur”.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine.
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Menopur is not indicated in any case for the treatment of pregnant or breastfeeding women.
Driving and using machines
It is very rare that Menopur affects the ability to drive and use machines.
Important information about some of the ingredients of Menopur:
Menopur contains less than 1 mmol of sodium chloride (23 mg) per dose, and is therefore essentially sodium-free.
Follow your doctor's instructions for administering Menopur exactly.
In case of doubt, consult your doctor or pharmacist again.
Treatment will begin within the first 7 days of the menstrual cycle (day 1 is the first day of the period). Treatment should be administered every day for at least 7 days.
The initial dose is usually 75-150 IU per day. This dose may be increased according to your response to treatment up to a maximum of 225 IU per day. A single dose should be administered at least 7 days before the dose is adjusted by the doctor. The recommended dose increase is 37.5 IU per adjustment (and no more than 75 IU). The treatment cycle should be abandoned if there is no adequate response after 4 weeks.
When an optimal response is obtained, a single injection of another hormone called human chorionic gonadotropin (hCG) will be administered, 5,000 to 10,000 IU, 1 day after the last dose of Menopur. It is recommended to have intercourse on the same day as the administration of hCG and the following day. Intrauterine insemination can be performed alternatively (injection of sperm directly into the uterus). Your doctor should closely monitor your progress for at least 2 weeks after the administration of hCG.
Your doctor will monitor the effect of Menopur treatment. Depending on progress, your doctor will decide to interrupt treatment with Menopur and not administer the hCG injection. In this case, you should use a contraceptive method (condom) or not have sexual intercourse until the next period begins.
ii. Women in assisted reproduction programs:
If you are also receiving treatment with GnRH agonists (a medication that helps the hormone called Gonadotropin-Releasing Hormone (GnRH) work), treatment with Menopur should begin approximately 2 weeks after starting GnRH agonist treatment.
If you are also receiving treatment with GnRH antagonists, treatment with Menopur should begin on day 2 or 3 of the menstrual cycle (day 1 is the first day of the period).
Menopur will be administered daily for at least 5 days. The recommended initial dose of Menopur is 150-225 IU. This dose may be increased according to your response to treatment up to a maximum of 450 IU per day. The dose should not be increased by more than 150 IU per adjustment. Normally, treatment is not recommended for more than 20 days.
If there are enough egg sacs, a single injection of a medication called human chorionic gonadotropin (hCG) will be administered at a dose of up to 10,000 IU to induce ovulation (release of an egg).
Your doctor should closely monitor your progress for at least 2 weeks after the administration of hCG.
Your doctor will monitor the effect of Menopur treatment. Depending on progress, your doctor will decide to interrupt treatment with Menopur and not administer the hCG injection. In this case, you should use a contraceptive method (condom) or not have sexual intercourse until the next period begins.
Male infertility:
Initially, 1,000 to 3,000 IU of human chorionic gonadotropin are administered, 3 times a week, until a normal serum testosterone level is reached.
Then, a dose of Menopur of 75-150 IU (1-2 vials) is administered 3 times a week, intramuscularly (IM), for several months.
Use in children
Menopur has no suitable indications for use in children.
INSTRUCTIONS FOR USE:
If your doctor tells you to inject Menopur yourself, you should follow any instructions they provide.
The first injection of this medication should be administered under the supervision of a doctor or nurse.
Menopur is provided as a powder in a vial and must be dissolved with two syringes with solvent before injection. The solvents to be used to dilute Menopur are provided in pre-filled syringes.
Menopur 1200 IU must be reconstituted with the two pre-filled syringes with solvent before use.
After dissolving the powder with the solvents, the vial contains medication for several days of treatment, so you must be sure to only extract the amount of medication prescribed by your doctor.
Your doctor has prescribed a dose of Menopur in IU (units). You should use one of the 18 graduated syringes in units IU (units) FSH/LH provided.

Follow these steps:



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Remove the rubber stopper from the second pre-filled syringe with solvent and firmly attach it to the needle fixed in the vial. Slowly injectallthe liquid to avoid forming bubbles (image 5).
Remove the syringe and reconstitution needle.






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Do not usethe reconstituted solution if it contains particles or is not transparent.
The powder vial is now dissolved with the two solvent syringes and ready to use.
REMEMBER: since the vial contains medication for several days of treatment, you must ensure that you only withdraw the amount of medication prescribed by your doctor.
If you have been prescribed Bravelle at the same time as Menopur, you can mix the two medications by reconstituting Menopur and injecting the prescribed dose of Menopur into the reconstituted Bravelle solution. Withdraw the mixed solution, so you can inject both medications together and not separately.
Your doctor or nurse will tell you where to inject (e.g., front of the thigh, abdomen, etc.). Before injection, clean the skin at the injection site with an alcohol swab.

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After removing the syringe, apply pressure to the injection site to contain any bleeding. A gentle massage at the injection site will help to disperse the solution under the skin.
Do not throw away used materials in the trash; they should be disposed of properly.
If you use more Menopur than you should.In case of overdose or if the solution is swallowed accidentally, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount used.
If you forget to use Menopur,do not use a double dose to make up for forgotten doses. Please tell your doctor or pharmacist.
If you have any other questions about using this medication, ask your doctor or pharmacist.
Like all medications, Menopur can cause side effects, although not everyone will experience them.
Treatment with Menopur may cause high levels of activity in the ovariesthat can lead to a disease called Ovarian Hyperstimulation Syndrome (OHSS), especially in women with polycystic ovaries .Symptoms include: abdominal distension and discomfort, nausea, vomiting, diarrhea, weight gain.In some severe cases of OHSS, rare complications have been reported, including fluid accumulation in the abdomen, pelvis, and/or pleural cavity,difficulty breathing, decreased urine production
blood clot formation in blood vessels (thromboembolism)and ovarian torsion. If you experience any of these symptoms, contact your doctor immediately, even if they develop some days after the last injection.
Allergic reactions (hypersensitivity)may occur when using this medication. Symptoms of these reactions may include: rash, itching, swelling of the throat, and difficulty breathing.If you experience any of these symptoms, contact your doctor immediately.
The following frequent side effectsaffect between 1 and 10 out of 100 patients treated:
The following infrequent side effectsaffect between 1 and 10 out of 1,000 patients treated:
The following rare side effectsaffect between 1 and 10 out of 10,000 patients treated:
In addition to the side effects listed above, the following side effects have been reported after marketing of Menopurwith an unknown frequency:
Reporting of side effects.
If you experience any side effects, consult your doctor or pharmacist, even if they are possible side effects that do not appear in this leaflet. You can also report them directly through the Spanish Medicines Monitoring System for Human Use https://www.notificaRAM.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep out of sight and reach of children.
Before reconstitution, store in the refrigerator (2°C – 8°C). Do not freeze. Store in the original package to protect from light.
After reconstitution, the solution can be stored for a maximum of 28 days at no more than 25°C.
The reconstituted solution should not be administered if it contains particles or is not transparent.
Do not use Menopur after the expiration date shown on the packaging after "EXP". The expiration date is the last day of the month indicated.
Medicines should not be thrown away in drains or trash. Deposit the packaging and unused medications in the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and unused medications. This will help protect the environment.
Composition of Menopur
The active ingredient is highly purified menotropin (human menopausal gonadotropin, hMG-HP) which corresponds to 1200 IU of follicle-stimulating hormone (FSH) activity and 1200 IU of luteinizing hormone (LH) activity.
After reconstitution, with the 2 ml of solvent, 1 ml of reconstituted solution contains 600 IU of highly purified menotropin.
The other components of the powder are: lactose monohydrate, polysorbate 20, disodium phosphate heptahydrate (as a buffering agent and pH adjuster), and phosphoric acid (for pH adjuster).
The components of the solvent are: metacresol and water for injection.
Appearance of the product and package contents.
Menopur is a powder and solvent for injectable solution.
Menopur is a lyophilized powder, white to grayish, which is presented in a glass vial along with two pre-filled syringes with solvent, a clear, colorless solution, for reconstitution, 1 reconstitution needle, and 18 disposable syringes graduated in units FSH/LH with pre-attached needles for administration.
Marketing authorization holder and manufacturer:
Marketing authorization holder
Ferring, S.A.U
C/ del Arquitecto Sánchez Arcas nº3, 1º
28040 Madrid
Manufacturer:
FERRING GmbH
Wittland 11,
D-24109 Kiel
GERMANY
This leaflet was approved inSeptember 2015
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
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