


Package Leaflet: Information for the User
Bemfola 75 IU/0.125 ml solution for injection in pre-filled pen
Bemfola 150 IU/0.25 ml solution for injection in pre-filled pen
Bemfola 225 IU/0.375 ml solution for injection in pre-filled pen
Bemfola 300 IU/0.50 ml solution for injection in pre-filled pen
Bemfola 450 IU/0.75 ml solution for injection in pre-filled pen
Follitropin alpha
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack
What is Bemfola
This medicine contains the active substance follitropin alpha, which is almost identical to a natural hormone produced by your body called ‘follicle stimulating hormone’ (FSH). FSH is a gonadotropin, a type of hormone that plays an important role in human reproduction and fertility. In women, FSH is necessary for the growth and development of the sacs (follicles) in the ovaries that contain the eggs. In men, FSH is necessary for sperm production.
What is Bemfola used for
In adult women,Bemfola is used:
«zygote intrafallopian transfer».
In adult men,Bemfola is used:
Before starting treatment, your fertility and that of your partner should be assessed by a doctor experienced in the treatment of fertility disorders.
Do not use Bemfola
Do not use Bemfola if you have any of these conditions. If you are not sure, ask your doctor before using this medicine.
Warnings and precautions
Consult your doctor or pharmacist before using Bemfola.
Porphyria
Tell your doctor before starting treatment if you or any member of your family has porphyria (an inability to break down porphyrins that can be passed from parents to children).
Tell your doctor immediately if:
In these cases, your doctor may recommend that you stop treatment.
Ovarian Hyperstimulation Syndrome (OHSS)
If you are a woman, this medicine increases the risk of you developing OHSS. This happens when your follicles develop too much and become large cysts. If you have pelvic pain, rapid weight gain, nausea, vomiting or difficulty breathing, consult your doctor immediately, who may stop treatment (see section 4).
If you do not ovulate and you follow the recommended dose and treatment schedule, this syndrome is less likely to occur. Treatment with Bemfola rarely causes a severe ovarian hyperstimulation syndrome, unless the medicine used for final follicular maturation (containing human chorionic gonadotropin, hCG) is also administered. If you develop OHSS, your doctor may not prescribe hCG in this treatment cycle and advise you to abstain from intercourse or use barrier contraceptives for at least 4 days.
Multiple Pregnancy
If you use Bemfola, you have a higher risk of becoming pregnant with more than one baby at the same time (‘multiple pregnancy’, usually twins), than if you were to become pregnant through natural conception. Multiple pregnancy can cause medical complications for you and your babies. You can reduce the risk of multiple pregnancy by using the correct dose of Bemfola at the right times. If you undergo assisted reproduction techniques, the risk of multiple pregnancy is related to your age and the quality and number of eggs fertilized or embryos placed inside you.
Abortion
If you undergo assisted reproduction techniques or ovarian stimulation to produce eggs, you are more likely to have a miscarriage than the average woman.
Blood Clotting Problems (Thromboembolic Events)
If you or a member of your family has had blood clots in the leg or lung, heart attack or stroke in the past or recently, you may have a higher risk of having these problems or of them getting worse with Bemfola treatment.
Men with High FSH Levels in the Blood
If you are a man, very high FSH levels in the blood can be a sign of testicular damage. Bemfola is usually not effective in these cases.
If your doctor decides to try treatment with Bemfola, your doctor may ask you to have a semen analysis 4 to 6 months after starting treatment.
Children and Adolescents
Bemfola is not indicated in children and adolescents under 18 years of age.
Using Bemfola with Other Medicines
Tell your doctor if you are taking, have recently taken or might take any other medicines.
Pregnancy and Breast-feeding
Do not use Bemfola if you are pregnant or breast-feeding.
Driving and Using Machines
Bemfola is not expected to affect your ability to drive or use machines.
Bemfola Contains Sodium
This medicine contains less than 1 mmol of sodium (23 mg) per dose, which is essentially ‘sodium-free’.
Follow the instructions for administration of this medicine exactly as told by your doctor. Ask your doctor or pharmacist if you are unsure.
Using this Medicine
How Much to Use
Your doctor will decide how much medicine to administer and how often. The doses described below are expressed in International Units (IU) and milliliters (ml).
Women
If you are not ovulating and have irregular periods or no periods
If your doctor does not observe the desired response after 4 weeks of treatment, the treatment cycle with Bemfola should be stopped. For the next cycle, your doctor will administer a higher starting dose of Bemfola than before.
If an excessive response is obtained, treatment will be stopped and hCG will not be administered (see section 2, “Ovarian Hyperstimulation Syndrome (OHSS)”). For the next cycle, your doctor will administer a lower dose of Bemfola than in the previous cycle.
If you need to develop several eggs before any assisted reproduction technique
In other cases, your doctor may first stop ovulation using a GnRH agonist or antagonist. In such cases, Bemfola administration is started about 2 weeks after starting treatment with the GnRH agonist, and both treatments are continued until adequate follicular development is achieved. For example, after 2 weeks of treatment with the GnRH agonist, 150 to 225 IU of Bemfola are administered for 7 days. The dose is then adjusted according to the response of the ovaries.
Men
If you use more Bemfola than you should
The effects of using too much Bemfola are not known. However, it can be expected that ovarian hyperstimulation syndrome may occur, which is described in section 4. However, this syndrome will only occur if hCG is also administered (see section 2, “Ovarian Hyperstimulation Syndrome (OHSS)”).
If you forget to use Bemfola
If you forget to use Bemfola, do not use a double dose to make up for forgotten doses. Consult your doctor as soon as you realize you have forgotten to administer a dose.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
Severe Adverse Effects in Women
Severe Adverse Effects in Men and Women
If you notice any of the above adverse effects, you should consult your doctor immediately, who may ask you to interrupt treatment with Bemfola.
Other Adverse Effects in Women
Very common (may affect more than 1 in 10 people):
Common (may affect up to 1 in 10 people):
Very rare (may affect up to 1 in 10,000 people):
Other Adverse Effects in Men
Very common (may affect more than 1 in 10 people):
Common (may affect up to 1 in 10 people):
Very rare (may affect up to 1 in 10,000 people):
Reporting Adverse Effects
If you experience any adverse effects, consult your doctor or pharmacist, even if they are possible adverse effects not listed in this leaflet. You can also report them directly through the national reporting system included in Appendix V. By reporting adverse effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiration date stated on the label or carton after CAD. The expiration date is the last day of the month indicated.
Store in a refrigerator (between 2°C and 8°C). Do not freeze. Store in the original packaging to protect it from light.
During its validity period, the unopened medicine can be stored at a temperature equal to or below 25°C for a maximum of 3 months without refrigeration and must be discarded if not used within 3 months.
Do not use this medicine if you notice any visible signs of deterioration, if the liquid contains particles, or if it is not transparent.
Once opened, the medicine will be injected immediately.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. This will help protect the environment.
Composition of Bemfola
Appearance of Bemfola and Package Contents
Marketing Authorization Holder and Manufacturer
Gedeon Richter Plc.
Gyömroi út 19-21.
1103 Budapest
Hungary
Date of Last Revision of this Leaflet
Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu.
Bemfola 75 UI/0.125 ml Pre-filled Pen
Bemfola 150 UI/0.25 ml Pre-filled Pen
Bemfola 225 UI/0.375 ml Pre-filled Pen
Bemfola 300 UI/0.50 ml Pre-filled Pen
Bemfola 450 UI/0.75 ml Pre-filled Pen
Instructions for Use
CONTENTS
Warning: Read and follow these Instructions for Use of the Bemfola pre-filled pen. Do not follow instructions from sources other than those provided in these Instructions for Use or by a healthcare professional, as this may compromise the proper use of the pre-filled pen and treatment. |
The Different Parts of Your Pre-filled Pen






You are now ready to administer the injection immediately: your doctor or nurse will have told you where to inject (e.g., in the abdomen, in the front of the thigh). To minimize skin irritation, choose a different injection site each day.



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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for BEMFOLA 150 IU/0.25ml injectable solution in a pre-filled pen – subject to medical assessment and local rules.