Femoston 2/10mg Tablets
Out of date information, search anotherRare (in less than 1 in 1,000, but more than 1 in 10,000 patients treated):
• liver disorders, which may include jaundice (yellowing of the skin), asthenia (feeling weak) and general malaise
• change in the surface of the eye
• intolerance to contact lenses
• pre-menstrual tension (PMT)
• swelling of the breasts
Very rare (in less than 1 in 10,000 patients treated, not known (cannot be estimated from the available data)):
• reduction in red blood cells which can make the skin pale and cause weakness or breathlessness (anaemia)
• chorea (muscle twitches)
• vomiting
• skin discolouration
• red or brown patches on the skin
• worsening of porphyria (a metabolic disease).
There is a slightly increased risk of developing the following diseases in women taking Hormone Replacement Therapy (HRT):
• dementia (there is no conclusive evidence that this can develop)
If unscheduled bleeding occurs after some time on HRT, you should contact your doctor. If unscheduled bleeding continues after stopping HRT, it may be necessary to perform tests to exclude disease of the endometrium (the lining of the uterus).
Changes can occur in the levels of certain proteins and hormones in the blood. The action of the hormones in the body is not affected. You should tell your doctor that you are taking HRT if you are to have a blood test.
The following side effects have been reported with other HRTs:
• various skin disorders:
- discoloration of the skin especially of the face or neck known as “pregnancy patches” (chloasma)
- painful reddish skin nodules (erythema nodosum)
- rash with target-shaped reddening or sores (erythema multiforme)
If any of the side effects gets serious , or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
6. Contents of the pack and other information
What Femoston contains
• Each pack of Femoston 2/1 Omg Tablets contains two different type of tablets. The arrows marked 1 and 2 show you which order to take the tablets in.
• Each round brick-red tablet contains 2mg of the active ingredient estradiol (as the hemihydrate).
• Each yellow tablet contains two ingredients: 2mg of estradiol (as the hemihydrate) and 10mg of dyhydrogesterone.
• The estradiols in the tablets are made from plant materials.
• Both the tablets also contain lactose, hypromellose, maize starch, colloidal anhydrous silica and magnesium stearate, macrogol 400, talc, titanium dioxide (E171) and yellow iron oxide (E172).
• The brick-red tablets also contain red iron oxide (E172) and black iron oxide (E172).
What Femoston looks like and contents of the pack
Each blister pack contains 14 round, biconvex, brick-red coated tablets marked ‘379’ on one side and plain on the other and 14 round, biconvex, yellow coated tablets marked ‘379’ on one side and plain on the other.
Femoston 2/1 Omg Tablets are available in packs containing 84 tablets.
Product Licence holder
Procured from within the EU and repackaged by the Parallel Import Product Licence holder: S&M Medical Ltd, Chemilines House, Alperton Lane, Wembley, HA0 1DX.
Manufacturer
This product is manufactured by Abbott Biologicals BV, Veerweg 12, NL-8121 AA Olst, The Netherlands.
|POM| PL No. 19488/0065
Leaflet revision date: 01 October 2012
Femoston is a registered trade mark of Solvay Pharmaceuticals BV, The Netherlands.
S065 LEAFLET Femoston 20121001
• Do not store above 30°C.
• Do not use after the expiry date printed on the carton label or blister strip.
• If your doctor tells you to stop taking the capsules, please take them back to the pharmacist for safe disposal. Only keep the capsules if your doctor tells you to.
• If the medicine become discoloured or show any other signs of deterioration, you should seek the advice of your pharmacist who will tell you what to do.
• Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.
PACKAGE LEAFLET: INFORMATION FOR THE USER FEMOSTON 2/1 Omg TABLETS (oestradiol hemihydrate and dydrogesterone)
Your medicine is known as Femoston 2/1 Omg Tablets but will be referred to as Femoston throughout the following patient information leaflet.
Information for other strengths of Femoston also may be present in this leaflet.
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, or 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 or nurse. This includes any possible side effects not listed in this leaflet.
What is in this leaflet
1. What Femoston is and what it is used for
2. What you need to know before you take Femoston
3. Howto take Femoston
4. Possible side effects
5. Howto store Femoston
6. Contents of the pack and other information
1. What Femoston is and what it is used for
Femoston is a Hormone Replacement Therapy (HRT). It contains two types of female hormones, an oestrogen and a progestogen. Femoston is used for:
Relief of symptoms occurring after menopause
During the menopause, the amount of the oestrogen produced by a woman’s body drops. This can cause symptoms such as hot face, neck and chest ("hot flushes"). Femoston alleviates these symptoms after menopause. You will only be prescribed Femoston if your symptoms seriously hinder your daily life.
Prevention of osteoporosis
After the menopause some women may develop fragile bones (osteoporosis). You should discuss all available options with your doctor.
If you are at an increased risk of fractures due to osteoporosis and other medicines are not suitable for you, you can use Femoston to prevent osteoporosis after menopause. 1
If any of the following applies to you. If you are not sure about any of the points below, talk to your doctor before taking Femoston, Do not take Femoston
• If you have or have ever had breast cancer, or if you are suspected of having it
• If you have cancer which is sensitive to oestrogens, such as cancer of the womb lining (endometrium), or if you are suspected of having it
• If you have any unexplained vaginal bleeding
• If you have excessive thickening of the womb lining
(endometrial hyperplasia) that is not being treated.
• If you have or have ever had a blood clot in a vein (thrombosis), such as in the legs (deep venous thrombosis) or the lungs (pulmonary embolism)
• If you have a blood clotting disorder (such as protein C, protein S, or antithrombin deficiency)
• If you have or recently have had a disease caused by blood clots in the arteries, such as a heart attack, stroke or angina
• If you have or have ever had a liver disease and your liver function tests have not returned to normal
• If you have a rare blood problem called “porphyria” which is passed down in families (inherited)
• If you are allergic (hypersensitive) to oestradiol/ dydrogesterone or any of the other ingredients of Femoston (listed in section 6 Further information)
If any of the above conditions appear for the first time while taking Femoston, stop taking it at once and consult your doctor immediately.
When to take special care with Femoston
Tell your doctor if you have ever had any of the following problems, before you start the treatment, as these may return or become worse during treatment with Femoston. If so, you should see your doctor more often for check-ups:
• fibroids inside your womb
• growth of womb lining outside your womb (endometriosis) or a history of excessive growth of the womb lining (endometrial hyperplasia)
• increased risk of developing blood clots (see “Blood clots in a vein (thrombosis)”)
• increased risk of getting a oestrogen-sensitive cancer (such as having a mother, sister or grandmother who has had breast cancer)
• high blood pressure.
• a liver disorder, such as a benign liver tumour
• diabetes
• gallstones
• migraine or severe headaches.
• a disease of the immune system that affects many organs of the body (systemic lupus erythematosus, SLE)
• epilepsy
• asthma
• a disease affecting the eardrum and hearing (otosclerosis)
• a very high level of fat in your blood (triglycerides)
• fluid retention due to cardiac or kidney problems Stop taking Femoston and see a doctor immediately If you notice any of the following when taking HRT:
- any of the conditions mentioned in the ‘Do not take Femoston’ section
- yellowing of your skin or the whites of your eyes (jaundice). These may be signs of a liver disease
- a large rise in your blood pressure (symptoms may be headache, tiredness, dizziness)
- migraine-like headaches which happen for the first time
- if you become pregnant
- if you notice signs of a blood clot, such as:
- painful swelling and redness of the legs
- sudden chest pain
- difficulty in breathing
For more information, see ‘Blood clots in a vein (thrombosis)’ Note: Femoston is not a contraceptive. If it is less than 12 months since your last menstrual period or you are under 50 years old, you may still need to use additional contraception to prevent pregnancy. Speak to your doctor for advice.
HRT and cancer
Excessive thickening of the lining of the womb (endometrial hyperplasia) and cancer of the lining of the womb (endometrial cancer)
Taking oestrogen-only FIRT will increase the risk of excessive thickening of the lining of the womb (endometrial hyperplasia) and cancer of the womb lining (endometrial cancer).
The progestogen in Femoston protects you from this extra risk. Irregular bleeding
You may have irregular bleeding or drops of blood (spotting) during the first 3-6 months of taking Femoston. However, if the irregular bleeding:
• carries on for more than the first 6 months
• starts after you have been taking Femoston for more than 6 months
• carries on after you have stopped taking Femoston see your doctor as soon as possible.
Unexpected bleeding
You will have a bleed once a month (so-called with-drawal bleed) while taking Femoston. But, if you have unexpected bleeding or drops of blood (spotting) besides your monthly bleeding, which:
• carries on for more than the first 6 months
• starts after you have been taking Femoston more than 6 months
• carries on after you have stopped taking Femoston see your doctor as soon as possible
Breast cancer
Evidence suggests that taking combined oestrogen-progestogen and possibly also oestrogen-only HRT increases the risk of breast cancer. The extra risk depends on how long you take HRT. The additional risk becomes clear within a few years. However, it returns to normal within a few years (at most 5) after stopping treatment. Compare
Women aged 50 to 79 who are not taking HRT, on average, 9 to 14 in 1000 will be diagnosed with breast cancer over a 5-year period. For women aged 50 to 79 who are taking oestrogen-progestogen HRT over 5 years, there will be 13 to 20 cases in 1000 users (i.e. an extra 4 to 6 cases).
• Regularly check your breasts. See your doctor if you notice any changes such as:
- dimpling of the skin
- changes in the nipple
- any lumps you can see or feel Ovarian cancer
Ovarian cancer is rare. A slightly increased risk of ovarian cancer has been reported in women taking HRT for at least 5 to 10 years. Women aged 50 to 69 who are not taking HRT, on average about 2 women in 1000 will be diagnosed with ovarian cancer over a 5-year period. For women who have been taking HRT for 5 years, there will be between 2 and 3 cases per 1000 users (i.e. up to 1 extra case).
Effect of HRT on heart and circulation Blood clots in a vein (thrombosis)
The risk of blood clots in the veins is about 1.3 to 3- times higher in HRT users than in non-users, especially during the first year of taking it.
Blood clots can be serious, and if one travels to the lungs, it can cause chest pain, breathlessness, fainting or even death.
You are more likely to get a blood clot in your veins as you get older and if any of the following applies to you.
Inform your doctor if any of these situations applies to you:
• you are unable to walk for a long time because of major surgery, injury or illness (see also section 3, If you need to have surgery)
• you are seriously overweight (BMI >30 kg/m1)
• you have any blood clotting problem that needs long-term treatment with a medicine used to prevent blood clots
• if any of your close relatives has ever had a blood clot in the leg, lung or an other organ
• you have systemic lupus erythematosus (SLE)
• you have cancer.
For signs of a blood clot, see “Stop taking Femoston and see a doctor immediately”.
Compare
Looking at women in their 50s who are not taking HRT, on average, over a 5-year period, 4 to 7 in 1000 would be expected to get a blood clot in a vein.
For women in their 50s who have been taking oestrogen-progestogen HRT for over 5 years, there will be 9 to 12 cases in 1000 users (i.e. an extra 5 cases).
Heart disease (heart attack)
There is no evidence that HRT will prevent a heart attack.
Women over the age of 60 years who use oestrogen-progestogen HRT are slightly more likely to develop heart disease than those not taking any HRT.
Stroke
The risk of getting stroke is about 1.5 times higher in HRT users than in non-users. The number of extra cases of stroke due to use of HRT will increase with age.
Compare
Looking at women in their 50s who are not taking HRT, on average, 8 in 1000 would be expected to have a stroke over a 5-year period. For women in their 50s who are taking HRT, there will be 11 cases in 1000 users, over 5 years (i.e. an extra 3 cases).
Other conditions
• HRT will not prevent memory loss. There is some evidence of a higher risk of memory loss in women who start using HRT after the age of 65. Speak to your doctor for advice.
Using other medicines
Some medicines may interfere with the effect of Femoston. This might lead to irregular bleeding. This applies to the following medicines:
• Medicines for epilepsy (such as phenobarbital, phenytoin and carbamazepin)
• Medicines for tuberculosis (such as rifampicin, rifabutin)
• Medicines for HIV infection (such as nevirapine,efavirenz, ritonavir and nelfinavir)
• Herbal remedies containing St John’s Wort (Hypericum perforatum).
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines including medicines obtained without a prescription, herbal medicines or other natural products. Laboratory tests
If you need a blood test, tell your doctor or the laboratory staff that you are taking Femoston, because this medicine can affect the results of some tests.
Pregnancy and breast-feeding
Femoston is for use in postmenopausal women only. If you become pregnant, stop taking Femoston and contact your doctor.
Important information about some of the ingredients of Femoston
This medicine contains lactose which is a type of sugar.
If you have been told by your doctor that you have a intolerance to some sugars, contact your doctor before taking this medicinal product.
3. How to take Femoston
Always take Femoston exactly as your doctor has told you.
You should check with your doctor or pharmacist if you are not sure.
Flow to take Femoston
Take one tablet every day, without a break between packs. Swallow the tablet with water and with or without food.
Your doctor will aim to give you the lowest dose for the shortest time to treat your symptoms. Speak to your doctor if you think this dose is too strong or not strong enough The usual starting dose is:
During day 1 to 14 of the cycle, 1 tablet daily containing 1 or 2 mg oestradiol.
During day 15 to 28 of the cycle, 1 tablet daily containing 1 or 2 mg oestradiol and 10 mg dydrogesterone.
Immediately after the 28-day cycle you should begin the next treatment.
The days of the week are printed on the back of the blister strips. The tablets from the part marked with arrow 1 should be taken first, then the tablets from the part marked with arrow 2 should be taken. If you are having regular periods you should start taking Femoston within five days of the start of bleeding.
If you are not having regular periods and are not taking any other Flormone Replacement Therapy (FHRT) preparations, or you are switching from a combined continuous FIRT product, you can start taking Femoston on any convenient day.
If you are currently using a ‘cyclic’ or ‘sequential’ FIRT preparation (which involves taking an oestrogen tablet or patch for part of the month, followed by both oestrogen and progestagen tablet or patch for up to 14 days) start taking Femoston the day after you finish the pack i.e. at the end of the progestagen phase.
The doctor may increase the dose later, if necessary. The different tablet strengths are colour-coded for your convenience.
If you are taking Femoston to treat symptoms of the menopause (change of life), your treatment should begin with the dosage Femoston 1/10.
Your doctor will then increase this dose according to your symptoms.
If you are taking Femoston to prevent osteoporosis, your doctor will adjust the dose individually according to your bone mass.
If you take more Femoston than you should If you or somebody else takes too many Femoston tablets, they are unlikely to come to any harm. Nausea (feeling sick), vomiting, sleepiness and dizziness may occur. No treatment is necessary, but if you are worried contact your doctor for advice.
If you forget to take Femoston
Take the missed tablet as soon as you remember. If it is more then 12 hours since you took the last one, take the next dose without taking the forgotten tablet.
Do not take a double dose. Bleeding or spotting may occur if you miss a dose.
If you stop taking Femoston
Do not stop taking Femoston without first talking to your doctor.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
If you need to have surgery
If you are going to have surgery, tell the surgeon that you are taking Femoston. You may need to stop taking Femoston about 4 to 6 weeks before the operation to reduce the risk of a blood clot (see section 2, Blood clots in a vein). Ask your doctor when you can start taking Femoston again.
4 Possible side effects
Like all medicines, Femoston can cause side effects, although not everybody gets them.
The following diseases are reported more often in women using FIRT compared to women not using FIRT:
• breast cancer
• abnormal growth or cancer of the lining of the womb (endometrial hyperplasia or cancer)
• ovarian cancer
• blood clots in the veins of the legs or lungs (venous thromboembolism)
• heart disease
• stroke
• probable memory loss if FIRT is started over the age of 65 For more information about these side effects, see Section 2.
The following serious side effects may occur during treatment with Femoston:
• swelling of the skin around the face and neck. This may cause difficulty breathing
• heart attack
• tumours that may be affected by the levels of progestagens (e.g. meningioma)
• heavy, irregular or painful genital bleeding
If any of these side effects occur you should stop treatment immediately and contact your doctor.
The following side effects may occur during treatment:
Common (in less than 1 in 10, but more than 1 in 100 patients treated):
• migraine
• headache
• feeling sick
• leg cramps
• breast pain or tenderness
• abdominal pain
• pelvic pain
• unscheduled bleeding or spotting
• wind (flatulence)
• feeling weak (asthenia)
• weight changes
Uncommon (in less than 1 in 100, but more than 1 in 1,000 patients treated):
• allergic skin reactions (including rash or itching)
• feeling down (depression)
• vaginal thrush (a vaginal infection due to a fungus called Candida albicans)
• symptoms of cystitis
• high blood pressure
• swelling of the ankles, feet or fingers (peripheral oedema)
• peripheral vascular disease
• varicose veins
• gallbladder disease
• change in sex drive
• back pain
• indigestion
• nervousness
• dizziness
• vaginal discharge
• fibroids get bigger (growths in the womb increase)
• changes in the cervix (the lower end of the womb)
S065 LEAFLET Femstor 20121001
Before you take Femoston
Medical history and regular check-ups
The use of HRT carries risks which need to be considered when deciding whether to start taking it, or whether to carry on taking it.
The experience in treating women with a premature menopause (due to ovarian failure or surgery) is limited. If you have a premature menopause the risks of using HRT may be different. Please talk to your doctor.
Before you start (or restart) HRT, your doctor will ask about your own and your family’s medical history. Your doctor may decide to perform a physical examination.
This may include an examination of your breasts and/ or an internal examination, if necessary.
Once you have started on Femoston you should see your doctor for regular check-ups (at least once a year). At these check-ups, discuss with your doctor the benefits and risks of continuing with Femoston.
Go for regular breast screening, as recommended by your doctor.