Finasteride 5mg Film Coated Tablets
Out of date information, search anotherPackage leaflet: Information for the user FINASTERIDE 5 mg Film-coated Tablets Finasteride
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.
• 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 effect talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.
What is in this leaflet:
1. What Finasteride is and what it is used for
2. What you need to know before you take Finasteride
3. How to take Finasteride
4. Possible side effects
5. How to store Finasteride
6. Contents of the pack and other Information
1. What Finasteride is and what it is used for
Finasteride belongs to a group of medicines called 5-alpha reductase inhibitors. They act by reducing the size of the prostate gland in men.
Finasteride is used in the treatment and control of benign enlargement of the prostate (benign prostatic hyperplasia - BPH). It causes regression of the enlarged prostate, improved urinary flow and symptoms caused by BPH, and reduced the risk of acute urinary retention and the need for surgery.
2. What you need to know before you take Finasteride Do NOT take Finasteride
- If you are allergic to finasteride or any of the other ingredients of this medicine (listed in section 6).
- If you are a woman (see also under “Pregnancy and breast-feeding”)
- If you are a child.
Warnings and precautions
Talk to your doctor or pharmacist before taking Finasteride.
- If you have a large amount of residual urine and/or severely reduced urinary flow. If this is the case, you should be closely monitored for narrowing of the urinary tract.
- If you have a reduced liver function. This finasteride plasma level may be increased in these patients.
Speak to your doctor if any of the above applies to you now or in the past.
You should promptly report to your doctor any changes in your breast tissue such as lumps, pain, enlargement of the breast tissue or nipple discharge as these may be signs of a serious condition, such as breast cancer.
A clinical examination (including digital rectal examination) and a determination of prostate-specific-antigen (PSA) in serum should be carried out prior to initiating therapy with finasteride and during treatment.
Other medicines and Finsteride
No significant drug interactions have been identified.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Pregnancy and breast-feeding
Finasteride is only intended for men.
Women who are pregnant or may become pregnant should not handle broken or crushed Finasteride tablets. If finasteride is absorbed through the skin or taken by mouth by a woman pregnant with a male foetus, the child may be born with malformed genital organs. The tablets are film-coated, which prevents contact with finasteride provided the tablets are not broken or crushed.
Driving and using machines
There are no data which suggest that Finasteride affects the ability to drive or use machines. Finsteride contains lactose
This medicine contains lactose. Patients with rare hereditary problems of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine. Please consult your doctor before taking Finasteride 5 mg if you know that you suffer from a sugar intolerance.
3. How to take Finasteride
Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.
The recommended dose is 1 tablet daily (equivalent to 5 mg finasteride).
The film-coated tablets can either be taken on an empty stomach or with a meal. The film-coated tablets should be swallowed whole and should not be divided or crushed. Although early improvement may be seen, treatment for at least six months may be necessary to assess whether a beneficial response has been achieved.
Your doctor will tell you how long you should continue to take Finasteride 5 mg. Do not interrupt treatment early or the symptoms may come back.
Patients with impaired liver function
There is no experience of the use of Finasteride 5 mg in patients with restricted liver function (see also “Take special care with Finasteride 5 mg”).
Patients with impaired kidney function
No dosage adjustment is required. The use of Finasteride 5 mg in patients who have to undergo haemodialysis has not been investigated to date.
Older people
No dosage adjustment is required.
Please speak to your doctor or pharmacist if you feel that the effect of Finasteride 5 mg is too strong or too weak.
If you take more Finasteride than you should
If you take more Finasteride 5 mg than you should or if children have been taking medicine by accident please notify your doctor immediately.
If you forget to take Finasteride
If you forget to take a dose of Finasteride 5 mg, you can take it as soon as you remember unless it is almost time for the next dose, in which case you should continue with your medication as prescribed. Do not take a double dose to make up for a forgotten dose.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Allergic reactions (frequency cannot be estimated from the available data)
If you have an allergic reaction, stop taking it and see your doctor straight away. The signs may include:
- skin rashes, itching, or lumps under your skin (hives)
- swelling of your lips_and face.
Other possible side effects during treatment:
Common side effects (may affect up to 1 in 10 people) may include:
- you may be unable to have an erection (impotence)
- you may have less desire to have sex
These side effects above may disappear after a while if you continue taking Finasteride. If not, they usually resolve after stopping Finasteride.
- you may have a decrease in the amount of semen released during sex. This decrease in the amount of semen does not appear to affect normal sexual function.
Uncommon (may affect up to 1 in 100 people)
- Rash,
- Sleepiness
- Breast swelling or tenderness
- Problems with ejaculation
Not known (frequency cannot be estimated from the available data)
- Palpitations (feeling your heartbeat)
- Changes in the way your liver is working, which can be shown by a blood test
- Pain in your testicles
- Male infertility and/or poor quality of semen.
- Depression
- Decrease in sex drive that may continue after stopping the medication
- Problems with erection that may continue after stopping the medication
You should promptly report to your doctor any changes in your breast tissue such as lumps, pain, enlargement or nipple discharge as these may be signs of a serious condition, such as breast cancer.
Finasteride may affect the result of PSA-laboratory test.
Reporting of side effects
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side
effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard
By reporting side effects you can help provide more information on the safety of this medicine.
5. How to store Finasteride
Keep this medicine out of the sight and reach of children.
Do not store above 30°C
Do not use this medicine after <EXP>. the expiry date which is stated on the container and the outer packaging. The expiry date refers to the last day of that month.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
6. Contents of the pack and other Information What Finasteride contains:
- The active substance is finasteride. Each film-coated tablet contains 5 mg finasteride.
- The other ingredients in the tablet core are lactose monohydrate, microcrystalline cellulose, Pregelatinised starch (maize), povidone K30, sodium starch glycolate (type A), magnesium stearate, sodium Laurilsulfate. The tablet coating Opadry 03G20795 Blue contains (hypromellose, (E464), titanium dioxide (E171), macrogol 6000, macrogol 400, indigo carmine lake (E132)
What Finasteride looks like and contents of the pack:
Finasteride 5 mg film-coated tablets are blue, capsule shaped tablets, with the inscription “FNT5” on one side and plain on the other Blister packs PVC/PVDC/Aluminium: 10, 14, 15, 20, 30, 50, 50x1, 56, 60, 98, 100, 100x1 tablets.
Not all pack sizes may be marketed.
Marketing Authorisation Holder and Manufacturer:
The marketing authorisation holder is TEVA UK Limited, Eastbourne, BN22 9AG and the Company responsible for manufacture:
Teva Pharmaceutical Works Private Limited Pallagi ut 13. Debrecen H-4042 Hungary or
TEVA UK Limited Brampton Road, Hampden Park, Eastbourne, East Sussex, BN22 9AG United Kingdom.
This leaflet was revised in September 2014
PL 00289/1024