BIFRIL 60MG FILM-COATED TABLETS
Active substance(s): ZOFENOPRIL CALCIUM
Bifril 30 mg 7.5 mg 15 mg 60 mg film-coated tablets
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. 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. This include any possible side effects not
listed in this leaflet. See section 4.
What is in this leaflet:
1. What Bifril is and what it is used for
2. What you need to know before you take Bifril
3. How to take Bifril
4. Possible side effects
5. How to store Bifril
6. Content of the pack and other information
1. WHAT BIFRIL IS AND WHAT IT IS USED FOR
Bifril contains zofenopril calcium 30 mg 7.5 mg 15 mg 60 mg which belongs to a group of blood pressure
lowering medicines called angiotensin converting enzyme (ACE) inhibitors.
Bifril is used to treat the following conditions:
• high blood pressure (hypertension).
• heart attack (acute myocardial infarction) in people who may or may not show signs and symptoms
of heart failure, and who have not received treatment that helps dissolve blood clots (thrombolytic
2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE BIFRIL
Do Not take Bifril if you:
• are allergic (hypersensitive) to any of the ingredients in the product (see Section 6 ‘What Bifril contains’)
• have had any previous allergic reaction to any other ACE inhibitor such as captopril or enalapril
• have a history of severe swelling and itching around the face, nose and throat (angioneurotic edema)
associated with previous ACE inhibitor therapy, or if you suffer from hereditary/idiopathic angioneurotic
oedema (rapid swelling of the skin, tissues, digestive tract and other organs)
• suffer from severe liver problems
• suffer from narrowing of the arteries to the kidneys
• are more than 3 months pregnant (It is also better to avoid Bifril in early pregnancy – see pregnancy
• are a woman of child-bearing age unless using effective contraception.
• have diabetes or impaired kidney function and you are treated with a blood pressure lowering medicine
Warning and precautions
Talk to your doctor before taking Bifril if you:
• have high blood pressure and liver or kidney problems
• have high blood pressure that is caused by a kidney problem or by narrowing of the artery leading to the
kidney (renovascular hypertension)
have recently had a kidney transplant
are undergoing dialysis
are on LDL apheresis (a procedure similar to kidney dialysis that clears your blood of harmful
have abnormally high levels of the hormone aldosterone in your blood (primary aldosteronism)
have a narrowing of the heart valve (aortic stenosis) or thickening of the heart walls (hypertrophic
suffer or have suffered from psoriasis (skin disease characterised by scaly pink patches)
are receiving desensitization treatment (‘allergy injections’) for insect stings.
are taking any of the following medicines used to treat high blood pressure:
- an “angiotensin II receptor blocker” (ARBs) (also known as sartans - for example valsartan,
telmisartan, irbesartan, etc.), in particular if you have diabetes-related kidney problems.
Your doctor may check your kidney function, blood pressure, and the amount of electrolytes (e.g. potassium)
in your blood at regular intervals.
See also information under the heading “Do not take Bifril’’
Your blood pressure may get too low with Bifril, especially after the first dose (this is more likely if you
are also taking diuretics, are dehydrated or on a low-salt diet). If this happens, tell your doctor immediately
and then lie down on your back.
If you are having an operation, tell your anaesthetist that you are taking Bifril before being anaesthetised.
This will help him/her to control your blood pressure and heart rate during the procedure.
In addition if you suffer from heart attack (acute myocardial infarction) and you:
• have low blood pressure (< 100mmHg) or are in a state of circulatory shock (as a result of your heart
problem) – Bifril is not recommended for you
• are over 75 years of age – Bifril should be used with special care.
You must tell your doctor if you think you are (or might become) pregnant. Bifril is not recommended in
early pregnancy, and must not be taken if you are more than 3 months pregnant, as it may cause serious harm
to your baby if used at that stage (see pregnancy section)
Children and adolescents
Do not give this medicine to children and adolescents under the age of 18 years because it is unlikely to be
Other medicines and Bifril
Tell your doctor if you are taking, have recently taken or might take any other medicines.
In particular, tell your doctor if you are taking:
• medicines that increase blood potassium levels( potassium sparing diuretics, such as spironolactone,
triamterene, amiloride or potassium supplements), potassium-containing salt substitutes
• lithium (used to treat mood disorders)
• narcotic drugs (such as morphine)
• antipsychotic drugs (used to treat schizophrenia and similar illnesses)
• antidepressants of the tricyclic type, e.g. amitriptyline and clomipramine
• other high blood pressure medicines and vasodilators (including beta-blockers, alpha-blockers and
diuretics such as hydrochlorothiazide, furosemide, torasemide).
Your doctor may need to change your dose and/or to take other precautions:
If you are taking an angiotensin II receptor blocker (ARB) or aliskiren (see also information under the
headings “Do not take Bifril” and “Warnings and precautions”)
• nitroglycerine and other nitrates used for chest pain (angina)
• antacids including cimetidine (used to treat heartburn and stomach ulcers)
• cyclosporin (used after organ transplants) and other immunosuppressant drugs (medicines that suppress
your body’s defence)
allopurinol (used to treat gout)
insulin or oral anti-diabetic medicines
cytostatic agents (used to treat cancer or diseases which affect the body’s defence system)
corticosteroids (powerful anti-inflammatory drugs)
procainamide (used to control an irregular heart beat)
nonsteroidal anti-inflammatory drugs (NSAIDs, such as aspirin or ibuprofen)
sympathomimetic drugs (medicines that act on the nervous system, including some used to treat asthma
or hay fever and pressor amines, e.g. adrenalin).
Bifril with food, drink and alcohol
Bifril can be taken with food or on an empty stomach, but the tablet is best taken with water. Alcohol
increases the hypotensive (lowering of blood pressure) effect of Bifril; ask your doctor for further advice on
drinking alcohol whilst on this medication.
Pregnancy and breast-feeding
If you are pregnant, if you think you may be pregnant or are planning to have a baby, ask your doctor for
advice before taking this medicine. Your doctor will normally advise you to stop taking Bifril before you
become pregnant or as soon as you know you are pregnant and will advise you to take another medicine
instead of Bifril.
Bifril is not recommended in early pregnancy, and must not be taken when more than 3 months pregnant, as
it may cause serious harm to your baby if used after the third month of pregnancy.
If you are breast-feeding or about to start breast-feeding ask your doctor for advice before taking this
medicine. Bifril is not recommended for mothers who are breast-feeding, and your doctor may choose
another treatment for you if you wish to breast-feed, especially if your baby is newborn, or was born
Driving and using machines
This medicine may cause dizziness or tiredness. If this happens to you, do not drive or operate machinery.
Bifril contains lactose
This product contains lactose - if you know you have an intolerance to some sugars, contact your doctor
before taking this medicine.
3. HOW TO TAKE BIFRIL
Always take Bifril exactly as your doctor has told you. Check with your doctor if you are not sure.
Bifril may be taken with food or on an empty stomach. The tablet is best taken with water.
Treatment of high blood pressure (hypertension)
The normal starting dose of Bifril is 15mg, once a day. Your doctor will gradually adjust the dosage (usually
at four weeks intervals) to find the dose that suits you best. Long-term antihypertensive effects are usually
obtained with 30mg of Bifril, once a day. The maximum dose is 60mg per day, taken in a single or two
If you are dehydrated, have a salt deficiency or are taking diuretics (water pills), it may be necessary to start
your treatment with 7.5mg of Bifril.
Liver or kidney problems
If you have mild to moderate liver impairment or moderate to severe kidney impairment, your doctor will
start your treatment with half the therapeutic dose of Bifril (15mg). If you are receiving dialysis, one-quarter
of the usual therapeutic dose (7.5mg) is needed at the start of your treatment.
Heart attack (acute myocardial infarction)
Bifril treatment should begin within the first 24 hours after the onset of symptoms.
You will receive Bifril tablets twice a day in the morning and evening, as follows:
• 7.5mg twice a day, on the first and second day of treatment
• 15mg twice a day, on the third and fourth day of treatment
• From the fifth day onwards, the dose should be increased to 30mg, twice a day
• Your doctor may adjust your dose or the maximum dose you receive on the basis of your blood pressure
• Treatment will then be continued for a further six weeks, or longer, if symptoms of heart failure persist.
If you take more Bifril than you should
If you accidentally take too many tablets, contact your doctor or nearest Accident & Emergency department
immediately (taking any remaining tablets, the carton or this leaflet with you if possible).
The most frequent symptoms and signs of an overdose are low blood pressure with fainting (hypotension),
very slow heart beat (bradycardia), changes in blood chemicals (electrolytes) and kidney dysfunction.
If you forget to take Bifril
If you miss a dose, take the next dose as soon as you remember. However if a long delay has occurred (e.g.
several hours) so that the next due dose is near, skip the forgotten dose and take the next, scheduled, normal
dose at the usual time. Do not take a double dose to make up for a forgotten tablet.
If you stop taking Bifril
Always consult your doctor before stopping Bifril treatment, whether you are taking it for high blood
pressure or following a heart attack.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
4. POSSIBLE SIDE EFFECTS
Like all medicines, Bifril can cause side effects, although not everybody gets them.
Most side effects associated with ACE inhibitors are reversible and disappear after treatment is finished.
Common side effects (affecting less than 1 person in every 10 treated):
• fatigue (tiredness)
• nausea and/or vomiting
Less common side effects (affecting less than 1 person in every 100 treated):
• general weakness
• muscle cramps
• skin rash.
Rare side effects (affecting less than 1 person in every 1000 treated):
• rapid swelling and itching, especially around the face, mouth and throat, with possible difficulty in
In addition to the side effects reported with Bifril, the following have generally been reported with ACE
• Severe low blood pressure at the start of treatment or when the dosage is increased, with dizziness,
impaired vision, fainting (syncope)
• Increased or irregular heartbeat, palpitations and chest pain (heart attack or angina pectoris)
• Impaired consciousness, sudden dizziness, suddenly impaired vision or weakness and/or loss of
sense of touch on one side of the body (transient ischaemic attack or stroke)
• Peripheral oedema (accumulation of water in the limbs), low blood pressure on standing, chest pain,
muscle aches and/or cramps
• Reduced kidney function, changes in the amount of daily urine, presence of proteins in the urine
• Abdominal pain, diarrhoea, constipation, dry mouth
• Allergic reactions like skin rash, hives (urticaria), itching, peeling, redness, loosening and blistering
of the skin (toxic epidermal necrolysis), worsening of psoriasis (a skin disease characterised by scaly
pink patches), hair loss (alopecia)
• Increased sweating and flushing
• Mood changes, depression, sleep disorders, altered skin sensations such as burning, prickling, or
tingling (paraesthesia), disorders of balance, confusion, ringing in the ears (tinnitus), taste disturbances,
• Difficulty in breathing, narrowing of the airways in the lung (bronchospasm), sinusitis, runny or
stuffy nose (rhinitis), inflammation of the tongue (glossitis), bronchitis
• Yellowing of the skin (jaundice), inflammation of the liver or pancreas (hepatitis, pancreatitis),
bowel obstruction (ileus)
• Changes in blood tests, such as red blood cell, white blood cell or platelet count or a reduction in all
kinds of blood cells (pancytopenia). Contact your doctor if you find that you bruise easily or develop
an unexplained sore throat or fever
• Increased blood levels of liver enzymes (transaminases) and bilirubin, increased blood urea and
• Anaemia due to rupture of red blood cells (haemolytic anaemia), which may occur if you suffer from
G6PD (glucose-6-phosphate dehydrogenase) deficiency.
If you get any side effects , talk to your doctor or pharmacist. This includes any possible side effects not
listed in this leaflet.
You can also report side effects directly via the national reporting system listed in Appendix 5.
By reporting side effects you can help provide more information on the safety of this medicine.
5. HOW TO STORE BIFRIL
Keep this medicine out of the sight and reach of children.
This medicinal product does not require any special storage condition.
Do not take Bifril after the expiry date (‘EXP’) which is stated on the box and blister pack.
Do not throw away any medicines via wastewater . Ask your pharmacist how to throw away medicines you
no longer use. These measures will help to protect the environment.
6. CONTENT OF THE PACK AND OTHER INFORMATION
What Bifril contains
The active substance is zofenopril calcium 30 mg 7.5 mg 15 mg 60 mg. The other ingredients are
microcrystalline cellulose, lactose monohydrate, croscarmellose sodium, magnesium stearate, colloidal
anhydrous silica, hypromellose, titanium dioxide (E171), macrogol 400, and macrogol 6000 (see Section 2
‘Bifril contains lactose’).
What Bifril looks like and contents of the pack
Bifril 30 is available as white, oblong film-coated tablets in packs of 7, 14, 15, 28, 30, 50, 56, 90 or 100 filmcoated tablets and in packs with perforated unit dose blisters of 50 and 56 film-coated tablets.
Bifril 7.5 is available as white, round film-coated tablets with convex faces in packs of 12, 14, 15, 28, 30, 48,
50, 56, 90 or 100 film-coated tablets and in packs with perforated unit dose blisters of 50 and 56 film-coated
Bifril 15 is available as white, oblong film-coated tablets in packs of 12, 14, 15, 28, 30, 50, 56, 90 or 100
film-coated tablets and in packs with perforated unit dose blisters of 50 and 56 film-coated tablets.
Bifril 60 is available as white, oblong film-coated tablets in packs of 14, 15, 28, 30, 50, 56, 90 or 100 filmcoated tablets and in packs with perforated unit dose blisters of 50 and 56 film-coated tablets.
Not all pack sizes may be marketed.
Marketing Authorisation Holder
To be completed nationally
A. MENARINI Manufacturing Logistics and Services Srl
Campo di Pile, L'Aquila, Italy.
Menarini –Von Heyden GmbH
Leipziger Strasse 7-13,
01097 – Dresden (Germany).
This medicinal product is authorised in the Member States of the EEA under the following names:
The Netherlands: Zopranol
United Kingdom: Bifril
This leaflet was last revised in MM/YYYY
National information, including pack sizes/presentations nationally approved and actually marketed, local
representatives and/or co-promotion, other sources of information (e.g. websites)
Source: Medicines and Healthcare Products Regulatory Agency
Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.