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Vfend®
Voriconazole
50 mg & 200 mg film-coated tablets
Reference Market: EMA
PACKAGE LEAFLET
Package Leaflet: Information for the user
VFEND® 50 mg film-coated tablets
VFEND® 200 mg film-coated tablets
Voriconazole
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
What is in this leaflet
VFEND contains the active substance voriconazole. VFEND is an antifungal medicine. It works by killing or stopping the growth of the fungi that cause infections.
It is used for the treatment of patients (adults and children over the age of 2) with:
VFEND is intended for patients with worsening, possibly life-threatening, fungal infections.
Prevention of fungal infections in high risk bone marrow transplant recipients.
This product should only be taken under the supervision of a doctor.
Do not take VFEND
If you are allergic to voriconazole or any of the other ingredients of this medicine (listed in section 6).
It is very important that you inform your doctor or pharmacist if you are taking or have taken any other medicines, even those that are obtained without a prescription, or herbal medicines.
The medicines in the following list must not be taken during your course of VFEND treatment:
Warnings and precautions
Talk to your doctor, pharmacist or nurse before taking VFEND if:
You should avoid any sunlight and sun exposure while being treated. It is important to cover sun exposed areas of skin and use sunscreen with high sun protection factor (SPF), as an increased sensitivity of skin to the sun’s UV rays can occur. These precautions are also applicable to children.
While being treated with VFEND:
If you develop skin disorders as described above, your doctor may refer you to a dermatologist, who after consultation may decide that it is important for you to be seen on a regular basis. There is a small chance that skin cancer could develop with long-term use of VFEND.
If you develop signs of ‘adrenal insufficiency’ where the adrenal glands do not produce adequate amounts of certain steroid hormones such as cortisol which may lead to symptoms such as: chronic, or long lasting fatigue, muscle weakness, loss of appetite, weight loss, abdominal pain, please tell your doctor.
If you develop signs of ‘Cushing’s syndrome’ where the body produces too much of the hormone cortisol
which may lead to symptoms such as: weight gain, fatty hump between the shoulders, a rounded face, darkening of the skin on the stomach, thighs breasts, and arms, thinning skin, bruising easily, high blood sugar, excessive hair growth, excessive sweating, please tell your doctor.
Your doctor should monitor the function of your liver and kidney by doing blood tests.
Children and adolescents
VFEND should not be given to children younger than 2 years of age.
Other medicines and VFEND
Please tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including those that are obtained without a prescription.
Some medicines, when taken at the same time as VFEND, may affect the way VFEND works or VFEND may affect the way they work.
Tell your doctor if you are taking the following medicine, as treatment with VFEND at the same time should be avoided if possible:
Tell your doctor if you are taking either of the following medicines, as treatment with VFEND at the same time should be avoided if possible, and a dose adjustment of voriconazole may be required:
Tell your doctor if you are taking any of the following medicines, as a dose adjustment or monitoring may be required to check that the medicines and/ or VFEND are still having the desired effect:
Pregnancy and breast-feeding
VFEND must not be taken during pregnancy, unless indicated by your doctor. Effective contraception must be used in women of childbearing potential. Contact your doctor immediately if you become pregnant while taking VFEND.
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Driving and using machines
VFEND may cause blurring of vision or uncomfortable sensitivity to light. While affected, do not drive or operate any tools or machines. Contact your doctor if you experience this.
VFEND contains lactose
If you have been told by your doctor that you have an intolerance to some sugars, tell your doctor before taking VFEND.
VFEND contains sodium
This medicine contains less than 1 mmol sodium (23 mg) per 50 mg tablet, that is to say essentially ‘sodium‑free’.
This medicine contains less than 1 mmol sodium (23 mg) per 200 mg tablet, that is to say essentially ‘sodium-free’.
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
Your doctor will determine your dose depending on your weight and the type of infection you have.
The recommended dose for adults (including elderly patients) is as follows:
Tablets |
||
Patients 40 kg and above |
Patients less than 40 kg |
|
Dose for the first 24 hours |
400 mg every 12 hours for |
200 mg every 12 hours for |
(Loading Dose) |
the first 24 hours |
the first 24 hours |
Dose after the first 24 hours |
200 mg twice a day |
100 mg twice a day |
(Maintenance Dose) |
Depending on your response to treatment, your doctor may increase the daily dose to 300 mg twice a day.
The doctor may decide to decrease the dose if you have mild to moderate cirrhosis.
Use in children and adolescents
The recommended dose for children and teenagers is as follows:
Tablets |
||
Children aged 2 to less than 12 years and teenagers aged 12 to 14 years weighing less than 50 kg |
Teenagers aged 12 to 14 years weighing 50 kg or more; and all teenagers older than 14 |
|
Dose for the first 24 hours (Loading Dose) |
Your treatment will be started as an infusion |
400 mg every 12 hours for the first 24 hours |
Dose after the first 24 hours (Maintenance Dose) |
9 mg/kg twice a day (a maximum dose of 350 mg twice daily) |
200 mg twice a day |
Depending on your response to treatment, your doctor may increase or decrease the daily dose.
Take your tablet at least one hour before, or one hour after a meal. Swallow the tablet whole with some water.
If you or your child are taking VFEND for prevention of fungal infections, your doctor may stop giving VFEND if you or your child develop treatment related side effects.
If you take more VFEND than you should
If you take more tablets than prescribed (or if someone else takes your tablets) you must seek medical advice or go to the nearest hospital casualty department immediately. Take your box of VFEND tablets with you. You may experience abnormal intolerance to light as a result of taking more VFEND than you should.
If you forget to take VFEND
It is important to take your VFEND tablets regularly at the same time each day. If you forget to take one dose, take your next dose when it is due. Do not take a double dose to make up for a forgotten dose.
If you stop taking VFEND
It has been shown that taking all doses at the appropriate times may greatly increase the effectiveness of your medicine. Therefore unless your doctor instructs you to stop treatment, it is important to keep taking VFEND correctly, as described above.
Continue taking VFEND until your doctor tells you to stop. Do not stop treatment early because your infection may not be cured. Patients with a weakened immune system or those with difficult infections may require long-term treatment to prevent the infection from returning.
When VFEND treatment is stopped by your doctor you should not experience any effects.
If you have any further questions on the use of this medicine, ask your doctor, pharmacist or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If any side effects occur, most are likely to be minor and temporary. However, some may be serious and need medical attention.
Serious side effects - Stop taking VFEND and see a doctor immediately
Other side effects
Very common: may affect more than 1 in 10 people
- Visual impairment (change in vision including blurred vision, visual color alterations, abnormal intolerance to visual perception of light, colour blindness, eye disorder, halo vision, night blindness, swinging vision, seeing sparks, visual aura, visual acuity reduced, visual brightness, loss of part of the usual field of vision, spots before the eyes)
- Fever
- Rash
- Nausea, vomiting, diarrhoea
- Headache
- Swelling of the extremities
- Stomach pains
- Breathing difficulties
- Elevated liver enzymes
Common: may affect up to 1 in 10 people
- Inflammation of the sinuses, inflammation of the gums, chills, weakness
- Low numbers of some types, including severe, of red (sometimes immune-related) and/or white blood cells (sometimes with fever), low numbers of cells called platelets that help the blood to clot
- Low blood sugar, low blood potassium, low sodium in the blood
- Anxiety, depression, confusion, agitation, inability to sleep, hallucinations
- Bleeding in the eye
- Low blood pressure, inflammation of a vein (which may be associated with the formation of a blood clot)
- Acute breathing difficulty, chest pain, swelling of the face (mouth, lips and around eyes), fluid accumulation in the lungs
- Jaundice, inflammation of the liver and liver injury
- Skin rashes which may lead to severe blistering and peeling of the skin characterized by a flat, red
area on the skin that is covered with small confluent bumps, redness of the skin
- Itchiness
- Hair loss
- Back pain
- Kidney failure, blood in the urine, changes in kidney function tests
Uncommon: may affect up to 1 in 100 people
- Very fast heart rate or skipped heartbeats, sometimes with erratic electrical impulses
Rare: may affect up to 1 in 1000 people
Side effects with frequency not known:
- Freckles and pigmented spots
Other significant side effects whose frequency is not known, but should be reported to your doctor immediately:
As VFEND has been known to affect the liver and the kidney, your doctor should monitor the function of your liver and kidney by doing blood tests. Please advise your doctor if you have any stomach pains or if your stools have a different consistency.
There have been reports of skin cancer in patients treated with VFEND for long periods of time.
Sunburn or severe skin reaction following exposure to light or sun was experienced more frequently in children. If you or your child develops skin disorders, your doctor may refer you to a dermatologist, who after consultation may decide that it is important for you or your child to be seen on a regular basis. Elevated liver enzymes were also observed more frequently in children.
If any of these side effects persist or are troublesome, please tell your doctor.
Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. By reporting side 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 Vfend after the expiry date which is stated on the label. The expiry date refers to the last day of that month.
Store below 30°C.
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.
What VFEND contains
What VFEND looks like and contents of the pack
VFEND 50 mg film-coated tablets are supplied as white to off-white round film-coated tablets with Pfizer marked on one side and VOR50 on the reverse.
VFEND 200 mg film-coated tablets are supplied as white to off-white capsule shaped film-coated tablets with Pfizer marked on one side and VOR200 on the reverse.
VFEND 50 mg film-coated tablets and 200 mg film-coated tablets are available as packs of 2, 10, 14, 20, 28, 30, 50, 56 and 100.
HDPE tablet containers containing 2, 30 or 100 film-coated tablets.
PVC / Aluminium blister in cartons of 2, 10, 14, 20, 28, 30, 50, 56 or 100 film-coated tablets.
PVC / Aluminium/PVC/PVDC blister in cartons of 2, 10, 14, 20, 28, 30, 50, 56 or 100 film-coated tablets
Not all pack sizes may be marketed.
Marketing Authorisation Holder
Pfizer Europe MA EEIG Boulevard de la Plaine 171050 Bruxelles Belgium
Manufacturing of the bulk, Packager & Releaser:
Pfizer Italia S.r.l.
LocalitÀ Marino del Tronto
63100 - Ascoli Piceno
Italy
The Leaflet was last revised in May 2022
THIS IS A MEDICAMENT
Keep all medicaments out of reach and sight of children Council of Arab Health Ministers Union of Arabic Pharmacists |
status: active
Domain: Human use
Combined pharmaceutical dose form:
Legal Status of Supply: Medicinal product subject to medical prescription
Clinical Information