Package leaflet: Information for the patient
IKERVIS 1 mg/mL, eye drops, emulsion
ciclosporin
1. What IKERVIS is and what it is used for
2. What you need to know before you use IKERVIS
3. How to use IKERVIS
4. Possible side effects
5. How to store IKERVIS
6. Contents of the pack and other information
1. What IKERVIS is and what it is used for
IKERVIS contains the active substance, ciclosporin. Ciclosporin belongs to a group of medicines known as immunosuppressive agents that are used to reduce inflammation.
IKERVIS is used to treat adults with severe keratitis (inflammation of the cornea, the transparent layer in the front part of the eye). It is used in those patients who have dry eye disease, which has not improved despite treatment with tear substitutes (artificial tears).
Talk to a doctor if you do not feel better or if you feel worse.
You should visit your doctor at least every 6 months to assess the effect of IKERVIS.
2. What you need to know before you use IKERVIS
Only use IKERVIS for dropping in your eye(s).
Talk to your doctor or pharmacist before using IKERVIS
Contact lenses can further damage the transparent front part of the eye (cornea). Therefore, you should remove your contact lenses at bedtime before using IKERVIS; you can reinsert them when you wake up.
IKERVIS should not be used in children and adolescents below 18 years old.
Tell your doctor or pharmacist if you are using, have recently used or might use any other medicines.
Talk to your doctor if you are using eye drops containing steroids with IKERVIS as these might increase the risk of side effects.
IKERVIS eye drops should be used at least 15 minutes after any other eye drops are used.
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 using this medicine.
IKERVIS should not be used if you are pregnant.
If you could become pregnant you must use contraception while using this medicine.
IKERVIS is likely to be present in breast milk in very small amounts. If you are breast feeding talk to your doctor before using this medicine.
Your vision may be blurred immediately after using IKERVIS eye drops. If this happens, wait until your vision clears before you drive or use machines.
IKERVIS contains cetalkonium chloride
This medicine contains 0.05 mg cetalkonium chloride in 1 mL. You should remove contact lenses before using this medicine and you can reinsert them when you wake up. Cetalkonium chloride may cause eye irritation. If you feel abnormal eye sensation, stinging or pain in the eye after using this medicine, talk to your doctor.
3. How to use IKERVIS
Always use 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 one drop in each affected eye, once daily at bedtime.
Follow these instructions carefully and ask your doctor or pharmacist if there is anything you do not understand.
If a drop misses your eye, try again.
If you use more IKERVIS than you should, rinse your eye with water. Do not put in any more drops until it is time for your next regular dose.
If you forget to use IKERVIS, continue with the next dose as planned. Do not use a double dose to make up for the forgotten dose. Do not use more than one drop each day in the affected eye(s).
If you stop using IKERVIS without speaking to your doctor, the inflammation of the transparent front part of your eye (known as keratitis) will not be controlled and could lead to impaired vision.
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.
The most common side effects are in and around the eyes.
Very common (may affect more than 1 in 10 people)
- Eye pain,
- Eye irritation
Common (may affect up to 1 in 10 people)
- Redness of the eyelid,
- Watery eyes,
- Eye redness,
- Blurred vision,
- Swelling of the eyelid,
- Redness of the conjunctiva (thin membrane covering the front part of the eye),
- Itching in the eye
Uncommon (may affect up to 1 in 100 people)
- Discomfort in or around the eye when the drops are put into the eye, including feeling that there is something in the eye,
- Irritation or swelling of the conjunctiva (thin membrane covering the front part of the eye),
- Tear disorder,
- Eye discharge,
- Irritation or inflammation of the conjunctiva (thin membrane covering the front part of the eye),
- Inflammation of the iris (coloured part of the eye) or eyelid,
- Deposits in the eye,
- Abrasion to the outer layer of the cornea,
- Red or swollen eyelids,
- Cyst in the eyelid
- Immune response or scarring in the cornea,
- Itching in the eyelid,
- Bacterial infection or inflammation of the cornea (transparent front part of the eye),
- Painful rash around the eye caused by the herpes zoster virus,
- Headache
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 (see contact details below).
HPRA Pharmacovigilance
By reporting side effects you can help provide more information on the safety of this medicine.
5. How to store IKERVIS
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the outer carton, the aluminium pouch and on the single-dose containers after “EXP”. The expiry date refers to the last day of that month.
Do not freeze.
Store below 25°C.
After opening of the aluminium pouches, the single-dose containers should be kept in the pouches in order to protect from light and avoid evaporation. Discard any opened individual single-dose container with any remaining emulsion immediately after use.
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
IKERVIS is a milky white eye drops emulsion.
It is supplied in single-dose containers made of a low-density polyethylene (LDPE).
Each single-dose container contains 0.3 mL eye drops, emulsion.
The single-dose containers are wrapped in a sealed aluminium pouch.
Pack sizes: 30 and 90 single-dose containers.
Not all pack sizes may be marketed.
SANTEN Oy
For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder: