Package Leaflet: Information for the Patient
Cibinqo 50 mg film-coated tablets
Cibinqo 100 mg film-coated tablets
Cibinqo 200 mg film-coated tablets
abrocitinib
This medicine is subject to additional monitoring, which will allow for quick identification of new safety information. You can help by reporting any side effects you may get. The last section of section 4 will tell you how to report side effects.
Read all of this leaflet carefully before you start taking this medicine, because it contains important information for you.
In addition to this leaflet, your doctor will give you a patient card, which contains important safety information that you should be aware of. Carry this patient card with you.
Contents of the pack
Cibinqo contains the active substance abrocitinib. It belongs to a group of medicines called Janus kinase inhibitors, which help reduce inflammation. It works by reducing the activity of an enzyme in the body called "Janus kinase", which is involved in inflammation.
Cibinqo is used to treat adults and adolescents from 12 years of age with moderate to severe atopic dermatitis, also known as atopic eczema. By reducing the activity of Janus kinase enzymes, Cibinqo reduces itching and skin inflammation. This, in turn, can reduce sleep disturbances and other consequences of atopic eczema, such as anxiety or depression, and improve overall quality of life.
Do not take Cibinqo
Warnings and precautions
Talk to your doctor or pharmacist before and during treatment with Cibinqo if:
Additional tests
Your doctor will perform blood tests before and during treatment with Cibinqo and may adjust the treatment if necessary.
Children
This medicine is not approved for use in children under 12 years of age, because the safety and benefits of Cibinqo have not yet been established.
Other medicines and Cibinqo
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
In particular, tell your doctor or pharmacist before taking Cibinqo if you are taking any of the following medicines to treat:
Your doctor may ask you to avoid taking or stop taking Cibinqo if you are taking any of the following medicines to treat:
If you are in any of the above situations or are unsure, talk to your doctor or pharmacist before taking Cibinqo.
Pregnancy, contraception, breastfeeding and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Contraception in women
If you are a woman of childbearing age, you should use an effective method of contraception during treatment with Cibinqo and for at least one month after your last dose of treatment. Your doctor may advise you on suitable methods of contraception.
Pregnancy
Do not take Cibinqo if you are pregnant, think you may be pregnant, or are planning to have a baby, as it may harm the unborn baby. Tell your doctor immediately if you become pregnant or think you may have become pregnant during treatment.
Breastfeeding
Do not take Cibinqo while breastfeeding, as it is not known whether this medicine passes into breast milk and may affect the baby. You and your doctor will decide whether to breastfeed or take this medicine.
Fertility
Cibinqo may cause a temporary reduction in fertility in women of childbearing age. This effect is reversible after stopping treatment.
Driving and using machines
Cibinqo has no effect on your ability to drive or use machines.
Cibinqo contains lactose monohydrate and sodium
If your doctor has told you that you have an intolerance to some sugars, contact them before taking this medicine.
This medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially "sodium-free".
Elderly patients
Patients aged 65 years and older may have a higher risk of infections, heart attack, and some types of cancer. Your doctor may decide that Cibinqo is not suitable for you.
Always take this medicine exactly as your doctor has told you. If you are not sure, check with your doctor or pharmacist.
Cibinqo is a tablet that is taken by mouth. It can be used with other eczema medicines that are applied to the skin or used alone.
The recommended initial dose for adults and adolescents (12 to 17 years) with a body weight of at least 59 kg is 100 mg or 200 mg once daily, as prescribed by your doctor. Your doctor may increase or decrease your dose depending on the effect of the medicine.
Some patients may need a lower initial dose, and your doctor may prescribe 100 mg once daily if:
If you have moderate to severe kidney problems, or if you are prescribed other medicines, the initial dose may be 50 mg or 100 mg once daily. The initial dose prescribed for you will be based on your needs and medical history or conditions, so you should always take this medicine exactly as your doctor has told you.
After starting treatment, your doctor may adjust the dose based on the effectiveness of the medicine and any side effects you experience. If the medicine works well, the dose may be reduced. Treatment may also be temporarily or permanently stopped if blood tests show a low white blood cell or platelet count.
If you have taken Cibinqo for 24 weeks and still show no improvement, your doctor may decide to permanently stop treatment.
Swallow the tablet whole with water. Do not break, crush, or chew the tablet before swallowing, as this may change the amount of medicine that enters your body.
You can take the tablet with or without food. If you feel sick (nauseous) while taking this medicine, it may help to take it with food. To help you remember to take your medicine, it is suggested that you take it at the same time every day.
If you take more Cibinqo than you should
If you take more Cibinqo than you should, contact your doctor. You may experience some of the side effects described in section 4.
If you forget to take Cibinqo
If you stop taking Cibinqo
Do not stop taking Cibinqo without talking to your doctor.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Serious side effects
See your doctor and seek medical help immediately if you notice any signs of:
Other side effects
Very common(may affect more than 1 in 10 people)
Common(may affect up to 1 in 10 people)
Uncommon(may affect up to 1 in 100 people)
Reporting of side effects
If you experience 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 through the national reporting system listed in the Appendix. 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 this medicine after the expiry date which is stated on the carton, bottle, and blister pack after "EXP". The expiry date is the last day of the month stated.
This medicine does not require any special storage conditions.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Cibinqo Composition
Each 50 mg tablet contains 50 mg of abrocitinib.
Each 100 mg tablet contains 100 mg of abrocitinib.
Each 200 mg tablet contains 200 mg of abrocitinib.
Tablet core: microcrystalline cellulose (E460i), anhydrous calcium hydrogen phosphate (E341ii), sodium starch glycolate, magnesium stearate (E470b).
Coating: hypromellose (E464), titanium dioxide (E171), lactose monohydrate, macrogol (E1521), triacetin (E1518), red iron oxide (E172) (see section 2 "Cibinqo contains lactose and sodium").
Product Appearance and Packaging Contents
Cibinqo 50 mg tablets are oval, pink tablets, approximately 11 mm long and 5 mm wide, engraved with "PFE" on one side and "ABR 50" on the other.
Cibinqo 100 mg tablets are round, pink tablets, approximately 9 mm in diameter, engraved with "PFE" on one side and "ABR 100" on the other.
Cibinqo 200 mg tablets are oval, pink tablets, approximately 18 mm long and 8 mm wide, engraved with "PFE" on one side and "ABR 200" on the other.
The 50 mg, 100 mg, and 200 mg tablets are available in polyvinylidene chloride (PVDC) blisters with an aluminum foil or high-density polyethylene (HDPE) bottles with a polypropylene cap. Each blister contains 14, 28, or 91 tablets. Each bottle contains 14 or 30 tablets.
Only some pack sizes may be marketed.
Marketing Authorization Holder
Pfizer Europe MA EEIG
Boulevard de la Plaine 17
1050 Bruxelles
Belgium
Manufacturer
Pfizer Manufacturing Deutschland GmbH
Mooswaldallee 1
79108 Freiburg Im Breisgau
Germany
You can request more information about this medicinal product by contacting the local representative of the marketing authorization holder:
| België/Belgique/Belgien Luxembourg/Luxemburg Pfizer NV/SA Tel: +32 (0)2 554 62 11 | Lietuva Pfizer Luxembourg SARL filialas Lietuvoje Tel: + 370 52 51 4000 | 
| 
 | Magyarország Pfizer Kft. Tel.: +36-1-488-37-00 | 
| Ceská republika Pfizer, spol. s r.o. Tel.: +420 283 004 111 | Malta Vivian Corporation Ltd. Tel: +356 21344610 | 
| Danmark Pfizer ApS Tlf.: +45 44 20 11 00 | Nederland Pfizer bv Tel: +31 (0)800 63 34 636 | 
| Deutschland PFIZER PHARMA GmbH Tel: +49 (0)30 550055-51000 | Norge Pfizer AS Tlf: +47 67 52 61 00 | 
| Eesti Pfizer Luxembourg SARL Eesti filiaal Tel: +372 666 7500 | Österreich Pfizer Corporation Austria Ges.m.b.H. Tel: +43 (0)1 521 15-0 | 
| Ελλ?δα Pfizer Ελλ?ς A.E. Τηλ: +30 210 6785 800 | Polska Pfizer Polska Sp. z o.o. Tel.:+48 22 335 61 00 | 
| España Pfizer, S.L. Tel: +34 91 490 99 00 | Portugal Laboratórios Pfizer, Lda. Tel: +351 21 423 5500 | 
| France Pfizer Tél: +33 (0)1 58 07 34 40 | România Pfizer Romania S.R.L. Tel: +40 (0) 21 207 28 00 | 
| Hrvatska Pfizer Croatia d.o.o. Tel: +385 1 3908 777 | Slovenija Pfizer Luxembourg SARL Pfizer, podružnica za svetovanje s podrocja farmacevtske dejavnosti, Ljubljana Tel: + 386 (0)1 52 11 400 | 
| Ireland Pfizer Healthcare Ireland Unlimited Company Tel: +1800 633 363 (toll free) +44 (0)1304 616161 | Slovenská republika Pfizer Luxembourg SARL, organizacná zložka Tel: + 421 2 3355 5500 | 
| Ísland Icepharma hf. Sími: +354 540 8000 | Suomi/Finland Pfizer Oy Puh/Tel: +358 (0)9 43 00 40 | 
| Italia Pfizer S.r.l. Tel: +39 06 33 18 21 | Sverige Pfizer AB Tel: +46 (0)8 550 520 00 | 
| K?προς Pfizer Ελλ?ς Α.Ε. (Cyprus Branch) Τηλ: +357 22 817690 | |
| Latvija Pfizer Luxembourg SARL filiale Latvija Tel: + 371 670 35 775 | 
Date of the last revision of this leaflet:
Other sources of information
Detailed information on this medicinal product is available on the European Medicines Agency website: https://www.ema.europa.eu.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for CIBINQO 50 mg FILM-COATED TABLETS – subject to medical assessment and local rules.