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TREMFYA 100 mg SOLUTION FOR INJECTION IN A PRE-FILLED PEN

TREMFYA 100 mg SOLUTION FOR INJECTION IN A PRE-FILLED PEN

Ask a doctor about a prescription for TREMFYA 100 mg SOLUTION FOR INJECTION IN A PRE-FILLED PEN

This page is for general information. Consult a doctor for personal advice. Call emergency services if symptoms are severe.
About the medicine

How to use TREMFYA 100 mg SOLUTION FOR INJECTION IN A PRE-FILLED PEN

Introduction

Package Leaflet: Information for the User

Tremfya 100 mg solution for injection in pre-filled pen

guselkumab

This medicine is subject to additional monitoring, which will allow for the 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 using this medicine because it contains important information for you.

Keep this leaflet, you may need to read it again.

  • Keep this leaflet, you may need to read it again.
  • If you have any further questions, ask your doctor, pharmacist, or nurse.
  • 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 effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

Contents of the pack

  1. What is Tremfya and what is it used for
  2. What you need to know before you use Tremfya
  3. How to use Tremfya
  4. Possible side effects
  5. Storage of Tremfya
  6. Contents of the pack and other information

1. What is Tremfya and what is it used for

Tremfya contains the active substance guselkumab, which is a type of protein called a monoclonal antibody.

This medicine works by blocking the activity of a protein called IL-23, which is found in higher amounts in people with psoriasis and psoriatic arthritis.

Plaque psoriasis

Tremfya is used to treat adults with moderate to severe plaque psoriasis, an inflammatory condition that affects the skin and nails.

Tremfya can improve skin and nail problems and reduce symptoms such as scaling, flaking, shedding, itching, pain, and stinging.

Psoriatic arthritis

Tremfya is used to treat a condition called psoriatic arthritis, an inflammatory disease of the joints, often accompanied by psoriasis. If you have psoriatic arthritis, you will first be given other medicines. If you do not respond well enough to these medicines, you will be given Tremfya to reduce the signs and symptoms of your disease. Tremfya can be used alone or with another medicine called methotrexate.

Using Tremfya for psoriatic arthritis will help you by reducing the signs and symptoms of the disease, slowing down the damage to the cartilage and bones of the joints, and improving your ability to perform normal daily activities.

2. What you need to know before you use Tremfya

Do not use Tremfya

  • If you are allergic to guselkumab or any of the other ingredients of this medicine (listed in section 6). If you think you may be allergic, talk to your doctor before using Tremfya.

If you have an active infection, including active tuberculosis.

  • If you have an active infection, including active tuberculosis.

Warnings and precautions

Talk to your doctor, pharmacist, or nurse before using Tremfya:

  • If you are being treated for an infection.
  • If you have a persistent or recurring infection.
  • If you have tuberculosis or have been in close contact with someone with tuberculosis.
  • If you think you have an infection or symptoms of an infection (see below "Monitoring for infections and allergic reactions").
  • If you have been vaccinated recently or are about to be vaccinated. You should not receive certain types of vaccines (live vaccines) while using Tremfya.

If you are not sure if any of the above conditions apply to you, talk to your doctor, pharmacist, or nurse before using Tremfya.

Following your doctor's instructions, before you receive Tremfya and when you are about to use it, you may need to have blood tests to check if you have high levels of liver enzymes. Increases in liver enzymes may be more frequent in patients who receive Tremfya every 4 weeks than in those who receive Tremfya every 8 weeks (see "How to use Tremfya" in section 3).

Monitoring for infections and allergic reactions

Tremfya has the potential to cause serious side effects, including allergic reactions and infections. You should monitor for signs of these conditions while you are receiving Tremfya.

Stop using Tremfya and talk to your doctor or seek medical help immediately if you notice any signs that may indicate a serious allergic reaction or infection.

Signs of infection may include fever or flu-like symptoms; muscle pain; cough; difficulty breathing; burning when urinating or urinating more frequently than usual; blood in the sputum; weight loss; diarrhea or stomach pain; hot, red, or painful skin, or sores on the body that are different from psoriasis lesions.

Serious allergic reactions have occurred with Tremfya, which may include the following symptoms: swelling of the face, lips, mouth, tongue, or throat; difficulty swallowing or breathing; and hives (see "Serious side effects" in section 4).

Children and adolescents

Tremfya is not recommended for use in children and adolescents under 18 years of age because there are no studies in this age group.

Other medicines and Tremfya

Talk to your doctor or pharmacist:

  • If you are using, have recently used, or might use any other medicine.

If you have been vaccinated recently or are about to be vaccinated. You should not receive certain types of vaccines (live vaccines) while using Tremfya.

  • If you have been vaccinated recently or are about to be vaccinated. You should not receive certain types of vaccines (live vaccines) while using Tremfya.

Pregnancy and breastfeeding

  • Tremfya must not be used during pregnancy, as the effects of this medicine in pregnant women are not known. If you are a woman of childbearing age, you are advised to avoid becoming pregnant and to use an effective method of contraception during treatment with Tremfya and for at least 12 weeks after the last dose of Tremfya.

Tell your doctor if you are pregnant, think you may be pregnant, or plan to become pregnant.

  • Tell your doctor if you are breastfeeding or plan to breastfeed. You and your doctor will decide if you can breastfeed or use Tremfya.

Driving and using machines

Tremfya is unlikely to affect your ability to drive or use machines.

3. How to use Tremfya

Follow the instructions for administration of this medicine exactly as your doctor or nurse has told you. If you are not sure, ask your doctor, nurse, or pharmacist.

How much to use and for how long

Your doctor will decide how long you need to use Tremfya.

Plaque psoriasis

  • The dose is 100 mg (the contents of 1 pre-filled pen) given as an injection under the skin (subcutaneous injection). Your doctor or nurse will probably give you this injection.
  • After the first dose, you will receive the next dose 4 weeks later and then every 8 weeks.

Psoriatic arthritis

  • The dose is 100 mg (the contents of 1 pre-filled pen) given as an injection under the skin (subcutaneous injection). Your doctor or nurse will probably give you this injection.
  • After the first dose, you will receive the next dose 4 weeks later and then every 8 weeks. In some patients, after the first dose, Tremfya may be given every 4 weeks. Your doctor will decide how often you can receive Tremfya.

At first, your doctor or nurse will inject Tremfya for you. However, you and your doctor may decide that you can inject Tremfya yourself. In this case, you will receive proper training on how to inject Tremfya. Talk to your doctor or nurse if you have any questions about injecting Tremfya. It is important that you do not try to inject yourself until your doctor or nurse has shown you how to do it.

To learn how to use Tremfya, read the "Instructions for use" leaflet carefully before using it, which is included in the package.

If you use more Tremfya than you should

If you have received more Tremfya than you should or the dose has been given before the scheduled time, tell your doctor.

If you forget to use Tremfya

If you have missed a dose of Tremfya, tell your doctor.

If you stop using Tremfya

Do not stop using Tremfya without talking to your doctor first. If you stop treatment, your symptoms may come back.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Serious side effects

Tell your doctor or seek medical help immediately if you get any of the following side effects:

Severe allergic reaction(may affect up to 1 in 100 people) - signs may include:

  • difficulty breathing or swallowing
  • swelling of the face, lips, mouth, tongue, or throat
  • intense itching of the skin, with a red rash or lumps

Other side effects

The following side effects are all mild to moderate. If any of these side effects gets serious, talk to your doctor, pharmacist, or nurse immediately.

Some side effects are very common (may affect more than 1 in 10 people):

  • respiratory tract infections

Some side effects are common (may affect up to 1 in 10 people):

  • headache
  • joint pain (arthralgia)
  • diarrhea
  • redness, irritation, or pain at the injection site
  • increased levels of liver enzymes in the blood

Some side effects are uncommon (may affect up to 1 in 100 people):

  • allergic reaction
  • skin rash
  • decrease in the number of a type of white blood cell called neutrophils
  • herpes simplex infections
  • fungal skin infections, such as athlete's foot
  • stomach upset (gastroenteritis)
  • hives

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 Spanish Medicines Monitoring System for Human Use: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of Tremfya

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 label of the pre-filled pen and on the carton after EXP. The expiry date is the last day of the month shown.

Store the pre-filled pen in the outer packaging to protect it from light.

Store in a refrigerator (2°C–8°C). Do not freeze.

Do not shake.

Do not use this medicine if you notice it is cloudy or has an unusual color, or contains large particles. Before using the medicine, take the package out of the refrigerator and keep the pre-filled pen inside until it reaches room temperature, waiting for 30 minutes.

This medicine is for single use only. 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.

6. Container Contents and Additional Information

Tremfya Composition

  • The active ingredient is guselkumab. Each pre-filled syringe contains 100 mg of guselkumab in 1 ml of solution.
  • The other components are histidine, histidine hydrochloride monohydrate, polysorbate 80, sucrose, and water for injectable preparations.

Appearance of Tremfya and Container Contents

Injectable solution (injection). Tremfya is a clear and colorless to light yellow solution. It is presented in a cardboard container containing a single-dose pre-filled syringe and as a multiple container containing 2 (2 containers of 1) single-dose pre-filled syringes. Not all pack sizes may be marketed.

Marketing Authorization Holder

Janssen-Cilag International NV

Turnhoutseweg 30

B-2340 Beerse

Belgium

Manufacturer

Janssen Biologics B.V.

Einsteinweg 101

2333CB Leiden

Netherlands

You can request more information about this medicinal product by contacting the local representative of the marketing authorization holder:

Belgium/Belgique/Belgie

Janssen-Cilag NV

Tel/Tél: +32 14 64 94 11

[email protected]

Lithuania

UAB "JOHNSON & JOHNSON"

Tel: +370 5 278 68 88

[email protected]

Bulgaria

Johnson & Johnson Bulgaria EOOD

Tel: +359 2 489 94 00

[email protected]

Luxembourg/Luxemburg

Janssen-Cilag NV

Tél/Tel: +32 14 64 94 11

[email protected]

Czech Republic

Janssen-Cilag s.r.o.

Tel.: +420 227 012 227

Hungary

Janssen-Cilag Kft.

Tel.: +36 1 884 2858

[email protected]

Denmark

Janssen-Cilag A/S

Tlf: +45 45 94 8282

[email protected]

Malta

AM MANGION LTD.

Tel: +356 2397 6000

Germany

Janssen-Cilag GmbH

Tel: +49 2137 955 955

[email protected]

Netherlands

Janssen-Cilag B.V.

Tel: +31 76 711 1111

[email protected]

Estonia

UAB "JOHNSON & JOHNSON" Estonian branch

Tel: +372 617 7410

[email protected]

Norway

Janssen-Cilag AS

Tlf: +47 24 12 65 00

[email protected]

Greece

Janssen-Cilag Φαρμακευτικη Α.Ε.Β.Ε.

Tηλ: +30 210 80 90 000

Austria

Janssen-Cilag Pharma GmbH

Tel: +43 1 610 300

Spain

Janssen-Cilag, S.A.

Tel: +34 91 722 81 00

[email protected]

Poland

Janssen-Cilag Polska Sp. z o.o.

Tel.: +48 22 237 60 00

France

Janssen-Cilag

Tél: 0 800 25 50 75 / +33 1 55 00 40 03

[email protected]

Portugal

Janssen-Cilag Farmacêutica, Lda.

Tel: +351 214 368 600

Croatia

Johnson & Johnson S.E. d.o.o.

Tel: +385 1 6610 700

[email protected]

Romania

Johnson & Johnson România SRL

Tel: +40 21 207 1800

Ireland

Janssen Sciences Ireland UC

Tel: +353 1 800 709 122

Slovenia

Johnson & Johnson d.o.o.

Tel: +386 1 401 18 00

[email protected]

Iceland

Janssen-Cilag AB

c/o Vistor hf.

Sími: +354 535 7000

[email protected]

Slovak Republic

Johnson & Johnson, s.r.o.

Tel: +421 232 408 400

Italy

Janssen-Cilag SpA

Tel: 800.688.777/+39 02 2510 1

[email protected]

Finland

Janssen-Cilag Oy

Puh/Tel: +358 207 531 300

[email protected]

Cyprus

Βαρνάβας Χατζηπαναγής Λτδ

Τηλ: +357 22 207 700

Sweden

Janssen-Cilag AB

Tel: +46 8 626 50 00

[email protected]

Latvia

UAB "JOHNSON & JOHNSON" Latvian branch

Tel: +371 678 93561

[email protected]

United Kingdom

Janssen-Cilag Ltd.

Tel: +44 1 494 567 444

Date of Last Revision of this Leaflet: 02/2021

Detailed information on this medicinal product is available on the European Medicines Agency website: http://www.ema.europa.eu, and on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/).

Pre-filled Tremfya syringe with white and blue color and activation button and label indicating single-use device

If your doctor decides that you or a caregiver can administer the Tremfya injections at home, you must learn to prepare and inject Tremfya correctly with the pre-filled syringe before attempting the injection.

Read these instructions for use before using the Tremfya pre-filled syringe and each time you renew the prescription for the pre-filled syringe. There may be new information. This instruction guide does not replace the need to talk to your doctor about your disease or treatment.

Also, read the package leaflet carefully before starting to inject yourself and discuss any questions you have with your doctor or nurse.

Storage information with a blue thermometer icon and blue text on a white background

Store in a refrigerator at 2 °C to 8 °C.

Do notfreeze.

Keep Tremfya and all medicines out of the reach of children.

Do notshake the pre-filled syringe at any time.

Blue logo with pill shape and text

Consult your doctor with any questions you may have. For additional help or to share your experience, see the contact information of your local representative in the package leaflet.

Pre-filled syringe with green body, upper push button, transparent window, and lower needle protector with cap

Clock showing 30 minutes next to a medication carton on a light gray background

Inspect the Carton

Remove the carton from the refrigerator.

Keep the pre-filled syringe in the carton and place it on a flat surface at room temperature for at least 30 minutesbefore using it.

Do notheat it in any other way.

Check the Expiration Date(EXP) on the carton.

Do notuse the medicine after the expiration date.

Do notinject the medicine if the carton punctures are broken.

Talk to your doctor or pharmacist to get a new pre-filled syringe.

Knee with three blue adhesive patches applied to the front and inner lateral side

Choose the Injection Site

Choose from the following areas to administer the injection:

  • Front of the thighs(recommended)
  • Lower abdomen

Do notuse the area within 5 cm around the navel.

  • Upper outer arm (if a caregiver is administering the injection)

Do notinject into painful, bruised, red, scaly, hard, or scarred skin.

Hand applying an adhesive patch to the skin after an injection and another hand holding a cotton ball over the injection site

Wash Your Hands

Wash your hands well with warm water and soap.

Clean the Injection Site

Clean the chosen injection site with an alcohol swab and let it dry.

Do nottouch, fan, or blow on the injection site after cleaning.

Injection needle with highlighted bevel in a blue circle and white plunger inside a transparent cylinder

Inspect the Liquid in the Window

Remove the pre-filled syringe from the carton.

Check the liquid in the viewing window. The liquid should be clear or light yellow and may contain tiny translucent or white particles. One or more air bubbles may also be visible.

This is normal.

Do notinject if the liquid is cloudy or has an abnormal color, or contains large particles. If you are unsure, consult your doctor or pharmacist to get a new pre-filled syringe.

Hand holding pre-filled syringe with blue arrows indicating downward pressure and rotation to inject Tremfya

Twist and Remove the Lower Cap

Keep your hands away from the needle guard after removing the cap.

Inject within 5 minutes of removing the needle cap.

Do notreplace the cap because the needle may be damaged.

Do notuse the pre-filled syringe if it falls after removing the cap.

Talk to your doctor or pharmacist to get a new pre-filled syringe.

Hand holding auto-injector with needle inserted perpendicularly into the skin at a 90-degree angle

Place it on the Skin

Place the pre-filled syringe directly on the skin (at a 90-degree angle to the injection site).

Hand holding applicator device with a blue arrow indicating the direction of insertion into the skin

Press the Push Button Down

The medicine is injected when you press. Perform these steps at a pace that feels comfortable for you.

Do notlift the pre-filled syringe during injection. The needle guard will lock, and the full dose will not be administered.

Hand holding applicator device with a short needle pointing downward on the skin

Injection Complete

The injection is complete when the push button is pressed all the way down, you hear a click, and the green body is no longer visible.

Hand holding auto-injector with a blue arrow pointing upward indicating the direction of injection

Lift the Syringe

The yellow line indicates that the needle guard has locked.

Used syringe being disposed of in a red container with a biological hazard symbol after injection

Dispose of the Used Pre-filled Syringe

Place the used pre-filled syringe in a puncture-resistant container after use.

When the container is full, dispose of the material according to the instructions of your doctor or nurse.

Hand holding a white cotton swab pressing on the injection site on the skin

Check the Injection Site

There may be a small amount of blood or liquid at the injection site.

Apply pressure to the skin with a cotton ball or gauze until the bleeding stops.

Do notrub the injection site.

If necessary, cover the injection site with a bandage.

Your injection is complete!

Online doctors for TREMFYA 100 mg SOLUTION FOR INJECTION IN A PRE-FILLED PEN

Discuss dosage, side effects, interactions, contraindications, and prescription renewal for TREMFYA 100 mg SOLUTION FOR INJECTION IN A PRE-FILLED PEN – subject to medical assessment and local rules.

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