Patient Information Leaflet

QUINUX20 mg/0.8 ml injectable solution in pre-filled syringe

Methotrexate

Read this leaflet carefully before you start using this medicine because it contains important information for you.

• Keep this leaflet, as you may need to read it again.
• If you have any questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you only. Do not give it to others even if they have the same symptoms as you, as it may harm them.
• If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this leaflet. See section 4.

Quinux contains methotrexate as the active ingredient.

Methotrexate is a substance with the following properties:

• interferes with the growth of certain cells in the body that reproduce quickly,
• reduces the activity of the immune system (the body's defense mechanism),
• has anti-inflammatory effects.

Quinux is indicated for the treatment of:

• active rheumatoid arthritis in adult patients,
• severe active polyarticular juvenile idiopathic arthritis (JIA), when the response to nonsteroidal anti-inflammatory drugs (NSAIDs) has not been adequate,
• severe and debilitating psoriasis that does not respond adequately to other treatments such as phototherapy, PUVA (psoralen + UVA radiation) and retinoids, and severe psoriatic arthritis in adult patients.

Rheumatoid arthritis (RA) is a chronic collagen disease characterized by inflammation of the synovial membranes (joint membranes). These membranes produce a fluid that acts as a lubricant in many joints. Inflammation causes the membrane to thicken and the joint to swell.

Juvenile arthritis affects children and adolescents under 16 years old. Polyarticular forms are indicated if there is involvement of 5 or more joints in the first 6 months of the disease.

Psoriatic arthritis is a type of arthritis with psoriatic lesions on the skin and nails, especially in the joints of the fingers of the hands and feet.

Poriasis is a chronic and frequent skin disease characterized by red patches covered with thick, dry, silver, and adherent scales.

Quinux modifies and slows the progression of the disease.

No use Quinux

• If you are allergic to methotrexate or any of the other components of this medication (listed in section 6),
• If you have severe liver or kidney disease or blood disorders,
• If you regularly consume large amounts of alcohol,
• If you have a severe infection, for example, tuberculosis, HIV, or other immunodeficiency syndromes,
• If you have a mouth ulcer, stomach ulcer, or intestinal ulcer,
• If you are pregnant or breastfeeding (see section "Pregnancy, breastfeeding, and fertility"),
• If you receive vaccines made with attenuated microorganisms at the same time.

Warnings and precautions

Consult your doctor or pharmacist before starting to use Quinux:

• If you are elderly or generally feel unwell and weak,
• If you have altered liver function,
• If you have dehydration (loss of fluids) problems.

A severe lung hemorrhage has been reported in patients with underlying rheumatological disease who received methotrexate. If you notice blood when coughing or spitting, you should contact your doctor immediately.

Recommended follow-up tests and safety measures

Even when Quinux is administered at low doses, severe side effects can occur. To detect them in time, your doctor will need to perform blood tests and checks.

Before starting treatment with Quinux

Before starting treatment, you will have blood tests to check that you have enough blood cells and tests to check liver function and to see if you have hepatitis (liver infection). In addition, your liver function, albumin serum concentration (a protein in the blood), hepatitis status, and kidney function will be monitored. Your doctor may also decide to perform other liver tests, some of which may be images of your liver and others may require a small sample of liver tissue for closer examination. Your doctor may also check if you have tuberculosis (an infectious disease with small nodules in the affected tissue) and may perform a chest X-ray or lung function test.

During treatment

Your doctor may perform the following tests:

• Examination of the mouth and throat to detect changes in the mucous membranes, such as inflammation or ulceration,
• Blood test/hemogram with blood cell count and measurement of serum methotrexate levels,
• Blood test to monitor liver function,
• Imaging tests to monitor liver condition,
• Small sample of liver tissue extracted for closer examination,
• Blood test to monitor kidney function,
• Review of the respiratory system and, if necessary, lung function test.

It is very important that you attend these scheduled tests.

If the results of any of these tests are notable, your doctor will adjust your treatment accordingly.

Methotrexate can affect the immune system and vaccine results.

It can also affect the results of immunological tests. It can intensify chronic inactive infections (for example, herpes zoster [“culebrillas”], tuberculosis, hepatitis B or C). During treatment with Quinux, do not receive vaccines made with attenuated microorganisms.

Methotrexate can make the skin more sensitive to sunlight. Avoid intense sunlight and do not use sunbeds or ultraviolet lamps without medical advice. To protect your skin from intense sunlight, wear suitable clothing or use a high-protection sunscreen.

During treatment with methotrexate, dermatitis caused by radiation and sunburn (recall reactions) may reappear. Psoriatic lesions can intensify during UV radiation (ultraviolet radiation) and simultaneous administration of methotrexate.

Lymph node enlargement (lymphoma) may occur, and treatment should be suspended in this case.

Diarrea can be a toxic effect of Quinux that requires suspension of treatment. If you have diarrhea, talk to your doctor.

Encephalopathy (a brain disorder) and leukoencephalopathy (a special disorder of the brain's white matter) have been reported in cancer patients receiving methotrexate treatment. These disorders cannot be ruled out for methotrexate treatment in other diseases.

If you, your partner, or caregiver notice the appearance or worsening of neurological symptoms, such as general muscle weakness, vision changes, changes in thought, memory, and orientation that cause confusion, and changes in personality, contact your doctor immediately, as these may be symptoms of a rare and severe brain infection called progressive multifocal leukoencephalopathy (PML).

Special precautions for Quinux treatment

Methotrexate temporarily affects the production of sperm and eggs, which is reversible in most cases. Methotrexate can cause severe birth defects. If you are a woman, avoid becoming pregnant while using methotrexate and for at least 6 months after completing treatment. If you are a man, avoid fathering a child while taking methotrexate and for at least 3 months after completing treatment. See also section "Pregnancy, breastfeeding, and fertility".

Older patients

Older patients on methotrexate treatment should be closely monitored by a doctor to detect any possible side effects as soon as possible.

The age-related deterioration of liver and kidney function, as well as the low body reserves of folic acid in the elderly, require a relatively low dose of methotrexate.

Other medications and Quinux

Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication.

The effect of treatment may be affected if Quinux is administered at the same time as certain medications:

• Medications that damage the liver or blood, for example, leflunomide
• Antibiotics (medications that prevent or combat certain infections) such as:tetracyclines,chloramphenicol,non-absorbable broad-spectrum antibiotics,penicillins,glucopetides,sulfonamides (medications containing sulfur that prevent or combat certain infections),ciprofloxacin, andcephalothin
• Non-steroidal anti-inflammatory drugs orsalicylates (medications for pain or inflammation)
• Probenecid (medication for gout)
• Weak organic acids such as diuretics of the asaor some medications used to treat pain and inflammatory diseases (for example, acetylsalicylic acid, diclofenac, and ibuprofen) and pyrazoles (for example, metamizol (synonyms novaminsulfon and dipirona) for intense pain and/or fever)
• Medications that can cause adverse effects on the bone marrow, for example, trimethoprim-sulfamethoxazole (an antibiotic) and pyrimethamine
• Sulfasalazine (anti-rheumatic)
• Azathioprine (immunosuppressant that is sometimes used to treat severe forms of rheumatoid arthritis)
• Mercaptopurine (cytostatic)
• Retinoids (medications for psoriasis and other skin diseases)
• Theophylline (medication for asthma and other respiratory diseases)
• Inhibitors of the proton pump (medications for stomach discomfort)
• Hypoglycemic medications (medications used to reduce blood sugar levels).

Vitamins containing folic acid may alter the effect of treatment and should only be taken as advised by your doctor.

Vaccinations with vaccines made with attenuated microorganisms should be avoided.

Use of Quinux with food, drinks, and alcohol

During treatment with Quinux, avoid consuming alcohol and large amounts of coffee, caffeinated soft drinks, and black tea.

Pregnancy, breastfeeding, and fertility

If you are pregnant or breastfeeding, or if you think you may be pregnant, consult your doctor or pharmacist before using this medication.

Pregnancy

Do not use Quinux during pregnancy or if you are planning to become pregnant. Methotrexate can cause birth defects, harm the fetus, or cause miscarriages. It is associated with skull, face, heart, and blood vessel malformations, brain, and limb malformations. Therefore, it is very important that methotrexate not be administered to pregnant patients or those planning to become pregnant. In fertile women, any possibility of pregnancy should be excluded with appropriate measures, for example, a pregnancy test before starting treatment. You should avoid becoming pregnant while taking methotrexate and for at least 6 months after stopping treatment, using reliable contraceptive methods during this time (see also section "Warnings and precautions").

If you become pregnant during treatment or suspect you may be pregnant, consult your doctor as soon as possible. You will be offered information on the risk of harm to the child during treatment.

If you want to become pregnant, consult your doctor, who may refer you to a specialist to inform you before the planned start of treatment.

As methotrexate may be genotoxic, all women who wish to become pregnant should consult a genetic counseling center, if possible, before treatment, and men should be informed about the possibility of preserving sperm before starting treatment.

Breastfeeding

Breastfeeding should be discontinuedduring treatment with Quinux.

Male fertility

The available data do not indicate a higher risk of malformations or miscarriages if the father takes a methotrexate dose of less than 30 mg/week. However, this risk cannot be completely ruled out. Methotrexate can be genotoxic, meaning it can cause genetic mutations. Methotrexate can affect sperm production and cause birth defects. Therefore, you should avoid fathering a child or donating sperm while taking methotrexate and for at least 3 months after stopping treatment.

Driving and operating machinery

Treatment with Quinux may cause adverse reactions that affect the central nervous system, such as fatigue and dizziness. Therefore, your ability to drive or operate machinery may be affected in some cases. If you feel tired or drowsy, do not drive or operate machinery.

Quinux contains sodium

This medication contains less than 1 mmol of sodium (23 mg) per dose unit; it is essentially "sodium-free".

Follow exactly the administration instructions of this medication as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.

Your doctor will determine the dose, which will be adjusted individually. Normally, treatment takes between 4 and 8 weeks to take effect.

The Quinux injection will be administered or supervised by your doctor or healthcare professionalonly once a week. Along with your doctor, you will choose a day of the week that suits you to receive the injection. Quinux can be injected intramuscularly (into a muscle) or subcutaneously (under the skin).

Useinchildrenandadolescents

Your doctor will decide what is the appropriate dose in children and adolescents with polyarticular idiopathic juvenile arthritis.

Quinux is not recommended for use in children under 3 years of age due to limited experience in this age group.

Duration and form of administration

Quinux is injectedonce a week.

Your doctor in charge will decide on the duration of treatment. The treatment of rheumatoid arthritis, idiopathic juvenile arthritis, psoriasis vulgaris, and psoriatic arthritis with Quinux is a long-term treatment.

At the beginning of treatment, Quinux may be injected by medical personnel. However, your doctor may decide that you can learn to inject Quinux yourself. You will receive the necessary training for this. Under no circumstances should you attempt to inject yourself unless you have been taught to do so.

See the usage instructions at the end of the prospectus.

The form of handling and eliminating the product will be done in accordance with the guidelines for other cytotoxic preparations in accordance with local regulations. Pregnant healthcare personnel should not handle or administer Quinux.

Methotrexate should not come into contact with the skin surface or mucous membranes. If it does come into contact, the affected area should be washed immediately with plenty of water.

If you feel that the effect of Quinux is too strong or too weak, consult your doctor or pharmacist.

IfyouusemoreQuinuxthanyoushould

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone: 91 562 04 20.

IfyouforgottouseQuinux

Do not use a double dose to compensate for the missed doses.

If you have any other doubts about the use of this medication, ask your doctor, pharmacist, or nurse.

Like all medicines, this medicine can cause side effects, although not everyone will experience them.

The frequency and severity of side effects will depend on the dose and frequency of administration. It is essential that your doctor performs regular check-ups, as severe side effects can occur even with low doses. Your doctor will perform tests to monitor abnormalities in the blood, such as low white blood cell counts (leukocytes), platelets, lymphoma, and changes in the kidneys and liver.

The most relevant side effects related to Quinux administration occur in the blood production system and the digestive tract.

Inform your doctor immediately if you experience any of the following symptoms, as they may indicate a severe side effect with potential life-threatening risk that may require urgent specific treatment:

• Severe respiratory distress (symptoms may include general discomfort, irritating and dry cough, difficulty breathing, feeling of lack of air at rest, chest pain, or fever).
• Bloody sputum or cough.
• Severe blistering or skin peeling.
• Unusual bleeding (including vomiting blood) or bruising.
• Severe diarrhea.
• Mouth ulcers.
• Black stools.
• Blood in urine or stools.
• Small red spots on the skin.
• Fever.
• Yellow discoloration of the skin (jaundice).
• Pain or difficulty urinating.
• Thirst and/or frequent urination.
• Seizures (convulsions).
• Loss of consciousness.
• Blurred vision or decreased vision.

The following side effects may occur:

Very common(may affect more than 1 in 10 people):

• Oral inflammation, indigestion, nausea (urge to vomit), loss of appetite.
• Increased liver enzymes.

Common(may affect up to 1 in 10 people):

• Mouth ulcers, diarrhea.
• Rash, skin redness, itching.
• Headache, fatigue, drowsiness.
• Decreased red blood cell formation with decreased white blood cell, red blood cell, or platelet count (leukopenia, anemia, thrombocytopenia).

Uncommon(may affect up to 1 in 100 people):

• Throat inflammation, intestinal inflammation, vomiting.
• Reactions similar to sunburn due to increased skin sensitivity to sunlight, hair loss, increased number of rheumatoid nodules, herpes zoster, inflammation of blood vessels, herpes-like rash, urticaria.
• Appearance of diabetes mellitus.
• Dizziness, confusion, depression.
• Urinary or vaginal tract inflammation or ulcers, decreased renal function, urinary disorders.
• Joint pain, muscle pain, osteoporosis (bone mass reduction).
• Decreased serum albumin.

Rare(may affect up to 1 in 10,000 people):

• Severe bleeding, toxic megacolon (acute and toxic dilation of the intestine).
• Sunburn-like syndrome, increased nail pigmentation, skin inflammation, furunculosis (deep infection of hair follicles), visible enlargement of small blood vessels.
• Local lesion at the injection site (sterile abscess formation, tissue destruction) after intramuscular injection or subcutaneous injection.
• Visual disturbances, pain, loss of strength or numbness/sensitivity to minor stimuli, altered taste (metallic taste), seizures, paralysis, severe headache with fever.
• Retinopathy (non-inflammatory eye disorder).
• Severe decrease in white blood cell count, severe bone marrow depression.
• Lymphoproliferative disorders (excessive increase in white blood cells).
• Loss of sexual appetite, impotence, increased male breast tissue (gynecomastia), altered sperm formation, menstrual disorders, vaginal secretion.
• Increased size of lymph nodes (lymphoma).

Frequency not known (cannot be estimated from available data):

• Leucoencephalopathy (a brain white matter disease).
• Pulmonary hemorrhage.
• Damage to jaw bones (secondary to excessive white blood cell increase).
• Redness and peeling of the skin.
• Tissue destruction at the injection site.
• Swelling.

When administered intramuscularly, metotrexate may cause frequent local reactions (burning sensation) or lesions (sterile abscess formation, tissue destruction) at the injection site. Subcutaneous metotrexate administration is well tolerated locally. Only mild local skin reactions were observed, which decreased during treatment.

Reporting of side effects

If you experience any type of side effect, consult your doctor,pharmacistornurse,even if it is a possible side effect not listed in this prospectus. You can also report them directly through the Spanish System of Pharmacovigilance of Medicines for Human Use. https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.

Keep this medication out of the sight and reach of children.

Do not store above 25 °C. Store pre-filled syringes in the outer packaging to protect them from light. Do not refrigerate or freeze.

Do not use this medication after the expiration date that appears on the packagingafter CAD. The expiration date is the last day of the month indicated.

Medicines should not be disposed of through drains or in the trash. Dispose of packaging and unused medicines at the SIGRE point of the pharmacyorany other medication waste collection system. If in doubt, ask your pharmacist how to dispose of packaging and unused medicines. In this way, you will help protect the environment.

Composition of Quinux

• The active ingredient is methotrexate. 1 ml of solution contains 25 mg of methotrexate(equivalenta27.42mgofmethotrexatedisodium).

1pre-filled syringeof0.8mlofsolutioncontains20mgofmethotrexate.

• The other components are sodium chloride, sodium hydroxide, water for injection.

Appearance of the product and contents of the pack

Quinux pre-filled syringes contain a yellowish and transparent solution.

The syringe is equipped with a safety system to help prevent needlestick injuries after use.

Each pack contains 1 or 4 pre-filled syringes with 0.8 ml of solution, with subcutaneous injection needles attached and alcohol-impregnated cotton wool.

Each pack contains 1 or 4 pre-filled syringes with 0.8 ml of solution, with subcutaneous injection needles attachedwith safety systemand alcohol-impregnated cotton wool.

Only some pack sizes may be marketed.

Marketing authorization holder and manufacturer responsible

Marketing authorization holder

Centrum Pharmaceutical Specialties, S.A.

C/ Sagitario, 14

03006, Alicante

Spain
GroupAsacpharma

Tel.: 965288160; Fax.: 965286434

Manufacturer responsible

Centrum Pharmaceutical Specialties, S.A.

C/ Sagitario, 14

03006, Alicante

Spain

Last review date of this leaflet: October 2024.

The detailed informationof this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) (http://www.aemps.gob.es)

Instructions for use

Read carefully the instructions before starting to administer the injection, and always use the recommended application technique advised by your doctor, nurse or pharmacist.

If you have any problems or questions, contact your doctor, nurse or pharmacist.

Preparation

Choose a clean, flat and well-lit work surface.

Gather all the necessary elements before starting:

• 1 Quinux pre-filled syringe
• 1 alcohol-impregnated cotton wool (supplied in the pack)

Wash your hands thoroughly. Before using it, inspect the Quinux pre-filled syringe for visible defects (or cracks).

Injection site

The best places for injection are:

• the upper thigh,
• the abdomen, except the area around the navel.

• If someone is helping you with the injection, you can also inject in the back of the arm, just below the shoulder.
• Change the injection site each time. This may reduce the risk of developing skin irritation at the injection site.
• Do not inject into skin that is painful, discolored, red, hardened or with scars or stretch marks. If you have psoriasis, do not attempt to inject directly into lesions or patches of skin that are raised, thickened, red or scaly.

Injecting the solution

1. Open the pack containing the pre-filled syringe of methotrexate and read the leaflet carefully. Remove the pre-filled syringe from the pack at room temperature.
2. Disinfection: select a place for the injection and disinfect it with the alcohol-impregnated cotton wool. Leave for 60 seconds to allow the disinfectant to dry.

1. Removecarefullythe plastic protective cap, turn it gently with a movement outward. Important: do not touch the needle of the pre-filled syringe.

1. Insertion of the cannula: with two fingers, form a fold in the skin and insert the needle quickly at an angle of 90 degrees.

1. Injection: insert the needle completely into the skin fold. Push the plunger slowly and inject the liquid under the skin. Hold the skin firmly until the injection is complete. Remove the needle carefully in a straight line.

A protective cap will automatically enclose the needle.

Methotrexate should not come into contact with the skin surface or mucous membranes. In case of contamination, the affected area should be washed immediately with plenty of water.

If you or someone in your environment are injured with the needle, consult your doctor immediately and do not use this pre-filled syringe.

Disposal and other manipulations

The manipulation and disposal of the medicine and the pre-filled syringe will be carried out in accordance with local regulationsforcytotoxic agents. Pregnant healthcare staff should not handle or administer Quinux.