Neotigason 10 mg hard capsules

Package leaflet: Information for the user

Introduction

Package leaflet: information for the user

Neotigason 10 mg hard capsules

Acitretin

WARNING

MAY SERIOUSLY HARM THE UNBORN BABY IF USED DURING PREGNANCY.

Women must use effective contraception throughout treatment.

Do not use if you are pregnant or think you might be pregnant.

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

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

Contents of this leaflet

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

1. What Neotigason is and what it is used for

Acitretin belongs to a group of medicines known as retinoids. Retinoids are derivatives of vitamin A.

This medicine is used to treat severe skin disorders in which the skin has become thickened, may appear scaly, and does not respond adequately to other conventional treatments.

Neotigason is indicated for the treatment of skin disorders such as psoriasis, ichthyosis (a skin condition characterized by dryness and formation of scale-like patches), and Darier's disease (a hereditary skin disorder affecting the skin, nails, and mucous membranes, manifested by the appearance of brown-colored spots on the face, chest, abdomen, and skin folds).

Acitretin should only be prescribed by physicians, preferably dermatologists, experienced in the use of systemic retinoids, who are able to properly assess the risks associated with acitretin during pregnancy and understand the required monitoring.

2. What you need to know before starting Neotigason

Do not take Neotigason

• If you are pregnant or breastfeeding.

• If there is any possibility that you could become pregnant, you must follow the precautions outlined in the “Pregnancy Prevention Programme”, see section “Warnings and precautions”.

• If you are allergic to acitretin or to any of the other ingredients of this medicine (listed in section 6), or if you are taking other “retinoid” medicines such as isotretinoin or tazarotene.

• If you have severe liver or kidney problems.

• If you have high levels of fats (lipids) in your blood.

• If you are taking vitamin A, see section “Other medicines and Neotigason”.

• If you are taking medicines called tetracyclines (a type of antibiotic used to treat infections) or methotrexate (used for skin conditions, arthritis or cancer), see section “Other medicines and Neotigason”.

• Acitretin is contraindicated in children.

Warnings and precautions

Treatment with acitretin must be supervised by a doctor specialized in treating the skin conditions for which it is indicated.

Acitretin should only be used as a last-resort treatment, i.e., when other treatments have failed.

Acitretin commonly increases blood fat levels, such as cholesterol or triglycerides, which has been associated with pancreatitis.

Inform your doctor if you experience severe abdominal or back pain (these may be signs of inflammation of the pancreas).

Due to the risk of fetal malformations, this medicine must not be given to anyone else. Any unused or expired medicine must be returned to the pharmacy for proper disposal.

Pregnancy Prevention Programme

Pregnant women must not take Neotigason.

This medicine can seriously harm the baby (it is considered "teratogenic") – it may cause serious abnormalities in the baby’s brain, face, ears, eyes, heart, and certain glands (thymus and parathyroid). It also increases the risk of miscarriage. This can occur even if Neotigason is taken for only a short time during pregnancy.

• Do not take this medicine if you are pregnant or think you might be pregnant.
• Do not take Neotigason if you are breastfeeding. The medicine is likely to pass into your milk and may harm your baby.
• Do not take Neotigason if you are capable of becoming pregnant during treatment.
• Do not become pregnant within 3 years after stopping treatment, as the medicine may still remain in your body.

Women who could become pregnant must be prescribed Neotigason under strict rules due to the risk of serious harm to the unborn child.

These rules are:

• Your doctor must explain the risk of harm to the unborn child – you must understand why you must not become pregnant and what you need to do to prevent pregnancy.
• You must have discussed contraception (birth control) with your doctor. Your doctor will provide information on how to avoid pregnancy and may refer you to a specialist for contraceptive advice.
• Before starting treatment, your doctor will require you to take a pregnancy test. The test must confirm that you are not pregnant when starting Neotigason treatment.

Women must use effective contraception before, during, and after taking Neotigason

• You must agree to use at least one highly reliable contraceptive method (e.g., an intrauterine device or contraceptive implant) or two effective methods that work in different ways (e.g., a hormonal contraceptive pill and a condom). Discuss with your doctor which methods are suitable for you.
• You must use contraception for one month before starting Neotigason, throughout treatment, and for 3 years after stopping treatment.
• You must use contraception even if you are not having periods or are not sexually active (unless your doctor determines it is not necessary).

Women must agree to undergo pregnancy tests before, during, and after taking Neotigason

• You must agree to attend regular follow-up visits, ideally every month.
• You must agree to undergo regular pregnancy tests, ideally monthly during treatment and, because the medicine may still remain in your body, every 1–3 months for 3 years after stopping Neotigason (unless your doctor determines otherwise).
• You must agree to undergo additional pregnancy tests if requested by your doctor.
• You must not become pregnant during treatment or within 3 years after stopping treatment, as the medicine may still be present in your body.
• Your doctor will discuss all these points with you using a checklist, and will ask you (or a parent/guardian) to sign it. This checklist confirms that you have been informed of the risks and that you will follow the above rules.

If you become pregnant while taking Neotigason, stop taking the medicine immediately and consult your doctor. Your doctor may refer you to a specialist for advice.

Additionally, if you become pregnant within 3 years after stopping Neotigason, you must consult your doctor. Your doctor may refer you to a specialist for advice.

Advice for men

The levels of oral retinoids in semen of men taking Neotigason are too low to harm a partner’s unborn child. However, you must never share your medicine with anyone.

Additional precautions

Never give this medicine to another person. Please return any unused capsules to your pharmacist at the end of treatment.

You must not donate blood during treatment with this medicine or for 3 years after stopping Neotigason, as a developing fetus could be harmed if a pregnant woman receives your blood.

Consult your doctor before starting Neotigason:

• If you have diabetes. You may need to monitor your blood sugar levels more frequently when starting Neotigason.
• If you have high blood fat levels or if you are obese. Your doctor may need to perform blood tests while you are taking Neotigason to monitor your blood fat levels.
• If you have cardiovascular problems. Your doctor may monitor you more closely, e.g., your blood pressure.
• If you drink large amounts of alcohol.
• If you have liver problems.
• If you notice a decrease in night vision.
• If you experience severe headache, nausea, vomiting, and/or vision problems. These may be symptoms of increased intracranial pressure, which must be evaluated by your doctor as soon as possible.
• If you will have significant sun exposure or use a sunbed. Neotigason may increase the effects of UV light on the skin. Before sun exposure, apply sunscreen (with a protection factor of at least SPF 15) to exposed skin areas. Uncontrolled use of sunlamps must be avoided.
• If you have ever had mental health problems, such as depression, aggressive tendencies, mood changes, or signs of psychosis (altered perception of reality, such as hearing voices or seeing things that are not there). This is because taking Neotigason may affect your mood and mental health.

Mental health problems

You may not notice some changes in your mood or behavior, so it is very important to inform your friends and family that this medicine could affect your mood and behavior. They may notice these changes and help you identify any issues that need to be discussed with your doctor.

Your liver function and blood fat (lipid) levels should be checked before starting treatment and regularly during treatment. Your doctor may also periodically monitor your bones, as Neotigason may cause bone changes, especially in children and elderly patients receiving long-term treatment.

Patients treated with Neotigason may experience hair loss.

Children and adolescents

Use of this medicine is not recommended in children and adolescents. If used under exceptional circumstances, careful monitoring for any abnormalities in muscle and bone development is required.

Other medicines and Neotigason

Inform your doctor or pharmacist if you are taking, have recently taken, or might need to take any other medicines.

Tetracyclines (a type of antibiotic): Concomitant treatment with tetracycline antibiotics is contraindicated during Neotigason therapy (see section “Do not take Neotigason”), as it may lead to increased intracranial pressure (benign intracranial hypertension).

Vitamin A: While taking Neotigason, you must not take medicines containing high doses of vitamin A (see section “Do not take Neotigason”). Daily intake of vitamin A should not exceed the recommended dose of 4000–5000 IU.

Methotrexate (a medicine used to treat psoriasis or certain types of cancer): Concomitant administration of methotrexate and Neotigason should be avoided due to the risk of hepatitis (liver inflammation) (see section “Do not take Neotigason”).

Phenytoin (a medicine for epilepsy): Neotigason partially reduces the binding of phenytoin to plasma proteins. The clinical significance of this is not fully known, but it should be considered when both drugs are used together.

Oral contraceptives (medicines used to prevent unwanted pregnancy): The contraceptive effect of low-dose progestogen-only preparations may be reduced due to interaction with Neotigason. Therefore, microdose progestogen preparations or “mini-pills” should not be used, as retinoids may interfere with their contraceptive effect.

To date, no interactions have been observed between Neotigason and other substances (e.g., digoxin, cimetidine).

Taking Neotigason with food, drinks, and alcohol

Women of childbearing potential must not consume alcohol (in beverages, food, or medicines) during Neotigason treatment or for the following 2 months after treatment ends. The combination of acitretin and alcohol may lead to the formation of a compound (etretinate), which may be harmful to the fetus and which, once formed, takes a long time to be completely eliminated from the body.

Capsules should be taken with food or milk.

Pregnancy, breastfeeding, and fertility

Neotigason causes severe fetal malformations and increases the incidence of spontaneous abortion. Do not take Neotigason if you are pregnant. If you become pregnant or think you may be pregnant while taking Neotigason, stop taking this medication immediately and contact your doctor. You must not become pregnant during the 3 years following completion of Neotigason treatment. In such a case, contact your doctor. Do not take Neotigason if you are breastfeeding.

For further information on pregnancy and contraception, see the section “Pregnancy Prevention Plan” under “Warnings and precautions”.

Driving and use of machines

Neotigason may in some cases cause reduced night vision, which resolves upon discontinuation of treatment. Therefore, caution should be exercised when driving vehicles or operating dangerous machinery during treatment.

Neotigason contains glucose

If your doctor has informed you that you have an intolerance to certain sugars, consult him before taking this medicine.

Neotigason contains sodium

This medicinal product contains less than 23 mg of sodium (1 mmol) per capsule; thus, it is essentially “sodium-free”.

3. How to take Neotigason

Follow exactly the instructions for use of this medicine provided by your doctor. If in doubt, consult your doctor or pharmacist again.

The capsules must be swallowed whole once daily, with food or milk.

The required dose of Neotigason varies from person to person, so your doctor will prescribe a dose appropriate for you. This medicine is administered orally.

Use in adults and elderly

For psoriasis, the recommended starting dose is 25 mg (1 capsule of 25 mg) or 30 mg (3 capsules of 10 mg).

After 2–4 weeks, your doctor may increase or reduce the dose, depending on the treatment's effectiveness and your response to it.

The maximum dose is 75 mg (3 capsules of 25 mg) per day. This maximum dose must not be exceeded. The capsule should preferably be taken once daily with a meal.

Most patients take acitretin for up to 3 months. However, your doctor may decide that you should take it for a longer period. Long-term treatment is not recommended in patients with psoriasis.

In patients with Darier’s disease, the usual starting dose is 10 mg, which may be increased by your doctor.

Use in children and adolescents

The use of this medicine is not recommended in children and adolescents unless, in the doctor’s judgment, the benefits clearly outweigh the risks.

The dose will be determined according to body weight.

Before starting treatment with this medicine, consult the section “Pregnancy Prevention Plan” in the “Warnings and precautions” section.

If you take more Neotigason than you should

If you take more acitretin than prescribed, you may experience severe headache, dizziness, nausea or vomiting, drowsiness, irritability, and itching. Stop taking the medicine immediately and consult your doctor without delay.

In case of overdose or accidental ingestion, contact your doctor or pharmacist immediately or call the Toxicology Information Service at telephone number 91 562 04 20, indicating the medicine and the amount ingested.

If you forget to take Neotigason

Do not take a double dose to make up for a missed dose. If you forget to take a dose, take it as soon as you remember and continue with your regular dosing schedule. However, if it is almost time for your next dose, skip the missed dose.

If you stop taking Neotigason

Your doctor is best qualified to decide whether treatment with acitretin should be stopped and how to do so. If you wish to discontinue the medicine, consult your doctor first.

If you have any further questions about the use of this medicine, ask your doctor or pharmacist.

4. Possible adverse effects

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

Most adverse effects of Neotigason are dose-dependent, which is why most patients experience some adverse effects during the initial period while the dose is being adjusted. These effects are generally well tolerated at the recommended doses and usually disappear once the dose is reduced or treatment is discontinued.

The most commonly affected parts are the skin and mucous membranes, with dryness sometimes accompanied by erosion observed in the lips, mouth, nasal or conjunctival mucosa. In rare cases, sensitivity to sunlight may increase.

Stop taking Neotigason and contact your doctor immediately if you experience the following adverse effects at the same time:

• severe headache;
• nausea or vomiting;
• vision problems.

The following adverse effects have been observed during treatment with Neotigason:

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

• dry, irritated or swollen eyes, which may cause intolerance to contact lenses;
• dry, irritated nose or runny nose, nosebleeds;
• dry mouth, thirst;
• dryness or inflammation of the lips, which can be relieved by applying a greasy ointment. Itching, hair loss, skin peeling on the palms of the hands or soles of the feet, or even elsewhere on the body;
• changes in liver function (shown in a blood test);
• increased blood lipid levels (shown in a blood test);
• elevated uric acid (shown in a blood test).

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

• headache;
• inflammation of the mouth mucosa, abdominal pain, diarrhea, nausea, vomiting;
• fragile skin, sticky sensation on the skin or rash, skin inflammation, changes in hair texture, brittle nails, nail area skin infection, skin redness, hair weakening;
• joint pain, muscle pain;
• swelling of hands, ankles and feet.

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

• dizziness;
• blurred vision;
• gum inflammation;
• liver inflammation;
• skin fissures, cracks or fine scarring, e.g. around the mouth (cheilitis), blisters and skin inflammation (bullous dermatitis), increased skin sensitivity to sunlight (photosensitivity reaction).

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

• damage to the peripheral nervous system, which may include symptoms such as muscle weakness, numbness and tingling in the feet and hands, or burning, stabbing pain.

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

• increased intracranial blood pressure;
• night blindness, eye cornea inflammation (ulcerative keratitis);
• yellowish skin, yellow coloration of the whites of the eyes (jaundice);
• bone pain, changes in bone growth.

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

• vaginal infection (also known as Candida or thrush);
• hearing problems, ringing in the ears (tinnitus);
• redness, decreased resistance of blood vessel walls, retinoic acid syndrome;
• changes in taste;
• rectal bleeding;
• small red bumps on the skin that may bleed easily (pyogenic granuloma), thinner skin, skin peeling (exfoliative dermatitis), cutaneous atrophy, angioedema, partial or complete loss of eyelashes or eyebrows (madarosis);
• improvement or worsening of glucose tolerance in diabetic patients;
• changes in voice tone, dysphonia;
• allergic reaction;
• mood disturbances;
• signs of psychosis: altered perception of reality, such as hearing voices or seeing things that are not there.

Reporting of adverse effects:

If you experience any adverse effects, consult your doctor or pharmacist, even if they are possible adverse effects not listed in this leaflet. You may also report them directly through the Spanish Pharmacovigilance System for Human Medicines: http://www.notificaram.es. By reporting adverse effects, you can help provide more information on the safety of this medicine.

5. Storage of Neotigason

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

Do not store above 25°C. Keep in the original packaging to protect from moisture.

Do not use this medicine after the expiry date stated on the container after EXP. The expiry date refers to the last day of the month indicated.

Return any unused capsules to your pharmacist. Keep them only if your doctor instructs you to do so.

Medicines must not be disposed of via wastewater or household waste. Dispose of unused medicines and their packaging at the SIGRE collection point at your pharmacy. If you have any doubts, ask your pharmacist how to properly dispose of medicines and packaging you no longer need. This will help protect the environment.

6. Contents of the container and additional information

Composition of Neotigason

• The active substance is acitretin. Each capsule contains 10 mg of acitretin.
• The other components are:

Capsule contents: glucose, sodium ascorbate (E-301), microcrystalline cellulose (E-460i), gelatin.

Capsule coating: black iron oxide (E-172), yellow iron oxide (E-172), red iron oxide (E-172), titanium dioxide (E-171), and gelatin.

Printing ink components: shellac, isopropyl alcohol, n-butyl alcohol, propylene glycol, ammonium hydroxide, black iron oxide (E-172).

Appearance of Neotigason and contents of the container

It is presented as hard capsules with a white body and brown cap, printed with the number "10" on the body, packed in blisters, in packs of 30 capsules.

Other presentations:

Neotigason 25 mg hard capsules: Pack of 30 capsules.

Marketing Authorization Holder

Aurovitas Spain, S.A.U.

Avda. de Burgos, 16-D

28036 Madrid

Spain

Manufacturer

Cenexi

52, Rue Marcel et Jacques Gaucher

94120 Fontenay-Sous-Bois

France

Or

Cenexi

17, Rue de Pontoise

95520 Osny

France

Date of the most recent review of this package leaflet: January 2025

Detailed and up-to-date information on this product is available by scanning the QR code included in the leaflet using a smartphone. The same information is also available at the following link: https://cima.aemps.es/info/60303 and on the website http://www.aemps.gob.es/.