ACTONEL 30 mg FILM-COATED TABLETS

2. What you need to know before you take Actonel

Do not take Actonel

• if you are allergic to sodium risedronate or any of the other ingredients of this medicine (listed in section 6)
• if your doctor has told you that you have a condition called hypocalcemia (low blood calcium levels)
• if you may be pregnant, are pregnant, or are planning to become pregnant
• if you are breastfeeding
• if you have severe kidney disease.

Warnings and precautions

Talk to your doctor or pharmacist before starting Actonel.

• If you cannot stay upright (sitting or standing) for at least 30 minutes.
• If you have bone or mineral metabolism problems (e.g., vitamin D deficiency, parathyroid hormone disorders, both causing low blood calcium levels).
• If you have or have had problems with your esophagus (the tube that connects the mouth to the stomach). At some point, you may have had or been told you have esophagitis (inflammation of the esophagus) or esophageal ulcers, or you may have been informed that you have Barrett's esophagus (a condition associated with changes in the cells lining the lower esophagus).
• If your doctor has told you that you have an intolerance to some sugars (such as lactose).
• If you have had or have pain, swelling, or numbness in the jaw or jawbone, or "a strong discomfort in the jaw" or a loose tooth.
• If you are undergoing dental treatment or are going to have a dental procedure, inform your dentist that you are taking Actonel.

Your doctor will advise you what to do if you take Actonel and have any of the problems mentioned above.

Children and adolescents

Sodium risedronate is not recommended for use in children and adolescents (under 18 years) due to insufficient data on safety and efficacy.

Taking Actonel with other medicines

Medicines containing any of the following substances reduce the effect of Actonel when taken at the same time:

• calcium
• magnesium
• aluminum (e.g., some antacids)
• iron

Take these medicines at least 30 minutes after taking Actonel.

Tell your doctor or pharmacist that you are taking, have recently taken, or might take any other medicines.

Taking Actonel with food and drinks

It is very important that you DO NOT take Actonel with food or drinks (other than plain water) because they can interfere. In particular, do not take this medicine at the same time as dairy products (such as milk) as they contain calcium (see section 2, "Taking Actonel with other medicines").

Take food and drinks (other than plain water) at least 30 minutes after Actonel.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or are planning to become pregnant, consult your doctor or pharmacist before using this medicine.

DO NOT take Actonel if you may be pregnant, are pregnant, or are planning to become pregnant (see section 2, "Do not take Actonel"). The potential risk associated with the use of sodium risedronate (the active ingredient in Actonel) in pregnant women is unknown.

DO NOT take Actonel if you are breastfeeding (see section 2, "Do not take Actonel").

Driving and using machines

It is not known if Actonel affects the ability to drive and use machines.

Actonel contains lactose

This medicine contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.

Actonel contains sodium

This medicine contains less than 1 mmol of sodium (23 mg) per film-coated tablet; this is essentially "sodium-free".

3. How to take Actonel

Follow exactly the administration instructions of this medicine given by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.

The recommended dose is:

One Actonel tablet (30 mg sodium risedronate) once a day.

The recommended treatment duration is usually 2 months.

The aluminum blister pack has the days of the week printed on it to help you take your medicine.

WHEN to take Actonel tablets

Take the Actonel tablet at least 30 minutes before the first food, drink, or other medicine of the day (except for plain water).

Although it is preferable to take this tablet before breakfast, if you were unable to take Actonel then, you can take it with an empty stomach, at the same time every day, in one of the following cases:

• Between meals: Actonel must be taken at least 2 hours before or at least 2 hours after taking any food, medicine, or drink (other than plain water).

OR:

• In the evening: Actonel must be taken at least 2 hours after taking the last food, medicine, or drink (other than plain water) of the day. Actonel must be taken at least 30 minutes before bedtime.

HOW to take Actonel tablets

• Take the tablet while standing or sitting upright to avoid heartburn.
• Swallow the tablet with at least one glass (120 ml) of plain water.
• Swallow the tablet whole. Do not chew or suck it.
• Do not lie down for at least 30 minutes after taking the tablet.

Your doctor will tell you if you should take calcium and vitamin supplements if you do not get enough from your diet.

Use in children and adolescents

Sodium risedronate is not recommended for use in children under 18 years due to insufficient data on safety and efficacy.

If you take more Actonel than you should

If you have taken more Actonel tablets than prescribed, drink a full glass of milk and consult your doctor.

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service (telephone 91 562 04 20), indicating the medicine and the amount taken.

If you forget to take Actonel

If you have forgotten to take the tablet at the scheduled time, you can take it as soon as possible, following the instructions above (e.g., before breakfast, between meals, or in the evening).

Do not take a double dose to make up for the forgotten dose.

If you stop taking Actonel

If you stop taking the treatment, you may start losing bone mass. Please consult your doctor before deciding to stop treatment.

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

4. Possible side effects

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

Stop taking Actonel and contact your doctor immediatelyif you experience any of the following symptoms:

• Symptoms of a severe allergic reaction, such as:
• • Swelling of the face, tongue, or throat
  • Difficulty swallowing
  • Hives and difficulty breathing.

The frequency of this side effect is not known (cannot be estimated from the available data).

• Severe skin reactions, including blistering of the skin. The frequency of this side effect is not known (cannot be estimated from the available data).

Tell your doctor as soon as possibleif you experience any of the following side effects:

• Eye inflammation, usually with pain, redness, and sensitivity to light. The frequency of this side effect is not known (cannot be estimated from the available data).
• Orbital inflammation - inflammation of the structures surrounding the eyeball. Symptoms may include: pain, swelling, redness, protrusion of the eyeball, and vision changes. The frequency of this side effect is not known (cannot be estimated from the available data)
• Jaw necrosis (osteonecrosis) associated with delayed healing and infection, often after a dental extraction (see section 2, "Warnings and precautions"). The frequency of this side effect is not known (cannot be estimated from the available data).
• Symptoms related to the esophagus, such as pain when swallowing, difficulty swallowing, chest pain, and worsening of heartburn. This side effect is uncommon (may affect up to 1 in 100 people).

Atypical fractures of the thigh bone (femur) may occur rarely, especially in patients on long-term treatment for osteoporosis. Tell your doctor if you notice pain, weakness, or discomfort in the thigh, hip, or groin, as these may be early symptoms of a possible fracture of the femur.

However, in clinical studies, the side effects observed were generally mild and did not cause the patient to stop treatment.

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

• Indigestion, nausea, stomach pain, discomfort or cramps in the stomach, heavy digestion, constipation, feeling of fullness, abdominal distension, diarrhea.
• Pain in your bones, muscles, or joints.
• Headache.

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

• Inflammation or ulcers of the esophagus (the tube that connects the mouth to the stomach) causing difficulty and pain when swallowing (see also section 2, "Warnings and precautions"), stomach inflammation and/or duodenal inflammation (the intestine where the stomach empties).
• Inflammation of the colored part of the eye (the iris) (red eyes, painful with possible changes in vision).

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

• Inflammation of the tongue (swollen, red, possibly painful), narrowing of the esophagus (the tube that connects the mouth to the stomach).
• Abnormal liver tests have been reported. This can only be diagnosed with blood tests.

During post-marketing use, the following have been reported:

• Very rare: Consult your doctor if you have ear pain, discharge from the ear, or an ear infection. These could be symptoms of damage to the bones of the ear.
• Frequency not known:
• Cases of hair loss
• Liver disorders, in some cases severe.

Rarely, at the start of treatment, a slight decrease in phosphate and calcium blood levels has been observed in some patients. These changes are usually small and do not cause symptoms.

The following side effects have also been observed in a clinical study in patients with Paget's disease: vision problems, breathing difficulties, cough, inflammation of the large intestine, eye surface wounds, cramps, dizziness, dry eyes, flu-like symptoms, muscle weakness, abnormal cell growth, nocturnal urinary incontinence, exceptionally blisters or swelling, chest pain, nasal discharge, rash, ringing in the ears, weight loss.

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

5. Storage of Actonel

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 after EXP. The expiry date refers to the last day of the month shown.

This medicine does not require any special storage conditions.

Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to your pharmacist. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.

6. Contents of the pack and further information

Composition of Actonel

• The active substance is sodium risedronate. Each tablet contains 30 mg of sodium risedronate (equivalent to 27.8 mg of risedronic acid).
• The other ingredients (excipients) are:

Tablet core: lactose monohydrate (see section 2), crospovidone, magnesium stearate, and microcrystalline cellulose.

Film coating: hypromellose, macrogol, hydroxypropylcellulose, colloidal anhydrous silica, and titanium dioxide (E171).

Appearance and packaging of the product

Actonel 30 mg film-coated tablets are oval, white tablets with the letters "RSN" on one face and "30 mg" on the other.

The tablets are available in blister packs of 1x3, 1x14, 28 (2x14) film-coated tablets.

Not all pack sizes may be marketed.

Marketing authorization holder

Theramex Ireland Limited

3rd Floor, Kilmore House,

Park Lane, Spencer Dock,

Dublin 1

D01 YE64

Ireland

Manufacturer

Balkanpharma-Dupnitsa AD

3, Samokovsko Shosse Str.

2600 Dupnitsa

Bulgaria

Local representative

Theramex Healthcare Spain, S.L.

Calle Martínez Villergas 52, Edificio C, 2ª planta izquierda.

28027 Madrid

Spain

This medicine is authorized in the Member States of the European Economic Area under the following names:

Belgium: Actonel 30 mg filmomhulde tabletten, Actonel 30 mg comprimé pelliculé, Actonel 30 mg Filmtabletten

France: Actonel 30 mg comprimé pelliculé

Germany: Actonel 30 mg Filmtabletten

Greece: Actonel 30 mg επικαλυμμ?να με λεπτ? υμ?νιο δισκ?α

Italy: Actonel 30 mg compresse rivestite con film

Luxembourg: Actonel 30 mg comprimé pelliculé

Netherlands: Actonel 30 mg, filmomhulde tabletten

Spain: Actonel 30 mg comprimidos recubiertos con película

Sweden: Optinate 30 mg filmdragerade tabletter

Date of last revision of this leaflet:October 2024

Detailed and up-to-date information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/