Amotaks Dis

Leaflet attached to the packaging: patient information

Amotaks Dis, 500 mg, tablets

Amotaks Dis, 750 mg, tablets

Amotaks Dis, 1 g, tablets

Amoxicillin

You should carefully read the contents of the leaflet before using the medicine, as it contains

important information for the patient.

• You should keep this leaflet, so that you can read it again if you need to.
• In case of any doubts, you should consult a doctor or pharmacist.
• This medicine has been prescribed to you as an adult patient (or child). Do not pass it on to others. The medicine may harm another person, even if their symptoms are the same.
• If the patient experiences any side effects, including any side effects not listed in this leaflet, they should tell their doctor or pharmacist. See section 4.

Table of contents of the leaflet

• 1. What is Amotaks Dis and what is it used for
• 2. Important information before taking Amotaks Dis
• 3. How to take Amotaks Dis
• 4. Possible side effects
• 5. How to store Amotaks Dis
• 6. Contents of the packaging and other information

1. What is Amotaks Dis and what is it used for

Amotaks Dis is an antibiotic. The active substance of the medicine is amoxicillin. Amoxicillin belongs to
a group of medicines called "penicillins".

What is Amotaks Dis used for

Amotaks Dis is used to treat infections caused by bacteria that are sensitive to amoxicillin.
Amotaks Dis is used to treat:

• acute bacterial sinusitis
• acute otitis media
• acute streptococcal pharyngitis and tonsillitis
• exacerbation of chronic bronchitis
• community-acquired pneumonia
• acute urinary tract infection
• asymptomatic bacteriuria during pregnancy
• acute pyelonephritis
• typhoid and paratyphoid fever
• dental abscess with spreading cellulitis
• infections related to joint prosthetics
• peptic ulcer disease caused by Helicobacter pylori bacteria
• Lyme disease.

Amotaks Dis can also be used to prevent endocarditis.

2. Important information before taking Amotaks Dis

When not to take Amotaks Dis:

If the above circumstances apply to the patient, they should not take Amotaks Dis. In case of doubt, before starting to take the medicine, the patient should consult their doctor or pharmacist before starting to take Amotaks Dis.

Warnings and precautions

Before starting to take Amotaks Dis, the patient should discuss it with their doctor or pharmacist if they:

• have infectious mononucleosis (fever, sore throat, swollen lymph nodes and extreme fatigue);
• have kidney disease;
• have irregular urination. In case of doubt whether the above circumstances apply to the patient, they should consult their doctor or pharmacist before starting to take Amotaks Dis.

Blood and urine tests

If the patient is to have:

• urine tests (to detect glucose) or blood tests to check liver function,
• estriol tests (performed during pregnancy to check if the baby is developing properly), they should inform their doctor or pharmacist that they are taking Amotaks Dis. Amoxicillin may affect the results of these tests.

Amotaks Dis and other medicines

The patient should tell their doctor or pharmacist about all the medicines they are taking now or have taken recently, as well as any medicines they plan to take.

• If the patient takes allopurinol (used to treat gout) at the same time as Amotaks Dis, they may be more likely to experience skin allergic reactions.
• If the patient takes probenecid (used to treat gout) - taking probenecid at the same time may reduce the excretion of amoxicillin and is not recommended. If, in the doctor's opinion, it is necessary to take both medicinal products, the doctor may decide to adjust the dose of Amotaks Dis.
• If the patient takes blood-thinning medicines (such as warfarin) at the same time as Amotaks Dis, they may need to have additional blood tests.
• If the patient takes other antibiotics (such as tetracycline) at the same time as Amotaks Dis, Amotaks Dis may be less effective.
• If the patient takes methotrexate (used to treat cancer and severe psoriasis), penicillins may increase the risk of side effects.

Pregnancy and breastfeeding

If the patient is pregnant or breastfeeding, thinks they may be pregnant or plans to have a baby, they should consult their doctor or pharmacist before taking this medicine.

Driving and using machines

Amotaks Dis may cause side effects and symptoms (such as allergic reactions, dizziness and seizures) that can affect the ability to drive and use machines.
The patient should not drive or use machines unless they feel well.

Amotaks Dis contains aspartame (E 951)

Each 500 mg tablet contains 3.40 mg of aspartame
Each 750 mg tablet contains 5.10 mg of aspartame
Each 1 g tablet contains 6.80 mg of aspartame
Aspartame is a source of phenylalanine. It may be harmful to patients with phenylketonuria.
This is a rare genetic disorder in which phenylalanine accumulates in the body due to its improper excretion.
Considering the dosage regimen presented in section 3, the maximum amount of aspartame that can be administered to a patient in a single dose is 20.4 mg, and in a daily dose it is 40.8 mg.
Amotaks Dis contains glucose(as one of the ingredients of strawberry, raspberry and tropical flavor)
Each 500 mg tablet contains 1.6 mg of glucose.
Each 750 mg tablet contains 2.4 mg of glucose.
Each 1 g tablet contains 3.1 mg of glucose.
If the patient has previously been diagnosed with intolerance to some sugars, they should consult their doctor before taking the medicine.

3. How to take Amotaks Dis

This medicine should be taken as directed by the doctor or pharmacist. In case of doubt, the patient should consult their doctor or pharmacist.

• Amotaks Dis tablets can be divided into two equal doses at the visible notch. The tablets can be swallowed whole or crushed and taken with a glass of water, sucked or drunk after preparing a suspension.

How to prepare the suspension
Put the appropriate number of tablets into a glass with a small amount of boiled, cooled water, mix well until the tablets are evenly distributed and drink immediately after preparation.

• Amotaks Dis can be taken before a meal, during or after a meal.
• The patient should maintain equal, at least 4-hour, intervals between doses taken during the day.

Usual dose

Children with a body weight of less than 40 kg

All doses are determined based on the child's body weight (in kilograms).

• The doctor will recommend the dose of Amotaks Dis to be given to the child.
• The usual dose is 40 mg to 90 mg per kilogram of body weight per day, given in two or three divided doses.
• The maximum recommended dose is 100 mg per kilogram of body weight per day.

Adults, elderly and children with a body weight of 40 kg or more

The usual dose of Amotaks Dis is 250 mg to 500 mg three times a day or 750 mg to 1 g every 12 hours, depending on the severity and type of infection.

• Severe infections:750 mg to 1 g three times a day.
• Acute urinary tract infection:3 g twice a day for one day.
• Lyme disease (borreliosis - tick-borne infection):single migrating erythema (early stage - a pinkish-red spot)

wandering erythema (early stage - a pinkish-red spot): 4 g per day. Systemic symptoms (late stage - more severe symptoms or when the disease affects multiple organs): up to 6 g per day.

• Peptic ulcer disease:750 mg or 1 g twice a day for 7 days in combination with other antibiotics and medicines used to treat stomach ulcers.
• Prevention of endocarditis during surgical procedures:the dose may vary depending on the type of surgical procedure. Other medicines may be given at the same time. For more detailed information, the patient should consult their doctor, pharmacist or nurse.
• The maximum recommended dose is 6 g per day.

Kidney disease

If the patient has kidney disease, the dose of the medicine may be lower than usual.

Taking a higher dose of Amotaks Dis than recommended

If the patient takes a higher dose of Amotaks Dis than recommended, they may experience symptoms such as stomach and intestinal irritation (nausea, vomiting or diarrhea) or crystals in the urine, which may be perceived as cloudy urine or problems with urination. The patient should contact their doctor as soon as possible. They should take the medicine with them to show it to the doctor.

Missing a dose of Amotaks Dis

• If the patient forgets to take a dose, they should take it as soon as they remember.
• The patient should not take the next dose too early, they should wait about 4 hours before taking the next dose.
• The patient should not take a double dose to make up for a missed dose.

How long to take Amotaks Dis

• The patient should continue taking Amotaks Dis for as long as their doctor recommends, even if they feel better. All doses of the medicine are needed to fight the infection. If some bacteria survive, they may cause a relapse of the infection.
• If the patient does not feel better after finishing the treatment with Amotaks Dis, they should consult their doctor.

In case of long-term use of Amotaks Dis, thrush (candidiasis - fungal infections of the mucous membranes causing local pain, itching and white discharge) may occur. In this case, the patient should consult their doctor.
If the patient takes Amotaks Dis for a long time, their doctor may order additional tests of kidney, liver and blood function.
In case of any further doubts about the use of this medicine, the patient should consult their doctor or pharmacist.

4. Possible side effects

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

If the patient experiences any of the following serious side effects, they should stop taking Amotaks Dis and contact their doctor immediately, as they may need urgent medical attention.

Very rare side effects (may occur in less than 1 in 10,000 patients)

• Allergic reactions, including: itching and skin rash, swelling of the face, lips, tongue, body or difficulty breathing. These symptoms can be severe, and in rare cases, they can be life-threatening.
• Rash or punctate, flat, red, round spots under the skin surface or bruising of the skin, which may be a sign of vasculitis due to an allergic reaction. This may be associated with joint pain (arthritis) and kidney disease.
• Delayed allergic reactions, usually occurring 7 to 12 days after taking Amotaks Dis, some of the observed symptoms include: rash, fever, joint pain and swollen lymph nodes, especially in the armpits.
• A skin reaction called erythema multiforme, characterized by itchy, reddish-purple patches on the skin, especially on the palms or soles, swelling of the skin (resembling urticaria), sensitive to touch areas in the mouth, eyes or genitals. Fever and fatigue may also occur.
• Other severe skin reactions include: changes in skin color, lumps under the skin, blisters, pustules, peeling of the skin, redness, pain, itching and flaking of the skin. They may be accompanied by fever, headache and body aches.
• Symptoms similar to flu with rash, fever, swollen lymph nodes and abnormal blood test results [including increased white blood cell count (eosinophilia) and increased liver enzyme activity]; drug reaction with eosinophilia and systemic symptoms (DRESS).
• Fever, chills, sore throat and other signs of infection or tendency to bruise. These may be signs of blood disorders.
• Jarisch-Herxheimer reaction. When taking Amotaks Dis to treat Lyme disease (borreliosis), the patient may experience fever, chills, muscle and headache, and skin rash.
• Colitis, causing diarrhea (sometimes with blood), abdominal pain and fever.
• Severe liver reactions may occur. They usually occur in patients who have been treated for a longer period, men and the elderly.

Side effects with unknown frequency (frequency cannot be estimated from the available data)

• Chest pain associated with an allergic reaction, which may be a sign of an allergy leading to a heart attack (Kounis syndrome).
• Rash with blisters arranged in a ring shape with crusts in the center or as a string of pearls (linear IgA dermatosis).
• Aseptic meningitis (inflammation of the membranes surrounding the brain and spinal cord).
• Drug-induced enteritis (DIES) Drug-induced enteritis occurred mainly in children receiving amoxicillin. It is a type of allergic reaction, the leading symptom of which is repeated vomiting (1-4 hours after taking the medicine). Further symptoms may include abdominal pain, lethargy, diarrhea and low blood pressure.

The patient should immediately inform their doctor if they experience:
o severe diarrhea with blood
o blisters, redness or bruising on the skin
o darker urine or pale stools
o yellowing of the skin and whites of the eyes (jaundice).
The patient should also read the information below about anemia that may be the cause of jaundice.
The above symptoms may occur during or up to a few weeks after stopping the medicine.

If the patient experiences any of these symptoms, they should stop taking the medicine and contact their doctor immediately.

Sometimes, less severe skin reactions may occur, such as:

• mildly itchy rash (round, pinkish-red patches), resembling urticaria, swelling on the forearms, legs, hands, feet or face. This occurs uncommonly (may occur in less than 1 in 100 patients).

If the patient experiences any of these symptoms, they should contact their doctor and stop taking Amotaks Dis.

Other possible side effects
Common side effects(may occur in less than 1 in 10 patients)

• skin rash
• nausea
• diarrhea.

Uncommon side effects(may occur in less than 1 in 100 patients)

• vomiting.

Very rare side effects(may occur in less than 1 in 10,000 patients)

• thrush (fungal infections of the vagina, mouth or skin folds), the doctor or pharmacist will advise on the treatment
• kidney function disorders
• seizures, especially in patients taking high doses or having kidney problems
• dizziness
• excessive activity
• tooth discoloration (in children), which can usually be removed by brushing
• yellow, brown or black, hairy tongue
• excessive breakdown of red blood cells, which can lead to anemia; symptoms include: fatigue, headaches, shortness of breath, dizziness, pallor and yellowing of the skin and whites of the eyes
• decreased white blood cell count
• decreased platelet count (blood cells involved in blood clotting)
• blood may clot longer than usual; this may be visible in case of nosebleeds or cuts. Side effect with unknown frequency(frequency cannot be estimated from the available data)
• crystals in the urine leading to acute kidney damage, visible as cloudy urine or difficulty or discomfort when urinating; to avoid these symptoms, the patient should drink plenty of fluids.

Reporting side effects

If the patient experiences any side effects, including any side effects not listed in this leaflet, they should tell their doctor, pharmacist or nurse. Side effects can be reported directly to the Department of Adverse Reaction Monitoring of Medicinal Products, Medical Devices and Biocidal Products
Al. Jerozolimskie 181C, 02-222 Warsaw
Phone: +48 22 49 21 301;
Fax: +48 22 49 21 309
website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
By reporting side effects, it is possible to gather more information on the safety of the medicine.

5. How to store Amotaks Dis

The medicine should be stored out of sight and reach of children.
Store in a temperature not exceeding 25°C. Protect from moisture.
Do not use this medicine after the expiry date (EXP) stated on the packaging. The expiry date refers to the last day of the month.
Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.

6. Contents of the packaging and other information

What Amotaks Dis contains

The active substance of the medicine is amoxicillin (in the form of amoxicillin trihydrate).
Amotaks Dis, 500 mg: each tablet contains 500 mg of amoxicillin.
Amotaks Dis, 750 mg: each tablet contains 750 mg of amoxicillin.
Amotaks Dis, 1 g: each tablet contains 1 g of amoxicillin.
Other ingredients of the medicine are: microcrystalline cellulose, crospovidone, magnesium stearate, strawberry flavor [maltodextrin, glucose, arabic gum (E 414), pectin (E 440)], raspberry flavor [maltodextrin, glucose, arabic gum (E 414), pectin (E 440)], tropical flavor [maltodextrin, glucose, arabic gum (E 414), pectin (E 440)], aspartame (E 951).

What Amotaks Dis looks like and what the pack contains

Tablets are almost white to cream-colored, oval, bi-convex with a notch in the middle allowing the tablet to be divided into two equal doses.
Packagingcontains 16 or 20 tablets.

Marketing authorization holder and manufacturer

Tarchomińskie Zakłady Farmaceutyczne „Polfa” Spółka Akcyjna
ul. A. Fleminga 2
03-176 Warsaw
Phone number: 22 811-18-14
To obtain more detailed information about this medicine, the patient should contact the marketing authorization holder.
Date of last revision of the leaflet:

General advice on the use of antibiotics

Antibiotics are used to treat bacterial infections. They are ineffective in treating viral infections.
Sometimes, bacterial infections do not respond to antibiotic treatment. One of the most common reasons for this phenomenon is that bacteria are resistant to the administered antibiotic. This means that bacteria can survive or multiply despite the use of an antibiotic.
Bacteria can become resistant to antibiotics for many reasons. Careful use of antibiotics can help reduce the likelihood of bacteria developing resistance.
The antibiotic prescribed by the doctor is intended solely for the treatment of the current illness. Paying attention to the following tips will help prevent the development of resistant bacteria that could render the antibiotic ineffective.

• 1. It is very important to take the antibiotic in the correct dose, at the right time and for the right number of days. The patient should read the instructions in the leaflet and if any of them are unclear, they should ask their doctor or pharmacist to explain.
• 2. The patient should not take an antibiotic that has not been prescribed specifically for them. They should only take it to treat the infection for which the antibiotic was prescribed.
• 3. The patient should not take an antibiotic prescribed for another person, even if they had a similar infection.
• 4. The patient should not give their antibiotics to other people.
• 5. If, after completing the treatment as recommended by the doctor, there are any remaining antibiotics, the patient should return them to the pharmacy for proper disposal.