Malarone

Leaflet accompanying the packaging: information for the user

Warning! Keep the leaflet, the information on the immediate packaging is in a foreign language!

Malarone

250 mg + 100 mg, film-coated tablets

Atovaquone + Proguanil hydrochloride

You should carefully read the contents of the leaflet before taking 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.
• If you have any doubts, you should consult a doctor or pharmacist.
• This medicine has been prescribed specifically for you. 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 Malarone and what is it used for
• 2. Important information before taking Malarone
• 3. How to take Malarone
• 4. Possible side effects
• 5. How to store Malarone
• 6. Contents of the packaging and other information

1. What is Malarone and what is it used for

Malarone belongs to a group of medicines called antimalarials. It contains two active substances: atovaquone and proguanil hydrochloride.

Indications for use of Malarone

Malarone has two uses:

• for the prevention of malaria
• for the treatment of malaria

Dosing recommendations for each indication can be found in section 3. How to take Malarone.
Malaria is spread through the bites of infected mosquitoes, which transmit the parasite
(Plasmodium falciparum) into the blood. Malarone prevents malaria by destroying the cells of this
parasite. In people who are already infected with malaria, Malarone also destroys the cells of these
parasites.

You should protect yourself against malaria infection.

Malaria can be contracted at any age. It is a serious disease, but it can be prevented.
It is very important to take measures to prevent mosquito bites in addition to taking Malarone.

• On exposed skin surfaces, insect repellents should be used.
• Light-colored clothing that covers most of the body should be worn,especially after sunset, as mosquitoes are most active at this time.
• Sleep in a protected roomor under a mosquito net impregnated with an insecticide.
• Windows and doors should be closed at sunset,if they are not screened.
• Consider using an insecticide(mats, aerosols, plugs) to clear the room of insects or prevent mosquitoes from entering the room.
• If you have any further doubts, you should consult a doctor or pharmacist.

Infection with malaria can occur despite taking the necessary precautions

of caution.In some types of malaria, the time from infection to the onset of symptoms can be long, so the disease may only become apparent after several days, weeks, or even months after returning from abroad.

• If symptoms such as high temperature, chills, headache, and fatigue occur after returning from abroad,you should contact a doctor immediately.

2. Important information before taking Malarone

When not to take Malarone

• If the patient is allergicto atovaquone, proguanil hydrochloride, or any of the other ingredients of this medicine (listed in section 6).
• In the prevention of malaria in patients with severe kidney disease.
• If these circumstances apply to the patient, they should tell their doctor.

When to exercise special caution when taking Malarone

Before starting to take Malarone, the patient should tell their doctor or pharmacist if:

• the patient has severe kidney disease
• the patient is a child being treated for malaria who weighs less than 11 kg. For the treatment of children weighing less than 11 kg, tablets with a different active substance content are available (see section
• 3).
• If these circumstances apply to the patient, they should tell their doctor or pharmacist.

Malarone and other medicines

The patient should tell their doctor or pharmacist about all medicinesthey are taking, or have recently taken, and about any medicines they plan to take, including those that are available without a prescription.
Some medicines may affect the action of Malarone or Malarone may increase or decrease the action of other medicines taken at the same time. These medicines include:

• metoclopramide, used to treat nausea and vomiting
• antibiotics, tetracycline, rifampicin, rifabutin
• efavirenzor certain protease inhibitorsused to treat HIV
• warfarinand other medicines that prevent blood clotting
• etoposide, used to treat cancer.
• If the patient is taking any of these medicines, they should tell their doctor. The doctor may decide that Malarone should not be taken or may recommend additional tests during its use.
• If the patient starts taking other medicines while taking Malarone, they should remember to tell their doctor.

Taking Malarone with food and drink

Malarone should be taken with food or a milk drink, if possible.
This will increase the absorption of Malarone and the effectiveness of the treatment.

Pregnancy and breastfeeding

If the patient is pregnant, they should not take Malarone,unless their doctor recommends otherwise.

• Before taking Malarone, the patient should consult their doctor or pharmacist.

The patient should not breastfeed while taking Malarone,as the active substances of Malarone pass into breast milk and may harm the baby.

Driving and using machines

The patient should not drive if they experience dizziness.

Malarone may cause dizziness in some people. If the patient experiences this symptom, they should not drive, operate any machinery, or perform any tasks that may pose a risk to themselves or others.

Malarone contains sodium

The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is essentially 'sodium-free'.

3. How to take Malarone

This medicine should always be taken according to the doctor's or pharmacist's recommendations.If in doubt, the patient should consult their doctor or pharmacist.
If possible, Malarone should be taken with food or a milk drink.
It is best to take Malarone at the same time every day.

If the patient vomits

During malaria prevention

• If the patient vomits within 1 hour of taking a Malarone tablet, they should take another dose immediately.
• It is essential to complete the full treatment cycle with Malarone. If the patient has taken extra doses due to vomiting, they may need an additional prescription.
• If the patient vomits,it is especially important to take additional precautions, such as using insect repellents and mosquito nets. Malarone may not be effective, as the amount of medicine absorbed may be reduced.

During malaria treatment

• If the patient vomits and has diarrhea,they should tell their doctor, who will recommend regular blood tests. Malarone may not be effective, as the amount of medicine absorbed may be reduced. Blood tests will allow the doctor to check if the malaria parasite has been removed from the patient's blood.

Malaria prevention

The recommended dose of Malarone for adultsis one tablet once a day, taken as follows.
Malarone is not recommended for malaria prevention in childrenor adults with a body weight below 40 kg.
For adults and children with a body weight below 40 kg, Malarone is recommended in the form of pediatric tablets.
To prevent malaria in adults, the patient should:

• start taking Malarone 1 to 2 days before traveling to a malaria-endemic area;
• continue taking Malarone every day during their stay;
• continue taking Malarone for 7 days after returning to a malaria-free area.

Malaria treatment

The recommended dose of Malarone for adultsis 4 tablets once a day for 3 days.
Dosing in childrendepends on body weight:

• 11-20 kg - 1 tablet once a day for three days
• 21-30 kg - 2 tablets in one daily dose for three days
• 31-40 kg - 3 tablets in one daily dose for three days
• over 40 kg - dosing as for adults.

This medicine is not recommended for the treatment of malaria in childrenwith a body weight below 11 kg.
If the child's body weight is below 11 kg, the patient should tell their doctor. In some countries, Malarone tablets with a different active substance content may be available.

Taking more than the recommended dose of Malarone

The patient should consult their doctor or pharmacist. If possible, they should show them the packaging of Malarone.

Missing a dose of Malarone

It is essential to complete the full treatment cycle with Malarone.

If the patient misses a dose of Malarone, they should take it as soon as possible and continue treatment as recommended.

The patient should not take a double dose to make up for a missed dose. They should take the next dose of Malarone at the usual time.

The patient should not stop taking Malarone without their doctor's recommendation.

The patient should continue taking Malarone for 7 days after returning to a malaria-free area.

to ensure maximum protection.To complete the full treatment cycle with Malarone, the patient should take it for 7 days after returning to a malaria-free area. Stopping the treatment early may put the patient at risk of malaria, as it takes 7 days to ensure that all parasites that may have appeared in the blood after a mosquito bite have been destroyed.
If the patient has any further doubts about taking this medicine, they should consult their doctor or pharmacist.

4. Possible side effects

Like all medicines, Malarone can cause side effects, although not everybody gets them.
The patient should be aware of the following serious side effects. They have occurred in a small number of people, but their frequency is unknown.
Severe allergic reactions- symptoms include:

• rash and itching
• sudden wheezing, chest tightness or throat tightness, or difficulty breathing
• swelling of the eyelids, face, lips, tongue, or other parts of the body.
• If the patient experiences any of the above symptoms of an allergic reaction, they should contact their doctor immediately. They should not take any further tablets.

Severe skin reactions

• a rash that may be blistering and looks like small targets (dark spots in the center, surrounded by a pale area with a dark ring around it) (erythema multiforme)
• a severe, widespread rash with blisters and peeling skin, especially around the mouth, nose, eyes, and genitals (Stevens-Johnson syndrome).
• If the patient experiences any of these symptoms, they should contact their doctor urgently.

Other side effects were mostly mild and temporary.

Very common side effects

May affect more than 1 in 10 patients:

• headache,
• nausea and vomiting,
• abdominal pain,
• diarrhea.

Common side effects

May affect less than 1 in 10 patients:

• dizziness,
• sleep disturbances (insomnia),
• unusual dreams,
• depression,
• loss of appetite,
• fever,
• rash that may be itchy,
• cough.

Common side effects that may appear in blood tests:

• decrease in red blood cell count (anemia), which may cause fatigue, headaches, and shortness of breath,
• decrease in white blood cell count (neutropenia), which may cause increased susceptibility to infections,
• decrease in sodium levels in the blood (hyponatremia),
• increase in liver enzyme activity.

Uncommon side effects

May affect less than 1 in 100 patients:

• anxiety,
• abnormal heartbeat (palpitations),
• swelling and redness of the mouth,
• hair loss,
• itchy rash with blisters (hives).

Uncommon side effects that may appear in blood tests:

• increase in amylase activity (an enzyme produced in the pancreas).

Rare side effects

May affect less than 1 in 1000 patients:

• seeing or hearing things that are not real (hallucinations).

Other side effects

Other side effects that have occurred in a small number of people, but their frequency is unknown.

• liver inflammation,
• bile duct obstruction (bile stasis),
• rapid heartbeat (tachycardia),
• blood vessel inflammation, which may appear as red or purple spots on the skin, but may also affect other parts of the body,
• seizures,
• panic attacks, crying,
• nightmares,
• severe mental health disorders, in which the patient loses contact with reality and is unable to think clearly and assess the situation,
• indigestion,
• mouth ulcers,
• blisters,
• skin peeling,
• increased sensitivity of the skin to sunlight.

Other side effects that may appear in blood tests:

• decrease in the number of all types of blood cells (pancytopenia).

Reporting side effects

If the patient experiences any side effects, including any side effects not listed in this leaflet, they should tell their doctor or pharmacist. Side effects can be reported directly to the Department of Medicinal Product Monitoring, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: + 48 22 49 21 301,
fax: + 48 22 49 21 309, website: https://smz.ezdrowie.gov.pl
By reporting side effects, more information can be collected on the safety of the medicine.

5. How to store Malarone

The medicine should be stored out of sight and reach of children.

The patient should not take this medicine after the expiry date stated on the packaging.The expiry date refers to the last day of the month stated.

There are no special precautions for storage.

Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines they no longer use. This will help protect the environment.

6. Contents of the packaging and other information

What Malarone contains

The active substances of Malarone are:atovaquone 250 mg and proguanil hydrochloride 100 mg, in each tablet.

Other ingredients of Malarone are:

tablet core:poloxamer 188, microcrystalline cellulose, low-substituted hydroxypropyl cellulose, povidone K 30, sodium carboxymethyl cellulose (type A), magnesium stearate;
tablet coating:hypromellose, titanium dioxide (E 171), red iron oxide (E 172), macrogol 400, macrogol 8000 (see section 2).

• If the patient is allergic to any of these ingredients, they should inform their doctor before taking Malarone.

What Malarone looks like and what the pack contains

Malarone film-coated tablets are pink and round, with the inscription "GX CM3" on one side.
They are packaged in blisters containing 12 tablets in a cardboard box.
For more detailed information, the patient should contact the marketing authorization holder or the parallel importer.

Marketing authorization holder in Ireland, the country of export:

GlaxoSmithKline (Ireland) Limited
12 Riverwalk
Citywest Business Campus
Dublin 24
Ireland

Manufacturer

Aspen Bad Oldesloe GmbH
Industriestrasse 32-36
23843 Bad Oldesloe
Germany
Glaxo Wellcome S.A.
Avenida de Extremadura, 3
09400 Aranda de Duero (Burgos)
Spain

Parallel importer:

Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź

Repackaged by:

Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
Marketing authorization number in Ireland, the country of export: PA1077/111/001
Parallel import authorization number: 139/25

This medicine is authorized in the Member States of the European Economic Area and in the United Kingdom (Northern Ireland) under the following names:

Austria, Belgium, Czech Republic, Finland, Germany, Greece, Spain, Netherlands, Ireland, Iceland, Lithuania, Luxembourg, Latvia, Malta, Norway, Poland, Portugal, Slovakia, Slovenia, Sweden, Hungary, Italy, United Kingdom (Northern Ireland): Malarone

Date of leaflet approval: 11.04.2025

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