PATIENT INFORMATION LEAFLET
Loitin 40 mg/ml powder for oral suspension
Fluconazole
Read this leaflet carefully before you start taking this medicine because it contains important information for you.
Loitin is one of the medications in the group called “antifungals”. The active ingredient is fluconazole.
Loitin is used to treat infections caused by fungi, and it may also be used to prevent the appearance of an infection byCandida. The most common cause of fungal infections is a yeast calledCandida.
Adults
Your doctor may prescribe this medication to treat the following types of fungal infections:
Your doctor may also prescribe Loitin for:
Children and adolescents (0 to 17 years)
Your doctor may prescribe this medication to treat the following types of fungal infections:
Your doctor may also prescribe Loitin for:
Warnings and precautions
Consult your doctor or pharmacist before starting to take Loitin
-if you have liver or kidney problems.
-if you have a heart condition, including heart rhythm problems.
-if you have abnormal levels of potassium, calcium, or magnesium in your blood.
-if you experience severe skin reactions (itching, skin redness, or difficulty breathing).
-if you experience signs of “adrenal insufficiency”, where the adrenal glands do not produce enough of certain hormones, such as cortisol (chronic fatigue or prolonged, muscle weakness, loss of appetite, weight loss, abdominal pain).
-if you have ever experienced severe skin rash or skin peeling, blisters, and/or mouth sores after taking Loitin.
Severe skin reactions, including drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported in relation to Loitin treatment. Stop taking Loitin and seek medical attention immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.
Speak with your doctor or pharmacist if the fungal infection does not improve, as an alternative antifungal treatment may be necessary.
Other medications and Loitin
Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication.
Informimmediatelyyour doctor if you are taking astemizole, terfenadine (an antihistamine for treating allergies), cisaprida (used for stomach discomfort), pimozida (used to treat mental health conditions), quinidina (used to treat heart arrhythmias), or erythromycin (an antibiotic for treating infections), as these medications should not be taken with Loitin (see section: “Do not take Loitin”).
There are some medications that may interact with Loitin.
Ensure your doctor knows if you are taking any of the following medications, as it may be necessary to adjust the dose or monitor for effectiveness:
Loitin with food and drinks
You can take the medication with or without food.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
If you plan to become pregnant, it is recommended to wait one week after a single dose of fluconazole before becoming pregnant.
For longer fluconazole treatment cycles, consult your doctor about the need to use appropriate contraceptive methods during treatment, which should be maintained for one week after the last dose.
You should not take Loitin if you are pregnant, think you may be pregnant, or plan to become pregnant, unless your doctor has told you to do so. If you become pregnant while taking this medication or within one week of the most recent dose, consult your doctor.
Fluconazole taken during the first or second trimester of pregnancy may increase the risk of spontaneous abortion. Fluconazole taken during the first trimester may increase the risk of congenital abnormalities affecting the heart, bones, and/or muscles.
Cases of babies born with congenital abnormalities affecting the skull, ears, and leg and elbow bones have been reported in women treated for three months or more with high doses (400-800 mg daily) of fluconazole for coccidioidomycosis. The relationship between fluconazole and these cases is unclear.
You can continue breastfeeding after taking a single dose of 150 mg of Loitin.
You should not continue breastfeeding if you are taking repeated doses of Loitin.
Driving and operating machines
When driving or operating machines, be aware that occasional dizziness or seizures may occur.
Important information about some Loitin components
This medication contains saccharose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Patients with diabetes mellitus should note that this medication contains 5.77 g (Loitin 10 mg/ml) or 5.46 (Loitin 40 mg/ml) of saccharose per 10 ml of oral suspension.
It may cause tooth decay if used for periods longer than 2 weeks.
This medication contains 2.96 mg of sodium benzoate per ml of oral suspension. Sodium benzoate may increase the risk of jaundice in newborns (up to 4 weeks of age).
Once reconstituted, a 20 ml dose of this medication contains less than 1 mmol of sodium (23 mg); this is essentially “sodium-free”.
It is better to take your medications always at the same time of the day.
The following are the recommended doses of this medication for different types of infections:
Adults
Condition | Dose |
To treat cryptococcal meningitis | 400 mg on the first day and subsequently 200 mg to 400 mg once a day for 6 to 8 weeks or longer if necessary. In some cases, the dose is increased to 800 mg. |
To prevent the recurrence of cryptococcal meningitis | 200 mg once a day until your doctor tells you to stop. |
To treat coccidioidomycosis | 200 mg to 400 mg once a day from 11 months to 24 months or longer if necessary. In some cases, the dose is increased to 800 mg. |
To treat internal fungal infections caused by Candida | 800 mg on the first day and subsequently 400 mg once a day until your doctor tells you to stop. |
To treat fungal infections of the mucous membranes affecting the mouth, throat, or associated with dental prostheses | 200 mg to 400 mg on the first day, and subsequently 100 mg to 200 mg once a day until your doctor tells you to stop. |
To treat mucosal candidiasis – the dose depends on the location of the infection | 50 mg to 400 mg once a day for 7 to 30 days until your doctor tells you to stop. |
To prevent the recurrence of mucosal infections affecting the mouth and throat | 100 mg to 200 mg once a day, or 200 mg three times a week, as long as you are at risk of developing an infection. |
To treat genital candidiasis | 150 mg as a single dose. |
To reduce the recurrence of vaginal candidiasis | 150 mg every three days for a total of 3 doses (days 1, 4, and 7) and then once a week as long as you are at risk of developing an infection. |
To treat fungal skin or nail infections | Depending on the location of the infection, 50 mg once a day, 150 mg once a week, 300 to 400 mg once a week for 1 to 4 weeks (for athlete's foot, up to 6 weeks may be necessary, for nail infections, continue treatment until a healthy nail grows). |
To prevent the transmission of an infection caused by Candida (if your immune system is weakened and does not function properly) | 200 mg to 400 mg once a day as long as you are at risk of developing an infection. |
Adolescents 12 to 17 years of ageold
Follow the dose indicated by your doctor (the adult dosage or the pediatric dosage).
Children up to 11 years old
The maximum daily dose for children is 400 mg.
The dose will be based on the child's weight in kilograms.
Condition | Daily dose |
Mucosal candidiasis and throat infections caused by Candida – the dose and duration of treatment depend on the severity of the infection and its location | 3 mg per kg of body weight once a day (the first day may be 6 mg per kg of body weight) |
Cryptococcal meningitis or internal fungal infections caused by Candida | 6 mg to 12 mg per kg of body weight once a day |
To prevent the recurrence of cryptococcal meningitis | 6 mg per kg of body weight once a day |
To prevent a child from contracting an infection caused by Candida (if their immune system does not function properly) | 3 mg to 12 mg per kg of body weight once a day |
Use in children 0 to 4 weeks old
Use in children 3 to 4 weeks old:
Use in children under 2 weeks old:
Elderly patients
The usual adult dose, unless you have kidney problems.
Patients with kidney problems
Your doctor may change your dose, depending on how well your kidneys are functioning.
Instructions for preparing the suspension:
Your pharmacist should reconstitute the powder for oral suspension before giving it to you. However, if the pharmacist does not reconstitute this product, the instructions are provided in the "The following information is only for doctors and other healthcare professionals or for patients (if the pharmacist does not reconstitute this product)" section at the end of this leaflet.
Instructions for use:
Shake the suspension bottle with the cap closed before each use.
In adults, calculate the dose in ml to administer according to the recommended dosage in mg and the product concentration.
If you take more Loitin than you should
Taking too much Loitin may make you feel unwell. Contact your doctor immediately or go to the nearest hospital. You can also call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount taken. Symptoms of a possible overdose may include hearing, seeing, feeling, and thinking things that are not real (hallucinations and paranoid behavior). It may be appropriate to initiate symptomatic treatment (with supportive measures and gastric lavage if necessary).
If you forget to take Loitin
Do not take a double dose to make up for the missed doses. If you have forgotten to take a dose, take it as soon as you remember. If it is almost time for the next dose, do not take the missed dose.
If you have any doubts about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicinecan cause side effects, although not everyone will experience them.
Stop taking Loitin and seek medical attention immediately if you notice any of the following symptoms:
Some people developallergic reactions,although severe allergic reactions are rare.If any side effect appears, talk to your doctor or pharmacist. This includes any possible side effect not mentioned in this leaflet. If you experience any of the following symptoms, informyour doctor immediately.
Loitin may affect your liver. Signs that indicate liver problems include:
-fatigue.
-loss of appetite.
-vomiting.
-yellowing of the skin or white of the eyes (jaundice).
If you experience any of these symptoms, stop taking Loitin andinform your doctor immediately.
Other side effects:
In addition, if you consider that any of the side effects you are experiencing are severe or if you notice any side effect not mentioned in this leaflet, inform your doctor or pharmacist.
Frequent side effects (may affect up to 1 in 10 patients) are:
Less frequent side effects (may affect up to1 in 100 patients) are:
Rare side effects (may affect up to 1 in 1000 patients) are:
Frequency not known, but may occur (cannot be estimated from available data):
Reporting side effects
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect not mentioned in this leaflet. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use:www.notificaRAM.es.
By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Medicines should not be disposed of through drains or in the trash. Dispose of the packaging and unused medications at the SIGRE collection point of the pharmacy. If in doubt, ask your pharmacist how to dispose of unused packaging and medications. By doing so, you will help protect the environment.
The active ingredient is fluconazole. Each 1 ml of reconstituted suspension contains 40 mg of fluconazole.
The other components are: sucrose, citric acid monohydrate (E-330), sodium citrate anhydrous (E-331), sodium benzoate (E-211), xanthan gum (E-415), colloidal silica (E-551), titanium dioxide (E-171), and orange aroma. See section 2 Important information about some of the components of Loitin.
Appearance of Loitin 40mg/ml oral powder and contents of the container
Loitin 40mg/ml oral powder is a dry white to off-white powder, packaged in a topaz-colored glass bottle. After adding water to the powder (following the instructions for healthcare professionals), it results in a white to off-white suspension with an orange flavor.
In each bottle, the mixture of powder with water produces 35 ml of suspension.
A measuring cup is also supplied to measure the correct dose.
It is presented in containers with 1 bottle and in clinical containers with 10 bottles.
The information in this leaflet only corresponds to Loitin 40 mg/ml oral powder.
For information on Loitin 10 mg/ml oral powder or Loitin capsules, please read the leaflet for these products.
Marketing authorization holder and responsible manufacturer
Marketing authorization holder:
Dari Pharma, S.L.U.
Gran Via Carles III, 98, 10th floor
08028 Barcelona – Spain
Responsible manufacturer:
Neuraxpharm Pharmaceuticals, S.L.
Avda. Barcelona, 69
08970 Sant Joan Despí (Barcelona)
Spain
Last review date of this leaflet: June 2024
The detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS): http://www.aemps.gob.es/
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This information is intended for healthcare professionals and patients (in case the pharmacist does not reconstitute this product):
Instructions for preparing the suspension:
The reconstituted suspension will consist of a white to off-white suspension with an orange flavor.
1. G ently shake the bottle to loosen the powder.
2. a dd a small amount of water and agitate vigorously. Add water up to the level marked on the bottle (this is achieved by adding 24 ml of water).
3. a gitate well for one or two minutes to obtain a uniform suspension.
4. E scribe the expiration date of the reconstituted suspension on the bottle label (the expiration date of the reconstituted suspension is 14 days). The remaining suspension cannot be used after this date and must be returned to the pharmacist.
Conversion of the dose of oral powder for suspension from mg/ml to ml/kg body weight:
Loitin 40 mg/ml oral powder:
In children, the dose of Loitin oral powder should be measured as accurately as possible according to the following equation:
The maximum daily dose should not exceed 400 mg in the pediatric population. The use of Loitin 40 mg/ml oral powder is not recommended for weights below 15 kg. For weights below 15 kg, Loitin 10 mg/ml oral powder is recommended.
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.