Package Insert: Information for the User
Fluconazole Normon 100 mg Hard Capsules EFG
Read this package insert carefully before starting to take the medicine.
Fluconazol Normon is one of the medications in the group called “antifungals”. The active ingredient is fluconazol.
Fluconazol 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 fluconazol 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 fluconazol for:
Do not take Fluconazol Normon if
-You are allergic (hypersensitive) to fluconazole, to other medicines you have taken to treat fungal infections or to any of the other ingredients of this medicine (listed in section 6).
The symptoms may include itching, skin redness or difficulty breathing.
-You are taking astemizole, terfenadine (antihistamines to treat allergies).
-You are taking cisapride (used to treat stomach discomfort).
-You are taking pimozide (used to treat mental illnesses).
-You are taking quinidine (used to treat heart arrhythmias).
-You are taking erythromycin (an antibiotic to treat infections).
Warnings and precautions
Consult your doctor or pharmacist before starting to take Fluconazol Normon
If you have ever had a severe skin rash or skin peeling, blisters and/or mouth sores after taking Fluconazol Normon.
Severe skin reactions, including drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported in association with fluconazole treatment. Stop using this medicine and seek medical attention immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.
Talk to your doctor or pharmacist if the fungal infection does not improve, an alternative antifungal treatment may be necessary.
Taking Fluconazol Normon with other medicines
Inform your doctor or pharmacist if you are using, have used recently or may need to use any other medicine.
Informimmediatelyyour doctor if you are taking astemizole, terfenadine (an antihistamine to treat allergies), cisapride (used to treat stomach discomfort), pimozide (used to treat mental illnesses), quinidine (used to treat heart arrhythmias) or erythromycin (an antibiotic to treat infections), as these medicines should not be taken with Fluconazol (see section: “Do not take FluconazolNormonif”).
There are some medicines that may interact with Fluconazol.
Make sure your doctor knows if you are taking any of the following medicines, as it may be necessary to adjust the dose or monitor to ensure the medicines continue to have the desired effect:
Taking Fluconazol Normon with food and drink
You can take the medicine with or without food.
Pregnancy, breastfeeding and fertility
If you are pregnant or breastfeeding, think you may be pregnant or are planning to become pregnant, consult your doctor or pharmacist before taking any medicine.
If you are planning to become pregnant, it is recommended that you wait one week after a single dose of fluconazole before becoming pregnant.
For longer treatment cycles with fluconazole, consult your doctor about the need to use suitable contraceptive methods during treatment, which should be continued for one week after the last dose.
You should not take Fluconazol if you are pregnant, think you may be pregnant or are planning to become pregnant, unless your doctor has told you to. If you become pregnant while taking this medicine 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 a baby being born with congenital abnormalities affecting the heart, bones and/or muscles.
Cases of babies born with congenital abnormalities affecting the skull, ears and leg and arm 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 fluconazole. Do not continue breastfeeding if you are taking repeated doses of fluconazole.
Driving and operating machinery
When driving or operating machinery, be aware that occasional dizziness or convulsions may occur.
Fluconazol Normon contains lactose and sodium
This medicine contains lactose. If your doctor has told you that you have a certain sugar intolerance, consult with them before taking this medicine.
This medicine contains less than 1 mmol of sodium (23 mg) per capsule; it is essentially “sodium-free”.
Follow exactly the administration instructions of this medication indicated by your doctor. If in doubt, consult your doctor or pharmacist again.
The capsules should be swallowed whole with the help of a glass of water. It is best to take your medications at the same time every day.
The following indicates the usual dose of this medication for different types of infections:
Adults
Illness | 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 lining of the mouth, throat, or associated with dental prostheses. | 200 mg to 400 mg on the first day, and then 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 lining of the mouth and throat | 100 mg to 200 mg once a day, or 200 mg 3 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 3 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 aged 12 to 17 years
Follow the dose indicated by your doctor (the adult dose or the pediatric dose).
Children up to 11 years
The maximum daily dose for children is 400 mg.
The dose will be based on the child's weight in kilograms.
Illness | 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 the transmission of an infection caused by Candida (if your immune system does not function properly) | 3 mg to 12 mg per kg of body weight |
Use in children 0 to 4 weeks of age
Use in children 3 to 4 weeks of age:
Use in children under 2 weeks of age:
Geriatric 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.
If you take more Fluconazol Normon than you should
Taking too many capsules at once 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 Fluconazol Normon
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 there is little time left 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.
Stop using Fluconazol and seek medical attentionimmediatelyif you notice any of the following symptoms:
•Generalized rash, high body temperature, and enlarged lymph nodes (DRESS syndrome or drug hypersensitivity syndrome).
Some people developallergic reactions, although severe allergic reactions are rare. If any side effect occurs, 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.
Fluconazol may affect your liver. Signs indicating liver problems include:
-Fatigue.
-Loss of appetite.
-Vomiting.
-Yellowing of the skin or the white part of the eyes (jaundice).
If you experience any of these symptoms, stop takingthis medicationand
inform your doctor immediately.
Other side effects:
In addition, if you consider that any of the side effects you experience 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 to 1 in 100 patients) are:
Rare side effects (may affect up to 1 in 1000 patients) are:
Unknown frequency, but may occur (cannot be estimated from available data):
Reporting side effects
If you experience any type ofside effect, consult your doctor, pharmacist, or nurse, even if it is a 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 medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
No special storage conditions are required.
Store in the original packaging.
Medications should not be disposed of through drains or in the trash. Dispose of the packaging and medications you no longer need at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition ofFluconazole Normon
The active ingredient is fluconazole.
Each hard capsule contains100mg of fluconazole.
The other components (excipients) are:
Content of the capsules:lactose monohydrate, cornstarch, silicon dioxidecolloid (E-551), magnesium stearate (E-572) and sodium lauryl sulfate (E-470a). See section 2
Fluconazole Normon contains lactose and sodium.
Composition of the capsule:titanium dioxide (E171), water and gelatin
Appearance ofFluconazole Normon100 mg hard capsules and packaging contents
The capsules have a white opaque body and cap.
It is presented in packagingwith 7 or 100 (EC) capsules in PVC-PVDC and Aluminum blisters.
Not all packaging sizes may be commercially available.
Marketing Authorization Holder and Responsible Manufacturer
Marketing Authorization Holder:
LABORATORIOS NORMON, S.A.
Ronda de Valdecarrizo, 6 – 28760 Tres Cantos – Madrid (Spain)
Responsible Manufacturer:
LICONSA, S.A.
Avda. Miralcampo, Nº 7, Industrial Estate Miralcampo
19200 Azuqueca de Henares (Guadalajara), Spain
This leaflet was approved in: August 2024
The detailed information of this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS):http://www.aemps.gob.es/
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.