Package Insert: Information for the User
Fluconazole Tarbis 150 mg Hard Capsules EFG
Read this package insert carefully before starting to take this medication, as it contains important information for you.
Fluconazol Tarbis is one of the medications in the group called “antifungals”. The active ingredient is fluconazol.
Fluconazol Tarbis is used to treat infections caused by fungi, and it may also be used to prevent the appearance of a fungal infection. The most common cause of fungal infections is a fungus called Candida.
Adults
Your doctor may prescribe this medication to treat the following types of fungal infections:
-Cryptococcal meningitis – a fungal infection in the brain.
-Coccidioidomycosis – a disease of the bronchopulmonary system.
-Infections caused by Candida localized in the bloodstream, in organs of the body (e.g. heart, lungs) or in the urinary tract.
-Mucosal candidiasis – an infection that affects the mucous membrane of the mouth, throat, or associated with dental prostheses.
-Genital candidiasis – an infection of the vagina or penis.
-Skin infections – e.g. athlete's foot, ringworm, inguinal ringworm, nail infection.
Your doctor may also prescribe Fluconazol Tarbis for:
-To prevent the recurrence of cryptococcal meningitis.
-To prevent the recurrence of mucosal infections.
-To reduce the recurrence of vaginal infections caused by Candida.
-To prevent the transmission of infections caused by Candida (if your immune system is weak and does not function properly).
Children and adolescents (0 to 17 years)
Your doctor may prescribe this medication to treat the following types of fungal infections:
-Mucosal candidiasis – an infection that affects the mucous membrane of the mouth or throat.
-Infections caused by Candida localized in the bloodstream, in organs of the body (e.g. heart, lungs) or in the urinary tract.
-Cryptococcal meningitis – a fungal infection in the brain.
Your doctor may also prescribe Fluconazol Tarbis for:
-To prevent the transmission of infections caused by Candida (if your immune system is weak and does not function properly).
-To prevent the recurrence of cryptococcal meningitis.
Do not take Fluconazol Tarbis if:
Warnings and precautions
Consult your doctor or pharmacist before starting to take Fluconazol Tarbis if
-You have liver or kidney problems.
-You have a heart condition, including heart rhythm problems.
-You have abnormal levels of potassium, calcium, or magnesium in your blood.
-You experience severe skin reactions (itching, skin redness, or difficulty breathing).
Severe skin reactions, including drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported in relation to Fluconazol Tarbis treatment. Stop taking Fluconazol Tarbis and seek medical attention immediately if you notice any symptoms related to these severe skin reactions described in section 4.
Use of Fluconazol Tarbis with other medications
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Notify your doctor immediately if you are taking astemizole, terfenadine (an antihistamine for allergies), cisaprida (used for stomach discomfort), pimozida (used to treat mental illnesses), quinidina (used to treat heart arrhythmias), or eritromicina (an antibiotic for infections), as these medications should not be taken with Fluconazol Tarbis (see section: “Do not take Fluconazol Tarbis if”).
There are some medications that may interact with Fluconazol Tarbis.
Make sure your doctor knows if you are taking any of the following medications:
Fluconazol Tarbis and food, drinks, and alcohol
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 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 maintained for one week after the last dose.
Do not take Fluconazol Tarbis if you are pregnant, think you may be pregnant, or plan to become pregnant or breastfeed, unless your doctor has instructed 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 during the first trimester may increase the risk of a baby being born with congenital anomalies affecting the heart, bones, and/or muscles.
Cases of babies born with congenital anomalies 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.
Consult your doctor or pharmacist before using any medication.
Driving and operating machines
When driving or operating machines, be aware that occasional dizziness or seizures may occur.
Fluconazol Tarbis contains lactose
This medication contains a small amount of lactose (milk sugar). If your doctor has told you that you have a certain sugar intolerance, consult with them before taking this medication.
Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The capsules should be swallowed whole with the help of a glass of water. It is better to take your medications always at the same time of the day.
The following indicates the usual dose of this medication for different types of infections:
Adults
Disease | 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 more 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 more if necessary. In some cases, the dose is increased to 800 mg. |
To treat internal fungal infections caused byCandida | 800 mg on the first day and subsequently 400 mg once a day until your doctor tells you to stop. |
To treat mucosal infections that affect the oral mucosa, pharynx, or associated with dental prostheses. | 200 mg to 400 mg on the first day, and then 100 mg to 200 mg 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 mucosal infections that affect the oral mucosa and pharynx | 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 infections of the skin or nails | 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 spread of an infection caused byCandida(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. |
Use in adolescents 12 to 17 years old
Follow the dose indicated by your doctor (the adult dose or the pediatric dose).
Use in 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.
Disease | Daily dose |
Mucosal candidiasis and pharyngeal infections caused byCandida– the dose and duration of treatment depend on the severity of the infection and its location. | 3 mg per kg of body weight (the first day may be 6 mg per kg of body weight) |
Cryptococcal meningitis or internal fungal infections caused byCandida | 6 mg to 12 mg per kg of body weight |
To prevent a child from contracting an infection caused byCandida(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 old
Use in children 3 to 4 weeks old:
Use in children under 2 weeks old:
In some cases, doctors may prescribe different doses than those described. Follow exactly the administration instructions indicated by your doctor. Consult your doctor or pharmacist if you have any doubts.
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 Tarbis than you should
Taking too many capsules at once may make you feel unwell. Contact your doctor or the nearest hospital immediately. You can also call the Toxicological 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 Tarbis
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 interrupt treatment with Fluconazol Tarbis
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medicationmay cause side effects, although not everyone will experience them.
Some people developallergic reactionsalthough severe allergic reactions are rare.If any of the following symptoms appear,inform your doctor immediately.
Fluconazol Tarbis 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 takingFluconazol Tarbisandinform your doctor immediately.
Stop taking Fluconazol Tarbis and seek medical attention immediately if you notice any of the following symptoms:
Other side effects:
In addition, if you consider any of the side effects you are experiencing to be severe or if you notice any side effect not mentioned in this leaflet, inform your doctor or pharmacist.
The following are common side effects that affect 1 to 10 of every 100 patients:
The following are infrequent side effects that affect 1 to 10 patients per 1,000:
The following are rare side effects, affecting 1 to 10 patients per 10,000:
Reporting side effects
If you experience any type of side effect, consult your doctor or pharmacist, 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 medication.
This medication does not require special conservation conditions.
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.
Medications should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at the SIGRE collection point of the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition ofFluconazol Tarbis
The active ingredient is fluconazole.
Each hard capsule contains 150mg of fluconazole.
The other components (excipients) are:
Hard capsule content: lactose monohydrate (lactose), pregelatinized cornstarch (cornstarch), hydrated colloidal silica, magnesium stearate, sodium lauryl sulfate.
Hard capsule composition: gelatin, titanium dioxide (E171) and quinoline (E 104).
Appearance of the product and contents of the packaging
The capsules have a green body and cap.
It is presented in packaging of 1 and 4 hard capsules and clinical packaging with 100 hard capsules.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization:
TARBIS FARMA, S.L.
Gran Vía Carlos III, 94
08028 - Barcelona
Spain
Responsible for manufacturing:
Neuraxpharm Pharmaceuticals, S.L
Avda. Barcelona, 69
08970 Sant Joan Despí (Barcelona)
Date of the last review of this leaflet:February 2024
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS):http://www.aemps.gob.es/
Есть вопросы по этому лекарству или вашим симптомам? Свяжитесь с лицензированным врачом для получения помощи и персонализированного ухода.