


Ask a doctor about a prescription for AZITHROMYCIN TARBIS 500 mg FILM-COATED TABLETS
Azithromycin Tarbis 500 mg film-coated tablets EFG
Azithromycin (dihydrate)
Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.
Contents of the Package Leaflet
Azithromycin belongs to a group of antibiotics called macrolide antibiotics.

It is used to treat the following infections:
Do not take Azithromycin Tarbis:
Warnings and Precautions
Consult your doctor or pharmacist before starting to take Azithromycin Tarbis:
Children
Azithromycin Tarbis should not be administered to children under 6 months of age.
Use of Azithromycin Tarbis with other medications
Inform your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication.
Azithromycin may interact with other medications. Inform your doctor or pharmacist if you are taking any of the following medications:
Pregnancy and Breastfeeding
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.
Azithromycin Tarbis is not recommended during pregnancy and breastfeeding, unless, in the doctor's opinion, the benefit outweighs the risk to the child.
Driving and Using Machines
There is no evidence that Azithromycin Tarbis affects the ability to drive or operate machinery.
Azithromycin Tarbis contains sucrose
This medication contains sucrose. 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 3.6 g of sucrose per 5 ml of reconstituted suspension.
Follow the instructions for administration of this medication indicated by your doctor. If in doubt, consult your doctor or pharmacist again.
Remember to take your medication.
Your doctor will indicate the duration of treatment with Azithromycin Tarbis. Do not stop treatment before completion, as there is a risk of relapse of the disease.
Azithromycin Tarbis is administered orally. The tablets should be swallowed whole, with a sufficient amount of liquid (a glass of water).
The dose will be determined by your doctor based on your individual needs and the type of infection. To achieve optimal efficacy, follow your doctor's instructions regarding dose and duration of treatment.
The recommended dose is:
Adults (including elderly patients): 500 mg (1 tablet) once a day for 3 consecutive days, with a total dose of 1500 mg (3 tablets).
For the treatment of sexually transmitted diseases, the dose is 1000 mg (2 tablets) taken as a single oral dose.
Children and adolescents: The dose of 500 mg of this formulation is only suitable for children and adolescents over 45 kg in weight, for whom the same dose as for adults is recommended. For those under 45 kg, other formulations are recommended.
If you think the effect of Azithromycin Tarbis is too strong or too weak, inform your doctor or pharmacist.
Consult your doctor or pharmacist immediately.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.
Do not take a double dose to make up for forgotten doses.
If you have any further questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication can cause side effects, although not everyone will experience them.
Most side effects observed in clinical trials were mild to moderate, reversible after discontinuation of the medication, and mainly affected the digestive system, consisting primarily of nausea, vomiting, diarrhea, or abdominal pain. Potentially serious side effects such as laryngeal edema (due to an allergic reaction) or changes in liver function accompanied by yellowing of the skin occurred rarely.
In addition, during treatment with Azithromycin Tarbis, any of the following side effects may occur, described for azithromycin when administered orally.
If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this package leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medications: https://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 shown on the blister pack and the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the Pharmacy Point. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
Azithromycin Tarbis 500 mg are film-coated tablets. Each package contains 3 tablets.
TARBIS FARMA, S.L.
Gran Vía Carlos III, 94
08028-BARCELONA (Spain)
KERN PHARMA, S.L.
Polígono Ind. Colón II Venus, 72
08228 Terrassa (Barcelona)
Industria Quimica y Farmaceutica VIR, S.A.
C/ Laguna 66-68-70, Polígono Industrial Urtinsa II
28923 Alcorcón (Madrid)
Spain
Date of the last revision of this package leaflet: July 2022
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
The average price of AZITHROMYCIN TARBIS 500 mg FILM-COATED TABLETS in November, 2025 is around 5.62 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for AZITHROMYCIN TARBIS 500 mg FILM-COATED TABLETS – subject to medical assessment and local rules.