Benzydamine hydrochloride
This medicine should always be used exactly as described in this patient leaflet or as directed by your doctor or pharmacist.
Tantum Verde, a spray for use in the mouth and throat, contains the active substance benzydamine, which belongs to the group of indole non-steroidal anti-inflammatory drugs (NSAIDs) for local and general use.
Benzydamine is characterized by its anti-inflammatory and analgesic effects, and it also has a local anesthetic and disinfectant effect. The medicine is well absorbed locally, reaching high concentrations in the tissues affected by the inflammatory process. The medicine is generally well tolerated and is suitable for local treatment of inflammation symptoms.
The medicine is for use on the mucous membrane of the mouth and throat.
The medicine is used to treat symptoms (pain, redness, swelling) associated with inflammation of the mouth and throat, such as bacterial and viral infections, inflammation of the mucous membranes after radiotherapy, post-operative conditions in laryngology and stomatology, as well as after intubation.
If after 7 days there is no improvement or the patient feels worse, you should consult a doctor.
Before starting to use Tantum Verde, you should discuss it with your doctor or pharmacist.
Using, especially long-term, medicines with local action may cause an allergic reaction. In such a case, the medicine should be discontinued and a doctor should be consulted, who will recommend appropriate action.
You should tell your doctor or pharmacist about all medicines that the patient is currently using or has recently used, as well as about medicines that the patient plans to use.
No interactions of Tantum Verde with other medicines are known.
If the patient is pregnant or breastfeeding, suspects that she may be pregnant, or plans to have a child, she should consult a doctor or pharmacist before using this medicine.
The medicine does not affect the ability to drive or use machines.
The medicine may cause allergic reactions (late-type reactions are possible).
This medicine contains 13.6 mg of alcohol (ethanol) in a single dose of 0.17 ml of solution, which is equivalent to 80 mg/ml. The amount of alcohol in a single dose of this medicine is equivalent to less than 1 ml of beer or 1 ml of wine. The small amount of alcohol in this medicine will not have noticeable effects.
The medicine contains a peppermint flavor with benzyl alcohol (E 1519), cinnamaldehyde, citral, citronellol, geraniol, isoeugenol, linalool, eugenol, and d-limonene, which may cause allergic reactions.
The medicine contains 0.024 mg of benzyl alcohol in each dose (0.17 ml). Benzyl alcohol may cause allergic reactions and mild local irritation.
Administering benzyl alcohol to small children is associated with a risk of serious side effects, including respiratory disorders (so-called "gasping syndrome"). Do not administer to newborns (up to 4 weeks of age) without a doctor's recommendation.
Do not administer to small children (under 3 years of age) for more than a week without a doctor's or pharmacist's recommendation.
Pregnant or breastfeeding women should consult a doctor before using the medicine, as a large amount of benzyl alcohol may accumulate in their body and cause side effects (so-called metabolic acidosis).
Patients with liver or kidney disease should consult a doctor before using the medicine, as a large amount of benzyl alcohol may accumulate in their body and cause side effects (so-called metabolic acidosis).
The medicine contains less than 1 mmol (23 mg) of sodium per dose, which means that the medicine is considered "sodium-free".
This medicine should always be used exactly as described in this patient leaflet or as directed by your doctor or pharmacist. In case of doubt, you should consult a doctor or pharmacist.
Tantum Verde should be sprayed onto the mucous membrane of the mouth and throat.
The recommended dose is:
Children under 6 years of age: 1 dose of the medicine (spray) per 4 kg of body weight, 2 to 6 times a day.
Regardless of body weight, do not exceed 4 doses at a time.
Children between 6 and 12 years of age: 4 doses of the medicine, 2 to 6 times a day.
Children over 12 years of age: 4 to 8 doses of the medicine, 2 to 6 times a day.
4 to 8 doses (sprays) of the medicine, 2 to 6 times a day.
Each dose of the medicine contains 0.17 ml of solution.
Do not use a higher dose than recommended. Continuous treatment should not be longer than 7 days, and any extension of treatment should be decided by a doctor.
Instructions for use:
Note: When using the medicine for the first time, the pump button should be pressed several times to fill the pump and obtain the correct spray.
If you feel that the effect of the medicine is too strong or too weak, you should consult a doctor.
Overdose of the medicine is unlikely due to the low concentration of the active substance in the medicine and the local route of administration.
No cases of overdose have been observed so far.
In case of using a higher dose than recommended or accidental ingestion of a large amount of the medicine, you should immediately consult a doctor or pharmacist.
You should not use a double dose to make up for a missed dose.
In case of any further doubts related to the use of this medicine, you should consult a doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Very rare(less than 1 in 10,000 people) and frequency not known(cannot be estimated from the available data):
Local symptoms are related to the pharmacodynamic effect of benzydamine, which, among other things, has a local anesthetic effect.
Local side effects are usually transient, resolve on their own, and rarely require additional treatment.
Benzydamine used locally is absorbed into the circulation in small amounts, and therefore general side effects occur very rarely.
If you experience any side effects, including any possible side effects not listed in this leaflet, you should tell your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the 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, you can help provide more information on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
There are no special precautions for storage.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the month stated.
Shelf life after first opening – 6 months.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Clear, colorless solution with a peppermint flavor.
HDPE container with a dosing pump with a foldable dosing nozzle (nozzle), in a cardboard box.
1 container - 30 ml
In order to obtain more detailed information, you should contact the marketing authorization holder or the parallel importer.
Angelini Pharma Österreich GmbH
Brigittenauer Lände 50-54
1200 Vienna
Austria
A.C.R.A.F. S.p.A
Via Vecchia del Pinocchio 22
60131 Ancona
Italy
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
Marketing authorization number in Lithuania, the country of export: LT/1/01/0257/005
Parallel import authorization number: 442/19
[Information about the trademark]
Need help understanding this medicine or your symptoms? Online doctors can answer your questions and offer guidance.