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About the medicine

Jak stosować ATSELASTINA E FLUTIKASONE VIATRIS

Treść ulotki

  1. Azelastina e Fluticasone Viatris 137 micrograms/50 micrograms per actuation nasal spray
  2. azelastine hydrochloride/fluticasone propionate
    1. What is Azelastina and Fluticasone Viatris nasal spray and what is it used for
    2. What you need to know before using Azelastina e Fluticasone Viatris nasal spray
    3. How to use Azelastina and Fluticasone Viatris nasal spray
    4. Possible side effects
    5. How to store Azelastina and Fluticasone Viatris nasal spray
    6. Package contents and other information

Azelastina e Fluticasone Viatris 137 micrograms/50 micrograms per actuation nasal spray

nasal, suspension

azelastine hydrochloride/fluticasone propionate

Read this leaflet carefully before you start using this medicine as it contains important
information for you.

  • Keep this leaflet. You may need to read it again.
  • If you have any questions, ask your doctor or pharmacist.
  • This medicine has been prescribed for you only. Do not pass it on to others, even if their symptoms are the same as yours, as it could be harmful.
  • If you get any side effects, even those not listed in this leaflet, tell your doctor or pharmacist. See section 4.

Contents of this leaflet

  • 1. What Azelastina e Fluticasone Viatris nasal spray is and what it is used for
  • 2. What you need to know before you use Azelastina e Fluticasone Viatris nasal spray
  • 3. How to use Azelastina e Fluticasone Viatris nasal spray
  • 4. Possible side effects
  • 5. How to store Azelastina e Fluticasone Viatris nasal spray
  • 6. Contents of the pack and other information

1. What is Azelastina and Fluticasone Viatris nasal spray and what is it used for

Azelastina and Fluticasone Viatris nasal spray contains two active ingredients: azelastine hydrochloride and
fluticasone propionate.

  • Azelastine hydrochloride belongs to the pharmacotherapeutic category of antihistamines. Antihistamines work by blocking the effects of substances such as histamine, which the body produces following an allergic reaction, thereby reducing the symptoms of allergic rhinitis.
  • Fluticasone propionate belongs to the pharmacotherapeutic category of corticosteroids, which reduce inflammation. Azelastina and Fluticasone Viatris nasal spray is used to relieve the symptoms of seasonal and perennial allergic rhinitis, from moderate to severe, when the use of antihistamine alone or corticosteroid alone via the intranasal route is not considered sufficient.

Seasonal or perennial allergic rhinitis are allergic reactions to substances such as pollen (hay fever), dust mites, molds, dust or pets.
Azelastina and Fluticasone Viatris nasal spray relieves allergy symptoms, such as excessive
nasal mucus production, runny nose, sneezing, itchy nose or stuffy nose.

2. What you need to know before using Azelastina e Fluticasone Viatris nasal spray

Do not use Azelastina e Fluticasone Viatris nasal spray:

  • if you are allergic to azelastine hydrochloride or fluticasone propionate or to any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions
Talk to your doctor or pharmacist before using Azelastina e Fluticasone Viatris nasal spray:

  • if you have recently had nasal surgery
  • if you have had a nasal infection. Nasal and airway infections must be treated with an antibacterial or antifungal medicine. If you have been given a medicine for a nasal infection, you can continue to use Azelastina e Fluticasone Viatris nasal spray to treat your allergies
  • if you have tuberculosis or an untreated infection
  • if you have had vision disorders or if you have a history of increased eye pressure, glaucoma and/or cataracts. If you have these conditions, you will be carefully monitored during the use of Azelastina e Fluticasone Viatris nasal spray
  • if you suffer from adrenal insufficiency. Extreme caution should be exercised when switching from systemic corticosteroid treatment to Azelastina e Fluticasone Viatris nasal spray
  • if you suffer from a severe liver disease. Your risk of developing undesirable systemic effects is greater.

In these cases, your doctor will decide whether or not you can use this medicine.
It is important that you take your dose, as indicated in the following section 3 or
as recommended by your doctor. Treatment with doses of inhaled corticosteroids higher than those
recommended can cause adrenal suppression, a condition that can cause weight loss, fatigue, muscle weakness, reduced blood sugar levels, craving for
salty foods, joint pain, depression and darkening of the skin. If these conditions occur, your doctor may recommend another medicine during periods of
stress or in case of elective surgery.
To avoid adrenal suppression, your doctor will advise you to take the lowest dose that can
effectively control your rhinitis symptoms.
If taken for long periods, inhaled corticosteroids (such as Azelastina e Fluticasone Viatris nasal spray) can cause a slowing of growth in children and adolescents. Your doctor will regularly check
your child's height and ensure they take the lowest effective dose possible.
Contact your doctor if you experience blurred vision or other visual disturbances.
If you are not sure whether the conditions mentioned above apply to you, talk to your doctor or
pharmacist before using this medicine.

Children
The use of this medicine is not recommended in children under 12 years of age.

Other medicines and Azelastina e Fluticasone Viatris nasal spray
Tell your doctor or pharmacist if you are taking, have recently taken or might take
any other medicines.
Some medicines can increase the effects of Azelastina e Fluticasone Viatris nasal spray and your
doctor may want to keep you under close observation if you are taking these medicines
(including some medicines for the treatment of HIV: ritonavir, cobicistat and medicines for the
treatment of fungal infections: ketoconazole).

Pregnancy and breastfeeding
If you are pregnant, suspect you are pregnant, are planning to become pregnant or are breastfeeding with
breast milk, ask your doctor or pharmacist for advice before using Azelastina e Fluticasone Viatris
nasal spray.

Driving and using machines
Azelastina e Fluticasone Viatris nasal spray negligibly alters the ability to drive vehicles
and use machines.
Very rarely, fatigue or dizziness may occur due to the disease itself or
the use of Azelastina e Fluticasone Viatris nasal spray. In these cases, avoid driving or
using machines. You should be aware that consuming alcohol can increase these
effects.

Azelastina e Fluticasone Viatris nasal spray contains benzalkonium chloride
This medicine contains 14 micrograms of benzalkonium chloride per actuation, equivalent to
0.014 mg/0.14 g. Benzalkonium chloride can cause irritation and swelling inside the nose,
especially if used for long periods.

3. How to use Azelastina and Fluticasone Viatris nasal spray

Use this medicine following the doctor's instructions exactly. If you have any doubts, consult your
doctor or pharmacist.
It is essential to use Azelastina and Fluticasone Viatris nasal spray regularly to obtain the
full therapeutic benefit.
Avoid contact with the eyes.

Adults and adolescents (from 12 years of age)

  • The recommended dose is one spray in each nostril in the morning and evening.

Use in children under 12 years of age

  • The use of this medicine is not recommended in children under 12 years of age.

Use in patients with impaired renal and hepatic function

  • No data are available on patients with renal and hepatic insufficiency.

Method of administration
For nasal use.
Read what is reported in this leaflet and follow the instructions.

INSTRUCTIONS FOR USE
Preparing the spray

  • 1. Gently shake the bottle for 5 seconds, tilting it up and down, then remove the protective cap (see figure 1).

Figure 1

Dark glass vial with white cap and cone-shaped top adapter black arrow indicates the direction
  • 2. The first time you use the nasal spray, you must prime the pump by spraying the product into the air.
  • 3. Prime the pump by placing two fingers on both sides of the spray pump and placing your thumb on the base of the bottle.
  • 4. Press down and release the pump 6 times, until a fine mist comes out (see figure 2).
  • 5. Now the pump is primed and ready for use. Figure 2
Hand holding a dark bottle with a white dropper and a black arrow indicates the direction downwards
  • 6. If the nasal spray has not been used for more than 7 days, you will need to re-prime the pump once, by pressing and releasing the pump itself.

Using the spray

  • 1. Gently shake the bottle for 5 seconds, tilting it up and down, then remove the protective cap (see figure 1).
  • 2. Blow your nose to clear your nostrils.
  • 3. Keep your head tilted downwards towards your feet. Do not tilt your head back.
  • 4. Hold the bottle upright and gently insert the tip of the spray into one nostril.
  • 5. Close the other nostril with a finger, press down quickly once, and at the same time, inhale gently (see figure 3).
  • 6. Exhale through your mouth.

Figure 3

Woman using a nasal spray held with the
  • 7. Repeat the same procedure for the other nostril.
  • 8. Inhale gently without tilting your head back after spraying. This will prevent the medicine from going down your throat, causing you to experience an unpleasant taste (see figure 4).

Figure 4

Woman looking down while holding a nasal spray in her hand ready to
  • 9. After each use, wipe the tip of the spray with a tissue or a clean cloth and then reinsert the protective cap.
  • 10. Do not poke the nozzle if you do not get the spray. Clean the tip of the spray with water.

It is important that you take your dose as recommended by your doctor. Use only the amount recommended
by your doctor.

Duration of treatment
Azelastina and Fluticasone Viatris nasal spray is indicated for long-term use. The duration of
treatment should correspond to the period in which the symptoms of allergy manifest.

If you use moreAzelastina and Fluticasone Viatris nasal spraythan you should
If you spray an excessive dose of this medicine into your nose, it is unlikely that any
problems will occur. If you are worried or if you have used higher doses than recommended for a long
period, contact your doctor. In case of accidental ingestion of Azelastina and Fluticasone Viatris nasal
spray, especially by a child, contact your doctor or the nearest
hospital emergency room as soon as possible.

If you forget to use Azelastina and Fluticasone Viatris nasal spray
Use the nasal spray as soon as you remember, then take the next dose as usual. Do not
take a double dose to make up for the missed dose.

If you stop using Azelastina and Fluticasone Viatris nasal spray
Do not stop using this medicine without asking your doctor, as this puts
the success of the treatment at risk.
If you have any doubts about the use of this medicine, consult your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Seek immediate medical assistance if you notice any of the following symptoms:

  • Swelling of the face, lips, tongue or throat, which can cause difficulty swallowing/breathing and sudden onset of rash. These could be signs of a severe allergic reaction.

Other side effects include:

Very common side effects(may affect more than 1 in 10 people) :

  • nosebleed

Common side effects(may affect up to 1 in 10 people) :

  • headache
  • bitter taste in the mouth, especially if you tilt your head back when using the nasal spray. This should disappear quickly if you sip a non-alcoholic beverage for a few minutes after using this medicine.
  • unpleasant smell

Uncommon side effects(may affect up to 1 in 100 people) :

  • mild irritation of the inside of the nose. This can cause a slight burning, itching or sneezing
  • nasal dryness, cough, dry throat or throat irritation

Rare side effects(may affect up to 1 in 1,000 people) :

  • dry mouth

Uncommon side effects(may affect up to 1 in 10,000 people) :

  • dizziness or drowsiness
  • cataract, glaucoma or increased eye pressure, resulting in loss of vision and/or red and painful eyes. These side effects have been reported after prolonged treatment with fluticasone propionate-based nasal sprays.
  • damage to the skin and mucous membrane of the nose
  • feeling unwell, exhaustion, fatigue or weakness
  • rash, itching or redness of the skin, raised itchy welts
  • bronchospasm (narrowing of the airways in the lungs)

Side effects with unknown frequency(frequency cannot be estimated based on available data) :

  • blurred vision
  • Nasal ulcers

It is possible that systemic side effects (side effects involving the whole body) may occur when this medicine is used at high doses for a long period. These effects are much less likely to occur if you use a corticosteroid nasal spray, compared to taking corticosteroids by mouth. These effects can vary in individual patients and between different corticosteroid preparations (see paragraph 2)
Nasal corticosteroids can affect the normal production of hormones in the body, particularly if you use high doses for a long period. In children and adolescents, this side effect can cause a slowing of growth.
In rare cases, a reduction in bone density (osteoporosis) has been observed when inhaled corticosteroids have been administered for a long period.

Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly through the national reporting system at https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse. By reporting side effects you can help provide more information on the safety of this medicine.

5. How to store Azelastina and Fluticasone Viatris nasal spray

Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the label of the bottle and on the
pack after “Exp.”. The expiry date refers to the last day of that month.
Do not refrigerate or freeze.
Shelf life after first opening: discard any unused medicine 6 months after the first
opening of the nasal spray.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist how to
dispose of medicines you no longer use. This will help protect the environment.

6. Package contents and other information

What Azelastina e Fluticasone Viatris nasal spray contains
The active ingredients are: azelastine hydrochloride and fluticasone propionate.
Each gram of suspension contains 1,000 micrograms of azelastine hydrochloride and
365 micrograms of fluticasone propionate.
Each actuation (0.14 g) delivers 137 micrograms of azelastine hydrochloride
(= 125 micrograms of azelastine) and 50 micrograms of fluticasone propionate.
The other ingredients are: disodium edetate, glycerol, microcrystalline cellulose, sodium carboxymethylcellulose,
polysorbate 80, benzalkonium chloride solution, phenyl ethyl alcohol and purified water.

Description of the appearance ofAzelastina e Fluticasone Viatris nasal sprayand contents of the
pack

Azelastina e Fluticasone Viatris nasal spray is a white, homogeneous suspension.
Azelastina e Fluticasone Viatris nasal spray is supplied in an amber glass bottle, equipped
with a spray pump, an applicator and a protective cap.
The 10 mL bottle contains 6.4 g of nasal spray, suspension (at least 28 actuations). The 25 mL bottle contains 23 g of nasal spray, suspension (at least 120 actuations).
Azelastina e Fluticasone Viatris nasal spray is available in:
Packs containing 1 bottle with 6.4 g of nasal spray, suspension
Packs containing 1 bottle with 23 g of nasal spray, suspension
Multipacks comprising 10 bottles, each containing 6.4 g of nasal spray, suspension
Multipacks comprising 3 bottles, each containing 23 g of nasal spray, suspension
Not all pack sizes may be marketed.

Marketing Authorisation Holder
Mylan S.p.A.
Via Vittor Pisani, 20
20124 Milan

Manufacturer
MEDA Pharma GmbH & Co. KG
Benzstraße 1
D-61352 Bad Homburg
Germany
Haupt Pharma Amareg GmbH
Donaustaufer Straße 378
D-93055 Regensburg
Germany

This medicinal product is authorised in the Member States of the European Economic Area with the following
names:

GermanyAzelastin/Fluticason Viatris 137 Mikrogramm/50 Mikrogramm pro Sprühstoß o Nasenspray, Suspension
Austriac Azeflu
Czech Republica Dymol
DenmarkFlutista
Greecem Flutista 137 microgram/50 microgram nasal spray, suspension
Finlandr Flutista
Francea AZÉLASTINE CHLORHYDRATE/FLUTICASONE PROPIONATE VIATRIS F 137 microgrammes/50 microgrammes, suspension pour pulvérisation nasale
HungaryAzelasztin/Flutikazon Viatris 137 mikrogramm / 50 mikrogramm szuszpenziós l orrspray
Italye Azelastina e Fluticasone Viatris
Netherlandsd Azelastine/ Fluticasonpropionaat Viatris 137 microgram/50 microgram per verstuiving, neusspray, suspensie
Norwaya Dymol
Polandn Dymol
Portugala Azelastine + Fluticasone Mylan
Romaniai AZEFLU 137 micrograme / 50 micrograme spray nazal, suspensie l
Swedena Flutista
Sloveniat Dymol 137 mikrogramov/50 mikrogramov na vpih pršilo za nos, suspenzija
SlovakiaI Dymol
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Odpowiedniki ATSELASTINA E FLUTIKASONE VIATRIS w innych krajach

Leki z tą samą substancją czynną dostępne w innych krajach.

Odpowiednik ATSELASTINA E FLUTIKASONE VIATRIS w Hiszpania

Postać farmaceutyczna: PREPARAT DO ZASTOSOWANIA DONOSOWEGO, 137 mikrogramów/50 mikrogramów
Substancja czynna: fluticasone, combinations
Producent: Day Zero Ehf.
Wymaga recepty
Postać farmaceutyczna: PREPARAT DO ZASTOSOWANIA DONOSOWEGO, 137 mikrogramów/50 mikrogramów/aplikacja
Substancja czynna: fluticasone, combinations
Postać farmaceutyczna: PREPARAT DO ZASTOSOWANIA DONOSOWEGO, 137 mikrogramów/50 mikrogramów/aplikacja
Substancja czynna: fluticasone, combinations
Wymaga recepty
Postać farmaceutyczna: PREPARAT DO ZASTOSOWANIA DONOSOWEGO, 137 mikrogramów/50 mikrogramów
Substancja czynna: fluticasone, combinations
Wymaga recepty
Postać farmaceutyczna: PREPARAT DO ZASTOSOWANIA DONOSOWEGO, 1 mg/g - 0,365 mg/g
Substancja czynna: fluticasone, combinations
Wymaga recepty
Postać farmaceutyczna: PREPARAT DO ZASTOSOWANIA DONOSOWEGO, 137 mikrogramów/50 mikrogramów/aktywacja
Substancja czynna: fluticasone, combinations
Producent: Teva B.V.
Wymaga recepty

Odpowiednik ATSELASTINA E FLUTIKASONE VIATRIS w Polska

Postać farmaceutyczna: Aerozol, (137 mcg + 50 mcg)/dawkę donosową
Substancja czynna: fluticasone, combinations
Importer: Adamed Pharma S.A. Farmaclair FARMEA
Wymaga recepty
Postać farmaceutyczna: Aerozol, (137 mcg + 50 mcg)/dawkę donosową
Substancja czynna: fluticasone, combinations
Importer: Farmaclair FARMEA
Wymaga recepty
Postać farmaceutyczna: Aerozol, (137 mcg + 50 mcg)/dawkę donosową
Substancja czynna: fluticasone, combinations
Importer: Farmaclair FARMEA
Wymaga recepty
Postać farmaceutyczna: Aerozol, (137 mcg + 50 mcg)/dawkę donosową
Substancja czynna: fluticasone, combinations
Importer: Farmea
Wymaga recepty
Postać farmaceutyczna: Aerozol, (137 mcg + 50 mcg)/dawkę donosową
Substancja czynna: fluticasone, combinations
Importer: Farmaclair FARMEA
Wymaga recepty
Postać farmaceutyczna: Aerozol, (137 mcg + 50 mcg)/ dawkę
Substancja czynna: fluticasone, combinations
Importer: Basic Pharma Manufacturing B.V.
Wymaga recepty

Odpowiednik ATSELASTINA E FLUTIKASONE VIATRIS w Ukraina

Postać farmaceutyczna: spray, 137 mcg/50 mcg per dose
Substancja czynna: fluticasone, combinations
Wymaga recepty
Postać farmaceutyczna: spray, 56, 120 or 240 doses in a polyethylene bottle
Wymaga recepty
Postać farmaceutyczna: spray, 75 or 150 doses in a bottle
Wymaga recepty

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Lekarz
5.0(1)

Tomasz Grzelewski

DermatologiaAlergologia21 lata doświadczenia

Lek. Tomasz Grzelewski, PhD, jest alergologiem, pediatrą, lekarzem rodzinnym i specjalistą medycyny sportowej, z klinicznym zainteresowaniem dermatologią, endokrynologią, alergologią i medycyną sportową. Ma ponad 20-letnie doświadczenie kliniczne. Ukończył Uniwersytet Medyczny w Łodzi, gdzie obronił pracę doktorską z wyróżnieniem. Jego badania zostały nagrodzone przez Polskie Towarzystwo Alergologiczne za innowacyjny wkład w rozwój alergologii. Od lat zajmuje się diagnostyką i leczeniem szerokiego zakresu schorzeń alergicznych i pediatrycznych, w tym nowoczesnymi metodami odczulania.

Przez pięć lat kierował dwoma oddziałami pediatrycznymi w Polsce, pracując z wymagającymi przypadkami klinicznymi i zespołami wielospecjalistycznymi. Pracował również w ośrodkach medycznych w Wielkiej Brytanii, zdobywając doświadczenie zarówno w podstawowej opiece zdrowotnej, jak i w opiece specjalistycznej. Od ponad dziesięciu lat prowadzi konsultacje online, doceniany za przejrzystość zaleceń i jakość porad.

Lek. Grzelewski aktywnie uczestniczy w programach klinicznych poświęconych nowoczesnym terapiom przeciwalergicznym. Jako główny badacz prowadzi projekty związane z odczulaniem podjęzykowym i doustnym, wspierając rozwój terapii opartych na aktualnych dowodach naukowych.

Ukończył także studia dermatologiczne w Cambridge Education Group (Royal College of Physicians of Ireland) oraz kurs endokrynologii klinicznej na Harvard Medical School, co poszerza jego kompetencje w zakresie zmian skórnych, atopii, pokrzywki, objawów endokrynnych i reakcji immunologicznych.

Pacjenci najczęściej zgłaszają się do lek. Grzelewskiego z takimi problemami jak:

  • alergie sezonowe i całoroczne
  • alergiczny nieżyt nosa i przewlekła niedrożność nosa
  • astma i trudności oddechowe
  • alergie pokarmowe i polekowe
  • pokrzywka, atopowe zmiany skórne, reakcje skórne
  • nawracające infekcje u dzieci
  • pytania dotyczące aktywności fizycznej i zdrowia sportowego
  • problemy ogólne w ramach medycyny rodzinnej
Lek. Tomasz Grzelewski jest ceniony za jasną komunikację, uporządkowane podejście i umiejętność tłumaczenia planów leczenia w sposób prosty i przystępny. Jego szerokie doświadczenie w alergologii, pediatrii, dermatologii i endokrynologii pozwala mu zapewniać pacjentom kompleksową i bezpieczną opiekę.
Umów wideokonsultację
zł366

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Często zadawane pytania

Czy ATSELASTINA E FLUTIKASONE VIATRIS wymaga recepty?

ATSELASTINA E FLUTIKASONE VIATRIS nie wymaga recepty w Włochy. Możesz skonsultować się z lekarzem online, aby sprawdzić, czy ten lek może być odpowiedni w Twojej sytuacji.

Jaka jest substancja czynna w ATSELASTINA E FLUTIKASONE VIATRIS?

Substancją czynną w ATSELASTINA E FLUTIKASONE VIATRIS jest fluticasone, combinations. Informacja ta pomaga rozpoznać leki o tym samym składzie, ale pod różnymi nazwami handlowymi.

Kto produkuje ATSELASTINA E FLUTIKASONE VIATRIS?

ATSELASTINA E FLUTIKASONE VIATRIS jest produkowany przez MYLAN S.P.A.. Nazwy handlowe i opakowania mogą się różnić w zależności od dystrybutora.

Którzy lekarze mogą ocenić stosowanie ATSELASTINA E FLUTIKASONE VIATRIS online?

Lekarze, tacy jak Lekarze rodzinni, Psychiatrzy, Dermatolodzy, Kardiolodzy, Endokrynolodzy, Gastroenterolodzy, Pulmonolodzy, Nefrolodzy, Reumatolodzy, Hematolodzy, Zakaźnicy, Alergolodzy, Geriatrzy, Pediatrzy, Onkolodzy, mogą ocenić, czy stosowanie ATSELASTINA E FLUTIKASONE VIATRIS jest odpowiednie w Twoim przypadku, w zależności od sytuacji klinicznej i lokalnych przepisów. Możesz umówić konsultację online, aby omówić objawy i możliwe dalsze kroki.

Jak kupić ATSELASTINA E FLUTIKASONE VIATRIS w Polsce?

Polska posiada dobrze rozwiniętą infrastrukturę ochrony zdrowia w dużych miastach, takich jak Warszawa, Kraków, Wrocław i Gdańsk. Apteki są łatwo dostępne i działają zgodnie z obowiązującymi przepisami, zapewniając dostęp do leków na receptę.

Możesz kupić ATSELASTINA E FLUTIKASONE VIATRIS w Warszawie, Krakowie, Wrocławiu lub Gdańsku w każdej aptece, posiadając ważną receptę.

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Jakie są alternatywy dla ATSELASTINA E FLUTIKASONE VIATRIS?

Inne leki zawierające tę samą substancję czynną (fluticasone, combinations) to m.in. ATSELASTINA E FLUTIKASONE SUBSTIPARM, ATSELASTINA E FLUTIKASONE TSENTIVA, DIPLORIN. Mogą one różnić się nazwą handlową lub postacią, ale zawierają ten sam składnik terapeutyczny. Przed zmianą lub rozpoczęciem nowego leku skonsultuj się z lekarzem.

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