SALMEX

This brand name is authorized in Finland, Malta, Poland, Romania

Active ingredients

The drug SALMEX contains a combination of these active pharmaceutical ingredients (APIs):

1 Fluticasone
UNII O2GMZ0LF5W - FLUTICASONE PROPIONATE

Fluticasone has anti-inflammatory and vasoconstrictive features. Fluticasone given by inhalation at recommended doses has a potent glucocorticoid anti-inflammatory action within the lungs, resulting in a reduction of both symptoms and exacerbations of asthma, with a lower incidence and severity of adverse effects than those observed when corticosteroids are administered systemically.

Read about Fluticasone
2 Salmeterol
UNII 6EW8Q962A5 - SALMETEROL XINAFOATE

Salmeterol is a selective long-acting (12 hour) β2 adrenoceptor agonist. These pharmacological properties of salmeterol offer more effective protection against histamine-induced bronchoconstriction and produce a longer duration of bronchodilation, lasting for at least 12 hours, than recommended doses of conventional short-acting β2 agonists.

Read about Salmeterol

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
SALMEX Inhalation powder, pre-dispensed Medicines Authority (MT) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
R03AK06 Salmeterol and fluticasone R Respiratory system → R03 Drugs for obstructive airway diseases → R03A Adrenergics, inhalants → R03AK Adrenergics and other drugs for obstructive airway diseases
Discover more medicines within R03AK06

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 029419, 077046, 107949, 131537, 488598, 508998
Country: MT Medicines Authority Identifier(s): MA1357/00101
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100291253, 100291260, 100291276
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W67890001, W67890002, W67890003, W67890004

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