MYSILDECARD

This brand name is authorized in Austria, Germany, Estonia, Spain, France, Ireland, Italy, Lithuania, Netherlands, Poland, Romania

Active ingredients

The drug MYSILDECARD contains one active pharmaceutical ingredient (API):

1 Sildenafil
UNII BW9B0ZE037 - SILDENAFIL CITRATE

Sildenafil is a potent and selective inhibitor of cyclic guanosine monophosphate (cGMP) specific phosphodiesterase type 5 (PDE5), the enzyme that is responsible for degradation of cGMP. Apart from the presence of this enzyme in the corpus cavernosum of the penis, PDE5 is also present in the pulmonary vasculature. Sildenafil, therefore, increases cGMP within pulmonary vascular smooth muscle cells resulting in relaxation.

Read about Sildenafil

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
MYSILDECARD Film-coated tablet European Medicines Agency (EU) 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
G04BE03 Sildenafil G Genito urinary system and sex hormones → G04 Urologicals → G04B Other urologicals, incl. antispasmodics → G04BE Drugs used in erectile dysfunction
Discover more medicines within G04BE03

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 12457176, 12661994
Country: EE Ravimiamet Identifier(s): 1729166, 1729177
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1161134003
Country: FR Base de données publique des médicaments Identifier(s): 69190025
Country: IE Health Products Regulatory Authority Identifier(s): 88036
Country: IT Agenzia del Farmaco Identifier(s): 045112036
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1081049, 1081050, 1081051
Country: NL Z-Index G-Standaard, PRK Identifier(s): 80365
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100377552
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W68188001

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