PEDEA

This brand name is authorized in Austria, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Italy, Lithuania, Netherlands, Poland, Romania, United Kingdom, South Africa

Active ingredients

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

1 Ibuprofen
UNII WK2XYI10QM - IBUPROFEN

Ibuprofen is a propionic acid derivative NSAID that has demonstrated its efficacy by inhibition of prostaglandin synthesis. In humans ibuprofen reduces inflammatory pain, swellings and fever. Furthermore, ibuprofen reversibly inhibits platelet aggregation.

Read about Ibuprofen

Medicine classification

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

ATC code Group title Classification
C01EB16 Ibuprofen C Cardiovascular system → C01 Cardiac therapy → C01E Other cardiac preparations → C01EB Other cardiac preparations
Discover more medicines within C01EB16
M02AA13 Ibuprofen M Musculo-skeletal system → M02 Topical products for joint and muscular pain → M02A Topical products for joint and muscular pain → M02AA Antiinflammatory preparations, non-steroids for topical use
Discover more medicines within M02AA13

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1197604
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 04284001
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 020662
Country: FR Base de données publique des médicaments Identifier(s): 67747504
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 95679
Country: HK Department of Health Drug Office Identifier(s): 66722
Country: IT Agenzia del Farmaco Identifier(s): 036602011
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1030196
Country: NL Z-Index G-Standaard Identifier(s): 15204103
Country: NL Z-Index G-Standaard, PRK Identifier(s): 81213
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100127105
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W69006001
Country: ZA Health Products Regulatory Authority Identifier(s): A40/3.1/0174

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