PEDEA

This brand name is authorized in Austria, Croatia, Estonia, Finland, France, Hong Kong SAR China, Ireland, Italy, Lithuania, Netherlands, Poland, Romania, South Africa, Spain, UK.

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 more about Ibuprofen

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
PEDEA Solution for injection	MPI, EU: SmPC	European Medicines Agency (EU)

Medicine classification

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

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