DYNASTAT

This brand name is authorized in Austria, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Lithuania, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, Spain, Tunisia, UK.

Active ingredients

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

1	Parecoxib UNII EB87433V6F - PARECOXIB SODIUM
	Parecoxib is a prodrug of valdecoxib. Valdecoxib is a selective COX-2 inhibitor within the clinical dose range. Cyclooxygenase is responsible for generation of prostaglandins. Two isoforms, COX-1 and COX-2, have been identified. COX-2 is the isoform of the enzyme that has been shown to be induced by pro-inflammatory stimuli and has been postulated to be primarily responsible for the synthesis of prostanoid mediators of pain, inflammation, and fever.
	Read more about Parecoxib

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
DYNASTAT Powder for 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
M01AH04	Parecoxib	M Musculo-skeletal system → M01 Antiinflammatory and antirheumatic products → M01A Antiinflammatory and antirheumatic products, non-steroids → M01AH Coxibs
Discover more medicines within M01AH04

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	469-MEE-1014
EE	Ravimiamet	1108785, 1108842, 1108853, 1108864
ES	Centro de información online de medicamentos de la AEMPS	02209005, 02209008
FI	Lääkealan turvallisuus- ja kehittämiskeskus	009192
FR	Base de données publique des médicaments	66278897
GB	Medicines & Healthcare Products Regulatory Agency	47349, 47777
HK	Department of Health Drug Office	50467, 58234
LT	Valstybinė vaistų kontrolės tarnyba	1015775, 1015776, 1015777, 1027881
MX	Comisión Federal para la Protección contra Riesgos Sanitarios	227M2001
NL	Z-Index G-Standaard	14748320
NL	Z-Index G-Standaard, PRK	65676
NZ	Medicines and Medical Devices Safety Authority	10168
PL	Rejestru Produktów Leczniczych	100126695, 100126703
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W64924001
SG	Health Sciences Authority	14148P, 14149P
TN	Direction de la Pharmacie et du Médicament	8013071