KONAKION

This brand name is authorized in Austria, Australia, Estonia, Spain, Finland, Hong Kong, Croatia, Ireland, Israel, Lithuania, Malta, Netherlands, New Zealand, Singapore, Turkey, South Africa

Active ingredients

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

1 Phytomenadione
UNII A034SE7857 - PHYTONADIONE

The presence of vitamin K (i.e. vitamin K or substances with vitamin K activity) is essential for the formation within the body of prothrombin, factor VII, factor IX and factor X. Lack of vitamin K leads to an increased tendency to haemorrhage. When an antidote to an anticoagulant is necessary it is essential to use vitamin K1 itself, as vitamin K analogues are much less effective.

Read about Vitamin K1

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
KONAKION MM PAEDIATRIC Solution (ampoules) Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC
KONAKION MM Solution (ampoules) Medicines & Healthcare Products Regulatory Agency (GB) 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
B02BA01 Phytomenadione B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics → B02BA Vitamin K
Discover more medicines within B02BA01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 10213M
Country: EE Ravimiamet Identifier(s): 1799242, 1803248, 1803350, 1803642, 1820652, 1870062
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 008776078IP, 21610, 27262, 8776078
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 404939
Country: HK Department of Health Drug Office Identifier(s): 30412, 38859
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-364029156
Country: IE Health Products Regulatory Authority Identifier(s): 30457, 30493
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 3032, 3677
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1090601, 1090602
Country: MT Medicines Authority Identifier(s): AA1411/01901, AA1456/00101, AA565/08802, AA565/08803, AA565/78201, AA729/00905
Country: NL Z-Index G-Standaard Identifier(s): 13577719, 14145804
Country: NL Z-Index G-Standaard, PRK Identifier(s): 48232
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 3780, 3781
Country: SG Health Sciences Authority Identifier(s): 08533P, 09412P
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8680979254035, 8680979254042
Country: ZA Health Products Regulatory Authority Identifier(s): 29/22/0492

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