AKINETON

This brand name is authorized in Austria, Brazil, Cyprus, Germany, Ecuador, Estonia, Spain, Finland, France, Croatia, Ireland, Japan, Lithuania, Mexico, Netherlands, Poland, Turkey

Active ingredients

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

1 Biperiden UNII K35N76CUHF - BIPERIDEN HYDROCHLORIDE

Biperiden is a predominantly centrally acting anti-cholinergic. It has a peripheral effect, which is low in comparison to atropine. Biperiden binds competitively to peripheral and central muscarinic receptors (primarily M1). Read about Biperiden

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
AKINETON Solution for injection	European Medicines Agency (EU)	MPI, EU: SmPC
AKINETON Tablets	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
N04AA02	Biperiden	N Nervous system → N04 Anti-parkinson drugs → N04A Anticholinergic agents → N04AA Tertiary amines
Discover more medicines within N04AA02

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: BR	Câmara de Regulação do Mercado de Medicamentos	Identifier(s): 559117100007817, 559117100007907
Country: DE	Bundesinstitut für Arzneimittel und Medizinprodukte	Identifier(s): 00660707, 00662356, 00662480, 00662528, 01607721, 01607738, 01607744, 01835066, 02033067, 02033073, 02033096, 02033104, 02126975, 02127199, 02127207, 02130497, 02237982, 02531931, 03035861, 03063969, 03063975, 03192282, 04954593, 04954601, 05023744, 06325387, 06325393, 07143493, 07143501, 07143518, 07202327, 07202333, 10353863, 10353886, 10839198, 10931188, 11229504, 15782155, 15782161, 16768507
Country: EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	Identifier(s): 364480313, 364490313
Country: EE	Ravimiamet	Identifier(s): 1017223, 1077005
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 26692, 28994, 51224
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 495152
Country: FR	Base de données publique des médicaments	Identifier(s): 66782153
Country: HR	Agencija za lijekove i medicinske proizvode	Identifier(s): HR-H-140280757, HR-H-182730030
Country: IE	Health Products Regulatory Authority	Identifier(s): 10783, 10834, 16032
Country: JP	医薬品医療機器総合機構	Identifier(s): 1162001C1043, 1162001F1066, 1162400A1059
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1010429
Country: MX	Comisión Federal para la Protección contra Riesgos Sanitarios	Identifier(s): 47958, 52899, 74405
Country: NL	Z-Index G-Standaard	Identifier(s): 15137937
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 1201, 3743
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100003389, 100003395, 100102660, 100164974, 100240416, 100240451, 100330898, 100333610, 100340997, 100341040, 100363892, 100366175, 100446945, 100451039, 100464388
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8699708011528, 8699708011542, 8699708011559, 8699708011566, 8699708751530, 8699708751547