AMPRES

This brand name is authorized in Austria, Finland, Ireland, Israel, Netherlands, Poland, Spain, UK.

Active ingredients

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

1
UNII LT7Z1YW11H - CHLOROPROCAINE HYDROCHLORIDE
 

Chloroprocaine is procaine in which one of the hydrogens ortho- to the carboxylic acid group is substituted by chlorine. Chloroprocaine, blocks the generation and the conduction of nerve impulses, presumably by increasing the threshold for electrical excitation in the nerve, by slowing the propagation of the nerve impulse and by reducing the rate of rise of the action potential. Chloroprocaine (like cocaine) has the advantage of constricting blood vessels which reduces bleeding, unlike other local anesthetics like lidocaine.

 
Read more about Chloroprocaine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 AMPRES 20 mg/ml Solution for injection MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)
 AMPRES 10 mg/ml Solution for injection MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group Classification
N01BA04 Chloroprocaine N Nervous system → N01 Anesthetics → N01B Anesthetics, local → N01BA Esters of aminobenzoic acid
Discover more medicines within N01BA04
N01BA05 Benzocaine N Nervous system → N01 Anesthetics → N01B Anesthetics, local → N01BA Esters of aminobenzoic acid
Discover more medicines within N01BA05

Authorization and marketing

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

Country Identification scheme Identifier(s)
ES Centro de información online de medicamentos de la AEMPS 76137
FI Lääkealan turvallisuus- ja kehittämiskeskus 075685
GB Medicines & Healthcare Products Regulatory Agency 220202, 383478
IL מִשְׂרַד הַבְּרִיאוּת 8815
NL Z-Index G-Standaard, PRK 205036
PL Rejestru Produktów Leczniczych 100284419

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