This brand name is authorized in Australia, Ireland, Japan, Malta, New Zealand, United Kingdom, United States
The drug CATAPRES contains one active pharmaceutical ingredient (API):
1
Clonidine
UNII W76I6XXF06 - CLONIDINE HYDROCHLORIDE
|
Clonidine has been shown to have both central and peripheral sites of action. With long-term treatment clonidine reduces the responsiveness of peripheral vessels to vasoconstrictor and vasodilator substances and to sympathetic nerve stimulation. Early in treatment, however, blood pressure reduction is associated with a central reduction of sympathetic outflow and increased vagal tone. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
CATAPRES Solution for injection | Health Products Regulatory Authority (IE) | MPI, EU: SmPC | |
CATAPRES Tablet | Health Products Regulatory Authority (IE) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
C02AC01 | Clonidine | C Cardiovascular system → C02 Antihypertensives → C02A Antiadrenergic agents, centrally acting → C02AC Imidazoline receptor agonists |
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): 3141H, 3145M |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 16313, 27799 |
Country: IE | Health Products Regulatory Authority | Identifier(s): 16690, 82872 |
Country: JP | 医薬品医療機器総合機構 | Identifier(s): 2149001F1034, 2149001F2065 |
Country: MT | Medicines Authority | Identifier(s): AA1442/00101, AA565/02803 |
Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 810, 811, 812, 813, 814 |
Country: US | FDA, National Drug Code | Identifier(s): 0597-0006, 0597-0007, 0597-0011, 0597-0031, 0597-0032, 0597-0033 |
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