C0032912 - A synthetic piperazine derivative and an alpha-1 adrenergic receptor inhibitor used primarily as an anti-hypertensive. Prazosin's effects are most pronounced in the large resistance vessels (i.e. arterioles) and result in a decrease in total systemic vascular resistance (SVR) without a rebound or reflex tachycardia. To a lesser extent, this agent also decreases the tone of the bladder sphincter, thereby allowing the opening of the bladder into the urethra and thus relieving the urinary conditions associated with benign prostatic hypertrophy. 4/10
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Terms, descriptions
CUI    C0032912
RussianMedical Subject Headings Russian D011224 L3364954preferred S3892438 Y ПРАЗОЗИН
RussianMedical Subject Headings Russian D011224 L0902530no S1106347 Y PRAZOZIN
RussianMedical Subject Headings Russian D011224 L1507740no S1803649 Y ADVERZUTEN
RussianMedical Subject Headings Russian D011224 L1520293no S1816202 Y FURAZOZIN
RussianMedical Subject Headings Russian D011224 L1537070no S1832979 Y PRATSIOL
RussianMedical Subject Headings Russian D011224 L3336974no S3864455 Y АДВЕРЗУТЕН
RussianMedical Subject Headings Russian D011224 L3364962no S3892446 Y ПРАТСИОЛ
RussianMedical Subject Headings Russian D011224 L3374984no S3902477 Y ФУРАЗОЗИН
Medical Subject Headings A0104284 AT127396400 A selective adrenergic alpha-1 antagonist used in the treatment of HEART FAILURE; HYPERTENSION; PHEOCHROMOCYTOMA; RAYNAUD DISEASE; PROSTATIC HYPERTROPHY; and URINARY RETENTION.
(CPTSP) CRISP Thesaurus A0487135 AT32350793 1-(4-amino-6,7-dimethoxy- 2-quinazolinyl) -4-(2-furoyl) piperazine.
Medical Subject Headings Czech A13042020 AT231382970 Lék užívaný k léčbě vysokého krevního tlaku (antihypertenzivum). Blokátor alfareceptoru (alfa 1). L.: Deprazolin. (cit. Velký lékařský slovník online, 2017 http://lekarske.slovniky.cz)
NCI Thesaurus A7573144 AT198145900 A synthetic piperazine derivative and an alpha-1 adrenergic receptor inhibitor used primarily as an anti-hypertensive. Prazosin's effects are most pronounced in the large resistance vessels (i.e. arterioles) and result in a decrease in total systemic vascular resistance (SVR) without a rebound or reflex tachycardia. To a lesser extent, this agent also decreases the tone of the bladder sphincter, thereby allowing the opening of the bladder into the urethra and thus relieving the urinary conditions associated with benign prostatic hypertrophy.