UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
L L L- L0 L1 L6 LA LB LC LD LE LF LG LH LI LK LL LM LN LO LP LR LS LT LU LV LX LY
LA LAB LAC LAD LAE LAF LAG LAJ LAK LAL LAM LAN LAP LAR LAS LAT LAU LAV LAW LAX LAY

Labetalol Hydrochloride

[The hydrochloride form of labetalol, a third generation selective alpha-1-adrenergic antagonist and non-selective beta-adrenergic antagonist with vasodilatory and antihypertensive properties. Labetalol competitively binds to alpha-1-adrenergic receptors in vascular smooth muscle, thereby inhibiting the adrenergic stimulation of endothelial cell function and vasoconstriction in peripheral blood vessels. This agent also binds to beta-receptors in the bronchial and vascular smooth muscle, resulting in a decrease in adrenergic stimulation. The result is a decrease in resting and exercise heart rates, cardiac output, and in both systolic and diastolic blood pressure, thereby resulting in vasodilation, and negative chronotropic and inotropic cardiac effects. ( NCI )]
UMLS (NCI) C0699440
 
Organic Chemical
Pharmacologic Substance
Relation/PAR: LABETALOL
Relation/CHD: LABETALOL HYDROCHLORIDE 100 MG
LABETALOL HYDROCHLORIDE 200 MG
LABETALOL HYDROCHLORIDE 300 MG
LABETALOL HYDROCHLORIDE 5 MG/ML

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