UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
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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
H H+ H1 HA HB HC HD HE HF HG HH HI HK HL HM HN HO HP HQ HR HS HT HU HV HX HY HZ
HD HDA HDD HDG HDI HDL HDN
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1. 13H-4,6:21,24-Dietheno-8,12-metheno-1H-pyrido(3',2':14,15)(1,11)dioxacycloeicosino(2,3,4-ij)isoquinolinium
[The chloride salt form of tubocurarine, a naturally occurring curare alkaloid isolated from the bark and stem of Chondodendron tomentosum with a muscle relaxant property. Tubocurarine chloride competes with acetylcholine for the nicotinic receptors at the neuromuscular junction of skeletal muscles, thereby inhibiting the action of acetylcholine and blocking the neural transmission without depolarizing the postsynaptic membrane. This may lead to skeletal muscle relaxation and paralysis. ( NCI )] (UMLS (NCI) C0282372) =Organic Chemical; Pharmacologic Substance ;
=Tubocurare;
=TUBOCURARINE CHLORIDE 3 MG/ML;
4. 5H-Dibenz(b,f)azepine, 10,11-dihydro-5-(3-(dimethylamino)-2-methylpropyl)-, Maleate(1:1)
[The maleate salt form of trimipramine, a tricyclic secondary amine of the dibenzazepine class, with an antidepressant property. Trimipramine maleate appears to inhibit serotonin transport and norepinephrine uptake by nerve terminals. This increases available norepinephrine or serotonin and prolongs its action. ( NCI )] (UMLS (NCI) C0242523) =Organic Chemical; Pharmacologic Substance =TRIMIPRAMINE;
=TRIMIPRAMINE MALEATE 100 MG;
TRIMIPRAMINE MALEATE 25 MG;
TRIMIPRAMINE MALEATE 50 MG
2. 3H-1,2-Dithiole-3-thione, 4-methyl-5-pyrazinyl-
[pyrazine with antiviral, schistosomicidal and anticarcinogenic properties. ( CSP )] (UMLS (NCI) C0069456) =Organic Chemical; Pharmacologic Substance ;
=thione;
5. 5H-Dibenz(b,f)azepine-5-carboxamide
[anticonvulsant and antineuralgic used in the treatment of pain associated with trigeminal neuralgia and in epilepsy manifested by tonic-clonic and partial seizures. ( CSP )] (UMLS (NCI) C0006949) =Organic Chemical; Pharmacologic Substance =[CN100] ANALGESICS;
[CN400] ANTICONVULSANTS;
azepine;
Dibenzazepines =10,11-Dihydro-10-oxo-5H-dibenz(b,f)azepine-5-carboxamide;
CARBAMAZEPINE 100 MG;
CARBAMAZEPINE 100 MG/5ML;
CARBAMAZEPINE 200 MG;
CARBAMAZEPINE 300 MG;
CARBAMAZEPINE 400 MG;
3. 4H-Dibenzo(de,g)quinoline-10,11-diol, 5,6,6a,7-Tetrahydro-6-methyl-, Hydrochloride,(6aR)-
[The hydrochloride salt form of apomorphine, a derivative of morphine and non-ergoline dopamine agonist with high selectivity for dopamine D2, D3, D4 and D5 receptors. Apomorphine hydrochloride acts by stimulating dopamine receptors in the nigrostriatal system, hypothalamus, limbic system, pituitary gland, and blood vessels. This enhances motor function, suppresses prolactin release, and causes vasodilation and behavioral effects. Apomorphine hydrochloride is used in the treatment of Parkinson's disease and erectile dysfunction. In addition, apomorphine hydrochloride acts on the chemoreceptor trigger zone and is used as a central emetic in the treatment of drug overdose. ( NCI )] (UMLS (NCI) C0237406) =Organic Chemical; Pharmacologic Substance =apomorphine;
TO BE DELETED INGREDIENT PREPARATIONS =APOMORPHINE HYDROCHLORIDE 6 MG;
6. 5H-Dibenzo(a,d)cycloheptene-5-propanamine, N-methyl-, Hydrochloride
[The hydrochloride salt form of protriptyline, a tricyclic secondary amine with antidepressant property. Protriptyline hydrochloride blocks the re-uptake of norepinephrine and serotonin by nerve terminals, thereby increasing available norepinephrine and serotonin. Protriptyline does not block dopamine transport but may have an indirect dopamine-facilitating effect through interactions of increased peri-synaptic abundance of norepinephrine, particularly in the cerebral cortex, where adrenergic terminals exceed dopaminergic terminals. This results in elevation of mood and behavioral activity. In addition, this agent exhibits anticholinergic activity. ( NCI )] (UMLS (NCI) C0700557) =Organic Chemical; Pharmacologic Substance ;
=PROTRIPTYLINE;
=PROTRIPTYLINE HYDROCHLORIDE 10 MG;
PROTRIPTYLINE HYDROCHLORIDE 5 MG;

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