UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
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R R R- R0 R1 R2 R3 R4 RA RB RC RD RE RF RG RH RI RK RM RN RO RP RQ RR RS RT RU RV RW RX RY
RRA RRC RRD RRE RRG RRM RRR RRS
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1. (2R,3R)-(R)-4-(2-Amino-1-hydroxyethyl)-1,2-benzenediol, 2,3-Dihydoxybutanedioate Monohydrate (1:1) (Salt)
[A bitartrate salt of norepinephrine, a synthetic phenylethylamine that mimics the sympathomimetic actions of the endogenous norepinephrine. Norepinephrine bitartrate acts directly on the alpha- and beta-adrenergic receptors. Clinically, norepinephrine is used as a peripheral vasoconstrictor that causes constriction of arterial and venous beds via its alpha-adrenergic action. It is also used as a potent inotropic and chronotropic stimulator of the heart mediated through its beta1 adrenergic action. ( NCI )] (UMLS (NCI) C0028333) =Organic Chemical; Pharmacologic Substance ;
=(.+-.)-Noradrenaline;
=NOREPINEPHRINE BITARTRATE 1 MG/ML;
5. (6R,7R)-7-(R)-Mandelamido-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-carboxylic Acid
[Semisynthetic wide-spectrum cephalosporin with prolonged action, probably due to beta-lactamase resistance. It is used also as the nafate. ( MSH )] (UMLS (NCI) C0007541) =Organic Chemical; Antibiotic =Cephalosporanic Acids;
[AM102] CEPHALOSPORINS, 2ND GENERATION =CEFOPERAZONE;
Cefamandole Nafate;
(6R-trans)-7-(((2-(Aminomethyl)phenyl)acetyl)amino)-3-(((1-(carboxymethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid;
Cefamandole Nafate;
2. (3R,3'R,6'R)-beta,epsilon-Carotene-3,3'-diol
[Lutein (LOO-teen) is a oxygenated carotenoid found in vegetables and fruits. lutein is found in the macula of the eye, where it is believed to act as a yellow filter. Lutein acts as an antioxidant, protecting cells against the damaging effects of free radicals. ( NCI )] (UMLS (NCI) C0043328) =Organic Chemical; Pharmacologic Substance; Biologically Active Substance
6. (6R,7R,8R,9S,10R,13S,14S,15S,16S,17S)-1,3',4',6,6a,7,8,9,10,11,12,13,14,15,15a,16-Hexadecahydro-10,13-dimethylspiro-(17H-dicyclopropa(6,7:15,16)cyclopenta(a)phenanthrene-17,2'(5'H)-furan)-3,5'(2H)-dione
[A synthetic spironolactone analogue and progestin with progestational and anti-mineralocorticoid activity. Drospirenone binds to the progesterone receptor, the resulting complex becomes activated and binds to specific sites on DNA. This results in a suppression of LH activity and an inhibition of ovulation as well as an alteration in the cervical mucus and endometrium. This leads to an increased difficulty of sperm entry into the uterus and implantation. This drug is used in oral contraceptives. ( NCI )] (UMLS (NCI) C0043822) =Organic Chemical; Pharmacologic Substance ;
=[HS200] CONTRACEPTIVES, SYSTEMIC;
Unclassified Ingredients =DROSPIRENONE 3 MG
3. (6R,7R)-7-(((2R)-Amino(4-hydroxyphenyl)acetyl)amino)-3-methyl-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid
[A semi-synthetic, beta-lactam, first-generation cephalosporin antibiotic with bactericidal activity. Cefadroxil binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. ( NCI )] (UMLS (NCI) C0007538) =Organic Chemical; Antibiotic =cephalexin;
[AM101] CEPHALOSPORINS, 1ST GENERATION =CEFADROXIL MONOHYDRATE;
Cefadroxil 100 MG/ML;
CEFADROXIL 1 GM;
CEFADROXIL 125 MG/5ML;
CEFADROXIL 250 MG/5ML;
CEFADROXIL 500 MG;
7. [2R-[2R*(4R*,8R*)]]-3,4-Dihydro-2,8-dimethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol
(UMLS (NCI) C0304915) =Organic Chemical; Pharmacologic Substance; Vitamin
4. (6R,7R)-7-((R)-2-Amino-2-(1,4-cyclohexadien-1-yl)acetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid
[A beta-lactam, first-generation cephalosporin antibiotic with bactericidal activity. Cephradine binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. PBPs participate in the terminal stages of assembling the bacterial cell wall, and in reshaping the cell wall during cell division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. ( NCI )] (UMLS (NCI) C0007738) =Organic Chemical; Antibiotic =cephalexin;
[AM101] CEPHALOSPORINS, 1ST GENERATION =CEPHRADINE 250 MG;
CEPHRADINE 500 MG;
CEPHRADINE 125 MG/5ML;
CEPHRADINE 250 MG/5ML

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