- 1. (1R,2R)-2-(2-Carboxyethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-veratrylisoquinolinium Benzenesulfonate, Pentamethylene Ester
- [A non-depolarizing skeletal muscle relaxant of the benzylisoquinolinium class. Cisatracurium besylate acts as a competitive acetylcholine antagonist that binds to nicotinic receptors at the neuromuscular junction. Compared to other neuromuscular blocking agents, it is intermediate in its onset and duration of action. Cisatracurium besylate is used to maintain neuromuscular relaxation during major surgical procedures, primarily to facilitate endotracheal intubation. Cisatracurium besylate can cause bronchospasms, hypotension, and bradycardia. ( NCI )] (UMLS (NCI) C0530105) =Organic Chemical; Pharmacologic Substance ;
=Atracurium;
CISATRACURIUM =CISATRACURIUM BESYLATE 10 MG/ML;
CISATRACURIUM BESYLATE 2 MG/ML;
| - 10. 3R,4R,5E,10E,12E,14S,26R,26aS)-26-((2-(Diethylamino)ethyl)sulfonyl)-8,9,14,15,24,25,26,26a-octahydro-14-hydroxy-3-isopropyl-4,12-dimethyl-3H-21,18-nitrilo-1H,22H-pyrrolo(2,1-c)(1,8,4,19)dioxadiazacyclotetracosine-1,7,16,22(4H,17H)-tetrone
- [A semi-synthetic derivative of streptogramin A produced by streptomycetes. Dalfopristin inhibits the early phase of protein synthesis in the bacterial ribosome by binding to the 70S subunit, and also alters the configuration of the ribosome to make it more susceptible for streptogramin B binding. Dalfopristin is used in combination with quinopristin, a streptogramin B derivative. This combination is active against most gram-positive organisms, including Enterococcus faecium, and is also active against some gram-negative organisms and mycoplasma. ( NCI )] (UMLS (NCI) C0756085) Dalfopristin;
DALFOPRISTIN PREPARATION;
Virginiamycin M1, 26-((2-(diethylamino)ethyl)sulfonyl)-26,27-dihydro-,(26R,27S)-;
=Amino Acid, Peptide, or Protein; Pharmacologic Substance =Mikamycin;
[AM900] ANTI-INFECTIVES, OTHER =DALFOPRISTIN 350 MG;
|
- 2. (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;
| - 11. RRA _ Pharmacy/treatment administration acknowledgment
- (UMLS (HL7) C1549254) =Health Care Activity =Event Type;
|
- 3. (2R,3R,4S)-4-(1,3-Benzodioxo-5-yl)-1-(2-(dibutylamino)-2-oxoethyl)-2-(4-methoxyphenyl)-3-pyrrolidinecarboxylic Acid
- [A substance that is being studied as a treatment for cancer. It belongs to the family of drugs called endothelin-1 protein receptor antagonists. ( NCI )] (UMLS (NCI) C0935914) ATRASENTAN;
=Organic Chemical; Pharmacologic Substance ;
| - 12. RRD _ Pharmacy/treatment dispense acknowledgment
- (UMLS (HL7) C1549250) =Health Care Activity =Event Type;
|
- 4. (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
| - 13. RRE - Pharmacy/Treatment Refill Authorization Acknowledgement
- (UMLS (HL7) C1549262) =Health Care Activity =Event Type;
|
- 5. (6R,7R)-3-(((5-Methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-7-(2-(1H-tetrazol-1-yl)acetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid
- [A beta-lactam antibiotic and first-generation cephalosporin with bactericidal activity. Cefazolin binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. 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) C0007546) =Organic Chemical; Antibiotic =Cephalosporanic Acids;
[AM101] CEPHALOSPORINS, 1ST GENERATION =(6R-trans)-3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-7-(((1H-tetrazol-1-yl)acetyl)amino)-5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, Sodium Salt | - 14. RRE _ Pharmacy/treatment encoded order acknowledgment
- (UMLS (HL7) C1549248) =Health Care Activity =Event Type;
|
- 6. (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;
| - 15. RRG _ Pharmacy/treatment give acknowledgment
- (UMLS (HL7) C1549252) =Health Care Activity =Event Type;
|
- 7. (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 | - 16. [(1R,-2R)-1,2-cyclohexanediamine-N,N'][oxalato (2--)-O,O']platinum
- [An anticancer drug that belongs to the family of drugs called platinum compounds. ( NCI )] (UMLS (NCI) C0069717) =Organic Chemical; Pharmacologic Substance =[AN000] ANTINEOPLASTICS;
Unclassified Ingredients =OXALIPLATIN 100MG VIAL (SDV,MDV OR ADDITIVE) (EA);
OXALIPLATIN 50 MG |
- 8. (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;
| - 17. [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
|
- 9. (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 | |
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