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
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
HBA HBE HBG HBI HBL HBS HBV
selected terms: 36 page 1 of 1

1. 10H-Benzo(4,5)cyclohepta(1,2-b)thiophen-10-one, 4,9-dihydro-4-(1-methyl-4-piperidinylidene)-,(E)-2-butenedioate(1:1)
[The fumarate salt of ketotifen, a cycloheptathiophene derivative with anti-allergic activity. Ketotifen selectively blocks histamine (H1) receptors and prevents the typical symptoms caused by histamine release. This agent also interferes with the release of inflammatory mediators from mast cells involved in hypersensitivity reactions, thereby decreasing chemotaxis and activation of eosinophils. ( NCI )] (UMLS (NCI) C0043443) =Organic Chemical; Pharmacologic Substance ;
=KETOTIFEN;
=KETOTIFEN FUMARATE 0.025 %
19. 5H-(1)Benzopyrano(2,3-b)pyridine-3-carboxylic Acid, 2-Amino-7-(1-methylethyl)-5-oxo-
[An anti-aphthous ulcer drug. Amlexanox inhibits the synthesis and release of inflammatory mediators, including leukotrienes and histamine, from mast cells, neutrophils, and mononuclear cells. Amlexanox also acts as a leukotriene D4 antagonist and a phosphodiesterase inhibitor. Amlexanox decreases the time ulcers take to heal as well as the pain associated with the ulcers. ( NCI )] (UMLS (NCI) C0103049) =Organic Chemical; Pharmacologic Substance =aminopyridine;
[OR900] DENTAL AND ORAL AGENTS, TOPICAL OTHER =AMLEXANOX 5 %;
2. 1H-1,4-Benzodiazepine-3-carboxylic acid, 7-chloro-2,3-dihydro-2-oxo-5-phenyl-, Monopotassium Salt, compound with Potassium Hydroxide
[A benzodiazepine with anxiolytic, sedative, hypnotic, and anticonvulsant properties. Clorazepate dipotassium exerts its effect by de-activating the nervous system through potentiation of the inhibitory effect of gamma-aminobutyric acid (GABA) on the GABA-A receptors by binding to a site that is distinct from the GABA binding site. Its inhibitory effect is caused by an increase in GABA-mediated chloride channel opening events, leading to hyperpolarization and synaptic inhibition. ( NCI )] (UMLS (NCI) C0009033) =Organic Chemical; Pharmacologic Substance ;
=benzodiazepine;
CLORAZEPATE PREPARATION =CLORAZEPATE DIPOTASSIUM 15 MG;
CLORAZEPATE DIPOTASSIUM 22.5 MG;
CLORAZEPATE DIPOTASSIUM 7.5 MG;
CLORAZEPATE DIPOTASSIUM 11.25 MG;
CLORAZEPATE DIPOTASSIUM 3.75 MG;
20. 5H-Benzo(5,6)cyclohepta(1,2-b)pyridine, 8-chloro-6,11-dihydro-11-(4-piperidinylidene)-
[A long-acting piperidine derivate with selective H1 antihistaminergic and non-sedating properties. Desloratadine diminishes the typical histaminergic effects on H1-receptors in bronchial smooth muscle, capillaries and gastrointestinal smooth muscle, including vasodilation, bronchoconstriction, increased vascular permeability, pain, itching and spasmodic contractions of gastrointestinal smooth muscle. Desloratadine is used to provide symptomatic relieve of allergic symptoms. ( NCI )] (UMLS (NCI) C0908935) Desloratadine;
DESLORATADINE PREPARATION;
=Organic Chemical; Pharmacologic Substance ;
=[AH900] ANTIHISTAMINES, OTHER;
Unclassified Ingredients =DESLORATADINE 5 MG;
3. 1H-Benz(de)isoquinolin-1-one, 2-(3S)-1-azabicyclo(2.2.2)oct-3-yl-2,3,3a,4,5,6-hexahydro-, Monohydrochloride,(3aS)-
[The hydrochloride salt form of palonosetron, a carbazole derivative and a selective serotonin receptor antagonist with antiemetic properties. Palonosetron competitively blocks the action of serotonin at 5-HT3 receptors located on vagal afferents in the chemoreceptor trigger zone (CTZ), resulting in suppression of chemotherapy-induced nausea and vomiting. ( NCI )] (UMLS (NCI) C1310734) PALONOSETRON HCL UNIDENTIFIED;
PALONOSETRON HCL UNIDENTIFIED;
PALONOSETRON HYDROCHLORIDE;
=Organic Chemical; Pharmacologic Substance ;
21. 7H-benzo(e)pyrido(4,3-b)indol-3-ol, 11-((3-(dimethylamino)propyl)amino)-8-methyl
[An anticancer drug that belongs to the family of drugs called topoisomerase inhibitors. ( NCI )] (UMLS (NCI) C0217476) =Organic Chemical; Pharmacologic Substance ;
4. 1H-benz(de)isoquinoline-1,3(2H)-dione, 5-amino-2-(2-(dimethylamino)ethyl)
(UMLS (NCI) C0051733) =Organic Chemical; Pharmacologic Substance
22. HB-S DIS W/O CRISIS NEC
[ ] (UMLS (ICD9CM) C1260401) Other sickle-cell disease without crisis =Disease or Syndrome
5. 1H-benzimidazol-2-ylcarbamic Acid Methyl Ester
[An anticancer drug that belongs to the family of drugs called antifungal agents. ( NCI )] (UMLS (NCI) C0065839) =Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance
23. Hb-S disease with mention of crisis
[broad term used to describe several different acute conditions occurring with sickle cell disease, including aplastic crisis, hemolytic crisis, and vasoocclusive crisis. ( CSP )] (UMLS (ICD9CM) C0238425) =Disease or Syndrome =Anemia, Sickle Cell;
6. 2H-1,2,4-Benzothiadiazine-7-sulfonamide, 3,4-Dihydro-3-(phenylmethyl)-6-(trifluoromethyl)-, 1,1-Dioxide
[A thiazide diuretic. Bendroflumethiazide directly inhibits sodium and chloride reabsorption on the luminal membrane of the early segment of the distal convoluted tubule in the kidney. This drug increases water, sodium, chloride, potassium and bicarbonate excretion and decreases calcium and uric acid secretion. Bendroflumethiazide is commonly used to treat hypertension, edema, and congestive heart failure. ( NCI )] (UMLS (NCI) C0004975) =Organic Chemical; Pharmacologic Substance
24. HB-S/HB-C DIS W CRISIS
[ ] (UMLS (ICD9CM) C1260398) Sickle-cell/Hb-C disease with crisis =Disease or Syndrome
7. 2H-1,2,4-Benzothiadiazine-7-sulfonamide, 3,4-dihydro-6-(trifluoromethyl)-, 1,1-Dioxide
[A thiazide diuretic with antihypertensive activity. Hydroflumethiazide directly inhibits sodium and chloride reabsorption on the luminal membrane of the early segment of the distal convoluted tubule in the kidney. This results in an increase in water, sodium, chloride, potassium and bicarbonate excretion and a decrease in calcium and uric acid secretion. (NCI05) ( NCI )] (UMLS (NCI) C0020273) =Organic Chemical; Pharmacologic Substance ;
=benzothiadiazine;
[CV701] THIAZIDES/RELATED DIURETICS =HYDROFLUMETHIAZIDE 50 MG
25. HB-SS DIS NEC W CRISIS
(UMLS (ICD9CM) C1260673) Other sickle-cell disease with crisis =Disease or Syndrome
8. 2H-1,2,4-Benzothiadiazine-7-sulfonamide, 6-chloro-3,4-dihydro-2-methyl-3-(((2,2,2-trifluoroethyl)thio)methyl)-, 1,1-Dioxide
[A sulfonamide derivative and a synthetic thiazide with diuretic, antihypertensive and anti-urolithic properties. By blocking the Na/Cl transporter, polythiazide inhibits reabsorption of sodium and chloride in the proximal and distal convoluted tubule of the kidney, resulting in increased excretion of water and electrolytes (sodium, potassium, chloride, magnesium, and bicarbonate) and subsequent reversal of hypertension. In addition, this agent exerts its anti-urolithic effect by decreasing calcium and uric acid excretion. ( NCI )] (UMLS (NCI) C0032613) =Organic Chemical; Pharmacologic Substance ;
=benzothiadiazine;
[CV701] THIAZIDES/RELATED DIURETICS =POLYTHIAZIDE 0.5 MG;
POLYTHIAZIDE 1 MG;
POLYTHIAZIDE 2 MG;
POLYTHIAZIDE 4 MG;
26. HB-SS DISEASE W/O CRISIS
[ ] (UMLS (ICD9CM) C0272078) =Disease or Syndrome
9. 2H-1,2,4-Benzothiadiazine-7-sulfonamide, 6-chloro-3-(chloromethyl)-3,4-dihydro-2-methyl-, 1,1-Dioxide
[A thiazide diuretic with antihypertensive activity. Methyclothiazide directly inhibits sodium and chloride reabsorption on the luminal membrane of the early segment of the distal convoluted tubule in the kidney. This results in an increase in water, sodium, chloride, potassium and bicarbonate excretion and a decrease in calcium and uric acid secretion. ( NCI )] (UMLS (NCI) C0025696) =Organic Chemical; Pharmacologic Substance ;
=benzothiadiazine;
[CV701] THIAZIDES/RELATED DIURETICS =NIVEA SKIN OIL;
METHYCLOTHIAZIDE 2.5 MG;
METHYCLOTHIAZIDE 5 MG
27. HB-SS/HB-C DIS W/O CRSIS
[One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia. ( MSH )] (UMLS (ICD9CM) C0019034) =Disease or Syndrome ;
=Anemia, Sickle Cell;
10. 2H-1,2,4-Benzothiadiazine-7-sulfonamide, 6-chloro-3-(dichloromethyl)-3,4-dihydro-, 1,1-Dioxide
[A thiazide diuretic with antihypertensive activity. Trichlormethiazide directly inhibits sodium and chloride reabsorption on the luminal membrane of the early segment in the distal convoluted tubule in the kidney. This leads to an increase in water, sodium, chloride, bicarbonate, and potassium secretion and a decrease in calcium and uric acid secretion. ( NCI )] (UMLS (NCI) C0040899) =Organic Chemical; Pharmacologic Substance =[CV701] THIAZIDES/RELATED DIURETICS;
6-Chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide =TRICHLORMETHIAZIDE 4 MG
28. HbA1c
[Minor hemoglobin components of human erythrocytes designated A1a, A1b, and A1c. Hemoglobin A1c is most important since its sugar moiety is glucose covalently bound to the terminal amino acid of the beta chain. Since normal glycohemoglobin concentrations exclude marked blood glucose fluctuations over the preceding three to four weeks, the concentration of glycosylated hemoglobin A is a more reliable index of the blood sugar average over a long period of time. ( MSH )] (UMLS (CSP) C0019018) =Amino Acid, Peptide, or Protein; Biologically Active Substance
11. 2H-1,4-Benzodiazepin-2-one, 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-
[benzodiazepine used in the treatment of anxiety, alcohol withdrawal, and insomnia. ( CSP )] (UMLS (NCI) C0029997) =Organic Chemical; Pharmacologic Substance ;
=benzodiazepine;
Benzodiazepinones;
tranquilizer;
[CN302] BENZODIAZEPINE DERIVATIVE, SEDATIVES/HYPNOTICS =OXAZEPAM 10 MG;
OXAZEPAM 15 MG;
OXAZEPAM 30 MG;
29. HBGF
[heparin binding growth factor that regulates endothelial cell proliferation; also acts as an angiogenic factor. ( CSP )] (UMLS (CSP) C0078058) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
=Growth Agents;
12. 2H-1,4-Benzodiazepine-2-thione, 7-chloro-5-(2-fluorophenyl)-1,3-dihydro-1-(2,2,2-trifluoroethyl)-
[A synthetic benzodiazepine derivative with anxiolytic, sedative and hypnotic properties. Quazepam and its major metabolite 2-oxoquazepam potentiate gamma-aminobutyric acid (GABA) activity by binding to the benzodiazepine-1 recognition site (BZ-1) within the GABA-A receptor, located in the limbic, neocortical and mesencephalic reticular system. This increases the frequency of GABA-activated chloride channel opening events, allowing the flow of chloride ions into the neuron leading to membrane hyperpolarization and decreased neuronal excitability. ( NCI )] (UMLS (NCI) C0072828) =Organic Chemical; Pharmacologic Substance =[CN302] BENZODIAZEPINE DERIVATIVE, SEDATIVES/HYPNOTICS;
Unclassified Ingredients =QUAZEPAM 15 MG;
QUAZEPAM 7.5 MG;
30. HBGF-8
[Heparin-Binding Neurotrophic Factors are a family of polypeptide growth factors produced by peripheral target tissues, as well as the nervous system, that block apoptosis and promote neuronal growth, regeneration, survival, and differentiation. Many growth factors appear to temporarily and non-covalently interact with the glycosaminoglycan heparin, which may affect growth factor activity. ( NCI )] (UMLS (NCI) C0084084) =Amino Acid, Peptide, or Protein; Biologically Active Substance
13. 2H-1-Benzopyran-2-one
[oxygen containing heterocyclic compound, obtainable naturally from several plants, or produced synthetically from an amino acid of phenylalanine; it is used for the preparation of drugs especially anticoagulants such as bishydroxycoumarin (dicoumarol) and warfarin (coumadin); coumarin glycosides such as dicoumarol and warfarin, are widely used as rodenticides. ( CSP )] (UMLS (NCI) C0010206) =Organic Chemical; Pharmacologic Substance =pyrone;
=furocoumarin;
1-(4'-Hydroxy-3'-coumarinyl)-1-phenyl-3-butanone;
31. HBIG
[hepatitis B immune globulin ( HL7V3.0 )] (UMLS (HL7) C0062525) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Immunologic Factor =[IM500] IMMUNOGLOBULINS;
Vaccines administered (code = CVX)(parenteral, unless oral is noted);
VaccineType;
=HEPATITIS B IMMUNE GLOBULIN;
14. 2H-Benzimidazol-2-one, 1-(1-(4,4-bis(4-fluorophenyl)butyl)-4-piperidinyl)-1,3-dihydro-
[diphenylbutylpiperidine that is used as an antipsychotic agent and as an alternative to haloperidol for the suppression of vocal and motor tics in patients with Tourette syndrome. ( CSP )] (UMLS (NCI) C0031935) =Organic Chemical; Pharmacologic Substance =benzimidazole;
[CN700] ANTIPSYCHOTICS;
[CN900] CNS MEDICATIONS, OTHER;
=PIMOZIDE 2 MG;
PIMOZIDE 1 MG;
32. HBL
[(HEP-a-toe-blas-TOE-ma) A type of liver tumor that occurs in infants and children. ( NCI )] (UMLS (NCI) C0206624) =Neoplastic Process ;
=hepatic neoplasm;
Neoplasms, Complex and Mixed
15. 3H-1,4-Benzodiazepin-2-amine, 7-chloro-N-methyl-5-phenyl, 4-oxide
[anxiolytic benzodiazepine derivative with anticonvulsant, sedative, and amnesic properties; also used in the symptomatic treatment of alcohol withdrawal. ( CSP )] (UMLS (NCI) C0008188) =Organic Chemical; Pharmacologic Substance ;
=benzodiazepine;
tranquilizer;
[CN302] BENZODIAZEPINE DERIVATIVE, SEDATIVES/HYPNOTICS;
=CHLORDIAZEPOXIDE HYDROCHLORIDE;
CHLORDIAZEPOXIDE 10 MG;
CHLORDIAZEPOXIDE 5 MG;
33. HBLV
[species of Roseolovirus isolated from patients with AIDS and other lymphoproliferative disorders; it appears to alter NK cell activity; HHV-6 is the cause of exanthema subitum and has been implicated in encephalitis. ( CSP )] (UMLS (CSP) C0019381) =Virus =herpes virus;
16. 4,4'-(3H-2,1-Benzoxathiol-3-ylidene)bis(2-bromo-3-methyl-6-(1-met-hylethyl)phenol) S,S-dioxide
[A dye used as an indicator in determining pH. Bromthymol blue is a weak acid. It can be in acid or base form, depending on the pH of the solution. This reagent is yellow in acidic solutions, blue in basic solutions and green in neutral solution. ( NCI )] (UMLS (NCI) C0006251) =Organic Chemical; Indicator, Reagent, or Diagnostic Aid
34. HBSAG
[A measurement of the surface antigen reaction of a biological specimen to the Hepatitis B virus. ( NCI )] (UMLS (NCI) C0201477) =Laboratory Procedure
17. 4H-1-benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-methoxy-
(UMLS (NCI) C0072562) =Organic Chemical
35. HBV
[A virus that causes hepatitis (inflammation of the liver). It is carried and passed to others through blood or sexual contact. Also, infants born to infected mothers may become infected with the virus. ( NCI )] (UMLS (NCI) C0019169) =Virus ;
18. 4H-1-benzopyran-8-acetic Acid, 4-Oxo-2-phenyl
[A synthetic flavonoid with vascular targeting properties. Flavone acetic acid exhibits an antiproliferative effect on endothelial cells as a result of a superoxide-dependent mechanism, which induces changes in permeability of the vasculature of the tumor. This agent may stimulate tumor necrosis and promote shunting of blood flow to viable regions of the tumor, increasing their oxygenation and rendering them more susceptible to the antitumor effects of hyperthermia and ionizing radiation. (NCI04) ( NCI )] (UMLS (NCI) C0060441) =Organic Chemical; Pharmacologic Substance
36. HBV-Activated Protein
[Encoded by human RARB Gene (NR1 Family), alternative isoforms of Retinoic Acid Receptor Beta (1-4) are composed of three domains: an N-terminal modulating domain, a central DNA-binding domain, and a C-terminal ligand-binding domain. RARB controls embryonic morphogenesis, cell proliferation, and differentiation by directly regulating gene transcription. RARB appears to limit growth of many cell types. (NCI) ( NCI )] (UMLS (NCI) C0140280) =Amino Acid, Peptide, or Protein; Receptor ;

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