Displaying drugs 976 - 1000 of 1190 in total
Bromfenac
Bromfenac is a nonsteroidal anti-inflammatory drug (NSAID) for ophthalmic use. Ophthalmic NSAIDs are becoming a cornerstone for the management of ocular pain and inflammation. Their well-characterized anti-inflammatory activity, analgesic property, and established safety record have also made NSAIDs an important tool for optimizing surgical outcomes. Non-ophthalmic formulations of bromfenac were...
Approved
Withdrawn
Matched Description: … Ophthalmic NSAIDs are becoming a cornerstone for the management of ocular pain and inflammation. ... Their well-characterized anti-inflammatory activity, analgesic property, and established safety record …
Matched Salts name: … Bromfenac sodium …
Matched Categories: … Hydrocarbons, Cyclic …
Matched Products: … Bromfenac Sodium …
Matched Salts name: … Bromfenac sodium …
Matched Categories: … Hydrocarbons, Cyclic …
Matched Products: … Bromfenac Sodium …
Myristica fragrans fruit
Myristica fragrans fruit allergenic extract is used in allergenic testing.
Approved
Matched Synonyms: … Myristica officinalis fruit …
Sulfadiazine
One of the short-acting sulfonamides used in combination with pyrimethamine to treat toxoplasmosis in patients with acquired immunodeficiency syndrome and in newborns with congenital infections.
Approved
Investigational
Vet approved
Matched Description: … combination with pyrimethamine to treat toxoplasmosis in patients with acquired immunodeficiency syndrome and …
Matched Mixtures name: … Trisulfaminic Sus …
Matched Salts name: … Sulfadiazine sodium …
Matched Categories: … Hydrocarbons, Cyclic ... sulfadiazine and tetroxoprim ... Sulfonamides and trimethoprim ... Genito Urinary System and Sex Hormones ... sulfadiazine and trimethoprim …
Matched Products: … Sulfadiazine Sodium …
Matched Mixtures name: … Trisulfaminic Sus …
Matched Salts name: … Sulfadiazine sodium …
Matched Categories: … Hydrocarbons, Cyclic ... sulfadiazine and tetroxoprim ... Sulfonamides and trimethoprim ... Genito Urinary System and Sex Hormones ... sulfadiazine and trimethoprim …
Matched Products: … Sulfadiazine Sodium …
Edetate calcium disodium anhydrous
Edetate calcium disodium is a metal ion chelator used to reduce blood concentrations and depot stores of lead from the body. It is on the World Health Organization Model List of Essential Medicines. Edetate calcium disodium was granted FDA approval on 16 July 1953.
Approved
Matched Description: … Edetate calcium disodium is a metal ion chelator used to reduce blood concentrations and depot stores …
Matched Categories: … Diet, Food, and Nutrition …
Matched Products: … Calcium Edetate de Sodium …
Matched Categories: … Diet, Food, and Nutrition …
Matched Products: … Calcium Edetate de Sodium …
Daptomycin
Daptomycin is a cyclic lipopeptide antibacterial agent with a broad spectrum of activity against Gram-positive bacteria, including methicillin-susceptible and -resistant Staphylococcus aureus (MSSA/MRSA) and vancomycin-resistant Enterococci (VRE).[A231379, A231384, L32534] Chemically, daptomycin comprises 13 amino acids, including several non-standard and D-amino acids, with the C-terminal 10 amino acids forming an ester-linked...
Approved
Investigational
Matched Description: … bacteria, including methicillin-susceptible and -resistant _Staphylococcus aureus_ (MSSA/MRSA) and vancomycin-resistant ... A231379, A231384, L32534] Chemically, daptomycin comprises 13 amino acids, including several non-standard and ... D-amino acids, with the C-terminal 10 amino acids forming an ester-linked ring and the N-terminal tryptophan …
Matched Categories: … Amino Acids, Peptides, and Proteins ... Peptides, Cyclic ... Cyclic Lipopeptides …
Matched Products: … Daptomycin in Sodium Chloride …
Matched Categories: … Amino Acids, Peptides, and Proteins ... Peptides, Cyclic ... Cyclic Lipopeptides …
Matched Products: … Daptomycin in Sodium Chloride …
Methylprednisolone hemisuccinate
A water-soluble ester of methylprednisolone used for cardiac, allergic, and hypoxic emergencies.
Approved
Matched Description: … A water-soluble ester of methylprednisolone used for cardiac, allergic, and hypoxic emergencies. …
Matched Salts name: … Methylprednisolone sodium succinate …
Matched Categories: … Hormones, Hormone Substitutes, and Hormone Antagonists ... Adrenals ... Adrenal Cortex Hormones …
Matched Products: … Methylprednisolone Sodium Succinate ... METHYLPREDNISOLONE SODIUM SUCCINATE ... Methylprednisolone sodium succinate …
Matched Salts name: … Methylprednisolone sodium succinate …
Matched Categories: … Hormones, Hormone Substitutes, and Hormone Antagonists ... Adrenals ... Adrenal Cortex Hormones …
Matched Products: … Methylprednisolone Sodium Succinate ... METHYLPREDNISOLONE SODIUM SUCCINATE ... Methylprednisolone sodium succinate …
BR-007
Investigational
Matched Synonyms: … -4H-pyrrolo[1,2-b]pyrazol-3-yl)quinolin-7-yl)oxy)ethoxy)carbonyl)amino)butane-1,1-diyl)bis(hydrogen phosphonate …
Matched Salts name: … BR-007 sodium …
Matched Salts name: … BR-007 sodium …
Choline alfoscerate
A component of phosphatidylcholines (lecithins), in which the two hydroxy groups of glycerol are esterified with fatty acids. (From Stedman, 26th ed) It counteracts the effects of urea on enzymes and other macromolecules. [PubChem]
Experimental
Investigational
Matched Synonyms: … (2R)-2,3-dihydroxypropyl 2-(trimethylammonio)ethyl phosphate …
Matched Description: … (From Stedman, 26th ed) It counteracts the effects of urea on enzymes and other macromolecules. …
Matched Description: … (From Stedman, 26th ed) It counteracts the effects of urea on enzymes and other macromolecules. …
N-Ethyl-5'-Carboxamido Adenosine
A stable adenosine A1 and A2 receptor agonist. Experimentally, it inhibits cAMP and cGMP phosphodiesterase activity. [PubChem]
Experimental
Matched Name: … N-Ethyl-5'-Carboxamido Adenosine …
Matched Description: … A stable adenosine A1 and A2 receptor agonist. ... Experimentally, it inhibits cAMP and cGMP phosphodiesterase activity. [PubChem] …
Matched Description: … A stable adenosine A1 and A2 receptor agonist. ... Experimentally, it inhibits cAMP and cGMP phosphodiesterase activity. [PubChem] …
Sodium 1,2-Dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol)
Approved
Matched Synonyms: … 1,2-dipalmitoyl-sn-glycero-3-phosphorylglycerol sodium salt …
Matched Name: … Sodium 1,2-Dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol) …
Matched Iupac: … sodium (2R)-1-[(2,3-dihydroxypropyl phosphono)oxy]-3-(hexadecanoyloxy)propan-2-yl hexadecanoate …
Matched Name: … Sodium 1,2-Dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol) …
Matched Iupac: … sodium (2R)-1-[(2,3-dihydroxypropyl phosphono)oxy]-3-(hexadecanoyloxy)propan-2-yl hexadecanoate …
Cyclo(his-pro)
Experimental
Matched Synonyms: … cyclo(L-His-L-Pro) ... cyclo(histidyl-prolyl) …
Matched Name: … Cyclo(his-pro) …
Matched Categories: … Amino Acids, Peptides, and Proteins …
Matched Name: … Cyclo(his-pro) …
Matched Categories: … Amino Acids, Peptides, and Proteins …
Amphotericin B
Amphotericin B shows a high order of in vitro activity against many species of fungi. Histoplasma capsulatum, Coccidioides immitis, Candida species, Blastomyces dermatitidis, Rhodotorula, Cryptococcus neoformans, Sporothrix schenckii, Mucor mucedo, and Aspergillus fumigatus are all inhibited by concentrations of amphotericin B ranging from 0.03 to 1.0 mcg/mL in vitro. While...
Approved
Investigational
Matched Description: … The antibiotic is without effect on bacteria, rickettsiae, and viruses. ... Pseudallescheria boydii and Fusarium sp. are often resistant to amphotericin B. ... Blastomyces dermatitidis, Rhodotorula, Cryptococcus neoformans, Sporothrix schenckii, Mucor mucedo, and …
Matched Categories: … Alimentary Tract and Metabolism ... Genito Urinary System and Sex Hormones ... Antiinfectives and Antiseptics for Local Oral Treatment ... Gynecological Antiinfectives and Antiseptics …
Matched Products: … SUS. ICEREN FLAKON, 1 ADET …
Matched Categories: … Alimentary Tract and Metabolism ... Genito Urinary System and Sex Hormones ... Antiinfectives and Antiseptics for Local Oral Treatment ... Gynecological Antiinfectives and Antiseptics …
Matched Products: … SUS. ICEREN FLAKON, 1 ADET …
Tranexamic acid
Tranexamic acid is a synthetic derivative of lysine used as an antifibrinolytic in the treatment and prevention of major bleeding. It possesses a similar mechanism of action to aminocaproic acid but is approximately 10-fold more potent. It was first patented in 1957 and received its initial US approval in 1986.
Approved
Matched International brands: … Cyclo-F …
Matched Description: … Tranexamic acid is a synthetic derivative of [lysine] used as an antifibrinolytic in the treatment and ... [L31883] It was first patented in 1957[A230108] and received its initial US approval in 1986. …
Matched Categories: … Amino Acids, Peptides, and Proteins ... Blood and Blood Forming Organs …
Matched Products: … Tranexamic Acid In Sodium Chloride …
Matched Description: … Tranexamic acid is a synthetic derivative of [lysine] used as an antifibrinolytic in the treatment and ... [L31883] It was first patented in 1957[A230108] and received its initial US approval in 1986. …
Matched Categories: … Amino Acids, Peptides, and Proteins ... Blood and Blood Forming Organs …
Matched Products: … Tranexamic Acid In Sodium Chloride …
MRK-003
MRK-003 is a potent and selective γ-secretase inhibitor developed by Merck. It is the preclinical analog of MK-0752, a drug in clinical development.
Investigational
Matched Synonyms: … 1-yl]prop-1-enyl]spiro[1,2,5-thiadiazolidine-4,13'-tricyclo[8.2.1.03,8]trideca-3(8),4,6-triene] 1,1-dioxide …
Matched Description: … MRK-003 is a potent and selective γ-secretase inhibitor developed by Merck. …
Matched Categories: … Gamma Secretase Inhibitors and Modulators …
Matched Description: … MRK-003 is a potent and selective γ-secretase inhibitor developed by Merck. …
Matched Categories: … Gamma Secretase Inhibitors and Modulators …
5'-O-[(L-methionyl)-sulphamoyl]adenosine
Experimental
Matched Name: … 5'-O-[(L-methionyl)-sulphamoyl]adenosine …
2'-O-Acetyl Adenosine-5-Diphosphoribose
Experimental
Matched Name: … 2'-O-Acetyl Adenosine-5-Diphosphoribose …
2',5'-DIDEOXY-ADENOSINE 3'-MONOPHOSPHATE
Experimental
Matched Name: … 2',5'-DIDEOXY-ADENOSINE 3'-MONOPHOSPHATE …
Rabeprazole
Rabeprazole is an antiulcer drug in the class of proton pump inhibitors. It is a prodrug - in the acid environment of the parietal cells it turns into active sulphenamide form. Rabeprazole inhibits the H+, K+ATPase of the coating gastric cells and dose-dependent oppresses basal and stimulated gastric acid secretion.
Approved
Investigational
Matched Description: … and stimulated gastric acid secretion. ... Rabeprazole inhibits the H+, K+ATPase of the coating gastric cells and dose-dependent oppresses basal …
Matched Salts name: … Rabeprazole sodium …
Matched Categories: … Alimentary Tract and Metabolism ... Antiinflammatory and Antirheumatic Products ... Antiinflammatory and Antirheumatic Products, Non-Steroids ... rabeprazole, amoxicillin and metronidazole ... rabeprazole, amoxicillin and clarithromycin …
Matched Products: … Rabeprazole sodium ... Rabeprazole Sodium ... Rabeprazole Sodium DR …
Matched Salts name: … Rabeprazole sodium …
Matched Categories: … Alimentary Tract and Metabolism ... Antiinflammatory and Antirheumatic Products ... Antiinflammatory and Antirheumatic Products, Non-Steroids ... rabeprazole, amoxicillin and metronidazole ... rabeprazole, amoxicillin and clarithromycin …
Matched Products: … Rabeprazole sodium ... Rabeprazole Sodium ... Rabeprazole Sodium DR …
ADH-1
Adherex's biotechnology compound, ADH-1, targets N-cadherin, a protein present on certain tumor cells and established tumor blood vessels. ADH-1 is currently in clinical development in a combination program with a range of chemotherapeutic agents to investigate the synergistic effects noted in our preclinical models. At the end of 2006, the...
Investigational
Matched Synonyms: … l-cysteinamide, n-acetyl-l-cysteinyl-l-histidyl-l-alanyl-l-valyl-, cyclic (1-5)-disulfide …
Matched Description: … and organisms. ... well-defined shape and become loosely adherent, flattened and migratory. ... Adherex's biotechnology compound, ADH-1, targets N-cadherin, a protein present on certain tumor cells and …
Matched Description: … and organisms. ... well-defined shape and become loosely adherent, flattened and migratory. ... Adherex's biotechnology compound, ADH-1, targets N-cadherin, a protein present on certain tumor cells and …
Displaying drugs 976 - 1000 of 1190 in total