Displaying drugs 301 - 325 of 10361 in total
Dexamethasone
Dexamethasone, or MK-125, is a corticosteroid fluorinated at position 9 used to treat endocrine, rheumatic, collagen, dermatologic, allergic, ophthalmic, gastrointestinal, respiratory, hematologic, neoplastic, edematous, and other conditions. Developed in 1957, it is structurally similar to other corticosteroids like hydrocortisone and prednisolone. Dexamethasone was granted FDA approval on 30 October 1958....
Approved
Investigational
Vet approved
Matched Mixtures name: … MOFLAG D ... MOFLAG D ... OCUTOB - D …
Chlorcyclizine
Chlorcyclizine is a first generation phenylpiperazine class antihistamine used to treat urticaria, rhinitis, pruritus, and other allergy symptoms. Chlorcyclizine also has some local anesthetic, anticholinergic, and antiserotonergic properties, and can be used as an antiemetic.
Approved
Matched Mixtures name: … biclora-D ... biclora-D ... Poly-tussin D …
Potassium Iodide
Saturated solution of Potassium Iodide (SSKI) is used pharmaceutically for emergency use in patients experiencing acute symptoms of severe hyperthyroidism (also known as thyroid storm or thyrotoxic crisis). SSKI can also be used for radioiodine-contamination emergencies or in preparation of thyrotoxic patients for thyroidectomy.
Approved
Matched Mixtures name: … I D M Expectorant Tab ... Iron Polysaccharides Folic Acid DHA …
Tiopronin
Tiopronin is a prescription thiol drug used primarily in the treatment of severe homozygous cystinuria. Patients with cystinuria excrete high levels of cystine in their urine and are at risk for kidney stone formation. Tiopronin is used as a second-line therapy to control the rate of cystine precipitation and excretion,...
Approved
Investigational
Matched Iupac: … 2-(2-sulfanylpropanamido)acetic acid …
Matched Description: … It is similar to d-penicillamine in use and efficacy, but offers the advantage of far less adverse effects …
Matched Description: … It is similar to d-penicillamine in use and efficacy, but offers the advantage of far less adverse effects …
Nateglinide
Nateglinide is an oral antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus (NIDDM). It belongs to the meglitinide class of short-acting insulin secretagogues, which act by binding to β cells of the pancreas to stimulate insulin release. Nateglinide is an amino acid derivative that induces an early insulin...
Approved
Investigational
Matched Iupac: … (2R)-3-phenyl-2-{[(1r,4r)-4-(propan-2-yl)cyclohexyl]formamido}propanoic acid …
Matched Description: … Nateglinide is an amino acid derivative that induces an early insulin response to meals decreasing postprandial …
Matched Description: … Nateglinide is an amino acid derivative that induces an early insulin response to meals decreasing postprandial …
Mepyramine
Mepyramine, or pyrilamine, targets the H1 receptor. It is a first generation antihistamine. However, it rapidly permeates the brain and so often causes drowsiness as a side effect. It has been found in over-the-counter combination products for colds and menstrual symptoms, but is considered to be an unapproved prescription medication...
Approved
Vet approved
Matched Mixtures name: … Zotex-D ... Pyril D ... Aldex D …
alpha-Tocopherol acetate
Alpha-tocopherol is the primary form of vitamin E that is preferentially used by the human body to meet appropriate dietary requirements. In particular, the RRR-alpha-tocopherol (or sometimes called the d-alpha-tocopherol stereoisomer) stereoisomer is considered the natural formation of alpha-tocopherol and generally exhibits the greatest bioavailability out of all of the...
Approved
Matched Description: … In particular, the RRR-alpha-tocopherol (or sometimes called the d-alpha-tocopherol stereoisomer) stereoisomer …
Matched Mixtures name: … Chunzam Silk Amino Acid Tooth …
Matched Mixtures name: … Chunzam Silk Amino Acid Tooth …
Toremifene
Toremifene is a selective estrogen receptor modulator (SERM) and a nonsteroidal antiestrogen used to treat estrogen receptor positive breast cancer. Like tamoxifen, toremifene is part of the first-generation triphenylethylene derivative chemical class of SERMs. Toremifene possesses tissue-specific actions: it has estrogenic (agonist) activity on the cardiovascular system and on bone...
Approved
Investigational
Matched Mixtures name: … FLOBACT - D ... FLOBACT - D …
Soy isoflavones
Approved
Experimental
Matched Mixtures name: … D-Cal SoyCal ... CALCIBON D SOYA FORTE TABLETAS …
Artenimol
Artenimol is an artemisinin derivative and antimalarial agent used in the treatment of uncomplicated Plasmodium falciparum infections [FDA Label]. It was first authorized for market by the European Medicines Agency in October 2011 in combination with DB13941 as the product Eurartesim. Artemisinin combination therapy is highly effective against malaria and...
Approved
Experimental
Investigational
Matched Mixtures name: … D-ARTEPP ... D-ARTEPP DISPERSIBLE …
Selenomethionine
Selenomethionine is a naturally occuring amino acid in some plant materials such as cereal grains, soybeans and enriched yeast but it cannot be synthesized from animals or humans. It can be produced from post-structural modifications. In vivo, selenomethionine plays an essential role in acting as an antioxidant, where it depletes...
Approved
Investigational
Matched Iupac: … (2S)-2-amino-4-(methylselanyl)butanoic acid …
Matched Description: … Selenomethionine is a naturally occuring amino acid in some plant materials such as cereal grains, soybeans …
Matched Mixtures name: … Vital-D Rx ... RenaPlex-D …
Matched Description: … Selenomethionine is a naturally occuring amino acid in some plant materials such as cereal grains, soybeans …
Matched Mixtures name: … Vital-D Rx ... RenaPlex-D …
Sotatercept
Sotatercept is an activin signalling inhibitor. It is a homodimeric recombinant fusion protein consisting of the extracellular domain of the human activin receptor type IIA (ActRIIA) linked to the human IgG1 Fc domain. On March 26, 2024, sotatercept was approved by the FDA for the treatment of pulmonary arterial hypertension...
Approved
Investigational
Magnesium silicate
Magnesium silicate is a compound of magnesium oxide and silicon. It is the magnesium salt of silicic acid containing an unspecified amount of water. The molecular formula can be expressed more clearly as MgSiO3.xH2O. It is known as talc and it presents many uses in the cosmetic industry, food industry...
Approved
Matched Description: … It is the magnesium salt of silicic acid containing an unspecified amount of water. …
Matched Categories: … Gastric Acid Lowering Agents ... Drugs for Acid Related Disorders …
Matched Categories: … Gastric Acid Lowering Agents ... Drugs for Acid Related Disorders …
Guaifenesin
Guaifenesin possesses a storied history, having been originally formally approved by the US FDA in 1952 and continues to be one of very few - if not perhaps the only drug that is readily available and used as an expectorant . Since that time the agent has been a combination...
Approved
Investigational
Vet approved
Matched Mixtures name: … Mucinex D ... Mucinex D ... Exall D …
Somatostatin
Somatostatin, also known as growth hormone-inhibiting hormone, is a naturally-occurring peptide hormone of 14 or 28 amino acid residues that regulates the endocrine system. It is secreted by the D cells of the islets to inhibit the release of insulin and glucagon, and is also generated in the hypothalamus, where...
Approved
Investigational
Matched Iupac: … 6,9,12,15,18,21,24,27,30,33,36-undecaoxo-1,2-dithia-5,8,11,14,17,20,23,26,29,32,35-undecaazacyclooctatriacontane-4-carboxylic acid …
Matched Description: … It is secreted by the D cells of the islets to inhibit the release of insulin and glucagon, and is also ... known as growth hormone-inhibiting hormone, is a naturally-occurring peptide hormone of 14 or 28 amino acid ... Somatostatin is initially secreted as a 116 amino acid precursor, preprosomatostatin, which undergoes …
Matched Description: … It is secreted by the D cells of the islets to inhibit the release of insulin and glucagon, and is also ... known as growth hormone-inhibiting hormone, is a naturally-occurring peptide hormone of 14 or 28 amino acid ... Somatostatin is initially secreted as a 116 amino acid precursor, preprosomatostatin, which undergoes …
Vonoprazan
Vonoprazan is a potassium-competitive acid blocker (PCAB) that inhibits H+, K+-ATPase-mediated gastric acid secretion. PCABs represent an alternative to proton-pump inhibitors for the treatment of acid-related disorders. Unlike proton-pump inhibitors, PCABs are not affected by CYP2C19 genetic polymorphisms and do not require acid-resistant formulations. Furthermore, vonoprazan is 350-times more potent...
Approved
Investigational
Matched Description: … ATPase-mediated gastric acid secretion. ... Vonoprazan is a potassium-competitive acid blocker (PCAB) that inhibits H+, K+- ... PCABs represent an alternative to proton-pump inhibitors for the treatment of acid-related disorders. …
Matched Categories: … Gastric Acid Lowering Agents ... Drugs for Acid Related Disorders ... Potassium-competitive Acid Blockers …
Matched Categories: … Gastric Acid Lowering Agents ... Drugs for Acid Related Disorders ... Potassium-competitive Acid Blockers …
Inositol nicotinate
Inositol nicotinate, also known as Inositol hexaniacinate/hexanicotinate or "no-flush niacin", is a niacin ester and vasodilator. It is used in food supplements as a source of niacin (vitamin B3), where hydrolysis of 1 g (1.23 mmol) inositol hexanicotinate yields 0.91 g nicotinic acid and 0.22 g inositol. Niacin exists in...
Approved
Withdrawn
Matched Description: … Niacin exists in different forms including nicotinic acid, nicotinamide and other derivatives such as ... niacin (vitamin B3), where hydrolysis of 1 g (1.23 mmol) inositol hexanicotinate yields 0.91 g nicotinic acid ... Nicotinic acid plays an essential role in many important metabolic processes and has been used as lipid-lowering …
Matched Categories: … Nicotinic Acid and Derivatives …
Matched Categories: … Nicotinic Acid and Derivatives …
Calcium levulinate
The relatively new calcium levulinate is produced from a direct reaction between L- or levulinic acid levulose and calcium hydroxide . The resultant calcium levulinate formulation, when used as a calcium supplement, possesses a high calcium content that is observed to be 14.8% higher than the content typically found in...
Approved
Experimental
Matched Description: … The relatively new calcium levulinate is produced from a direct reaction between L- or levulinic acid …
Colesevelam
Colesevelam is a bile acid sequestrant. Colesevelam is used with exercise and diet changes (restriction of cholesterol and fat intake) to reduce the amount of cholesterol and certain fatty substances in the blood. It works by binding bile acids in the intestine. Bile acids are made when cholesterol is broken...
Approved
Matched Description: … Colesevelam is a bile acid sequestrant. …
Matched Categories: … Bile Acid Sequestrants ... Bile-acid Binding Activity …
Matched Categories: … Bile Acid Sequestrants ... Bile-acid Binding Activity …
Odevixibat
Odevixibat, or A4250, is an ileal sodium/bile acid cotransporter inhibitor indicated for the treatment of pruritus in patients older than 3 months, with progressive familial intrahepatic cholestasis (PFIC).[A236808,L34793] Odevixibat is the first approved non-surgical treatment option for PFIC. Previous therapies for PFIC included a bile acid sequestrant such as ursodeoxycholic...
Approved
Investigational
Matched Iupac: … tetrahydro-1lambda6,2,5-benzothiadiazepin-8-yl]oxy}acetamido)-2-(4-hydroxyphenyl)acetamido]butanoic acid …
Matched Description: … [L34803] Previous therapies for PFIC included a bile acid sequestrant such as [ursodeoxycholic acid]. ... Odevixibat, or A4250, is an ileal sodium/bile acid cotransporter inhibitor indicated for the treatment …
Matched Categories: … Ileal bile acid transport inhibitor ... Ileal Bile Acid Transporter Inhibitor …
Matched Description: … [L34803] Previous therapies for PFIC included a bile acid sequestrant such as [ursodeoxycholic acid]. ... Odevixibat, or A4250, is an ileal sodium/bile acid cotransporter inhibitor indicated for the treatment …
Matched Categories: … Ileal bile acid transport inhibitor ... Ileal Bile Acid Transporter Inhibitor …
Phosphorus
Approved
Experimental
Matched Mixtures name: … Calci A and D Tab ... Calcium Phosphorus & Vitamin D …
Safflower oil
Safflower (Carthamus tinctorius L) is a herbaceous plant in the Asteraceae family. Extracted from the seeds of safflowers, safflower oil is a rich source of various saturated fatty acids, monounsaturated fatty acid (oleic acid) or essential n-6 polyunsaturated fatty acid (PUFA) linoleic acid [A32677, A32679], depending on the flower type....
Approved
Investigational
Matched Description: … (oleic acid) or essential n-6 polyunsaturated fatty acid (PUFA) linoleic acid [A32677, A32679], depending ... Gamma linolenic acid (GLA) safflower oil is marketed as an over-the-counter dietary supplement. ... safflowers, safflower oil is a rich source of various saturated fatty acids, monounsaturated fatty acid …
Raltitrexed
Raltitrexed (brand name Tomudex®) is a chemotherapy drug manufactured AstraZeneca Company, is an antimetabolite used in chemotherapy. It is an inhibitor of thymidylate synthase.
Approved
Investigational
Matched Iupac: … methyl[(2-methyl-4-oxo-1,4-dihydroquinazolin-6-yl)methyl]amino}thiophen-2-yl)formamido]pentanedioic acid …
Matched Categories: … Folic Acid Analogues ... Folic Acid Antagonists …
Matched Categories: … Folic Acid Analogues ... Folic Acid Antagonists …
Manganese cation
Manganese is a transition metal that was first described in the 19th and 20th centuries. It is environmentally abundant, being the fifth most abundant metal and the twelfth most abundant element overall on Earth.[A263657, A263667] Manganese intake primarily occurs through the diet, as it is found at low levels in...
Approved
Nutraceutical
Matched Mixtures name: … C & D ... Liquid Opti-minplex +d ... Multi Mega Minerals With Vitamin D …
Oxaliplatin
Oxaliplatin is a platinum-based chemotherapy drug in the same family as cisplatin and carboplatin. Compared to cisplatin the two amine groups are replaced by diamino cyclohexane (DACH) group to provide a greater antitumor effect. However, this leads to poorer water solubility, which was compensated by the addition of the chloride...
Approved
Investigational
Matched Iupac: … (3aR,7aR)-octahydro-2',5'-dioxaspiro[cyclohexa[d]1,3-diaza-2-platinacyclopentane-2,1'-cyclopentane]-3 …
Displaying drugs 301 - 325 of 10361 in total