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Previously treated with a PD-1 blocking antibody
go.drugbank.com/conditions/DBCOND0164672Drugs: LifileucelSynonyms: Previously treated with a PD-1 blocking antibodySymptomatic Botulism caused by Clostridium botulinum serotype A
go.drugbank.com/conditions/DBCOND0093883Synonyms: Symptomatic Botulism caused by Clostridium botulinum serotype APovidone-iodine
go.drugbank.com/drugs/DB06812ApprovedInvestigationalThis unique complex was discovered in 1955 at the Industrial Toxicology Laboratories in Philadelphia by H. A. Shelanski and M. V. Shelanski. … Povidone-iodine is a stable chemical complex of polyvinylpyrrolidone (povidone, PVP) and elemental iodine. It contains from 9.0% to 12.0% available iodine, calculated on a dry basis.
Synonyms: PVP-IMixtures: Mlp A-2, Mlp A-1Diphenidol
go.drugbank.com/drugs/DB01231ApprovedWithdrawnDiphenidol is an antiemetic agent used in the treatment of vomiting and vertigo. Diphenidol overdose may result in serious toxicity in children.
Categories: Heterocyclic Compounds, 1-RingSynonyms: Diphenyl(3-(1-piperidyl)propyl)carbinol, alpha,alpha-Diphenyl-1-piperidinebutanolGliclazide
go.drugbank.com/drugs/DB01120ApprovedInvestigationala sulfonamide group able to release a proton and the presence of one aromatic group. … [A39546] On the other hand, based on the pharmacological efficacy, gliclazide is considered a second-generation sulfonylurea which presents a higher potency and a shorter half-life.
Synonyms: 1-(3-azabicyclo(3.3.0)oct-3-yl)-3-(p-tolylsulfonyl)urea, 1-(hexahydrocyclopenta(c)pyrrol-2(1H)-yl)-3-(p-tolylsulfonyl)ureaCategories: Drugs Used in Diabetes, Cytochrome P-450 SubstratesProphylaxis of prevention of subtype A viruses contained in the 2015 formula Influenza A Virus Infection
go.drugbank.com/conditions/DBCOND0112776Synonyms: Prophylaxis of prevention of subtype A viruses contained in the 2015 formula Influenza A Virus InfectionLetrozole
go.drugbank.com/drugs/DB01006ApprovedInvestigational[A190543,A1559,L11623,L11626] It is a third generation aromatase inhibitor like [exemestane] and [anastrozole], meaning it does not significantly affect cortisol, aldosterone, and thyroxine. … Letrozole, or CGS 20267, is an oral non-steroidal type II aromatase inhibitor first described in the literature in 1990.
Categories: P-glycoprotein substrates, Cytochrome P-450 SubstratesProducts: LETROZOL 1A PHARMA 2.5MG, Letrozole SunAnkle spasticity following a stroke or traumatic brain injury
go.drugbank.com/conditions/DBCOND0133858Drugs: Clostridium botulinumSynonyms: Ankle spasticity following a stroke or traumatic brain injurySIS-101-ADO
go.drugbank.com/drugs/DB18085ExperimentalSIS-101-ADO is a siRNA therapeutic under investigation for the treatment of Autosomal Dominant Osteopetrosis Type 2 (ADO2).[L48091]
Benzocaine
go.drugbank.com/drugs/DB01086ApprovedInvestigationalBenzocaine is an ester local anesthetic that acts by preventing transmission of impulses along nerve fibers and at nerve endings. … [A231219] It is commonly used for local anesthesia in many over the counter products.[L32454,L32459,L32464] Benzocaine was first used for local anesthesia in dentistry.[A231259]
Synonyms: p-Carbethoxyaniline, Ethyl p-aminobenzoateMixtures: Kank-A, Blistex Kank-A