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Fenticonazole
go.drugbank.com/drugs/DB13434InvestigationalFenticonazole has a broad spectrum of antimycotic activity against dermatophytes and yeasts.
Products: LOMEXIN 600 MG OVULOS, JİNOMED 600 MG OVÜL, 2 OVÜLArtemisia vulgaris root
go.drugbank.com/drugs/DB14170ApprovedArtemisia vulgaris root allergenic extract is used in allergenic testing.
Products: LAIS Beifuß 1000 UA SublingualtablettenEcamsule
go.drugbank.com/drugs/DB09534ApprovedEcamsule has been approved for use in the U.S. since 2006, but only at a specific concentration and only in a few products manufactured by L'Oreal. … It is a benzylidene camphor derivative, many of which are known for their excellent photostability.
Mixtures: Anthelios-creme Solaire SPF 10, Gelee Fraiche Hydratante SPF 10Besifloxacin
go.drugbank.com/drugs/DB06771ApprovedFDA approved on May 28, 2009.
Products: BESIVANCE % 0,6 OFTALMIK SÜSPANSIYON, 5 MLMephentermine
go.drugbank.com/drugs/DB01365ApprovedWithdrawn(From Martindale, The Extra Pharmacopoeia, 30th ed, p1248) … It is used to maintain blood pressure in hypotensive states, for example, following spinal anesthesia.
Products: Wyamine Sulfate Injection Liq 30mg/mlGlutamic acid
go.drugbank.com/drugs/DB00142ApprovedInvestigationalNutraceuticalA peptide that is a homopolymer of glutamic acid.
Synonyms: L-Glutamate, L-Glutamic acidMixtures: PEPZAN 225 MG/225 MG FİLM TABLET, 20 ADET, NUMETA PED G16 % E İNFÜZYONLUK EMÜLSİYON, 500 MLCilgavimab
go.drugbank.com/drugs/DB16393ApprovedInvestigationalmay be exposed to the virus. … Cilgavimab, in combination with [tixagevimab], was issued an FDA emergency use authorization (EUA) on December 9, 2021, for the pre-exposure prophylaxis of COVID-19 in individuals at increased risk for
Tixagevimab
go.drugbank.com/drugs/DB16394ApprovedInvestigationalmay be exposed to the virus. … Tixagevimab, in combination with [cilgavimab], was issued an FDA emergency use authorization (EUA) on December 9, 2021, for the pre-exposure prophylaxis of COVID-19 in individuals at increased risk for
Daclizumab
go.drugbank.com/drugs/DB00111ApprovedInvestigationalWithdrawnDaclizumab is a composite of human (90%) and murine (10%) antibody sequences. … On 22 April 2008, Roche Registration Limited chose to voluntarily withdraw the marketing authorization for their product Zenapax (daclizumab), as indicated for the prophylaxis of acute organ rejection
Products: Zenapax 5mg/mlPhysostigmine
go.drugbank.com/drugs/DB00981ApprovedIt can be applied topically to the conjunctiva. … It also can cross the blood-brain barrier and is used when central nervous system effects are desired, as in the treatment of severe anticholinergic toxicity.
Products: Antilirium Inj 1mg/ml