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Halazepam is a benzodiazepine derivative. It is no longer marketed in the United States. It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. It is a trifluoroethyl derivative of nordazepam. While its structure may be similar to chlordiazepoxide and diazepam, it has both less toxicity and less tendency to cause paradoxical hostility and aggression than either of them. It has active benzodiazepine metabolites.
Halcinonide is a corticosteroid.It is used topically in the treatment of certain skin conditions.
Halobetasol propionate is thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid. It is used for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.
Halofantrine is a drug used to treat malaria. Its structure contains a substituted phenanthrene, and is related to the antimalarial drugs quinine and lumefantrine. It is only used to treat malaria. It is not used to prevent malaria because of the risk of toxicity and unreliable absorption.
Halometasone is a corticosteroid. It can be used as topical glucocorticoid drug which has a significant and rapid anti-inflammatory, anti-allergic, anti-itch, anti-exudative and anti-proliferative effect.
Halomon is a polyhalogenated monoterpene first isolated from the marine red algae Portieria hornemannii. It has attracted research interest because of its promising profile of selective cytotoxicity that suggests its potential use as an antitumor agent. It is in a class of chemical compounds known as halocarbons, which are often potent alkylating agents which may be toxic to individual cells or to living organisms. The red algae that naturally produce halomon and other related compounds probably do so as a poisonous defense against fish or other marine life that may see it as a potential source of food. Halomon, however, is a selective toxin; studies at the National Cancer Institute have indicated that it is more toxic to certain types of tumor cells than to other cells.
Haloperidol is a phenyl-piperidinyl-butyrophenone that is used primarily to treat schizophrenia and other psychoses. It is also used in schizoaffective disorder, delusional disorders, ballism, and tourette syndrome (a drug of choice) and occasionally as adjunctive therapy in mental retardation and the chorea of huntington disease. It is a potent antiemetic and is used in the treatment of intractable hiccups.
Haloperidol decanoate is the decanoate ester of the butyrophenone, haloperidol. It is available in sesame oil in sterile form for intramuscular (IM) injection. Haloperidol decanoate is the long-acting form of haloperidol. It is used for the treatment of schizophrenic patients who require prolonged parenteral antipsychotic therapy. Haloperidol decanoate belongs to a group of medicines known as the butyrophenone antipsychotics. It acts by blocking a variety of receptors in the brain, particularly dopamine receptors.
Haloprogin is an antifungal drug used to treat athlete's foot and other fungal infections.
Halothane is an inhalational general anesthetic. It is the only inhalational anesthetic agent containing a bromine atom; there are several other halogenated anesthesia agents which lack the bromine atom and do contain the fluorine and chlorine atoms present in halothane. It is a core medicine in the World Health Organization's "Essential Drugs List", which is a list of minimum medical needs for a basic health care system. Its use in developed countries, however, has been almost entirely superseded by newer inhalational anaesthetic agents.
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