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Levorphanol tartrate

Children-Safety and efficacy have not been established. LEVORPHANOL TARTRATE ... [Pg.854]

Oral- Recommended starting dose is 2 mg. Repeat in 6 to 8 hours Levo-Dromoran) or 3 to 6 hours Levorphanol Tartrate) as needed, provided the patient is assessed for signs of hypoventilation and excessive sedation. [Pg.854]

Levorphanol Tartrate The effective daily dosage range, depending on the severity of the pain, is 8 to 16 mg in 24 hours in the nontolerant patient. Total oral daily doses of more than 16 mg in 24 hours are generally not recommended as starting doses in non-opioid-tolerant patients. [Pg.854]

Levorphanol tartrate is used for the relief of severe pain in cancer, trauma, colic, and myocardial infarction, as well as pre- and postoperatively. It is administered orally or subcutaneously in doses of 2 to 3 mg according to the age and weight of the patient and the severity of pain. [Pg.467]

Levorphanol Tartrate 462.0 Diprenorphine Hydrochloride Oxedrine Tartrate... [Pg.1082]

Ro 1-5431 Levo-Dromoran ) is the (-)-form of hydroxy-Af-methylmorphinan, and is an opioid receptor agonist and OPIOID ANALGESIC. It is used orally or by injection to treat moderate to severe pain, levorphanol tartrate levorphanol. [Pg.165]

Codeine (sulfate, phosphate), CSS II Hydromorphone HC1 (Dilaudid) CSS II Levorphanol tartrate (Levo-Dromoran) CSS II Meperidine (Demerol) Synthetic narcotic CSS II Fentanyl (Duragesic, Sublimaze) CSS II... [Pg.250]

Effect of levorphanol tartrate on ribonucleic acid synthesis in normal and regenerating rat liver... [Pg.149]

Grewe (1946) introduced a vital alkylation reaction via a very specific stereo-selective (trans) synthesis followed by acid-catalyzed intramolecular, aromatic substitution, which caused the B/C-c/s CfD-trans ring fusions found to be common in either morphine or its natural congeners. This study has paved the way for an altogether new morphinan analogues known as benzomorphans . A few classical examples of this group of compoimds are listed below, viz., levorphanol tartrate dextromethorphan hydrobromide butorphanol tartrate ... [Pg.317]

The raeemie mixture dl) of l-(p-hydroxybenzyl)-2-methyl-1,2,3,4,5,6,7,8-octahydro-isoquinoline may be obtained exactly in the same manner as described for levorphanol tartrate (in 1 above). This is now resolved to get the J-enantiomorph and then treated with phenyltrimethyl ammonium hydroxide to cause methylation and yield the dextromethorphan base. Treatment of the base with appropriate amount of hydrobromide gives the eorresponding hydrobromide. [Pg.319]

Levorphanol tartrate (Levo-Dromoran) CSS II For moderate to severe pain... [Pg.334]

A nephelometric method was developed for the analysis of levallorphan tartrate in the presence of levorphanol tartrate. The method takes advantage of the kinetics of bromination of the allyl function on levallorphan which in acidic aqueous medium is faster than the bromination of the levorphanol. The bromination product is insoluble and hence lends itself to a turbidimetric determination (21). The procedure involves adding 1 mg of levallorphan tartrate (along with up to 10 mg of levorphanol tartrate) to 5 ml of 2.5N HCl and 15 ml of water in a glass stoppered 25-ml graduated cylinder. Bring to 25°C and add... [Pg.360]

Levorphanol tartrate, Ci7H230N,C4Hg06,2H20, Mol. Wt. 443-5. The official B.P,C, method of assay is the following ... [Pg.500]


See other pages where Levorphanol tartrate is mentioned: [Pg.633]    [Pg.833]    [Pg.842]    [Pg.620]    [Pg.704]    [Pg.704]    [Pg.750]    [Pg.855]    [Pg.1746]    [Pg.165]    [Pg.916]    [Pg.388]    [Pg.168]    [Pg.317]    [Pg.166]   
See also in sourсe #XX -- [ Pg.467 ]

See also in sourсe #XX -- [ Pg.704 ]

See also in sourсe #XX -- [ Pg.237 ]

See also in sourсe #XX -- [ Pg.388 , Pg.389 ]

See also in sourсe #XX -- [ Pg.317 , Pg.318 , Pg.319 , Pg.336 ]

See also in sourсe #XX -- [ Pg.500 ]




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