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Drugs used in Hypertension
Drugs used in Hypertension

... • More effective than the thiazides. • Act more rapidly, but shorter duration of action. • Ususally furosemide – used orally to decr peripheral and pulmonary edema in moderate and severe HF. • Given i.v. for pulmonary edema resulting from acute ventricular failure. • Effective in patients with decr ...
Drugs acting on the uterus
Drugs acting on the uterus

... Drugs acting on the uterus ...
HypertenDiur
HypertenDiur

... • More effective than the thiazides. • Act more rapidly, but shorter duration of action. • Ususally furosemide – used orally to decr peripheral and pulmonary edema in moderate and severe HF. • Given i.v. for pulmonary edema resulting from acute ventricular failure. • Effective in patients with decr ...
Analgesic
Analgesic

... fentanyl transdermal system • should be used for longterm (chronic) pain requiring continuous narcotic pain • Is designed to release the drug into the skin at a constant rate ranging from 25 to 100 micrograms/h, ...
Adverse reactions
Adverse reactions

... • Five dopaminergic systems or pathways are important for understanding schizophrenia and the mechanism of action of antipsychotic drugs: 1) Mesolimbic-mesocortical pathway: the one most closely related to behavior and psychosis 2) Nigrostriatal pathway: it is involved in the coordination of volunta ...
Recreational Drugs
Recreational Drugs

...  MS: Paresthesias, muscle rigidity, motor agitation, rhabdomyolysis. LSD or d-lysergic acid diethylamide  Discovered in 1938.  Manufactured from lysergic acid found in ergot, a fungus that grows on rye and other grains.  It is by weight the most potent drug discovered. ...
Endocrine aspects of anabolic steroids
Endocrine aspects of anabolic steroids

... results in disturbances in menstrual function and infertility is, in contrast, reversible. Stimulation of the sebaceous glands appears to be dose-related: Increasing testosterone beyond the physiological range in normal men results in further increases in the sebum excretion rate. Consequently AAS u ...
Cholinoceptor blocking drugs
Cholinoceptor blocking drugs

... •Marked reflex vagal discharge sometimes accompanies the pain of MI and may result in sufficient depression of SA- and AV- nodal functions to impair cardiac out put. ...
Characterization of the Analgesic and Anti
Characterization of the Analgesic and Anti

... brain barrier in either rats or humans (Mroszczak et al., 1987), evidence that (R,S)-ketorolac acts at sites in the central as well as the peripheral nervous system to produce analgesia has accumulated. For example, after intrathecal (i.t.) administration, (R,S)-ketorolac blocks pain states associat ...
The cannabinoids: An overview. Therapeutic implications in
The cannabinoids: An overview. Therapeutic implications in

... search for additional therapies, one of which is cannabis. Cannabis is used currently by MS patients, although it is not an approved drug (36). Several animal studies involving cannabinoids have been described using an experimental model of MS. This model, known as experimental autoimmune encephalom ...
Date Prepared Name  Office Address
Date Prepared Name Office Address

... A monkey model of human mu-opioid receptor physiogenetics NIDA/ R21 021180 PI ($457,399) To explore comparable functionality of rhesus and human opioid receptor polymorphisms. ...
New Tuberculosis Therapeutics: A Growing
New Tuberculosis Therapeutics: A Growing

... for the first 8 weeks of therapy, the Tuberculosis Trials Consortium reported that, even though the primary end point of an increase in the rate of sputum conversion at 8 weeks was not met, a post hoc analysis of sputum conversion at earlier points in time suggested that a quicker time to sputum con ...
Narcotics and Analgesics
Narcotics and Analgesics

... Drugs used for migraines  Drugs vary in onset with sub q sumatriptan acting the most rapidly and starting within 10 minutes; most clients get relief within 1-2 hours  Drugs are metabolized in the liver by monoamine oxidase or by cytochrome ...
comparison ofsuppressive activity of the central nervous system from
comparison ofsuppressive activity of the central nervous system from

Synergistic Interaction between the Two Mechanisms of Action of
Synergistic Interaction between the Two Mechanisms of Action of

... systemic as well as spinal combination of morphine with the ␣2-adrenoceptor agonist clonidine resulted in synergistic antinociception (Ossipov et al., 1990; Fairbanks and Wilcox, 1999). In clinical settings, morphine analgesia was potentiated by systemic tricyclic antidepressants (Levine et al., 198 ...
Final - lgh
Final - lgh

... acetylcholinesterases so their concentration in the synaptic cleft does not fall rapidly  Continuous end plate potential depolarization will leads to muscle relaxation  End plate cannot repolarized as long as depolarizing agent binds to Ach receptors  Recovery only occur when drug diffuses away f ...
DESIGN, SYNTHESIS AND MOLECULAR DOCKING STUDIES OF BENZOTHIAZOLE  Research Article
DESIGN, SYNTHESIS AND MOLECULAR DOCKING STUDIES OF BENZOTHIAZOLE Research Article

... spectrum of biodynamic properties having potent clinical significance [4]. Schiff bases are currently been applied for the treatment of a number of disease condition. Though extensive research work has been reported on benzothiazole with Schiff base, relatively very little is known about the substit ...
Full Prescribing Information
Full Prescribing Information

... narrow therapeutic index cannot be avoided. BCRP Substrates with a Narrow Therapeutic Index (e.g., methotrexate, topotecan, or irinotecan): Increased plasma concentrations of BCRP substrates may result in potential adverse reactions. Monitor for adverse reactions related to the concomitant drug if u ...
Journal of Chemical and Pharmaceutical Research __________________________________________________
Journal of Chemical and Pharmaceutical Research __________________________________________________

... dopaminergic stimulation. Moreover sympathomimetics may increase alertness and thereby counterbalance the sedative effects of vestibular suppressants. Amphetamines are little used because of their addiction potential. Miscellaneous agents: Acetyl-leucine and Ginkgo Biloba are said to act as vestibul ...
general pharmacology
general pharmacology

... ◦ Antimuscarinic action (atropine like effects) ◦Blocks muscarinic receptor in SA node ◦ NE release from adrenergic nerve endings. ◦Avoid in patient with coronary diseases. ...
Document
Document

... research has advanced our knowledge of the role played by neuropeptides in the methamphetamineinduced striatal injury. Recently, we are investigating the role of other striatal neuropeptides such as neuropeptide Y and somatostatin on the cellular mechanisms of methamphetamine-induced neural damage. ...
Additivity Versus Synergy: A Theoretical Analysis of - Area-c54
Additivity Versus Synergy: A Theoretical Analysis of - Area-c54

Drug/Application
Drug/Application

... membram (gram neg)  Presence of an efflux pump ...
Clinical Data, Inc. Licenses Adenosine A2A Agonist to Santen for
Clinical Data, Inc. Licenses Adenosine A2A Agonist to Santen for

Principles of early drug discovery
Principles of early drug discovery

... analysing the data generated (reviewed in Zanders et al., 2002). The ultimate goal of this approach is to provide chemical tools against every protein encoded by the genome. The aim is to use these tools to evaluate cellular function prior to full investment in the target and commitment to a screeni ...
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NK1 receptor antagonist

Neurokinin 1 (NK1) antagonists are a novel class of medications that possesses unique antidepressant, anxiolytic, and antiemetic properties. The discovery of neurokinin 1 (NK1) receptor antagonists was a turning point in the prevention of nausea and vomiting associated with cancer chemotherapy.An example of a drug in this class is aprepitant. Chemotherapy-induced emesis appears to consist of acute and delayed phases. So far, the acute phase emesis responds to 5-HT3 antagonists while the delayed phase remains difficult to control. The discovery and development of NK1 receptor antagonists have elicited antiemetic effect in both acute and especially in delayed phases of emesis.The first registered clinical use of NK1 receptor antagonists was the treatment of emesis, associated with cancer chemotherapy.
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