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Clinical Pharmacology

2022
This chapter provides an overview of the general principles and miscellaneous topics of clinical pharmacology that are relevant to pain medicine. This involves the World Health Organization (WHO) analgesic ladder which is mainly used for acute and cancer pain.
Sabina Bachtold   +6 more
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Rapacuronium: clinical pharmacology

European Journal of Anaesthesiology, 2001
The need for a rapid-acting non-depolarizing neuromuscular blocking agent with a short duration of action resulted in the synthesis of rapacuronium. The onset of maximum block with rapacuronium occurs in 60-90 s with doses of 1.5-2.5 mg kg-1 with a duration of clinical relaxation of 15-30 min.
R K, Mirakhur, K C, McCourt
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Omapatrilat: Clinical pharmacology

Drugs of Today, 2000
Omapatrilat is the most clinically advanced member of a new class of cardiovascular agents known as vasopeptidase inhibitors. Omapatrilat acts by inhibiting two key enzymes responsible for blood pressure regulation: neutral endopeptidase and angiotensin-converting enzyme.
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Clinical pharmacology: Foscarnet

The American Journal of Medicine, 1992
Foscarnet exerts its antiviral effects via reversible inhibition of viral polymerases. Pharmacodynamic data indicate that herpesvirus and human immunodeficiency virus replication is inhibited by therapeutically achievable concentrations of foscarnet; however, the concentrations of foscarnet required for such inhibition have been found to vary widely ...
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Clinical Pharmacology Of Caffeine

Annual Review of Medicine, 1990
Caffeine is the most widely consumed stimulant drug in the world. This chapter reviews the human pharmacology of caffeine; the evidence for its role in causing human disease, including addiction; and its potential usefulness as a therapeutic agent.
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CLINICAL PHARMACOLOGY OF BENZODIAZEPINES

Annual Review of Medicine, 1987
The benzodiazepines are the most widely used anxiolytic drugs. Their pharmacokinetic properties differ widely. Side effects are usually mild but dependence can supervene after long-term administration, even if normal therapeutic doses are not exceeded. Careful monitoring of use is essential.
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Pharmacology and Clinical Pharmacology of Vigabatrin

Journal of Child Neurology, 1991
Vigabatrin is an enzyme-activated, irreversible inhibitor of γ-aminobutyric acid (GABA) aminotransferase, which causes a marked increase in cerebral GABA concentration and a resulting anticonvulsant action. Recovery from its effects requires the synthesis of new enzyme, and this may take several days following a single dose.
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Clinical pharmacology overview

2012
Abstract The first chapter of the book provides an introduction to pharmacology and its implementation in clinical practice.
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Clinical pharmacology

Medical Journal of Australia, 1961
Gillian M, Shenfield   +2 more
openaire   +3 more sources

CLINICAL PHARMACOLOGY

The Lancet, 1964
A.C. Dornhorst   +2 more
openaire   +3 more sources

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