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Slide () - Access Emergency Medicine
Slide () - Access Emergency Medicine

... CYP2C9 and CYP1A9 to primary metabolites that retain affinity and ability to bind with cannabinoid receptors. One JWH-018 primary metabolite, acts as a antagonist at CB1. Secondary metabolites are formed by conjugation. These metabolites may retain ability to bind to cannabinoid receptors but at thi ...
International Journal of Phytopharmacology
International Journal of Phytopharmacology

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Predicting drug pharmacokinetics in humans from in vitro
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... the last decade have highlighted the importance of assessing the potential for inhibition [1] and induction of drug metabolism [2]. In addition, identification of the drug-metabolizing enzymes responsible for the biotransformations commonly encountered in drug development may predict interindividual ...
Tutorial - 5: Cardiovascular Drug Development: ACE inhibitors, Beta
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Module One: The Family as a Dynamic System
Module One: The Family as a Dynamic System

... drugs within each class often produce similar effects. However, all controlled substances, regardless of class, share a number of common features. With the exception of anabolic steroids, drugs in the other classes are utilized to alter mood, thought, and feeling through their actions on the central ...
*****************#***********#******|6******7#**8#**9
*****************#***********#******|6******7#**8#**9

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Ecstasy - TroxelToxicology
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pharmacokinetics

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Key to Problems for Drug Design Courses (II)
Key to Problems for Drug Design Courses (II)

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Pharmacologyonline 1: 613-624 (2011) Thanigavelan et al.

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ANTICONVULSANT ACTIVITY OF METHANOLIC EXTRACT OF MELISSA PARVIFLORA IN
ANTICONVULSANT ACTIVITY OF METHANOLIC EXTRACT OF MELISSA PARVIFLORA IN

... neurological condition seen by neurologists. Incidence of epilepsy in developed countries is approximately 50 per 100, 000 while that of developing country is 100 per 100, 000[1].India is home to about 10 million people with epilepsy (prevalence of about 1%)[2]. The number of Epilepsy Specialists an ...
The Expanding Role of Microsomal Enzyme Induction, and Its
The Expanding Role of Microsomal Enzyme Induction, and Its

... enzyme induction are drugs and xenobiotics. Factors modulating the extent of enzyme induction by a given agent include age and nutrition, and wide species variations are encountered with different inducing agents. Markers for microsomal enzyme induction include determination of the plasma half-life ...
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Drug interaction



A drug interaction is a situation in which a substance (usually another drug) affects the activity of a drug when both are administered together. This action can be synergistic (when the drug's effect is increased) or antagonistic (when the drug's effect is decreased) or a new effect can be produced that neither produces on its own. Typically, interactions between drugs come to mind (drug-drug interaction). However, interactions may also exist between drugs and foods (drug-food interactions), as well as drugs and medicinal plants or herbs (drug-plant interactions). People taking antidepressant drugs such as monoamine oxidase inhibitors should not take food containing tyramine as hypertensive crisis may occur (an example of a drug-food interaction). These interactions may occur out of accidental misuse or due to lack of knowledge about the active ingredients involved in the relevant substances.It is therefore easy to see the importance of these pharmacological interactions in the practice of medicine. If a patient is taking two drugs and one of them increases the effect of the other it is possible that an overdose may occur. The interaction of the two drugs may also increase the risk that side effects will occur. On the other hand, if the action of a drug is reduced it may cease to have any therapeutic use because of under dosage. Notwithstanding the above, on occasion these interactions may be sought in order to obtain an improved therapeutic effect. Examples of this include the use of codeine with paracetamol to increase its analgesic effect. Or the combination of clavulanic acid with amoxicillin in order to overcome bacterial resistance to the antibiotic. It should also be remembered that there are interactions that, from a theoretical standpoint, may occur but in clinical practice have no important repercussions.The pharmaceutical interactions that are of special interest to the practice of medicine are primarily those that have negative effects for an organism. The risk that a pharmacological interaction will appear increases as a function of the number of drugs administered to a patient at the same time.It is possible that an interaction will occur between a drug and another substance present in the organism (i.e. foods or alcohol). Or in certain specific situations a drug may even react with itself, such as occurs with dehydration. In other situations, the interaction does not involve any effect on the drug. In certain cases, the presence of a drug in an individual's blood may affect certain types of laboratory analysis (analytical interference).It is also possible for interactions to occur outside an organism before administration of the drugs has taken place. This can occur when two drugs are mixed, for example, in a saline solution prior to intravenous injection. Some classic examples of this type of interaction include that Thiopentone and Suxamethonium should not be placed in the same syringe and same is true for Benzylpenicillin and Heparin. These situations will all be discussed under the same heading due to their conceptual similarity.Drug interactions may be the result of various processes. These processes may include alterations in the pharmacokinetics of the drug, such as alterations in the absorption, distribution, metabolism, and excretion (ADME) of a drug. Alternatively, drug interactions may be the result of the pharmacodynamic properties of the drug, e.g. the co-administration of a receptor antagonist and an agonist for the same receptor.
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