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2015 PK and PD
2015 PK and PD

... • At the cellular level: Most drugs exert their effects on the body by interacting with macromolecule “targets” which are usually on the surface or within cells. ...
06_Synthetic Organic..
06_Synthetic Organic..

... to students of chemistry attending the lectures “Synthetic organic drugs”. The major goal in their education is preparation for the design of new drugs so the major intention of this study guide is to get an idea about the strategies of pharmaceutical therapy and drug action. Since it is not possibl ...
- University of Mississippi
- University of Mississippi

... have some type of modulating capabilities over opioid analgesia, which is still not fully understood. Perhaps the best result of these studies is the evidence that shows that the side effects, like tolerance, withdrawal symptoms, and constipation were not also potentiated (Vidal-Torres et al., 2013) ...
PLACE IN THERAPY OF TWO NEW DRUGS
PLACE IN THERAPY OF TWO NEW DRUGS

... function and asthma symptoms. There is some evidence of reduced local (oropharyngeal) side effects, but more long-term data is needed before we can determine if Alvesco ® reduces systemic adverse effects as well. Given the available evidence, Alvesco® does not currently offer any significant advanta ...
Conformational aspects of drug-DNA interactions: Studies on
Conformational aspects of drug-DNA interactions: Studies on

... ones. We are confident in concluding that derivatives I, III, IV and V intercalate into DNA, while compound II, notwithstanding its chemical structure, represents an example of non-intercalated, outside-bound drug. In addition to this unexpected finding, our results indicate that the coumarin deriva ...
Uptravi
Uptravi

... • No difference in mortality between groups • Addition of selexipag to baseline regimen of two meds gave benefits consistent with overall treatment effect • Similar efficacy regardless of dose range Sitbon O, et al. N Engl J Med. 2015;373(26):2522-33. ...
Chapter 5 Over the counter drugs[1].
Chapter 5 Over the counter drugs[1].

... Adverse reactions: sedation. Uncoordination, lack of concentration and lassitude. Central and peripheral antimuscarinic action such as blurred vision, constipation and urinary retention. ...
Drug chirality: Stereoselectivity in the action and disposition
Drug chirality: Stereoselectivity in the action and disposition

... Neuroprotective- prevents entry of heavy metal ions across blood brain barrier. Neurotoxic at high doses Effects of Gantacurium, a chlorofumarate muscle relaxant, can be rapidly reveresed by L-cysteine. Not been introduced in clinical practice. ...
Thromboxane Receptors Antagonists and/or Synthase Inhibitors
Thromboxane Receptors Antagonists and/or Synthase Inhibitors

... TXA2 is the major product of the arachidonic acid (AA) metabolism in platelets that, in response to various stimuli, is produced via the consequent actions of cyclooxygenase (COX) and TX synthase (TXS). Through its interaction with TP receptors on platelets, TXA2 is a potent inducer of platelet acti ...
I. Adrenergic Nervous System: Overview
I. Adrenergic Nervous System: Overview

... cannot breathe. Anaphylactic shock requires immediate advanced medical care; but other first aid measures include rescue breathing (part of CPR) and administration of epinephrine (adrenaline). Rescue breathing may be hindered by the constricted airways but is essential if the victim stops breathing ...
Allergic Rhinitis
Allergic Rhinitis

... Ketotifen ...
Bibliographic Information The action of certain esters and ethers of
Bibliographic Information The action of certain esters and ethers of

Medication Strategies for Behavior Patients Lynne Seibert DVM, MS
Medication Strategies for Behavior Patients Lynne Seibert DVM, MS

... humans, tricyclic antidepressants can cause cardiovascular, neurological, hematologic, gastrointestinal, and endocrine side effects. Testicular hypoplasia has also been reported. Tricyclic antidepressants should never be used in combination with MAO inhibitors, and should be used cautiously, if at a ...
JWH018, a common constituent of Spice herbal blends, is a potent
JWH018, a common constituent of Spice herbal blends, is a potent

... and EPSC amplitude. Cultured autaptic neurons are heterogeneous, with some expressing CB1 receptors and others not. The presence of DSE (which requires CB1 receptors) was used as a marker for neuronal cannabinoid sensitivity. DSE was induced as previously described (Straiker and Mackie, 2005). Recor ...
Identification of Epidermal Growth Factor
Identification of Epidermal Growth Factor

... National Cancer Institute (NCI) drug screen database. Methods: The levels of mRNAs were measured and used to generate a molecular target database for the 60 cell lines of the NCI anticancer drug screen. The computer analysis program, COMPARE, was used to search for cytotoxicity patterns in the NCI d ...
a comparative study between palonosetron and granisetron to
a comparative study between palonosetron and granisetron to

... Granisetron is a selective 5 hydroxytryptamine receptor antagonist (5HT3 RA). Granisetron is shown to be effective in preventing chemotherapy induced nausea & vomiting.7,12 Later it’s antiemetic efficacy was also tested in postoperative nausea and vomiting and was found to be effective in preventing ...
INTRODUCTION to Pharmacology
INTRODUCTION to Pharmacology

... subunits alpha, beta, and gamma • Based on alpha subunits they are further classified into 3 main subtypes Gs, Gi, and Gq ...
Sheet#14,Dr.Alia,Rawan Majali
Sheet#14,Dr.Alia,Rawan Majali

... Somatostatin is a regulator of gastrin release; it inhibits gastrin release. The vagus nerve has an inhibitory action on these cells; inhibiting the inhibitory effect on gastrin, thus we have more gastrin secretion. Histamine release is controlled by two factors; vagal stimulation (acetylcholine bin ...
Hyperlipotrotinemia
Hyperlipotrotinemia

... Statins – other potential cardioprotective effects:  On endothelial cell function – increase NO synthesis  On plaque stability – reduce degradation of matrix by metalloproteinases  On inflammation – antiinflammatory?  On lipoprotein oxidation – reduce oxidation of LDL and uptake by macrophages ...
Altered Glutamate Receptor Function during Recovery of Bladder
Altered Glutamate Receptor Function during Recovery of Bladder

... animals had laminectomies but was left uninjured (n ⫽ 15). Additional groups of subacutely injured animals (n ⫽ 7) and uninjured controls (n ⫽ 3) were generated for studies of histopathology of the injury site and immunohistochemistry of the lumbosacral micturition centers (see methods below). Anima ...
Suggestion from clinicians
Suggestion from clinicians

... This review provides a reasonable amount of data to assess the trough BP lowering effect of 9 different ARBs. When the different ARBs are compared, there is a similarity in their BP lowering effects at trough. When the best estimate of the near maximal BP lowering efficacy of these 9 drugs is compar ...
Selexipag for the treatment of pulmonary arterial hypertension
Selexipag for the treatment of pulmonary arterial hypertension

... in patients with World Health Organization functional class (FC) II or III disease. The recommended initial selexipag dosage is 200 mg twice daily. Like prostanoid analogs, selexipag has a dose-dependent adverse-effect profile that includes nausea, vomiting, diarrhea, headache, and musculoskeletal p ...
ANXIOLYTICS AND HYPNOTICS
ANXIOLYTICS AND HYPNOTICS

... decrease neuronal excitability via agonist effect at the GABAA receptor. b. Classification: by duration of action as short-acting (e.g., triazolam), intermediate-acting (e.g., temazepam) and long-acting (flurazepam). ...
Pharmaceutical chemistry 1. Naming chemical
Pharmaceutical chemistry 1. Naming chemical

... C2H5OSO2OH + C2H5OH ...
ANTI-PSYCHOTIC DRUGS
ANTI-PSYCHOTIC DRUGS

... to accumulation of amines in presynaptic stores for the amino neurotransmitters and increase release ...
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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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