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Mobicam - Beximco Pharmaceuticals Ltd.
Mobicam - Beximco Pharmaceuticals Ltd.

... Caution should be exercised in patients have symptoms of gastrointestinal diseases. If peptic ulceration or gastrointestinal bleeding occurs, Tenoxicam should be immediately withdrawn. It is necessary to adequately monitor the patient with increased risk of developing renal failure, impaired renal f ...
C-13 Part II Non-Mendelian inheritance
C-13 Part II Non-Mendelian inheritance

... relationship between the alleles Most genes do not meet these criteria. ...
Drug Treatment Choice in Older Adults with Urinary Incontinence
Drug Treatment Choice in Older Adults with Urinary Incontinence

Chapter 4
Chapter 4

... Principle of segregation Genes (alleles) occur in pairs (because chromosomes occur in pairs). During gamete production, the members of each gene pair separate, so each gamete contains one member of each pair. During fertilization, the full number of chromosomes is restored, and members of gene or al ...
OPIOIDS
OPIOIDS

... prescribing opiates for pain became more common during the last decade of the 20th Century • Opioid therapy became accepted (although often inadequately) for treating acute pain, pain due to cancer, & pain caused by a terminal disease • Still disputed is the use of opioids for chronic pain not assoc ...
BSc in Medical Sciences with PHARMACOLOGY Course Director Dr
BSc in Medical Sciences with PHARMACOLOGY Course Director Dr

... The macrophage as a pharmacological target in airway disease Airway mucus production and pharmacotherapy of overproduction Glucocorticoids and the cardiovascular system Stress and the cardiovascular system ...
29 October 2014
29 October 2014

... Dr Kim first portrayed the evolution of concepts from the old belief that medication response is universal to the current understanding that variations are indeed present and that awareness of such would help to build therapeutic alliance in medication treatment. Dr Kim then clarified a number of ea ...
Document
Document

... ...
Initial IND Submission Checklist
Initial IND Submission Checklist

... ii) Description of the drug product iii) Description of any placebo used in the studies v) Specify any environmental analysis performed on investigational product or indicate a claim for exclusion under 21 CFR 25.30 or 21 CFR 25.31 Pharmacology and Toxicology Information The section should include i ...
Synergistic stabilization of BCS Class II drug
Synergistic stabilization of BCS Class II drug

... Department of Chemical, Biological and Pharmaceutical Engineering, New Jersey Institute of Technology ...
BLIND A condition imposed on an individual (or group of individuals
BLIND A condition imposed on an individual (or group of individuals

... the above into account, and makes a statistically significant result likely within the prescribed amount of time. TREATMENT 1. The act of treating, as in caring for a patient. 2. The specific regimen, method, or procedure being tested in a clinical trial. TREATMENT ARM Term sometimes used in place o ...
Slide 1
Slide 1

... mainly by two aspects: •general concerns do exist regarding potentially harmful effects of drugs on the embryo. The fear of a second disaster as with thalidomide still present; ...
Phase I Issues for Novel TB Drugs
Phase I Issues for Novel TB Drugs

... Exposure-Response Studies • FDA Guidance for Industry: Exposure-Response Relationships — Study Design, Data Analysis, and Regulatory Applications • Objective: explore relationship of drug exposure to response (e.g., biomarkers, potentially valid surrogate endpoints, clinical effects, adverse events ...
EU Core Safety Profile
EU Core Safety Profile

... Use in Hepatically Impaired Patients: As with any drug wholly metabolised by the liver, doxazosin should be administered with particular caution to patients with evidence of impaired hepatic function. Since there is no clinical experience in patients with severe hepatic impairment use in these patie ...
Checklist of Information to be Included When Reporting a Clinical
Checklist of Information to be Included When Reporting a Clinical

... 1 The title identifies the drug(s) and patient population(s) studied. 2 The abstract includes the name of the drug(s) studied, the route of administration, the population in whom it was studied, and the results of the primary objective and major clinical pharmacokinetic findings. Background 3 Pharma ...
HST-151 Final Exam p
HST-151 Final Exam p

... What is the explanation for this? What implication does it have for patient care? [6] The drug obeys dose-dependent (saturation) kinetics rather than first order. Half-life is lengthening as dose is raised. Non-linear kinetics means that a small dosage increment can potentially cause a very large in ...
17-19
17-19

... CYP2D6 isoenzyme —This isoenzyme metabolizes a variety of drugs. There are clear phenotypes of this enzyme, there are racial differences in this expression. As an example, up to 8 to 10 percent of Caucasians are deficient in this enzyme and are called poor metabolizers of those drugs eliminated thro ...
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... OTC Drug Products’ letter of August 28,200O concerning an Application for Exemption for BC Analgesic Powder (two doses). My call was returned by Michelle Butler, Esquire. I informed Ms. Butler that we would like an explanation of a sentence that appears on the second page of Mr. Dormer’s letter that ...
Introduction to Genomics, Bioinformatics - UNC
Introduction to Genomics, Bioinformatics - UNC

... Alignments between the query sequence and any given database sequence, allowing for mismatches and gaps, indicate their degree of similarity ...
zero order kinetics.
zero order kinetics.

... • Microsomal enzymes (monooxygenase, cytochrome P450 and glucoronyl transferase) may be induced or inhibited by other drugs whereas nonmicrosomal enzymes are not subjected to these interactions. ...
FACTORS MODIFYING DRUG EFFECTS
FACTORS MODIFYING DRUG EFFECTS

... Such as: respond differently to drugs both from time to time and from other individuals. ...
File
File

... qualitatively (e.g., grain yields). ...
Nursing Process Focus: Patients Receiving Lorazepam (Ativan
Nursing Process Focus: Patients Receiving Lorazepam (Ativan

... restoration of normal sleep/wake pattern. • Demonstrate understanding of sleep hygiene and factors that facilitate sleep. • Demonstrate understanding of the drug's action by accurately describing drug side effects and precautions. • Remain free of injury during course of drug therapy. ...
Human Research Involving Drugs and Biologics  1.0 Purpose:
Human Research Involving Drugs and Biologics 1.0 Purpose:

... including pilot studies) will require that the investigator seek consultation with FDA regarding the need for an IND or BLA. Documentation of the FDA’s response (e.g., an IND or BLA number or a letter exempting the research from such requirement) must be presented to the IRB at the time of initial r ...
Nursing Process Focus: Lorazepam (Ativan)
Nursing Process Focus: Lorazepam (Ativan)

... (The drug's affect on the hippocampus and cerebral cortex may cause confusion or amnesia.) Monitor mental health status and evaluate risk potential for suicide. Monitor the environment for signs of hoarding medication. Obtain a noself harm verbal contract from patients identified as being at risk of ...
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Pharmacogenomics

Pharmacogenomics (a portmanteau of pharmacology and genomics) is the study of the role of genetics in drug response. It deals with the influence of acquired and inherited genetic variation on drug response in patients by correlating gene expression or single-nucleotide polymorphisms with drug absorption, distribution, metabolism and elimination, as well as drug receptor target effects. The term pharmacogenomics is often used interchangeably with pharmacogenetics. Although both terms relate to drug response based on genetic influences, pharmacogenetics focuses on single drug-gene interactions, while pharmacogenomics encompasses a more genome-wide association approach, incorporating genomics and epigenetics while dealing with the effects of multiple genes on drug response.Pharmacogenomics aims to develop rational means to optimize drug therapy, with respect to the patients' genotype, to ensure maximum efficacy with minimal adverse effects. Through the utilization of pharmacogenomics, it is hoped that drug treatments can deviate from what is dubbed as the “one-dose-fits-all” approach. It attempts to eliminate the trial-and-error method of prescribing, allowing physicians to take into consideration their patient’s genes, the functionality of these genes, and how this may affect the efficacy of the patient’s current and/or future treatments (and where applicable, provide an explanation for the failure of past treatments). Such approaches promise the advent of ""personalized medicine""; in which drugs and drug combinations are optimized for each individual's unique genetic makeup. Whether used to explain a patient’s response or lack thereof to a treatment, or act as a predictive tool, it hopes to achieve better treatment outcomes, greater efficacy, minimization of the occurrence of drug toxicities and adverse drug reactions (ADRs). For patients who have lack of therapeutic response to a treatment, alternative therapies can be prescribed that would best suit their requirements. In order to provide pharmacogenomic-based recommendations for a given drug, two possible types of input can be used: genotyping or exome or whole genome sequencing. Sequencing provides many more data points, including detection of mutations that prematurely terminate the synthesized protein (early stop codon).
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