• Study Resource
  • Explore Categories
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
DEVELOPMENT OF A VALIDATED STABILITY-INDICATING HPLC ASSAY METHOD FOR DEXKETOPROFEN TROMETAMOL
DEVELOPMENT OF A VALIDATED STABILITY-INDICATING HPLC ASSAY METHOD FOR DEXKETOPROFEN TROMETAMOL

... presence of its degradation products was noticed. The peaks obtained were sharp and have clear baseline separation. The resolution factor for drug from nearest resolving was > 3. The photodiode array scanned all the components present in the mixture in whole wavelength range from 200 to 400 nm and i ...
ProposalForMedsAllergiesLabsSDWG_WG_2012_10_4
ProposalForMedsAllergiesLabsSDWG_WG_2012_10_4

... classifications that can identify drug concepts intended for specific therapeutic uses and thereby potentially not only identify drugs missed in RxNorm based extensional value sets but also suppress reporting on patients that are on same ingredient drugs that do not meet the therapeutic intent (such ...
RECENT DEVELOPMENTS IN TARGETED DRUG DELIVERY SYSTEM FOR CROSSING BLOOD-
RECENT DEVELOPMENTS IN TARGETED DRUG DELIVERY SYSTEM FOR CROSSING BLOOD-

... physicochemical properties. But the main important factor is lipophilicity of drug 8, 12. Increasing lipophilicity of a drug may cause increase in its volume of distribution. Other pharmacokinetic parameters are also be affected by lipophilicity of drug. As lipophilicity of drug increases, the rate ...
QA171_3_Liver_ADRs_April_2014_update
QA171_3_Liver_ADRs_April_2014_update

... The nature and severity of the liver disease in a specific patient will determine the clinical relevance of the adverse effect profile of a drug. It is therefore important to have a thorough understanding of a patient’s liver condition (i.e. through knowledge of laboratory, scan and biopsy results a ...
Small Is Beautiful: Issues in Nanomedicine
Small Is Beautiful: Issues in Nanomedicine

... scientific information on health risks and general failure on the part of regulatory agencies and patent offices. As  usual,  the  reality  is  somewhere  between  such  extremes.  Whatever  your  stance,  nano  has  already  permeated  virtually  every  sector  of  the  global  economy,  with  pote ...
Interactions between five candidate genes and antihypertensive
Interactions between five candidate genes and antihypertensive

Modeling Variation in Repeated Measures Data
Modeling Variation in Repeated Measures Data

... Figure 1. The graph shows that means for the three treatment groups are essentially the same at HR=O (baseline). At. HR=l the mean for drug B is larger than the mean for drug A, and both of the drug means are much larger than the placebo mean. Means for drugs A and B continue to be larger than the p ...
Party DRUGS - Australian Doctor
Party DRUGS - Australian Doctor

... last one to two days but it can take up to a week for users to feel normal again while serotonin levels are being restored. Symptoms are more intense in those using high doses, injecting the drug and using several different drugs at the same time. Sexual effects ...
1946814726Revised review article greety
1946814726Revised review article greety

... Rivaroxaban is the second new oral anticoagulant approved in September 2008 by European Medicines Agency (EMA) and by the FDA based on the results of the ROCKET AF (Rivaroxaban Versus Warfarin in Non valvular Atrial Fibrillaion) trial. It is a direct factor x a inhibitor, which connects reversibly t ...
DEPARTMENT OF  HEALTH  AND  HWAN  SE&VICES
DEPARTMENT OF HEALTH AND HWAN SE&VICES

... Schering ...
Predictability of Idiosyncratic Drug Toxicity Risk for Carboxylic Acid
Predictability of Idiosyncratic Drug Toxicity Risk for Carboxylic Acid

N receptors
N receptors

... • At the NMJ, N receptors Pentameric with four types of subunits, two a subunits bind ACh for ligand gating • All other nAChRs, including those at the peripheral ganglia, have 2 a’s and 3 b’s ...
adrenergic agents - NC State Veterinary Medicine
adrenergic agents - NC State Veterinary Medicine

... cardiovascular and pulmonary systems, both of which are heavily dependent upon adrenergic stimulation. Cardiac rate, rhythm, and force are controlled primarily by β 1 -receptors, while pulmonary function is dependent upon β 2 -receptors. The vasculature of both the cardiac and the pulmonary systems ...
Semantic integration of medication data into the EHOP Clinical Data
Semantic integration of medication data into the EHOP Clinical Data

... a DKDB (here Theriaque) rather than a unique terminology. Many other DKDB exist (e.g. in France: Banque Claude Bernard, Vidal) but these systems are not as open as Theriaque. RxNorm 7, which is based on UMLS, appears to us as the "ideal" DKDB for integrating and exploiting medication data, since it ...
Case Presentation - EZ
Case Presentation - EZ

... • Easily arousable and responsive to stimulation without becoming uncomfortable and quick return to sleep-like state- COOPERATIVE PATIENT – Patients receiving Precedex have been observed to be arousable and alert when stimulated. This alone should not be considered as evidence of lack of efficacy in ...
the side effects of common psychiatric drugs
the side effects of common psychiatric drugs

... serotonin—in the brain that was theorized to influence depression. This has remained a theory only. Serotonin (of which about only 5% is found in the brain) is one of the chemicals by which brain cells signal each other. SSRIs prevent serotonin from being naturally reabsorbed and thus create continu ...
Pharmacology of stimulant substances
Pharmacology of stimulant substances

... ⚝ Binding of parent and M1 metabolite to μopioid receptors ⚝ Weak inhibition of reuptake of norepinephrine and serotonin. ...
Cholestasis - Yorkshire and the Humber Deanery
Cholestasis - Yorkshire and the Humber Deanery

... risk of hepatotoxic reaction ...
Drugs and the Elderly: Practical Considerations
Drugs and the Elderly: Practical Considerations

... Water soluble drugs: lithium, aminoglycosides, alcohol, digoxin ...
How predictive is ocular toxicology?
How predictive is ocular toxicology?

... Take home message from Dr Chambers who is a practicing ophthalmologist “If there is any pharmacologic activity due to the drug product, there is also a risk of adverse events from it due to known or unknown pharmacologic activity” “While the events observed in non-human studies may not be duplicate ...
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS)
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS)

... freeze-dried and are able to achieve with success tissue targeting of many drugs (antibiotics, cytostatics, peptides and proteins, nucleic acids, etc.).In addition, nanoparticles were able to protect drugs against chemical and enzymatic degradation and were also able to reduce side effects of some a ...
antihistamines
antihistamines

... The future of antihistamines • The anti-inflammatory activity of second generation antihistamines, about which little is known, will continue to be researched and possibly lead to an effective alternative to corticosteriods in the treatment of allergic airways conditions. • The action of the H4 rec ...
Cytochrome P450 Drug Interactions Table
Cytochrome P450 Drug Interactions Table

... Inhibitors: drugs that prevent the enzyme from metabolizing the substrates Activators: drugs that increase the enzyme’s ability to metabolize the substrates • The table contains lists of drugs in columns under the designation of specific cytochrome P450 isoforms. A drug appears in a column if there ...
Yohimbine: Old Drug with New Interactions
Yohimbine: Old Drug with New Interactions

... increases sympathetic outflow to these neurons. A hypertensive crisis is possible. This potential interaction is based primarily on theoretical considerations, but it appears likely that it would occur. Yohimbine may also interact in patients receiving other MAOIs, such as furazolidone or methylene ...
Page 1 of 6 Bezalip 200mg Tablets - (eMC) print friendly 17/06/2016
Page 1 of 6 Bezalip 200mg Tablets - (eMC) print friendly 17/06/2016

... be informed of symptoms and monitored for signs of myopathy and increased CPK activity and combination therapy discontinued if signs of myopathy develop. Combination therapy should not be used in patients with predisposing factors for myopathy (see section 4.3 and 4.5). - Bezafibrate alters the comp ...
< 1 ... 330 331 332 333 334 335 336 337 338 ... 578 >

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.
  • studyres.com © 2026
  • DMCA
  • Privacy
  • Terms
  • Report