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Creatinine Clearance When Does It Matter?
Creatinine Clearance When Does It Matter?

...  At this time, it MAY be best to use CG in the elderly (>70 years) and with drugs with narrow therapeutic index such as new oral anticoagulants  MDRD should be “normalized” at extremes of body mass.  Not for everyone:  Amputees, low muscle mass (paraplegic), AKI, malnourished, ...
Clinically relevant drug interactions with antiepileptic drugs
Clinically relevant drug interactions with antiepileptic drugs

WHO Drug Information - World Health Organization
WHO Drug Information - World Health Organization

... entered into therapeutic use. In the 1980s, the development of biotechnology products based on recombinant techniques led to highly novel therapeutic agents, thus creating a new need for adaptation of the INN system. The present article describes the ways that the INN Programme has responded to the ...
ICH E10 - Duke People
ICH E10 - Duke People

... The decision to approve a drug is based on its having a satisfactory balance of benefits and risks within the conditions specified in the product labeling. This decision is based on the information available at the time of approval. The knowledge related to the safety profile of the product can chan ...
The Řie-Tozer Model of Drug D
The Řie-Tozer Model of Drug D

... elimination). The scheme of the 3-pool model of drug distribution is shown in Figure 1. Equation 2 has been derived by Øie and Tozer based on law of mass action and assumption that unbound drug concentrations in different body fluids are equal. According to this equation, volumes of the individual b ...
Solid Dispersion: Methods and Polymers to increase the solubility of
Solid Dispersion: Methods and Polymers to increase the solubility of

... industry combines solid solution/dispersion technology with nanotechnology. In this procedure, a liquid stream of a drug/polymer solution is subjected to a potential between 5 and 30 kV. When electrical forces prevail over the surface tension of the drug/polymer solution at the air interface, fibers ...
Protein Ligand Interactions: A Method and its Application to Drug Discovery
Protein Ligand Interactions: A Method and its Application to Drug Discovery

... • The truth is we know very little about how the major drugs we take work – receptors are unknown • We know even less about what side effects they might have - receptors are unknown • Drug discovery seems to be approached in a very consistent and conventional way • The cost of bringing a drug to mar ...
Drug Interaction and Food - KSU Faculty Member websites
Drug Interaction and Food - KSU Faculty Member websites

... of many molecular entities and often a complete characterization of all the chemical constituents from a natural product is not possible (Pal and Mitra, 2006). Additionally, chemical constituents of natural product may vary depending on the part of the plant processed (stems, leaves, roots), seasona ...
The Top 6 June specials 2015
The Top 6 June specials 2015

... hence efficacy, bioavailability and excipients. Special medicines can be very expensive (several hundred pounds for one bottle) and may not represent a cost effective treatment. A special may have a short expiry date e.g. seven days. The GMC have produced some guidance on prescribing specials http:/ ...
, 0 Memorandum
, 0 Memorandum

... FDA has carefully evaluated the information in your submission and the agency has significant concerns about the evidence on which you rely to support your conclusion that a dietary supplement containing Ganoderma lucidum mycelium will reasonably be expected to be safe. The notification states that ...
STUDIES ON FORMULATION AND EVALUATION OF OSMOTICALLY CONTROLLED DRUG Research Article
STUDIES ON FORMULATION AND EVALUATION OF OSMOTICALLY CONTROLLED DRUG Research Article

... Present investigation is to develop controlled osmotic tablet of Carbamazepine with an aim of increasing its therapeutic effectiveness for extended period of time thus reducing dose frequency and side effects. As new innovation in oral controlled plasma drug delivery it avoids fluctuation in drug co ...
Prescribing for Pregnant or Lactating Women
Prescribing for Pregnant or Lactating Women

... To best address all of these potential concerns, recommendations for drug use during pregnancy are often criteria-based using data and results from available studies. These criteria often include: - what (if any) information is known from studies conducted in humans and/or animals - if the nature of ...
REDUCING OF ERROR IN THE MEDICATION PROCESS OF A PRIVATE... NORTHEAST OF THAILAND  Original Article
REDUCING OF ERROR IN THE MEDICATION PROCESS OF A PRIVATE... NORTHEAST OF THAILAND Original Article

... the same place or near each other, make confusion occur. The Pharmacy Department modified drug shelf and rearrange drugs alphabetically with tall man letter especially for LASA drug [9]. In addition, the pink reflect sticker was used for identified and is of concern for both pharmacists and pharmaci ...
safety reporting requirements for clinical drug trials
safety reporting requirements for clinical drug trials

... the Clinical Trials Branch. Therefore, special medical or administrative criteria are needed to define reactions that, either due to their nature (“serious”) or due to significant, unexpected information they provide, justify expedited reporting. To ensure no confusion or misunderstanding of the dif ...
Generics and public health - WHO archives
Generics and public health - WHO archives

... Pharmaceutical equivalents: Products that contain the same amount of the same active substance(s) in the same dosage form; meet the same or comparable standards; are intended to be administered by the same route. Pharmaceutical equivalence does not necessarily imply therapeutic equivalence as differ ...
Document
Document

... 10. A 45-year s-old man with dislocation of shoulder joint was admitted to the hospital. What drug can be used to relax skeletal muscles and set the bone? A. *Dithylinum (suxamethonium) B. Dimedrolum (diphenhydramine) C. Analginum (methamizole) D. Promedolum (trimeperidine) E. Acetylsalicylic acid 1 ...
Research Article DEVELOPMENT AND CHARACTERIZATION OF COMPRESSED ODT FORMULATION OF  INSOLUBLE LOW BITTER DRUG 
Research Article DEVELOPMENT AND CHARACTERIZATION OF COMPRESSED ODT FORMULATION OF  INSOLUBLE LOW BITTER DRUG 

... rapidly, usually  within a  matter of seconds, when  placed  under  the  tongue.  ODT  delayed  release  is  a  solid  dosage  form  containing  medicinal  substances  which  disintegrates  rapidly,  usually  within  matter of seconds, when place upon the tongue, but which releases a  drug (or drugs ...
DEVELOPMENT OF NIR METHOD FOR DETERMINATION OF RHEOLOGICAL BEHAVIOR AND
DEVELOPMENT OF NIR METHOD FOR DETERMINATION OF RHEOLOGICAL BEHAVIOR AND

... Transmittance measures the decrease in radiation intensity as function of wave length when radiation is passed through the sample. Conversely, reflectance measures the ratio of the intensity of light reflected from the sample [5]. There are many studies [6, 7, 8, 9, 10] that demonstrate the efficacy ...
PHYSICOCHEMICAL CHARACTERIZATION OF SPRAY DRIED FORMULATION CONTAINING AMORPHOUS DRUG Research Article
PHYSICOCHEMICAL CHARACTERIZATION OF SPRAY DRIED FORMULATION CONTAINING AMORPHOUS DRUG Research Article

... uniform in size with fewer sharp edges than those produced by conventional granulation methods6, 7, 8, 9. There are many articles in the literature related to spray drying10, 11, 12, 13. However the effect of spray drying on the solid state and phase transformation of the drug is not completely expl ...
DEPARTMENT OF  HEALTH  AND  HUMAN  SERVICES
DEPARTMENT OF HEALTH AND HUMAN SERVICES

... remains unclear whether L-Arginine alpha-ketoglutarate (2: 1) is a dietary ingredient that may lawfully be marketed as a dietary supplement. Nevertheless, FDA has carefully evaluated the information in your submission and the agency has significant concerns about the evidence upon which you rely to ...
Pelagia Research Library Hydroxypropyl methylcellulose
Pelagia Research Library Hydroxypropyl methylcellulose

... retention, and as a binder. HPMC imparts little or no flavor to food. The historical record in the literature is not entirely clear on when HPMC was first introduced into food or any other commercial use. However, references point to a US patent on its preparation having been issued in 1960 to the D ...
Classification of research and development activities
Classification of research and development activities

Beware: Clinically Significant Drug Interactions in the Treatment of HIV
Beware: Clinically Significant Drug Interactions in the Treatment of HIV

... interactions with non-nucleoside reverse transcriptase inhibitors (NNRTIs), protease inhibitors (PIs), and integrase strand transfer inhibitors (INSTIs). Evaluate the consequences of drug interactions associated with antiretroviral drugs and determine the incidence of clinical adverse effects from i ...
Click here B. Pharmacy Syllabus
Click here B. Pharmacy Syllabus

... Note: Examiner to set eight questions and the candidates are required to attempt any five. 1. Introduction: Definition, history, scope and development of Pharmacognosy. (2) 2. Sources of drugs: Biological, marine, geographical and plant tissue cultures. (4) 3. Classification of drugs: Alphabetical, ...
Hormone Products and Prescription
Hormone Products and Prescription

... precautions for use and information for patients, an expiration date, an identifying lot or control number, and information about the quantity of the container (21 CFR 201.1, 201.10, 201.17, 201.18, 201.50, ...
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Compounding

Pharmaceutical compounding (done in compounding pharmacies) is the creation of a particular pharmaceutical product to fit the unique need of a patient. To do this, compounding pharmacists combine or process appropriate ingredients using various tools. This may be done for medically necessary reasons, such as to change the form of the medication from a solid pill to a liquid, to avoid a non-essential ingredient that the patient is allergic to, or to obtain the exact dose(s) needed or deemed best of particular active pharmaceutical ingredient(s). It may also be done for more optional reasons, such as adding flavors to a medication or otherwise altering taste or texture. Compounding is most routine in the case of intravenous/parenteral medication, typically by hospital pharmacists, but is also offered by privately owned compounding pharmacies and certain retail pharmacies for various forms of medication. Whether routine or rare, intravenous or oral, etc., when a given drug product is made or modified to have characteristics that are specifically prescribed for an individual patient, it is known as ""traditional"" compounding.Due to the rising cost of compounding and the shortage of drugs, many hospitals have shown a tendency to rely more upon large-scale compounding pharmacies to meet their regular requirement, particularly of sterile-injectable medications. When compounding is done on bulk production of a given formulation rather than patient-specific production, it is known as ""non-traditional"" compounding (which, as discussed below, is arguably not ""compounding"" but rather ""manufacturing""). This development raises concerns about patient safety and makes a case for proper regulatory control and monitoring.
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