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Average, population and individual bioequivalence
Average, population and individual bioequivalence

... individuals and formulations and intra-subject variance are not considered either.7,11,15 Consequently, ABE criterion cannot fully answer all questions related to interchangeability – whether related to a new patient (prescribability) or to a patient in treatment (switchability) – for low therapeuti ...
sohn-presentation-on-opioids
sohn-presentation-on-opioids

How FDA Approves Drugs and Regulates Their Safety and
How FDA Approves Drugs and Regulates Their Safety and

... effectiveness, address product integrity, labeling, reporting of research and adverse events, surveillance, drug studies, risk management, information dissemination, off-label use, and directto-consumer advertising, all topics in which Congress has traditionally been interested. FDA seeks to ensure ...
FAQ in Word format - Help for Headaches
FAQ in Word format - Help for Headaches

Enabling Pharmacists To Respond To The Health Needs Of
Enabling Pharmacists To Respond To The Health Needs Of

... established place regularly registered by the State Board of Pharmacy, in which prescriptions, drugs, medicines, chemicals and poisons 1. are compounded, dispensed, vended or sold at retail. (b) The term "pharmacist" shall mean a natural person licensed by the State Board of Pharmacy to prepare, com ...
Is there an interaction between erythromycin and statins?
Is there an interaction between erythromycin and statins?

... the patient had experienced a delayed interaction between a past completed four week course of erythromycin and simvastatin. The patient made a full recovery [20]. A man aged 83-years who was receiving stable therapy with simvastatin 80mg per day was hospitalized with rhabdomyolysis for 1 to 2 weeks ...
Prescriptions Pain Medications FAQs
Prescriptions Pain Medications FAQs

ALFENTANIL 500 MICROGRAMS / ML SOLUTION FOR INJECTION
ALFENTANIL 500 MICROGRAMS / ML SOLUTION FOR INJECTION

... use before and during anaesthesia. It is indicated for use in short procedures and outpatient surgery; and procedures of medium and long duration when given as a bolus followed by supplemental doses, or by continuous infusion. At very high doses, Alfentanil 500 micrograms/ml Solution for Injection m ...
This Item - Mid Essex Hospital Services NHS Trust
This Item - Mid Essex Hospital Services NHS Trust

... Heybridge or Rayne ...
Enhancement of Taste Masking by A newly
Enhancement of Taste Masking by A newly

... important factor in ensuring the likelihood that the recipients will intake the pharmaceuticals. A constant problem in treatment of patients is their inability or unwillingness to swallow solid dosage forms such as tablets especially in children and the elderly. These types of dosage forms permit pe ...
FORMULATION OF RAPID MOUTH DISSOLVING TABLETS OF CETIRIZINE di HCL USING  SUBLIMATION METHOD  Research Article   
FORMULATION OF RAPID MOUTH DISSOLVING TABLETS OF CETIRIZINE di HCL USING  SUBLIMATION METHOD  Research Article   

... Patient compliance is a prerequisite for the success of any drug delivery system which culminated into the design of mouth dissolving drug delivery  system beside older NDDS. Cetirizine dihydrochloride is a non‐sedative antihistamine with potent antiallergic action. The purpose of this study was  to ...
Dissolution Stability of Cephalexin Extemporaneous Suspensions
Dissolution Stability of Cephalexin Extemporaneous Suspensions

... tested tablets, but only the CE peak area was quantified. Chemical stability of CE in the stressed formulations was examined against a CE reference standard, which was run simultaneously each time samples were evaluated. The CE concentration measured in the assay of each formulation remained within ...
DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION
DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION

... condition and % Assay was calculated for each condition (Table 6). ...
an-update-of-taste-m.. - Scholars Research Library
an-update-of-taste-m.. - Scholars Research Library

... saliva so the drug concentration in saliva will remain below taste threshold value. The desire for improved palatability of formulations has prompted the development of various new technologies for taste abatement. Many of these technologies have been successfully commercialized. But, the ideal solu ...
A SURVEY BASED STUDY IN CURRENT SCENARIO OF GENERIC AND... Research Article
A SURVEY BASED STUDY IN CURRENT SCENARIO OF GENERIC AND... Research Article

... medicines allow more patients to be treated with the same amount of money and mobilizes fund to finance other treatment modalities [5]. While manufacturing generic drugs, the drug companies use the same active ingredients and are shown to work the same way in the body, they have the same risks and b ...
VOLTAMMETRIC BEHAVIOR OF GEFITINIB AND ITS ADSORPTIVE STRIPPING  VOLTAMMETRIC DETERMINATION IN PHARMACEUTICAL FORMULATIONS AND URINE 
VOLTAMMETRIC BEHAVIOR OF GEFITINIB AND ITS ADSORPTIVE STRIPPING  VOLTAMMETRIC DETERMINATION IN PHARMACEUTICAL FORMULATIONS AND URINE 

... colored  powder. Gefitinib is  a  free  base. Gefitinib  can be  defined  as  sparingly soluble at pH 1.0, but is practically insoluble above pH 7.0,  with the solubility dropping sharply between pH 4.0 and pH 6.0. In  non‐aqueous solvents, gefitinib is freely soluble in glacial acetic acid  and  di ...
sustained and controlled drug delivery system - as a part
sustained and controlled drug delivery system - as a part

Antihistamines - Take Control of your Health
Antihistamines - Take Control of your Health

HerbalDrugs_Thailand
HerbalDrugs_Thailand

... Section 3 Background and Justification a. Brief description of the situation before the innovative experience Since 1980, the office of Primary Health Care System, Ministry of Public Health, had proposed herbal drugs as Essential Drugs which could be used as one of the strategies to achieve “Health ...
Ping Zhao CV
Ping Zhao CV

... clinical pharmacokinetic (PK) and pharmacodynamic (PD) studies using clinical pharmacology principles and standard (e.g., compartmental and population PK/PD) as well as contemporary (e.g., populationbased PBPK) modeling tools o Authored/co-authored PBPK reviews (Examples available online for drugs l ...
National Conference on Nanoscience and Nanotechnology (NCNN
National Conference on Nanoscience and Nanotechnology (NCNN

... other existing compounds. Fullerene is a carbon allotrope like diamond and graphite. All the electrons in fullerene are delocalized and spread over the whole molecule periphery as clouds. These electrons demonstrate antioxidative potency when they react with free radicals and active oxygen. Its use ...
Zyprexa/Zyprexa Zydis (olanzapine)
Zyprexa/Zyprexa Zydis (olanzapine)

... the medication develops, these side effects usually subside. Taking Zyprexa in a single bedtime dose may minimize daytime sedation. For dry mouth, chewing sugarless gum or sucking on sugarless candy may promote salivation. To prevent constipation, patients should increase fluid intake and dietary fi ...
SIMULTANEOUS DETERMINATION OF CLOPIDOGREL AND
SIMULTANEOUS DETERMINATION OF CLOPIDOGREL AND

... selectivity. Initially methanol: water in the ratio of (80: 20) was tried but both the peaks merged. Later methanol: water: Acetonitrile in the ratio of (80: 10:10) was tried and it was found that both the peaks were well separated with acceptable resolution. Hence methanol: water: Acetonitrile in t ...
Pharmacy - Beirut Arab University
Pharmacy - Beirut Arab University

IND, NDA, ANDA, CONCEPT OF PARA I TO IV,
IND, NDA, ANDA, CONCEPT OF PARA I TO IV,

... EXCLUSIVITY:CONTENT, FORMAT & APPLICATION NEW DRUG APPLICATION (N. D. A.) Introduction: The New Drug Application (NDA) is the vehicle in the United States through which drug sponsors formally propose that the FDA approve a new pharmaceutical for sale and marketing. The goals of the NDA are to provid ...
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Pharmaceutical marketing

Pharmaceutical marketing, sometimes called medico-marketing or pharma marketing in some countries, is the business of advertising or otherwise promoting the sale of pharmaceuticals or drugs.Many countries have measures in place to limit advertising by pharmaceutical companies.Pharmaceutical company spending on marketing far exceeds that of its research budget. In Canada, $1.7 billion was spent in 2004 to market drugs to physicians; in the United States, $21 billion was spent in 2002. In 2005, money spent on pharmaceutical marketing in the United States was estimated at $29.9 billion with one estimate as high as $57 billion. When the U.S. numbers are broken down, 56% was free samples, 25% was pharmaceutical sales representative ""detailing"" (promoting drugs directly to) physicians, 12.5% was direct to user advertising, 4% on detailing to hospitals, and 2% on journal ads. There is some evidence that marketing practices can negatively affect both patients and the health care profession.
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