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Marine Origin Polysaccharides in Drug Delivery Systems
Marine Origin Polysaccharides in Drug Delivery Systems

... For example, alginate extracted from Laminaria digitata and Ascophyllum nodosum have been shown to have M/G ratios of 1.16 and 1.82, respectively [30]. Alginate is biocompatible, has low toxicity and high bioavailability as well. These are the main advantages that make alginate one of the biopolymer ...
An overview of interactions between grapefruit juice and drugs ReView Abstract
An overview of interactions between grapefruit juice and drugs ReView Abstract

... reduce the formation of artherosclerotic plaques.3,4 It may also inhibit cancer cell proliferation.5,6 As many as 15 years ago, investigators found that grapefruit juice can markedly augment oral drug bioavailability. This was an unexpected observation from an interaction study between the dihydropy ...
PART II - United Nations Office on Drugs and Crime
PART II - United Nations Office on Drugs and Crime

... have caused serious disease or other problems (WHO). A “brief intervention” is a structured therapy of short duration aimed at assisting an individual to cease or reduce the use of a psychoactive substance or to deal with other life issues (WHO). “Coverage” describes the extent to which an intervent ...
PART II
PART II

... have caused serious disease or other problems (WHO). A “brief intervention” is a structured therapy of short duration aimed at assisting an individual to cease or reduce the use of a psychoactive substance or to deal with other life issues (WHO). “Coverage” describes the extent to which an intervent ...
Prescription medicine use by one million Canadian children
Prescription medicine use by one million Canadian children

... have included drug analysis using very small sample volumes, pharmacokinetic techniques such as sparse sampling, development of surrogate markers and use of novel clinical trial designs including ‘n of one’ studies and clinical trials simulations in silico. These have provided investigators with the ...
If your drug is not “on the list” just give us a call for a price. Ask us for
If your drug is not “on the list” just give us a call for a price. Ask us for

... $37/6 months • $70/1 year Simvastatin (generic Zocor®) • Clopidogrel (generic Plavix®) Alendronate (generic Fosamax®) • Pantoprazole (generic Protonix®) Omeprazole (generic Prilosec®) • Citalopram (generic Celexa®) Losartan and Losartan/HCTZ (generic Cozaar and Hyzar®) Escitalopram (generic Lexapro® ...
How Criminal Law Affects Health Care and Religious Freedom
How Criminal Law Affects Health Care and Religious Freedom

... because of the affordability, consistency, low profile and access afforded to it by its legal status, it turns out that recreational users report that they will still buy legal highs even when their legal status changes (McElrath & Van Hout, 2011, 498). Since recreational Salvia smokers tend to be c ...
The PBAC agenda primarily consists of applications relating
The PBAC agenda primarily consists of applications relating

... circumstances, consumers will be able to comment on items in other sections of the agenda. The submissions for which input is sought will be listed in alphabetical order by drug name. There is no provision for consumer comments to the PBAC on agenda item 8 which relates to pricing matters. Pharmaceu ...
March 2016 PBAC Meeting Agenda
March 2016 PBAC Meeting Agenda

... circumstances, consumers will be able to comment on items in other sections of the agenda. The submissions for which input is sought will be listed in alphabetical order by drug name. There is no provision for consumer comments to the PBAC on agenda item 8 which relates to pricing matters. Pharmaceu ...
Amphetamine-Type Stimulants: A Global Review, 1996
Amphetamine-Type Stimulants: A Global Review, 1996

... the easy access to a variety of potential starting materials. While it is clear that there is sufficient basis to justify an international review, the utility of such a review will depend on resolving a number of fundamental questions at the outset. What are the magnitudes, in absolute and relative ...
the preparation and administration of blincyto ® brochure
the preparation and administration of blincyto ® brochure

... disorders, disturbances in consciousness, confusion and disorientation, and coordination and balance disorders. The median time to onset of any neurological toxicity was 7 days. Monitor patients for signs or symptoms and interrupt or discontinue BLINCYTO® as outlined in the PI. • Infections: Approx ...
The Socio-Economic Impact of Amphetamine Type Stimulants in
The Socio-Economic Impact of Amphetamine Type Stimulants in

... Arrestees reported that the use of these drug types was a factor in their criminal offending and increased their likelihood of becoming angry. About a quarter of the arrestees who recently used amphetamines considered their use of these drugs to have played a major part in the activities they were s ...
Salvia divinorum use and phenomenology: results from an online
Salvia divinorum use and phenomenology: results from an online

... investigations of S. divinorum and other hallucinogens, this study surveyed 154 recent users and questioned them on their use behaviours, consequences of use and other attitudinal measures. Although reporting an extensive substance use history, and considering the limitations of online surveys, ther ...
Veterinary Anesthetic and Analgesic Formulary
Veterinary Anesthetic and Analgesic Formulary

... by the drugs used, strain, age, sex, body weight, procedure performed and the amount of stimulus  during the procedure. As a result, any published duration of action would be a generalization. For  assistance in judging duration of action, consultation with a veterinarian is ideal when developing an ...
Review of cough and cold medicines in children
Review of cough and cold medicines in children

... Cough and cold medicines in children are used for acute or recurrent cough, usually without a definite diagnosis, and for cough and other symptoms believed by a parent to be due to the common cold. The brief discussion to follow refers to causes of these symptoms and to symptom patterns associated w ...
Read Document - MotherToBaby
Read Document - MotherToBaby

... become pregnant during oral retinoid treatment. • Link between use in pregnancy and serious birth defects: Isotretinoin is a potent teratogen. • The FDA should diligently monitor effectiveness of the new mandatory risk management plan and report findings of pregnancy exposures or system failures in ...
PHARMACEUTICAL BENEFITS ADVISORY COMMITTEE (PBAC
PHARMACEUTICAL BENEFITS ADVISORY COMMITTEE (PBAC

... circumstances, consumers will be able to comment on items in other sections of the agenda. The submissions for which input is sought will be listed in alphabetical order by drug name. There is no provision for consumer comments to the PBAC on agenda item 8 which relates to pricing matters. Pharmaceu ...
November 2016 PBAC Meeting Agenda
November 2016 PBAC Meeting Agenda

... circumstances, consumers will be able to comment on items in other sections of the agenda. The submissions for which input is sought will be listed in alphabetical order by drug name. There is no provision for consumer comments to the PBAC on agenda item 8 which relates to pricing matters. Pharmaceu ...
pharmaceutical informations on the web
pharmaceutical informations on the web

... Number, active ingredient, ATC code, dosage form • Price Info: Factory / Wholesaler / Public • Prescription / Reimbursement Information • Calculated Info: Daily Therapy Price (NTK), WHO DDD PHARMACEUTICAL INFORMATIONS ON THE WEB ...
MAXIDOL® Liquid Gels
MAXIDOL® Liquid Gels

... capsule every 12 hours. Do not take more than 2 capsules in a 24 hour period. Drink a full glass of water with each dose. Under 12 years: Children under 12 should not take this drug. The safety in pediatric use has not been established. OVERDOSAGE Significant overdose can be characterized by drowsin ...
opioid codrugs for pain management - UKnowledge
opioid codrugs for pain management - UKnowledge

... were studied in aqueous solutions from pH 1.3-7.4, in simulated gastrointestinal fluids, in rat plasma and in brain homogenate. Only the ester-linked codrugs showed sign of hydrolysis in different solutions. Carbamate-linked codrugs didn’t cleave under any hydrolytic condition. Pharmacokinetic study ...
The Medical History of Psychedelic Drugs
The Medical History of Psychedelic Drugs

... 2.1 INTRODUCTION............................................................................................................................................ 4 ...
focusing in on adderall - Institute for Food Laws and Regulations
focusing in on adderall - Institute for Food Laws and Regulations

... When the United States Congress passed the Controlled Substance Act in 1970, amphetamines were listed as Schedule II drugs, meaning that they have a high potential for abuse, and that such abuse leads to severe psychological or physical dependence.1 Cocaine, opium, and morphine are examples of drugs ...
Preview the material
Preview the material

... component, which includes building relationships with patients in order to glean important information from patients and to serve as educators for both the patient and the patient’s family. Nurses must relate patient information to safety measures of avoiding drug-drug and drug-food interactions, al ...
M P D U
M P D U

... Medicare Part B Payments for Prescription Drugs CMS contracts with private companies (i.e., contractors) to process and pay Medicare Part B claims, including those for prescription drugs. 3 To obtain payment for covered outpatient prescription drugs, health care providers submit claims to their Medi ...
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Orphan drug

An orphan drug is a pharmaceutical agent that has been developed specifically to treat a rare medical condition, the condition itself being referred to as an orphan disease.In the US and EU it is easier to gain marketing approval for an orphan drug, and there may be other financial incentives, such as extended exclusivity periods, all intended to encourage the development of drugs which might otherwise lack a sufficient profit motive. The assignment of orphan status to a disease and to any drugs developed to treat it is a matter of public policy in many countries, and has resulted in medical breakthroughs that may not have otherwise been achieved due to the economics of drug research and development.According to Thomson Reuters in their 2012 publication ""The Economic Power of Orphan Drugs"", there has been increased investing in orphan drug Research and Development partly due to the U. S. Orphan Drug Act (ODA) 1983 and similar Acts in other regions of the world and also driven by ""high-profile philanthropic funding."" The period between 2001 to 2011 was the ""most productive period in the history of orphan drug development, in terms of average annual orphan drug designations and orphan drug approvals."" For the same decade the compound annual growth rate (CAGR) of the orphan drugs was an ""impressive 25.8 percent, compared to only 20.1 percent for a matched control group of non-orphan drugs."" By 2012 the market for orphan drugs was worth USD$637 million compared to the USD$638 million matched control group of non-orphan drugs, Thomson Reuters.By 2012, ""the revenue-generating potential of orphan drugs [was] as great as for non-orphan drugs, even though patient populations for rare diseases are significantly smaller. Moreover, we suggest that orphan drugs have greater profitability when considered in the full context of developmental drivers including government financial incentives, smaller clinical trial sizes, shorter clinical trial times and higher rates of regulatory success.""
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