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presentation ( format)
presentation ( format)

...  As with other antidepressants, risk of suicide increased and highest age < 18 Khan A, et al. J Clin Psychiatry 2011;72:441-47. Rickels K, et al. J Clin Psychiatry 2009;70:326-33. ...
pharmacology 2008 - addiction education home
pharmacology 2008 - addiction education home

... Background: The abuse and diversion of pharmacological agents with CNS mechanisms of action is an important concern from governmental, regulatory, public health and safety perspectives. In recent years, there have been an increased number of reports concerning the abuse and diversion of quetiapine i ...
Formulation
Formulation

... GIT or unnecessary systemic absorption. The colon is attracting interest as a site where poorly absorbed drug molecule may have an improved bioavailability. The region of colon is recognized as having a somewhat less hostile environment with less diversity and intensity of activity than the stomach ...
Bulletin #86
Bulletin #86

... (d) Patients must discontinue all drugs with anticholinergic activity at least 14 days before the MMSE and FAQ are administered. Drugs with anticholinergic activity are not to be used concurrently with rivastigmine therapy. List all current medications patient was taking at the time of assessment. ( ...
3: Respiratory system - Gateshead Health NHS Foundation Trust
3: Respiratory system - Gateshead Health NHS Foundation Trust

... Theophylline has a narrow margin between therapeutic and toxic effects; therapy should be monitored. ...
Slide 1
Slide 1

... below the level of the arrangement between a Plan Sponsor and a first tier entity. These written arrangements continue down to the level of the ultimate provider of both health and administrative services. Examples include pharmacies, marketing firms, quality assurance companies, claims processing f ...
ESSENTIAL MEDICINES and COUNTERFEIT MEDICINES
ESSENTIAL MEDICINES and COUNTERFEIT MEDICINES

... manufacturing process by a known manufacturer, SFFC medicines are  made by people with the intent to mislead. • The  extreme  difficulty  in  tracing  the  manufacturing  and  distribution  channels  of  SFFC  medicines  makes  their  circulation  on  markets  difficult to stop.  • Even  a  single  ...
NuLev Tablet Prescribing Information
NuLev Tablet Prescribing Information

... NuLev® is effective as adjunctive therapy in the treatment of peptic ulcer. It can also be used to control gastric secretion, visceral spasm and hypermotility in spastic colitis, spastic bladder, cystitis, pylorospasm, and associated abdominal cramps. May be used in functional intestinal disorders t ...
Metabolic Fate of Pharmaceuticals: A Focus on Slow Metabolizers
Metabolic Fate of Pharmaceuticals: A Focus on Slow Metabolizers

... Inter–Individual Variability in Drug Response When prescribing therapy, it is important for physicians to recognize that each individual is genetically unique. Variability in drug efficacy may be up to 100-fold among individuals within the general population.1 Inter-individual variability is also ob ...
Short Note on Receptors
Short Note on Receptors

... In 1901 Langley challenged the dominant hypothesis that drugs act at nerve endings by demonstrating that nicotine acted at sympathetic ganglia even after the degeneration of the severed preganglionic nerve endings.[1] In 1905 he introduced the concept of a receptive substance on the surface of skele ...
$doc.title

... the  fact  that  other  potentially  harmful   drugs  (including  synthetic  cathinones,   the  psychoactive  ingredients  in  “bath   salts”)  are  sometimes  sold  as  ecstasy.   These  drugs  can  be  neurotoxic  or  pose   other  unpredic ...
Herb-drug interactions - Weatherford High School
Herb-drug interactions - Weatherford High School

... Asian ginseng (Panax ginseng) – ginsenosides may inhibit platelet aggregation (anticoagulant). RCTs in in healthy volunteers & cardiac patients showed no effect of Asian ginseng on INR, platelet aggregation. Monitor closely. American ginseng (Panax quinquefolius) – RCT in healthy ...
PREPARATION AND EVALUATION OF FLUOXEITINE HYDROCHLORIDE ORAL DISPERSIBLE TABLETS Research Article
PREPARATION AND EVALUATION OF FLUOXEITINE HYDROCHLORIDE ORAL DISPERSIBLE TABLETS Research Article

... The tablets were formulated employing direct compression method using 8mm flat-faced punches. It is the process by which tablets are compressed directly from mixtures of the drug and excipients without preliminary treatment such as granulation. Preparation of fluoxeitine hydrochloride oro dispersibl ...
EVALUATION OF REPAGLINIDE ENCAPSULATED NANOPARTICLES PREPARED BY SONICATION METHOD  Research Article
EVALUATION OF REPAGLINIDE ENCAPSULATED NANOPARTICLES PREPARED BY SONICATION METHOD Research Article

... The formulation was optimized for further studies, on the basis of particle size and high encapsulation efficiency. Ethyl acetate was used as an organic solvent because both drug and polymer are soluble in it. Due to the high solubility of solvent in water it diffused faster in external phase and pr ...
PowerPoint Presentation - Lecture 7
PowerPoint Presentation - Lecture 7

... • SE & adverse reactions of Penicillins 1. Hypersensitivity - mild or severe Mild = rash, pruritus, & hives - Rx w/ antihistamines Severe = anaphylactic shock - occurs w/ in 20 min. - Rx w/ epinephrine ...
Design and statistical optimization of circadian rhythm
Design and statistical optimization of circadian rhythm

... effect. HPMC K100M was selected for its swelling behaviour. These two polymers were individually tested for their influence over t10% and t90%. S1 did not show any significant lag time and revealed rupturable/erodible polymer alone cannot provide desired pulsatile release pattern. So Formulations S2 ...
Disparate practical way of doing solubility enhancement study to
Disparate practical way of doing solubility enhancement study to

... Bioavailability is the rate and extent to which the active ingredient or active moiety is absorbed from a drug product and becomes available at the site of action. Traditionally, nearly 40% of the new chemical entities (NCEs) identified by pharmaceutical industry screening programs have failed to be ...
Janus-Opioid-Conference-Summit-Keynote
Janus-Opioid-Conference-Summit-Keynote

... force to represent to health care providers that OxyContin did not cause euphoria and was less addictive than immediaterelease opiates; and allowed health care providers to entertain the erroneous belief that OxyContin was less addictive than ...
Quantitative Structure-Activity Relationship Modeling to Predict Drug-Drug Interactions
Quantitative Structure-Activity Relationship Modeling to Predict Drug-Drug Interactions

... United States, bringing a single drug to market typically takes 10-15 years, and its cost can range from $800 million to $1 billion. For every one drug approved, there have been up to 10,000 drugs rejected and even after a drug has made it to market, there is still a potential for it to be removed [ ...
New Goals and New Drugs for People With Heavy Anti-HIV
New Goals and New Drugs for People With Heavy Anti-HIV

... For example, if you have HIV resistant to nucleosides, nonnucleosides, and protease inhibitors, a combination including a CCR5 inhibitor and an integrase inhibitor would have a very good chance of stopping that multidrug-resistant HIV. ...
GPhA Overview and Assessment: Food and Drug Administration`s
GPhA Overview and Assessment: Food and Drug Administration`s

... requirements for generic drug manufacturers continue to be in effect and were not changed by Mensing. Second, GPhA believes it is not the regulatory obligations that lead most of our members to “conduct robust postmarketing surveillance, evaluation, and reporting, and to ensure that the labeling fo ...
RSPT 1410 Common Respiratory Drugs
RSPT 1410 Common Respiratory Drugs

... terbutaline, albuterol, bitolterol, pirbuterol, levalbuterol ...
9th International Workshop on Clinical
9th International Workshop on Clinical

... average concentration was found to significantly affect the half-life describing the decline in mycobacterial load. The estimated EC50 was 1.42 µg/mL (95%CI 1.02-1.99) which is higher than the typical observed average concentration in the continuation phase, but falls within the observed range of ex ...
EXTENDED RELEASE ROPINIROLE TABLET FORMULATION PREPARED BY MELT GRANULATION TECHNIQUE  Research Article
EXTENDED RELEASE ROPINIROLE TABLET FORMULATION PREPARED BY MELT GRANULATION TECHNIQUE Research Article

... The present work was aimed to develop an extended release matrix tablet formulation of Ropinirole hydrochloride (ROH) using polymers like polyox WSR 301, carbopol 71G, kollicoat SR 30 D and waxes like cetyl alcohol (CA), carnauba wax (CW), glyceryl monostearate (GMS). Wet granulation, direct compres ...
The mechanism of action of aspirin
The mechanism of action of aspirin

... different from that of the anti-inflammatory steroids, and their analgesic action was of a different nature than that produced by opiates. Aspirin-like drugs are weak analgesics compared with ‘‘strong’’ narcotic analgesics like morphine. They are effective in clinical pain of low or moderate but not ...
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