CURRICULUM VITAE Stacey C. Sigmon, Ph.D. February 2014
... Higgins, S.T., Sigmon, S.C., & Heil, S.H. (2011). Contingency management in the treatment of substance use disorders: Trends in the literature. In P. Ruiz & E. Strain (Eds.), Lowinson & Ruiz’s Substance Abuse: A Comprehensive Textbook, Fifth Edition. Maryland: Lippincott Williams & Wilkins, pp. 603- ...
... Higgins, S.T., Sigmon, S.C., & Heil, S.H. (2011). Contingency management in the treatment of substance use disorders: Trends in the literature. In P. Ruiz & E. Strain (Eds.), Lowinson & Ruiz’s Substance Abuse: A Comprehensive Textbook, Fifth Edition. Maryland: Lippincott Williams & Wilkins, pp. 603- ...
AIPLA Spring Meeting 2017 - REMS and Citizen Petitions (Amy
... The expected benefit of the drug with respect to such disease or condition; The expected or actual duration of treatment with the drug; The seriousness of any known or potential adverse events that may be related to the drug and the background incidence of such events in the patient population for t ...
... The expected benefit of the drug with respect to such disease or condition; The expected or actual duration of treatment with the drug; The seriousness of any known or potential adverse events that may be related to the drug and the background incidence of such events in the patient population for t ...
The final publication is available at Copyright - RiuNet
... There is little information relating to free amino acids in Stevia. Rafiq et al. [17] only identified eight of ...
... There is little information relating to free amino acids in Stevia. Rafiq et al. [17] only identified eight of ...
A Comparison of Thermodynamic Parameters for Vinorelbine
... (Lobert and Correia, 1992; Chabner et al., 1996). However, clinical doses also are based on dose-limiting side effects. The clinical toxicity of vincristine is mostly neurological, with predictable cumulative effects, whereas vinorelbine is the least neurotoxic vinca alkaloid (Chabner et al., 1996). ...
... (Lobert and Correia, 1992; Chabner et al., 1996). However, clinical doses also are based on dose-limiting side effects. The clinical toxicity of vincristine is mostly neurological, with predictable cumulative effects, whereas vinorelbine is the least neurotoxic vinca alkaloid (Chabner et al., 1996). ...
Chapter 8
... Calculations Using Mass of Reactants and Products In the laboratory we work with masses of reactants and products. However, as we have seen, chemical equations give relationships among moles of reactants and products. We therefore need a method for going back and forth between moles of substance an ...
... Calculations Using Mass of Reactants and Products In the laboratory we work with masses of reactants and products. However, as we have seen, chemical equations give relationships among moles of reactants and products. We therefore need a method for going back and forth between moles of substance an ...
Determination of Atorvastatin Pharmacokinetic
... metabolism of many drugs by known popular juices like grapefruit, orange, and pomegranate juices [10-15]. Generally, drug – food interactions and in particularly, drug – beverages interactions are the most causes of alterations of pharmacokinetics or pharmacodynamics of drugs [9], either by inducing ...
... metabolism of many drugs by known popular juices like grapefruit, orange, and pomegranate juices [10-15]. Generally, drug – food interactions and in particularly, drug – beverages interactions are the most causes of alterations of pharmacokinetics or pharmacodynamics of drugs [9], either by inducing ...
Hyperforin as a natural antidepressant: an overview
... Now a days herbal drugs are too in demand and interaction of herbal medicine with synthetic drugs are like a particular area of interest for research. St. John’s wort an herbal drug also known as hyperforin, basically hyperforin is not a drug it is isolated from the flowering tops of the perennial p ...
... Now a days herbal drugs are too in demand and interaction of herbal medicine with synthetic drugs are like a particular area of interest for research. St. John’s wort an herbal drug also known as hyperforin, basically hyperforin is not a drug it is isolated from the flowering tops of the perennial p ...
patrick_tb_ch22
... carboxylate ion interacting through ionic and hydrogen bonding interactions. Page reference: 648-649 a. Ionic binding theory b. Hydrogen bonding theory *c. Chelation binding theory d. Complexation binding theory Type: multiple choice question Title: Chapter 22 Question 15 15) The following structure ...
... carboxylate ion interacting through ionic and hydrogen bonding interactions. Page reference: 648-649 a. Ionic binding theory b. Hydrogen bonding theory *c. Chelation binding theory d. Complexation binding theory Type: multiple choice question Title: Chapter 22 Question 15 15) The following structure ...
S02 Techno2 Hard Gelatin Capsules
... D: Lubricants: reduce powder to metal adhesion, such as magnesium stearate. They exert their effect by coating the surface of other ingredients. Lubricants are usually hydrophobic materials that achieve their activity by coating the surface of pharmaceutical powders. At high levels they can reduce t ...
... D: Lubricants: reduce powder to metal adhesion, such as magnesium stearate. They exert their effect by coating the surface of other ingredients. Lubricants are usually hydrophobic materials that achieve their activity by coating the surface of pharmaceutical powders. At high levels they can reduce t ...
DRUG NAME: Octreotide SYNONYM(S): COMMON TRADE NAME(S):
... later trimesters.5 Breastfeeding: Although octreotide is likely digested when taken orally,5 breastfeeding should be avoided unless ...
... later trimesters.5 Breastfeeding: Although octreotide is likely digested when taken orally,5 breastfeeding should be avoided unless ...
Identification of the date-rape drug GHB and its precursor GBL by
... Previous analysis of GHB and GBL (Fig. 1) in a forensic context has been studied by HPLC,[7] GC-MS,[6] NMR[8] and infrared spectroscopy[8] and often involves removing the drug from the liquid matrix prior to analysis. Raman spectroscopy is a suitable method for this type of analysis as it is a non-d ...
... Previous analysis of GHB and GBL (Fig. 1) in a forensic context has been studied by HPLC,[7] GC-MS,[6] NMR[8] and infrared spectroscopy[8] and often involves removing the drug from the liquid matrix prior to analysis. Raman spectroscopy is a suitable method for this type of analysis as it is a non-d ...
Thiazide and Thiazide
... 1) The 2-position can tolerate small alkyl groups as CH3. 2) Substitutents in the 3-position determine the potency and duration of action of the thiazides. 3) Saturation of C-N bond between the 3 and 4 positions of the benzothiadiazine-1,1-dioxide nucleus increases the potency of this class of diure ...
... 1) The 2-position can tolerate small alkyl groups as CH3. 2) Substitutents in the 3-position determine the potency and duration of action of the thiazides. 3) Saturation of C-N bond between the 3 and 4 positions of the benzothiadiazine-1,1-dioxide nucleus increases the potency of this class of diure ...
biologically important isotope hybrid
... laboratory, but in the case of complicated compounds of biological importance, as, for example, biopolymers, biosynthesis is the only practical way in which they can be secured. We have shown that organisms can be grown in 99.8% 2H20 on suitably selected 'H-substrates, so that the compounds extracte ...
... laboratory, but in the case of complicated compounds of biological importance, as, for example, biopolymers, biosynthesis is the only practical way in which they can be secured. We have shown that organisms can be grown in 99.8% 2H20 on suitably selected 'H-substrates, so that the compounds extracte ...
Isotopes of Volatile Organic Compounds: An Emerging Approach for
... Although the radioactive isotopes, including 14C and 3H, are much less abundant than the stable isotopes, they can still provide useful information if enough sample is available. For example, Currie et al.15 pioneered the use of 14C to differentiate between natural and anthropogenic sources of carbo ...
... Although the radioactive isotopes, including 14C and 3H, are much less abundant than the stable isotopes, they can still provide useful information if enough sample is available. For example, Currie et al.15 pioneered the use of 14C to differentiate between natural and anthropogenic sources of carbo ...
Republic of Palau - World Health Organization
... FUNCTION IS IMPAIRED The use of drugs in patients with reduced renal function can give rise to problems for several reasons: -failure to excrete the drug or its metabolite may produce toxicity - sensitivity to some drugs is increased even if elimination is not impaired - many side effects are poorly ...
... FUNCTION IS IMPAIRED The use of drugs in patients with reduced renal function can give rise to problems for several reasons: -failure to excrete the drug or its metabolite may produce toxicity - sensitivity to some drugs is increased even if elimination is not impaired - many side effects are poorly ...
CIR Report Data Sheet - Cosmetic Ingredient Review
... including: acute and long-term biocompatibility testing for cytotoxicity, irritation or intracutaneous reactivity, sensitization, systemic toxicity, implantation effects, and hematocompatibility. The FDA found those data to be adequate and determined that alumina and was safe and effective for use i ...
... including: acute and long-term biocompatibility testing for cytotoxicity, irritation or intracutaneous reactivity, sensitization, systemic toxicity, implantation effects, and hematocompatibility. The FDA found those data to be adequate and determined that alumina and was safe and effective for use i ...
AHRN PSI Overdose Prevention Report Final
... High Risk Overdose • Cocktail (a mix) of different drugs (opiates, ATS, alcohol…) o strongly enhances the risk for an OD (some drugs like Heroin are ‘downers’, o ATS are uppers: very hard on t ...
... High Risk Overdose • Cocktail (a mix) of different drugs (opiates, ATS, alcohol…) o strongly enhances the risk for an OD (some drugs like Heroin are ‘downers’, o ATS are uppers: very hard on t ...
Dear Sir/Madam - University of Michigan College of Pharmacy
... Professional Expertise and Research Conducted remarkable research with approximately 40 manuscripts published in peer reviewed journals in areas of: (1) pharmacokinetics-pharmacodynamics (PK/PD) modeling and population pharmacokinetics (POPPK), (2) interspecies scaling and human PK projection, (3) ...
... Professional Expertise and Research Conducted remarkable research with approximately 40 manuscripts published in peer reviewed journals in areas of: (1) pharmacokinetics-pharmacodynamics (PK/PD) modeling and population pharmacokinetics (POPPK), (2) interspecies scaling and human PK projection, (3) ...
A Review on Natural Plant: Aerva lanata
... A phytochemical constituent of A. lanata is identified by qualitative phytochemical screening. The A. lanata comprises the alkaloid, flavonoids, phenol, tannin, proteins, amino acids and carbohydrates respectively. The percentage of crude chemical constituents in A. lanata estimated quantitatively. ...
... A phytochemical constituent of A. lanata is identified by qualitative phytochemical screening. The A. lanata comprises the alkaloid, flavonoids, phenol, tannin, proteins, amino acids and carbohydrates respectively. The percentage of crude chemical constituents in A. lanata estimated quantitatively. ...
09107sgp06
... Clearly, the fact heroin was legal and widely prescribed for common use such as coughs and colds, as well as a pain killer, had not led to the sort of widespread dependency those opponents of legalization fear it would do if legalized today. In fact, heroin's emergence on to the medical stage was so ...
... Clearly, the fact heroin was legal and widely prescribed for common use such as coughs and colds, as well as a pain killer, had not led to the sort of widespread dependency those opponents of legalization fear it would do if legalized today. In fact, heroin's emergence on to the medical stage was so ...
navigating the fda
... • Clinical data not supportive of indications for use – need more data •Inadequacy on how people respond to various dosages – need more data •“Approvable” – probably be approved, provided certain issues get resolved •Labeling •Safety issues •Manufacturing issues – can delay or deny application. Prod ...
... • Clinical data not supportive of indications for use – need more data •Inadequacy on how people respond to various dosages – need more data •“Approvable” – probably be approved, provided certain issues get resolved •Labeling •Safety issues •Manufacturing issues – can delay or deny application. Prod ...
Comparative Evaluation of in vitro Diclofenac Sodium
... vehicles and excipients on drug availability since physicochemical properties of vehicles strongly influence drug release topically.9 Several in vitro skin permeation studies have done to investigate the vehicle effect on various topical drug deliveries.7; 10-14 In the present study, diclofenac sodi ...
... vehicles and excipients on drug availability since physicochemical properties of vehicles strongly influence drug release topically.9 Several in vitro skin permeation studies have done to investigate the vehicle effect on various topical drug deliveries.7; 10-14 In the present study, diclofenac sodi ...
BCBSM Prior Authorization and Step Therapy Guidelines
... Off-Label / High-Cost Specialty program-Off-label means a drug is being used in a way that has not been approved by the U.S. Food and Drug Administration. Drugs with potential for off-label use and high-cost specialty drugs on this list require prior authorization for Blue Cross to cover them. ...
... Off-Label / High-Cost Specialty program-Off-label means a drug is being used in a way that has not been approved by the U.S. Food and Drug Administration. Drugs with potential for off-label use and high-cost specialty drugs on this list require prior authorization for Blue Cross to cover them. ...
Drug misuse and dependence: UK guidelines on clinical
... The working group considered NICE clinical guidelines and technology appraisals in drafting the 2007 Clinical Guidelines. The working group interpreted and incorporated the NICE suite of guidance as appropriate, but the 2007 Clinical Guidelines cover the management and treatment of drug misusers in ...
... The working group considered NICE clinical guidelines and technology appraisals in drafting the 2007 Clinical Guidelines. The working group interpreted and incorporated the NICE suite of guidance as appropriate, but the 2007 Clinical Guidelines cover the management and treatment of drug misusers in ...
Drug discovery
In the fields of medicine, biotechnology and pharmacology, drug discovery is the process by which new candidate medications are discovered. Historically, drugs were discovered through identifying the active ingredient from traditional remedies or by serendipitous discovery. Later chemical libraries of synthetic small molecules, natural products or extracts were screened in intact cells or whole organisms to identify substances that have a desirable therapeutic effect in a process known as classical pharmacology. Since sequencing of the human genome which allowed rapid cloning and synthesis of large quantities of purified proteins, it has become common practice to use high throughput screening of large compounds libraries against isolated biological targets which are hypothesized to be disease modifying in a process known as reverse pharmacology. Hits from these screens are then tested in cells and then in animals for efficacy.Modern drug discovery involves the identification of screening hits, medicinal chemistry and optimization of those hits to increase the affinity, selectivity (to reduce the potential of side effects), efficacy/potency, metabolic stability (to increase the half-life), and oral bioavailability. Once a compound that fulfills all of these requirements has been identified, it will begin the process of drug development prior to clinical trials. One or more of these steps may, but not necessarily, involve computer-aided drug design. Modern drug discovery is thus usually a capital-intensive process that involves large investments by pharmaceutical industry corporations as well as national governments (who provide grants and loan guarantees). Despite advances in technology and understanding of biological systems, drug discovery is still a lengthy, ""expensive, difficult, and inefficient process"" with low rate of new therapeutic discovery. In 2010, the research and development cost of each new molecular entity (NME) was approximately US$1.8 billion. Drug discovery is done by pharmaceutical companies, with research assistance from universities. The ""final product"" of drug discovery is a patent on the potential drug. The drug requires very expensive Phase I, II and III clinical trials, and most of them fail. Small companies have a critical role, often then selling the rights to larger companies that have the resources to run the clinical trials.Discovering drugs that may be a commercial success, or a public health success, involves a complex interaction between investors, industry, academia, patent laws, regulatory exclusivity, marketing and the need to balance secrecy with communication. Meanwhile, for disorders whose rarity means that no large commercial success or public health effect can be expected, the orphan drug funding process ensures that people who experience those disorders can have some hope of pharmacotherapeutic advances.