How to Use the Drug Store to Treat Coughs and Colds By: Raymond
... Aspirin is an analgesic as well as an antipyretic. It may cause gastrointestinal upset and has been linked to ulcers. One advantage is that it is not expensive. It is not recommended in those who are under 18 especially in those with the flu, chickenpox or another viral illness as there is a risk of ...
... Aspirin is an analgesic as well as an antipyretic. It may cause gastrointestinal upset and has been linked to ulcers. One advantage is that it is not expensive. It is not recommended in those who are under 18 especially in those with the flu, chickenpox or another viral illness as there is a risk of ...
The Drug Store - NurseCe4Less.com
... Aspirin is an analgesic as well as an antipyretic. It may cause gastrointestinal upset and has been linked to ulcers. One advantage is that it is not expensive. It is not recommended in those who are under 18 especially in those with the flu, chickenpox or another viral illness as there is a risk of ...
... Aspirin is an analgesic as well as an antipyretic. It may cause gastrointestinal upset and has been linked to ulcers. One advantage is that it is not expensive. It is not recommended in those who are under 18 especially in those with the flu, chickenpox or another viral illness as there is a risk of ...
Site-specific conjugation of a cytotoxic drug to an antibody improves
... fractions for in vivo efficacy, tolerability in mice and pharmacokinetics8. The most heavily conjugated species had the lowest maximum tolerated IgG dose and most rapid clearance but did not confer a proportional increase in efficacy. This suggests that it would be desirable to selectively generate ...
... fractions for in vivo efficacy, tolerability in mice and pharmacokinetics8. The most heavily conjugated species had the lowest maximum tolerated IgG dose and most rapid clearance but did not confer a proportional increase in efficacy. This suggests that it would be desirable to selectively generate ...
A Rapid Differentiation of Pseudoephedrine and Ephedrine by
... and dissolved with 1M H2SO4. Some binder remains visible in the solution. An equal volume 1chlorobutane is added to the tube. The mixture is centrifuged and vortexed for five minutes. The top (1-chlorobutane) layer is taken off with a Pasteur filter pipette and discarded. The solution is made basic ...
... and dissolved with 1M H2SO4. Some binder remains visible in the solution. An equal volume 1chlorobutane is added to the tube. The mixture is centrifuged and vortexed for five minutes. The top (1-chlorobutane) layer is taken off with a Pasteur filter pipette and discarded. The solution is made basic ...
Side Effects of Ritalin
... was caught by his father taking an extra 10 mg tablet of Ritalin before playing in a Pop Warner football game. He said it made him feel "sharper," though his father felt he was "acting strange." In a culture where professional athletes still attempt to use performanceenhancing drugs despite stiff pe ...
... was caught by his father taking an extra 10 mg tablet of Ritalin before playing in a Pop Warner football game. He said it made him feel "sharper," though his father felt he was "acting strange." In a culture where professional athletes still attempt to use performanceenhancing drugs despite stiff pe ...
Chapter 4
... Water molecules attract each other equally in all directions. Water molecules on the surface, however, can only be pulled into the bulk water by water molecules underneath, since there are no water molecules to pull in the opposite direction. The surface tension of water is strong enough to support ...
... Water molecules attract each other equally in all directions. Water molecules on the surface, however, can only be pulled into the bulk water by water molecules underneath, since there are no water molecules to pull in the opposite direction. The surface tension of water is strong enough to support ...
Drug-Induced Hepatotoxicity: A Review
... Hepatotoxicity implies chemical-driven liver damage. Certain medicinal agents, when taken in overdoses and sometimes even when introduced within therapeutic ranges, may injure the organ. Other chemical agents, such as those used in laboratories and industries, natural chemicals (e.g., microcystins) ...
... Hepatotoxicity implies chemical-driven liver damage. Certain medicinal agents, when taken in overdoses and sometimes even when introduced within therapeutic ranges, may injure the organ. Other chemical agents, such as those used in laboratories and industries, natural chemicals (e.g., microcystins) ...
Multiple-Drug Toxicity Caused by the Coadministration of 4
... acute overdose potential, long-term effects, or allergic reactions. Structural similarities with methcathinone and user reported experiences would suggest that mephedrone shares many of the same euphoric and stimulant effects. Recently, there were two reported deaths in Sweden and Denmark related to ...
... acute overdose potential, long-term effects, or allergic reactions. Structural similarities with methcathinone and user reported experiences would suggest that mephedrone shares many of the same euphoric and stimulant effects. Recently, there were two reported deaths in Sweden and Denmark related to ...
51th ICAAC Chicago, IL September 17
... expression of viral genes. Integrase performs two related reactions: the enzyme-catalyzed hydrolysis of a dinucleotide from the 3'-end of each viral LTR DNA and the strand transfer reaction that integrates the viral DNA into the host cell's DNA. In a high throughput screening campaigns at Boehringer ...
... expression of viral genes. Integrase performs two related reactions: the enzyme-catalyzed hydrolysis of a dinucleotide from the 3'-end of each viral LTR DNA and the strand transfer reaction that integrates the viral DNA into the host cell's DNA. In a high throughput screening campaigns at Boehringer ...
A Warning on Gemcitabine Generics Used For
... potential to generate significant cost savings and ...
... potential to generate significant cost savings and ...
Do You Know... Anabolic Steroids
... body to recover normal hormone levels ·· Pyramiding: taking doses in cycles of six to 12 weeks, starting with a low dose, then slowly increasing it, and then decreasing the amount to zero, believing this allows the body time to adjust to the high doses ·· Stacking: taking two or more types of steroi ...
... body to recover normal hormone levels ·· Pyramiding: taking doses in cycles of six to 12 weeks, starting with a low dose, then slowly increasing it, and then decreasing the amount to zero, believing this allows the body time to adjust to the high doses ·· Stacking: taking two or more types of steroi ...
Crucial Considerations to Ensure the Safety of IV Therapy
... interest is any entity producing, marketing, re-selling, or distributing health care goods or services consumed by, or used on, patients. A person has a relevant financial relationship if the individual or his or her spouse/partner has a financial relationship (e.g., employee, consultant, research g ...
... interest is any entity producing, marketing, re-selling, or distributing health care goods or services consumed by, or used on, patients. A person has a relevant financial relationship if the individual or his or her spouse/partner has a financial relationship (e.g., employee, consultant, research g ...
Modifying effects of boswellia carteri on clarithromycine action: In
... inhibition of Boswellia carteri ranged from 6mmfor Pseudomonas aeruginosa to 14mm for Klebsiella pneumonia the p value was insignificant p ˃0.05 but the combined mixture showed significant differences from either clarithromycine or boswellia carteri p ˂0.05. The MIC ranged from 8-32mg/ml,8-64mg/ml a ...
... inhibition of Boswellia carteri ranged from 6mmfor Pseudomonas aeruginosa to 14mm for Klebsiella pneumonia the p value was insignificant p ˃0.05 but the combined mixture showed significant differences from either clarithromycine or boswellia carteri p ˂0.05. The MIC ranged from 8-32mg/ml,8-64mg/ml a ...
pKa Prediction of Monoprotic Small Molecules the SMARTS Way
... All in all, approximately 50% of all drug failures have been attributed to poor ADME, and in 2003 approximately $8 billion was lost due to the inability to predict the toxic nature of a substance during the early stages of drug development.12-14 The main advantage of in silico pKa prediction is that ...
... All in all, approximately 50% of all drug failures have been attributed to poor ADME, and in 2003 approximately $8 billion was lost due to the inability to predict the toxic nature of a substance during the early stages of drug development.12-14 The main advantage of in silico pKa prediction is that ...
Talwin Nx (pentazocine and naloxone hydrochlorides)
... CNS Effect. Caution should be used when pentazocine is administered to patients prone to seizures; seizures have occurred in a few such patients in association with the use of pentazocine though no cause and effect relationship has been established. Porphyria. Particular caution should be exercised ...
... CNS Effect. Caution should be used when pentazocine is administered to patients prone to seizures; seizures have occurred in a few such patients in association with the use of pentazocine though no cause and effect relationship has been established. Porphyria. Particular caution should be exercised ...
Pharmacognosy-I (Part-8)
... Balsams • Balsams are resinous mixtures that contain large proportions of cinnamic acid, benzoic acid or both or esters of these acids. • The term “balsam” is often wrongly applied to oleoresins and should be reserved for such substances as balsam of Peru, balsam of Tolu and storax, which contain a ...
... Balsams • Balsams are resinous mixtures that contain large proportions of cinnamic acid, benzoic acid or both or esters of these acids. • The term “balsam” is often wrongly applied to oleoresins and should be reserved for such substances as balsam of Peru, balsam of Tolu and storax, which contain a ...
drugs and cosmetics (iind amendment) rules, 2005
... (i) Clinical trial on a new drug shall be initiated only after the permission has been granted by the Licensing Authority under rule 21 (b), and the approval obtained from the respective ethics committee(s). The Licensing Authority as defined shall be informed of the approval of the respective insti ...
... (i) Clinical trial on a new drug shall be initiated only after the permission has been granted by the Licensing Authority under rule 21 (b), and the approval obtained from the respective ethics committee(s). The Licensing Authority as defined shall be informed of the approval of the respective insti ...
1 Phenol Synonym: carbolic acid CAS: 108-95
... reaction with uridine diphosphate (UDP)-glucuronic acid, in the presence of UDPglucuronate transferase [6]. Small amounts of phenol are oxidized to catechol and quinol, which are mainly conjugated [1]. Excretion: Phenol is rapidly secreted through the kidney, primarily conjugated with glucosiduronid ...
... reaction with uridine diphosphate (UDP)-glucuronic acid, in the presence of UDPglucuronate transferase [6]. Small amounts of phenol are oxidized to catechol and quinol, which are mainly conjugated [1]. Excretion: Phenol is rapidly secreted through the kidney, primarily conjugated with glucosiduronid ...
From the Metal to the Molecule
... 1) With the exception of cobalt, these elements form intermetallic phases with bismuth. Previous studies suggest that this is a basic requirement for the formation of the corresponding subhalides. Consequently, we can speak of the partial oxidation of intermetallic phases. 2) The electronegativities ...
... 1) With the exception of cobalt, these elements form intermetallic phases with bismuth. Previous studies suggest that this is a basic requirement for the formation of the corresponding subhalides. Consequently, we can speak of the partial oxidation of intermetallic phases. 2) The electronegativities ...
development and validation of high performance liquid
... After a number of trials with mobile phases of different composition, 0.05 M potassium dihydrogen phosphate : methanol 60:40 v/v pH adjusted to 4.5 with orthophosphoric acid was selected as mobile phase because of better resolution and symmetric peaks. CEF and SUL were found to show appreciable abso ...
... After a number of trials with mobile phases of different composition, 0.05 M potassium dihydrogen phosphate : methanol 60:40 v/v pH adjusted to 4.5 with orthophosphoric acid was selected as mobile phase because of better resolution and symmetric peaks. CEF and SUL were found to show appreciable abso ...
Inconspicuous and Miscalculated Opioid Risks
... Courtesy of Dr. Jeffrey Fudin (http://www.paindr.com) ...
... Courtesy of Dr. Jeffrey Fudin (http://www.paindr.com) ...
Medical Marijuana? - Commonwealth Prevention Alliance
... American Cancer Society says: "While it shows promise for controlling cancer pain among some patients, there is still concern that marijuana may cause toxic side effects in some people and that the benefits of THC must be carefully weighed against its potential risks. There is no available scientif ...
... American Cancer Society says: "While it shows promise for controlling cancer pain among some patients, there is still concern that marijuana may cause toxic side effects in some people and that the benefits of THC must be carefully weighed against its potential risks. There is no available scientif ...
asean guidelines for - Food and Drug Administration Philippines
... composition in terms of active substances, of having the same pharmaceutical form, and of being bioequiva lent unless it is apparent in the light of scientific knowledge that it differs from the original original product as regards safety and efficacy". By extension, it is generally considered that ...
... composition in terms of active substances, of having the same pharmaceutical form, and of being bioequiva lent unless it is apparent in the light of scientific knowledge that it differs from the original original product as regards safety and efficacy". By extension, it is generally considered that ...
Journal Citation Studies. 46. Physical Chemistry and Chemical
... The 1983 impact factor for a j oumal is the average number of citations received in 1983 by the articles published in that journal in 1981 and 1982. When we first began calculating impact over 10 years ago, we chose to use a 2-year period for articles to equalize the difference between those article ...
... The 1983 impact factor for a j oumal is the average number of citations received in 1983 by the articles published in that journal in 1981 and 1982. When we first began calculating impact over 10 years ago, we chose to use a 2-year period for articles to equalize the difference between those article ...
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.