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• Wood Gas
  ...sifier or [[wood gas generator]]. It is the result of two high-temperature reactions (above {{convert|700|C}}): an exothermic reaction where carbon burns to CO< ...y somewhat from sample to sample. The same source reports the following chemical composition by volume which most likely is also variable:
  11 KB (1,707 words) - 18:26, 24 June 2010
• Halothane
  ...thers]] such as [[enflurane]] and [[isoflurane]]. The incidence of hepatic reactions with these agents is lower. The exact degree of [[hepatotoxic]] potential o ...was first synthesised by [[Charles Suckling|C. W. Suckling]] of [[Imperial Chemical Industries]] (ICI) in 1951 and was first used clinically by M. Johnstone in
  6 KB (845 words) - 11:06, 20 September 2010
• Mefloquine
  ...Hoffmann–La Roche|F. Hoffmann–La Roche]]) or '''Mefaquin''' and by the chemical name mefloquine hydrochloride (formulated with HCl). Mefloquine was develop ...is review was prompted by the manufacturer's request to revise the Adverse Reactions - Postmarketing section of the label to include pneumonitis of possible all
  13 KB (1,807 words) - 16:41, 27 September 2010
• Lidocaine
  Etymology: from one of its many chemical names - [alpha-Diethylamino-2,6-dimethylacetani- ] - lide + ~ocaine. === Adverse drug reactions ===
  15 KB (2,006 words) - 16:41, 27 September 2010
• Dexamethasone
  ...paired wound-healing, increased sweating, rash, [[striae]], suppression of reactions to skin tests, thin fragile skin, thinning scalp hair, [[urticaria]]. * Allergic reactions (though infrequently): [[Anaphylactoid reactions|Anaphylactoid reaction]], [[anaphylaxis]], [[angioedema]].
  18 KB (2,498 words) - 16:41, 27 September 2010
• Sodium thiosulfate
  ==Principal reactions and applications== This reaction is known as a "[[Chemical clock|clock reaction]]", because when the sulfur reaches a certain concentr
  12 KB (1,720 words) - 16:42, 27 September 2010
• Chloramphenicol
  Chloramphenicol poisoning can cause sensitivity reactions to organic acids and salicylates. ...the main pathway conjugational excretion, which leads to a buildup of the chemical in infants system- contraindication.{{Citation needed|date=November 2009}}
  29 KB (3,876 words) - 16:42, 27 September 2010
• Erythromycin
  ...esearch group, posthumously reported the first stereocontrolled asymmetric chemical synthesis of Erythromycin A. ...ired dithiadecalin product (9) through a series of reduction and oxidation reactions. (9) is then converted to both a ketone (10) and an aldehyde (11).
  19 KB (2,731 words) - 17:52, 18 September 2010
• Isoniazid
  Adverse reactions include [[rash]], abnormal [[liver function tests]], [[hepatitis]], [[sider Hepatotoxicity of INH is by nitrogen group in its chemical structure,as it is metabolized in liver and gets converted in to ammonium m
  12 KB (1,566 words) - 16:43, 27 September 2010
• Amphotericin B
  ...he [[Orinoco River]] region of [[Venezuela]]. Its name originates from the chemical's [[amphoteric]] properties. Two amphotericins, Amphotericin A and Amphote ...brillation]]), and even frank [[cardiac failure]] have been reported. Skin reactions, including serious forms, are also possible.
  13 KB (1,785 words) - 16:44, 27 September 2010
• Potassium iodide
  '''Potassium iodide''' is an [[inorganic compound]] with [[chemical formula|formula]] [[potassium|K]][[iodide|I]]. This white salt is the most KI is a precursor to [[silver iodide]] (AgI) an important chemical in photography. KI is a component in some disinfectants and hair treatment
  23 KB (3,281 words) - 16:44, 27 September 2010
• Aciclovir
  ...[United States Adopted Name|USAN]], former [[British Approved Name|BAN]]), chemical name '''acycloguanosine''', abbreviated as '''ACV''',<ref name=deClercq2005 ...istered IV, include [[encephalopathy]] (1% of patients) and injection site reactions. The injection formulation is [[alkaline]] ([[pH]] 11), and [[extravasation
  14 KB (1,878 words) - 16:44, 27 September 2010
• Abacavir
  |caption=Chemical structure of abacavir == Adverse reactions ==
  8 KB (1,124 words) - 16:44, 27 September 2010
• Atropine
  ...and [[VX (nerve agent)|VX]]. Troops that are likely to be attacked with [[chemical weapon]]s often carry [[autoinjector]]s with atropine and [[obidoxime]], wh Adverse reactions to atropine include ventricular [[fibrillation]], supraventricular or ventr
  16 KB (2,198 words) - 16:46, 27 September 2010
• Methylene blue
  ...blue''' is a [[Heterocyclic ring|heterocyclic]] [[aromaticity|aromatic]] [[chemical compound]] with the [[molecular formula]] [[carbon|C]]₁₆[[hydrog ...tration of [[chemical kinetics]] in general chemistry, the "[[Blue bottle (chemical reaction)|blue bottle]]" experiment. Typically, a solution is made of [[dex
  27 KB (3,650 words) - 16:46, 27 September 2010
• Fluoxetine
  ...article about fluoxetine in 1974. A year later, it was given the official chemical name fluoxetine and the Eli Lilly and Company gave it the trade name Prozac ...ph.17302}}</ref><ref>{{cite journal |author=Caley CF |title=Extrapyramidal reactions and the selective serotonin-reuptake inhibitors |journal=Ann Pharmacother |
  52 KB (7,168 words) - 16:47, 27 September 2010
• Activated carbon
  ...us to have a very large [[surface area]] available for [[adsorption]] or [[chemical reaction]]s.<ref>[http://www.activated-carbon.com/1-3.html "Properties of A ...ul applications may come solely from the high surface area, though further chemical treatment often enhances the absorbing properties of the material. Activat
  41 KB (5,738 words) - 16:47, 27 September 2010
• Aspirin
  ...preparation of aspirin ("salicylic-acetic anhydride") was one of the many reactions Gerhardt conducted for his paper on anhydrides and he did not pursue it fur ...te) and von Gilm's (from salicylic acid) syntheses and concluded that both reactions gave the same compound—acetylsalicylic acid. They were first to assign to
  78 KB (10,918 words) - 16:52, 27 September 2010
• Prussian blue
  '''Prussian blue''' is a dark blue [[pigment]] with the idealized [[chemical formula|formula]] Fe₇(CN)₁₈⋅14H₂O.<ref n * Insoluble Prussian blue is produced if in the reactions above an excess of Fe³⁺ or Fe²⁺, respectively, is add
  20 KB (3,004 words) - 16:47, 27 September 2010
• Atenolol
  ...replacement for [[propranolol]] in the treatment of [[hypertension]]. The chemical works by slowing down the heart and reducing its workload. Unlike [[propran ...However, due to its cardioselective properties, the risk of bronchospastic reactions if using atenolol is reduced compared to nonselective drugs as [[propranolo
  12 KB (1,720 words) - 16:48, 27 September 2010

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