A self defense weapon formed as a memo pad and which is easily held by a person's fingers, therefore making it possible to provide protection from a mugger and also to quickly and easily write a record or a message without failure of missing or forgetting significant information under a stressful situation.
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| Number | Title | Issue Date |
| 8153601 | Azithromycin-containing aqueous pharmaceutical composition and a method for the preparation of the same The invention provides an azithromycin-containing aqueous pharmaceutical composition, which comprises at least one member selected from the group consisting of azithromycin, and pharmaceutically acceptable salts thereof, and at least one member selected from the gro... | 04/10/2012 |
| 7612115 | Aqueous pharmaceutical compositions The present invention has an object to provide an antibacterial aqueous pharmaceutical composition and an aqueous pharmaceutical composition which have a sufficiently low gelation temperature even when new quinolone antibacterial agents such as ofloxacin as the acti... | 11/03/2009 |
| 7225949 | Liquid drug container A liquid drug container comprises a container body 1; a nozzle member 2 liquid-tightly mounted on the container body 1; and a nozzle cap 6 fitted on the nozzle member 2. A nozzle hole 231 of the nozzle member 2 is cov... | 06/05/2007 |
| 7150986 | Lactic acid bacteria-containing probiotics products The present invention provides a probiotics product comprising, as an effective component, lactic acid bacteria belonging to Lactobacillus salivarius possessing high adhesiveness to mucous membrane, a high proliferation ability and a high resistance to acids,... | 12/19/2006 |
| 7105512 | Ophthalmic aqueous pharmaceutical preparation The present invention provides an ophthalmic aqueous pharmaceutical preparation, which is excellent in anti-inflammatory effect, which is less stimulative and which has high safety and excellent storage stability. The ophthalmic aqueous pharmaceutical preparation co... | 09/12/2006 |
| 6849419 | Monoclonal antibody hybridoma immunoassay method and diagnosis kit The object of the present invention is to provide a diagnostic method by which Helicobacter pylori infection can be diagnosed at low cost without causing pain on subjects and without requiring particular equipment and which is free of cross reactivity and exc... | 02/01/2005 |
| 6777197 | Method and test kit for measuring immunoglobulins reactive with amylase as indication of crohn's disease A method for diagnosing Crohn's disease by detecting the presence of immunoglobulins, reactive with an amylase, in a specimen by an immunologic or enzymologic method using the amylase, and a test kit for this method. ... | 08/17/2004 |
| 6495603 | Anti-inflammatory eye drop The present invention relates to an anti-inflammatory eye drop comprising a drug selectively inhibiting COX-2, selected from the group consisting of etodolac, N-(2-(cyclohexyloxy)-4-nitrophenyl) methane-sulfonamide and meloxicam, which only slightly damag... | 12/17/2002 |
| 6432439 | O/W emulsion composition An O/W emulsion composition comprising fluorometholone or clobetasone butyrate, a phospholipid, an oil, a nonionic water-soluble cellulose derivative, and water. The O/W composition has advantages that fluorometholone or clobetasone butyrate contained the... | 08/13/2002 |
| 6225306 | Biphenyl derivatives and drug composition A biphenyl derivative represented by the following general formula (1) and a pharmaceutically acceptable salt thereof: ##STR1## [In the formula (1), A represents a single bond, --CH2 --, --CO--, --CS-- or --SO2 --; B represents a sin... | 05/01/2001 |
| 6132751 | O/W emulsion composition for eye drops An O/W emulsion composition for eye drops comprises a drug selected from the group consisting of fluorometholone, clobetasone butyrate and clobetasol propionate; a phospholipid; liquid paraffine; and water. The O/W emulsion composition is excellent in sol... | 10/17/2000 |
| 5929115 | Anti-inflammatory eye drop An anti-inflammatory eye drop comprises (a) 0.05 to 0.7 weight/volume % of diclofenac sodium; (b) 1 to 10 weight/volume % of γ-cyclodextrin; (c) 1 to 20 weight/volume % of polyvinyl pyrrolidone; and (d) 0.002 to 0.01 weight/volume % of benzethonium chloride or 0.002 to... | 07/27/1999 |
| 5756552 | Lyophilized pharmaceutical preparations capable of providing aqueous drug composition having property of reversible thermosetting gelation Herein disclosed is a lyophilized pharmaceutical preparation obtained by lyophilizing an aqueous composition having property of reversible thermosetting gelation and comprising an effective amount of a drug, 0.2 to 2.1 (W/V)% of methylcellulose (the conte... | 05/26/1998 |
| 5693337 | Stable lipid emulsion A lipid emulsion which comprises (A) an oil component, (B) an emulsifying agent containing yolk lecithin and/or soybean lecithin, and (C) water, wherein the lipid emulsion further comprises citric acid or a pharmaceutically acceptable salt thereof and at ... | 12/02/1997 |
| 5648455 | Antibiotic WAP-8294A, method for preparing the same and antibacterial composition Antibiotics WAP-8294A, A1, A2, A4, AX, AX-8, AX-9 and AX-13 or pharmeceutically acceptable salts thereof produced by a strain belonging to the genus Lysobacter; a method for producing the foregoing antibiotic WAP-8294A com... | 07/15/1997 |
| 5624962 | Aqueous drug composition having property of reversible thermosetting gelation An aqueous drug composition having property of reversible thermosetting gelation for ophthalmic, dermatological and body cavitical use which comprises effective amount of drugs used for pharmaceutical therapy or diagnosis, methylcellulose, citric acid and... | 04/29/1997 |
| 5602161 | Tetrazolylphenyl pivalate derivatives and medicinal composition containing the same as effective component The tetrazolylphenyl pivalate of the the following general formula or a pharmaceutically acceptable salt thereof: ##STR1## wherein R1 and R2 each represents a hydrogen atom, a lower alkyl group or other substituents; an elastase... | 02/11/1997 |
| 5569464 | Stable aqueous dispersions containing liposomes An aqueous dispersion containing liposomes comprising yolk lecithin and/or soybean lecithin as lipids for forming liposomes wherein the dispersion contains a hydroxy acid and an amino acid, which hardly shows coloration, shows little leak of drugs encapsu... | 10/29/1996 |
| 5356916 | 1,2,4-oxadiazole derivatives having monoamine oxidase B enzyme-inhibitory activity A 1,2,4-oxadiazole derivative is represented by the following general formula (I): ##STR1## wherein R1 represents a lower alkyl or cycloalkyl group, a lower alkyl group substituted with a halogen atom, a lower alkylamino group or a ph... | 10/18/1994 |
| 5262433 | Tetrazoleacetic acid derivatives and method of aldose reductase inhibition therewith A tetrazoleacetic acid derivative represented by the following general formula I: ##STR1## wherein in the formula I, R represents a hydrogen atom or a lower alkyl group; A is an alkylene group having 2 to 5 carbon atoms; Ar is selected from the ... | 11/16/1993 |
| 5252592 | Tetrazoleacetic acid derivatives having aldose reductase inhibitory activity A tetrazoleacetic acid derivative represented by the following general formula (I): ##STR1## [in Formula (I), R1 represents a hydrogen atom or a lower alkyl group; R2, R3 and R4 are the same or different fr... | 10/12/1993 |
| 5246835 | Method of diagnosing renal diseases A method of diagnosing renal diseases by detecting fragments of albumin in human urine. The detection of the fragments is carried out by, for example, immunological methods or liquid chromatography techniques.... | 09/21/1993 |
| 5068239 | Tetrazoleacetic acid derivatives and use for aldose reductase inhibitory activity A tetrazoleacetic acid derivative represented by the following general formula (I): ##STR1## [in Formula (I), R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralkyl group, a ... | 11/26/1991 |
| 5055481 | Tetrazole derivatives and aldose reductase inhibition therewith The present invention relates to an aldose reductase inhibitor having the following formula: ##STR1## R1 is a hydrogen atom or --A--COOR5 (A is an alkylene group having 1 to 4 carbon atoms and R5 is a hydrogen atom or... | 10/08/1991 |
| 4861718 | Gene coding for thermostable beta-galactosidase, bacillus subtilis having the gene, enzyme coded by the gene and a process for the production thereof A novel gene coding for thermostable ଲ-galactosidase, novel recombinant DNA in which a DNA fragment containing the above gene is inserted, novel Bacillus subtilis in which the above recombinant DNA is introduced, and novel thermostable ଲ-galac... | 08/29/1989 |
| 4795754 | 3-(1H-tetrazol-5-y1)oxanilic acid and salts thereof and pharmaceutical compositions containing them A new compound, 3-(1H-tetrazol-5-yl)oxanilic acid and pharmaceutically acceptable salts thereof are herein disclosed, which can be prepared by reacting 3-(1H-tetrazol-5-yl)aniline with a compound represented by the general formula: A--CO--CO--B (wherein A... | 01/03/1989 |
| 4778816 | Anti-asthmatic composition and process for preparing the same 5-(3-n-Butyloxalylaminophenyl) tetrazole having an excellent SRS-A release-inhibiting effect is used as an effective component for an anti-asthmatic agent, and a pharmaceutical preparation obtained by mixing the tetrazole with a specific dispersant such a... | 10/18/1988 |
| 4587254 | 1,3,4-thiadiazole derivatives, process for the production thereof and use thereof as antiulcer agent New 1,3,4-thiadiazole derivatives of the general formula (I): ##STR1## wherein R1 represents a group of the formula: ##STR2## and R2 represents an amino, lower alkylamino, cyclohexylamino, benzoylamino, mercapto or lower al... | 05/06/1986 |
| 4537967 | 1-Oxo-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid derivatives The following new isocarbostyryl derivatives represented by the general formula [I]: ##STR1## wherein R1 is a hydrogen atom or a lower alkyl group, are provided, said derivatives having excellent angiotensin converting enzyme inhibitory ... | 08/27/1985 |