摘要:
An external adhesive preparation comprising a steroid for treatment of skin diseases in admixture with an adhesive gel base comprising as essential components a water-soluble high molecular weight compound, water and a water-retaining agent. The external adhesive preparation is useful for treatment of skin diseases by applying the preparation spread on a soft support directly to diseased parts on the skin, thereby administering the contained steroid to the skin.
摘要:
A shared object is newly created in a unified format with respect to past medical information that is effective in a photographing step or a report creating step. Since the shared object can include a position determination image, unique object information, body coordinates information, a photographing condition, a image creating condition, and key image information, it is possible to automatically set the same photographing condition, photographing range, a tomographic position to be photographed, and image creating condition as those in a past test by using the information described above.
摘要:
There are provided an input unit which inputs an object with scan information attached thereto into an image of a subject acquired on the basis of the scan information, and an insertion unit which inserts report information to the object when preparation of an image interpretation report of a study based on the image is completed.
摘要:
A report check apparatus includes an input unit which inputs data of a diagnostic reading report as a check target, a check unit which checks whether the input diagnostic reading report contains a semantic error related to diagnostic reading, and a display unit which displays a check result by the check unit.
摘要:
A long-acting diclofenac sodium preparation is disclosed. The preparation comprises a sustained-release diclofenac sodium component which is prepared by coating a sustained-release coat onto a pharmaceutical composition comprising diclofenac sodium and an organic acid. It can decrease the maximum blood concentration of diclofenac by suppressing and controlling the rate of release of diclofenac sodium and maintain the blood concentration of diclofenac constant for a considerably long period of time. The risk of side-effect occurrences is reduced and patients is released from frequent administration of the medicine.
摘要:
A link corresponding range is identified in a string in a finding section of a medical report display screen. A content is specified and dragged and dropped onto the area in which link corresponding range is displayed. When the string is specified, address information on the content is attached to the string. At the same time, the string in the link corresponding range is identified and displayed. The present apparatus subsequently determines whether or not to display information related to the linked reference content. If a display instruction has been given, a protocol that allows the related information to be automatically acquired and displayed is embedded in the hyperlink. When report production is completed, a file is saved to finish the series of processing operations. The file is then transferred to, for example, a trace reading report production requester.
摘要:
A preparation for oral administration which comprises S-(3-hydroxypropyl)-L-cysteine and one or more excipients, where the excipients do not cause discoloration of S-(3-hydroxypropyl)-L-cysteine is disclosled. According to an embodiment of the invention, the excipient may comprise a starch and/or a cyclodextrin. Typical starches used in the invention include corn starch, potato starch, wheat starch, and rice starch. Typical cyclodextrins used in the invention include &agr;-cyclodextrin, &bgr;-cyclodextrin, and &ggr;-cyclodextrin. Other excipients, such as saccharides, sugar alcohols and cellulose are not present in amounts that cause discoloration of the HPCY.
摘要:
The present invention relates to a sustained-release suppository preparation characterized by comprising an acidic drug or a salt thereof which can be absorbed by rectal administration and an acidic compound or a pH buffering agent. The sustained-release suppository preparation of the present invention exhibits no rapid increase in blood concentration immediately after the administration and maintains its action for a long period of time. Thus, it is safer and exhibits a better therapeutic effect.
摘要:
An antiinflammatory and analgesic gel preparation comprising diclofenac or its salts, an ester of dibasic acid, a lower alcohol, and a nonionic polymer or a mixture of nonionic polymers selected from the group consisting of (a) 1.5-4% by weight of hydroxypropyl cellulose having a molecular weight of 500,000 or greater, (b) 2-4% by weight of hydroxyethyl cellulose having a molecular weight of 1,250,000 or greater, and (c) 1.5-4% by weight of a mixture of hydroxypropyl cellulose having a molecular weight of 500,000 or greater and hydroxyethyl cellulose having a molecular weight of 1,250,000 or greater, and having a viscosity of 5,000-35,000 cps and an yield value of 5 dyn/cm.sup.2 or greater. The gel preparation is excellent in the percutaneous absorption of diclofenac or its salts and provides good properties upon use and superior medical effects of diclofenac or its salts.
摘要翻译:包含双氯芬酸或其盐的抗炎和镇痛凝胶制剂,二元酸的酯,低级醇和非离子聚合物或非离子聚合物的混合物,其选自(a)1.5-4重量%的羟丙基纤维素 分子量为500,000以上,(b)2-4重量%的分子量为1,250,000以上的羟乙基纤维素,(c)1.5-4重量%的具有分子量的羟丙基纤维素的混合物 500,000以上的羟乙基纤维素和分子量为1,250,000以上的羟乙基纤维素,粘度为5,000〜35,000cps,屈服值为5dyn / cm 2以上。 凝胶制剂在双氯芬酸或其盐的经皮吸收方面是优异的,并且在使用时提供良好的性质和双氯芬酸或其盐的优异的医学效果。
摘要:
A composition for foaming preparation comprising (a) an organic acid of which the crystal surface is coated with a sugar and (b) a carbonate is disclosed. In the composition, an organic acid is completely shut off from a carbonate by a sugar coating so that the acid does not react with the carbonate over a prolonged storage time. When the composition is put into mouth, the sugar which covers the acid is readily dissolved, allowing the acid and the carbonate to react and to generate carbon oxide gas. An excellent foaming calcium preparation can be produced by using calcium carbonate as the carbonate or by adding other salt of calcium to the composition. Such a calcium preparation gives a good taste and favorable feeling upon administration. It is especially suitable for regular administration of calcium over an extended period of time.