(i) a breath-actuated inhaler comprising a medicament reservoir (6) mounted within a housing (2) which comprises a mouthpiece (4) and breath-actuation means which prevents dispensing from the reservoir until a patient inhales through the mouthpiece, and (ii) a protective casing (34) surrounding the breath actuated inhaler, the casing comprising a body portion (36) and a movable cover (38) which may be displaced to allow a patient access to the mouthpiece (4) to use the breath-actuated inhaler whilst it is within the casing, the breath-actuated inhaler being removable from the protective casing and operable outside the casing.
摘要翻译:一种吸入装置,包括:(i)呼吸致动吸入器,其包括安装在壳体(2)内的药物储存器(6),所述药剂容器包括接口(4)和呼吸致动装置,所述呼吸致动装置防止从所述储存器分配,直到患者吸入 所述接口管,以及(ii)围绕所述呼吸致动吸入器的保护壳体(34),所述壳体包括主体部分(36)和可移动盖(38),所述主体部分可移动以允许患者接近所述接口管(4) 呼吸致动的吸入器在其位于壳体内时使用,呼吸致动吸入器可从保护壳体移除并且可在壳体外部操作。 H
摘要:
A self-propelling aerosol formulation which may be free from CFC's which comprises a medicament, 1,1,1,2-tetrafluoroethane, a surface active agent and at least one compound having a higher polarity than 1,1,1,2-tetrafluoroethane.
摘要:
Novel 1-substituted 1H-imidazo-[4,5-c]quinolin-4-amines are disclosed. These compounds function as antiviral agents, and they are potential synthetic intermediates in the preparation of known antiviral agents and labeled known antiviral agents. This invention also provides intermediates for preparing such compounds, pharmaceutical compositions containing such compounds, and pharmacological methods of using such compounds.
摘要:
Pharmaceutical formulations and adhesive-coated sheet materials for the topical and/or transdermal delivery of 1-isobutyl-1H-imidazo[4,5-c]quinolin-4-amine, including creams, ointments and pressure-sensitive adhesive compositions. Pharmacological methods of using the formulations and the adhesive-coated sheet materials of the invention in the treatment of viral infections.
摘要:
Novel compounds which are 2,6-di-tertiary-butylphenols substituted in the 4 position by an acylaminophenyl group, which acylaminophenyl group is substituted by a moiety which includes a carboxyl group, are useful as inhibitors of leukotriene biosynthesis and as antiallergic agents.
摘要:
Novel compounds which are 2, 6-di-t-butylphenols substituted on the 4 position by a thenoyl group, which thenoyl group is substituted by an acid group are useful as inhibitors of leukotriene synthesis and as antiallergic agents.
摘要:
L'invention concerne des suspensions aqueuses contenant au moins un composé choisi parmi les acides 6,7-dihydro-benzoquinolizine-carboxyliques, en particulier l'acide [1H-5H] dihydro-6,7-fluoro-9 méthyl-5 oxo-1 benzo [i,j] quinolizine carboxylique-2, suspensions caractérisées en ce qu'elles renferment une quantité importante d'un tel composé cristallisé sous forme d'aiguilles non dissoutes et qu'elles présentent un pH inférieur ou égal à 7, ces suspensions étant particulièrement efficaces pour lutter, dans le régime végétal, contre les bactéries gram⁻ et gram⁺.
摘要:
Novel compounds which are 2,6-di-t-butytphenols substituted on the 4 position by an anilino group, which anilino group is substituted by a group which includes carboxyl, tetrazolyl or N-methyltetrazolyl are useful as inhibitors of leukotriene synthesis and as antiallergic agents. Pharmaceutical compositions containing such compounds and pharmacological methods for use of such compounds are also disclosed.
摘要:
Microfibrous heparin salts, nonwoven webs (22) of such fibers, a process for preparing the fibers and the use of the webs for the rapid heparinization of blood are disclosed.
摘要:
An aerosol formulation comprising a medicament, 1,1,1,2-tetrafluoroethane, a surface active agent and at least one compound having a higher polarity than 1,1,1,2-tetrafluoroethane.