ipratropium_salbutamol

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  • 7/28/2019 Ipratropium_salbutamol

    1/1

    Ipratropium salbutamol (Duavent) nebule, 1 nebule PRN for dyspnea

    DRUGNAME

    MECHANISM OF ACTION INDICATION ADVERSE EFFECT OVERDOSAGE CONTRAINDICATION

    NURSINGRESPONSIBILITY

    IpratropiumSalbutamol

    Duavent500 mcg /2.5 mg per2.5 ml

    pulmoneb

    Solunon fornebulizano

    n

    FORMULA

    TION:Each 2.5mL

    pulmonebcontains:Ipratropium

    bromide(anhydrous) 500 mcgSalbutamol(as sulfate)

    2.5 mg

    Anticholinergic / Beta,-agonistIpratropium bromide

    Antiasthmatic & COPD PreparationsPharmacology: Ipratropium bromide:Ipratropium bromide is a quaternaryammonium compound with

    anticholinergic (parasympatholytic)properties. Similar to atropine, it is a

    nonselective competitive antagonistof muscarinic receptors present in

    airways and other organs. Ipratropiumbromide relaxes smooth muscles of

    bronchi and bronchioles by blocking

    acetylcholine-induced stimulation ofguanyl cyclase, thus reducingformation of cyclic guanosinemonophosphate (cGMP), a mediatorof bronchoconstriction.

    Salbutamol: Salbutamol stimulatesadenyl cyclase, the enzyme whichcatalyzes the formation of cyclic-3',5'-adenosine monophosphate (cAMP)from adenosine triphosphate (ATP).

    The cAMP thus formed mediates thecellular response eg, bronchialsmooth muscle relaxation.Invitro and in vivo pharmacologicstudies have demonstrated thatsalbutamol has a preferential effect on-adrenergic receptors that areespecially found in respiratory tractcompared with isoproterenol.

    Managementofreversiblebro

    nchospasm associated withobstructiveairway

    diseases (eg,bronchial

    asthma).For patients

    withchronic obstru

    ctive

    pulmonarydisease (COPD) on aregularinhaled

    bronchodilatorwho continueto haveevidenceofbronchospasm and who

    require asecondbronchodilator.

    Gastrointestinal:Nausea.Respiratory: Bronchitis,

    dyspnea, coughing,pneumonia,bronchospasm,pharyngitis, sinusitis,

    rhinitis.Additional adverse

    reactions, reported in