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Final Salbu-Ipra

Combivent is a combination of albuterol sulfate and ipratropium bromide used to treat chronic obstructive pulmonary disease. It works by relaxing bronchial smooth muscle through stimulation of beta-2 receptors and inhibition of acetylcholine. Common side effects include dizziness, nausea, dry mouth, and bronchospasms. Nurses should monitor for side effects, educate patients on proper use, and assess for contraindications like hypersensitivity prior to administration.

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0% found this document useful (0 votes)
483 views3 pages

Final Salbu-Ipra

Combivent is a combination of albuterol sulfate and ipratropium bromide used to treat chronic obstructive pulmonary disease. It works by relaxing bronchial smooth muscle through stimulation of beta-2 receptors and inhibition of acetylcholine. Common side effects include dizziness, nausea, dry mouth, and bronchospasms. Nurses should monitor for side effects, educate patients on proper use, and assess for contraindications like hypersensitivity prior to administration.

Uploaded by

Gwyn Rosales
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as DOCX, PDF, TXT or read online on Scribd
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Name of Drug Classification Mechanism of Action Indication Contraindication Side Effects Nursing Responsibilities

Generic Name: Pharmacologic Class: Ipratropium bromide is an General Indications: Hypersensitivity to CNS: dizziness,blurred vision Before
Salbutamol + Anitcholinergic anticholinergic - patients with chronic salbutamol, ipratropium 1. Check the doctor’s order
Ipratropium (parasympatholytic) agent obstructive pulmonary or fenoterol, atropine or GI: nausea, drymouth 2. Assess allergy to the drug
which, based on animal disease (COPD) on a its 3. Caution patient of the
Trade/Brand Name: studies, appears to inhibit regular aerosol derivatives.Hypertrophic Respi: different side effects
Combivent, DuoNeb, vagally-mediated reflexes bronchodilator who obstructive dyspnea,bronchospasms,horsenes 4. Obtain baseline vital
Breva Therapeutic Class: by antagonizing the action continue to have cardiomyopathy, s signs
Bronchodilator of acetylcholine, the evidence of tachyarrhythmia. 5. Prepare drugs properly at
Patients’ Dose: transmitter agent released bronchospasm and who CV: palpitations,chest pain the right dosage.
at the neuromuscular require a second Drug to Drug
junctions in the lung. bronchodilator. Interactions:Increased
Route: Anticholinergics prevent adverse effects with During
Inhalation the increases in corticosteroids, xanthine 1. Verify patient’s identity
Pregnancy Category: intracellular concentration derivatives, diuretics. 2. Explain to patient the
Form: C of Ca++ which is caused purpose of medication
by interaction of Special Precaution: 3. Advise patient to swallow
acetylcholine with the Patient’s Indication: Patient with CV medication as a whole
Maximum dose: muscarinic receptors on disorders (e.g. ischaemic 4. Give drug with full glass
<6 times/24 hours bronchial smooth muscle. heart disease, arrhythmia, of water to reduce risk of
severe heart failure), tablet or capsule lodging in
Salbutamol relaxes severe airway the esophagus.
Minimum dose: bronchial, uterine, and obstruction, cystic 5.Do not crush, and ensure
4 times/24 hours vascular smooth muscle by fibrosis, prostatic that patient does not chew
stimulating beta 2 hyperplasia or bladder- SR preparations.
receptors. neck obstruction,
Availability: convulsive disorders,
Inhalation Solution hyperthyroidism, After
Pharmacokinetics diabetes mellitus. 1. Monitor vital signs noting
Absorption: Ipratropium: Pregnancy and lactation. hypotension andan irregular
Content: Rapidly absorbed after orabnormal pulse.
Albuterol Sulfate 2.5 mg inhalation. Bioavailability: 2. Monitor for adverse
in 3mL <10%; Salbutamol: effects.
Ipratropium Bromide 0.5 Rapidly and completely 3. Maintain aquiet,
mg in 3mL absorbed after inhalation. comfortableenvironment
Time to peak plasma tominimize anxietyand
concentration: Within 3 perhapsdecreasepalpitations.
hours. 4. Document correctly and
Distribution: Ipratropium: accordingly.
Plasma protein binding:
<20%.
Metabolism: Ipratropium:
Partially metabolised to
inactive ester hydrolysis
products; Salbutamol:
Undergoes first-pass
metabolism in the liver
and possibly in the gut
wall. Metabolised to
inactive sulfate conjugate.
Excretion: Ipratropium:
Via urine and faeces.
Terminal elimination half-
life: 1.6 hours.
Salbutamol: Via urine (as
metabolites and
unchanged drug); faeces
(small amounts).
Elimination half-life: 3-7
hours.

Half life:
- Salbutamol: 4 hr;
Ipratropium: 2 hr
Peak:
- Salbutamol: 2-3 hr;
Ipratropium: 1-2 hr
Onset:
- Salbutamol: 15-30
minutes; Ipratropium: 5-15
minutes
Duration
-- Salbutamol: 4-8 hr;
Ipratropium: 3-6 hr

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Wilkins Wilkins Wilkins Wilkins Wilkins JONES & BARTLETT Wilkins
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JONES & BARTLETT JONES & BARTLETT JONES & BARTLETT JONES & BARTLETT JONES & BARTLETT Drug Handbook. SUDBURY. JONES & BARTLETT
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