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Effects of short-acting agents usually last only 4 to 6 hours whereas those of LABAs last 12 hours.
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Treatment with theophylline may cause a small improvement in FEV 1; however, it is poorly tolerated, requires monitoring, and does not improve patient-oriented outcomes such as breathlessness.
Patients should follow the instructions in the patient information leaflet provided with the product.
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User-generated content areas are not reviewed by a WebMD physician or any member of the WebMD editorial staff for accuracy, balance, objectivity, or any other reason except for compliance with our Terms and Conditions.
Testing consisted of pulmonary function testing, dyspnea evaluation, and symptom-limited constant-load cycle exercise tests with measurements of cardiopulmonary parameters, symptom intensity and pulmonary mechanics.
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In these studies, Spiriva HANDIHALER, administered once-daily in the morning, provided improvement in lung function (FEV 1), with peak effect occurring within 3 hours following the first dose.
This material does not endorse drugs, diagnose patients, or recommend therapy.
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The HandiHaler device is an inhalation device used to inhale the dry powdercontained in the SPIRIVA capsule.
Spiriva, which will maintain patent protection into 2014, is one go-to treatment for chronic obstructive pulmonary disease, or COPD.
Some patients find that they are more difficult to manage than MDIs.
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Go to the program website and find out if you are eligible.
However, this list may not represent all companies that are involved in the production of this medication.
This product contains tiotropium bromide and is used to treat bronchospasm associated with chronic obstructive pulmonary disease.
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Turn your HANDIHALER device upside down and gently, but firmly, tap to remove the Spiriva capsule pieces.
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SPIRIVA RESPIMAT consists of a SPIRIVA RESPIMAT inhaler and an aluminum cylinder (SPIRIVA RESPIMAT cartridge) containing tiotropium bromide (as the monohydrate).
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Tashkin, MD, FACP, FCCP, Professor of Medicine, David Geffen School of Medicine at the University of California at Los Angeles and lead clinical investigator, presented the results from "Addition of Nebulized Formoterol Fumarate to Tiotropium Treatment Relieves Dyspnea and Symptoms in COPD Patients" in a poster session today.
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The drug information contained herein is subject to change and is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects.
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SPIRIVA RESPIMAT 5 mcg also has been compared to placebo in seven placebo-controlled parallel-group trials ranging from 12 to 52 weeks of treatment duration in 4149 adult patients (aged 18 to 75 years) with asthma and in two placebo-controlled parallel-group trials ranging from 12 to 48 weeks of treatment duration in 789 adolescent patients (1370 adults and 264 adolescents receiving SPIRIVA RESPIMAT 5 mcg once-daily).
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