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At first, lung function was markedly improved, then I started having rapid and irregular heart problems, along with high blood pressure. Because I was also taking Atrovent, my Doctor told me that I shouldn't take both. He decreased the Spiriva and my heart problems subsided. Unfortunately, I have lost some lung function, my activity level has decreased probably 70% and I am living on inhalers every 3hrs. And I feel like an elephant has parked himself on my chest! Quality of life is minimal so I'm ready to resume taking Spiriva.

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Vital status information was collected for patients who discontinued the trial prematurely to assess the effects of differential discontinuation and a potential healthy-survivor effect.

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The FDA announced that it is investigating the results from several recent clinical studies involving Spiriva (tiotropium), including the UPLIFT trial that the FDA first notified the public about in March 2008.

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When taking SPIRIVA RESPIMAT, patients should breathe out slowly and fully, then patients should take a slow, deep breath through their mouth, press the dose-release button, and continue to breathe in slowly for as long as they can.

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These trials further support the improvement in pulmonary function (FEV 1) with Spiriva HANDIHALER, which persisted over the spirometric observational period.

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NMS can cause hyperpyrexia, muscle rigidity, altered mental status and evidence of autonomic instability (irregular pulse or blood pressure, tachycardia, diaphoresis and cardiac dysrhythmia).

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Out of 100% of people surveyed, these results show the distribution in percentages of the severity of side effects experienced by users.

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Spiriva capsules contain 18 mcg of tiotropium in a light green, hard gelatin capsule with TI 01 printed on one side and Boehringer Ingelheim company logo on the other side.

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