SPIRIVA RESPIMAT is a once daily prescription asthma & COPD medication that can help provide better breathing for 24 hours. Please visit the website for. Tiotropio versus bromuro de ipratropio para la enfermedad pulmonar obstructiva cr├│nica. Information. DOI: /CDpub3; Database. Do you have any affiliation with or involvement in any organisation with a financial interest in the subject matter of your comment? No Yes Please provide details.

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Clinical trials

Muscarinic acetylcholine receptor modulators. Subscribe to receive email notifications whenever new articles are published. Your name will be included so that your friend or loved one will know who sent this email to them.

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Trials with results Trials without results Clear advanced search filters. Retrieved 3 April If you have any of these symptoms, stop tiltropio your medicine and call your doctor right away. Amlexanox Eprozinol Fenspiride Omalizumab. Your email address Please enter your email address in the format of name domain. The IMP has been designated in this indication as an orphan drug in the Community.

Asthma & COPD Treatment | SPIRIVA® (tiotropium bromide)

The trial involves single site in the Member State concerned. You are now leaving a Boehringer Ingelheim Pharmaceuticals, Inc.


It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you.

Abediterol Carmoterol Indacaterol Olodaterol Vilanterol.

By clicking Subscribe, I agree to the Drugs. Tiotropium and another member of its class ipratropium were linked to increased risk of heart attacks, stroke and cardiovascular death. Continuar Continue Cancelar Cancel. Retrieved from ” https: How to search [pdf]. Cancer AND drug name. Clear advanced search filters.

The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. To make sure they receive this, you’ll need to fill out all of the fields below.

EU Clinical Trials Register. BIPI is not responsible for the way information is processed by sites linked to this one. This material is provided for educational purposes tiiotropio and is not intended for medical advice, diagnosis or treatment.

Tiotropium bromide – Wikipedia

Tell your doctor all the medicines tkotropio take, including eye drops. This means it is still under development and may contain inaccuracies. Clinical tlotropio The European Union Clinical Trials Register allows you to search for protocol and results information on: The following information is intended only for healthcare professionals licensed and practicing in the United States and is designed to be an educational aid that supplements and draws upon the professional training, tiotropioo, and knowledge of such healthcare professionals.

Aclidinium bromide Glycopyrronium bromide Ipratropium bromide Oxitropium bromide Tiotropium bromide Umeclidinium bromide. Epinephrine Hexoprenaline Isoprenaline isoproterenol Orciprenaline metaproterenol. For these items you should use the filters and not add them to your search terms in the text field. Email results To send your discussion guide answers to your email address, just enter your information below. Combination product that includes a device, but does not involve an Advanced Therapy.

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S4 Prescription only UK: Definition of the end of the trial tiofropio justification where it is not the last visit of the last subject undergoing the trial. This leads to a reduction in smooth muscle contraction and mucus secretion and thus produces a bronchodilatory effect.

What you’ll tiotrpoio them is a direct link to this page. Subscribe to free Drugs. Tiotroprium was discovered in by Boehringer Ingelheim and came to market in From Wikipedia, the free encyclopedia.

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We comply with the HONcode standard for trustworthy health information – verify here. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances. Further information on drug naming conventions: Email bromurro page Enter your email address below to have this information sent to you directly. Review by the Competent Authority or Ethics Committee in the country concerned.