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  • Interactive

    Stroke eLearning prescribers' module

    Thrombolysing with Actilyse®  (alteplase): case studies

  • Prescribing Information

    Actilyse®
    (alteplase)
    Actilyse® Cathflo® 2mg
    (alteplase)
    GIOTRIF®
    (afatinib dimaleate)
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    (empagliflozin)
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    (dabigatran etexilate)
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    (idarucizumab)
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    (tiotropium & olodaterol)
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    (tiotropium)
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    (tiotropium)
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    (olodaterol)
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    (linagliptin)
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    UK Stroke Forum 2018: BI Symposium
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    Stroke eLearning module

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    Actilyse® (alteplase) dosing and administration poster

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    Actilyse® (alteplase) reconstitution video

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    Actilyse® (alteplase) mode of action

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Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard.
Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 0800 328 1627 (freephone).

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MORE INFORMATION ON BOEHRINGER INGELHEIM MEDICINES

Reporting adverse events

Adverse events should be reported. Reporting form and information can be found at www.mhra.gov.uk/yellowcard

Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 0800 328 1627 (freephone).

Reporting side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any side effects not listed in package leaflet.

You can also report side effects directly to the Yellow Card scheme of www.mhra.gov.uk/yellowcard

By reporting side effects you can help provide more information on the safety of the medicine.

For more information, or to access the current prescriber guides and summary of product characteristics, please visit www.medicines.org.uk/emc

NP-UK-100172 V1 – March 2019

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PC-UK-101781 date of prep July 2019