| Take a look around the novoMEDLINK™ experience. |
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| Indicated for congenital hemophilia A or B with inhibitors, congenital Factor VII deficiency, Glanzmann’s thrombasthenia with refractoriness to platelets, and acquired hemophilia. |
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| Success Speaks for Itself | Hospital Series |
| Help your hospital team stay prepared with NovoSeven® RT. |
| Explore novoMEDLINK™ for bleeding disorders tools and resources built for your hospital team. You’ll find information on treating a broad range of bleeding disorders with NovoSeven® RT. You can also access a dosing calculator for bleeding episodes, clinical pathways for emergent bleeds and acquired hemophilia, and more educational resources. |
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| All the resources you need, all in one place. |
| novoMEDLINK™ is your go-to source for bleeding disorder resources, Novo Nordisk products, educational tools, and disease state information to help patients with rare bleeding disorders and the people who treat them. |
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| Selected Important Safety Information |
| WARNING: THROMBOSIS |
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Serious arterial and venous thrombotic events following administration
of NovoSeven® RT have been reported
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Discuss the risks and explain the signs and symptoms of thrombotic and
thromboembolic events to patients who will receive
NovoSeven® RT
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Monitor patients for signs or symptoms of activation of the coagulation
system and for thrombosis
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| Warnings and Precautions |
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Serious arterial and venous thrombotic events have been reported in clinical trials
and postmarketing surveillance
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Patients with congenital hemophilia receiving concomitant treatment with aPCCs
(activated prothrombin complex concentrates), older patients particularly with
acquired hemophilia and receiving other hemostatic agents, and patients with a
history of cardiac and vascular disease may have an increased risk of developing
thrombotic events
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| Please click here or scroll below for additional Important Safety Information. |
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| novoMEDLINK™ clinical education curated for you: |
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| A Glanzmann’s Thrombasthenia Patient Regains Her Autonomy |
| Angela Kellum, a hospital pharmacist at Tulane University School of Medicine, explains how NovoSeven® RT was chosen as part of the comprehensive treatment plan for a patient with Glanzmann’s Thrombasthenia with platelet refractoriness. |
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| A Patient Shows Signs of Newly Developed Inhibitors |
| Dr. Lisa Boggio, a hematologist at Rush University, shares how and why her hospital team prescribed NovoSeven® RT for a hemophilia patient who arrived displaying signs of inhibitors. |
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| Have you created an account on novoMEDLINK™? |
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| Keep up with important information about treatments for rare bleeding disorders. |
| Receive the latest news about rare bleeding disorders from Novo Nordisk. |
| Download, order, and share educational materials for you and your patients. |
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| Indications and Usage |
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NovoSeven® RT (coagulation Factor VIIa, recombinant) is a coagulation factor
indicated for:
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Treatment of bleeding episodes and perioperative management in adults and children
with hemophilia A or B with inhibitors, congenital Factor VII (FVII)
deficiency, and Glanzmann’s thrombasthenia with refractoriness to platelet
transfusions, with or without antibodies to platelets
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Treatment of bleeding episodes and perioperative management in adults with acquired
hemophilia
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| Important Safety Information (cont’d) |
| Warnings and Precautions |
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Hypersensitivity reactions, including anaphylaxis, can occur with
NovoSeven® RT. Patients with a known hypersensitivity to mouse,
hamster, or bovine proteins may be at a higher risk of hypersensitivity reactions.
Discontinue infusion and administer appropriate treatment when hypersensitivity
reactions occur
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Factor VII deficient patients should be monitored for prothrombin time (PT) and
factor VII coagulant activity (FVII:C). If FVII:C fails to reach the expected level,
or PT is not corrected, or bleeding is not controlled after treatment with the
recommended doses, antibody formation may be suspected and analysis for antibodies
should be performed
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Laboratory coagulation parameters (PT/INR, aPTT, FVII:C) have shown no direct
correlation to achieving hemostasis
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| Adverse Reactions |
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The most common and serious adverse reactions in clinical trials are thrombotic
events. Thrombotic adverse reactions following the administration of
NovoSeven® RT in clinical trials occurred in 4% of patients with
acquired hemophilia and 0.2% of bleeding episodes in patients with congenital
hemophilia
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| Drug Interactions |
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Thrombosis may occur if NovoSeven® RT is administered
concomitantly with Coagulation Factor XIII
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Please click here for
Prescribing Information, including boxed Warning.
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NovoSeven® is a registered trademark of Novo Nordisk Health Care AG.
novoMEDLINK™ is a trademark of Novo Nordisk A/S.
Novo Nordisk is a registered trademark of Novo Nordisk A/S.
© 2022 Novo Nordisk All rights reserved. US22NSVN00038 July 2022 |
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