Report Code: A15408 | Pages: NA | Mar 2023 | 790 Views | ||
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Pandemic disrupted the entire world and affected many industries.
Get detailed COVID-19 impact analysis on the Factor V Leiden Thrombophilia Treatment Market
Request Now !Factor V Leiden thrombophilia is a genetic disease that increases the likelihood of developing a blood clot at some point in life. Despite this, it is expected that a clot will not form in 95% of Factor V Leiden patients. When a clot does form, it usually occurs in the legs (deep venous thrombosis or DVT) or the lungs (pulmonary embolism or PE). The name Factor V Leiden refers to a specific gene mutation in the F5 gene, which is involved in the creation of blood clots following an injury. The Factor V Leiden gene mutation can be inherited in one or two copies. This disorder is sometimes misdiagnosed as Factor V deficiency, a genetic bleeding problem that can result in severe bleeding after surgery or trauma. Factor V Leiden thrombophilia may increase the risk of heart attacks, strokes, and pregnancy problems.
COVID-19 Impact Analysis:
Pharmaceutical and biotech companies together with governments globally are working to address the COVID-19 outbreak, from supporting the development of vaccines to planning for medicine supply chain challenges.
Currently, about 115 vaccine candidates and 155 molecules are in the R&D pipeline. Moreover, commonly used drugs such as Hydroxychloroquine have witnessed a dramatic surge in demand for the management of COVID-19. Such high demand for these drugs has presented huge opportunities for manufacturers of COVID-19 management drugs, as many developed countries are facing shortage of these drugs. Thus, the pharmaceutical and biotechnology industry is expected to witness a significant growth in the future owing to the demand for vaccine and treatment drugs for COVID-19. This in turn, is expected to have a significant impact on the global Factor V Leiden thrombophilia treatment market.
Top Impacting Factors:
Market Trends:
New Product Launches to Flourish Factor V Leiden Thrombophilia Market
In October 2019, Johnson & Johnson’s Xarelto was approved by the FDA to help prevent blood clots in acutely ill patients without a high risk of bleeding during and after hospitalization.Â
In December 2020, Glenmark Pharmaceuticals received a tentative approval by the United States Food and Drug Administration (USFDA) for Dabigatran Etexilate capsules in the strengths of 75 mg, 110 mg, and 150 mg. The approved product is a generic version of Boehringer Ingelheim Pharmaceuticals' Pradaxa capsules.
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Key Benefits of Report:
Questions Answered in Factor V Leiden Thrombophilia Treatment Market Report:
Factor V Leiden Thrombophilia Treatment Market Report Highlights
Aspects | Details |
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By Type of Blood Clot |
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By Diagnosis |
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By Treatment |
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By Region |
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Key Market Players | Bristol-Myers Squibb, Portola Pharmaceuticals, C. H. Boehringer Sohn, Pfizer, Roche, CoaguSense, Siemens, Alere, Abbott, Bayer Group, Johnson & Johnson, Daiichi Sankyo |
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