Natalizumab (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Natalizumab" in English language version.

refsWebsite

Global rank English rank

33web.archive.org

1^st place

21nih.gov

4^th place

16doi.org

2^nd place

10fda.gov

447^th place

338^th place

10europa.eu

68^th place

117^th place

7semanticscholar.org

11^th place

8^th place

2medscape.com

719^th place

636^th place

2tga.gov.au

3,984^th place

2,622^nd place

1drugs.com

399^th place

333^rd place

1canada.ca

1,712^th place

1,063^rd place

1medicines.org.uk

3,823^rd place

2,387^th place

1ectrims-congress.eu

low place

1webmd.com

1,169^th place

1,075^th place

1fiercepharma.com

low place

8,921^st place

1bloomberg.com

99^th place

77^th place

1nelm.nhs.uk

low place

1healthcentral.com

low place

1medpagetoday.com

9,274^th place

5,856^th place

1boston.com

310^th place

208^th place

1nytimes.com

7^th place

1gazette.gc.ca

low place

1pmlive.com

low place

bloomberg.com

Greene RT (15 December 2008). "Biogen, Elan Report Brain Illness in Tysabri Patient". Bloomberg.com. Retrieved 21 December 2008.

boston.com

"Biogen Idec testing Tysabri as a cancer treatment". The Boston Globe. 5 September 2008. Archived from the original on 29 October 2013. Retrieved 5 September 2008.

canada.ca

health-products.canada.ca

"Tysabri Product information". Health Canada. 22 October 2009. Archived from the original on 25 August 2023. Retrieved 25 August 2023.

doi.org

Hutchinson M (June 2007). "Natalizumab: A new treatment for relapsing remitting multiple sclerosis". Therapeutics and Clinical Risk Management. 3 (2): 259–268. doi:10.2147/tcrm.2007.3.2.259. PMC 1936307. PMID 18360634.
Pucci E, Giuliani G, Solari A, Simi S, Minozzi S, Di Pietrantonj C, et al. (October 2011). "Natalizumab for relapsing remitting multiple sclerosis". The Cochrane Database of Systematic Reviews (10): CD007621. doi:10.1002/14651858.CD007621.pub2. PMID 21975773.
Van Assche G, Van Ranst M, Sciot R, Dubois B, Vermeire S, Noman M, et al. (July 2005). "Progressive multifocal leukoencephalopathy after natalizumab therapy for Crohn's disease". The New England Journal of Medicine. 353 (4): 362–368. doi:10.1056/NEJMoa051586. PMID 15947080.
Bloomgren G, Richman S, Hotermans C, Subramanyam M, Goelz S, Natarajan A, et al. (May 2012). "Risk of natalizumab-associated progressive multifocal leukoencephalopathy". The New England Journal of Medicine. 366 (20): 1870–1880. doi:10.1056/NEJMoa1107829. PMID 22591293.
Kappos L, Bates D, Edan G, Eraksoy M, Garcia-Merino A, Grigoriadis N, et al. (August 2011). "Natalizumab treatment for multiple sclerosis: updated recommendations for patient selection and monitoring". Lancet Neurology. 10 (8): 745–58. doi:10.1016/S1474-4422(11)70149-1. PMID 21777829. S2CID 15639613.
Rice GP, Hartung HP, Calabresi PA (2005). "Anti-alpha4 integrin therapy for multiple sclerosis: mechanisms and rationale". Neurology. 64 (8): 1336–42. doi:10.1212/01.WNL.0000158329.30470.D0. PMID 15851719. S2CID 39916466.
Zohren F, Toutzaris D, Klarner V, Hartung HP, Kieseier B, Haas R (2008). "The monoclonal anti-VLA4 antibody natalizumab mobilizes CD34+ hematopoietic progenitor cells in humans". Blood. 111 (7): 3893–5. doi:10.1182/blood-2007-10-120329. PMID 18235044. S2CID 206866717.
Kleinschmidt-DeMasters BK, Tyler KL (July 2005). "Progressive multifocal leukoencephalopathy complicating treatment with natalizumab and interferon beta-1a for multiple sclerosis". The New England Journal of Medicine. 353 (4): 369–374. doi:10.1056/NEJMoa051782. PMID 15947079.
Langer-Gould A, Atlas SW, Green AJ, Bollen AW, Pelletier D (July 2005). "Progressive multifocal leukoencephalopathy in a patient treated with natalizumab". The New England Journal of Medicine. 353 (4): 375–381. doi:10.1056/NEJMoa051847. PMID 15947078.
Van Assche G, Van Ranst M, Sciot R, Dubois B, Vermeire S, Noman M, et al. (July 2005). "Progressive multifocal leukoencephalopathy after natalizumab therapy for Crohn's disease". The New England Journal of Medicine. 353 (4): 362–368. doi:10.1056/NEJMoa051586. PMID 15947080.
Yousry TA, Major EO, Ryschkewitsch C, Fahle G, Fischer S, Hou J, et al. (March 2006). "Evaluation of patients treated with natalizumab for progressive multifocal leukoencephalopathy". The New England Journal of Medicine. 354 (9): 924–933. doi:10.1056/NEJMoa054693. PMC 1934511. PMID 16510746.
Berger JR (October 2006). "Natalizumab". Drugs of Today. 42 (10): 639–655. doi:10.1358/dot.2006.42.10.1042190. PMID 17136224.
Ransohoff RM (August 2007). ""Thinking without thinking" about natalizumab and PML". Journal of the Neurological Sciences. 259 (1–2): 50–52. doi:10.1016/j.jns.2006.04.011. PMID 17521672. S2CID 28808262.
Aksamit AJ (November 2006). "Review of progressive multifocal leukoencephalopathy and natalizumab". The Neurologist. 12 (6): 293–298. doi:10.1097/01.nrl.0000250948.04681.96. PMID 17122725. S2CID 25003597.
Kappos L, Bates D, Hartung HP, Havrdova E, Miller D, Polman CH, et al. (May 2007). "Natalizumab treatment for multiple sclerosis: recommendations for patient selection and monitoring". The Lancet. Neurology. 6 (5): 431–441. doi:10.1016/S1474-4422(07)70078-9. PMID 17434098. S2CID 18131415.
Fiore D (2007). "Multiple sclerosis and Natalizumab". American Journal of Therapeutics. 14 (6): 555–560. doi:10.1097/MJT.0b013e31804bfa6a. PMID 18090880. S2CID 22339176.

drugs.com

"Natalizumab (Tysabri) Use During Pregnancy". Drugs.com. 24 September 2019. Archived from the original on 23 November 2020. Retrieved 4 May 2020.

ectrims-congress.eu

onlinelibrary.ectrims-congress.eu

"Incidence of natalizumab-associated progressive multifocal leucoencephalopathy and its relationship with the pattern of natalizumab exposure over time". ECTRIMS. 10 October 2018. Archived from the original on 28 October 2021. Retrieved 18 July 2019.

europa.eu

ema.europa.eu

"Tyruko EPAR". European Medicines Agency. 28 September 2023. Archived from the original on 28 October 2023. Retrieved 6 October 2023.
"Tysabri EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 6 August 2020. Retrieved 4 May 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
"EMA confirms recommendations to minimise risk of brain infection PML with Tysabri". European Medicines Agency. 25 April 2016. Archived from the original on 23 January 2021. Retrieved 29 November 2019.
"European Medicines Agency: Committee for Medicinal Products for Human Use 24–27 April 2006" (PDF) (Press release). European Medicines Agency (EMA). 28 April 2006. Archived (PDF) from the original on 10 July 2007. Retrieved 2 April 2008.
"Tyruko: Pending EC decision". European Medicines Agency (EMA). 21 July 2023. Archived from the original on 25 August 2023. Retrieved 25 August 2023. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.

emea.europa.eu

"Meeting highlights from the Committee for Medicinal Products for Human Use" (PDF). European Medicines Agency. 22 October 2009. Archived from the original (PDF) on 27 December 2009. Retrieved 31 August 2010.
"Annex: Conditions or restrictions with regard to the safe and effective use of the medicinal product to be implemented by the member states" (PDF). European Medicines Agency. Archived from the original (PDF) on 20 August 2007. Retrieved 9 March 2008.
"EMEA concludes new advice to doctors and patients for Tysabri (natalizumab) needed" (PDF). European Medicines Agency. 20 March 2008. Retrieved 5 April 2008.^{[dead link]}
"Questions and answers on Tysabri and liver injury" (PDF). European Medicines Agency. 20 March 2008. Retrieved 14 April 2008.^{[permanent dead link]} ; lay-summary Archived 11 June 2008 at the Wayback Machine, second summary Archived 5 December 2008 at the Wayback Machine
"Refusal CHMP assessment report for natalizumab" (PDF). European Medicines Agency. 15 November 2007. Retrieved 2 April 2008.^{[permanent dead link]} "lay-summary" (PDF). Archived (PDF) from the original on 18 July 2009. Retrieved 4 April 2008. (78.5 KB)

fda.gov

"FDA Approves First Biosimilar to Treat Multiple Sclerosis". U.S. Food and Drug Administration (FDA) (Press release). 24 August 2023. Archived from the original on 25 August 2023. Retrieved 25 August 2023. This article incorporates text from this source, which is in the public domain.
U.S. Food and Drug Administration (August 2008). "Natalizumab Injection for Intraveneous {{sic}} Use (marketed as Tysabri)". U.S. Food and Drug Administration (FDA). Archived from the original on 19 December 2008. Retrieved 22 December 2008.
"FDA Drug Safety Communication: Risk of Progressive Multifocal Leukoencephalopathy (PML) with the use of Tysabri (natalizumab)". FDA. 2 May 2010. Archived from the original on 24 April 2019. Retrieved 31 August 2010.
"FDA MedWatch - 2008 Safety Information Alerts". U.S. Food and Drug Administration (FDA). 28 February 2008. Archived from the original on 25 May 2009. Retrieved 5 April 2008.
Panzara M, Francis V (1 February 2008). "Important safety information: Dear Healthcare Practitioner letter" (PDF). Biogen Idec and Élan. Archived (PDF) from the original on 12 May 2009. Retrieved 11 April 2008.; lay summary Archived 11 June 2008 at the Wayback Machine
"Errata to FDA Background document for the Tysabri (natalizumab) Advisory Committee on July 31, 2007" (PDF). U.S. Food and Drug Administration (FDA). 20 July 2007. Archived (PDF) from the original on 17 May 2017. Retrieved 9 March 2008.
"FDA Approves Tysabri to Treat Moderate-to-Severe Crohn's Disease". U.S. Food and Drug Administration (FDA). 14 January 2008. Archived from the original on 23 May 2009. Retrieved 9 March 2008.
"Biosimilar Drug Information". U.S. Food and Drug Administration (FDA). 1 November 2023. Archived from the original on 28 August 2021. Retrieved 26 November 2023.

accessdata.fda.gov

"Tyruko (natalizumab-sztn) injection, for intravenous use" (PDF). Archived (PDF) from the original on 25 August 2023. Retrieved 25 August 2023.

nctr-crs.fda.gov

"FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 October 2023.

fiercepharma.com

Staton T (26 October 2009). "Tysabri safety falls under EMEA scrutiny". Fierce Pharma. Archived from the original on 23 January 2021. Retrieved 20 November 2018.

gazette.gc.ca

"SOR/2008-101: Food and Drug Act; Regulations Amending the Food and Drug Regulations (1528—Schedule F)" (PDF). Canada Gazette Part I. 142 (8): 649. 16 April 2008. Archived (PDF) from the original on 18 August 2011. Retrieved 18 December 2010.

healthcentral.com

Gross K (3 March 2008). "Multiple Sclerosis - Natalizumab (Tysabri) Can Rarely Cause Liver Problems". Archived from the original on 7 November 2016. Retrieved 5 April 2008.

medicines.org.uk

"Tysabri 300 mg concentrate for solution for infusion - Summary of Product Characteristics (SmPC)". (emc). 14 November 2019. Archived from the original on 22 October 2020. Retrieved 4 May 2020.

medpagetoday.com

Panzara M, Francis V (1 February 2008). "Important safety information: Dear Healthcare Practitioner letter" (PDF). Biogen Idec and Élan. Archived (PDF) from the original on 12 May 2009. Retrieved 11 April 2008.; lay summary Archived 11 June 2008 at the Wayback Machine

medscape.com

Jeffrey S (5 February 2010). "PML Risk Increases With Repeated Natalizumab Infusions: FDA". Medscape. Archived from the original on 26 January 2012. Retrieved 31 August 2010.
"Questions and answers on Tysabri and liver injury" (PDF). European Medicines Agency. 20 March 2008. Retrieved 14 April 2008.^{[permanent dead link]} ; lay-summary Archived 11 June 2008 at the Wayback Machine, second summary Archived 5 December 2008 at the Wayback Machine

nelm.nhs.uk

"Questions and answers on Tysabri and liver injury" (PDF). European Medicines Agency. 20 March 2008. Retrieved 14 April 2008.^{[permanent dead link]} ; lay-summary Archived 11 June 2008 at the Wayback Machine, second summary Archived 5 December 2008 at the Wayback Machine

nih.gov

pubmed.ncbi.nlm.nih.gov

"Natalizumab: new drug. Multiple sclerosis: risky market approval". Prescrire International. 17 (93): 7–10. February 2008. PMID 18354844.
Hutchinson M (June 2007). "Natalizumab: A new treatment for relapsing remitting multiple sclerosis". Therapeutics and Clinical Risk Management. 3 (2): 259–268. doi:10.2147/tcrm.2007.3.2.259. PMC 1936307. PMID 18360634.
Pucci E, Giuliani G, Solari A, Simi S, Minozzi S, Di Pietrantonj C, et al. (October 2011). "Natalizumab for relapsing remitting multiple sclerosis". The Cochrane Database of Systematic Reviews (10): CD007621. doi:10.1002/14651858.CD007621.pub2. PMID 21975773.
Van Assche G, Van Ranst M, Sciot R, Dubois B, Vermeire S, Noman M, et al. (July 2005). "Progressive multifocal leukoencephalopathy after natalizumab therapy for Crohn's disease". The New England Journal of Medicine. 353 (4): 362–368. doi:10.1056/NEJMoa051586. PMID 15947080.
Bloomgren G, Richman S, Hotermans C, Subramanyam M, Goelz S, Natarajan A, et al. (May 2012). "Risk of natalizumab-associated progressive multifocal leukoencephalopathy". The New England Journal of Medicine. 366 (20): 1870–1880. doi:10.1056/NEJMoa1107829. PMID 22591293.
Kappos L, Bates D, Edan G, Eraksoy M, Garcia-Merino A, Grigoriadis N, et al. (August 2011). "Natalizumab treatment for multiple sclerosis: updated recommendations for patient selection and monitoring". Lancet Neurology. 10 (8): 745–58. doi:10.1016/S1474-4422(11)70149-1. PMID 21777829. S2CID 15639613.
Horga A, Horga de la Parte JF (2007). "[Natalizumab in the treatment of multiple sclerosis]". Rev Neurol (in Spanish). 45 (5): 293–303. PMID 17876741.
Rice GP, Hartung HP, Calabresi PA (2005). "Anti-alpha4 integrin therapy for multiple sclerosis: mechanisms and rationale". Neurology. 64 (8): 1336–42. doi:10.1212/01.WNL.0000158329.30470.D0. PMID 15851719. S2CID 39916466.
Zohren F, Toutzaris D, Klarner V, Hartung HP, Kieseier B, Haas R (2008). "The monoclonal anti-VLA4 antibody natalizumab mobilizes CD34+ hematopoietic progenitor cells in humans". Blood. 111 (7): 3893–5. doi:10.1182/blood-2007-10-120329. PMID 18235044. S2CID 206866717.
Kleinschmidt-DeMasters BK, Tyler KL (July 2005). "Progressive multifocal leukoencephalopathy complicating treatment with natalizumab and interferon beta-1a for multiple sclerosis". The New England Journal of Medicine. 353 (4): 369–374. doi:10.1056/NEJMoa051782. PMID 15947079.
Langer-Gould A, Atlas SW, Green AJ, Bollen AW, Pelletier D (July 2005). "Progressive multifocal leukoencephalopathy in a patient treated with natalizumab". The New England Journal of Medicine. 353 (4): 375–381. doi:10.1056/NEJMoa051847. PMID 15947078.
Van Assche G, Van Ranst M, Sciot R, Dubois B, Vermeire S, Noman M, et al. (July 2005). "Progressive multifocal leukoencephalopathy after natalizumab therapy for Crohn's disease". The New England Journal of Medicine. 353 (4): 362–368. doi:10.1056/NEJMoa051586. PMID 15947080.
Yousry TA, Major EO, Ryschkewitsch C, Fahle G, Fischer S, Hou J, et al. (March 2006). "Evaluation of patients treated with natalizumab for progressive multifocal leukoencephalopathy". The New England Journal of Medicine. 354 (9): 924–933. doi:10.1056/NEJMoa054693. PMC 1934511. PMID 16510746.
Berger JR (October 2006). "Natalizumab". Drugs of Today. 42 (10): 639–655. doi:10.1358/dot.2006.42.10.1042190. PMID 17136224.
Ransohoff RM (August 2007). ""Thinking without thinking" about natalizumab and PML". Journal of the Neurological Sciences. 259 (1–2): 50–52. doi:10.1016/j.jns.2006.04.011. PMID 17521672. S2CID 28808262.
Aksamit AJ (November 2006). "Review of progressive multifocal leukoencephalopathy and natalizumab". The Neurologist. 12 (6): 293–298. doi:10.1097/01.nrl.0000250948.04681.96. PMID 17122725. S2CID 25003597.
Kappos L, Bates D, Hartung HP, Havrdova E, Miller D, Polman CH, et al. (May 2007). "Natalizumab treatment for multiple sclerosis: recommendations for patient selection and monitoring". The Lancet. Neurology. 6 (5): 431–441. doi:10.1016/S1474-4422(07)70078-9. PMID 17434098. S2CID 18131415.
Fiore D (2007). "Multiple sclerosis and Natalizumab". American Journal of Therapeutics. 14 (6): 555–560. doi:10.1097/MJT.0b013e31804bfa6a. PMID 18090880. S2CID 22339176.

ncbi.nlm.nih.gov

Hutchinson M (June 2007). "Natalizumab: A new treatment for relapsing remitting multiple sclerosis". Therapeutics and Clinical Risk Management. 3 (2): 259–268. doi:10.2147/tcrm.2007.3.2.259. PMC 1936307. PMID 18360634.
Yousry TA, Major EO, Ryschkewitsch C, Fahle G, Fischer S, Hou J, et al. (March 2006). "Evaluation of patients treated with natalizumab for progressive multifocal leukoencephalopathy". The New England Journal of Medicine. 354 (9): 924–933. doi:10.1056/NEJMoa054693. PMC 1934511. PMID 16510746.

dailymed.nlm.nih.gov

"Tysabri- natalizumab injection". DailyMed. 12 August 2019. Archived from the original on 27 March 2020. Retrieved 4 May 2020.

nytimes.com

Pollack (9 March 2006). "F.D.A. Panel Recommends M.S. Drug Despite Lethal Risk". The New York Times. Archived from the original on 11 January 2016. Retrieved 13 March 2008.

pmlive.com

"Sandoz granted positive CHMP opinion for multiple sclerosis biosimilar". PMLive. 24 July 2023. Archived from the original on 24 July 2023. Retrieved 24 July 2023.

semanticscholar.org

api.semanticscholar.org

Kappos L, Bates D, Edan G, Eraksoy M, Garcia-Merino A, Grigoriadis N, et al. (August 2011). "Natalizumab treatment for multiple sclerosis: updated recommendations for patient selection and monitoring". Lancet Neurology. 10 (8): 745–58. doi:10.1016/S1474-4422(11)70149-1. PMID 21777829. S2CID 15639613.
Rice GP, Hartung HP, Calabresi PA (2005). "Anti-alpha4 integrin therapy for multiple sclerosis: mechanisms and rationale". Neurology. 64 (8): 1336–42. doi:10.1212/01.WNL.0000158329.30470.D0. PMID 15851719. S2CID 39916466.
Zohren F, Toutzaris D, Klarner V, Hartung HP, Kieseier B, Haas R (2008). "The monoclonal anti-VLA4 antibody natalizumab mobilizes CD34+ hematopoietic progenitor cells in humans". Blood. 111 (7): 3893–5. doi:10.1182/blood-2007-10-120329. PMID 18235044. S2CID 206866717.
Ransohoff RM (August 2007). ""Thinking without thinking" about natalizumab and PML". Journal of the Neurological Sciences. 259 (1–2): 50–52. doi:10.1016/j.jns.2006.04.011. PMID 17521672. S2CID 28808262.
Aksamit AJ (November 2006). "Review of progressive multifocal leukoencephalopathy and natalizumab". The Neurologist. 12 (6): 293–298. doi:10.1097/01.nrl.0000250948.04681.96. PMID 17122725. S2CID 25003597.
Kappos L, Bates D, Hartung HP, Havrdova E, Miller D, Polman CH, et al. (May 2007). "Natalizumab treatment for multiple sclerosis: recommendations for patient selection and monitoring". The Lancet. Neurology. 6 (5): 431–441. doi:10.1016/S1474-4422(07)70078-9. PMID 17434098. S2CID 18131415.
Fiore D (2007). "Multiple sclerosis and Natalizumab". American Journal of Therapeutics. 14 (6): 555–560. doi:10.1097/MJT.0b013e31804bfa6a. PMID 18090880. S2CID 22339176.

tga.gov.au

"Tysabri natalizumab 150 mg/1 mL injection solution pre-filled syringe (353845)". Therapeutic Goods Administration (TGA). 12 August 2022. Archived from the original on 25 August 2023. Retrieved 25 August 2023.

ebs.tga.gov.au

"Tysabri Product and Consumer Medicine Information Licence". TGA eBS. Archived from the original on 3 July 2022. Retrieved 25 August 2023.

web.archive.org

"Tyruko (natalizumab-sztn) injection, for intravenous use" (PDF). Archived (PDF) from the original on 25 August 2023. Retrieved 25 August 2023.
"Tyruko EPAR". European Medicines Agency. 28 September 2023. Archived from the original on 28 October 2023. Retrieved 6 October 2023.
"Natalizumab (Tysabri) Use During Pregnancy". Drugs.com. 24 September 2019. Archived from the original on 23 November 2020. Retrieved 4 May 2020.
"Tysabri natalizumab 150 mg/1 mL injection solution pre-filled syringe (353845)". Therapeutic Goods Administration (TGA). 12 August 2022. Archived from the original on 25 August 2023. Retrieved 25 August 2023.
"Tysabri Product and Consumer Medicine Information Licence". TGA eBS. Archived from the original on 3 July 2022. Retrieved 25 August 2023.
"Tysabri Product information". Health Canada. 22 October 2009. Archived from the original on 25 August 2023. Retrieved 25 August 2023.
"Tysabri 300 mg concentrate for solution for infusion - Summary of Product Characteristics (SmPC)". (emc). 14 November 2019. Archived from the original on 22 October 2020. Retrieved 4 May 2020.
"Tysabri- natalizumab injection". DailyMed. 12 August 2019. Archived from the original on 27 March 2020. Retrieved 4 May 2020.
"Tysabri EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 6 August 2020. Retrieved 4 May 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
"Meeting highlights from the Committee for Medicinal Products for Human Use" (PDF). European Medicines Agency. 22 October 2009. Archived from the original (PDF) on 27 December 2009. Retrieved 31 August 2010.
Jeffrey S (5 February 2010). "PML Risk Increases With Repeated Natalizumab Infusions: FDA". Medscape. Archived from the original on 26 January 2012. Retrieved 31 August 2010.
"Incidence of natalizumab-associated progressive multifocal leucoencephalopathy and its relationship with the pattern of natalizumab exposure over time". ECTRIMS. 10 October 2018. Archived from the original on 28 October 2021. Retrieved 18 July 2019.
Hitti M (1 August 2008). "MS Drug Tysabri Tied to Brain Infection". WebMD. Archived from the original on 20 November 2018. Retrieved 31 August 2010.
Staton T (26 October 2009). "Tysabri safety falls under EMEA scrutiny". Fierce Pharma. Archived from the original on 23 January 2021. Retrieved 20 November 2018.
"FDA Approves First Biosimilar to Treat Multiple Sclerosis". U.S. Food and Drug Administration (FDA) (Press release). 24 August 2023. Archived from the original on 25 August 2023. Retrieved 25 August 2023. This article incorporates text from this source, which is in the public domain.
"Annex: Conditions or restrictions with regard to the safe and effective use of the medicinal product to be implemented by the member states" (PDF). European Medicines Agency. Archived from the original (PDF) on 20 August 2007. Retrieved 9 March 2008.
U.S. Food and Drug Administration (August 2008). "Natalizumab Injection for Intraveneous {{sic}} Use (marketed as Tysabri)". U.S. Food and Drug Administration (FDA). Archived from the original on 19 December 2008. Retrieved 22 December 2008.
"FDA Drug Safety Communication: Risk of Progressive Multifocal Leukoencephalopathy (PML) with the use of Tysabri (natalizumab)". FDA. 2 May 2010. Archived from the original on 24 April 2019. Retrieved 31 August 2010.
"EMA confirms recommendations to minimise risk of brain infection PML with Tysabri". European Medicines Agency. 25 April 2016. Archived from the original on 23 January 2021. Retrieved 29 November 2019.
"FDA MedWatch - 2008 Safety Information Alerts". U.S. Food and Drug Administration (FDA). 28 February 2008. Archived from the original on 25 May 2009. Retrieved 5 April 2008.
"Questions and answers on Tysabri and liver injury" (PDF). European Medicines Agency. 20 March 2008. Retrieved 14 April 2008.^{[permanent dead link]} ; lay-summary Archived 11 June 2008 at the Wayback Machine, second summary Archived 5 December 2008 at the Wayback Machine
Gross K (3 March 2008). "Multiple Sclerosis - Natalizumab (Tysabri) Can Rarely Cause Liver Problems". Archived from the original on 7 November 2016. Retrieved 5 April 2008.
Panzara M, Francis V (1 February 2008). "Important safety information: Dear Healthcare Practitioner letter" (PDF). Biogen Idec and Élan. Archived (PDF) from the original on 12 May 2009. Retrieved 11 April 2008.; lay summary Archived 11 June 2008 at the Wayback Machine
"Biogen Idec testing Tysabri as a cancer treatment". The Boston Globe. 5 September 2008. Archived from the original on 29 October 2013. Retrieved 5 September 2008.
Pollack (9 March 2006). "F.D.A. Panel Recommends M.S. Drug Despite Lethal Risk". The New York Times. Archived from the original on 11 January 2016. Retrieved 13 March 2008.
"Errata to FDA Background document for the Tysabri (natalizumab) Advisory Committee on July 31, 2007" (PDF). U.S. Food and Drug Administration (FDA). 20 July 2007. Archived (PDF) from the original on 17 May 2017. Retrieved 9 March 2008.
"European Medicines Agency: Committee for Medicinal Products for Human Use 24–27 April 2006" (PDF) (Press release). European Medicines Agency (EMA). 28 April 2006. Archived (PDF) from the original on 10 July 2007. Retrieved 2 April 2008.
"SOR/2008-101: Food and Drug Act; Regulations Amending the Food and Drug Regulations (1528—Schedule F)" (PDF). Canada Gazette Part I. 142 (8): 649. 16 April 2008. Archived (PDF) from the original on 18 August 2011. Retrieved 18 December 2010.
"Refusal CHMP assessment report for natalizumab" (PDF). European Medicines Agency. 15 November 2007. Retrieved 2 April 2008.^{[permanent dead link]} "lay-summary" (PDF). Archived (PDF) from the original on 18 July 2009. Retrieved 4 April 2008. (78.5 KB)
"FDA Approves Tysabri to Treat Moderate-to-Severe Crohn's Disease". U.S. Food and Drug Administration (FDA). 14 January 2008. Archived from the original on 23 May 2009. Retrieved 9 March 2008.
"Tyruko: Pending EC decision". European Medicines Agency (EMA). 21 July 2023. Archived from the original on 25 August 2023. Retrieved 25 August 2023. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
"Sandoz granted positive CHMP opinion for multiple sclerosis biosimilar". PMLive. 24 July 2023. Archived from the original on 24 July 2023. Retrieved 24 July 2023.
"Biosimilar Drug Information". U.S. Food and Drug Administration (FDA). 1 November 2023. Archived from the original on 28 August 2021. Retrieved 26 November 2023.

webmd.com

Hitti M (1 August 2008). "MS Drug Tysabri Tied to Brain Infection". WebMD. Archived from the original on 20 November 2018. Retrieved 31 August 2010.