Inducing Remission in GPA & MPA Patients | Rituxan® GPA & MPA

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Inducing Remission in GPA & MPA Patients | Rituxan® GPA & MPA | HCP

www.rituxan-hcp.com/

Find information for healthcare professionals about Rituxan® (rituximab), the only FDA-approved treatment proven to induce remission in patients with GPA ...

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Where is www.rituxan-hcp.com hosted?

Country:

United States

City:

South San Francisco

Registrar:

SafeNames Ltd

Latitude:

37.65

Longitude:

-122.42

IP address:

72.34.128.84

IP Binary address:

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IP Octal address:

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IP Hexadecimal address:

48228054

Context analysis of rituxan-hcp.com

Number of letters on this page:

20 866

Number of words on this page:

3 662

Number of sentences on this page:

160

Average words per sentences on this page:

23

Number of syllables on this page:

7 387

Number of Strong texts:

74

Domain name architecture

Domain name length:

15

Hyphens:

Domain contain 1 hyphens!

Domain name with Hindi letters:

र इ ट उ ख़ अ ञ - (h) च प . च ओ म

Domain name with Hebrew letters:

ר (i) ת (u) כס (a) נ - ה ק(c) פּ . ק(c) (ο) מ

Domain name with Cyrillic letters:

р и т у ξ a н - х ц п . ц о м

Domain name with Arabic letters:

ر (i) ت (u) (x) ا ن - ح (c) (p) . (c) (o) م

Domain name with Greek letters:

ρ ι τ υ ξ α ν - (h) χ π . χ ο μ

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艾儿艾提伊吾艾克斯诶艾娜 - 艾尺西屁 . 西哦艾马

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rtxn-hcp.cm

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iuxa-.o

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r¹⁸ i⁹ t²⁰ u²¹ x²⁴ a¹ n¹⁴ h⁸ c³ p¹⁶ . c³ o¹⁵ m¹³

Domain name pattern:
V: Vowel, C: Consonant, N: Number

C V C V C V C C C C . C V C

<HEAD> DATA INFORMATION

Encoding:

utf-8

keywords:

Rituxan, rituximab, rheumatoid arthritis treatment, ra treatment, ra medication, rheumatoid arthritis infusion treatment, rheumatoid arthritis symptoms, ra symptoms

description:

Find information for healthcare professionals about Rituxan® (rituximab), the only FDA-approved treatment proven to induce remission in patients with GPA and MPA. INDICATION STATEMENT - Rituxan® (rituximab), in combination with glucocorticoids, is indicated for the treatment of adult patients with Granulomatosis with Polyangiitis (GPA) (Wegener’s Granulomatosis) and Microscopic Polyangiitis (MPA) - Limitations of Use: Rituxan is not recommended for use in patients with severe, active infections BOXED WARNINGS and Additional Important Safety Information BOXED WARNINGS Infusion Reactions: Rituxan administration can result in serious, including fatal, infusion reactions. Deaths within 24 hours of Rituxan infusion have occurred. Approximately 80% of fatal infusion reactions occurred in association with the first infusion. Monitor patients closely. Discontinue Rituxan infusion for severe reactions and provide medical treatment for Grade 3 or 4 infusion reactions. Severe Mucocutaneous Reactions: Severe, including fatal, mucocutaneous reactions can occur in patients receiving Rituxan. Hepatitis B Virus (HBV) Reactivation: HBV reactivation can occur in patients treated with Rituxan, in some cases resulting in fulminant hepatitis, hepatic failure, and death. Screen all patients for HBV infection before treatment initiation, and monitor patients during and after treatment with Rituxan. Discontinue Rituxan and concomitant medications in the event of HBV reactivation. Progressive Multifocal Leukoencephalopathy (PML): PML, including fatal PML, can occur in patients receiving Rituxan. Warnings and Precautions Rituxan administration can also result in additional serious, including fatal, adverse reactions including: - Tumor lysis syndrome (TLS): Administer aggressive intravenous hydration, anti‑hyperuricemic agents, monitor renal function - Infections: Withhold Rituxan and institute appropriate anti-infective therapy - Cardiac arrhythmias and angina: Discontinue infusions in case of serious or life-threatening events - Bowel obstruction and perforation: Consider and evaluate for abdominal pain, vomiting, or related symptoms - Live virus vaccines: Do not administer live virus vaccines prior to or during Rituxan - Cytopenias: Monitor blood counts at regular intervals Granulomatosis With Polyangiitis (GPA) (Wegener’s Granulomatosis) and Microscopic Polyangiitis (MPA) - Use of concomitant immunosuppressants other than corticosteroids has not been studied in GPA or MPA patients exhibiting peripheral B-cell depletion following treatment with Rituxan. Observe patients with GPA and MPA closely for signs of infection if immunosuppressants other than corticosteroids are used concomitantly - The safety and efficacy of retreatment with Rituxan have not been established in patients with GPA and MPA - Common adverse reactions (≥15%) in the clinical study were infections, nausea, diarrhea, headache, muscle spasms, anemia, and peripheral edema. Other important adverse reactions include infusion reactions You may report side effects to the FDA at (800) FDA-1088 or www.fda.gov/medwatch. You may also report side effects to Genentech at (888) 835-2555. For additional safety information, please see the Rituxan full prescribing information, including BOXED WARNINGS.

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External links in rituxan-hcp.com

https://www.gene.com/download/pdf/rituxan_prescribing.pdf
http://www.rituxanforgpampa.com
http://rituxanforra-hcp.com
http://rituxanforGPAMPA.com
http://www.fda.gov/medwatch
http://www.gene.com/gene/privacy.html
http://www.gene.com/terms-conditions
https://www.gene.com/contact-us
https://www.biogen.com/en_us/about-biogen/contact.html?ID=5973
http://www.gene.com/
https://www.biogen.com/

Possible email addresses for rituxan-hcp.com

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email@rituxan-hcp.com
support@rituxan-hcp.com
contact@rituxan-hcp.com
admin@rituxan-hcp.com
postmaster@rituxan-hcp.com
hostmaster@rituxan-hcp.com
domain@rituxan-hcp.com
abuse@rituxan-hcp.com

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