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interferon alfa-n3

   Also found in: Dictionary/thesaurus, Encyclopedia, Wikipedia 0.03 sec.
interferon alfa-n3,
a highly purified mixture of natural human interferon proteins that acts as a biologic response modifier, used in the treatment of venereal warts. It is administered intralesionally.

interferon [in″ter-fēr´on]
any of a family of glycoprotein biological response modifiers used as antineoplastic agents and immunoregulators; they inhibit cellular growth, alter the state of cellular differentiation, have effects on the cell cycle, interfere with oncogene expression, alter cell surface antigen expression, have effects on antibody production, and regulate cytotoxic effector cells.
interferon-α the major interferon produced by virus-induced leukocyte cultures; its primary producer cells are null cells, and its major activities are antiviral activity and activation of NK cells.
interferon alfa-2a a synthetic form of interferon-α produced by recombinant technology that acts as a biologic response modifier, used as an antineoplastic in the treatment of hairy cell leukemia and AIDS-related Kaposi's sarcoma; administered intramuscularly or subcutaneously.
interferon alfa-2b a synthetic form of interferon-α produced by recombinant technology that acts as a biologic response modifier, used in the treatment of veneral warts, hepatitis B, and chronic hepatitis C and as an antineoplastic in the treatment of hairy cell leukemia, malignant melanoma, non-Hodgkin's lymphomas, multiple myeloma, mycosis fungoides, and AIDS-related Kaposi's sarcoma; administered intramuscularly, subcutaneously, or intralesionally.
interferon alfacon-1 a synthetic interferon related to both α and β interferons, produced by recombinant DNA technology; used in the treatment of chronic hepatitis C virus infection, administered subcutaneously.
interferon alfa-n3 a highly purified mixture of natural human interferon proteins that acts as a biologic response modifier; used in the treatment of venereal warts, administered intralesionally.
interferon-β the major interferon produced by double-stranded RNA-induced fibroblast cultures; the major producer cells are fibroblasts, epithelial cells, and macrophages, and its major activity is antiviral.
interferon beta-1a a synthetic form of interferon-β produced by recombinant DNA techniques that acts as a biologic response modifier; used in the treatment of relapsing forms of multiple sclerosis; administered intramuscularly.
interferon beta-1b a synthetic modified form of interferon-β produced by recombinant DNA techniques; used as a biologic response modifier in the treatment of relapsing forms of multiple sclerosis; administered subcutaneously.
interferon-γ the major interferon produced by lymphocyte cultures that have been immunologically stimulated by mitogens or antigens; the major producer cells are T lymphocytes, and its major activity is immunoregulation.
interferon gamma-1b a synthetic form of interferon-γ produced by recombinant technology that acts as a biologic response modifier and antineoplastic. It is used to reduce the frequency and severity of serious infections associated with chronic granulomatous disease, administered subcutaneously.

interferon alfa-n3 Warning - Hazardous drug!

Alferon N

Pharmacologic class: Immunomodulator

Therapeutic class: Immunologic agent, antiviral

Pregnancy risk category C

FDA Boxed Warning

• Drug may cause or worsen fatal or life-threatening neuropsychiatric, autoimmune, ischemic, and infectious disorders. Monitor patient closely with periodic clinical and laboratory evaluations. Discontinue drug in patients with persistently severe or worsening signs or symptoms of these conditions. In many cases, these disorders resolve after withdrawal.

Action

Binds to membrane receptors on viral cells, inducing protein synthesis, inhibiting viral replication, and suppressing cell proliferation. Increases phagocytosis by macrophages, enhances expression of human leukocyte antigen, and augments lymphocyte cytotoxicity.

Availability

Injection: 5 million international units/ml

Indications and dosages

Refractory or recurring external condylomata acuminata (genital warts)

Adults ages 18 and older: 0.05 ml (250,000 international units) injected intralesionally into base of each wart twice weekly for up to 8 weeks

Contraindications

• Hypersensitivity to human interferon alfa proteins or any product component
• Anaphylactic sensitivity to mouse immunoglobulin, egg protein, or neomycin

Precautions

Use cautiously in:
• fertile males and females
• debilitated patients
• pregnant or breastfeeding patients
• children younger than age 18.

Administration

• Use 30G needle to administer intralesional injection.

RouteOnsetPeakDuration
Intrales.-Not measurable-

Adverse reactions

CNS: vasovagal reaction, fatigue, dizziness, insomnia, decreased concentration, depression, nervousness, malaise, headache

EENT: visual disturbances, nasal and sinus drainage, pharyngitis, epistaxis, throat tightness, tongue hyperesthesia

GI: increased salivation

GU: dysuria

Musculoskeletal: arthralgia, back pain, myalgia, muscle cramps

Skin: sweating, generalized pruritus, papular rash on neck, photosensitivity

Other: strange taste in mouth, fever, chills, swollen left inguinal lymph node, tingling sensation of legs and feet, hot sensation of soles, heat intolerance, hot flashes, flulike symptoms, itching and pain at injection site, hypersensitivity reactions including anaphylaxis

Interactions

Drug-diagnostic tests. White blood cells (WBCs): decreased

Patient monitoring

• Monitor WBC count.
Watch closely for hypersensitivity reactions, including anaphylaxis.

Patient teaching

• Assure patient that flulike symptoms will subside with repeated doses.
Tell patient to immediately report signs and symptoms of hypersensitivity reaction, such as hives, difficulty breathing, wheezing, and tightness in chest.
• Tell female patient to inform prescriber if she is or plans to become pregnant. Caution her not to breastfeed.
• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the tests mentioned above.



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AMEX: HEB) has initiated clinical trials as part of an accelerated evaluation of the experimental bio-therapeutic Alferon LDO (Low Dose Oral Interferon Alfa-n3 (Human Leukocyte Derived)) as a potential new experimental therapy for Avian Flu and other lethal viral diseases, which have high acute death rates.
Amex:HEB) continues the evaluation of Alferon LDO (Low Dose Oral Interferon Alfa-n3 (Human Leukocyte Derived)) as a potential therapy for Avian Flu.
AMEX: HEB) announced today that the institutional review board of Hong Kong has approved a protocol for a randomized, dose-ranging study of Alferon(R) LDO (Low Dose Oral Interferon Alfa-n3 (Human Leukocyte Derived)) in normal volunteers and/or asymtomatic subjects with exposure to a person known to have SARS or possible SARS.
 
 
 
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