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Interferon gamma

Generic Medicine Info
Indications and Dosage
Subcutaneous
Chronic granulomatous disease, Malignant osteopetrosis
Adult: Patients with BSA >0.5 m2: 50 mcg/m2 (1 million units/m2) 3 times weekly. Patients with BSA ≤0.5 m2: 1.5 mcg/kg 3 times weekly.
Elderly: Initiate at the lower end of the dosing range.
Child: Same as adult dose. Dose recommendation may vary between countries (refer to local guidelines).
Contraindications
Hypersensitivity to interferon gamma, products derived from Escherichia coli.
Special Precautions
Patient with myelosuppression, history of seizure disorder or compromised CNS function, pre-existing CV disease (e.g. ischaemia, heart failure, arrhythmia), seizure disorder. Severe renal and hepatic impairment. Children and elderly. Pregnancy and lactation.
Adverse Reactions
Significant: Dose-related reversible neutropenia and thrombocytopenia, neurologic disorders (e.g. dizziness, decreased mental status, gait disturbances), flu-like symptoms (e.g. fever, headache, chills, myalgia, fatigue), increased AST and/or ALT, acute serious hypersensitivity reactions, transient cutaneous rashes, renal toxicity, risk of drug accumulation (particularly in severe renal and hepatic impairment).
Gastrointestinal disorders: Nausea, vomiting, diarrhoea, abdominal pain.
General disorders and administration site conditions: Inj site pain, erythema, tenderness.
Musculoskeletal and connective tissue disorders: Arthralgia, back pain.
Psychiatric disorders: Depression.
Patient Counseling Information
This drug may cause fatigue, convulsion, confusion, disorientation or hallucination, if affected, do not drive or operate machinery.
Monitoring Parameters
Monitor CBC with differential, platelet count, LFTs, electrolytes, BUN, creatinine, and urinalysis before treatment and every 3 months thereafter.
Drug Interactions
Increased risk for unexpected amplified immune response with other heterologous serum protein or immunological preparations (e.g. vaccines). May prolong the half-lives of drugs that are metabolised by CYP450 system. May increase toxicity with drugs that have neurotoxic, haematotoxic, myelosuppressive, or cardiotoxic effects.
Action
Description:
Overview: Interferon gamma, a biosynthetic form of endogenous human interferon gamma, is a cytokine with antiviral and immunomodulating effects.
Mechanism of Action: Interferon gamma increases macrophage cytotoxicity by enhancing the respiratory burst via generation of toxic oxygen metabolites, which mediate the killing of intracellular microorganisms. It increases HLA-DR expression and augments Fc receptors expression, thereby causing an increased antibody-dependent cell mediated cytotoxicity. However, the exact mechanism of action remains unknown.
Synonym(s): Interferon gamma-1b.
Pharmacodynamics: Studies have demonstrated an increase on oxidative capacity of cells in patients with chronic granulomatous disease, which suggests increased superoxide production, leading to enhanced microbial killing and reduced risk of serious infections. In patients with severe malignant osteoporosis, interferon gamma-1b has been shown to enhance phagocytic superoxide production and osteoclast function in vivo. Additionally, in vitro studies have demonstrated a threefold increase in superoxide generation in osteoclasts from affected patients compared with minimal changes in healthy cells. In both disorders, the exact mechanism has not been clearly established.
Pharmacokinetics:
Absorption: Time to peak plasma concentration: Approx 7 hours (SC).
Excretion: Elimination half-life: Approx 6 hours (SC).
Storage
Intact vial: Store between 2-8°C. Do not freeze. Discard if intact vial is left at room temperature for >12 hours before use.
MIMS Class
Cancer Immunotherapy / Disease-Modifying Anti-Rheumatic Drugs (DMARDs)
ATC Classification
L03AB03 - interferon gamma ; Belongs to the class of interferons. Used as immunostimulants.
References
Actimmune Injection, Solution (Horizon Therapeutics USA, Inc.). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed. Accessed 10/10/2025.

Brayfield A, Cadart C (eds). Interferon Gamma. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 10/10/2025.

Immukin 2 x 10^6 IU (0.1 mg) Solution for Injection (Clinigen Healthcare Limited). MHRA. https://products.mhra.gov.uk. Accessed 10/10/2025.

Interferon Gamma-1b. Gold Standard Drug Database in ClinicalKey [online]. Elsevier Inc. https://www.clinicalkey.com. Accessed 10/10/2025.

Interferon Gamma-1b. UpToDate Lexidrug, Lexi-Drugs Multinational Online. Waltham, MA. UpToDate, Inc. https://online.lexi.com. Accessed 10/10/2025.

Interferon Gamma. UpToDate Lexidrug, AHFS DI (Adult and Pediatric) Online. American Society of Health-System Pharmacists, Inc. Waltham, MA. UpToDate, Inc. https://online.lexi.com. Accessed 10/10/2025.

Joint Formulary Committee. Interferon Gamma-1b. British National Formulary [online]. London. BMJ Group and Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 10/10/2025.

Paediatric Formulary Committee. Interferon Gamma-1b. BNF for Children [online]. London. BMJ Group, Pharmaceutical Press, and RCPCH Publications. https://www.medicinescomplete.com. Accessed 20/11/2025.

Disclaimer: This information is independently developed by MIMS based on Interferon gamma from various references and is provided for your reference only. Therapeutic uses, prescribing information and product availability may vary between countries. Please refer to MIMS Product Monographs for specific and locally approved prescribing information. Although great effort has been made to ensure content accuracy, MIMS shall not be held responsible or liable for any claims or damages arising from the use or misuse of the information contained herein, its contents or omissions, or otherwise. Copyright © 2025 MIMS. All rights reserved. Powered by MIMS.com
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