Finished product reference
Interferon Gamma-1b
Injection, Solution · Parenteral · 100 µg/0.5mL
- List code
- 686
- Pharmacologic class
- Immunomodulator: recombinant interferon gamma-1b
What it is and how it works
Interferon gamma-1b is a recombinant type II interferon that activates macrophages and phagocytes, enhancing oxidative (respiratory burst) killing of microorganisms, antigen presentation and cytokine production. In osteopetrosis it is thought to enhance osteoclast superoxide production and bone resorption.
Indications
Reduction of the frequency and severity of serious infections in chronic granulomatous disease; delaying progression of severe malignant osteopetrosis.
Dosage and administration (summary)
50 micrograms/m² by subcutaneous injection three times weekly in patients with body surface area above 0.5 m² (1.5 micrograms/kg in smaller patients); dosing is supervised by a specialist.
Contraindications
Hypersensitivity to interferon gamma, closely related interferons or excipients (including E. coli-derived proteins).
Warnings and precautions
Flu-like symptoms (fever, headache, chills, myalgia) are common and may exacerbate pre-existing cardiac disease; caution in patients with seizure disorders, CNS disease or myelosuppression. Monitor blood counts, liver function and renal function periodically. Avoid concomitant myelosuppressive drugs where possible.
Pregnancy
Use only if the potential benefit justifies the potential risk.
Storage and supply
Store at 2–8 °C; do not freeze; do not shake.
Source: reference summary prepared from the EU SmPC/EPAR, BNF and WHO Model Formulary. The approved product information in Iran governs.
Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.
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