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Tremfya is an FDA-approved biologic medication that blocks interleukin-23 (IL-23), a protein that drives inflammation in psoriasis, psoriatic arthritis, and inflammatory bowel disease. Manufactured by Janssen (Johnson & Johnson), it is delivered as a 100mg subcutaneous injection via prefilled syringe, One-Press injector, or Tremfya Pen, and is intended for use under physician supervision.
Tremfya is indicated for adults and children 6 years and older (weighing at least 40 kg) with moderate-to-severe plaque psoriasis, active psoriatic arthritis, Crohn’s disease, and ulcerative colitis.
Tremfya works by selectively blocking IL-23, a signaling protein that triggers the inflammatory cascade behind psoriasis and related autoimmune conditions. By neutralizing IL-23 specifically, it interrupts inflammation upstream, which is why it’s classified as an interleukin inhibitor rather than a broader immunosuppressant.
The standard maintenance dose is 100mg by subcutaneous injection at Week 0, Week 4, and every 8 weeks thereafter.
Patients should be evaluated for tuberculosis and brought up to date on age-appropriate vaccinations before starting Tremfya, since it affects immune function.
The most common side effects of Tremfya include upper respiratory infections, headache, injection site reactions, joint pain, and diarrhea.
Because Tremfya affects immune response, patients should contact their care team promptly if signs of infection, fever, or allergic reaction develop.
For psoriasis and psoriatic arthritis, Tremfya is injected at Week 0, Week 4, and then every 8 weeks as ongoing maintenance. Crohn’s disease and ulcerative colitis follow a different induction schedule before settling into maintenance dosing.
Yes, adults can self-inject Tremfya using the prefilled syringe, One-Press injector, or Tremfya Pen after receiving proper training from a healthcare provider. Pediatric patients should have the injection administered by a healthcare professional or trained caregiver.
Some patients notice improvement within a few weeks, but full effect can take several months. Response time varies by condition and individual patient factors.
Yes — tuberculosis screening is required before starting Tremfya, and liver enzyme testing is recommended, particularly for Crohn’s disease and ulcerative colitis patients.
Tremfya selectively targets IL-23, distinguishing it from biologics that target TNF-alpha or IL-17, and it is the only IL-23 inhibitor approved with both subcutaneous and intravenous induction options for Crohn’s disease.
Medically reviewed. Last updated: [20/06/2026]. This content is for informational purposes and does not replace consultation with a licensed physician.
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Estimated delivery: 3–7 business days to UK. 7–10 business days to UAE, Saudi Arabia and Gulf countries. 10–15 days for USA and Asian countries.
All packages arrive in plain, unmarked brown boxes. No pharmacy name or medication details on the outside.
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