Moderate-to-severe plaque psoriasis in patients who are candidates for phototherapy or systemic therapy.
Binds to the p19 protein subunit of the interleukin (IL)-23 cytokine to prevent its interaction with the IL-23 receptor. This cytokine is normally involved in inflammatory and immune responses. Binding to interleukins antagonizes their effects, inhibiting the release of proinflammatory cytokines and chemokines.
Decrease in area and severity of psoriatic lesions.
Absorption: 49% absorbed following subcutaneous administration.
Distribution: Well distributed to tissues.
Metabolism and Excretion: Broken down by catabolic processes into peptides and amino acids.
Half-life: 15–18 days
TIME/ACTION PROFILE (plasma concentrations)
|Subcut||unknown||5.5 days||8 wk|
- Active, untreated infection.
Use Cautiously in:
- History of tuberculosis (possibility of reactivation);
- OB: Use only if potential maternal benefit justifies potential risk to fetus;
- Lactation: Safety not established;
- Pedi: Safety and effectiveness not established.
Exercise Extreme Caution in:
Chronic infection or history of recurrent infection.
Adverse Reactions/Side Effects
GI: diarrhea, ↑ liver enzymes
Local: injection site reactions
* CAPITALS indicate life-threatening.
Underline indicate most frequent.
- May ↓ antibody response to and ↑ risk of adverse reactions from live vaccines; avoid use during therapy.
- May affect the activity of CYP450 drug-metabolizing enzymes; appropriate monitoring and dose adjustment should be carried out when treatment is started in patients receiving concurrent treatment with CYP450 substrate, especially those with a narrow therapeutic index, including warfarin and cyclosporine.
SC (Adults) 100 mg initially and 4 wk later, then 100 mg every 8 wk.
Solution for subcutaneous injection: 100 mg/mL in prefilled syringes and patient-controlled injectors
- Assess affected area(s) prior to and periodically during therapy.
- Assess patient for latent tuberculosis with a tuberculin skin test prior to initiation of therapy. Treatment of latent tuberculosis should be started before therapy with guselkumab.
- Assess for signs of infection (fever, dyspnea, flu-like symptoms, frequent or painful urination, redness or swelling at the site of a wound), including tuberculosis, prior to injection. Monitor new infections closely; most common are upper respiratory tract infections, bronchitis, and urinary tract infections.
Lab Test Considerations:
May cause ↑ liver enzymes.
- Impaired skin integrity (Indications)
- Update immunizations to current prior to initiating therapy. Patients on guselkumab may receive concurrent vaccinations, except for live vaccines.
- SC Allow syringe and solution to reach room temperature, for 30 min before injecting. Solution is clear and colorless to light yellow solution and may contain small translucent particles; do not administer solutions that are cloudy, discolored or contain large particles. Store solution in refrigerator in original carton to protect from light; do not shake or freeze. Inject full amount (1 mL) of One Press injector in front of thigh, abdomen, or upper arm. Avoid areas that are tender, bruised, red, hard, thick, scaly, or affected by psoriasis.
- Instruct patient on correct technique for self-injection, care and disposal of equipment. Review Medication Guide with patient before starting therapy and with each injection.
- Advise patient to notify health care professional if signs and symptoms of infection (fever, chills, sore throat, painful urination) occur.
- Instruct patient to avoid receiving live vaccines during therapy.
- Instruct patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and consult health care professional before taking any new medications.
- Instruct patient to notify health care professional of medication regimen prior to treatment or surgery.
- Advise female patient to notify health care professional if pregnancy is planned or suspected or if breast feeding.
Decrease in extent and severity of psoriatic lesions.
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