Ustekinumab Stelara (us-te-kin′u-mab)
Classification: IMMUNOMODULATOR; MONOCLONAL ANTIBODY; INTERLEUKIN-12 AND INTERLEUKIN-23 RECEPTOR ANTAGONIST
Therapeutic: IMMUNOSUPPRESSANT
ACTION & THERAPEUTIC EFFECT
A human monoclonal antibody that disrupts IL-12
and IL-23 mediated signaling and cytokine cascades. Inhibits inflammatory and immune responses
associated with plaque psoriasis thereby improving psoriasis.
Treatment of moderate to severe plaque
psoriasis.
Clinically significant hypersensitivity to ustekinumab;
active infection (e.g., active TB); live vaccines; BCG vaccines within 1 y
prior to, during, or l y following drug treatment; reversible posterior
leukoencephalopathy syndrome (RPLS).
Chronic infection or history of recurrent
infection (e.g., latent TB); prior malignancy; phototherapy; older adults;
pregnancy (category B); lactation. Safety and efficacy under 18 y not
established.
Subcutaneous 45 mg initially and 4wk later, followed by
45 mg q12wk
Subcutaneous 90 mg initially and 4 wk later, followed by
90 mg q12wk
- Solution may contain a few small translucent or
white particles. Do NOT shake.
- Note: Needle cover on prefilled syringe is
natural rubber and should not be handled by latexsensitive persons.
- When using a single-use vial, withdraw dose
using a 27 gauge syringe with a one-half inch needle.
- Rotate injection sites and do not inject into an
area that is tender, bruised, red, or irritated.
- Store unopened vials upright in refrigerator.
Discard unused portions in single-use vials.
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Nursing Implications for Ustekinumab Stelara |
CNS: Depression, dizziness, fatigue, headache. GI: Diarrhea, pharyngolaryngeal pain. Musculoskeletal: Back pain, myalgia. Respiratory: Nasopharyngitis, upper respiratory tract infection. Skin: Injection-site erythema, pruritis.
Drug: LIVE VACCINES should not be administered concurrently with
ustekinumab
therapy. Closely monitor use with narrow
therapeutic index drugs (e.g., warfarin, cyclosporine).
Peak: 7–13.5 days. Metabolism:
Degraded to smaller proteins. Half-Life: 14.9–45.6 days.
Assessment & Drug Effects
- Monitor for and promptly report S&S of TB or
other infection.
- Monitor neurologic status and report promptly:
Seizures, problems with vision, headaches, or confusion.
- Note: BCG vaccines should not be given during
treatment, for one year prior to initiating treatment, or one year following
discontinuation of treatment.
- Montior lab tests: Prior to initiation of
therapy, test for latent TB.
Patient & Family Education
- Do not accept vaccinations with live vaccines
while taking this drug. Note that non-live vaccines may not be effective if given
during a course of ustekinumab.
- You should be tested for TB prior to taking this
drug.
- Report promptly S&S of infection including:
Chills, fever, cough, shortness of breath, diarrhea, stomach or abdominal pain,
burning on urination, sores anywhere on your body, unexplained or excessive fatigue.
- Report immediately seizures, problems with
vision, headaches, or confusion.
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