Inebilizumab-cdon

From WikiMD's Food, Medicine & Wellness Encyclopedia

What is inebilizumab-cdon?[edit | edit source]



What are the uses of this medicine?[edit | edit source]

How does this medicine work?[edit | edit source]

The precise mechanism by which inebilizumab-cdon exerts its therapeutic effects in NMOSD is unknown but is presumed to involve binding to CD19, a cell surface antigen presents on pre-B and mature B lymphocytes. Following cell surface binding to B lymphocytes, inebilizumab-cdon results in antibody-dependent cellular cytolysis.

Who Should Not Use this medicine ?[edit | edit source]

This medicine cannot be used in patients if:

  • had a life-threatening infusion reaction to UPLIZNA.
  • an active hepatitis B virus infection.
  • active or untreated inactive (latent) tuberculosis.

What drug interactions can this medicine cause?[edit | edit source]

Is this medicine FDA approved?[edit | edit source]

  • It was approved for use in the United States in 2020.

How should this medicine be used?[edit | edit source]

  • Prior to initiating UPLIZNA, perform Hepatitis B virus (HBV) screening. UPLIZNA is contraindicated in patients with active HBV .
  • Prior to initiating UPLIZNA, evaluate for active tuberculosis and test for latent infection.
  • Administer all immunizations according to immunization guidelines at least 4 weeks prior to initiation of UPLIZNA for live or live-attenuated vaccines.
  • Prior to every infusion of UPLIZNA, determine whether there is an active infection. In case of active infection, delay infusion of UPLIZNA until the infection resolves
  • Premedicate with a corticosteroid, an antihistamine, and an antipyretic.
  • UPLIZNA must be diluted in 250 mL of 0.9% Sodium Chloride Injection, USP prior to administration.

The recommended dose is:

  • Initial dose: 300 mg intravenous infusion followed two weeks later by a second 300 mg intravenous infusion
  • Subsequent doses (starting 6 months from the first infusion): single 300 mg intravenous infusion every 6 months

Administration

  • UPLIZNA is given through a needle placed in a vein (IV or intravenous infusion) in your arm.
  • Before treatment with UPLIZNA, your healthcare provider will give you a corticosteroid medicine, an antihistamine, and a fever prevention medicine to help infusion reactions become less frequent and less severe. See “What is the most important information I should know about UPLIZNA?”
  • Your first dose of UPLIZNA will be given as 2 separate infusions, 2 weeks apart.
  • Your next doses of UPLIZNA will be given as one infusion every 6 months.
  • Each infusion will last about 1 hour and 30 minutes. After each infusion, you will be monitored by a healthcare provider for at least 1 hour.

What are the dosage forms and brand names of this medicine?[edit | edit source]

This medicine is available in fallowing doasage form:

  • As Injection: 100 mg/10 mL (10 mg/mL) solution in a single-dose vial

This medicine is available in fallowing brand namesː

  • UPLIZNA

What side effects can this medication cause?[edit | edit source]

Common possible side effects of this medicine include:

  • urinary tract infection
  • arthralgia
  • Headache
  • Back pain

UPLIZNA can cause serious side effects, including:

  • Infusion reactions
  • Hepatitis B virus (HBV) reactivation
  • Progressive Multifocal Leukoencephalopathy (PML)

What special precautions should I follow?[edit | edit source]

  • UPLIZNA can cause infusion reactions, which can include headache, nausea, somnolence, dyspnea, fever, myalgia, rash, or other signs or symptoms.
  • Administer pre-medication with a corticosteroid, an antihistamine, and an anti-pyretic.
  • Management recommendations for infusion reactions depend on the type and severity of the reaction. For life-threatening infusion reactions, immediately and permanently stop UPLIZNA and administer appropriate supportive treatment. For less severe infusion reactions, management may involve temporarily stopping the infusion, reducing the infusion rate, and/or administering symptomatic treatment.
  • Delay UPLIZNA administration in patients with an active infection until the infection is resolved.
  • Vaccination with live-attenuated or live vaccines is not recommended during treatment and after discontinuation, until B-cell repletion.
  • Monitor the level of immunoglobulins at the beginning, during, and after discontinuation of treatment with UPLIZNA until B-cell repletion. Consider discontinuing UPLIZNA if a patient develops a serious opportunistic infection or recurrent infections if immunoglobulin levels indicate immune compromise.
  • Advise females of reproductive potential of the potential risk to a fetus and to use an effective method of contraception during treatment and for 6 months after stopping UPLIZNA.

What to do in case of emergency/overdose?[edit | edit source]

  • In case of overdose, call the poison control helpline of your country. In the United States, call 1-800-222-1222.

Can this medicine be used in pregnancy?[edit | edit source]

  • There are no adequate data on the developmental risk associated with the use of UPLIZNA in pregnant women.

Can this medicine be used in children?[edit | edit source]

  • Safety and effectiveness in pediatric patients have not been established.

What should I know about storage and disposal of this medication?[edit | edit source]

  • Store in a refrigerator at 2°C to 8°C (36°F to 46°F) in original carton to protect from light.
  • Do not freeze.
  • Do not shake.
  • Store vials upright.


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