DANYELZA

Generic Name/API: naxitamab-gqgk

Manufacturer: Y-mAbs Therapeutics, Inc

Dosage Forms & Strength:
Injection: 40 mg/10 mL (4 mg/mL) in a single-dose vial.

Storage:
Store DANYELZA vial refrigerated at 2°C to 8°C (36°F to 46°F) in the outer carton to protect from light until time
of use.

  • INDICATION
  • IMPORTANT SAFETY INFORMATION

INDICATIONS
WHAT IS DANYELZA?
DANYELZA is a prescription medicine used in combination with a medicine called granulocyte-macrophage colony-stimulating factor (GM-CSF) to treat children 1-year of age and older and adults with high-risk neuroblastoma in the bone or bone marrow that:

has come back (relapsed) or that did not respond to previous treatment (refractory), and
has shown a partial response, minor response, or stable disease to prior therapy.
DANYELZA is approved based on two clinical studies that looked at reducing tumor size. DANYELZA is still being studied to confirm the study results and the clinical benefit of treatment.

IMPORTANT SAFETY INFORMATION
What is the most important information I should know about DANYELZA?
DANYELZA may cause serious side effects, including:
Serious infusion-related reactions. DANYELZA can cause serious infusion-related reactions that require immediate medical attention. Infusion-related reactions are common with DANYELZA. Tell your healthcare provider right away if you get any signs or symptoms during or after your DANYELZA infusion, including:

swelling of your face, eyes, lips, mouth, or tongue
itching
redness on your face (flushing)
skin rash or hives
trouble breathing
cough or wheezing
noisy high-pitched breathing
feeling faint or dizziness (low blood pressure)

Nervous system problems. Talk to your healthcare provider right away if you have new symptoms or worsening of nervous system problems, including:
Severe pain from nerves (neuropathic pain), including pain in the belly (abdomen), bone, neck, legs, or arms. Pain is common with DANYELZA and can be severe.
Inflammation of the spinal cord. Signs or symptoms may include:
weakness in your legs or arms
bladder and bowel problems
pain in back, legs, or stomach (abdomen)
numbness
tingling
burning sensation
Reversible Posterior Leukoencephalopathy Syndrome (RPLS – also known as Posterior Reversible Encephalopathy Syndrome – PRES). PRES is a condition that affects the brain. Your healthcare provider will monitor your blood pressure and check for any neurologic symptoms after your DANYELZA infusion. Signs or symptoms of PRES may include:
severe headache
vision changes
changes in mental status, such as confusion, disorientation, or decreased alertness
difficulty speaking
weakness in your arms or legs
seizures
Numbness, tingling, or burning sensation in the arms or legs.
Nervous system problems of the eye. Signs or symptoms may include:
unequal pupil size
blurred vision
trouble focusing your eyes
larger pupil size (dilated)
decreased ability to see
sensitivity to light
Problems urinating or emptying your bladder (prolonged urinary retention).
Do not receive DANYELZA if you have had a severe allergic reaction to naxitamab-gqgk (the active ingredient in DANYELZA). Ask your healthcare provider if you are not sure.

Before receiving DANYELZA, tell your healthcare provider about all your medical conditions, including if you:

have high blood pressure
are pregnant or plan to become pregnant. DANYELZA may harm your unborn baby.
Your healthcare provider will do a pregnancy test before you start treatment with DANYELZA.
Females who are able to become pregnant should use effective birth control (contraception) during treatment and for 2 months after your last dose of DANYELZA. Talk to your healthcare provider about birth control choices that may be right for you during this time.
Tell your healthcare provider right away if you become pregnant or think you might be pregnant during treatment with DANYELZA.
are breastfeeding or plan to breastfeed. It is not known if DANYELZA passes into your breast milk. Do not breastfeed during treatment and for 2 months after your last dose of DANYELZA.
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

What are the possible side effects of DANYELZA?
DANYELZA may cause serious side effects, including:
See “What is the most important information I should know about DANYELZA?”
High blood pressure (hypertension). High blood pressure is common in people who receive DANYELZA. Your blood pressure will be monitored during your DANYELZA infusion, and at least each day on Days 1 to 8 of each DANYELZA treatment cycle. Tell your healthcare provider right away if you get any signs or symptoms of high blood pressure, including:
headaches
seizures
nausea or vomiting
chest pain
dizziness
visual changes
shortness of breath
feeling that your heart is pounding or racing (palpitations)
nose bleeds
The most common side effects of DANYELZA include:
fast heart rate
vomiting
cough
nausea
decreased white blood cell, red blood cell, and platelet counts
diarrhea
decreased appetite
tiredness
skin rashes
decreased level of potassium, sodium, and phosphate in the blood
hives
fever
headache
injection site reaction
swelling of the body or only in one part of the body
anxiety
irritability
increased liver function blood tests
decreased blood sugar level
decreased calcium levels in the blood
decreased protein levels (albumin) in the blood

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