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HYQVIA
Immune Globulin Infusion (human) 10% With Recombinant Human Hyaluronidase
$383.00
2.5G/25ML · 1 syringes
BrandBranded medicine· By Takeda
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2.5G/25ML
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FDA boxed warningThrombosis
Thrombosis may occur with immune globulin products, including HYQVIA. Risk factors may include advanced age, prolonged immobilization, hypercoagulable conditions, history of venous or arterial thrombosis, use of estrogens, indwelling vascular catheters, hyperviscosity and cardiovascular risk factors. Thrombosis may occur in the absence of known risk factors.
For patients at risk of thrombosis, administer HYQVIA at the minimum dose and infusion rate practicable. Ensure adequate hydration in patients before administration.
Monitor for signs and symptoms of thrombosis and assess blood viscosity in patients at risk of hyperviscosity.
About HYQVIA
Overview
HYQVIA combines human immune globulin with recombinant human hyaluronidase. It is used to treat primary immunodeficiency in adults and children aged two years and older, and as maintenance therapy for adults with chronic inflammatory demyelinating polyneuropathy (CIDP). The immune globulin supplies antibodies against bacteria and viruses, while hyaluronidase helps it spread and be absorbed under the skin; how immune globulin works in CIDP is not fully understood.
What it treats
- Primary immunodeficiency (PI) in adults and children aged 2 years and older. - Maintenance treatment of chronic inflammatory demyelinating polyneuropathy (CIDP) in adults.
Safety information
Side effects
Common side effects include reactions at the infusion site, headache, tiredness, nausea and fever. Vomiting was also common in patients treated for primary immunodeficiency (PI). Redness and itching were also common in patients treated for chronic inflammatory demyelinating polyneuropathy (CIDP). Contact a doctor immediately for a severe allergic reaction, a blood clot, aseptic meningitis (inflammation around the brain and spinal cord), breakdown of red blood cells that may cause anemia, or an acute lung injury related to treatment. People with IgA deficiency who have antibodies against IgA have a greater risk of severe allergic reactions, including anaphylaxis. Treatment must be stopped if symptoms of aseptic meningitis appear. Antibodies against the recombinant human hyaluronidase component can develop and were common in patients treated for PI. These may react with the body’s own hyaluronidase; their clinical significance and possible effects on human fertilization are unknown. Infusion into or around an infected area can spread the infection. HYQVIA may also carry a risk of transmitting infectious agents, including viruses and agents associated with variant Creutzfeldt-Jakob disease and, theoretically, Creutzfeldt-Jakob disease.
FDA boxed warning
Thrombosis
Thrombosis may occur with immune globulin products, including HYQVIA. Risk factors may include advanced age, prolonged immobilization, hypercoagulable conditions, history of venous or arterial thrombosis, use of estrogens, indwelling vascular catheters, hyperviscosity and cardiovascular risk factors. Thrombosis may occur in the absence of known risk factors.
For patients at risk of thrombosis, administer HYQVIA at the minimum dose and infusion rate practicable. Ensure adequate hydration in patients before administration.
Monitor for signs and symptoms of thrombosis and assess blood viscosity in patients at risk of hyperviscosity.
A boxed warning is the strongest warning the US Food and Drug Administration requires on a medicine label. Text is taken from the official label, with internal section references removed.
Before taking this medicine
Do not use HYQVIA if you have: • A history of anaphylaxis or a severe whole-body allergic reaction to human immune globulin (IgG). • IgA deficiency with antibodies against IgA and a history of allergic reactions. • A known whole-body allergic reaction to hyaluronidase, including the recombinant human hyaluronidase in HYQVIA, or to human albumin in the hyaluronidase solution. Special caution is needed if you are over 65 or at risk of kidney problems. People with IgA deficiency and anti-IgA antibodies have a greater risk of severe allergic reactions, including anaphylaxis. HYQVIA can cause blood clots, aseptic meningitis, red blood cell breakdown and acute lung injury. Monitoring for signs of red blood cell breakdown and lung reactions is needed. Treatment should be stopped if symptoms of aseptic meningitis appear. Infusion into or around an infected area can spread the infection. Antibodies to recombinant human hyaluronidase may develop and could react with the body’s own hyaluronidase. Whether this affects fertilization in humans is unknown, and the clinical significance is unclear. HYQVIA may carry a risk of transmitting infectious agents, including viruses and the agents associated with variant Creutzfeldt-Jakob disease and, theoretically, Creutzfeldt-Jakob disease.
Interactions
HYQVIA can temporarily reduce the immune response to live virus vaccines. This may last up to 6 months for mumps, rubella and varicella (chickenpox) vaccines, and a year or more for measles vaccines. Tell your doctor if you are planning any live virus vaccinations. HYQVIA components must not be mixed or administered with other products. Mixing HYQVIA with other drug solutions has not been evaluated.
Using HYQVIA
Dosing
Dosing is set by your prescriber. Each health care professional may prescribe medication differently according to a patient's medical history and condition, so follow the directions on your prescription label and speak to your doctor or pharmacist before changing anything.
Storage
Store in the original carton to protect it from light. Check the pack for whether it must be refrigerated before first use. Keep all medicines out of the sight and reach of children.
Clinical information on this page is summarised from the US FDA label HYQVIA (IMMUNE GLOBULIN INFUSION (HUMAN), 10% WITH RECOMBINANT HUMAN HYALURONIDASE) KIT [TAKEDA PHARMACEUTICALS AMERICA, INC.] (DailyMed, retrieved 21 September 2026).
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