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Medical Topics
This is a common story we hear from patients. An IDF survey reports the average time it takes for diagnosis of PI is… Read More Ask a question
Kimberly Duff, R.N., B.S.N.
Answers Medical Questions
Families and PI
Let me start by saying congratulations for being an advocate on your son’s behalf. Missing school can be very difficult… Read More Ask a question
Dayna Fladhammer
Answers Family and PI Questions
Therapeutic Play
From my experience, withholding important information from children can be extremely stressful. Children can handle more… Read More Ask a question
Adina Bodolay, Certified Child Life Specialist
Answers Therapeutic Play Questions
Insurance
Depending on which state you reside in, there have been some legislative changes that impact the age category your… Read More Ask a question
Kimberly Jones, R.N.
Answers Insurance Questions
Plasma Safety
How are donors screened to ensure the safety of plasma?
All plasma donors must undergo a pre-donation selection process, including verification of good health, medical history, and risk behavior questions… Read More Ask a question
Thomas R. Kreil, Ph.D.
Answers Plasma Safety Questions
Important Risk Information for GAMMAGARD LIQUID
GAMMAGARD LIQUID is contraindicated in patients with known anaphylactic or severe hypersensitivity responses to Immune Globulin (Human). Patients with severe selective IgA deficiency (IgA < 0.05 g/L) may develop anti-IgA antibodies that can result in a severe anaphylactic reaction.
Immune Globulin Intravenous (Human) products have been reported to be associated with renal dysfunction, acute renal failure, osmotic nephrosis, and death. IGIV products should be administered at the minimum concentration available and the minimum rate of infusion practicable in at risk patients.
GAMMAGARD LIQUID is made from human plasma. It may carry a risk of transmitting infectious agents, e.g. viruses, and theoretically, the Creutzfeldt-Jakob disease (CJD) agent. Some viruses, such as B19V or hepatitis A, are particularly difficult to remove or inactivate.
GAMMAGARD LIQUID should only be administered intravenously.
Immediate anaphylactic and hypersensitivity reactions are a remote possibility.
IGIV products can contain blood group antibodies which may act as hemolysins and induce in vivo coating of red blood cells with immunoglobulin causing a positive direct antiglobulin reaction and, rarely, hemolysis. Hemolytic anemia can develop subsequent to IGIV therapy due to enhanced red blood cell sequestration.
There have been reports of noncardiogenic pulmonary edema (Transfusion Related Acute Lung Injury [TRALI]) in patients administered IGIV.
Thrombotic events have been reported in association with IGIV. The potential risks and benefits of IGIV should be weighed against those of alternative therapies.
Aseptic meningitis syndrome (AMS) has been reported to occur infrequently in association with GAMMAGARD LIQUID treatment. Discontinuation of IGIV treatment has resulted in remission of AMS within several days without sequelae.
Please see the detailed Important Risk Information and Full Prescribing Information for GAMMAGARD LIQUID [Immune Globulin Intravenous (Human)] for full prescribing details.
The PI Panel cannot respond to questions about individual medical cases, provide second opinions or make specific recommendations regarding therapy. The information our experts provide is from their own experiences. Always seek the advice of your own physician or other qualified healthcare professional regarding any medical condition. We will do our best to address as many questions as possible. We will not publish the names of any patients, physicians, or therapies.



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