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Human Immunoglobulin G side effects: what 20,354 FDA adverse event reports show

Human Immunoglobulin G · Qivigy Kthm · 1,184 reaction terms · 146,376 drug–reaction co-reports · data 2026-09-14
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Drug class

Human Immunoglobulin G

FDA label (Established Pharmacologic Class)

Brand names

Qivigy Kthm

openFDA label

Who reports

20,354 reports · 92% serious · 2,729 with death outcome · 63% female

openFDA FAERS counts, all years, deduplication not applied

Used for

QIVIGY (immune globulin intravenous, human-kthm) 10% solution is indicated for the treatment of adults with Primary Humoral Immunodeficiency (PI). This includes, but is not limited to, congenital agammaglobulinemia, common variable immunodeficiency (CVID), X-linked agammaglobulinemia, Wiskott-Aldrich syndrome, and severe combined immunodeficiencies.

FDA label, Indications and Usage

What it is

QIVIGY (immune globulin intravenous, human-kthm) is a ready-to-use, sterile, non-pyrogenic liquid solution of human immune globulin (IgG) for intravenous administration. QIVIGY is clear or slightly opalescent, colorless or pale yellow.

FDA label, Description section

Boxed warning

THROMBOSIS, RENAL DYSFUNCTION, AND ACUTE RENAL FAILURE Thrombosis may occur with immune globulin products, including QIVIGY. Risk factors may include: advanced age, prolonged immobilization, hypercoagulable condition.

FDA label
How to read this page. FAERS is a spontaneous-reporting system: counts are not incidence rates and a signal is not proof of causation. Each reaction below is run through an automated screen — is the term in the FDA label (known), in the indications (the disease being treated), an administrative/coding term, or none of these (unlabeled)? That screen is mechanical text matching, not a causality assessment. The 30 hand-written Bradford Hill assessments are on the causality assessment page. Not medical advice.

Causality screen of the 40 strongest signals

Labeled adverse reaction 2Labeled (related wording) 6Reporting / coding artifact 4Lab value / disease marker 8Not in label — unassessed 20
What the badges mean

Strongest disproportionality signals

Flagged terms (PRR ≥ 2, χ² ≥ 4, n ≥ 10), ranked by PRR; infinite PRRs (no comparator reports) excluded. The EBGM column is a second, shrinkage-based estimate (MGPS) with its 5th percentile EB05 and the BCPNN IC025; a pair flagged by PRR alone is marked PRR-only and should be read as fragile. The strata column recomputes the PRR on serious reports only (and, for the 300 most-reported drugs, adjusted for age band), and flags pairs whose reports are unusually skewed by sex or come mostly from consumers. Each row also shows the PRR against the other drugs of the same FDA class, which removes most confounding by the condition being treated, and a calibrated p-value: on validation, known non-causes average an ROR of about 2, so significance is judged against that empirical null (✓ = p < 0.05 after calibration). 1,144 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.

Show:
ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Allergy to immunoglobulin therapy44764.5
516.8–1,131.0ROR 766.2 · calibrated p 5e-15 ✓
365.8 EB05 283.8 · IC025 +5.7
3/3 methods agree
Reporting / coding artifactserious n=42 · ♀ 100% (drug 63%)no trial arm names this drug
Blood immunoglobulin g abnormal44379.0
268.1–535.9ROR 379.8 · calibrated p 4e-12 ✓
246.3 EB05 191.0 · IC025 +5.6
3/3 methods agree
Lab value / disease markerserious n=42no trial arm names this drug
Inspiratory capacity decreased74376.7
288.5–491.8ROR 378.0 · calibrated p 2e-12 ✓
256.3 EB05 210.9 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=74 · ♀ 0% (drug 63%) · 100% clinicianno trial arm names this drug
Amaurosis fugax209248.7
213.9–289.1ROR 251.2 · calibrated p 6e-11 ✓
196.1 EB05 174.8 · IC025 +6.9
3/3 methods agree
Not in label — unassessedserious n=209 · 94% clinicianno trial arm names this drug
Human antichimeric antibody positive62228.9
173.8–301.4ROR 229.6 · calibrated p 2e-10 ✓
176.6 EB05 142.7 · IC025 +5.8
3/3 methods agree
Lab value / disease markerserious n=62 · ♀ 100% (drug 63%)no trial arm names this drug
Infusion site mass184213.1
181.9–249.7ROR 215.1 · calibrated p 3e-10 ✓
173.0 EB05 153.0 · IC025 +6.7
3/3 methods agree
Not in label — unassessedserious n=178 · 70% consumerno trial arm names this drug
Infusion site discharge282202.1
178.0–229.5ROR 204.9 · calibrated p 4e-10 ✓
166.6 EB05 150.9 · IC025 +6.8
3/3 methods agree
Not in label — unassessedserious n=268 · 78% consumerno trial arm names this drug
Infusion site bruising334190.7
169.8–214.2ROR 193.9 · calibrated p 6e-10 ✓
159.1 EB05 145.3 · IC025 +6.8
3/3 methods agree
Not in label — unassessedserious n=319no trial arm names this drug
Infusion site scar65178.0
136.8–231.6ROR 178.6 · calibrated p 2e-9 ✓
145.1 EB05 117.8 · IC025 +5.7
3/3 methods agree
Not in label — unassessedserious n=60no trial arm names this drug
Ankle arthroplasty46150.5
110.4–205.1ROR 150.9 · calibrated p 1e-8 ✓
124.4 EB05 97.1 · IC025 +5.3
3/3 methods agree
Not in label — unassessedserious n=46 · ♀ 100% (drug 63%) · 100% clinicianno trial arm names this drug
Short stature31137.6
94.6–200.3ROR 137.8 · calibrated p 3e-8 ✓
112.9 EB05 83.4 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=31 · ♀ 100% (drug 63%) · 100% clinicianno trial arm names this drug
Stiff person syndrome38128.9
92.0–180.7ROR 129.2 · calibrated p 4e-8 ✓
108.3 EB05 82.4 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=38no trial arm names this drug
Coronary artery aneurysm26126.6
84.2–190.3ROR 126.7 · calibrated p 6e-8 ✓
104.2 EB05 74.7 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=25 · 100% clinicianno trial arm names this drug
Transfusion-related acute lung injury31117.5
81.0–170.3ROR 117.6 · calibrated p 9e-8 ✓
99.0 EB05 73.1 · IC025 +4.7
3/3 methods agree
Labeled adverse reaction
exact term
serious n=30 · 100% clinicianno trial arm names this drug
Blood immunoglobulin g decreased251117.4
103.1–133.7ROR 118.9 · calibrated p 3e-8 ✓
104.5 EB05 94.1 · IC025 +6.2
3/3 methods agree
Lab value / disease markerserious n=239no trial arm names this drug
Coombs direct test positive32117.3
81.3–169.1ROR 117.5 · calibrated p 9e-8 ✓
99.1 EB05 73.5 · IC025 +4.7
3/3 methods agree
Labeled adverse reaction
exact term
serious n=32 · 100% clinicianno trial arm names this drug
Blood immunoglobulin a decreased66115.3
89.4–148.7ROR 115.6 · calibrated p 6e-8 ✓
100.6 EB05 81.8 · IC025 +5.5
3/3 methods agree
Lab value / disease markerserious n=65no trial arm names this drug
Infusion site haemorrhage323113.2
101.0–126.9ROR 115.0 · calibrated p 4e-8 ✓
101.3 EB05 92.3 · IC025 +6.3
3/3 methods agree
Not in label — unassessedserious n=314no trial arm names this drug
Immunoglobulins abnormal26112.9
75.3–169.4ROR 113.1 · calibrated p 1e-7 ✓
94.8 EB05 68.0 · IC025 +4.5
3/3 methods agree
Lab value / disease markerserious n=24no trial arm names this drug
Infusion site discomfort101112.1
91.3–137.6ROR 112.7 · calibrated p 6e-8 ✓
99.1 EB05 83.9 · IC025 +5.8
3/3 methods agree
Not in label — unassessedserious n=94no trial arm names this drug
Immunoglobulins decreased129106.6
88.9–127.7ROR 107.2 · calibrated p 8e-8 ✓
95.1 EB05 82.1 · IC025 +5.8
3/3 methods agree
Lab value / disease markerserious n=129 · ♀ 84% (drug 63%)no trial arm names this drug
Joint destruction144103.7
87.4–123.0ROR 104.4 · calibrated p 1e-7 ✓
93.0 EB05 80.9 · IC025 +5.9
3/3 methods agree
Not in label — unassessedserious n=144 · ♀ 100% (drug 63%) · 94% clinicianno trial arm names this drug
Body height below normal59102.0
78.1–133.3ROR 102.3 · calibrated p 2e-7 ✓
90.1 EB05 72.4 · IC025 +5.3
3/3 methods agree
Reporting / coding artifactserious n=59 · ♀ 100% (drug 63%)no trial arm names this drug
Chronic inflammatory demyelinating polyradiculoneuropathy12598.8
82.3–118.7ROR 99.4 · calibrated p 1e-7 ✓
88.9 EB05 76.6 · IC025 +5.8
3/3 methods agree
Not in label — unassessedserious n=124no trial arm names this drug
Infusion site swelling53697.5
89.3–106.4ROR 100.1 · calibrated p 1e-7 ✓
88.7 EB05 82.6 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=511no trial arm names this drug
Device infusion issue20794.4
81.9–108.7ROR 95.3 · calibrated p 2e-7 ✓
85.7 EB05 76.3 · IC025 +5.9
3/3 methods agree
Reporting / coding artifactserious n=202 · 72% consumerno trial arm names this drug
Incorrect drug administration rate35794.3
84.7–105.0ROR 95.9 · calibrated p 2e-7 ✓
85.9 EB05 78.7 · IC025 +6.1
3/3 methods agree
Reporting / coding artifactserious n=340no trial arm names this drug
Immunisation reaction5788.5
67.5–116.0ROR 88.8 · calibrated p 4e-7 ✓
79.4 EB05 63.5 · IC025 +5.1
3/3 methods agree
Not in label — unassessedserious n=56 · ♀ 86% (drug 63%)no trial arm names this drug
Bone density increased2568.1
45.4–102.1ROR 68.2 · calibrated p 4e-6 ✓
61.0 EB05 43.5 · IC025 +4.2
3/3 methods agree
Lab value / disease markerserious n=25 · ♀ 100% (drug 63%)no trial arm names this drug
Blood immunoglobulin m decreased6166.5
51.4–86.2ROR 66.7 · calibrated p 3e-6 ✓
61.3 EB05 49.5 · IC025 +5.0
3/3 methods agree
Lab value / disease markerserious n=61no trial arm names this drug
Insurance issue90266.1
61.9–70.6ROR 69.1 · calibrated p 2e-6 ✓
62.0 EB05 58.7 · IC025 +5.8
3/3 methods agree
Not in label — unassessedserious PRR 75.8 · 71% consumerno trial arm names this drug
Death of relative2463.8
42.3–96.4ROR 63.9 · calibrated p 7e-6 ✓
57.5 EB05 40.6 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=24no trial arm names this drug
Smooth muscle cell neoplasm2462.8
41.6–94.9ROR 62.9 · calibrated p 7e-6 ✓
56.7 EB05 40.1 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=24 · ♀ 100% (drug 63%) · 100% clinicianno trial arm names this drug
Multiple allergies44861.9
56.3–68.0ROR 63.2 · calibrated p 3e-6 ✓
58.2 EB05 53.8 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=432 · ♀ 85% (drug 63%) · 78% consumerno trial arm names this drug

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Human Immunoglobulin G only as a background or rescue medication (NCT00433511, NCT00096278); no trial listing it as the tested intervention was cached, so no trial cross-check is shown.

Most frequently reported reactions

By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Off label use (used outside approved label)4,4875.3
5.2–5.4ROR 6.5 · calibrated p 0.121
5.3 EB05 5.2 · IC025 +2.4
3/3 methods agree
Reporting / coding artifactserious PRR 5.8no trial arm names this drug
Drug ineffective (drug did not work)2,4861.9
1.9–2.0ROR 2.1 · calibrated p 0.977
1.9 EB05 1.9 · IC025 +0.9Reporting / coding artifactserious PRR 3.3no trial arm names this drug
Fatigue (tiredness)2,4793.3
3.2–3.4ROR 3.6 · calibrated p 0.465
3.3 EB05 3.2 · IC025 +1.6
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.6no trial arm names this drug
Headache2,2873.7
3.6–3.9ROR 4.1 · calibrated p 0.362
3.7 EB05 3.6 · IC025 +1.8
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 4.4no trial arm names this drug
Covid-192,17012.7
12.2–13.2ROR 14.1 · calibrated p 0.009 ✓
12.5 EB05 12.1 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious PRR 13.2no trial arm names this drug
Sinusitis1,89319.2
18.4–20.0ROR 21.0 · calibrated p 0.002 ✓
18.8 EB05 18.1 · IC025 +4.2
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 22.2no trial arm names this drug
Product dose omission issue1,8566.7
6.4–7.0ROR 7.3 · calibrated p 0.089
6.7 EB05 6.4 · IC025 +2.7
3/3 methods agree
Reporting / coding artifactserious PRR 14.8no trial arm names this drug
Nausea1,6032.1
2.0–2.2ROR 2.2 · calibrated p 0.966
2.1 EB05 2.0 · IC025 +1.0Labeled adverse reaction
exact term
serious PRR 2.4no trial arm names this drug
Inappropriate schedule of product administration1,5839.2
8.8–9.7ROR 9.9 · calibrated p 0.033 ✓
9.1 EB05 8.8 · IC025 +3.1
3/3 methods agree
Reporting / coding artifactserious PRR 13.6no trial arm names this drug
Malaise (feeling unwell)1,5213.5
3.4–3.7ROR 3.8 · calibrated p 0.427
3.5 EB05 3.4 · IC025 +1.7
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.6no trial arm names this drug
Pyrexia (fever)1,4814.4
4.2–4.6ROR 4.7 · calibrated p 0.276
4.4 EB05 4.2 · IC025 +2.0
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.3no trial arm names this drug
Fall1,3644.2
4.0–4.4ROR 4.4 · calibrated p 0.306
4.2 EB05 4.0 · IC025 +2.0
3/3 methods agree
Not in label — unassessedserious PRR 3.1no trial arm names this drug
Pain1,3042.2
2.1–2.3ROR 2.2 · calibrated p 0.928
2.2 EB05 2.1 · IC025 +1.0
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 2.0 · ♀ 83% (drug 63%)no trial arm names this drug
Illness1,22712.6
12.0–13.3ROR 13.4 · calibrated p 0.011 ✓
12.5 EB05 11.9 · IC025 +3.5
3/3 methods agree
Reporting / coding artifactserious PRR 16.1no trial arm names this drug

Unlabeled candidate signals

These flagged terms were not found in the FDA label text and do not match an artifact pattern. They are the pairs that would merit a structured assessment (temporality, dose-response, biological plausibility, consistency across databases, trial or cohort evidence). The screen has not done that; string-matching misses label wording, and a strong PRR can still be stimulated reporting, co-medication, or the disease itself.

Want to assess one of these properly? The runbook describes the Bradford Hill / trial-evidence workflow used on the assessment page, and handoff_top1000_signals.csv lists the strongest unassessed pairs across all drugs.

Common questions

What are the most reported side effects of Human Immunoglobulin G?

In FDA FAERS, the most frequently co-reported reaction terms for Human Immunoglobulin G are fatigue, headache, covid-19, pneumonia, sinusitis, nausea. These are report counts, not rates: FAERS has no denominator, reporting is voluntary and uneven, and a term can be reported because of the illness being treated rather than the drug.

Does Human Immunoglobulin G have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: THROMBOSIS, RENAL DYSFUNCTION, AND ACUTE RENAL FAILURE Thrombosis may occur with immune globulin products, including QIVIGY. Risk factors may include: advanced age, prolonged immobilization, hypercoagulable condition.

Do FAERS signals prove that Human Immunoglobulin G causes these side effects?

No. A disproportionality signal (PRR, ROR) means a reaction is reported more often with this drug than with others in the database. That can reflect a real effect, but also the disease being treated, stimulated reporting after news or litigation, co-medications, or how reports are coded. Causality needs temporality, dose-response, biological plausibility, consistency across data sources and, ideally, trial or cohort evidence. This page screens each term against the FDA label and ClinicalTrials.gov results; it does not establish causation.

Sources & methods

Page generated 2026-10-14. Label and PubChem text are retrieved automatically and may lag the current label; always check the current prescribing information. OpenPV is a beta research tool of the Open Source Medicine Foundation.