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Drug · FAERS side-effect profile with label screen

Insulin Human side effects: what 39,515 FDA adverse event reports show

Insulin Human · Afrezza · 1,209 reaction terms · 146,609 drug–reaction co-reports · data 2026-09-14
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Drug class

Insulin

FDA label (Established Pharmacologic Class)

Brand names

Afrezza

openFDA label

Who reports

39,515 reports · 60% serious · 2,907 with death outcome · 56% female

openFDA FAERS counts, all years, deduplication not applied

Used for

AFREZZA ® is indicated to improve glycemic control in adult and pediatric patients 6 years of age and older with diabetes mellitus. AFREZZA ® is a rapid acting inhaled human insulin indicated to improve glycemic control in adult and pediatric patients 6 years of age and older with diabetes mellitus.

FDA label, Indications and Usage

What it is

11.1 AFREZZA Cartridges Human insulin is a rapid acting human insulin produced by recombinant DNA technology utilizing a non-pathogenic laboratory strain of Escherichia coli (K12).

FDA label, Description section

Boxed warning

RISK OF ACUTE BRONCHOSPASM IN PATIENTS WITH CHRONIC LUNG DISEASE Acute bronchospasm has been observed in AFREZZA-treated patients with asthma and Chronic Obstructive Pulmonary Disease (COPD) [see Warnings and Precautions ( 5.1 )]. AFREZZA is contraindicated in patients with chronic lung disease such as asthma or COPD [see Contraindications ( 4 )].

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 — boxed warning 3Labeled adverse reaction 2Labeled (related wording) 8Likely indication confounding 6Reporting / coding artifact 4Lab value / disease marker 4Not in label — unassessed 13
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). 1,169 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
Hypoglycaemia unawareness69126.1
97.0–164.0ROR 126.3 · calibrated p 3e-8 ✓
99.1 EB05 80.9 · IC025 +5.5
3/3 methods agree
Not in label — unassessedserious n=65 · 71% consumerno trial arm names this drug
Shock hypoglycaemic7193.0
72.3–119.7ROR 93.2 · calibrated p 3e-7 ✓
77.5 EB05 63.5 · IC025 +5.3
3/3 methods agree
Not in label — unassessedserious n=68 · 100% consumerno trial arm names this drug
Increased insulin requirement3282.4
56.8–119.6ROR 82.5 · calibrated p 1e-6 ✓
68.5 EB05 50.8 · IC025 +4.5
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
–no trial arm names this drug
Insulin resistance25776.1
66.8–86.7ROR 76.5 · calibrated p 9e-7 ✓
66.2 EB05 59.7 · IC025 +5.7
3/3 methods agree
Reporting / coding artifactserious n=158 · 83% consumerno trial arm names this drug
Coronary artery surgery3464.9
45.4–92.6ROR 64.9 · calibrated p 5e-6 ✓
56.1 EB05 42.0 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=34no trial arm names this drug
Anti-insulin antibody positive2055.6
35.1–88.2ROR 55.6 · calibrated p 2e-5 ✓
48.2 EB05 32.9 · IC025 +3.8
3/3 methods agree
Lab value / disease markerserious n=20no trial arm names this drug
Hypoglycaemic unconsciousness15946.1
39.2–54.2ROR 46.3 · calibrated p 2e-5 ✓
42.2 EB05 37.0 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=159 · 86% consumerno trial arm names this drug
Blood glucose fluctuation79241.2
38.3–44.2ROR 42.0 · calibrated p 4e-5 ✓
38.2 EB05 36.0 · IC025 +5.1
3/3 methods agree
Lab value / disease markerserious n=525 · 86% consumerno trial arm names this drug
Blood glucose decreased3,29938.9
37.6–40.3ROR 42.4 · calibrated p 4e-5 ✓
36.3 EB05 35.3 · IC025 +5.1
3/3 methods agree
Labeled — boxed warning
synonym match
serious PRR 40.5 · 90% consumerno trial arm names this drug
Multi-organ disorder13037.1
31.1–44.3ROR 37.2 · calibrated p 9e-5 ✓
34.6 EB05 29.9 · IC025 +4.7
3/3 methods agree
Not in label — unassessedserious n=130 · ♀ 100% (drug 56%)no trial arm names this drug
Neuropathic arthropathy3732.3
23.2–45.1ROR 32.4 · calibrated p 3e-4 ✓
30.1 EB05 22.8 · IC025 +3.9
3/3 methods agree
Not in label — unassessedserious n=36 · 100% consumerno trial arm names this drug
Diabetic gastroparesis2030.6
19.5–48.0ROR 30.6 · calibrated p 5e-4 ✓
28.2 EB05 19.3 · IC025 +3.4
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=20no trial arm names this drug
Blood glucose increased10,00829.6
29.1–30.1ROR 39.3 · calibrated p 6e-5 ✓
28.1 EB05 27.6 · IC025 +4.8
3/3 methods agree
Labeled — boxed warning
synonym match
serious PRR 30.6 · 90% consumerno trial arm names this drug
Neuropathy8627.8
22.4–34.5ROR 27.9 · calibrated p 4e-4 ✓
26.3 EB05 22.0 · IC025 +4.2
3/3 methods agree
Labeled adverse reaction
exact term
serious n=84no trial arm names this drug
Blood glucose abnormal91527.5
25.8–29.4ROR 28.2 · calibrated p 4e-4 ✓
26.2 EB05 24.8 · IC025 +4.6
3/3 methods agree
Lab value / disease markerserious PRR 28.4 · 89% consumerno trial arm names this drug
Intercepted drug dispensing error7427.4
21.7–34.5ROR 27.4 · calibrated p 5e-4 ✓
25.9 EB05 21.3 · IC025 +4.1
3/3 methods agree
Not in label — unassessed100% consumerno trial arm names this drug
Intercepted product selection error6127.0
20.9–35.0ROR 27.1 · calibrated p 5e-4 ✓
25.6 EB05 20.6 · IC025 +4.0
3/3 methods agree
Not in label — unassessed100% consumerno trial arm names this drug
Stress symptoms2125.6
16.5–39.6ROR 25.6 · calibrated p 0.001 ✓
24.0 EB05 16.5 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=21no trial arm names this drug
Diabetic complication11825.6
21.3–30.7ROR 25.6 · calibrated p 7e-4 ✓
24.3 EB05 20.9 · IC025 +4.2
3/3 methods agree
Reporting / coding artifactserious n=110 · 88% consumerno trial arm names this drug
Diabetic coma12123.7
19.7–28.4ROR 23.8 · calibrated p 1e-3 ✓
22.6 EB05 19.4 · IC025 +4.1
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=121 · 88% consumerno trial arm names this drug
Retinopathy15723.2
19.8–27.3ROR 23.3 · calibrated p 0.001 ✓
22.2 EB05 19.5 · IC025 +4.1
3/3 methods agree
Labeled adverse reaction
exact term
serious n=142 · 76% consumerno trial arm names this drug
Large for dates baby3723.1
16.6–32.1ROR 23.1 · calibrated p 0.001 ✓
21.9 EB05 16.6 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=32 · 100% consumerno trial arm names this drug
Incorrect drug dosage form administered2522.3
15.0–33.3ROR 22.3 · calibrated p 0.002 ✓
21.1 EB05 15.0 · IC025 +3.3
3/3 methods agree
Reporting / coding artifact100% consumerno trial arm names this drug
Glycosylated haemoglobin increased96721.2
19.8–22.5ROR 21.7 · calibrated p 0.001 ✓
20.4 EB05 19.3 · IC025 +4.2
3/3 methods agree
Lab value / disease markerserious PRR 20.1 · 85% consumerno trial arm names this drug
Hypoglycaemic coma10720.3
16.8–24.7ROR 20.4 · calibrated p 0.002 ✓
19.6 EB05 16.6 · IC025 +3.9
3/3 methods agree
Not in label — unassessedserious n=106no trial arm names this drug
Wrong drug administered32920.0
17.9–22.3ROR 20.2 · calibrated p 0.002 ✓
19.3 EB05 17.6 · IC025 +4.0
3/3 methods agree
Reporting / coding artifactserious n=142 · 83% consumerno trial arm names this drug
Eye haemorrhage47119.3
17.7–21.2ROR 19.6 · calibrated p 0.002 ✓
18.7 EB05 17.3 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious PRR 20.0 · 73% consumerno trial arm names this drug
Blood insulin increased1918.9
12.0–29.9ROR 18.9 · calibrated p 0.004 ✓
17.8 EB05 11.8 · IC025 +2.9
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
–no trial arm names this drug
Diabetic foot9817.5
14.3–21.4ROR 17.5 · calibrated p 0.004 ✓
16.9 EB05 14.3 · IC025 +3.6
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=95 · 76% consumerno trial arm names this drug
Diabetic ulcer2317.4
11.5–26.4ROR 17.4 · calibrated p 0.005 ✓
16.5 EB05 11.4 · IC025 +3.0
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=22no trial arm names this drug
Hypoglycaemia neonatal5117.4
13.2–23.0ROR 17.4 · calibrated p 0.004 ✓
16.8 EB05 13.2 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=50no trial arm names this drug
Hypoglycaemia (low blood sugar)1,52617.2
16.4–18.1ROR 17.8 · calibrated p 0.003 ✓
16.7 EB05 16.0 · IC025 +4.0
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 15.5no trial arm names this drug

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Insulin Human only as a background or rescue medication (NCT00659295, NCT05214573); 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
Blood glucose increased10,00829.6
29.1–30.1ROR 39.3 · calibrated p 6e-5 ✓
28.1 EB05 27.6 · IC025 +4.8
3/3 methods agree
Labeled — boxed warning
synonym match
serious PRR 30.6 · 90% consumerno trial arm names this drug
Blood glucose decreased3,29938.9
37.6–40.3ROR 42.4 · calibrated p 4e-5 ✓
36.3 EB05 35.3 · IC025 +5.1
3/3 methods agree
Labeled — boxed warning
synonym match
serious PRR 40.5 · 90% consumerno trial arm names this drug
Drug ineffective (drug did not work)3,0521.2
1.2–1.3ROR 1.2 · calibrated p 0.474
1.2 EB05 1.2 · IC025 +0.2Reporting / coding artifactserious PRR 1.6 · 82% consumerno trial arm names this drug
Incorrect dose administered1,9004.5
4.3–4.7ROR 4.7 · calibrated p 0.271
4.5 EB05 4.3 · IC025 +2.1
3/3 methods agree
Reporting / coding artifactserious PRR 5.0 · 88% consumerno trial arm names this drug
Hypoglycaemia (low blood sugar)1,52617.2
16.4–18.1ROR 17.8 · calibrated p 0.003 ✓
16.7 EB05 16.0 · IC025 +4.0
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 15.5no trial arm names this drug
Nausea1,4811.0
0.9–1.0ROR 1.0 · calibrated p 0.304
1.0 EB05 1.0 · IC025 -0.1
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 1.1no trial arm names this drug
Visual impairment1,3696.0
5.7–6.3ROR 6.1 · calibrated p 0.141
5.9 EB05 5.6 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious PRR 4.8 · 93% consumerno trial arm names this drug
Fall1,2352.0
1.9–2.1ROR 2.0 · calibrated p 0.948
2.0 EB05 1.9 · IC025 +0.9Not in label — unassessedserious PRR 2.0no trial arm names this drug
Diarrhoea (diarrhea)1,1911.0
0.9–1.0ROR 1.0 · calibrated p 0.295
1.0 EB05 0.9 · IC025 -0.1
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 1.2no trial arm names this drug
Malaise (feeling unwell)1,1481.4
1.3–1.5ROR 1.4 · calibrated p 0.574
1.4 EB05 1.3 · IC025 +0.4Not in label — unassessedserious PRR 1.4 · 81% consumerno trial arm names this drug
Wrong technique in product usage process1,1433.0
2.8–3.2ROR 3.1 · calibrated p 0.603
3.0 EB05 2.9 · IC025 +1.5
3/3 methods agree
Reporting / coding artifactserious PRR 4.5 · 89% consumerno trial arm names this drug
Dizziness1,0951.2
1.1–1.2ROR 1.2 · calibrated p 0.421
1.2 EB05 1.1 · IC025 +0.1Not in label — unassessedserious PRR 1.3 · 72% consumerno trial arm names this drug
Fatigue (tiredness)1,0530.7
0.7–0.8ROR 0.7 · calibrated p 0.136
0.7 EB05 0.7 · IC025 -0.6
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 0.9no 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.

✓ A hand-written Bradford Hill causality assessment exists for this drug: Insulin glargine ↔ Hypoglycaemia (blood glucose decreased).

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 Insulin Human?

In FDA FAERS, the most frequently co-reported reaction terms for Insulin Human are blood glucose increased, blood glucose decreased, hypoglycaemia, nausea, visual impairment, weight decreased. 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 Insulin Human have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: RISK OF ACUTE BRONCHOSPASM IN PATIENTS WITH CHRONIC LUNG DISEASE Acute bronchospasm has been observed in AFREZZA-treated patients with asthma and Chronic Obstructive Pulmonary Disease (COPD) [see Warnings and Precautions ( 5.1 )]. AFREZZA is contraindicated in patients with chronic lung disease such as asthma or COPD [see Contraindications ( 4 )].

Do FAERS signals prove that Insulin Human 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.