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Adalimumab-Aaty side effects: what 47,048 FDA adverse event reports show

Adalimumab-Aaty · Adalimumab · 1,265 reaction terms · 496,955 drug–reaction co-reports · data 2026-09-14
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Drug class

Tumor necrosis factor (tnf) blocker

FDA label, Indications wording

Brand names

Adalimumab

openFDA label

Who reports

47,048 reports · 94% serious · 6,925 with death outcome · 67% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Adalimumab-aaty is a tumor necrosis factor (TNF) blocker indicated for: Reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in adult patients with moderately to severely active r heumatoid arthritis .

FDA label, Indications and Usage

What it is

Adalimumab-aaty is a tumor necrosis factor blocker. Adalimumab-aaty is a recombinant human IgG1 monoclonal antibody created using phage display technology resulting in an antibody with human derived heavy and light chain variable regions and human IgG1:k constant regions.

FDA label, Description section

Boxed warning

SERIOUS INFECTIONS and MALIGNANCY WARNING: SERIOUS INFECTIONS and MALIGNANCY See full prescribing information for complete boxed warning. SERIOUS INFECTIONS ( 5.1 , 6.1 ): Increased risk of serious infections leading.

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 (related wording) 4Likely indication confounding 3Reporting / coding artifact 2Lab value / disease marker 9Not in label — unassessed 22
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). 1,225 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
Anti-cyclic citrullinated peptide antibody4691,083.1
915.3–1,281.6ROR 1,094.0 · calibrated p 1e-17 ✓
309.0 EB05 286.3 · IC025 +7.7
3/3 methods agree
Lab value / disease markerserious n=469 · ♀ 100% (drug 67%) · 94% clinicianno trial arm names this drug
Lupus vulgaris795918.0
812.6–1,037.0ROR 933.7 · calibrated p 7e-17 ✓
295.4 EB05 278.6 · IC025 +7.9
3/3 methods agree
Not in label — unassessedserious n=795 · ♀ 100% (drug 67%) · 96% clinicianno trial arm names this drug
Grip strength139677.7
519.9–883.3ROR 679.7 · calibrated p 6e-15 ✓
257.5 EB05 223.5 · IC025 +6.8
3/3 methods agree
Not in label — unassessedserious n=139 · ♀ 100% (drug 67%) · 100% clinicianno trial arm names this drug
Red blood cell sedimentation rate167660.1
519.4–839.1ROR 662.5 · calibrated p 6e-15 ✓
256.4 EB05 225.4 · IC025 +7.0
3/3 methods agree
Lab value / disease markerserious n=167no trial arm names this drug
Human antichimeric antibody positive185541.2
436.4–671.1ROR 543.3 · calibrated p 4e-14 ✓
236.9 EB05 209.6 · IC025 +7.0
3/3 methods agree
Lab value / disease markerserious n=185 · ♀ 100% (drug 67%)no trial arm names this drug
Deep vein thrombosis postoperative1,063534.3
488.7–584.0ROR 546.6 · calibrated p 2e-14 ✓
240.4 EB05 228.5 · IC025 +7.7
3/3 methods agree
Not in label — unassessedserious n=1,063 · ♀ 100% (drug 67%) · 95% clinicianno trial arm names this drug
Synovial fluid analysis46504.6
330.3–770.8ROR 505.1 · calibrated p 5e-13 ✓
214.4 EB05 167.2 · IC025 +5.6
3/3 methods agree
Reporting / coding artifactserious n=46 · ♀ 100% (drug 67%) · 100% clinicianno trial arm names this drug
Chronic recurrent multifocal osteomyelitis57471.9
324.7–685.8ROR 472.5 · calibrated p 6e-13 ✓
211.8 EB05 169.5 · IC025 +5.8
3/3 methods agree
Not in label — unassessedserious n=56no trial arm names this drug
Swollen joint count increased1,585465.5
434.0–499.3ROR 481.7 · calibrated p 9e-14 ✓
225.8 EB05 216.6 · IC025 +7.6
3/3 methods agree
Lab value / disease markerserious n=1,584 · ♀ 100% (drug 67%) · 95% clinicianno trial arm names this drug
C-reactive protein449440.7
386.8–502.2ROR 445.0 · calibrated p 2e-13 ✓
218.3 EB05 201.9 · IC025 +7.3
3/3 methods agree
Lab value / disease markerserious n=449 · ♀ 100% (drug 67%) · 96% clinicianno trial arm names this drug
Rheumatic fever2,133429.5
404.9–455.6ROR 449.9 · calibrated p 2e-13 ✓
217.1 EB05 209.5 · IC025 +7.6
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=2,132 · ♀ 100% (drug 67%) · 94% clinicianno trial arm names this drug
Facet joint syndrome1,478396.9
370.1–425.6ROR 409.7 · calibrated p 5e-13 ✓
208.3 EB05 199.5 · IC025 +7.5
3/3 methods agree
Not in label — unassessedserious n=1,478 · ♀ 100% (drug 67%) · 95% clinicianno trial arm names this drug
Swollen joint count106339.5
263.5–437.4ROR 340.3 · calibrated p 6e-12 ✓
185.5 EB05 157.7 · IC025 +6.3
3/3 methods agree
Not in label — unassessedserious n=106 · ♀ 100% (drug 67%) · 100% clinicianno trial arm names this drug
Adjustment disorder with depressed mood868339.4
310.8–370.7ROR 345.8 · calibrated p 3e-12 ✓
191.0 EB05 180.6 · IC025 +7.3
3/3 methods agree
Not in label — unassessedserious n=868 · ♀ 100% (drug 67%) · 97% clinicianno trial arm names this drug
Paradoxical psoriasis177324.9
267.6–394.6ROR 326.2 · calibrated p 6e-12 ✓
183.4 EB05 161.9 · IC025 +6.7
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=168 · 95% clinicianno trial arm names this drug
Hypocholesterolaemia127314.8
250.7–395.4ROR 315.7 · calibrated p 1e-11 ✓
178.8 EB05 154.2 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=127 · ♀ 100% (drug 67%) · 100% clinicianno trial arm names this drug
Retinitis668299.1
271.2–329.9ROR 303.4 · calibrated p 9e-12 ✓
177.4 EB05 166.4 · IC025 +7.2
3/3 methods agree
Not in label — unassessedserious n=668 · ♀ 100% (drug 67%) · 94% clinicianno trial arm names this drug
Anti-cyclic citrullinated peptide antibody positive2,718277.5
264.8–290.9ROR 294.5 · calibrated p 1e-11 ✓
170.2 EB05 164.9 · IC025 +7.3
3/3 methods agree
Lab value / disease markerserious PRR 104.2 · ♀ 100% (drug 67%) · 94% clinicianno trial arm names this drug
Dislocation of vertebra822262.5
240.9–286.1ROR 267.1 · calibrated p 3e-11 ✓
164.0 EB05 154.8 · IC025 +7.1
3/3 methods agree
Not in label — unassessedserious n=822 · ♀ 100% (drug 67%) · 96% clinicianno trial arm names this drug
Rheumatoid factor positive2,121260.4
247.0–274.6ROR 272.6 · calibrated p 2e-11 ✓
163.5 EB05 157.8 · IC025 +7.2
3/3 methods agree
Lab value / disease markerserious n=2,120 · ♀ 100% (drug 67%) · 94% clinicianno trial arm names this drug
X-ray abnormal652257.7
234.1–283.8ROR 261.3 · calibrated p 4e-11 ✓
162.0 EB05 151.8 · IC025 +7.0
3/3 methods agree
Lab value / disease markerserious n=652 · ♀ 100% (drug 67%) · 96% clinicianno trial arm names this drug
Musculoskeletal deformity86256.7
196.8–334.9ROR 257.2 · calibrated p 8e-11 ✓
156.7 EB05 130.8 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious n=86 · ♀ 100% (drug 67%)no trial arm names this drug
Subcutaneous drug absorption impaired194247.4
207.6–295.0ROR 248.5 · calibrated p 8e-11 ✓
156.2 EB05 138.6 · IC025 +6.6
3/3 methods agree
Not in label — unassessedserious n=194 · ♀ 100% (drug 67%) · 96% clinicianno trial arm names this drug
Ileocaecal resection100192.4
152.2–243.4ROR 192.9 · calibrated p 9e-10 ✓
130.8 EB05 110.6 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious n=100 · 100% clinicianno trial arm names this drug
Body height below normal188181.7
153.3–215.3ROR 182.4 · calibrated p 1e-9 ✓
127.1 EB05 112.6 · IC025 +6.3
3/3 methods agree
Reporting / coding artifactserious n=188 · ♀ 100% (drug 67%)no trial arm names this drug
Pemphigus3,547178.4
171.8–185.3ROR 192.9 · calibrated p 5e-10 ✓
127.0 EB05 123.6 · IC025 +6.9
3/3 methods agree
Not in label — unassessedserious PRR 77.7 · ♀ 100% (drug 67%) · 93% clinicianno trial arm names this drug
C-reactive protein abnormal1,782172.1
163.1–181.7ROR 178.9 · calibrated p 1e-9 ✓
123.8 EB05 119.0 · IC025 +6.8
3/3 methods agree
Lab value / disease markerserious n=1,782 · ♀ 93% (drug 67%) · 93% clinicianno trial arm names this drug
Seronegative arthritis297160.7
140.7–183.5ROR 161.7 · calibrated p 3e-9 ✓
117.0 EB05 106.3 · IC025 +6.4
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=297 · ♀ 100% (drug 67%) · 93% clinicianno trial arm names this drug
Short stature69160.2
121.6–211.0ROR 160.4 · calibrated p 5e-9 ✓
114.0 EB05 93.1 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=69no trial arm names this drug
Helicobacter infection2,690160.1
153.3–167.2ROR 169.8 · calibrated p 2e-9 ✓
117.5 EB05 113.8 · IC025 +6.8
3/3 methods agree
Not in label — unassessedserious PRR 75.7 · ♀ 100% (drug 67%) · 95% clinicianno trial arm names this drug
Hand deformity3,385155.9
150.0–161.9ROR 167.9 · calibrated p 2e-9 ✓
115.2 EB05 112.0 · IC025 +6.8
3/3 methods agree
Not in label — unassessedserious PRR 76.4 · ♀ 100% (drug 67%) · 94% clinicianno trial arm names this drug
Cutaneous leishmaniasis62145.5
109.2–193.9ROR 145.7 · calibrated p 1e-8 ✓
106.0 EB05 85.6 · IC025 +5.5
3/3 methods agree
Not in label — unassessedserious n=61 · ♀ 33% (drug 67%) · 100% clinicianno trial arm names this drug
Vaginal flatulence75145.0
111.7–188.2ROR 145.2 · calibrated p 1e-8 ✓
106.3 EB05 87.6 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=75 · ♀ 100% (drug 67%)no trial arm names this drug
Folliculitis2,512143.5
137.3–149.9ROR 151.5 · calibrated p 4e-9 ✓
108.3 EB05 104.8 · IC025 +6.7
3/3 methods agree
Not in label — unassessedserious PRR 77.6 · ♀ 99% (drug 67%) · 96% clinicianno trial arm names this drug
Steroid dependence206142.8
122.1–167.1ROR 143.4 · calibrated p 8e-9 ✓
106.9 EB05 95.2 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=206 · ♀ 27% (drug 67%) · 93% clinicianno trial arm names this drug
Bone erosion797129.5
119.7–140.1ROR 131.7 · calibrated p 1e-8 ✓
100.0 EB05 94.3 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=796 · ♀ 99% (drug 67%) · 96% clinicianno trial arm names this drug

Clinical concept groups

MedDRA splits one clinical problem across several terms (e.g. "neutropenia", "neutrophil count decreased", "agranulocytosis"), which dilutes term-level signals. These rows count reports with any term in a concept group (an exact union, not a sum), compared with all other drugs. Groups are hand-built and listed in the methods.

ConceptReportsPRR 95% CIReading
Interstitial lung disease1,7158.17.7–8.5signal
Liver injury5,3558.07.8–8.2signal
Hyperglycaemia / diabetes2,9743.93.7–4.0signal
Serious infection6,2803.63.6–3.7signal
Depression2,1493.43.3–3.6signal
Tendon disorder2753.22.9–3.6signal
Opportunistic infection9303.12.9–3.3signal
Pancreatitis5012.82.5–3.0signal
Gi bleeding1,0642.62.5–2.8signal
Anaphylaxis / angioedema5311.91.7–2.1raised
Rhabdomyolysis / myopathy3391.91.7–2.1raised
Malignancy1,3071.51.5–1.6raised
Osteonecrosis1961.51.3–1.7raised
Fall / fracture1,2201.41.4–1.5raised
Stroke7071.31.2–1.4raised
Venous thromboembolism5981.21.1–1.3raised

Trial evidence (ClinicalTrials.gov)

No completed trial with posted adverse-event results was found on ClinicalTrials.gov for Adalimumab-Aaty (searched ADALIMUMAB-AATY).

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
Drug ineffective (drug did not work)10,5653.6
3.5–3.7ROR 4.3 · calibrated p 0.319
3.6 EB05 3.5 · IC025 +1.8
3/3 methods agree
Reporting / coding artifactage-adj. PRR 4.1 · serious PRR 6.0no trial arm names this drug
Off label use (used outside approved label)8,3054.3
4.2–4.4ROR 5.0 · calibrated p 0.234
4.3 EB05 4.2 · IC025 +2.1
3/3 methods agree
Reporting / coding artifactage-adj. PRR 4.3 · serious PRR 4.7no trial arm names this drug
Rheumatoid arthritis5,74523.8
23.2–24.4ROR 27.0 · calibrated p 5e-4 ✓
22.6 EB05 22.2 · IC025 +4.5
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
age-adj. PRR 20.6 · serious PRR 16.8 · ♀ 95% (drug 67%)no trial arm names this drug
Pain5,4714.0
3.9–4.1ROR 4.4 · calibrated p 0.313
4.0 EB05 3.9 · IC025 +1.9
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 3.9 · serious PRR 3.8 · ♀ 90% (drug 67%)no trial arm names this drug
Arthralgia (joint pain)5,2505.7
5.6–5.9ROR 6.3 · calibrated p 0.132
5.6 EB05 5.5 · IC025 +2.5
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 5.1 · serious PRR 6.2 · ♀ 91% (drug 67%)no trial arm names this drug
Rash4,6684.8
4.7–5.0ROR 5.3 · calibrated p 0.208
4.8 EB05 4.7 · IC025 +2.2
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 4.6 · serious PRR 6.5 · ♀ 92% (drug 67%)no trial arm names this drug
Condition aggravated4,5316.8
6.6–7.0ROR 7.4 · calibrated p 0.084
6.7 EB05 6.5 · IC025 +2.7
3/3 methods agree
Reporting / coding artifactage-adj. PRR 6.1 · serious PRR 6.1no trial arm names this drug
Drug intolerance4,27020.7
20.1–21.3ROR 22.6 · calibrated p 0.001 ✓
19.8 EB05 19.3 · IC025 +4.3
3/3 methods agree
Reporting / coding artifactage-adj. PRR 23.4 · serious PRR 19.5 · ♀ 93% (drug 67%)no trial arm names this drug
Nausea4,1182.3
2.3–2.4ROR 2.5 · calibrated p 0.830
2.3 EB05 2.3 · IC025 +1.2
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 2.1 · serious PRR 2.7 · ♀ 91% (drug 67%)no trial arm names this drug
Diarrhoea (diarrhea)4,0852.8
2.8–2.9ROR 3.0 · calibrated p 0.621
2.8 EB05 2.8 · IC025 +1.4
3/3 methods agree
Not in label — unassessedage-adj. PRR 2.7 · serious PRR 3.0 · ♀ 89% (drug 67%)no trial arm names this drug
Headache4,0842.9
2.8–3.0ROR 3.1 · calibrated p 0.594
2.9 EB05 2.8 · IC025 +1.5
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 2.4 · serious PRR 3.6no trial arm names this drug
Alopecia (hair loss)3,8969.0
8.7–9.3ROR 9.7 · calibrated p 0.036 ✓
8.8 EB05 8.6 · IC025 +3.1
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 8.0 · serious PRR 11.5 · ♀ 98% (drug 67%) · 90% clinicianno 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: TNF-inhibitors (adalimumab) ↔ Drug-induced lupus.

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 Adalimumab-Aaty?

In FDA FAERS, the most frequently co-reported reaction terms for Adalimumab-Aaty are rheumatoid arthritis, fatigue, pain, arthralgia, rash, 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 Adalimumab-Aaty have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: SERIOUS INFECTIONS and MALIGNANCY WARNING: SERIOUS INFECTIONS and MALIGNANCY See full prescribing information for complete boxed warning. SERIOUS INFECTIONS ( 5.1 , 6.1 ): Increased risk of serious infections leading.

Do FAERS signals prove that Adalimumab-Aaty 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.