Adalimumab-Aaty side effects: what 47,048 FDA adverse event reports show
Drug class
Tumor necrosis factor (tnf) blocker
Brand names
Adalimumab
Who reports
47,048 reports · 94% serious · 6,925 with death outcome · 67% female
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 .
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.
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.
Causality screen of the 40 strongest signals
What the badges mean
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Likely indication confounding The term appears in the label's indications: reports probably describe the disease being treated (or its progression), not a drug effect. Classic confounding by indication.
- Reporting / coding artifact An administrative, monitoring or exposure term (product issue, off-label use, 'test normal', overdose...). Not a biological reaction; a high PRR here reflects how reports are coded.
- Lab value / disease marker A laboratory result, investigation or disease-activity marker (antibody positive, CRP abnormal, swollen joint count) not described in the label. These usually mirror the monitored disease or testing protocol rather than a drug effect; not screened further.
- Not in label — unassessed Not found in the label text, not an artifact pattern. This is a genuine candidate for a formal causality assessment (Bradford Hill / WHO-UMC); it has NOT had one here.
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.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Anti-cyclic citrullinated peptide antibody | 469 | 1,083.1 915.3–1,281.6ROR 1,094.0 · calibrated p 1e-17 ✓ | 309.0 EB05 286.3 · IC025 +7.7 3/3 methods agree | Lab value / disease marker | serious n=469 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Lupus vulgaris | 795 | 918.0 812.6–1,037.0ROR 933.7 · calibrated p 7e-17 ✓ | 295.4 EB05 278.6 · IC025 +7.9 3/3 methods agree | Not in label — unassessed | serious n=795 · ♀ 100% (drug 67%) · 96% clinician | no trial arm names this drug |
| Grip strength | 139 | 677.7 519.9–883.3ROR 679.7 · calibrated p 6e-15 ✓ | 257.5 EB05 223.5 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious n=139 · ♀ 100% (drug 67%) · 100% clinician | no trial arm names this drug |
| Red blood cell sedimentation rate | 167 | 660.1 519.4–839.1ROR 662.5 · calibrated p 6e-15 ✓ | 256.4 EB05 225.4 · IC025 +7.0 3/3 methods agree | Lab value / disease marker | serious n=167 | no trial arm names this drug |
| Human antichimeric antibody positive | 185 | 541.2 436.4–671.1ROR 543.3 · calibrated p 4e-14 ✓ | 236.9 EB05 209.6 · IC025 +7.0 3/3 methods agree | Lab value / disease marker | serious n=185 · ♀ 100% (drug 67%) | no trial arm names this drug |
| Deep vein thrombosis postoperative | 1,063 | 534.3 488.7–584.0ROR 546.6 · calibrated p 2e-14 ✓ | 240.4 EB05 228.5 · IC025 +7.7 3/3 methods agree | Not in label — unassessed | serious n=1,063 · ♀ 100% (drug 67%) · 95% clinician | no trial arm names this drug |
| Synovial fluid analysis | 46 | 504.6 330.3–770.8ROR 505.1 · calibrated p 5e-13 ✓ | 214.4 EB05 167.2 · IC025 +5.6 3/3 methods agree | Reporting / coding artifact | serious n=46 · ♀ 100% (drug 67%) · 100% clinician | no trial arm names this drug |
| Chronic recurrent multifocal osteomyelitis | 57 | 471.9 324.7–685.8ROR 472.5 · calibrated p 6e-13 ✓ | 211.8 EB05 169.5 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious n=56 | no trial arm names this drug |
| Swollen joint count increased | 1,585 | 465.5 434.0–499.3ROR 481.7 · calibrated p 9e-14 ✓ | 225.8 EB05 216.6 · IC025 +7.6 3/3 methods agree | Lab value / disease marker | serious n=1,584 · ♀ 100% (drug 67%) · 95% clinician | no trial arm names this drug |
| C-reactive protein | 449 | 440.7 386.8–502.2ROR 445.0 · calibrated p 2e-13 ✓ | 218.3 EB05 201.9 · IC025 +7.3 3/3 methods agree | Lab value / disease marker | serious n=449 · ♀ 100% (drug 67%) · 96% clinician | no trial arm names this drug |
| Rheumatic fever | 2,133 | 429.5 404.9–455.6ROR 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% clinician | no trial arm names this drug |
| Hepatic enzyme | 68 | 426.2 305.3–595.0ROR 426.9 · calibrated p 1e-12 ✓ | 204.3 EB05 166.7 · IC025 +6.0 3/3 methods agree | Labeled (related wording) related wording | serious n=68 · ♀ 100% (drug 67%) · 100% clinician | no trial arm names this drug |
| Facet joint syndrome | 1,478 | 396.9 370.1–425.6ROR 409.7 · calibrated p 5e-13 ✓ | 208.3 EB05 199.5 · IC025 +7.5 3/3 methods agree | Not in label — unassessed | serious n=1,478 · ♀ 100% (drug 67%) · 95% clinician | no trial arm names this drug |
| Swollen joint count | 106 | 339.5 263.5–437.4ROR 340.3 · calibrated p 6e-12 ✓ | 185.5 EB05 157.7 · IC025 +6.3 3/3 methods agree | Not in label — unassessed | serious n=106 · ♀ 100% (drug 67%) · 100% clinician | no trial arm names this drug |
| Adjustment disorder with depressed mood | 868 | 339.4 310.8–370.7ROR 345.8 · calibrated p 3e-12 ✓ | 191.0 EB05 180.6 · IC025 +7.3 3/3 methods agree | Not in label — unassessed | serious n=868 · ♀ 100% (drug 67%) · 97% clinician | no trial arm names this drug |
| Paradoxical psoriasis | 177 | 324.9 267.6–394.6ROR 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% clinician | no trial arm names this drug |
| Hypocholesterolaemia | 127 | 314.8 250.7–395.4ROR 315.7 · calibrated p 1e-11 ✓ | 178.8 EB05 154.2 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=127 · ♀ 100% (drug 67%) · 100% clinician | no trial arm names this drug |
| Retinitis | 668 | 299.1 271.2–329.9ROR 303.4 · calibrated p 9e-12 ✓ | 177.4 EB05 166.4 · IC025 +7.2 3/3 methods agree | Not in label — unassessed | serious n=668 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Anti-cyclic citrullinated peptide antibody positive | 2,718 | 277.5 264.8–290.9ROR 294.5 · calibrated p 1e-11 ✓ | 170.2 EB05 164.9 · IC025 +7.3 3/3 methods agree | Lab value / disease marker | serious PRR 104.2 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Dislocation of vertebra | 822 | 262.5 240.9–286.1ROR 267.1 · calibrated p 3e-11 ✓ | 164.0 EB05 154.8 · IC025 +7.1 3/3 methods agree | Not in label — unassessed | serious n=822 · ♀ 100% (drug 67%) · 96% clinician | no trial arm names this drug |
| Rheumatoid factor positive | 2,121 | 260.4 247.0–274.6ROR 272.6 · calibrated p 2e-11 ✓ | 163.5 EB05 157.8 · IC025 +7.2 3/3 methods agree | Lab value / disease marker | serious n=2,120 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| X-ray abnormal | 652 | 257.7 234.1–283.8ROR 261.3 · calibrated p 4e-11 ✓ | 162.0 EB05 151.8 · IC025 +7.0 3/3 methods agree | Lab value / disease marker | serious n=652 · ♀ 100% (drug 67%) · 96% clinician | no trial arm names this drug |
| Musculoskeletal deformity | 86 | 256.7 196.8–334.9ROR 257.2 · calibrated p 8e-11 ✓ | 156.7 EB05 130.8 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=86 · ♀ 100% (drug 67%) | no trial arm names this drug |
| Duodenal ulcer perforation | 2,657 | 254.0 242.4–266.3ROR 269.2 · calibrated p 3e-11 ✓ | 161.1 EB05 156.0 · IC025 +7.2 3/3 methods agree | Labeled (related wording) related wording | serious PRR 98.1 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Subcutaneous drug absorption impaired | 194 | 247.4 207.6–295.0ROR 248.5 · calibrated p 8e-11 ✓ | 156.2 EB05 138.6 · IC025 +6.6 3/3 methods agree | Not in label — unassessed | serious n=194 · ♀ 100% (drug 67%) · 96% clinician | no trial arm names this drug |
| Ileocaecal resection | 100 | 192.4 152.2–243.4ROR 192.9 · calibrated p 9e-10 ✓ | 130.8 EB05 110.6 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=100 · 100% clinician | no trial arm names this drug |
| Body height below normal | 188 | 181.7 153.3–215.3ROR 182.4 · calibrated p 1e-9 ✓ | 127.1 EB05 112.6 · IC025 +6.3 3/3 methods agree | Reporting / coding artifact | serious n=188 · ♀ 100% (drug 67%) | no trial arm names this drug |
| Pemphigus | 3,547 | 178.4 171.8–185.3ROR 192.9 · calibrated p 5e-10 ✓ | 127.0 EB05 123.6 · IC025 +6.9 3/3 methods agree | Not in label — unassessed | serious PRR 77.7 · ♀ 100% (drug 67%) · 93% clinician | no trial arm names this drug |
| C-reactive protein abnormal | 1,782 | 172.1 163.1–181.7ROR 178.9 · calibrated p 1e-9 ✓ | 123.8 EB05 119.0 · IC025 +6.8 3/3 methods agree | Lab value / disease marker | serious n=1,782 · ♀ 93% (drug 67%) · 93% clinician | no trial arm names this drug |
| Peripheral venous disease | 1,097 | 169.2 157.9–181.3ROR 173.2 · calibrated p 1e-9 ✓ | 122.1 EB05 116.2 · IC025 +6.8 3/3 methods agree | Labeled (related wording) related wording | serious n=1,097 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Seronegative arthritis | 297 | 160.7 140.7–183.5ROR 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% clinician | no trial arm names this drug |
| Short stature | 69 | 160.2 121.6–211.0ROR 160.4 · calibrated p 5e-9 ✓ | 114.0 EB05 93.1 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=69 | no trial arm names this drug |
| Helicobacter infection | 2,690 | 160.1 153.3–167.2ROR 169.8 · calibrated p 2e-9 ✓ | 117.5 EB05 113.8 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious PRR 75.7 · ♀ 100% (drug 67%) · 95% clinician | no trial arm names this drug |
| Hand deformity | 3,385 | 155.9 150.0–161.9ROR 167.9 · calibrated p 2e-9 ✓ | 115.2 EB05 112.0 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious PRR 76.4 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Cutaneous leishmaniasis | 62 | 145.5 109.2–193.9ROR 145.7 · calibrated p 1e-8 ✓ | 106.0 EB05 85.6 · IC025 +5.5 3/3 methods agree | Not in label — unassessed | serious n=61 · ♀ 33% (drug 67%) · 100% clinician | no trial arm names this drug |
| Vaginal flatulence | 75 | 145.0 111.7–188.2ROR 145.2 · calibrated p 1e-8 ✓ | 106.3 EB05 87.6 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=75 · ♀ 100% (drug 67%) | no trial arm names this drug |
| Folliculitis | 2,512 | 143.5 137.3–149.9ROR 151.5 · calibrated p 4e-9 ✓ | 108.3 EB05 104.8 · IC025 +6.7 3/3 methods agree | Not in label — unassessed | serious PRR 77.6 · ♀ 99% (drug 67%) · 96% clinician | no trial arm names this drug |
| Steroid dependence | 206 | 142.8 122.1–167.1ROR 143.4 · calibrated p 8e-9 ✓ | 106.9 EB05 95.2 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=206 · ♀ 27% (drug 67%) · 93% clinician | no trial arm names this drug |
| Muscle injury | 1,962 | 140.2 133.4–147.4ROR 146.3 · calibrated p 6e-9 ✓ | 106.4 EB05 102.5 · IC025 +6.6 3/3 methods agree | Labeled (related wording) related wording | serious PRR 70.3 · ♀ 100% (drug 67%) · 96% clinician | no trial arm names this drug |
| Bone erosion | 797 | 129.5 119.7–140.1ROR 131.7 · calibrated p 1e-8 ✓ | 100.0 EB05 94.3 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=796 · ♀ 99% (drug 67%) · 96% clinician | no 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.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Interstitial lung disease | 1,715 | 8.17.7–8.5 | signal |
| Liver injury | 5,355 | 8.07.8–8.2 | signal |
| Hyperglycaemia / diabetes | 2,974 | 3.93.7–4.0 | signal |
| Serious infection | 6,280 | 3.63.6–3.7 | signal |
| Depression | 2,149 | 3.43.3–3.6 | signal |
| Tendon disorder | 275 | 3.22.9–3.6 | signal |
| Opportunistic infection | 930 | 3.12.9–3.3 | signal |
| Pancreatitis | 501 | 2.82.5–3.0 | signal |
| Gi bleeding | 1,064 | 2.62.5–2.8 | signal |
| Anaphylaxis / angioedema | 531 | 1.91.7–2.1 | raised |
| Rhabdomyolysis / myopathy | 339 | 1.91.7–2.1 | raised |
| Malignancy | 1,307 | 1.51.5–1.6 | raised |
| Osteonecrosis | 196 | 1.51.3–1.7 | raised |
| Fall / fracture | 1,220 | 1.41.4–1.5 | raised |
| Stroke | 707 | 1.31.2–1.4 | raised |
| Venous thromboembolism | 598 | 1.21.1–1.3 | raised |
Trial evidence (ClinicalTrials.gov)
Most frequently reported reactions
By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Drug ineffective (drug did not work) | 10,565 | 3.6 3.5–3.7ROR 4.3 · calibrated p 0.319 | 3.6 EB05 3.5 · IC025 +1.8 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 4.1 · serious PRR 6.0 | no trial arm names this drug |
| Off label use (used outside approved label) | 8,305 | 4.3 4.2–4.4ROR 5.0 · calibrated p 0.234 | 4.3 EB05 4.2 · IC025 +2.1 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 4.3 · serious PRR 4.7 | no trial arm names this drug |
| Rheumatoid arthritis | 5,745 | 23.8 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 |
| Fatigue (tiredness) | 5,525 | 3.2 3.1–3.3ROR 3.5 · calibrated p 0.491 | 3.2 EB05 3.1 · IC025 +1.6 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 2.9 · serious PRR 3.7 · ♀ 91% (drug 67%) | no trial arm names this drug |
| Pain | 5,471 | 4.0 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) | 5,250 | 5.7 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 |
| Rash | 4,668 | 4.8 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 aggravated | 4,531 | 6.8 6.6–7.0ROR 7.4 · calibrated p 0.084 | 6.7 EB05 6.5 · IC025 +2.7 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 6.1 · serious PRR 6.1 | no trial arm names this drug |
| Drug intolerance | 4,270 | 20.7 20.1–21.3ROR 22.6 · calibrated p 0.001 ✓ | 19.8 EB05 19.3 · IC025 +4.3 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 23.4 · serious PRR 19.5 · ♀ 93% (drug 67%) | no trial arm names this drug |
| Nausea | 4,118 | 2.3 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 |
| Systemic lupus erythematosus | 4,118 | 58.7 56.9–60.5ROR 64.2 · calibrated p 3e-6 ✓ | 51.9 EB05 50.5 · IC025 +5.6 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 53.1 · serious PRR 32.4 · ♀ 96% (drug 67%) · 93% clinician | no trial arm names this drug |
| Diarrhoea (diarrhea) | 4,085 | 2.8 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 — unassessed | age-adj. PRR 2.7 · serious PRR 3.0 · ♀ 89% (drug 67%) | no trial arm names this drug |
| Headache | 4,084 | 2.9 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 3.6 | no trial arm names this drug |
| Joint swelling | 4,070 | 15.6 15.1–16.0ROR 16.9 · calibrated p 0.004 ✓ | 15.1 EB05 14.7 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 14.3 · serious PRR 15.7 · ♀ 96% (drug 67%) | no trial arm names this drug |
| Alopecia (hair loss) | 3,896 | 9.0 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% clinician | no 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.
- Lupus vulgaris — n=795, PRR 918.0
- Grip strength — n=139, PRR 677.7
- Deep vein thrombosis postoperative — n=1,063, PRR 534.3
- Chronic recurrent multifocal osteomyelitis — n=57, PRR 471.9
- Facet joint syndrome — n=1,478, PRR 396.9
- Swollen joint count — n=106, PRR 339.5
- Adjustment disorder with depressed mood — n=868, PRR 339.4
- Hypocholesterolaemia — n=127, PRR 314.8
- Retinitis — n=668, PRR 299.1
- Dislocation of vertebra — n=822, PRR 262.5
✓ 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
- FDA label via openFDA (set ID c44365e9-d470-4e35-978d-8565a9e3471e, effective 20260708; matched on
openfda.generic_name.exact:"ADALIMUMAB-AATY" AND openfda.product_type:"HUMAN PRESCRIPTION DRUG") - Bayesian shrinkage measures computed offline over all 1,317,300 cached pairs: BCPNN information component (IC, with Norén closed-form IC025) and MGPS empirical-Bayes geometric mean (EBGM, EB05) with a two-component gamma prior fitted by maximum marginal likelihood (α₁=0.57, β₁=0.02, α₂=1.42, β₂=0.70, w=0.17); unstratified
- FAERS pair statistics from the OpenPV build of 2026-09-14 (openFDA
count=aggregation, fieldpatient.drug.openfda.generic_name.exact, 1,265 reaction terms, min 3 co-reports); PRR/ROR with 95% CI, chi-square with Yates correction - Serious-only and stratified counts (serious:1, patient.patientsex, primarysource.qualification) from openFDA count queries; serious-only PRR uses the drug serious report total and the term global serious total (N_serious=11,882,979); strata shown only when n ≥ 20
- Seriousness and sex counts from openFDA
count=serious,patient.patientsex,seriousnessdeath - ClinicalTrials.gov API v2 (query
ADALIMUMAB-AATY, results-bearing studies sorted by enrollment)
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.