Adalimumab-Fkjp side effects: what 46,046 FDA adverse event reports show
Drug class
Tumor necrosis factor (tnf) blocker
Brand names
Adalimumab
Who reports
46,046 reports · 95% serious · 6,734 with death outcome · 67% female
Used for
Adalimumab-fkjp is a tumor necrosis factor (TNF) blocker indicated for: Rheumatoid Arthritis (RA) ( 1.1 ): 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 RA.
What it is
Adalimumab-fkjp is a tumor necrosis factor blocker. Adalimumab-fkjp is a recombinant human IgG1 monoclonal antibody. Adalimumab-fkjp is produced by recombinant DNA technology in a mammalian ce.
Boxed warning
SERIOUS INFECTIONS and MALIGNANCY SERIOUS INFECTIONS Patients treated with adalimumab products including Adalimumab-fkjp are at increased risk for developing serious infections that may lead to hospitalization or death [see Warnings and Precautions (5.1) ] .
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 flags pairs whose reports are unusually skewed by sex or come mostly from consumers rather than clinicians. 1,236 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 | 1,106.7 935.3–1,309.6ROR 1,118.1 · χ² 149,063 / p <1e-300 | 315.7 EB05 292.4 · 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 | 938.0 830.3–1,059.6ROR 954.4 · χ² 240,357 / p <1e-300 | 301.8 EB05 284.6 · 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 | 692.4 531.2–902.6ROR 694.5 · χ² 37,447 / p <1e-300 | 262.9 EB05 228.2 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious n=139 · ♀ 100% (drug 67%) · 96% clinician | no trial arm names this drug |
| Red blood cell sedimentation rate | 167 | 674.5 530.7–857.4ROR 677.0 · χ² 44,576 / p <1e-300 | 261.8 EB05 230.2 · IC025 +7.0 3/3 methods agree | Lab value / disease marker | serious n=167 | no trial arm names this drug |
| Human antichimeric antibody positive | 186 | 559.7 451.3–694.1ROR 561.9 · χ² 45,888 / p <1e-300 | 243.3 EB05 215.3 · IC025 +7.0 3/3 methods agree | Lab value / disease marker | serious n=186 · ♀ 100% (drug 67%) | no trial arm names this drug |
| Deep vein thrombosis postoperative | 1,063 | 545.9 499.4–596.8ROR 558.8 · χ² 260,501 / p <1e-300 | 245.6 EB05 233.5 · 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 | 515.6 337.5–787.6ROR 516.1 · χ² 10,750 / p <1e-300 | 218.6 EB05 170.5 · 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 | 482.2 331.8–700.8ROR 482.8 · χ² 12,956 / p <1e-300 | 216.0 EB05 172.9 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious n=56 | no trial arm names this drug |
| Swollen joint count increased | 1,586 | 476.3 444.0–510.8ROR 493.2 · χ² 364,562 / p <1e-300 | 230.8 EB05 221.4 · IC025 +7.7 3/3 methods agree | Lab value / disease marker | serious n=1,585 · ♀ 100% (drug 67%) · 95% clinician | no trial arm names this drug |
| C-reactive protein | 449 | 450.3 395.2–513.2ROR 454.8 · χ² 100,210 / p <1e-300 | 223.0 EB05 206.3 · 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 | 2,134 | 439.3 414.1–466.0ROR 460.6 · χ² 471,223 / p <1e-300 | 221.9 EB05 214.1 · IC025 +7.7 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=2,133 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Hepatic enzyme | 68 | 435.5 312.0–608.0ROR 436.2 · χ² 14,734 / p <1e-300 | 208.5 EB05 170.1 · 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 | 405.5 378.2–434.8ROR 419.0 · χ² 313,001 / p <1e-300 | 212.8 EB05 203.9 · IC025 +7.6 3/3 methods agree | Not in label — unassessed | serious n=1,478 · ♀ 100% (drug 67%) · 95% clinician | no trial arm names this drug |
| Adjustment disorder with depressed mood | 869 | 347.6 318.2–379.6ROR 354.2 · χ² 168,979 / p <1e-300 | 195.4 EB05 184.7 · IC025 +7.4 3/3 methods agree | Not in label — unassessed | serious n=869 · ♀ 100% (drug 67%) · 97% clinician | no trial arm names this drug |
| Swollen joint count | 106 | 346.9 269.3–446.9ROR 347.7 · χ² 20,417 / p <1e-300 | 189.4 EB05 161.0 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=106 · ♀ 100% (drug 67%) · 100% clinician | no trial arm names this drug |
| Hypocholesterolaemia | 127 | 321.7 256.2–404.0ROR 322.6 · χ² 23,453 / p <1e-300 | 182.6 EB05 157.5 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=127 · ♀ 100% (drug 67%) · 100% clinician | no trial arm names this drug |
| Paradoxical psoriasis | 169 | 306.8 252.3–373.0ROR 307.9 · χ² 30,400 / p <1e-300 | 178.9 EB05 157.4 · IC025 +6.6 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=161 · 96% clinician | no trial arm names this drug |
| Retinitis | 668 | 305.6 277.1–337.0ROR 310.1 · χ² 120,431 / p <1e-300 | 181.2 EB05 170.0 · 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 | 2,719 | 283.8 270.7–297.5ROR 301.5 · χ² 469,160 / p <1e-300 | 174.0 EB05 168.5 · IC025 +7.3 3/3 methods agree | Lab value / disease marker | serious PRR 105.7 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Dislocation of vertebra | 822 | 268.2 246.1–292.3ROR 273.1 · χ² 136,770 / p <1e-300 | 167.5 EB05 158.2 · 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 | 2,122 | 266.3 252.5–280.7ROR 279.1 · χ² 351,765 / p <1e-300 | 167.2 EB05 161.3 · IC025 +7.3 3/3 methods agree | Lab value / disease marker | serious n=2,121 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| X-ray abnormal | 652 | 263.4 239.2–290.0ROR 267.1 · χ² 107,192 / p <1e-300 | 165.5 EB05 155.1 · IC025 +7.1 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 | 262.3 201.0–342.2ROR 262.8 · χ² 13,959 / p <1e-300 | 160.0 EB05 133.6 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious n=86 · ♀ 100% (drug 67%) | no trial arm names this drug |
| Duodenal ulcer perforation | 2,658 | 259.7 247.8–272.2ROR 275.6 · χ² 433,770 / p <1e-300 | 164.6 EB05 159.4 · IC025 +7.3 3/3 methods agree | Labeled (related wording) related wording | serious PRR 99.6 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Subcutaneous drug absorption impaired | 194 | 252.8 212.1–301.4ROR 253.9 · χ² 30,956 / p <1e-300 | 159.5 EB05 141.5 · 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 | 196.6 155.5–248.7ROR 197.1 · χ² 13,395 / p <1e-300 | 133.5 EB05 113.0 · 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 | 190 | 188.5 159.1–223.2ROR 189.2 · χ² 24,812 / p <1e-300 | 131.3 EB05 116.3 · IC025 +6.4 3/3 methods agree | Reporting / coding artifact | serious n=190 · ♀ 100% (drug 67%) | no trial arm names this drug |
| Pemphigus | 3,550 | 182.5 175.7–189.6ROR 197.7 · χ² 455,601 / p <1e-300 | 129.9 EB05 126.4 · IC025 +6.9 3/3 methods agree | Not in label — unassessed | serious PRR 78.9 · ♀ 100% (drug 67%) · 93% clinician | no trial arm names this drug |
| C-reactive protein abnormal | 1,784 | 176.2 166.9–186.0ROR 183.2 · χ² 223,024 / p <1e-300 | 126.6 EB05 121.7 · IC025 +6.9 3/3 methods agree | Lab value / disease marker | serious n=1,784 · ♀ 93% (drug 67%) · 93% clinician | no trial arm names this drug |
| Peripheral venous disease | 1,097 | 172.9 161.3–185.2ROR 177.1 · χ² 135,192 / p <1e-300 | 124.8 EB05 118.7 · 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 |
| Short stature | 69 | 163.7 124.3–215.6ROR 163.9 · χ² 8,054 / p <1e-300 | 116.4 EB05 95.1 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=69 | no trial arm names this drug |
| Helicobacter infection | 2,690 | 163.6 156.7–170.8ROR 173.7 · χ² 318,532 / p <1e-300 | 120.0 EB05 116.3 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious PRR 76.8 · ♀ 100% (drug 67%) · 95% clinician | no trial arm names this drug |
| Seronegative arthritis | 294 | 161.9 141.8–185.0ROR 163.0 · χ² 34,428 / p <1e-300 | 118.3 EB05 107.4 · IC025 +6.4 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=294 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Hand deformity | 3,387 | 159.4 153.4–165.6ROR 172.0 · χ² 393,450 / p <1e-300 | 117.8 EB05 114.5 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious PRR 77.5 · ♀ 100% (drug 67%) · 94% clinician | no trial arm names this drug |
| Cutaneous leishmaniasis | 62 | 148.6 111.6–198.1ROR 148.8 · χ² 6,718 / p <1e-300 | 108.2 EB05 87.4 · 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 | 148.1 114.1–192.3ROR 148.4 · χ² 8,128 / p <1e-300 | 108.6 EB05 89.5 · 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 | 146.6 140.3–153.2ROR 155.0 · χ² 273,751 / p <1e-300 | 110.6 EB05 107.0 · IC025 +6.7 3/3 methods agree | Not in label — unassessed | serious PRR 78.7 · ♀ 99% (drug 67%) · 96% clinician | no trial arm names this drug |
| Steroid dependence | 206 | 145.9 124.7–170.7ROR 146.6 · χ² 22,259 / p <1e-300 | 109.2 EB05 97.3 · 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 | 1,963 | 143.4 136.4–150.7ROR 149.7 · χ² 210,271 / p <1e-300 | 108.8 EB05 104.8 · IC025 +6.7 3/3 methods agree | Labeled (related wording) related wording | serious PRR 71.3 · ♀ 100% (drug 67%) · 96% clinician | no trial arm names this drug |
| Bone erosion | 799 | 132.8 122.8–143.6ROR 135.1 · χ² 80,532 / p <1e-300 | 102.4 EB05 96.6 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=798 · ♀ 99% (drug 67%) · 95% clinician | no trial arm names this drug |
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) | 10,627 | 3.7 3.6–3.8ROR 4.5 · χ² 22,127 / p <1e-300 | 3.7 EB05 3.6 · IC025 +1.8 3/3 methods agree | Reporting / coding artifact | serious PRR 6.1 | no trial arm names this drug |
| Off label use (used outside approved label) | 8,523 | 4.5 4.4–4.6ROR 5.3 · χ² 24,016 / p <1e-300 | 4.5 EB05 4.4 · IC025 +2.1 3/3 methods agree | Reporting / coding artifact | serious PRR 4.9 | no trial arm names this drug |
| Rheumatoid arthritis | 5,753 | 24.4 23.8–25.0ROR 27.7 · χ² 122,934 / p <1e-300 | 23.2 EB05 22.7 · IC025 +4.5 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 17.1 · ♀ 95% (drug 67%) | no trial arm names this drug |
| Fatigue (tiredness) | 5,474 | 3.2 3.1–3.3ROR 3.5 · χ² 8,659 / p <1e-300 | 3.2 EB05 3.1 · IC025 +1.6 3/3 methods agree | Labeled (related wording) related wording | serious PRR 3.7 · ♀ 91% (drug 67%) | no trial arm names this drug |
| Pain | 5,458 | 4.1 4.0–4.2ROR 4.5 · χ² 12,885 / p <1e-300 | 4.0 EB05 3.9 · IC025 +2.0 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 3.8 · ♀ 90% (drug 67%) | no trial arm names this drug |
| Arthralgia (joint pain) | 5,202 | 5.8 5.6–5.9ROR 6.4 · χ² 20,694 / p <1e-300 | 5.7 EB05 5.6 · IC025 +2.5 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 6.3 · ♀ 91% (drug 67%) | no trial arm names this drug |
| Rash | 4,644 | 4.9 4.8–5.1ROR 5.4 · χ² 14,644 / p <1e-300 | 4.9 EB05 4.8 · IC025 +2.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 6.5 · ♀ 92% (drug 67%) | no trial arm names this drug |
| Condition aggravated | 4,449 | 6.8 6.6–7.0ROR 7.4 · χ² 21,972 / p <1e-300 | 6.7 EB05 6.5 · IC025 +2.7 3/3 methods agree | Reporting / coding artifact | serious PRR 6.1 | no trial arm names this drug |
| Drug intolerance | 4,263 | 21.1 20.5–21.7ROR 23.1 · χ² 78,173 / p <1e-300 | 20.2 EB05 19.7 · IC025 +4.3 3/3 methods agree | Reporting / coding artifact | serious PRR 19.8 · ♀ 93% (drug 67%) | no trial arm names this drug |
| Systemic lupus erythematosus | 4,111 | 59.8 58.0–61.7ROR 65.6 · χ² 210,145 / p <1e-300 | 52.9 EB05 51.6 · IC025 +5.7 3/3 methods agree | Labeled (related wording) related wording | serious PRR 32.8 · ♀ 96% (drug 67%) · 93% clinician | no trial arm names this drug |
| Diarrhoea (diarrhea) | 4,109 | 2.9 2.8–3.0ROR 3.1 · χ² 5,320 / p <1e-300 | 2.9 EB05 2.8 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious PRR 3.1 · ♀ 89% (drug 67%) | no trial arm names this drug |
| Nausea | 4,062 | 2.4 2.3–2.4ROR 2.5 · χ² 3,260 / p <1e-300 | 2.3 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.7 · ♀ 91% (drug 67%) | no trial arm names this drug |
| Joint swelling | 4,048 | 15.8 15.3–16.3ROR 17.2 · χ² 54,523 / p <1e-300 | 15.3 EB05 14.9 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 15.9 · ♀ 96% (drug 67%) | no trial arm names this drug |
| Headache | 4,025 | 2.9 2.9–3.0ROR 3.1 · χ² 5,274 / p <1e-300 | 2.9 EB05 2.9 · IC025 +1.5 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 3.6 · ♀ 87% (drug 67%) | no trial arm names this drug |
| Alopecia (hair loss) | 3,895 | 9.2 8.9–9.5ROR 9.9 · χ² 28,066 / p <1e-300 | 9.0 EB05 8.8 · IC025 +3.1 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 11.6 · ♀ 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 938.0
- Grip strength — n=139, PRR 692.4
- Deep vein thrombosis postoperative — n=1,063, PRR 545.9
- Chronic recurrent multifocal osteomyelitis — n=57, PRR 482.2
- Facet joint syndrome — n=1,478, PRR 405.5
- Adjustment disorder with depressed mood — n=869, PRR 347.6
- Swollen joint count — n=106, PRR 346.9
- Hypocholesterolaemia — n=127, PRR 321.7
- Retinitis — n=668, PRR 305.6
- Dislocation of vertebra — n=822, PRR 268.2
✓ 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-Fkjp?
In FDA FAERS, the most frequently co-reported reaction terms for Adalimumab-Fkjp are rheumatoid arthritis, fatigue, pain, arthralgia, rash, systemic lupus erythematosus. 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-Fkjp have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: SERIOUS INFECTIONS and MALIGNANCY SERIOUS INFECTIONS Patients treated with adalimumab products including Adalimumab-fkjp are at increased risk for developing serious infections that may lead to hospitalization or death [see Warnings and Precautions (5.1) ] .
Do FAERS signals prove that Adalimumab-Fkjp 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 5cde907d-6747-0e62-db25-1718ee717fe7, effective 20260112; matched on
openfda.generic_name.exact:"ADALIMUMAB-FKJP" 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, 1,276 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-FKJP, results-bearing studies sorted by enrollment)
Page generated 2026-10-08. 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.