Pomalidomide side effects: what 101,956 FDA adverse event reports show
Drug class
Thalidomide Analog
Who reports
101,956 reports · 62% serious · 14,025 with death outcome · 48% female
Used for
Pomalidomide capsules are a thalidomide analogue indicated for the treatment of adult patients: in combination with dexamethasone, for patients with multiple myeloma (MM) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy ( 1.1 ).
What it is
Pomalidomide is a thalidomide analog.
Boxed warning
EMBRYO-FETAL TOXICITY and VENOUS AND ARTERIAL THROMBOEMBOLISM WARNING: EMBRYO-FETAL TOXICITY and VENOUS AND ARTERIAL THROMBOEMBOLISM See full prescribing information for complete boxed warning EMBRYO-FETAL TOXICITY Pomalidomide capsules are contraindicated in pregnancy. Pomalidomide capsules are a thalidomide analogue.
Causality screen of the 40 strongest signals
What the badges mean
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- 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). 1,076 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 |
|---|---|---|---|---|---|---|
| Cellulitis enterococcal | 18 | 604.5 239.9–1,522.7ROR 604.6 · calibrated p 7e-11 ✓ | 131.1 EB05 87.7 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=18 | not reported in cached trials |
| Plasma cell myeloma refractory | 358 | 78.3 69.3–88.5ROR 78.6 · calibrated p 7e-7 ✓ | 56.5 EB05 51.8 · IC025 +5.5 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=357 · 92% clinician | not reported in cached trials |
| Clonal haematopoiesis | 18 | 65.9 38.7–112.3ROR 66.0 · calibrated p 9e-6 ✓ | 47.6 EB05 31.8 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | serious n=18 | not reported in cached trials |
| Plasma cell myeloma | 8,060 | 53.2 52.0–54.5ROR 57.7 · calibrated p 5e-6 ✓ | 42.3 EB05 41.5 · IC025 +5.4 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious PRR 38.1 | NCT01712789: 4/676 (0.6%) on Pomalidomide (serious AE) |
| Monoclonal immunoglobulin increased | 51 | 45.1 33.3–61.1ROR 45.1 · calibrated p 4e-5 ✓ | 36.6 EB05 28.9 · IC025 +4.3 3/3 methods agree | Lab value / disease marker | serious n=28 | NCT01712789: 3/676 (0.4%) on Pomalidomide (serious AE) |
| Corneal epithelial microcysts | 28 | 42.4 28.2–63.8ROR 42.4 · calibrated p 7e-5 ✓ | 34.5 EB05 25.0 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=27 · 100% consumer | not reported in cached trials |
| Plasma cell leukaemia | 102 | 42.0 34.0–52.0ROR 42.1 · calibrated p 5e-5 ✓ | 34.7 EB05 29.4 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=102 · 92% clinician | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Light chain analysis increased | 171 | 40.9 34.7–48.2ROR 41.0 · calibrated p 5e-5 ✓ | 34.1 EB05 30.0 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=91 | not reported in cached trials |
| Plasmacytoma | 301 | 39.1 34.5–44.2ROR 39.2 · calibrated p 6e-5 ✓ | 32.8 EB05 29.8 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious n=289 | NCT01712789: 10/676 (1.5%) on Pomalidomide (serious AE) |
| Plasma cell myeloma recurrent | 513 | 38.1 34.7–41.8ROR 38.3 · calibrated p 7e-5 ✓ | 32.2 EB05 29.9 · IC025 +4.8 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=431 | not reported in cached trials |
| Light chain disease | 23 | 38.0 24.3–59.3ROR 38.0 · calibrated p 1e-4 ✓ | 31.4 EB05 22.0 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | serious n=22 | not reported in cached trials |
| Light chain analysis abnormal | 30 | 34.7 23.6–51.2ROR 34.7 · calibrated p 2e-4 ✓ | 29.3 EB05 21.5 · IC025 +3.7 3/3 methods agree | Reporting / coding artifact | serious n=15 | not reported in cached trials |
| Ivth nerve paralysis | 31 | 32.4 22.1–47.3ROR 32.4 · calibrated p 3e-4 ✓ | 27.6 EB05 20.4 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | serious n=31 · ♀ 0% (drug 48%) · 100% clinician | not reported in cached trials |
| Human chorionic gonadotropin increased | 110 | 28.7 23.5–35.1ROR 28.7 · calibrated p 4e-4 ✓ | 25.2 EB05 21.5 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=74 · ♀ 100% (drug 48%) · 95% clinician | not reported in cached trials |
| Pneumonia parainfluenzae viral | 21 | 28.4 18.0–44.8ROR 28.4 · calibrated p 7e-4 ✓ | 24.5 EB05 16.9 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=21 · 100% clinician | NCT01734928: 1/278 (0.4%) on Pomalidomide (serious AE) |
| Monoclonal immunoglobulin present | 86 | 25.9 20.7–32.4ROR 25.9 · calibrated p 7e-4 ✓ | 23.0 EB05 19.2 · IC025 +4.0 3/3 methods agree | Lab value / disease marker | serious n=43 | NCT01712789: 3/676 (0.4%) on Pomalidomide (serious AE) |
| Paraproteinaemia | 34 | 24.9 17.4–35.6ROR 24.9 · calibrated p 1e-3 ✓ | 22.0 EB05 16.5 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=33 · 100% clinician | not reported in cached trials |
| Full blood count decreased | 1,764 | 19.6 18.7–20.6ROR 19.9 · calibrated p 0.002 ✓ | 17.9 EB05 17.3 · IC025 +4.1 3/3 methods agree | Lab value / disease marker | serious PRR 14.3 | not reported in cached trials |
| Emergency care examination | 55 | 18.1 13.7–23.8ROR 18.1 · calibrated p 0.004 ✓ | 16.6 EB05 13.2 · IC025 +3.4 3/3 methods agree | Reporting / coding artifact | – | not reported in cached trials |
| Full blood count increased | 96 | 17.8 14.5–22.0ROR 17.9 · calibrated p 0.004 ✓ | 16.4 EB05 13.8 · IC025 +3.6 3/3 methods agree | Lab value / disease marker | serious n=15 | not reported in cached trials |
| Pneumonia respiratory syncytial viral | 62 | 16.6 12.8–21.5ROR 16.6 · calibrated p 0.005 ✓ | 15.3 EB05 12.3 · IC025 +3.4 3/3 methods agree | Labeled adverse reaction exact term | serious n=62 · ♀ 21% (drug 48%) | NCT01712789: 2/676 (0.3%) on Pomalidomide (serious AE) |
| Laboratory test abnormal | 1,309 | 9.5 9.0–10.0ROR 9.6 · calibrated p 0.037 ✓ | 9.1 EB05 8.7 · IC025 +3.1 3/3 methods agree | Reporting / coding artifact | serious PRR 5.6 | not reported in cached trials |
| Pneumonia influenzal | 52 | 9.3 7.0–12.3ROR 9.3 · calibrated p 0.045 ✓ | 8.5 EB05 6.7 · IC025 +2.6 3/3 methods agree | Not in label — unassessed | serious n=52 | NCT01712789: 3/676 (0.4%) on Pomalidomide (serious AE) |
| Crystal nephropathy | 25 | 9.1 6.1–13.6ROR 9.1 · calibrated p 0.053 | 7.9 EB05 5.5 · IC025 +2.3 3/3 methods agree | Not in label — unassessed | serious n=25 · ♀ 100% (drug 48%) · 100% clinician | not reported in cached trials |
| Osteolysis | 85 | 8.8 7.1–11.0ROR 8.8 · calibrated p 0.051 | 8.3 EB05 6.8 · IC025 +2.7 3/3 methods agree | Not in label — unassessed | serious n=82 · 91% clinician | NCT01712789: 2/676 (0.3%) on Pomalidomide (serious AE) |
| Product distribution issue | 367 | 8.8 8.0–9.8ROR 8.9 · calibrated p 0.049 ✓ | 8.4 EB05 7.7 · IC025 +2.9 3/3 methods agree | Reporting / coding artifact | serious n=39 · 77% consumer | not reported in cached trials |
| Amyloidosis | 69 | 8.5 6.7–10.8ROR 8.5 · calibrated p 0.058 | 7.9 EB05 6.4 · IC025 +2.6 3/3 methods agree | Not in label — unassessed | serious n=67 | NCT01712789: 2/676 (0.3%) on Pomalidomide (serious AE) |
| Vertebral lesion | 20 | 8.3 5.3–13.0ROR 8.3 · calibrated p 0.071 | 7.1 EB05 4.7 · IC025 +2.0 3/3 methods agree | Not in label — unassessed | serious n=13 | not reported in cached trials |
| Blood immunoglobulin a increased | 21 | 8.3 5.4–12.9ROR 8.3 · calibrated p 0.071 | 7.1 EB05 4.8 · IC025 +2.1 3/3 methods agree | Lab value / disease marker | – | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Pneumococcal sepsis | 25 | 8.2 5.5–12.2ROR 8.2 · calibrated p 0.073 | 7.1 EB05 5.0 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious n=25 · 100% clinician | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Parainfluenzae virus infection | 57 | 7.8 6.0–10.2ROR 7.8 · calibrated p 0.076 | 7.2 EB05 5.7 · IC025 +2.4 3/3 methods agree | Not in label — unassessed | serious n=54 · 93% clinician | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Bone lesion | 128 | 7.5 6.3–9.0ROR 7.5 · calibrated p 0.082 | 7.1 EB05 6.1 · IC025 +2.5 3/3 methods agree | Not in label — unassessed | serious n=100 | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| White blood cell count decreased | 3,664 | 7.1 6.9–7.4ROR 7.4 · calibrated p 0.085 | 6.9 EB05 6.7 · IC025 +2.7 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 4.5 | NCT01712789: 2/676 (0.3%) on Pomalidomide (serious AE) |
| Cytopenia | 401 | 7.1 6.4–7.8ROR 7.1 · calibrated p 0.095 | 6.8 EB05 6.3 · IC025 +2.6 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 6.2 · 93% clinician | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Pneumonia pneumococcal | 47 | 6.7 5.0–9.0ROR 6.7 · calibrated p 0.119 | 6.2 EB05 4.8 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious n=47 · 100% clinician | NCT01712789: 5/676 (0.7%) on Pomalidomide (serious AE) |
| Jc virus infection | 50 | 6.6 5.0–8.7ROR 6.6 · calibrated p 0.123 | 6.1 EB05 4.8 · IC025 +2.1 3/3 methods agree | Labeled (related wording) related wording | serious n=50 · 100% clinician | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Blood immunoglobulin m increased | 19 | 6.5 4.1–10.3ROR 6.5 · calibrated p 0.138 | 5.6 EB05 3.8 · IC025 +1.7 3/3 methods agree | Lab value / disease marker | serious n=13 | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Protein total increased | 81 | 6.4 5.2–8.0ROR 6.4 · calibrated p 0.129 | 6.1 EB05 5.0 · IC025 +2.2 3/3 methods agree | Lab value / disease marker | serious n=32 | not reported in cached trials |
| Keratopathy | 48 | 6.4 4.8–8.6ROR 6.4 · calibrated p 0.133 | 5.9 EB05 4.6 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious n=47 · ♀ 28% (drug 48%) | not reported in cached trials |
| Listeriosis | 33 | 6.3 4.5–8.9ROR 6.3 · calibrated p 0.142 | 5.7 EB05 4.2 · IC025 +1.9 3/3 methods agree | Not in label — unassessed | serious n=31 · 91% clinician | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Pomalidomide as a study intervention. The right-hand column of the signal table shows whether each FAERS term was also recorded in these trials, with a real denominator (20 of 40 signal terms matched).
- NCT01712789 — Evaluation of Safety of Pomalidomide in Combination With Dexamethasone (Low Dose) in Patients With Refractory (N=682, PHASE3; 345 AE terms posted; arms: Pomalidomide Plus Low Dose Dexamethasone)
- NCT01734928 — Safety and Efficacy of Pomalidomide, Bortezomib and Low-dose Dexamethasone in Subjects With Relapsed or Refrac (N=559, PHASE3; 347 AE terms posted; arms: Treatment 1: POM + BTZ + LD-DEX; Treatment 2: BTZ + LD-DEX)
Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.
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 |
|---|---|---|---|---|---|---|
| Plasma cell myeloma | 8,060 | 53.2 52.0–54.5ROR 57.7 · calibrated p 5e-6 ✓ | 42.3 EB05 41.5 · IC025 +5.4 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious PRR 38.1 | NCT01712789: 4/676 (0.6%) on Pomalidomide (serious AE) |
| Death | 7,703 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.895 | 1.8 EB05 1.8 · IC025 +0.8 | Outcome field, not a reaction boxed warning mentions mortality | serious PRR 1.7 | NCT01712789: 4/676 (0.6%) on Pomalidomide (serious AE) |
| Fatigue (tiredness) | 7,499 | 2.0 1.9–2.0ROR 2.1 · calibrated p 0.981 | 2.0 EB05 1.9 · IC025 +0.9 | Labeled adverse reaction exact term | serious PRR 1.3 | NCT01712789: 5/676 (0.7%) on Pomalidomide (serious AE) |
| Pneumonia (lung infection) | 6,314 | 4.1 4.0–4.2ROR 4.3 · calibrated p 0.331 | 4.0 EB05 3.9 · IC025 +2.0 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 3.9 | NCT01712789: 4/676 (0.6%) on Pomalidomide (serious AE) |
| Off label use (used outside approved label) | 4,578 | 1.1 1.1–1.1ROR 1.1 · calibrated p 0.364 | 1.1 EB05 1.1 · IC025 +0.1 | Reporting / coding artifact | serious PRR 1.1 | not reported in cached trials |
| Diarrhoea (diarrhea) | 3,909 | 1.2 1.2–1.3ROR 1.3 · calibrated p 0.480 | 1.2 EB05 1.2 · IC025 +0.3 | Labeled adverse reaction exact term | serious PRR 0.9 | NCT01712789: 6/676 (0.9%) on Pomalidomide (serious AE) |
| White blood cell count decreased | 3,664 | 7.1 6.9–7.4ROR 7.4 · calibrated p 0.085 | 6.9 EB05 6.7 · IC025 +2.7 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 4.5 | NCT01712789: 2/676 (0.3%) on Pomalidomide (serious AE) |
| Neutropenia (low neutrophils (infection-fighting cells)) | 3,342 | 5.2 5.0–5.3ROR 5.3 · calibrated p 0.204 | 5.1 EB05 4.9 · IC025 +2.3 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 4.4 · 92% clinician | NCT01712789: 34/676 (5.0%) on Pomalidomide (serious AE) |
| Rash | 3,064 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.620 | 1.4 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | serious PRR 1.0 | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Dyspnoea (shortness of breath) | 2,846 | 1.0 1.0–1.1ROR 1.0 · calibrated p 0.328 | 1.0 EB05 1.0 · IC025 -0.0 PRR-only: not supported by EBGM or IC | Labeled adverse reaction exact term | serious PRR 0.8 | NCT01712789: 15/676 (2.2%) on Pomalidomide (serious AE) |
| Asthenia (weakness) | 2,684 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.629 | 1.5 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | serious PRR 1.1 | NCT01712789: 5/676 (0.7%) on Pomalidomide (serious AE) |
| Neuropathy peripheral (nerve damage in hands/feet) | 2,669 | 5.9 5.7–6.2ROR 6.1 · calibrated p 0.146 | 5.8 EB05 5.6 · IC025 +2.5 3/3 methods agree | Labeled (related wording) related wording | serious PRR 5.5 | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Constipation | 2,668 | 2.5 2.5–2.6ROR 2.6 · calibrated p 0.775 | 2.5 EB05 2.4 · IC025 +1.3 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 1.6 | NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE) |
| Nausea | 2,565 | 0.7 0.6–0.7ROR 0.7 · calibrated p 0.110 | 0.7 EB05 0.6 · IC025 -0.6 PRR-only: not supported by EBGM or IC | Labeled adverse reaction exact term | serious PRR 0.5 | NCT01712789: 3/676 (0.4%) on Pomalidomide (serious AE) |
| Product dose omission issue | 2,275 | 1.6 1.6–1.7ROR 1.7 · calibrated p 0.744 | 1.6 EB05 1.6 · IC025 +0.6 | Reporting / coding artifact | serious PRR 1.3 · 71% consumer | not reported in cached trials |
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.
- Corneal epithelial microcysts — n=28, PRR 42.4
- Plasma cell leukaemia — n=102, PRR 42.0 (also seen in trial arm)
- Light chain analysis increased — n=171, PRR 40.9
- Plasmacytoma — n=301, PRR 39.1 (also seen in trial arm)
- Light chain disease — n=23, PRR 38.0
- Ivth nerve paralysis — n=31, PRR 32.4
- Human chorionic gonadotropin increased — n=110, PRR 28.7
- Pneumonia parainfluenzae viral — n=21, PRR 28.4 (also seen in trial arm)
- Paraproteinaemia — n=34, PRR 24.9
- Pneumonia influenzal — n=52, PRR 9.3 (also seen in trial arm)
✓ A hand-written Bradford Hill causality assessment exists for this drug: Pomalidomide ↔ Plasma Cell Myeloma.
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 Pomalidomide?
In FDA FAERS, the most frequently co-reported reaction terms for Pomalidomide are plasma cell myeloma, fatigue, pneumonia, diarrhoea, white blood cell count decreased, neutropenia. 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 Pomalidomide have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: EMBRYO-FETAL TOXICITY and VENOUS AND ARTERIAL THROMBOEMBOLISM WARNING: EMBRYO-FETAL TOXICITY and VENOUS AND ARTERIAL THROMBOEMBOLISM See full prescribing information for complete boxed warning EMBRYO-FETAL TOXICITY Pomalidomide capsules are contraindicated in pregnancy. Pomalidomide capsules are a thalidomide analogue.
Do FAERS signals prove that Pomalidomide 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 41400b90-b64e-447b-90f3-1cad58050eba, effective 20260304; matched on
openfda.generic_name.exact:"POMALIDOMIDE") - 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, 1,116 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
POMALIDOMIDE, 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.