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Pomalidomide side effects: what 101,956 FDA adverse event reports show

Pomalidomide · 1,116 reaction terms · 210,693 drug–reaction co-reports · data 2026-09-14
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Drug class

Thalidomide Analog

FDA label (Established Pharmacologic Class)

Who reports

101,956 reports · 62% serious · 14,025 with death outcome · 48% female

openFDA FAERS counts, all years, deduplication not applied

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 ).

FDA label, Indications and Usage

What it is

Pomalidomide is a thalidomide analog.

FDA label, Description section

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.

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 adverse reaction 3Labeled (related wording) 1Likely indication confounding 3Reporting / coding artifact 4Lab value / disease marker 7Not 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). 1,076 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
Cellulitis enterococcal18604.5
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 — unassessedserious n=18not reported in cached trials
Plasma cell myeloma refractory35878.3
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% cliniciannot reported in cached trials
Clonal haematopoiesis1865.9
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 — unassessedserious n=18not reported in cached trials
Plasma cell myeloma8,06053.2
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 38.1NCT01712789: 4/676 (0.6%) on Pomalidomide (serious AE)
Monoclonal immunoglobulin increased5145.1
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 markerserious n=28NCT01712789: 3/676 (0.4%) on Pomalidomide (serious AE)
Corneal epithelial microcysts2842.4
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 — unassessedserious n=27 · 100% consumernot reported in cached trials
Plasma cell leukaemia10242.0
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 — unassessedserious n=102 · 92% clinicianNCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE)
Light chain analysis increased17140.9
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 — unassessedserious n=91not reported in cached trials
Plasmacytoma30139.1
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 — unassessedserious n=289NCT01712789: 10/676 (1.5%) on Pomalidomide (serious AE)
Plasma cell myeloma recurrent51338.1
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=431not reported in cached trials
Light chain disease2338.0
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 — unassessedserious n=22not reported in cached trials
Light chain analysis abnormal3034.7
23.6–51.2ROR 34.7 · calibrated p 2e-4 ✓
29.3 EB05 21.5 · IC025 +3.7
3/3 methods agree
Reporting / coding artifactserious n=15not reported in cached trials
Ivth nerve paralysis3132.4
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 — unassessedserious n=31 · ♀ 0% (drug 48%) · 100% cliniciannot reported in cached trials
Human chorionic gonadotropin increased11028.7
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 — unassessedserious n=74 · ♀ 100% (drug 48%) · 95% cliniciannot reported in cached trials
Pneumonia parainfluenzae viral2128.4
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 — unassessedserious n=21 · 100% clinicianNCT01734928: 1/278 (0.4%) on Pomalidomide (serious AE)
Monoclonal immunoglobulin present8625.9
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 markerserious n=43NCT01712789: 3/676 (0.4%) on Pomalidomide (serious AE)
Paraproteinaemia3424.9
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 — unassessedserious n=33 · 100% cliniciannot reported in cached trials
Full blood count decreased1,76419.6
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 markerserious PRR 14.3not reported in cached trials
Emergency care examination5518.1
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 increased9617.8
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 markerserious n=15not reported in cached trials
Pneumonia respiratory syncytial viral6216.6
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 abnormal1,3099.5
9.0–10.0ROR 9.6 · calibrated p 0.037 ✓
9.1 EB05 8.7 · IC025 +3.1
3/3 methods agree
Reporting / coding artifactserious PRR 5.6not reported in cached trials
Pneumonia influenzal529.3
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 — unassessedserious n=52NCT01712789: 3/676 (0.4%) on Pomalidomide (serious AE)
Crystal nephropathy259.1
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 — unassessedserious n=25 · ♀ 100% (drug 48%) · 100% cliniciannot reported in cached trials
Osteolysis858.8
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 — unassessedserious n=82 · 91% clinicianNCT01712789: 2/676 (0.3%) on Pomalidomide (serious AE)
Product distribution issue3678.8
8.0–9.8ROR 8.9 · calibrated p 0.049 ✓
8.4 EB05 7.7 · IC025 +2.9
3/3 methods agree
Reporting / coding artifactserious n=39 · 77% consumernot reported in cached trials
Amyloidosis698.5
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 — unassessedserious n=67NCT01712789: 2/676 (0.3%) on Pomalidomide (serious AE)
Vertebral lesion208.3
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 — unassessedserious n=13not reported in cached trials
Blood immunoglobulin a increased218.3
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 sepsis258.2
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 — unassessedserious n=25 · 100% clinicianNCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE)
Parainfluenzae virus infection577.8
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 — unassessedserious n=54 · 93% clinicianNCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE)
Bone lesion1287.5
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 — unassessedserious n=100NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE)
White blood cell count decreased3,6647.1
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 4.5NCT01712789: 2/676 (0.3%) on Pomalidomide (serious AE)
Cytopenia4017.1
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% clinicianNCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE)
Pneumonia pneumococcal476.7
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 — unassessedserious n=47 · 100% clinicianNCT01712789: 5/676 (0.7%) on Pomalidomide (serious AE)
Blood immunoglobulin m increased196.5
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 markerserious n=13NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE)
Protein total increased816.4
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 markerserious n=32not reported in cached trials
Keratopathy486.4
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 — unassessedserious n=47 · ♀ 28% (drug 48%)not reported in cached trials
Listeriosis336.3
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 — unassessedserious n=31 · 91% clinicianNCT01712789: 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).

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.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Plasma cell myeloma8,06053.2
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 38.1NCT01712789: 4/676 (0.6%) on Pomalidomide (serious AE)
Death7,7031.8
1.8–1.9ROR 1.9 · calibrated p 0.895
1.8 EB05 1.8 · IC025 +0.8Outcome field, not a reaction
boxed warning mentions mortality
serious PRR 1.7NCT01712789: 4/676 (0.6%) on Pomalidomide (serious AE)
Fatigue (tiredness)7,4992.0
1.9–2.0ROR 2.1 · calibrated p 0.981
2.0 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
serious PRR 1.3NCT01712789: 5/676 (0.7%) on Pomalidomide (serious AE)
Pneumonia (lung infection)6,3144.1
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 3.9NCT01712789: 4/676 (0.6%) on Pomalidomide (serious AE)
Off label use (used outside approved label)4,5781.1
1.1–1.1ROR 1.1 · calibrated p 0.364
1.1 EB05 1.1 · IC025 +0.1Reporting / coding artifactserious PRR 1.1not reported in cached trials
Diarrhoea (diarrhea)3,9091.2
1.2–1.3ROR 1.3 · calibrated p 0.480
1.2 EB05 1.2 · IC025 +0.3Labeled adverse reaction
exact term
serious PRR 0.9NCT01712789: 6/676 (0.9%) on Pomalidomide (serious AE)
White blood cell count decreased3,6647.1
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 4.5NCT01712789: 2/676 (0.3%) on Pomalidomide (serious AE)
Neutropenia (low neutrophils (infection-fighting cells))3,3425.2
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% clinicianNCT01712789: 34/676 (5.0%) on Pomalidomide (serious AE)
Rash3,0641.5
1.4–1.5ROR 1.5 · calibrated p 0.620
1.4 EB05 1.4 · IC025 +0.5Labeled adverse reaction
exact term
serious PRR 1.0NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE)
Dyspnoea (shortness of breath)2,8461.0
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 0.8NCT01712789: 15/676 (2.2%) on Pomalidomide (serious AE)
Asthenia (weakness)2,6841.5
1.4–1.5ROR 1.5 · calibrated p 0.629
1.5 EB05 1.4 · IC025 +0.5Labeled adverse reaction
exact term
serious PRR 1.1NCT01712789: 5/676 (0.7%) on Pomalidomide (serious AE)
Constipation2,6682.5
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 1.6NCT01712789: 1/676 (0.1%) on Pomalidomide (serious AE)
Nausea2,5650.7
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 0.5NCT01712789: 3/676 (0.4%) on Pomalidomide (serious AE)
Product dose omission issue2,2751.6
1.6–1.7ROR 1.7 · calibrated p 0.744
1.6 EB05 1.6 · IC025 +0.6Reporting / coding artifactserious PRR 1.3 · 71% consumernot 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.

✓ 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

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.