← All drugs
Drug · FAERS side-effect profile with label screen

Fosaprepitant Dimeglumine side effects: what 13,667 FDA adverse event reports show

Fosaprepitant Dimeglumine · Fosaprepitant · 1,046 reaction terms · 91,170 drug–reaction co-reports · data 2026-09-14
Share: X Facebook Reddit Email

Drug class

Substance p/neurokinin-1 (nk 1 ) receptor antagonist

FDA label, Indications wording

Brand names

Fosaprepitant

openFDA label

Who reports

13,667 reports · 86% serious · 2,220 with death outcome · 63% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Fosaprepitant for Injection, in combination with other antiemetic agents, is indicated in adults and pediatric patients 6 months of age and older for the prevention of: • acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy (HEC) including high-dose cisplatin.

FDA label, Indications and Usage

What it is

Fosaprepitant for Injection is a sterile, lyophilized formulation containing fosaprepitant dimeglumine, a prodrug of aprepitant, a substance P/neurokinin-1 (NK 1 ) receptor antagonist, an anti.

FDA label, Description section

Boxed warning

None in the current 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) 3Reporting / coding artifact 1Lab value / disease marker 8Not in label — unassessed 28
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). 1,006 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
Grip strength1181,608.0
1,241.6–2,082.6ROR 1,622.0 · calibrated p 2e-19 ✓
691.8 EB05 593.2 · IC025 +7.2
3/3 methods agree
Not in label — unassessedserious n=118 · ♀ 100% (drug 63%) · 96% cliniciannot reported in cached trials
Testicular germ cell cancer metastatic131,404.6
660.3–2,987.6ROR 1,405.9 · calibrated p 3e-15 ✓
351.4 EB05 218.5 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=13not reported in cached trials
Computerised tomogram thorax23940.3
558.9–1,581.8ROR 941.9 · calibrated p 3e-15 ✓
391.0 EB05 274.4 · IC025 +4.7
3/3 methods agree
Not in label — unassessedserious n=23 · ♀ 100% (drug 63%) · 100% cliniciannot reported in cached trials
Swollen joint count77701.6
535.8–918.9ROR 705.6 · calibrated p 4e-15 ✓
428.4 EB05 353.9 · IC025 +6.5
3/3 methods agree
Not in label — unassessedserious n=77 · ♀ 100% (drug 63%) · 97% cliniciannot reported in cached trials
Procalcitonin decreased12318.4
170.9–593.3ROR 318.7 · calibrated p 3e-10 ✓
185.9 EB05 113.3 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=12not reported in cached trials
Acquired porphyria11282.0
148.2–536.7ROR 282.2 · calibrated p 8e-10 ✓
168.8 EB05 100.6 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=11not reported in cached trials
Lupus vulgaris165247.1
209.8–291.1ROR 250.1 · calibrated p 7e-11 ✓
207.5 EB05 182.2 · IC025 +6.8
3/3 methods agree
Not in label — unassessedserious n=165 · ♀ 100% (drug 63%) · 95% cliniciannot reported in cached trials
Pulmonary septal thickening12235.7
128.3–433.0ROR 235.9 · calibrated p 2e-9 ✓
154.5 EB05 94.2 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=12not reported in cached trials
Porphyria acute159199.8
169.5–235.5ROR 202.1 · calibrated p 5e-10 ✓
172.9 EB05 151.5 · IC025 +6.6
3/3 methods agree
Not in label — unassessedserious n=159 · ♀ 100% (drug 63%) · 97% cliniciannot reported in cached trials
X-ray abnormal192185.0
159.4–214.7ROR 187.6 · calibrated p 8e-10 ✓
162.3 EB05 143.9 · IC025 +6.6
3/3 methods agree
Lab value / disease markerserious n=192 · ♀ 100% (drug 63%) · 98% cliniciannot reported in cached trials
Anti-cyclic citrullinated peptide antibody67171.2
133.0–220.3ROR 172.0 · calibrated p 3e-9 ✓
147.5 EB05 120.2 · IC025 +5.8
3/3 methods agree
Lab value / disease markerserious n=67 · ♀ 100% (drug 63%) · 99% cliniciannot reported in cached trials
C-reactive protein89166.8
134.1–207.5ROR 167.9 · calibrated p 3e-9 ✓
145.7 EB05 122.0 · IC025 +6.0
3/3 methods agree
Lab value / disease markerserious n=89 · ♀ 100% (drug 63%) · 98% cliniciannot reported in cached trials
Deep vein thrombosis postoperative192166.5
143.6–193.1ROR 168.9 · calibrated p 2e-9 ✓
147.9 EB05 131.2 · IC025 +6.5
3/3 methods agree
Not in label — unassessedserious n=192 · ♀ 100% (drug 63%) · 94% cliniciannot reported in cached trials
Adjustment disorder with depressed mood186156.0
134.2–181.2ROR 158.1 · calibrated p 4e-9 ✓
139.5 EB05 123.4 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=186 · ♀ 100% (drug 63%) · 96% cliniciannot reported in cached trials
Retinitis153154.8
131.2–182.7ROR 156.5 · calibrated p 4e-9 ✓
138.1 EB05 120.7 · IC025 +6.3
3/3 methods agree
Not in label — unassessedserious n=153 · ♀ 100% (drug 63%) · 95% cliniciannot reported in cached trials
Nail bed inflammation28148.1
100.5–218.2ROR 148.4 · calibrated p 2e-8 ✓
123.8 EB05 89.9 · IC025 +4.7
3/3 methods agree
Not in label — unassessedserious n=27 · ♀ 100% (drug 63%)not reported in cached trials
Dislocation of vertebra189142.4
122.8–165.2ROR 144.4 · calibrated p 7e-9 ✓
128.6 EB05 113.9 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=189 · ♀ 100% (drug 63%) · 95% cliniciannot reported in cached trials
Facet joint syndrome244128.7
113.0–146.5ROR 131.0 · calibrated p 2e-8 ✓
117.6 EB05 105.7 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=244 · ♀ 100% (drug 63%) · 95% cliniciannot reported in cached trials
Duodenal ulcer perforation546123.3
113.2–134.3ROR 128.4 · calibrated p 2e-8 ✓
113.6 EB05 105.8 · IC025 +6.6
3/3 methods agree
Not in label — unassessedserious PRR 76.6 · ♀ 100% (drug 63%) · 94% clinicianNCT00619359: 1/1,143 (0.1%) on Fosaprepitant Dimeglumine (serious AE)
Tonsillar haemorrhage11123.3
66.7–227.8ROR 123.3 · calibrated p 3e-7 ✓
95.6 EB05 57.0 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=11not reported in cached trials
Sleep disorder due to general medical condition, insomnia type466119.7
109.1–131.3ROR 123.9 · calibrated p 2e-8 ✓
110.5 EB05 102.3 · IC025 +6.5
3/3 methods agree
Not in label — unassessedserious n=466 · ♀ 100% (drug 63%) · 95% cliniciannot reported in cached trials
Swollen joint count increased219115.8
101.1–132.8ROR 117.7 · calibrated p 4e-8 ✓
106.7 EB05 95.3 · IC025 +6.2
3/3 methods agree
Lab value / disease markerserious n=219 · ♀ 100% (drug 63%) · 96% cliniciannot reported in cached trials
Anti-cyclic citrullinated peptide antibody positive482111.6
101.9–122.2ROR 115.6 · calibrated p 4e-8 ✓
103.6 EB05 96.1 · IC025 +6.4
3/3 methods agree
Lab value / disease markerserious PRR 70.2 · ♀ 100% (drug 63%) · 94% cliniciannot reported in cached trials
Eosinophil percentage decreased12100.8
56.2–180.8ROR 100.9 · calibrated p 9e-7 ✓
82.6 EB05 50.3 · IC025 +3.3
3/3 methods agree
Lab value / disease markerserious n=12not reported in cached trials
Computerised tomogram thorax abnormal43100.8
74.1–137.2ROR 101.2 · calibrated p 2e-7 ✓
90.9 EB05 70.3 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=43 · ♀ 100% (drug 63%) · 100% cliniciannot reported in cached trials
Rheumatic fever25996.7
85.3–109.5ROR 98.5 · calibrated p 1e-7 ✓
90.3 EB05 81.5 · IC025 +6.1
3/3 methods agree
Not in label — unassessedserious n=259 · ♀ 100% (drug 63%) · 96% cliniciannot reported in cached trials
Muscle injury47694.4
86.2–103.4ROR 97.8 · calibrated p 1e-7 ✓
88.6 EB05 82.1 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious PRR 64.8 · ♀ 100% (drug 63%) · 94% cliniciannot reported in cached trials
Colony stimulating factor therapy1294.0
52.5–168.5ROR 94.1 · calibrated p 1e-6 ✓
78.0 EB05 47.5 · IC025 +3.3
3/3 methods agree
Reporting / coding artifactserious n=12not reported in cached trials
Seminoma1387.0
49.8–152.1ROR 87.1 · calibrated p 2e-6 ✓
73.8 EB05 45.9 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=13not reported in cached trials
Folliculitis54986.1
79.1–93.7ROR 89.7 · calibrated p 3e-7 ✓
81.3 EB05 75.7 · IC025 +6.1
3/3 methods agree
Not in label — unassessedserious PRR 64.4 · ♀ 99% (drug 63%) · 95% cliniciannot reported in cached trials
Helicobacter infection53184.3
77.3–91.8ROR 87.6 · calibrated p 3e-7 ✓
79.7 EB05 74.1 · IC025 +6.1
3/3 methods agree
Not in label — unassessedserious PRR 56.8 · ♀ 100% (drug 63%) · 94% cliniciannot reported in cached trials
Rheumatoid factor positive27877.6
68.9–87.5ROR 79.2 · calibrated p 7e-7 ✓
73.5 EB05 66.6 · IC025 +5.8
3/3 methods agree
Lab value / disease markerserious n=278 · ♀ 100% (drug 63%) · 96% cliniciannot reported in cached trials
Bone erosion16574.9
64.1–87.5ROR 75.8 · calibrated p 1e-6 ✓
70.9 EB05 62.2 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=165 · ♀ 100% (drug 63%) · 98% cliniciannot reported in cached trials
Nasal mucosal disorder2774.3
50.5–109.2ROR 74.4 · calibrated p 2e-6 ✓
67.6 EB05 48.8 · IC025 +4.3
3/3 methods agree
Not in label — unassessedserious n=27 · ♀ 100% (drug 63%)not reported in cached trials
Peripheral venous disease17369.4
59.7–80.8ROR 70.3 · calibrated p 2e-6 ✓
66.0 EB05 58.1 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=172 · ♀ 100% (drug 63%) · 94% cliniciannot reported in cached trials
Blood creatine decreased1368.5
39.3–119.4ROR 68.6 · calibrated p 8e-6 ✓
60.1 EB05 37.4 · IC025 +3.3
3/3 methods agree
Lab value / disease markerserious n=13not reported in cached trials
Subcutaneous drug absorption impaired2367.6
44.5–102.5ROR 67.7 · calibrated p 5e-6 ✓
61.6 EB05 43.2 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=23 · ♀ 100% (drug 63%) · 91% cliniciannot reported in cached trials

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Fosaprepitant Dimeglumine 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 (1 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
Nausea1,4782.9
2.7–3.0ROR 3.1 · calibrated p 0.593
2.9 EB05 2.8 · IC025 +1.4
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 3.0NCT00619359: 4/1,143 (0.3%) on Fosaprepitant Dimeglumine (serious AE)
Dyspnoea (shortness of breath)1,2693.4
3.3–3.6ROR 3.7 · calibrated p 0.439
3.4 EB05 3.3 · IC025 +1.7
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 2.8NCT00619359: 2/1,143 (0.2%) on Fosaprepitant Dimeglumine (serious AE)
Pyrexia (fever)1,1295.0
4.7–5.3ROR 5.4 · calibrated p 0.198
5.0 EB05 4.8 · IC025 +2.2
3/3 methods agree
Not in label — unassessedserious PRR 4.2 · 91% clinicianNCT00619359: 1/1,143 (0.1%) on Fosaprepitant Dimeglumine (serious AE)
Diarrhoea (diarrhea)1,1102.6
2.5–2.8ROR 2.8 · calibrated p 0.697
2.6 EB05 2.5 · IC025 +1.3
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.0NCT00619359: 3/1,143 (0.3%) on Fosaprepitant Dimeglumine (serious AE)
Vomiting1,0813.5
3.3–3.8ROR 3.8 · calibrated p 0.425
3.5 EB05 3.4 · IC025 +1.7
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 3.2NCT00619359: 13/1,143 (1.1%) on Fosaprepitant Dimeglumine (serious AE)
Fatigue (tiredness)1,0802.1
2.0–2.3ROR 2.2 · calibrated p 0.936
2.1 EB05 2.0 · IC025 +1.0
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 2.5 · ♀ 86% (drug 63%)NCT00619359: 1/1,169 (0.1%) on Fosaprepitant Dimeglumine (serious AE)
Off label use (used outside approved label)8911.6
1.5–1.7ROR 1.6 · calibrated p 0.716
1.6 EB05 1.5 · IC025 +0.5Reporting / coding artifactserious PRR 1.9not reported in cached trials
Alopecia (hair loss)8866.9
6.5–7.4ROR 7.3 · calibrated p 0.086
6.9 EB05 6.5 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious PRR 8.5 · ♀ 99% (drug 63%)NCT00619359: 12/1,143 (1.0%) on Fosaprepitant Dimeglumine
Rash8633.1
2.9–3.3ROR 3.2 · calibrated p 0.566
3.0 EB05 2.9 · IC025 +1.5
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 4.3 · ♀ 83% (drug 63%)not reported in cached trials
Hypersensitivity (allergic reaction)8356.9
6.5–7.4ROR 7.3 · calibrated p 0.087
6.9 EB05 6.5 · IC025 +2.7
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 8.4 · ♀ 84% (drug 63%) · 94% clinicianNCT01594749: 1/504 (0.2%) on Fosaprepitant Dimeglumine (serious AE)
Febrile neutropenia81919.2
18.0–20.5ROR 20.4 · calibrated p 0.002 ✓
19.0 EB05 17.9 · IC025 +4.1
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 12.8 · 92% clinicianNCT00619359: 18/1,143 (1.6%) on Fosaprepitant Dimeglumine (serious AE)
Pruritus (itching)7443.0
2.8–3.2ROR 3.1 · calibrated p 0.583
3.0 EB05 2.8 · IC025 +1.5
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 4.7 · ♀ 89% (drug 63%) · 91% cliniciannot reported in cached trials
Infusion related reaction (reaction during infusion)74017.4
16.2–18.6ROR 18.3 · calibrated p 0.003 ✓
17.2 EB05 16.2 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious PRR 14.0 · ♀ 90% (drug 63%) · 94% cliniciannot reported in cached trials
Stomatitis (mouth sores)68417.5
16.2–18.8ROR 18.3 · calibrated p 0.003 ✓
17.3 EB05 16.2 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious PRR 17.1 · ♀ 88% (drug 63%) · 91% clinicianNCT00619359: 1/1,169 (0.1%) on Fosaprepitant Dimeglumine (serious AE)
Pain6561.6
1.5–1.8ROR 1.7 · calibrated p 0.750
1.6 EB05 1.5 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.7 · ♀ 90% (drug 63%)NCT00619359: 1/1,143 (0.1%) on Fosaprepitant Dimeglumine (serious AE)

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.

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 Fosaprepitant Dimeglumine?

In FDA FAERS, the most frequently co-reported reaction terms for Fosaprepitant Dimeglumine are nausea, dyspnoea, pyrexia, diarrhoea, vomiting, fatigue. 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 Fosaprepitant Dimeglumine have an FDA boxed warning?

No. The FDA label retrieved for Fosaprepitant Dimeglumine has no boxed warning; see the label's Warnings and Precautions for the recognised risks.

Do FAERS signals prove that Fosaprepitant Dimeglumine 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.