Fosaprepitant Dimeglumine side effects: what 13,667 FDA adverse event reports show
Drug class
Substance p/neurokinin-1 (nk 1 ) receptor antagonist
Brand names
Fosaprepitant
Who reports
13,667 reports · 86% serious · 2,220 with death outcome · 63% female
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.
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.
Boxed warning
None in the current label
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.
- 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). 1,006 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 |
|---|---|---|---|---|---|---|
| Grip strength | 118 | 1,608.0 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 — unassessed | serious n=118 · ♀ 100% (drug 63%) · 96% clinician | not reported in cached trials |
| Testicular germ cell cancer metastatic | 13 | 1,404.6 660.3–2,987.6ROR 1,405.9 · calibrated p 3e-15 ✓ | 351.4 EB05 218.5 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=13 | not reported in cached trials |
| Computerised tomogram thorax | 23 | 940.3 558.9–1,581.8ROR 941.9 · calibrated p 3e-15 ✓ | 391.0 EB05 274.4 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=23 · ♀ 100% (drug 63%) · 100% clinician | not reported in cached trials |
| Swollen joint count | 77 | 701.6 535.8–918.9ROR 705.6 · calibrated p 4e-15 ✓ | 428.4 EB05 353.9 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=77 · ♀ 100% (drug 63%) · 97% clinician | not reported in cached trials |
| Injection site vasculitis | 12 | 403.4 213.4–762.4ROR 403.7 · calibrated p 4e-11 ✓ | 211.7 EB05 129.1 · IC025 +3.6 3/3 methods agree | Labeled (related wording) related wording | serious n=11 | not reported in cached trials |
| Infusion site streaking | 15 | 319.6 183.1–557.6ROR 319.9 · calibrated p 1e-10 ✓ | 197.9 EB05 127.3 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | serious n=15 | not reported in cached trials |
| Procalcitonin decreased | 12 | 318.4 170.9–593.3ROR 318.7 · calibrated p 3e-10 ✓ | 185.9 EB05 113.3 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=12 | not reported in cached trials |
| Acquired porphyria | 11 | 282.0 148.2–536.7ROR 282.2 · calibrated p 8e-10 ✓ | 168.8 EB05 100.6 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=11 | not reported in cached trials |
| Lupus vulgaris | 165 | 247.1 209.8–291.1ROR 250.1 · calibrated p 7e-11 ✓ | 207.5 EB05 182.2 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious n=165 · ♀ 100% (drug 63%) · 95% clinician | not reported in cached trials |
| Pulmonary septal thickening | 12 | 235.7 128.3–433.0ROR 235.9 · calibrated p 2e-9 ✓ | 154.5 EB05 94.2 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=12 | not reported in cached trials |
| Porphyria acute | 159 | 199.8 169.5–235.5ROR 202.1 · calibrated p 5e-10 ✓ | 172.9 EB05 151.5 · IC025 +6.6 3/3 methods agree | Not in label — unassessed | serious n=159 · ♀ 100% (drug 63%) · 97% clinician | not reported in cached trials |
| Injection site phlebitis | 26 | 190.0 126.4–285.6ROR 190.4 · calibrated p 3e-9 ✓ | 150.4 EB05 107.9 · IC025 +4.7 3/3 methods agree | Labeled (related wording) related wording | serious n=25 · ♀ 100% (drug 63%) | not reported in cached trials |
| X-ray abnormal | 192 | 185.0 159.4–214.7ROR 187.6 · calibrated p 8e-10 ✓ | 162.3 EB05 143.9 · IC025 +6.6 3/3 methods agree | Lab value / disease marker | serious n=192 · ♀ 100% (drug 63%) · 98% clinician | not reported in cached trials |
| Anti-cyclic citrullinated peptide antibody | 67 | 171.2 133.0–220.3ROR 172.0 · calibrated p 3e-9 ✓ | 147.5 EB05 120.2 · IC025 +5.8 3/3 methods agree | Lab value / disease marker | serious n=67 · ♀ 100% (drug 63%) · 99% clinician | not reported in cached trials |
| C-reactive protein | 89 | 166.8 134.1–207.5ROR 167.9 · calibrated p 3e-9 ✓ | 145.7 EB05 122.0 · IC025 +6.0 3/3 methods agree | Lab value / disease marker | serious n=89 · ♀ 100% (drug 63%) · 98% clinician | not reported in cached trials |
| Deep vein thrombosis postoperative | 192 | 166.5 143.6–193.1ROR 168.9 · calibrated p 2e-9 ✓ | 147.9 EB05 131.2 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=192 · ♀ 100% (drug 63%) · 94% clinician | not reported in cached trials |
| Adjustment disorder with depressed mood | 186 | 156.0 134.2–181.2ROR 158.1 · calibrated p 4e-9 ✓ | 139.5 EB05 123.4 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=186 · ♀ 100% (drug 63%) · 96% clinician | not reported in cached trials |
| Retinitis | 153 | 154.8 131.2–182.7ROR 156.5 · calibrated p 4e-9 ✓ | 138.1 EB05 120.7 · IC025 +6.3 3/3 methods agree | Not in label — unassessed | serious n=153 · ♀ 100% (drug 63%) · 95% clinician | not reported in cached trials |
| Nail bed inflammation | 28 | 148.1 100.5–218.2ROR 148.4 · calibrated p 2e-8 ✓ | 123.8 EB05 89.9 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=27 · ♀ 100% (drug 63%) | not reported in cached trials |
| Dislocation of vertebra | 189 | 142.4 122.8–165.2ROR 144.4 · calibrated p 7e-9 ✓ | 128.6 EB05 113.9 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=189 · ♀ 100% (drug 63%) · 95% clinician | not reported in cached trials |
| Facet joint syndrome | 244 | 128.7 113.0–146.5ROR 131.0 · calibrated p 2e-8 ✓ | 117.6 EB05 105.7 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=244 · ♀ 100% (drug 63%) · 95% clinician | not reported in cached trials |
| Duodenal ulcer perforation | 546 | 123.3 113.2–134.3ROR 128.4 · calibrated p 2e-8 ✓ | 113.6 EB05 105.8 · IC025 +6.6 3/3 methods agree | Not in label — unassessed | serious PRR 76.6 · ♀ 100% (drug 63%) · 94% clinician | NCT00619359: 1/1,143 (0.1%) on Fosaprepitant Dimeglumine (serious AE) |
| Tonsillar haemorrhage | 11 | 123.3 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 — unassessed | serious n=11 | not reported in cached trials |
| Sleep disorder due to general medical condition, insomnia type | 466 | 119.7 109.1–131.3ROR 123.9 · calibrated p 2e-8 ✓ | 110.5 EB05 102.3 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=466 · ♀ 100% (drug 63%) · 95% clinician | not reported in cached trials |
| Swollen joint count increased | 219 | 115.8 101.1–132.8ROR 117.7 · calibrated p 4e-8 ✓ | 106.7 EB05 95.3 · IC025 +6.2 3/3 methods agree | Lab value / disease marker | serious n=219 · ♀ 100% (drug 63%) · 96% clinician | not reported in cached trials |
| Anti-cyclic citrullinated peptide antibody positive | 482 | 111.6 101.9–122.2ROR 115.6 · calibrated p 4e-8 ✓ | 103.6 EB05 96.1 · IC025 +6.4 3/3 methods agree | Lab value / disease marker | serious PRR 70.2 · ♀ 100% (drug 63%) · 94% clinician | not reported in cached trials |
| Eosinophil percentage decreased | 12 | 100.8 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 marker | serious n=12 | not reported in cached trials |
| Computerised tomogram thorax abnormal | 43 | 100.8 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 — unassessed | serious n=43 · ♀ 100% (drug 63%) · 100% clinician | not reported in cached trials |
| Rheumatic fever | 259 | 96.7 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 — unassessed | serious n=259 · ♀ 100% (drug 63%) · 96% clinician | not reported in cached trials |
| Muscle injury | 476 | 94.4 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 — unassessed | serious PRR 64.8 · ♀ 100% (drug 63%) · 94% clinician | not reported in cached trials |
| Colony stimulating factor therapy | 12 | 94.0 52.5–168.5ROR 94.1 · calibrated p 1e-6 ✓ | 78.0 EB05 47.5 · IC025 +3.3 3/3 methods agree | Reporting / coding artifact | serious n=12 | not reported in cached trials |
| Seminoma | 13 | 87.0 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 — unassessed | serious n=13 | not reported in cached trials |
| Folliculitis | 549 | 86.1 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 — unassessed | serious PRR 64.4 · ♀ 99% (drug 63%) · 95% clinician | not reported in cached trials |
| Helicobacter infection | 531 | 84.3 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 — unassessed | serious PRR 56.8 · ♀ 100% (drug 63%) · 94% clinician | not reported in cached trials |
| Rheumatoid factor positive | 278 | 77.6 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 marker | serious n=278 · ♀ 100% (drug 63%) · 96% clinician | not reported in cached trials |
| Bone erosion | 165 | 74.9 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 — unassessed | serious n=165 · ♀ 100% (drug 63%) · 98% clinician | not reported in cached trials |
| Nasal mucosal disorder | 27 | 74.3 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 — unassessed | serious n=27 · ♀ 100% (drug 63%) | not reported in cached trials |
| Peripheral venous disease | 173 | 69.4 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 — unassessed | serious n=172 · ♀ 100% (drug 63%) · 94% clinician | not reported in cached trials |
| Blood creatine decreased | 13 | 68.5 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 marker | serious n=13 | not reported in cached trials |
| Subcutaneous drug absorption impaired | 23 | 67.6 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 — unassessed | serious n=23 · ♀ 100% (drug 63%) · 91% clinician | not 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).
- NCT00619359 — Evaluation of Fosaprepitant (MK0517) in Single Dose Schedule (0517-017) (N=2322, PHASE3; 184 AE terms posted; arms: Fosaprepitant; Aprepitant)
- NCT01594749 — Efficacy and Safety of Fosaprepitant Dimeglumine in Preventing Chemotherapy-Induced Nausea and Vomiting (MK-05 (N=1015, PHASE3; 64 AE terms posted; arms: Fosaprepitant Regimen; Control Regimen)
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 |
|---|---|---|---|---|---|---|
| Nausea | 1,478 | 2.9 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 3.0 | NCT00619359: 4/1,143 (0.3%) on Fosaprepitant Dimeglumine (serious AE) |
| Dyspnoea (shortness of breath) | 1,269 | 3.4 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 2.8 | NCT00619359: 2/1,143 (0.2%) on Fosaprepitant Dimeglumine (serious AE) |
| Pyrexia (fever) | 1,129 | 5.0 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 — unassessed | serious PRR 4.2 · 91% clinician | NCT00619359: 1/1,143 (0.1%) on Fosaprepitant Dimeglumine (serious AE) |
| Diarrhoea (diarrhea) | 1,110 | 2.6 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 3.0 | NCT00619359: 3/1,143 (0.3%) on Fosaprepitant Dimeglumine (serious AE) |
| Vomiting | 1,081 | 3.5 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 3.2 | NCT00619359: 13/1,143 (1.1%) on Fosaprepitant Dimeglumine (serious AE) |
| Fatigue (tiredness) | 1,080 | 2.1 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) | 891 | 1.6 1.5–1.7ROR 1.6 · calibrated p 0.716 | 1.6 EB05 1.5 · IC025 +0.5 | Reporting / coding artifact | serious PRR 1.9 | not reported in cached trials |
| Alopecia (hair loss) | 886 | 6.9 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 — unassessed | serious PRR 8.5 · ♀ 99% (drug 63%) | NCT00619359: 12/1,143 (1.0%) on Fosaprepitant Dimeglumine |
| Rash | 863 | 3.1 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) | 835 | 6.9 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% clinician | NCT01594749: 1/504 (0.2%) on Fosaprepitant Dimeglumine (serious AE) |
| Febrile neutropenia | 819 | 19.2 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% clinician | NCT00619359: 18/1,143 (1.6%) on Fosaprepitant Dimeglumine (serious AE) |
| Pruritus (itching) | 744 | 3.0 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% clinician | not reported in cached trials |
| Infusion related reaction (reaction during infusion) | 740 | 17.4 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 — unassessed | serious PRR 14.0 · ♀ 90% (drug 63%) · 94% clinician | not reported in cached trials |
| Stomatitis (mouth sores) | 684 | 17.5 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 — unassessed | serious PRR 17.1 · ♀ 88% (drug 63%) · 91% clinician | NCT00619359: 1/1,169 (0.1%) on Fosaprepitant Dimeglumine (serious AE) |
| Pain | 656 | 1.6 1.5–1.8ROR 1.7 · calibrated p 0.750 | 1.6 EB05 1.5 · IC025 +0.6 | Labeled 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.
- Grip strength — n=118, PRR 1,608.0
- Computerised tomogram thorax — n=23, PRR 940.3
- Swollen joint count — n=77, PRR 701.6
- Lupus vulgaris — n=165, PRR 247.1
- Porphyria acute — n=159, PRR 199.8
- Deep vein thrombosis postoperative — n=192, PRR 166.5
- Adjustment disorder with depressed mood — n=186, PRR 156.0
- Retinitis — n=153, PRR 154.8
- Nail bed inflammation — n=28, PRR 148.1
- Dislocation of vertebra — n=189, PRR 142.4
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
- FDA label via openFDA (set ID 3ed3e0a9-a0a8-4555-9f73-2043e79e3398, effective 20260529; matched on
openfda.generic_name.exact:"FOSAPREPITANT DIMEGLUMINE") - 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, 1,046 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
FOSAPREPITANT DIMEGLUMINE, 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.