Fludarabine side effects: what 39,092 FDA adverse event reports show
Drug class
Nucleotide metabolic inhibitor
Label matched
Fludarabine Phosphate (Fludarabine Phosphate)
Who reports
39,092 reports · 98% serious · 11,956 with death outcome · 40% female
Used for
Fludarabine Phosphate Injection is a nucleotide metabolic inhibitor indicated for: The treatment of adult patients with B-cell chronic lymphocytic leukemia (CLL) who have not responded to or whose disease has progressed during treatment with at least one standard alkylating-agent containing regimen. Benefit in treatment-naïve or non-refractory CLL patients is not established.
What it is
Fludarabine Phosphate Injection contains fludarabine phosphate, a nucleotide metabolic inhibitor. Fludarabine phosphate is a fluorinated nucleotide analog of the antiviral agent vidarabine, 9- ß -D-arabinofuranosyladenine (ara-A), that is relatively resistant to deamination by adenosine deaminase.
Boxed warning
CNS TOXICITY, HEMOLYTIC ANEMIA, AND PULMONARY TOXICITY WARNING: CNS TOXICITY, HEMOLYTIC ANEMIA, AND PULMONARY TOXICITY See full prescribing information for complete boxed warning. Severe central nervous system toxicity occurred in 36% of patients treated with doses approximately four times greater (96 mg/m 2 /day for 5 to 7 days) than the recommended dose.
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.
- 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). 1,106 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 |
|---|---|---|---|---|---|---|
| Pre-engraftment immune reaction | 64 | 2,254.2 1,284.8–3,955.0ROR 2,257.9 · calibrated p 5e-19 ✓ | 380.0 EB05 308.1 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=64 · 91% clinician | not reported in cached trials |
| Adenovirus reactivation | 99 | 1,376.4 947.1–2,000.5ROR 1,379.9 · calibrated p 7e-18 ✓ | 356.1 EB05 301.0 · IC025 +6.7 3/3 methods agree | Not in label — unassessed | serious n=98 · 100% clinician | not reported in cached trials |
| Meningomyelitis herpes | 20 | 880.6 430.5–1,801.1ROR 881.0 · calibrated p 1e-13 ✓ | 251.5 EB05 171.9 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=20 | not reported in cached trials |
| Cytokine increased | 69 | 578.7 411.3–814.1ROR 579.7 · calibrated p 6e-14 ✓ | 257.0 EB05 210.0 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious n=69 · 100% clinician | NCT00281918: 1/402 (0.2%) on Fludarabine (serious AE) |
| Chimerism | 40 | 440.3 289.4–669.7ROR 440.7 · calibrated p 2e-12 ✓ | 215.9 EB05 165.4 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=40 · 100% clinician | not reported in cached trials |
| Protothecosis | 41 | 416.6 276.7–627.2ROR 417.0 · calibrated p 3e-12 ✓ | 210.6 EB05 161.8 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=41 · ♀ 100% (drug 40%) · 90% clinician | not reported in cached trials |
| Cystitis viral | 159 | 387.1 315.6–474.9ROR 388.7 · calibrated p 1e-12 ✓ | 218.0 EB05 191.0 · IC025 +6.8 3/3 methods agree | Labeled (related wording) related wording | serious n=158 · 96% clinician | not reported in cached trials |
| Acute graft versus host disease in skin | 1,138 | 379.1 351.5–408.8ROR 390.4 · calibrated p 8e-13 ✓ | 220.3 EB05 209.8 · IC025 +7.6 3/3 methods agree | Labeled (related wording) related wording | serious n=1,135 · 97% clinician | not reported in cached trials |
| Viral haemorrhagic cystitis | 291 | 378.7 325.9–440.1ROR 381.5 · calibrated p 1e-12 ✓ | 217.8 EB05 197.6 · IC025 +7.1 3/3 methods agree | Labeled (related wording) related wording | serious n=290 · 98% clinician | not reported in cached trials |
| Juvenile chronic myelomonocytic leukaemia | 20 | 364.4 206.1–644.0ROR 364.6 · calibrated p 5e-11 ✓ | 179.3 EB05 122.6 · IC025 +4.4 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=20 | not reported in cached trials |
| Acute graft versus host disease in intestine | 559 | 357.6 321.3–397.9ROR 362.7 · calibrated p 2e-12 ✓ | 212.1 EB05 197.7 · IC025 +7.3 3/3 methods agree | Not in label — unassessed | serious n=556 · 99% clinician | not reported in cached trials |
| Autoimmune lymphoproliferative syndrome | 21 | 292.0 171.4–497.5ROR 292.1 · calibrated p 2e-10 ✓ | 161.1 EB05 111.1 · IC025 +4.4 3/3 methods agree | Labeled (related wording) related wording | serious n=21 | not reported in cached trials |
| Idiopathic pneumonia syndrome | 104 | 289.2 227.7–367.2ROR 290.0 · calibrated p 2e-11 ✓ | 181.1 EB05 153.7 · IC025 +6.3 3/3 methods agree | Not in label — unassessed | serious n=104 · 96% clinician | not reported in cached trials |
| Engraftment syndrome | 205 | 288.8 243.7–342.3ROR 290.3 · calibrated p 2e-11 ✓ | 183.9 EB05 163.7 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious n=202 | not reported in cached trials |
| Malignant genitourinary tract neoplasm | 21 | 284.5 167.4–483.5ROR 284.6 · calibrated p 3e-10 ✓ | 158.8 EB05 109.6 · IC025 +4.4 3/3 methods agree | Labeled (related wording) related wording | serious n=21 · 100% clinician | not reported in cached trials |
| Chronic lymphocytic leukaemia recurrent | 237 | 280.1 239.4–327.8ROR 281.8 · calibrated p 2e-11 ✓ | 180.8 EB05 162.2 · IC025 +6.8 3/3 methods agree | Labeled (related wording) related wording | serious n=237 · 99% clinician | not reported in cached trials |
| Human herpesvirus 6 encephalitis | 97 | 278.5 217.8–356.1ROR 279.2 · calibrated p 4e-11 ✓ | 176.4 EB05 148.9 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=97 · 100% clinician | not reported in cached trials |
| Encephalitis cytomegalovirus | 145 | 271.7 222.4–331.8ROR 272.7 · calibrated p 4e-11 ✓ | 175.6 EB05 152.9 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=145 · ♀ 10% (drug 40%) · 97% clinician | not reported in cached trials |
| Acute graft versus host disease | 1,528 | 266.4 250.7–283.1ROR 277.2 · calibrated p 2e-11 ✓ | 177.1 EB05 169.7 · IC025 +7.3 3/3 methods agree | Labeled (related wording) related wording | serious n=1,520 · 96% clinician | not reported in cached trials |
| Bone marrow transplant rejection | 72 | 257.0 194.0–340.6ROR 257.5 · calibrated p 9e-11 ✓ | 165.7 EB05 136.0 · IC025 +5.9 3/3 methods agree | Not in label — unassessed | serious n=70 · 96% clinician | not reported in cached trials |
| Viruria | 34 | 256.6 170.4–386.5ROR 256.8 · calibrated p 2e-10 ✓ | 157.9 EB05 118.1 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=34 · 100% clinician | not reported in cached trials |
| Acute graft versus host disease in liver | 230 | 252.1 215.5–294.9ROR 253.6 · calibrated p 6e-11 ✓ | 168.6 EB05 151.1 · IC025 +6.7 3/3 methods agree | Labeled (related wording) related wording | serious n=229 · 96% clinician | not reported in cached trials |
| Chronic graft versus host disease in intestine | 59 | 249.4 183.0–339.8ROR 249.7 · calibrated p 1e-10 ✓ | 161.0 EB05 129.4 · IC025 +5.7 3/3 methods agree | Not in label — unassessed | serious n=59 · 100% clinician | not reported in cached trials |
| Graft versus host disease in gastrointestinal tract | 673 | 249.0 227.3–272.7ROR 253.3 · calibrated p 5e-11 ✓ | 168.8 EB05 158.3 · IC025 +7.1 3/3 methods agree | Labeled (related wording) related wording | serious n=673 · 97% clinician | not reported in cached trials |
| Chronic graft versus host disease in skin | 280 | 239.0 207.6–275.1ROR 240.7 · calibrated p 9e-11 ✓ | 163.0 EB05 147.6 · IC025 +6.8 3/3 methods agree | Labeled (related wording) related wording | serious n=280 · 99% clinician | not reported in cached trials |
| Graft versus host disease in skin | 676 | 238.6 218.0–261.1ROR 242.8 · calibrated p 7e-11 ✓ | 163.9 EB05 153.8 · IC025 +7.1 3/3 methods agree | Labeled (related wording) related wording | serious n=675 · 97% clinician | not reported in cached trials |
| Disseminated toxoplasmosis | 35 | 234.1 157.2–348.4ROR 234.3 · calibrated p 4e-10 ✓ | 149.4 EB05 112.3 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=35 · 94% clinician | not reported in cached trials |
| Adenoviral hepatitis | 69 | 227.8 171.8–302.1ROR 228.2 · calibrated p 3e-10 ✓ | 152.8 EB05 124.9 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious n=69 · ♀ 79% (drug 40%) · 97% clinician | not reported in cached trials |
| Retinitis viral | 35 | 222.8 150.1–330.7ROR 223.0 · calibrated p 7e-10 ✓ | 144.8 EB05 108.8 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=35 · ♀ 100% (drug 40%) · 91% clinician | not reported in cached trials |
| Cytomegalovirus infection reactivation | 1,240 | 220.4 206.4–235.3ROR 227.5 · calibrated p 1e-10 ✓ | 155.4 EB05 148.3 · IC025 +7.1 3/3 methods agree | Labeled (related wording) related wording | serious n=1,237 · 98% clinician | not reported in cached trials |
| Cord blood transplant therapy | 25 | 220.1 138.1–351.0ROR 220.3 · calibrated p 1e-9 ✓ | 139.3 EB05 99.3 · IC025 +4.6 3/3 methods agree | Reporting / coding artifact | serious n=25 | not reported in cached trials |
| Adenovirus infection | 816 | 214.0 197.4–231.9ROR 218.5 · calibrated p 2e-10 ✓ | 152.0 EB05 143.5 · IC025 +7.0 3/3 methods agree | Not in label — unassessed | serious n=805 · 96% clinician | not reported in cached trials |
| Blood stem cell transplant failure | 61 | 212.0 157.6–285.3ROR 212.4 · calibrated p 5e-10 ✓ | 144.8 EB05 116.8 · IC025 +5.7 3/3 methods agree | Not in label — unassessed | serious n=60 · 98% clinician | not reported in cached trials |
| Bronchiolitis obliterans syndrome | 47 | 206.9 147.7–289.9ROR 207.2 · calibrated p 8e-10 ✓ | 140.6 EB05 110.0 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=47 · ♀ 62% (drug 40%) · 100% clinician | not reported in cached trials |
| Chronic lymphocytic leukaemia transformation | 58 | 202.9 149.9–274.7ROR 203.2 · calibrated p 8e-10 ✓ | 140.2 EB05 112.4 · IC025 +5.6 3/3 methods agree | Labeled (related wording) related wording | serious n=58 · ♀ 15% (drug 40%) | not reported in cached trials |
| Chronic graft versus host disease in eye | 53 | 197.2 143.9–270.3ROR 197.5 · calibrated p 1e-9 ✓ | 136.9 EB05 108.6 · IC025 +5.5 3/3 methods agree | Labeled (related wording) related wording | serious n=53 · 98% clinician | not reported in cached trials |
| Epstein-barr virus infection reactivation | 338 | 196.0 173.1–222.0ROR 197.7 · calibrated p 5e-10 ✓ | 142.1 EB05 129.8 · IC025 +6.7 3/3 methods agree | Labeled (related wording) related wording | serious n=336 · 96% clinician | not reported in cached trials |
| Engraft failure | 76 | 194.9 149.9–253.5ROR 195.3 · calibrated p 9e-10 ✓ | 137.8 EB05 113.7 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious n=76 · 97% clinician | not reported in cached trials |
| Chronic graft versus host disease | 938 | 186.7 173.4–201.0ROR 191.3 · calibrated p 6e-10 ✓ | 137.8 EB05 130.6 · IC025 +6.9 3/3 methods agree | Labeled (related wording) related wording | serious n=928 · 98% clinician | not reported in cached trials |
| Adenoviral haemorrhagic cystitis | 52 | 176.1 128.7–241.0ROR 176.3 · calibrated p 3e-9 ✓ | 126.3 EB05 100.0 · IC025 +5.4 3/3 methods agree | Labeled (related wording) related wording | serious n=52 · 100% 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 Fludarabine 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).
- NCT00281918 — Fludarabine and Cyclophosphamide With or Without Rituximab in Patients With Previously Untreated Chronic B-Cel (N=817, PHASE3; 226 AE terms posted; arms: Fludarabine+Cyclophosphamide (FC); Fludarabine+Cyclophosphamide+Rituximab ()
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 |
|---|---|---|---|---|---|---|
| Off label use (used outside approved label) | 4,350 | 2.7 2.6–2.8ROR 2.9 · calibrated p 0.656 | 2.7 EB05 2.6 · IC025 +1.4 3/3 methods agree | Reporting / coding artifact | serious PRR 2.9 · 95% clinician | not reported in cached trials |
| Drug ineffective (drug did not work) | 2,971 | 1.2 1.2–1.3ROR 1.2 · calibrated p 0.459 | 1.2 EB05 1.2 · IC025 +0.2 | Reporting / coding artifact | serious PRR 2.0 · 97% clinician | not reported in cached trials |
| Pyrexia (fever) | 2,930 | 4.6 4.4–4.7ROR 4.9 · calibrated p 0.250 | 4.5 EB05 4.4 · IC025 +2.1 3/3 methods agree | Labeled (related wording) related wording | serious PRR 3.3 · 94% clinician | NCT00281918: 18/402 (4.5%) on Fludarabine (serious AE) |
| Cytokine release syndrome | 2,905 | 96.5 92.9–100.3ROR 104.2 · calibrated p 8e-8 ✓ | 81.7 EB05 79.3 · IC025 +6.3 3/3 methods agree | Not in label — unassessed | serious PRR 48.7 · 96% clinician | NCT00281918: 1/402 (0.2%) on Fludarabine (serious AE) |
| Febrile neutropenia | 2,826 | 23.9 23.0–24.8ROR 25.7 · calibrated p 6e-4 ✓ | 22.9 EB05 22.2 · IC025 +4.4 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 13.5 · 95% clinician | NCT00281918: 31/402 (7.7%) on Fludarabine (serious AE) |
| Product use in unapproved indication | 2,243 | 5.0 4.8–5.2ROR 5.2 · calibrated p 0.214 | 4.9 EB05 4.8 · IC025 +2.2 3/3 methods agree | Reporting / coding artifact | serious PRR 5.7 · 97% clinician | not reported in cached trials |
| Neutropenia (low neutrophils (infection-fighting cells)) | 2,012 | 8.1 7.7–8.4ROR 8.5 · calibrated p 0.056 | 8.0 EB05 7.7 · IC025 +2.9 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 4.8 · 96% clinician | NCT00281918: 31/402 (7.7%) on Fludarabine (serious AE) |
| Cytomegalovirus infection | 1,682 | 60.3 57.4–63.4ROR 63.0 · calibrated p 3e-6 ✓ | 54.2 EB05 52.1 · IC025 +5.7 3/3 methods agree | Not in label — unassessed | serious PRR 32.0 · 96% clinician | NCT00281918: 1/402 (0.2%) on Fludarabine (serious AE) |
| Thrombocytopenia (low platelets) | 1,635 | 8.0 7.6–8.4ROR 8.3 · calibrated p 0.060 | 7.9 EB05 7.5 · IC025 +2.9 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 4.8 · 96% clinician | NCT00281918: 6/402 (1.5%) on Fludarabine (serious AE) |
| Sepsis (blood infection) | 1,542 | 7.5 7.1–7.9ROR 7.8 · calibrated p 0.073 | 7.4 EB05 7.1 · IC025 +2.8 3/3 methods agree | Not in label — unassessed | serious PRR 4.4 · 94% clinician | NCT00281918: 5/402 (1.2%) on Fludarabine (serious AE) |
| Acute graft versus host disease | 1,528 | 266.4 250.7–283.1ROR 277.2 · calibrated p 2e-11 ✓ | 177.1 EB05 169.7 · IC025 +7.3 3/3 methods agree | Labeled (related wording) related wording | serious n=1,520 · 96% clinician | not reported in cached trials |
| Pneumonia (lung infection) | 1,457 | 2.4 2.3–2.5ROR 2.5 · calibrated p 0.822 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 1.5 · 95% clinician | NCT00281918: 18/402 (4.5%) on Fludarabine (serious AE) |
| Mucosal inflammation | 1,413 | 30.7 29.1–32.4ROR 31.8 · calibrated p 2e-4 ✓ | 29.1 EB05 27.8 · IC025 +4.8 3/3 methods agree | Labeled (related wording) related wording | serious PRR 18.1 · 96% clinician | NCT00281918: 1/402 (0.2%) on Fludarabine (serious AE) |
| Infection | 1,386 | 5.2 4.9–5.5ROR 5.4 · calibrated p 0.200 | 5.1 EB05 4.9 · IC025 +2.3 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 3.8 · 96% clinician | NCT00281918: 5/402 (1.2%) on Fludarabine (serious AE) |
| Pancytopenia (all blood cells low) | 1,382 | 13.6 12.9–14.4ROR 14.1 · calibrated p 0.009 ✓ | 13.3 EB05 12.7 · IC025 +3.6 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 7.9 · 93% clinician | NCT00281918: 7/402 (1.7%) on Fludarabine (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.
- Pre-engraftment immune reaction — n=64, PRR 2,254.2
- Adenovirus reactivation — n=99, PRR 1,376.4
- Meningomyelitis herpes — n=20, PRR 880.6
- Cytokine increased — n=69, PRR 578.7 (also seen in trial arm)
- Chimerism — n=40, PRR 440.3
- Protothecosis — n=41, PRR 416.6
- Acute graft versus host disease in intestine — n=559, PRR 357.6
- Idiopathic pneumonia syndrome — n=104, PRR 289.2
- Engraftment syndrome — n=205, PRR 288.8
- Human herpesvirus 6 encephalitis — n=97, PRR 278.5
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 Fludarabine?
In FDA FAERS, the most frequently co-reported reaction terms for Fludarabine are pyrexia, cytokine release syndrome, febrile neutropenia, neutropenia, cytomegalovirus infection, thrombocytopenia. 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 Fludarabine have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: CNS TOXICITY, HEMOLYTIC ANEMIA, AND PULMONARY TOXICITY WARNING: CNS TOXICITY, HEMOLYTIC ANEMIA, AND PULMONARY TOXICITY See full prescribing information for complete boxed warning. Severe central nervous system toxicity occurred in 36% of patients treated with doses approximately four times greater (96 mg/m 2 /day for 5 to 7 days) than the recommended dose.
Do FAERS signals prove that Fludarabine 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 8039c2e3-ffe5-3997-e053-2991aa0ad9d0, effective 20230214; matched on
openfda.generic_name.exact:"FLUDARABINE PHOSPHATE") - 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, 1,146 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
FLUDARABINE, 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.