Escitalopram Oxalate side effects: what 72,460 FDA adverse event reports show
Drug class
Selective serotonin reuptake inhibitor (ssri)
Brand names
Escitalopram
Who reports
72,460 reports · 78% serious · 7,343 with death outcome · 66% female
Used for
Escitalopram tablets are indicated for the treatment of: major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older. generalized anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older. Escitalop.
What it is
Escitalopram tablets contain escitalopram, a selective serotonin reuptake inhibitor (SSRI), present as escitalopram oxalate salt. Escitalopram is the pure S- enantiomer (single isomer) of the racemic bicyclic phthalane derivative citalopram.
Boxed warning
SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behaviors in pediatric and young adult patients in short-term studies. Closely monitor all antidepressant-treated patients for clinical worsening, and for emergence of suicidal thoughts and behaviors [see Warnings and Precautions (5.1) ] .
Causality screen of the 40 strongest signals
What the badges mean
- Labeled — boxed warning The term (or its clinical synonym) appears in the FDA boxed warning: causality is regulator-recognised and considered serious.
- 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.
- 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). 1,158 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 |
|---|---|---|---|---|---|---|
| Spirometry abnormal | 286 | 276.7 235.2–325.6ROR 277.8 · calibrated p 3e-11 ✓ | 139.5 EB05 126.4 · IC025 +6.6 3/3 methods agree | Lab value / disease marker | serious n=286 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Mite allergy | 274 | 218.9 187.1–256.2ROR 219.8 · calibrated p 2e-10 ✓ | 123.1 EB05 111.3 · IC025 +6.5 3/3 methods agree | Labeled (related wording) related wording | serious n=273 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Total lung capacity abnormal | 131 | 152.1 123.0–188.0ROR 152.4 · calibrated p 6e-9 ✓ | 98.1 EB05 84.8 · IC025 +5.9 3/3 methods agree | Not in label — unassessed | serious n=130 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Mycotic allergy | 271 | 137.4 118.9–158.8ROR 137.9 · calibrated p 1e-8 ✓ | 92.4 EB05 83.5 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious n=270 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Pulmonary vasculitis | 155 | 120.1 99.6–144.9ROR 120.4 · calibrated p 3e-8 ✓ | 83.9 EB05 73.4 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious n=155 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Dust allergy | 272 | 113.8 98.9–130.9ROR 114.2 · calibrated p 5e-8 ✓ | 81.1 EB05 73.3 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=271 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Capillaritis | 66 | 94.3 71.4–124.6ROR 94.4 · calibrated p 3e-7 ✓ | 69.7 EB05 56.7 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=66 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Amaurosis fugax | 242 | 84.6 73.3–97.6ROR 84.8 · calibrated p 4e-7 ✓ | 65.1 EB05 58.5 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=242 · 100% clinician | no trial arm names this drug |
| Vital capacity decreased | 100 | 82.5 66.0–103.0ROR 82.6 · calibrated p 6e-7 ✓ | 63.4 EB05 53.6 · IC025 +5.3 3/3 methods agree | Not in label — unassessed | serious n=100 · ♀ 100% (drug 66%) | no trial arm names this drug |
| Reversible airways obstruction | 102 | 71.5 57.5–88.8ROR 71.6 · calibrated p 2e-6 ✓ | 56.7 EB05 48.1 · IC025 +5.2 3/3 methods agree | Not in label — unassessed | serious n=102 · ♀ 100% (drug 66%) | no trial arm names this drug |
| Conjunctivitis allergic | 288 | 70.9 62.3–80.6ROR 71.1 · calibrated p 1e-6 ✓ | 56.7 EB05 51.4 · IC025 +5.5 3/3 methods agree | Not in label — unassessed | serious n=288 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Steroid dependence | 167 | 70.7 59.7–83.7ROR 70.9 · calibrated p 2e-6 ✓ | 56.5 EB05 49.6 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=167 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Genital anaesthesia | 51 | 68.1 50.2–92.4ROR 68.2 · calibrated p 3e-6 ✓ | 54.1 EB05 42.7 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=51 · ♀ 0% (drug 66%) · 100% consumer | no trial arm names this drug |
| Catarrh | 153 | 60.0 50.4–71.5ROR 60.2 · calibrated p 5e-6 ✓ | 49.5 EB05 43.2 · IC025 +5.2 3/3 methods agree | Not in label — unassessed | serious n=153 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Antineutrophil cytoplasmic antibody positive | 105 | 48.6 39.6–59.8ROR 48.7 · calibrated p 2e-5 ✓ | 41.4 EB05 35.2 · IC025 +4.8 3/3 methods agree | Lab value / disease marker | serious n=105 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Rapid eye movement sleep behaviour disorder | 51 | 42.3 31.5–56.8ROR 42.3 · calibrated p 5e-5 ✓ | 36.5 EB05 28.8 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious n=49 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Sputum culture positive | 103 | 41.2 33.5–50.7ROR 41.3 · calibrated p 5e-5 ✓ | 35.9 EB05 30.5 · IC025 +4.6 3/3 methods agree | Lab value / disease marker | serious n=103 · ♀ 100% (drug 66%) | no trial arm names this drug |
| Physical deconditioning | 295 | 38.5 34.1–43.5ROR 38.7 · calibrated p 7e-5 ✓ | 34.0 EB05 30.9 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious n=294 | no trial arm names this drug |
| Neuritis | 147 | 30.5 25.7–36.1ROR 30.5 · calibrated p 3e-4 ✓ | 27.5 EB05 24.0 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=147 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Normochromic normocytic anaemia | 286 | 30.4 26.9–34.3ROR 30.5 · calibrated p 3e-4 ✓ | 27.5 EB05 24.9 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=286 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Burns second degree | 158 | 28.6 24.3–33.7ROR 28.7 · calibrated p 4e-4 ✓ | 26.0 EB05 22.8 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious n=158 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Bronchial secretion retention | 112 | 28.0 23.1–34.0ROR 28.1 · calibrated p 4e-4 ✓ | 25.5 EB05 21.8 · IC025 +4.2 3/3 methods agree | Labeled (related wording) related wording | serious n=112 · ♀ 100% (drug 66%) | no trial arm names this drug |
| Reversible cerebral vasoconstriction syndrome | 165 | 26.5 22.6–31.1ROR 26.5 · calibrated p 5e-4 ✓ | 24.3 EB05 21.3 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=165 · 100% clinician | no trial arm names this drug |
| Eosinophilic granulomatosis with polyangiitis | 159 | 24.7 21.0–29.0ROR 24.7 · calibrated p 8e-4 ✓ | 22.7 EB05 19.9 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=159 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Serotonin syndrome | 1,460 | 23.8 22.6–25.1ROR 24.3 · calibrated p 8e-4 ✓ | 22.1 EB05 21.1 · IC025 +4.4 3/3 methods agree | Labeled — boxed warning exact term | age-adj. PRR 15.3 · serious PRR 16.4 | no trial arm names this drug |
| Genital hypoaesthesia | 61 | 18.6 14.4–24.1ROR 18.7 · calibrated p 0.003 ✓ | 17.5 EB05 14.1 · IC025 +3.5 3/3 methods agree | Labeled (related wording) related wording | serious n=60 · ♀ 0% (drug 66%) · 100% consumer | no trial arm names this drug |
| Major depression | 434 | 18.2 16.5–20.0ROR 18.3 · calibrated p 0.003 ✓ | 17.1 EB05 15.8 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 13.1 | no trial arm names this drug |
| Pseudomonal bacteraemia | 49 | 17.9 13.4–23.9ROR 17.9 · calibrated p 0.004 ✓ | 16.8 EB05 13.1 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=49 · 100% clinician | no trial arm names this drug |
| Respiratory symptom | 161 | 17.6 15.0–20.6ROR 17.6 · calibrated p 0.004 ✓ | 16.6 EB05 14.5 · IC025 +3.7 3/3 methods agree | Labeled (related wording) related wording | serious n=159 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Intrusive thoughts | 60 | 16.2 12.5–21.0ROR 16.2 · calibrated p 0.006 ✓ | 15.3 EB05 12.2 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=59 · ♀ 0% (drug 66%) · 100% consumer | no trial arm names this drug |
| Forced expiratory volume decreased | 142 | 15.2 12.8–18.0ROR 15.2 · calibrated p 0.007 ✓ | 14.4 EB05 12.5 · IC025 +3.5 3/3 methods agree | Lab value / disease marker | serious n=141 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Hypopnoea | 172 | 15.1 12.9–17.6ROR 15.1 · calibrated p 0.007 ✓ | 14.3 EB05 12.6 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=170 · ♀ 28% (drug 66%) | no trial arm names this drug |
| Clonus | 135 | 14.9 12.6–17.7ROR 15.0 · calibrated p 0.007 ✓ | 14.2 EB05 12.3 · IC025 +3.5 3/3 methods agree | Labeled adverse reaction exact term | serious n=134 · 100% clinician | no trial arm names this drug |
| Alcohol poisoning | 130 | 14.9 12.5–17.7ROR 14.9 · calibrated p 0.008 ✓ | 14.1 EB05 12.2 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=129 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Urinary tract disorder | 219 | 14.8 12.9–16.9ROR 14.8 · calibrated p 0.008 ✓ | 14.0 EB05 12.5 · IC025 +3.5 3/3 methods agree | Labeled (related wording) related wording | serious n=218 · 100% clinician | no trial arm names this drug |
| Respiratory disorder neonatal | 72 | 13.7 10.8–17.3ROR 13.7 · calibrated p 0.011 ✓ | 12.9 EB05 10.6 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=72 | no trial arm names this drug |
| Sleep talking | 76 | 13.4 10.7–16.9ROR 13.4 · calibrated p 0.012 ✓ | 12.7 EB05 10.4 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=73 · ♀ 0% (drug 66%) · 100% consumer | no trial arm names this drug |
| Suspected suicide | 212 | 13.4 11.7–15.4ROR 13.5 · calibrated p 0.011 ✓ | 12.8 EB05 11.4 · IC025 +3.4 3/3 methods agree | Labeled (related wording) related wording | serious n=212 · 100% clinician | no trial arm names this drug |
| Hyperreflexia | 152 | 13.1 11.1–15.4ROR 13.1 · calibrated p 0.012 ✓ | 12.5 EB05 10.9 · IC025 +3.3 3/3 methods agree | Labeled adverse reaction exact term | serious n=151 · 100% clinician | no trial arm names this drug |
| Emotional poverty | 76 | 13.1 10.4–16.4ROR 13.1 · calibrated p 0.013 ✓ | 12.4 EB05 10.1 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=72 · ♀ 0% (drug 66%) · 100% consumer | no trial arm names this drug |
Clinical concept groups
MedDRA splits one clinical problem across several terms (e.g. "neutropenia", "neutrophil count decreased", "agranulocytosis"), which dilutes term-level signals. These rows count reports with any term in a concept group (an exact union, not a sum), compared with all other drugs. Groups are hand-built and listed in the methods.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Suicidality | 5,521 | 6.66.5–6.8 | signal |
| Hyponatraemia | 1,282 | 4.74.4–4.9 | signal |
| Depression | 3,549 | 3.73.6–3.8 | signal |
| Extrapyramidal | 1,246 | 3.53.3–3.6 | signal |
| Arrhythmia / qt | 2,008 | 3.02.9–3.2 | signal |
| Rhabdomyolysis / myopathy | 689 | 2.52.3–2.7 | signal |
| Fall / fracture | 3,176 | 2.42.3–2.5 | signal |
| Gi bleeding | 1,246 | 2.01.9–2.1 | raised |
| Seizure | 1,294 | 1.91.8–2.0 | raised |
| Venous thromboembolism | 1,333 | 1.81.7–1.9 | raised |
| Kidney injury | 2,572 | 1.61.6–1.7 | raised |
| Stroke | 1,344 | 1.61.5–1.6 | raised |
| Severe cutaneous reaction | 376 | 1.51.3–1.6 | raised |
| Anaphylaxis / angioedema | 633 | 1.51.4–1.6 | raised |
| Serious infection | 3,755 | 1.41.4–1.5 | raised |
| Interstitial lung disease | 448 | 1.41.2–1.5 | raised |
Trial evidence (ClinicalTrials.gov)
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 |
|---|---|---|---|---|---|---|
| Drug ineffective (drug did not work) | 4,822 | 1.1 1.0–1.1ROR 1.1 · calibrated p 0.348 | 1.1 EB05 1.0 · IC025 +0.0 | Reporting / coding artifact | age-adj. PRR 1.2 · serious PRR 1.5 | no trial arm names this drug |
| Fatigue (tiredness) | 4,608 | 1.7 1.7–1.8ROR 1.8 · calibrated p 0.811 | 1.7 EB05 1.7 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.7 | no trial arm names this drug |
| Nausea | 4,374 | 1.6 1.6–1.7ROR 1.6 · calibrated p 0.736 | 1.6 EB05 1.6 · IC025 +0.6 | Labeled adverse reaction exact term | age-adj. PRR 1.3 · serious PRR 1.7 | no trial arm names this drug |
| Off label use (used outside approved label) | 3,899 | 1.3 1.3–1.3ROR 1.3 · calibrated p 0.520 | 1.3 EB05 1.3 · IC025 +0.3 | Reporting / coding artifact | age-adj. PRR 1.2 · serious PRR 1.4 | no trial arm names this drug |
| Headache | 3,746 | 1.7 1.7–1.8ROR 1.8 · calibrated p 0.815 | 1.7 EB05 1.7 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 2.0 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 3,735 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.782 | 1.7 EB05 1.6 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.6 | no trial arm names this drug |
| Drug interaction | 3,118 | 5.8 5.6–6.0ROR 6.0 · calibrated p 0.150 | 5.7 EB05 5.5 · IC025 +2.4 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 4.6 · serious PRR 4.6 | no trial arm names this drug |
| Dizziness | 3,098 | 1.8 1.7–1.9ROR 1.8 · calibrated p 0.854 | 1.8 EB05 1.7 · IC025 +0.8 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.9 | no trial arm names this drug |
| Fall | 3,062 | 2.7 2.6–2.8ROR 2.8 · calibrated p 0.712 | 2.7 EB05 2.6 · IC025 +1.4 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 2.2 · serious PRR 2.1 | no trial arm names this drug |
| Anxiety | 2,977 | 3.0 2.9–3.1ROR 3.1 · calibrated p 0.586 | 3.0 EB05 2.9 · IC025 +1.5 3/3 methods agree | Likely indication confounding term in indications; also in warnings | age-adj. PRR 3.0 · serious PRR 2.8 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 2,908 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.648 | 1.5 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | age-adj. PRR 1.2 · serious PRR 1.3 | no trial arm names this drug |
| Vomiting | 2,738 | 1.7 1.6–1.8ROR 1.7 · calibrated p 0.782 | 1.7 EB05 1.6 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.6 | no trial arm names this drug |
| Condition aggravated | 2,703 | 2.6 2.5–2.7ROR 2.7 · calibrated p 0.745 | 2.6 EB05 2.5 · IC025 +1.3 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 2.3 · serious PRR 2.5 | no trial arm names this drug |
| Depression | 2,618 | 3.3 3.2–3.5ROR 3.4 · calibrated p 0.502 | 3.3 EB05 3.2 · IC025 +1.7 3/3 methods agree | Labeled — boxed warning synonym match | age-adj. PRR 3.1 · serious PRR 2.9 | no trial arm names this drug |
| Pain | 2,496 | 1.2 1.1–1.2ROR 1.2 · calibrated p 0.427 | 1.2 EB05 1.1 · IC025 +0.2 | Labeled adverse reaction exact term | age-adj. PRR 1.2 · serious PRR 1.1 | no trial arm names this drug |
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.
- Total lung capacity abnormal — n=131, PRR 152.1
- Mycotic allergy — n=271, PRR 137.4
- Pulmonary vasculitis — n=155, PRR 120.1
- Dust allergy — n=272, PRR 113.8
- Capillaritis — n=66, PRR 94.3
- Amaurosis fugax — n=242, PRR 84.6
- Vital capacity decreased — n=100, PRR 82.5
- Reversible airways obstruction — n=102, PRR 71.5
- Conjunctivitis allergic — n=288, PRR 70.9
- Steroid dependence — n=167, PRR 70.7
✓ A hand-written Bradford Hill causality assessment exists for this drug: Escitalopram ↔ QT prolongation.
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 Escitalopram Oxalate?
In FDA FAERS, the most frequently co-reported reaction terms for Escitalopram Oxalate are fatigue, nausea, headache, diarrhoea, dizziness, fall. 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 Escitalopram Oxalate have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behaviors in pediatric and young adult patients in short-term studies. Closely monitor all antidepressant-treated patients for clinical worsening, and for emergence of suicidal thoughts and behaviors [see Warnings and Precautions (5.1) ] .
Do FAERS signals prove that Escitalopram Oxalate 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 09945404-e4cf-6269-e063-6294a90a5b8d, effective 20260602; matched on
openfda.generic_name.exact:"ESCITALOPRAM OXALATE") - 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, 1,198 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
ESCITALOPRAM OXALATE, 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.