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Drug · FAERS side-effect profile with label screen

Escitslopram side effects: what 57,813 FDA adverse event reports show

Escitslopram · Escitalopram · 1,205 reaction terms · 236,230 drug–reaction co-reports · data 2026-09-14
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Drug class

Selective serotonin reuptake inhibitor (ssri)

FDA label, Indications wording

Brand names

Escitalopram

openFDA label

Who reports

57,813 reports · 80% serious · 6,033 with death outcome · 65% female

openFDA FAERS counts, all years, deduplication not applied

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. Additional pediatric use information is approved for AbbVie Inc.'s LEXAPRO (escitalopram) tablets. However, due to AbbVie Inc.'s marketing exclusivity rights, this drug product is not labeled with that information.

FDA label, Indications and Usage

What it is

Escitalopram tablets USP contains 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.

FDA label, Description section

Boxed warning

SUICIDAL THOUGHTS AND BEHAVIORS WARNING: SUICIDAL THOUGHTS AND BEHAVIORS See full prescribing information for complete boxed warning. Increased risk of suicidal thoughts and behavior in pediatric and young adult patients taking antidepressants.

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 — boxed warning 1Labeled adverse reaction 2Labeled (related wording) 4Lab value / disease marker 3Not in label — unassessed 30
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). 1,165 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
Total lung capacity abnormal98125.8
99.9–158.4ROR 126.0 · calibrated p 3e-8 ✓
91.7 EB05 77.4 · IC025 +5.7
3/3 methods agree
Not in label — unassessedserious n=97 · ♀ 0% (drug 65%)no trial arm names this drug
Spirometry abnormal130103.1
84.8–125.3ROR 103.3 · calibrated p 1e-7 ✓
79.3 EB05 68.5 · IC025 +5.7
3/3 methods agree
Lab value / disease markerserious n=130 · ♀ 0% (drug 65%)no trial arm names this drug
Pulmonary vasculitis11398.6
80.1–121.4ROR 98.8 · calibrated p 2e-7 ✓
76.5 EB05 65.4 · IC025 +5.5
3/3 methods agree
Not in label — unassessedserious n=113 · ♀ 0% (drug 65%)no trial arm names this drug
Capillaritis5389.2
66.0–120.5ROR 89.3 · calibrated p 5e-7 ✓
69.8 EB05 55.4 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=53 · ♀ 0% (drug 65%) · 100% clinicianno trial arm names this drug
Genital anaesthesia4981.3
59.6–110.9ROR 81.4 · calibrated p 9e-7 ✓
64.8 EB05 51.0 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=49 · ♀ 0% (drug 65%) · 100% consumerno trial arm names this drug
Steroid dependence13870.3
58.5–84.3ROR 70.4 · calibrated p 2e-6 ✓
58.4 EB05 50.7 · IC025 +5.3
3/3 methods agree
Not in label — unassessedserious n=138 · ♀ 21% (drug 65%) · 100% clinicianno trial arm names this drug
Amaurosis fugax16767.0
56.8–79.1ROR 67.2 · calibrated p 2e-6 ✓
56.3 EB05 49.4 · IC025 +5.3
3/3 methods agree
Not in label — unassessedserious n=167 · 100% clinicianno trial arm names this drug
Catarrh13162.6
52.0–75.3ROR 62.7 · calibrated p 4e-6 ✓
53.0 EB05 45.8 · IC025 +5.2
3/3 methods agree
Not in label — unassessedserious n=131 · ♀ 24% (drug 65%) · 100% clinicianno trial arm names this drug
Mycotic allergy11859.0
48.5–71.6ROR 59.1 · calibrated p 6e-6 ✓
50.4 EB05 43.2 · IC025 +5.1
3/3 methods agree
Not in label — unassessedserious n=117 · ♀ 0% (drug 65%)no trial arm names this drug
Rapid eye movement sleep behaviour disorder5051.9
38.6–69.8ROR 51.9 · calibrated p 2e-5 ✓
44.7 EB05 35.2 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=48 · ♀ 0% (drug 65%) · 100% clinicianno trial arm names this drug
Dust allergy11850.5
41.6–61.2ROR 50.6 · calibrated p 1e-5 ✓
44.1 EB05 37.8 · IC025 +4.9
3/3 methods agree
Not in label — unassessedserious n=118 · ♀ 0% (drug 65%)no trial arm names this drug
Antineutrophil cytoplasmic antibody positive7843.4
34.3–54.9ROR 43.5 · calibrated p 4e-5 ✓
38.5 EB05 31.8 · IC025 +4.6
3/3 methods agree
Lab value / disease markerserious n=78 · ♀ 0% (drug 65%) · 100% clinicianno trial arm names this drug
Conjunctivitis allergic13637.1
31.1–44.3ROR 37.2 · calibrated p 9e-5 ✓
33.6 EB05 29.1 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious n=136 · ♀ 0% (drug 65%)no trial arm names this drug
Autoscopy4533.2
24.4–45.0ROR 33.2 · calibrated p 2e-4 ✓
30.1 EB05 23.4 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=44 · ♀ 0% (drug 65%) · 100% consumerno trial arm names this drug
Burns second degree13630.5
25.6–36.3ROR 30.6 · calibrated p 3e-4 ✓
28.1 EB05 24.3 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=136 · ♀ 23% (drug 65%) · 100% clinicianno trial arm names this drug
Reversible cerebral vasoconstriction syndrome14929.7
25.2–35.1ROR 29.8 · calibrated p 3e-4 ✓
27.4 EB05 23.9 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=149 · 100% clinicianno trial arm names this drug
Neuritis10626.8
22.0–32.6ROR 26.8 · calibrated p 5e-4 ✓
24.9 EB05 21.1 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=106 · ♀ 0% (drug 65%)no trial arm names this drug
Resting tremor4023.8
17.2–32.7ROR 23.8 · calibrated p 0.001 ✓
22.1 EB05 16.9 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=37 · ♀ 0% (drug 65%) · 100% clinicianno trial arm names this drug
Serotonin syndrome1,17123.6
22.3–25.0ROR 24.1 · calibrated p 8e-4 ✓
22.2 EB05 21.1 · IC025 +4.4
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 16.1no trial arm names this drug
Pseudomonal bacteraemia4822.0
16.4–29.4ROR 22.0 · calibrated p 0.002 ✓
20.6 EB05 16.1 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=48 · ♀ 100% (drug 65%)no trial arm names this drug
Oromandibular dystonia4121.8
15.9–29.9ROR 21.8 · calibrated p 0.002 ✓
20.4 EB05 15.7 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=41 · 100% clinicianno trial arm names this drug
Physical deconditioning13821.1
17.8–25.0ROR 21.1 · calibrated p 0.002 ✓
19.9 EB05 17.3 · IC025 +3.9
3/3 methods agree
Not in label — unassessedserious n=138no trial arm names this drug
Eosinophilic granulomatosis with polyangiitis10620.0
16.5–24.4ROR 20.1 · calibrated p 0.002 ✓
19.0 EB05 16.1 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=106 · ♀ 0% (drug 65%)no trial arm names this drug
Intrusive thoughts5518.5
14.1–24.3ROR 18.6 · calibrated p 0.003 ✓
17.6 EB05 14.0 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=54no trial arm names this drug
Agitation neonatal4317.1
12.6–23.2ROR 17.1 · calibrated p 0.005 ✓
16.2 EB05 12.4 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=43 · ♀ 0% (drug 65%)no trial arm names this drug
Respiratory disorder neonatal7016.6
13.1–21.1ROR 16.7 · calibrated p 0.005 ✓
15.9 EB05 12.9 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=70no trial arm names this drug
Clonus12016.6
13.8–19.9ROR 16.6 · calibrated p 0.005 ✓
15.8 EB05 13.6 · IC025 +3.6
3/3 methods agree
Labeled adverse reaction
exact term
serious n=119 · 100% clinicianno trial arm names this drug
Normochromic normocytic anaemia13116.5
13.9–19.7ROR 16.5 · calibrated p 0.005 ✓
15.8 EB05 13.6 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=131 · ♀ 0% (drug 65%)no trial arm names this drug
Hypopnoea14615.9
13.5–18.8ROR 16.0 · calibrated p 0.006 ✓
15.3 EB05 13.3 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=144 · ♀ 29% (drug 65%) · 90% clinicianno trial arm names this drug
Sleep terror17115.3
13.2–17.9ROR 15.4 · calibrated p 0.007 ✓
14.7 EB05 12.9 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=166 · ♀ 0% (drug 65%)no trial arm names this drug
Small for dates baby20015.1
13.1–17.4ROR 15.2 · calibrated p 0.007 ✓
14.5 EB05 12.9 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=199no trial arm names this drug
Sleep talking6714.8
11.6–18.9ROR 14.8 · calibrated p 0.008 ✓
14.1 EB05 11.4 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=65 · ♀ 0% (drug 65%)no trial arm names this drug
Reduced facial expression3914.7
10.6–20.2ROR 14.7 · calibrated p 0.009 ✓
13.9 EB05 10.4 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=38 · ♀ 0% (drug 65%) · 100% clinicianno trial arm names this drug
Hyperreflexia13514.5
12.2–17.2ROR 14.5 · calibrated p 0.008 ✓
13.9 EB05 12.0 · IC025 +3.5
3/3 methods agree
Labeled adverse reaction
exact term
serious n=134 · 100% clinicianno trial arm names this drug
Electrocardiogram qrs complex prolonged19414.3
12.4–16.5ROR 14.3 · calibrated p 0.009 ✓
13.7 EB05 12.2 · IC025 +3.5
3/3 methods agree
Lab value / disease markerserious n=194 · 100% clinicianno trial arm names this drug
Alcohol poisoning9713.7
11.2–16.8ROR 13.7 · calibrated p 0.011 ✓
13.2 EB05 11.1 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=96 · ♀ 0% (drug 65%) · 100% clinicianno trial arm names this drug

Trial evidence (ClinicalTrials.gov)

No completed trial with posted adverse-event results was found on ClinicalTrials.gov for Escitslopram (searched ESCITSLOPRAM).

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
Drug ineffective (drug did not work)3,8501.1
1.0–1.1ROR 1.1 · calibrated p 0.349
1.1 EB05 1.0 · IC025 +0.0Reporting / coding artifactserious PRR 1.5no trial arm names this drug
Fatigue (tiredness)3,5311.7
1.6–1.7ROR 1.7 · calibrated p 0.765
1.6 EB05 1.6 · IC025 +0.7Labeled adverse reaction
exact term
serious PRR 1.6no trial arm names this drug
Nausea3,3601.5
1.5–1.6ROR 1.6 · calibrated p 0.694
1.5 EB05 1.5 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.6no trial arm names this drug
Off label use (used outside approved label)3,1321.3
1.3–1.4ROR 1.3 · calibrated p 0.527
1.3 EB05 1.3 · IC025 +0.3Reporting / coding artifactserious PRR 1.4no trial arm names this drug
Diarrhoea (diarrhea)2,8541.6
1.6–1.7ROR 1.6 · calibrated p 0.734
1.6 EB05 1.6 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.5no trial arm names this drug
Headache2,6841.6
1.5–1.6ROR 1.6 · calibrated p 0.696
1.6 EB05 1.5 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.8no trial arm names this drug
Drug interaction2,5856.0
5.8–6.2ROR 6.2 · calibrated p 0.136
5.9 EB05 5.7 · IC025 +2.5
3/3 methods agree
Reporting / coding artifactserious PRR 4.6no trial arm names this drug
Anxiety2,4473.1
3.0–3.3ROR 3.2 · calibrated p 0.558
3.1 EB05 3.0 · IC025 +1.6
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 2.8no trial arm names this drug
Fall2,4382.7
2.6–2.8ROR 2.7 · calibrated p 0.715
2.7 EB05 2.6 · IC025 +1.3
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 2.1no trial arm names this drug
Dizziness2,3871.7
1.7–1.8ROR 1.8 · calibrated p 0.814
1.7 EB05 1.7 · IC025 +0.7Labeled adverse reaction
exact term
serious PRR 1.8no trial arm names this drug
Depression2,1903.5
3.4–3.6ROR 3.6 · calibrated p 0.461
3.5 EB05 3.4 · IC025 +1.7
3/3 methods agree
Labeled — boxed warning
synonym match
serious PRR 3.0no trial arm names this drug
Vomiting2,0991.6
1.6–1.7ROR 1.7 · calibrated p 0.738
1.6 EB05 1.6 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.5no trial arm names this drug
Condition aggravated2,0582.5
2.4–2.6ROR 2.5 · calibrated p 0.798
2.5 EB05 2.4 · IC025 +1.2
3/3 methods agree
Reporting / coding artifactserious PRR 2.4no trial arm names this drug
Dyspnoea (shortness of breath)2,0401.3
1.3–1.4ROR 1.3 · calibrated p 0.522
1.3 EB05 1.3 · IC025 +0.3Labeled adverse reaction
exact term
serious PRR 1.1no trial arm names this drug
Somnolence (drowsiness)1,9523.5
3.4–3.7ROR 3.6 · calibrated p 0.453
3.5 EB05 3.4 · IC025 +1.7
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.8no 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.

✓ A hand-written Bradford Hill causality assessment exists for this drug: Escitslopram ↔ Suicidal Ideation.

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 Escitslopram?

In FDA FAERS, the most frequently co-reported reaction terms for Escitslopram are fatigue, nausea, diarrhoea, headache, anxiety, 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 Escitslopram have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: SUICIDAL THOUGHTS AND BEHAVIORS WARNING: SUICIDAL THOUGHTS AND BEHAVIORS See full prescribing information for complete boxed warning. Increased risk of suicidal thoughts and behavior in pediatric and young adult patients taking antidepressants.

Do FAERS signals prove that Escitslopram 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.