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L-Lysine side effects: what 731 FDA adverse event reports show

L-Lysine · L-Lysine 7415 · 18 reaction terms · 104 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Brand names

L-Lysine 7415

openFDA label

Who reports

731 reports · 53% serious · 15 with death outcome · 78% female

openFDA FAERS counts, all years, deduplication not applied

Used for

For the temporary relief of itchy, painful, red, or irritated skin, anxiousness, diarrhea, or indigestion.

FDA label, Indications and Usage

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 9 strongest signals

Reporting / coding artifact 1No label text to screen 8
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 flags pairs whose reports are unusually skewed by sex or come mostly from consumers rather than clinicians. 9 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
Mouth ulceration1216.4
9.4–28.7ROR 16.7 · χ² 158 / p 1e-36
15.3 EB05 8.4 · IC025 +2.4
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 11.9no trial data cached
Oral herpes1116.3
9.0–29.2ROR 16.5 · χ² 143 / p 3e-33
15.0 EB05 7.9 · IC025 +2.3
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 7.6no trial data cached
Hair texture abnormal714.9
7.1–31.2ROR 15.0 · χ² 77 / p 7e-19
12.0 EB05 5.0 · IC025 +1.6
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious n=2no trial data cached
Gastrointestinal pain513.1
5.5–31.4ROR 13.2 · χ² 45 / p 1e-11
8.8 EB05 3.3 · IC025 +1.1
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 21.8no trial data cached
Tendonitis712.9
6.2–27.0ROR 13.0 · χ² 66 / p 3e-16
9.9 EB05 4.3 · IC025 +1.5
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 18.0no trial data cached
Oral pain1012.8
6.9–23.7ROR 13.0 · χ² 97 / p 3e-23
10.8 EB05 5.4 · IC025 +2.0
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 12.8no trial data cached
Impaired driving ability512.6
5.3–30.2ROR 12.7 · χ² 43 / p 3e-11
8.3 EB05 3.2 · IC025 +1.1
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 18.4no trial data cached
Palmar-plantar erythrodysaesthesia syndrome56.1
2.6–14.7ROR 6.2 · χ² 17 / p 2e-5
4.2 EB05 2.0 · IC025 +0.5No label text to screen
label has no adverse-reaction text
–no trial data cached
Product substitution issue115.5
3.1–9.9ROR 5.6 · χ² 36 / p 9e-10
4.6 EB05 2.7 · IC025 +1.2
3/3 methods agree
Reporting / coding artifactserious PRR 9.3no trial data cached

Trial evidence (ClinicalTrials.gov)

Trial cross-check not yet run for this drug (ClinicalTrials.gov pull covers the 800 most-reported drugs first).

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
Mouth ulceration1216.4
9.4–28.7ROR 16.7 · χ² 158 / p 1e-36
15.3 EB05 8.4 · IC025 +2.4
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 11.9no trial data cached
Product substitution issue115.5
3.1–9.9ROR 5.6 · χ² 36 / p 9e-10
4.6 EB05 2.7 · IC025 +1.2
3/3 methods agree
Reporting / coding artifactserious PRR 9.3no trial data cached
Oral herpes1116.3
9.0–29.2ROR 16.5 · χ² 143 / p 3e-33
15.0 EB05 7.9 · IC025 +2.3
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 7.6no trial data cached
Oral pain1012.8
6.9–23.7ROR 13.0 · χ² 97 / p 3e-23
10.8 EB05 5.4 · IC025 +2.0
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 12.8no trial data cached
Tendonitis712.9
6.2–27.0ROR 13.0 · χ² 66 / p 3e-16
9.9 EB05 4.3 · IC025 +1.5
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 18.0no trial data cached
Hair texture abnormal714.9
7.1–31.2ROR 15.0 · χ² 77 / p 7e-19
12.0 EB05 5.0 · IC025 +1.6
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious n=2no trial data cached
Palmar-plantar erythrodysaesthesia syndrome56.1
2.6–14.7ROR 6.2 · χ² 17 / p 2e-5
4.2 EB05 2.0 · IC025 +0.5No label text to screen
label has no adverse-reaction text
–no trial data cached
Impaired driving ability512.6
5.3–30.2ROR 12.7 · χ² 43 / p 3e-11
8.3 EB05 3.2 · IC025 +1.1
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 18.4no trial data cached
Gastrointestinal pain513.1
5.5–31.4ROR 13.2 · χ² 45 / p 1e-11
8.8 EB05 3.3 · IC025 +1.1
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious PRR 21.8no trial data cached
Metrorrhagia46.6
2.5–17.7ROR 6.7 · χ² 14 / p 9e-5
4.2 EB05 1.8 · IC025 +0.3No label text to screen
label has no adverse-reaction text
serious n=3no trial data cached
Blood count abnormal47.5
2.8–19.9ROR 7.5 · χ² 16 / p 3e-5
4.5 EB05 1.9 · IC025 +0.4Lab value / disease marker–no trial data cached
Hair colour changes49.1
3.4–24.3ROR 9.2 · χ² 21 / p 2e-6
5.3 EB05 2.1 · IC025 +0.5
3/3 methods agree
No label text to screen
label has no adverse-reaction text
–no trial data cached
Breast pain410.8
4.1–28.7ROR 10.8 · χ² 26 / p 1e-7
6.3 EB05 2.4 · IC025 +0.6
3/3 methods agree
No label text to screen
label has no adverse-reaction text
serious n=3no trial data cached
Menorrhagia (heavy periods)34.3
1.4–13.4ROR 4.3 · χ² 5 / p 0.015
2.9 EB05 1.2 · IC025 -0.5
PRR-only: not supported by EBGM or IC
No label text to screen
label has no adverse-reaction text
serious PRR 10.6no trial data cached
Amenorrhoea (missed periods)35.2
1.7–16.0ROR 5.2 · χ² 6 / p 0.006
3.3 EB05 1.3 · IC025 -0.4
PRR-only: not supported by EBGM or IC
No label text to screen
label has no adverse-reaction text
serious PRR 12.9no trial data cached

Unlabeled candidate signals

Every screened signal with n ≥ 20 was either labeled, an indication term, or an artifact pattern — no unlabeled candidate stood out in the top signals.

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 L-Lysine?

In FDA FAERS, the most frequently co-reported reaction terms for L-Lysine are mouth ulceration, oral herpes, oral pain, tendonitis, hair texture abnormal, palmar-plantar erythrodysaesthesia syndrome. 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 L-Lysine have an FDA boxed warning?

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

Do FAERS signals prove that L-Lysine 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 2026-10-08. 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.