Valacyclovir side effects: what 41,440 FDA adverse event reports show
Drug class
Not stated in label
Who reports
41,440 reports · 74% serious · 3,715 with death outcome · 56% female
Used for
Valacyclovir tablets are a deoxynucleoside analogue DNA polymerase inhibitor indicated for: Adult Patients ( 1.1 ) Cold Sores (Herpes Labialis) Genital Herpes Treatment in immunocompetent patients (initial or recurrent episode) Suppression in immunocom.
What it is
Valacyclovir hydrochloride, USP is the hydrochloride salt of the L ‑valyl ester of the antiviral drug acyclovir. Valacyclovir tablets, USP are for oral administration. Each film-coated tablet .
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- 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.
- 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.
- 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). 1,164 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 |
|---|---|---|---|---|---|---|
| Cryopyrin associated periodic syndrome | 32 | 99.6 68.2–145.6ROR 99.7 · calibrated p 3e-7 ✓ | 79.4 EB05 58.9 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=32 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Multisystem inflammatory syndrome | 23 | 79.0 50.9–122.6ROR 79.0 · calibrated p 2e-6 ✓ | 64.8 EB05 45.5 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=23 | not reported in cached trials |
| Human herpesvirus 6 encephalitis | 26 | 50.8 33.9–76.0ROR 50.8 · calibrated p 3e-5 ✓ | 44.8 EB05 32.1 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=26 · 100% clinician | not reported in cached trials |
| Mantle cell lymphoma recurrent | 34 | 43.5 30.7–61.8ROR 43.6 · calibrated p 5e-5 ✓ | 39.3 EB05 29.4 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=34 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Microsporidia infection | 28 | 43.2 29.3–63.5ROR 43.2 · calibrated p 6e-5 ✓ | 38.8 EB05 28.2 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=28 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Ophthalmic herpes simplex | 39 | 36.9 26.6–51.0ROR 36.9 · calibrated p 1e-4 ✓ | 33.9 EB05 25.9 · IC025 +4.1 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=37 · 100% clinician | not reported in cached trials |
| Klebsiella bacteraemia | 51 | 29.3 22.1–38.8ROR 29.3 · calibrated p 4e-4 ✓ | 27.5 EB05 21.7 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=51 · ♀ 30% (drug 56%) · 100% clinician | not reported in cached trials |
| Respiratory tract infection bacterial | 26 | 27.7 18.6–41.1ROR 27.7 · calibrated p 6e-4 ✓ | 25.8 EB05 18.5 · IC025 +3.5 3/3 methods agree | Labeled (related wording) related wording | serious n=26 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Periorbital pain | 41 | 27.2 19.9–37.2ROR 27.2 · calibrated p 6e-4 ✓ | 25.6 EB05 19.6 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | 100% consumer | not reported in cached trials |
| Cytokine release syndrome | 861 | 23.9 22.3–25.6ROR 24.4 · calibrated p 8e-4 ✓ | 22.8 EB05 21.6 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious PRR 17.9 · 98% clinician | not reported in cached trials |
| Crystalluria | 24 | 23.2 15.4–34.9ROR 23.2 · calibrated p 0.002 ✓ | 21.8 EB05 15.4 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=24 · 100% clinician | not reported in cached trials |
| Alpha haemolytic streptococcal infection | 39 | 22.1 16.0–30.4ROR 22.1 · calibrated p 0.002 ✓ | 21.0 EB05 16.0 · IC025 +3.5 3/3 methods agree | Labeled (related wording) related wording | serious n=39 · ♀ 34% (drug 56%) · 100% clinician | not reported in cached trials |
| Necrotising retinitis | 25 | 20.6 13.8–30.7ROR 20.6 · calibrated p 0.003 ✓ | 19.5 EB05 13.8 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=25 · 100% clinician | not reported in cached trials |
| Hepatic cytolysis | 470 | 20.2 18.4–22.1ROR 20.4 · calibrated p 0.002 ✓ | 19.4 EB05 18.0 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious PRR 15.2 · 97% clinician | not reported in cached trials |
| Streptococcal bacteraemia | 41 | 20.0 14.7–27.3ROR 20.0 · calibrated p 0.002 ✓ | 19.1 EB05 14.7 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=41 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Febrile bone marrow aplasia | 158 | 19.8 16.9–23.2ROR 19.9 · calibrated p 0.002 ✓ | 19.0 EB05 16.7 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=158 · 100% clinician | not reported in cached trials |
| Immune effector cell-associated neurotoxicity syndrome | 205 | 19.1 16.6–22.0ROR 19.2 · calibrated p 0.002 ✓ | 18.4 EB05 16.4 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=205 · 100% clinician | not reported in cached trials |
| Escherichia bacteraemia | 72 | 16.2 12.8–20.5ROR 16.2 · calibrated p 0.006 ✓ | 15.6 EB05 12.8 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=72 · 100% clinician | not reported in cached trials |
| Bone demineralisation | 33 | 16.2 11.4–22.9ROR 16.2 · calibrated p 0.006 ✓ | 15.5 EB05 11.4 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious n=25 · ♀ 0% (drug 56%) | not reported in cached trials |
| Pseudomonal bacteraemia | 26 | 16.1 10.9–23.9ROR 16.2 · calibrated p 0.007 ✓ | 15.3 EB05 10.8 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious n=26 · 100% clinician | not reported in cached trials |
| Dilated cardiomyopathy | 28 | 15.7 10.8–22.8ROR 15.7 · calibrated p 0.008 ✓ | 14.9 EB05 10.6 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious n=28 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Herpes ophthalmic | 38 | 15.1 11.0–20.9ROR 15.1 · calibrated p 0.008 ✓ | 14.5 EB05 10.9 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious n=35 | not reported in cached trials |
| Genital herpes | 44 | 14.9 11.0–20.1ROR 14.9 · calibrated p 0.008 ✓ | 14.3 EB05 11.0 · IC025 +3.2 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=24 | not reported in cached trials |
| Aplastic anaemia | 150 | 14.9 12.6–17.5ROR 14.9 · calibrated p 0.007 ✓ | 14.4 EB05 12.6 · IC025 +3.5 3/3 methods agree | Labeled adverse reaction exact term | serious n=150 · ♀ 31% (drug 56%) · 95% clinician | not reported in cached trials |
| Mixed liver injury | 80 | 14.3 11.4–17.8ROR 14.3 · calibrated p 0.009 ✓ | 13.8 EB05 11.4 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=80 · 100% clinician | not reported in cached trials |
| Immunoglobulins decreased | 37 | 14.0 10.1–19.5ROR 14.1 · calibrated p 0.011 ✓ | 13.4 EB05 10.0 · IC025 +3.0 3/3 methods agree | Lab value / disease marker | serious n=34 | not reported in cached trials |
| Herpes virus infection | 156 | 14.0 12.0–16.4ROR 14.1 · calibrated p 0.009 ✓ | 13.6 EB05 11.9 · IC025 +3.4 3/3 methods agree | Likely indication confounding term in indications | serious n=88 | not reported in cached trials |
| Eyelid pain | 52 | 13.9 10.6–18.3ROR 13.9 · calibrated p 0.011 ✓ | 13.4 EB05 10.5 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | ♀ 83% (drug 56%) · 100% consumer | not reported in cached trials |
| Toxic encephalopathy | 131 | 13.8 11.6–16.4ROR 13.8 · calibrated p 0.010 ✓ | 13.4 EB05 11.5 · IC025 +3.4 3/3 methods agree | Labeled (related wording) related wording | serious n=131 · 100% clinician | not reported in cached trials |
| Graft versus host disease in gastrointestinal tract | 55 | 13.4 10.2–17.5ROR 13.4 · calibrated p 0.012 ✓ | 12.9 EB05 10.2 · IC025 +3.1 3/3 methods agree | Labeled (related wording) related wording | serious n=55 · ♀ 31% (drug 56%) · 100% clinician | not reported in cached trials |
| Neurotoxicity | 443 | 13.2 12.0–14.5ROR 13.3 · calibrated p 0.011 ✓ | 12.9 EB05 11.9 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious PRR 10.1 · 98% clinician | not reported in cached trials |
| Herpes simplex | 165 | 13.2 11.3–15.4ROR 13.2 · calibrated p 0.012 ✓ | 12.8 EB05 11.2 · IC025 +3.4 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=132 | not reported in cached trials |
| Aplasia | 50 | 13.0 9.8–17.2ROR 13.0 · calibrated p 0.014 ✓ | 12.4 EB05 9.7 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious n=50 · 100% clinician | not reported in cached trials |
| Febrile neutropenia | 1,651 | 12.9 12.3–13.5ROR 13.4 · calibrated p 0.011 ✓ | 12.6 EB05 12.1 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | serious PRR 9.9 · 94% clinician | not reported in cached trials |
| Pneumonia influenzal | 29 | 12.5 8.7–18.1ROR 12.6 · calibrated p 0.017 ✓ | 11.7 EB05 8.3 · IC025 +2.7 3/3 methods agree | Not in label — unassessed | serious n=28 | not reported in cached trials |
| Ophthalmic herpes zoster | 41 | 11.9 8.7–16.2ROR 11.9 · calibrated p 0.020 ✓ | 11.2 EB05 8.4 · IC025 +2.8 3/3 methods agree | Not in label — unassessed | serious n=41 | not reported in cached trials |
| Dermatitis exfoliative generalised | 76 | 11.4 9.1–14.3ROR 11.4 · calibrated p 0.022 ✓ | 11.0 EB05 9.0 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious n=76 · ♀ 20% (drug 56%) · 100% clinician | not reported in cached trials |
| Rhinovirus infection | 83 | 11.3 9.1–14.0ROR 11.3 · calibrated p 0.022 ✓ | 10.9 EB05 9.0 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious n=81 · ♀ 36% (drug 56%) | not reported in cached trials |
| Diffuse large b-cell lymphoma | 161 | 10.9 9.3–12.7ROR 10.9 · calibrated p 0.024 ✓ | 10.6 EB05 9.2 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious PRR 8.3 · 95% clinician | not reported in cached trials |
| Mantle cell lymphoma | 32 | 10.9 7.7–15.4ROR 10.9 · calibrated p 0.028 ✓ | 10.1 EB05 7.3 · IC025 +2.6 3/3 methods agree | Not in label — unassessed | serious n=32 · ♀ 0% (drug 56%) | NCT03134196: 1/266 (0.4%) on Valacyclovir (serious AE) |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Valacyclovir 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).
- NCT00306787 — Efficacy and Safety of Famciclovir 1-day Treatment Compared to 3-day Treatment With Valacyclovir in Adults Wit (N=1179, PHASE3; 8 AE terms posted; arms: Famciclovir; Valacyclovir)
- NCT03134196 — Zoster Eye Disease Study (N=527, PHASE4; 45 AE terms posted; arms: Placebo; Masked Oral Valacyclovir 1000 mg Daily)
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) | 2,721 | 1.6 1.5–1.6ROR 1.6 · calibrated p 0.725 | 1.6 EB05 1.5 · IC025 +0.6 | Reporting / coding artifact | serious PRR 1.8 | not reported in cached trials |
| Fatigue (tiredness) | 2,434 | 1.6 1.5–1.6ROR 1.6 · calibrated p 0.721 | 1.6 EB05 1.5 · IC025 +0.6 | Labeled adverse reaction exact term | serious PRR 1.5 | not reported in cached trials |
| Diarrhoea (diarrhea) | 2,241 | 1.8 1.7–1.8ROR 1.8 · calibrated p 0.835 | 1.8 EB05 1.7 · IC025 +0.7 | Labeled adverse reaction exact term | serious PRR 1.6 | NCT00306787: 5/385 (1.3%) on Valacyclovir |
| Drug ineffective (drug did not work) | 2,004 | 0.8 0.7–0.8ROR 0.8 · calibrated p 0.160 | 0.8 EB05 0.7 · IC025 -0.5 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | serious PRR 0.9 | not reported in cached trials |
| Nausea | 1,970 | 1.3 1.2–1.3ROR 1.3 · calibrated p 0.492 | 1.3 EB05 1.2 · IC025 +0.3 | Labeled adverse reaction exact term | serious PRR 1.2 | NCT00306787: 18/385 (4.7%) on Valacyclovir |
| Febrile neutropenia | 1,651 | 12.9 12.3–13.5ROR 13.4 · calibrated p 0.011 ✓ | 12.6 EB05 12.1 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | serious PRR 9.9 · 94% clinician | not reported in cached trials |
| Pyrexia (fever) | 1,580 | 2.3 2.2–2.4ROR 2.4 · calibrated p 0.872 | 2.3 EB05 2.2 · IC025 +1.1 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.1 | not reported in cached trials |
| Pneumonia (lung infection) | 1,528 | 2.4 2.3–2.5ROR 2.5 · calibrated p 0.834 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled (related wording) related wording | serious PRR 1.9 | NCT03134196: 1/261 (0.4%) control (serious AE) |
| Headache | 1,475 | 1.2 1.1–1.3ROR 1.2 · calibrated p 0.439 | 1.2 EB05 1.1 · IC025 +0.2 | Labeled adverse reaction exact term | serious PRR 1.2 · ♀ 80% (drug 56%) | NCT00306787: 17/385 (4.4%) on Valacyclovir |
| Pain | 1,364 | 1.1 1.1–1.2ROR 1.1 · calibrated p 0.390 | 1.1 EB05 1.1 · IC025 +0.1 | Labeled adverse reaction exact term | serious PRR 1.0 | NCT00306787: 4/385 (1.0%) on Valacyclovir |
| Rash | 1,303 | 1.5 1.4–1.6ROR 1.5 · calibrated p 0.667 | 1.5 EB05 1.5 · IC025 +0.5 | Likely indication confounding term in indications; also in warnings | serious PRR 1.5 | not reported in cached trials |
| Neutropenia (low neutrophils (infection-fighting cells)) | 1,224 | 4.6 4.4–4.9ROR 4.7 · calibrated p 0.268 | 4.6 EB05 4.4 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious PRR 3.5 · 94% clinician | not reported in cached trials |
| Acute kidney injury (sudden kidney damage) | 1,170 | 3.9 3.7–4.1ROR 4.0 · calibrated p 0.379 | 3.9 EB05 3.7 · IC025 +1.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 3.0 · 94% clinician | NCT03134196: 1/261 (0.4%) control (serious AE) |
| Dyspnoea (shortness of breath) | 1,132 | 1.0 1.0–1.1ROR 1.0 · calibrated p 0.315 | 1.0 EB05 1.0 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Labeled adverse reaction exact term | serious PRR 0.9 | not reported in cached trials |
| Asthenia (weakness) | 1,125 | 1.5 1.4–1.6ROR 1.5 · calibrated p 0.661 | 1.5 EB05 1.4 · IC025 +0.5 | Not in label — unassessed | serious PRR 1.3 | not reported in cached trials |
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.
- Cryopyrin associated periodic syndrome — n=32, PRR 99.6
- Multisystem inflammatory syndrome — n=23, PRR 79.0
- Human herpesvirus 6 encephalitis — n=26, PRR 50.8
- Mantle cell lymphoma recurrent — n=34, PRR 43.5
- Microsporidia infection — n=28, PRR 43.2
- Klebsiella bacteraemia — n=51, PRR 29.3
- Periorbital pain — n=41, PRR 27.2
- Cytokine release syndrome — n=861, PRR 23.9
- Crystalluria — n=24, PRR 23.2
- Necrotising retinitis — n=25, PRR 20.6
✓ A hand-written Bradford Hill causality assessment exists for this drug: Valacyclovir ↔ Acute kidney injury.
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 Valacyclovir?
In FDA FAERS, the most frequently co-reported reaction terms for Valacyclovir are fatigue, diarrhoea, nausea, febrile neutropenia, pyrexia, pneumonia. 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 Valacyclovir have an FDA boxed warning?
No. The FDA label retrieved for Valacyclovir has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Valacyclovir 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 26634bf1-c6d8-4d48-9a4e-845c47df07f8, effective 20260604; matched on
openfda.generic_name.exact:"VALACYCLOVIR") - 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, 1,204 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
VALACYCLOVIR, 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.