Lovastatin side effects: what 25,522 FDA adverse event reports show
Drug class
HMG-CoA Reductase Inhibitor
Who reports
25,522 reports · 57% serious · 2,065 with death outcome · 58% female
Used for
Therapy with lovastatin tablets USP should be a component of multiple risk factor intervention in those individuals with dyslipidemia at risk for atherosclerotic vascular disease. Lovastatin tablets USP should be used in addition to a diet restricted i.
What it is
DESCRIPTION Lovastatin is a cholesterol lowering agent isolated from a strain of Aspergillus terreus. After oral ingestion, lovastatin, which is an inactive lactone, is hydrolyzed to the corresponding β-hydroxyacid form.
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.
- 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). 1,096 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 |
|---|---|---|---|---|---|---|
| Type iia hyperlipidaemia | 56 | 269.9 199.5–365.1ROR 270.5 · calibrated p 7e-11 ✓ | 189.6 EB05 151.5 · IC025 +5.7 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=56 · 100% clinician | no trial arm names this drug |
| Chronic kidney disease-mineral and bone disorder | 30 | 23.5 16.4–33.8ROR 23.6 · calibrated p 0.001 ✓ | 22.6 EB05 16.6 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=30 | no trial arm names this drug |
| Nephrogenic anaemia | 129 | 23.3 19.6–27.7ROR 23.4 · calibrated p 0.001 ✓ | 22.6 EB05 19.5 · IC025 +4.1 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=129 | no trial arm names this drug |
| Hyperparathyroidism secondary | 59 | 19.6 15.1–25.3ROR 19.6 · calibrated p 0.003 ✓ | 19.0 EB05 15.3 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | serious n=59 | no trial arm names this drug |
| Myasthenic syndrome | 17 | 18.7 11.6–30.3ROR 18.7 · calibrated p 0.004 ✓ | 17.8 EB05 11.4 · IC025 +2.8 3/3 methods agree | Not in label — unassessed | serious n=17 | no trial arm names this drug |
| Rebound acid hypersecretion | 61 | 16.7 12.9–21.5ROR 16.7 · calibrated p 0.005 ✓ | 16.2 EB05 13.1 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=61 | no trial arm names this drug |
| Left atrial dilatation | 17 | 11.0 6.8–17.8ROR 11.0 · calibrated p 0.031 ✓ | 9.7 EB05 6.0 · IC025 +2.3 3/3 methods agree | Not in label — unassessed | serious n=17 | no trial arm names this drug |
| Dilatation atrial | 15 | 10.6 6.3–17.6ROR 10.6 · calibrated p 0.037 ✓ | 9.1 EB05 5.4 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious n=15 | no trial arm names this drug |
| End stage renal disease | 211 | 9.5 8.3–10.9ROR 9.6 · calibrated p 0.038 ✓ | 9.3 EB05 8.3 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious PRR 9.5 | no trial arm names this drug |
| Diabetic neuropathy | 57 | 9.5 7.3–12.3ROR 9.5 · calibrated p 0.041 ✓ | 9.0 EB05 7.2 · IC025 +2.7 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=52 | no trial arm names this drug |
| Haemorrhagic anaemia | 44 | 8.2 6.1–11.0ROR 8.2 · calibrated p 0.068 | 7.6 EB05 5.9 · IC025 +2.4 3/3 methods agree | Not in label — unassessed | serious n=44 · 76% consumer | no trial arm names this drug |
| Chronic kidney disease | 749 | 8.1 7.5–8.7ROR 8.3 · calibrated p 0.059 | 8.0 EB05 7.5 · IC025 +2.9 3/3 methods agree | Not in label — unassessed | serious PRR 8.3 | no trial arm names this drug |
| Kyphosis | 16 | 7.5 4.6–12.2ROR 7.5 · calibrated p 0.100 | 6.3 EB05 4.1 · IC025 +1.8 3/3 methods agree | Not in label — unassessed | serious n=15 | no trial arm names this drug |
| Myopathy | 74 | 7.1 5.6–8.9ROR 7.1 · calibrated p 0.100 | 6.8 EB05 5.6 · IC025 +2.4 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 7.1 | no trial arm names this drug |
| Lumbar spinal stenosis | 25 | 7.1 4.8–10.5ROR 7.1 · calibrated p 0.109 | 6.3 EB05 4.5 · IC025 +2.0 3/3 methods agree | Not in label — unassessed | serious n=23 | no trial arm names this drug |
| Dilatation ventricular | 18 | 7.0 4.4–11.1ROR 7.0 · calibrated p 0.116 | 6.0 EB05 4.0 · IC025 +1.8 3/3 methods agree | Not in label — unassessed | serious n=18 | no trial arm names this drug |
| Renal failure chronic | 64 | 6.8 5.3–8.7ROR 6.8 · calibrated p 0.112 | 6.5 EB05 5.2 · IC025 +2.3 3/3 methods agree | Labeled (related wording) related wording | serious PRR 6.8 · 100% clinician | no trial arm names this drug |
| Neck mass | 22 | 6.4 4.2–9.8ROR 6.4 · calibrated p 0.141 | 5.7 EB05 4.0 · IC025 +1.8 3/3 methods agree | Not in label — unassessed | serious n=21 · ♀ 0% (drug 58%) | no trial arm names this drug |
| Ischaemic cardiomyopathy | 24 | 6.4 4.3–9.6ROR 6.4 · calibrated p 0.141 | 5.7 EB05 4.0 · IC025 +1.8 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=24 | no trial arm names this drug |
| Essential hypertension | 20 | 6.4 4.1–9.9ROR 6.4 · calibrated p 0.145 | 5.6 EB05 3.8 · IC025 +1.7 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=17 | no trial arm names this drug |
| Hyperlipidaemia | 92 | 6.3 5.2–7.8ROR 6.4 · calibrated p 0.132 | 6.1 EB05 5.1 · IC025 +2.3 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious PRR 5.9 | no trial arm names this drug |
| Aortic arteriosclerosis | 19 | 6.1 3.9–9.6ROR 6.1 · calibrated p 0.164 | 5.3 EB05 3.6 · IC025 +1.7 3/3 methods agree | Not in label — unassessed | serious n=19 | no trial arm names this drug |
| Peripheral vascular disorder | 38 | 6.1 4.4–8.3ROR 6.1 · calibrated p 0.156 | 5.6 EB05 4.3 · IC025 +2.0 3/3 methods agree | Not in label — unassessed | serious n=36 | no trial arm names this drug |
| Diverticulum | 52 | 6.0 4.5–7.8ROR 6.0 · calibrated p 0.159 | 5.7 EB05 4.5 · IC025 +2.0 3/3 methods agree | Not in label — unassessed | serious n=49 | no trial arm names this drug |
| Carotid artery stenosis | 25 | 5.9 4.0–8.7ROR 5.9 · calibrated p 0.173 | 5.3 EB05 3.8 · IC025 +1.7 3/3 methods agree | Not in label — unassessed | serious n=25 | no trial arm names this drug |
| Amyotrophic lateral sclerosis | 15 | 5.8 3.5–9.7ROR 5.8 · calibrated p 0.187 | 5.0 EB05 3.2 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious n=12 | no trial arm names this drug |
| Lipoma | 18 | 5.7 3.6–9.1ROR 5.8 · calibrated p 0.189 | 5.0 EB05 3.4 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious n=16 | no trial arm names this drug |
| Blood cholesterol abnormal | 32 | 5.7 4.0–8.1ROR 5.7 · calibrated p 0.181 | 5.3 EB05 3.9 · IC025 +1.8 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=22 · 81% consumer | no trial arm names this drug |
| Renal injury | 207 | 5.7 5.0–6.5ROR 5.7 · calibrated p 0.170 | 5.6 EB05 5.0 · IC025 +2.3 3/3 methods agree | Labeled (related wording) related wording | serious PRR 5.8 | no trial arm names this drug |
| Spinal osteoarthritis | 58 | 5.4 4.2–7.0ROR 5.4 · calibrated p 0.200 | 5.2 EB05 4.2 · IC025 +1.9 3/3 methods agree | Not in label — unassessed | serious PRR 5.5 | no trial arm names this drug |
| Psychological trauma | 57 | 5.4 4.2–7.0ROR 5.4 · calibrated p 0.203 | 5.1 EB05 4.1 · IC025 +1.9 3/3 methods agree | Not in label — unassessed | serious PRR 5.5 · ♀ 100% (drug 58%) · 100% consumer | no trial arm names this drug |
| Potentiating drug interaction | 21 | 5.3 3.4–8.1ROR 5.3 · calibrated p 0.225 | 4.7 EB05 3.3 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious n=20 · 100% clinician | no trial arm names this drug |
| Body height decreased | 69 | 5.3 4.2–6.7ROR 5.3 · calibrated p 0.212 | 5.1 EB05 4.1 · IC025 +1.9 3/3 methods agree | Not in label — unassessed | serious n=35 · ♀ 79% (drug 58%) · 75% consumer | no trial arm names this drug |
| Type 2 diabetes mellitus | 212 | 5.2 4.5–5.9ROR 5.2 · calibrated p 0.214 | 5.1 EB05 4.6 · IC025 +2.1 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 4.7 | no trial arm names this drug |
| Excoriation | 16 | 5.1 3.1–8.4ROR 5.1 · calibrated p 0.247 | 4.5 EB05 2.9 · IC025 +1.3 3/3 methods agree | Not in label — unassessed | serious n=14 | no trial arm names this drug |
| Actinic keratosis | 16 | 5.1 3.1–8.3ROR 5.1 · calibrated p 0.254 | 4.4 EB05 2.9 · IC025 +1.3 3/3 methods agree | Not in label — unassessed | serious n=16 | no trial arm names this drug |
| Thrombocytosis | 22 | 5.0 3.3–7.6ROR 5.0 · calibrated p 0.256 | 4.5 EB05 3.1 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious n=22 | no trial arm names this drug |
| Cerebral atrophy | 24 | 5.0 3.3–7.4ROR 5.0 · calibrated p 0.257 | 4.5 EB05 3.2 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious n=24 | no trial arm names this drug |
| Lower gastrointestinal haemorrhage | 44 | 4.9 3.6–6.6ROR 4.9 · calibrated p 0.255 | 4.6 EB05 3.6 · IC025 +1.7 3/3 methods agree | Not in label — unassessed | serious PRR 5.0 · 81% consumer | no trial arm names this drug |
| Hair disorder | 49 | 4.9 3.7–6.4ROR 4.9 · calibrated p 0.259 | 4.6 EB05 3.6 · IC025 +1.7 3/3 methods agree | Labeled (related wording) related wording | ♀ 100% (drug 58%) | no trial arm names this drug |
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) | 1,683 | 1.1 1.0–1.1ROR 1.1 · calibrated p 0.342 | 1.1 EB05 1.0 · IC025 -0.0 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | serious PRR 1.0 | no trial arm names this drug |
| Fatigue (tiredness) | 1,537 | 1.6 1.5–1.7ROR 1.7 · calibrated p 0.749 | 1.6 EB05 1.6 · IC025 +0.6 | Labeled (related wording) related wording | serious PRR 1.6 | no trial arm names this drug |
| Nausea | 1,402 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.633 | 1.5 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | serious PRR 1.5 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 1,274 | 1.6 1.5–1.7ROR 1.7 · calibrated p 0.745 | 1.6 EB05 1.6 · IC025 +0.6 | Labeled adverse reaction exact term | serious PRR 1.5 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 1,227 | 1.8 1.7–1.9ROR 1.8 · calibrated p 0.844 | 1.8 EB05 1.7 · IC025 +0.7 | Labeled adverse reaction exact term | serious PRR 1.6 | no trial arm names this drug |
| Dizziness | 1,161 | 1.9 1.8–2.0ROR 2.0 · calibrated p 0.923 | 1.9 EB05 1.8 · IC025 +0.8 | Labeled adverse reaction exact term | serious PRR 1.9 | no trial arm names this drug |
| Pain | 1,070 | 1.4 1.3–1.5ROR 1.4 · calibrated p 0.608 | 1.4 EB05 1.4 · IC025 +0.4 | Labeled adverse reaction exact term | serious PRR 1.4 | no trial arm names this drug |
| Headache | 1,015 | 1.3 1.3–1.4ROR 1.3 · calibrated p 0.539 | 1.3 EB05 1.3 · IC025 +0.3 | Labeled adverse reaction exact term | serious PRR 1.4 | no trial arm names this drug |
| Asthenia (weakness) | 985 | 2.2 2.0–2.3ROR 2.2 · calibrated p 0.951 | 2.2 EB05 2.0 · IC025 +1.0 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.2 | no trial arm names this drug |
| Fall | 909 | 2.2 2.1–2.4ROR 2.3 · calibrated p 0.905 | 2.2 EB05 2.1 · IC025 +1.1 3/3 methods agree | Not in label — unassessed | serious PRR 2.3 | no trial arm names this drug |
| Arthralgia (joint pain) | 818 | 1.6 1.5–1.7ROR 1.6 · calibrated p 0.734 | 1.6 EB05 1.5 · IC025 +0.6 | Labeled adverse reaction exact term | serious PRR 1.8 | no trial arm names this drug |
| Off label use (used outside approved label) | 817 | 0.8 0.7–0.8ROR 0.8 · calibrated p 0.165 | 0.8 EB05 0.7 · IC025 -0.5 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | serious PRR 0.7 | no trial arm names this drug |
| Death | 797 | 0.8 0.7–0.8ROR 0.8 · calibrated p 0.158 | 0.8 EB05 0.7 · IC025 -0.5 PRR-only: not supported by EBGM or IC | Outcome field, not a reaction | serious PRR 0.8 | no trial arm names this drug |
| Pain in extremity | 754 | 2.1 2.0–2.3ROR 2.1 · calibrated p 0.984 | 2.1 EB05 2.0 · IC025 +0.9 | Not in label — unassessed | serious PRR 2.5 | no trial arm names this drug |
| Vomiting | 753 | 1.3 1.2–1.4ROR 1.3 · calibrated p 0.528 | 1.3 EB05 1.2 · IC025 +0.3 | Labeled adverse reaction exact term | serious PRR 1.3 | 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.
- Chronic kidney disease-mineral and bone disorder — n=30, PRR 23.5
- Hyperparathyroidism secondary — n=59, PRR 19.6
- Rebound acid hypersecretion — n=61, PRR 16.7
- End stage renal disease — n=211, PRR 9.5
- Haemorrhagic anaemia — n=44, PRR 8.2
- Chronic kidney disease — n=749, PRR 8.1
- Lumbar spinal stenosis — n=25, PRR 7.1
- Neck mass — n=22, PRR 6.4
- Peripheral vascular disorder — n=38, PRR 6.1
- Diverticulum — n=52, PRR 6.0
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 Lovastatin?
In FDA FAERS, the most frequently co-reported reaction terms for Lovastatin are fatigue, nausea, diarrhoea, dyspnoea, dizziness, pain. 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 Lovastatin have an FDA boxed warning?
No. The FDA label retrieved for Lovastatin has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Lovastatin 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 02aae38d-ee9d-4c09-a155-b69f221ed3e9, effective 20241015; matched on
openfda.generic_name.exact:"LOVASTATIN") - 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, 1,136 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
LOVASTATIN, 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.