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Drug · FAERS side-effect profile with label screen

Lovastatin side effects: what 25,522 FDA adverse event reports show

Lovastatin · 1,136 reaction terms · 95,262 drug–reaction co-reports · data 2026-09-14
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Drug class

HMG-CoA Reductase Inhibitor

FDA label (Established Pharmacologic Class)

Who reports

25,522 reports · 57% serious · 2,065 with death outcome · 58% female

openFDA FAERS counts, all years, deduplication not applied

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.

FDA label, Indications and Usage

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.

FDA label, Description section

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 40 strongest signals

Labeled adverse reaction 1Labeled (related wording) 3Likely indication confounding 8Not in label — unassessed 28
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). 1,096 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
Type iia hyperlipidaemia56269.9
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% clinicianno trial arm names this drug
Chronic kidney disease-mineral and bone disorder3023.5
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 — unassessedserious n=30no trial arm names this drug
Nephrogenic anaemia12923.3
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=129no trial arm names this drug
Hyperparathyroidism secondary5919.6
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 — unassessedserious n=59no trial arm names this drug
Myasthenic syndrome1718.7
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 — unassessedserious n=17no trial arm names this drug
Rebound acid hypersecretion6116.7
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 — unassessedserious n=61no trial arm names this drug
Left atrial dilatation1711.0
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 — unassessedserious n=17no trial arm names this drug
Dilatation atrial1510.6
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 — unassessedserious n=15no trial arm names this drug
End stage renal disease2119.5
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 — unassessedserious PRR 9.5no trial arm names this drug
Diabetic neuropathy579.5
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=52no trial arm names this drug
Haemorrhagic anaemia448.2
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 — unassessedserious n=44 · 76% consumerno trial arm names this drug
Chronic kidney disease7498.1
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 — unassessedserious PRR 8.3no trial arm names this drug
Kyphosis167.5
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 — unassessedserious n=15no trial arm names this drug
Myopathy747.1
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 7.1no trial arm names this drug
Lumbar spinal stenosis257.1
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 — unassessedserious n=23no trial arm names this drug
Dilatation ventricular187.0
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 — unassessedserious n=18no trial arm names this drug
Neck mass226.4
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 — unassessedserious n=21 · ♀ 0% (drug 58%)no trial arm names this drug
Ischaemic cardiomyopathy246.4
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=24no trial arm names this drug
Essential hypertension206.4
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=17no trial arm names this drug
Hyperlipidaemia926.3
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 5.9no trial arm names this drug
Aortic arteriosclerosis196.1
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 — unassessedserious n=19no trial arm names this drug
Peripheral vascular disorder386.1
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 — unassessedserious n=36no trial arm names this drug
Diverticulum526.0
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 — unassessedserious n=49no trial arm names this drug
Carotid artery stenosis255.9
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 — unassessedserious n=25no trial arm names this drug
Amyotrophic lateral sclerosis155.8
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 — unassessedserious n=12no trial arm names this drug
Lipoma185.7
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 — unassessedserious n=16no trial arm names this drug
Blood cholesterol abnormal325.7
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% consumerno trial arm names this drug
Spinal osteoarthritis585.4
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 — unassessedserious PRR 5.5no trial arm names this drug
Psychological trauma575.4
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 — unassessedserious PRR 5.5 · ♀ 100% (drug 58%) · 100% consumerno trial arm names this drug
Potentiating drug interaction215.3
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 — unassessedserious n=20 · 100% clinicianno trial arm names this drug
Body height decreased695.3
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 — unassessedserious n=35 · ♀ 79% (drug 58%) · 75% consumerno trial arm names this drug
Type 2 diabetes mellitus2125.2
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 4.7no trial arm names this drug
Excoriation165.1
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 — unassessedserious n=14no trial arm names this drug
Actinic keratosis165.1
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 — unassessedserious n=16no trial arm names this drug
Thrombocytosis225.0
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 — unassessedserious n=22no trial arm names this drug
Cerebral atrophy245.0
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 — unassessedserious n=24no trial arm names this drug
Lower gastrointestinal haemorrhage444.9
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 — unassessedserious PRR 5.0 · 81% consumerno trial arm names this drug

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Lovastatin only as a background or rescue medication (NCT00461630, NCT00202878); no trial listing it as the tested intervention was cached, so no trial cross-check is shown.

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)1,6831.1
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 artifactserious PRR 1.0no trial arm names this drug
Nausea1,4021.5
1.4–1.5ROR 1.5 · calibrated p 0.633
1.5 EB05 1.4 · IC025 +0.5Labeled adverse reaction
exact term
serious PRR 1.5no trial arm names this drug
Diarrhoea (diarrhea)1,2741.6
1.5–1.7ROR 1.7 · calibrated p 0.745
1.6 EB05 1.6 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.5no trial arm names this drug
Dyspnoea (shortness of breath)1,2271.8
1.7–1.9ROR 1.8 · calibrated p 0.844
1.8 EB05 1.7 · IC025 +0.7Labeled adverse reaction
exact term
serious PRR 1.6no trial arm names this drug
Dizziness1,1611.9
1.8–2.0ROR 2.0 · calibrated p 0.923
1.9 EB05 1.8 · IC025 +0.8Labeled adverse reaction
exact term
serious PRR 1.9no trial arm names this drug
Pain1,0701.4
1.3–1.5ROR 1.4 · calibrated p 0.608
1.4 EB05 1.4 · IC025 +0.4Labeled adverse reaction
exact term
serious PRR 1.4no trial arm names this drug
Headache1,0151.3
1.3–1.4ROR 1.3 · calibrated p 0.539
1.3 EB05 1.3 · IC025 +0.3Labeled adverse reaction
exact term
serious PRR 1.4no trial arm names this drug
Asthenia (weakness)9852.2
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 2.2no trial arm names this drug
Fall9092.2
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 — unassessedserious PRR 2.3no trial arm names this drug
Arthralgia (joint pain)8181.6
1.5–1.7ROR 1.6 · calibrated p 0.734
1.6 EB05 1.5 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.8no trial arm names this drug
Off label use (used outside approved label)8170.8
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 artifactserious PRR 0.7no trial arm names this drug
Death7970.8
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 reactionserious PRR 0.8no trial arm names this drug
Pain in extremity7542.1
2.0–2.3ROR 2.1 · calibrated p 0.984
2.1 EB05 2.0 · IC025 +0.9Not in label — unassessedserious PRR 2.5no trial arm names this drug
Vomiting7531.3
1.2–1.4ROR 1.3 · calibrated p 0.528
1.3 EB05 1.2 · IC025 +0.3Labeled adverse reaction
exact term
serious PRR 1.3no 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.

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

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.