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Atorvastatin side effects: what 245,741 FDA adverse event reports show

Atorvastatin Calcium · 1,174 reaction terms · 905,519 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Label matched

Atorvastatin Calcium (Atorvastatin Calcium)

closest FDA label found for this product string; brand list suppressed because the label is a related product, not an exact match

Who reports

245,741 reports · 65% serious · 18,671 with death outcome · 54% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Therapy with lipid-altering agents should be only one component of multiple risk factor intervention in individuals at significantly increased risk for atherosclerotic vascular disease due to hypercholesterolemia. Drug therapy is recommended as an adjunct to diet when the response to a diet restricted in saturated fat and cholesterol and other nonpharmacologic measures alone has been inadequate.

FDA label, Indications and Usage

What it is

Atorvastatin is a dihydroxy monocarboxylic acid that is a member of the drug class known as statins, used primarily for lowering blood cholesterol and for preventing cardiovascular diseases.

PubChem CID 60823 (ChEBI)

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) 4Likely indication confounding 8Lab value / disease marker 5Not in label — unassessed 22
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). 1,134 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
Vaginal flatulence16397.5
77.8–122.3ROR 97.6 · calibrated p 2e-7 ✓
45.2 EB05 39.7 · IC025 +5.1
3/3 methods agree
Not in label — unassessedserious n=163 · ♀ 100% (drug 54%) · 100% clinicianno trial arm names this drug
Neurologic neglect syndrome25370.1
59.3–82.9ROR 70.2 · calibrated p 2e-6 ✓
38.4 EB05 34.6 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=253 · ♀ 100% (drug 54%) · 100% clinicianno trial arm names this drug
Carotid artery thrombosis25536.1
31.1–41.8ROR 36.1 · calibrated p 1e-4 ✓
25.4 EB05 22.9 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=255 · ♀ 100% (drug 54%) · 100% clinicianno trial arm names this drug
Adjustment disorder26121.1
18.4–24.2ROR 21.2 · calibrated p 0.002 ✓
17.0 EB05 15.4 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=258 · ♀ 100% (drug 54%) · 100% clinicianno trial arm names this drug
Amaurosis fugax17316.3
13.8–19.2ROR 16.3 · calibrated p 0.005 ✓
13.7 EB05 12.1 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=173 · 100% clinicianno trial arm names this drug
Chronic kidney disease-mineral and bone disorder14312.9
10.8–15.4ROR 12.9 · calibrated p 0.013 ✓
11.2 EB05 9.7 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=143 · ♀ 0% (drug 54%)no trial arm names this drug
Nephrogenic anaemia56911.7
10.7–12.8ROR 11.7 · calibrated p 0.018 ✓
10.3 EB05 9.7 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=568no trial arm names this drug
High density lipoprotein decreased39711.4
10.3–12.6ROR 11.4 · calibrated p 0.021 ✓
10.1 EB05 9.3 · IC025 +3.2
3/3 methods agree
Lab value / disease markerserious n=277no trial arm names this drug
Hyperparathyroidism secondary29211.0
9.7–12.4ROR 11.0 · calibrated p 0.023 ✓
9.8 EB05 8.9 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=289no trial arm names this drug
Personality disorder29310.6
9.3–11.9ROR 10.6 · calibrated p 0.027 ✓
9.4 EB05 8.5 · IC025 +3.0
3/3 methods agree
Not in label — unassessedserious n=289 · ♀ 100% (drug 54%) · 100% clinicianno trial arm names this drug
Diabetic neuropathy5099.6
8.8–10.5ROR 9.6 · calibrated p 0.037 ✓
8.7 EB05 8.1 · IC025 +3.0
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=485no trial arm names this drug
Female genital tract fistula1759.5
8.2–11.2ROR 9.6 · calibrated p 0.039 ✓
8.5 EB05 7.5 · IC025 +2.8
3/3 methods agree
Not in label — unassessedserious n=175 · ♀ 100% (drug 54%) · 100% clinicianno trial arm names this drug
Radiculopathy2639.3
8.2–10.6ROR 9.4 · calibrated p 0.041 ✓
8.4 EB05 7.6 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=257 · ♀ 100% (drug 54%)no trial arm names this drug
Myocardial necrosis marker increased1579.0
7.7–10.7ROR 9.0 · calibrated p 0.047 ✓
8.1 EB05 7.1 · IC025 +2.7
3/3 methods agree
Lab value / disease markerserious n=155 · ♀ 0% (drug 54%) · 100% clinicianno trial arm names this drug
Blood cholesterol decreased1758.8
7.5–10.2ROR 8.8 · calibrated p 0.051
7.9 EB05 6.9 · IC025 +2.7
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
♀ 0% (drug 54%) · 100% consumerno trial arm names this drug
Ischaemic cardiomyopathy2898.7
7.7–9.8ROR 8.7 · calibrated p 0.052
7.9 EB05 7.1 · IC025 +2.8
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=291 · ♀ 32% (drug 54%)no trial arm names this drug
Blood pressure systolic abnormal2328.7
7.6–9.9ROR 8.7 · calibrated p 0.053
7.9 EB05 7.0 · IC025 +2.8
3/3 methods agree
Lab value / disease markerserious n=230 · ♀ 100% (drug 54%) · 100% clinicianno trial arm names this drug
Myopathy7918.5
7.9–9.1ROR 8.5 · calibrated p 0.055
7.8 EB05 7.3 · IC025 +2.8
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 6.5no trial arm names this drug
Difficulty in walking3068.1
7.2–9.1ROR 8.1 · calibrated p 0.064
7.4 EB05 6.7 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious n=271no trial arm names this drug
Arterial occlusive disease6858.0
7.4–8.7ROR 8.0 · calibrated p 0.066
7.4 EB05 6.9 · IC025 +2.8
3/3 methods agree
Not in label — unassessedserious PRR 6.7no trial arm names this drug
Chronic sinusitis3217.9
7.1–8.9ROR 7.9 · calibrated p 0.070
7.2 EB05 6.6 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious n=315 · ♀ 100% (drug 54%)no trial arm names this drug
Polymyositis1487.7
6.5–9.1ROR 7.7 · calibrated p 0.076
7.0 EB05 6.1 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=144 · 100% clinicianno trial arm names this drug
Blood pressure diastolic abnormal2137.6
6.6–8.8ROR 7.6 · calibrated p 0.078
7.0 EB05 6.2 · IC025 +2.6
3/3 methods agree
Lab value / disease markerserious n=212 · ♀ 100% (drug 54%) · 100% clinicianno trial arm names this drug
Low density lipoprotein increased6357.6
7.0–8.2ROR 7.6 · calibrated p 0.078
7.0 EB05 6.6 · IC025 +2.7
3/3 methods agree
Lab value / disease markerserious n=436no trial arm names this drug
Macular degeneration9817.6
7.1–8.1ROR 7.6 · calibrated p 0.078
7.0 EB05 6.6 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious PRR 6.6 · ♀ 89% (drug 54%)no trial arm names this drug
Multi-organ disorder1607.4
6.3–8.7ROR 7.4 · calibrated p 0.086
6.8 EB05 5.9 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=157 · ♀ 100% (drug 54%)no trial arm names this drug
Coronary artery occlusion1,1057.4
6.9–7.8ROR 7.4 · calibrated p 0.085
6.8 EB05 6.5 · IC025 +2.7
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious PRR 6.1no trial arm names this drug
Angina unstable5247.3
6.7–8.0ROR 7.3 · calibrated p 0.087
6.8 EB05 6.3 · IC025 +2.6
3/3 methods agree
Not in label — unassessedserious n=522no trial arm names this drug
Carotid artery stenosis2777.2
6.4–8.2ROR 7.2 · calibrated p 0.091
6.7 EB05 6.0 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=274no trial arm names this drug
Rebound acid hypersecretion2427.2
6.3–8.2ROR 7.2 · calibrated p 0.091
6.7 EB05 6.0 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=242no trial arm names this drug
Coronary artery stenosis3917.1
6.4–7.9ROR 7.1 · calibrated p 0.096
6.6 EB05 6.0 · IC025 +2.5
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=387 · ♀ 32% (drug 54%)no trial arm names this drug
Essential hypertension1997.0
6.1–8.1ROR 7.0 · calibrated p 0.099
6.5 EB05 5.7 · IC025 +2.5
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=178no trial arm names this drug
Hyperlipidaemia8706.6
6.2–7.1ROR 6.6 · calibrated p 0.116
6.2 EB05 5.8 · IC025 +2.5
3/3 methods agree
Likely indication confounding
term in indications
serious PRR 5.6no trial arm names this drug
Carotid artery occlusion2606.5
5.7–7.3ROR 6.5 · calibrated p 0.125
6.0 EB05 5.4 · IC025 +2.4
3/3 methods agree
Not in label — unassessedserious n=256no trial arm names this drug
Proctitis1966.3
5.5–7.3ROR 6.3 · calibrated p 0.131
5.9 EB05 5.2 · IC025 +2.3
3/3 methods agree
Not in label — unassessedserious n=195 · ♀ 100% (drug 54%) · 100% clinicianno trial arm names this drug
Blood cholesterol abnormal3216.3
5.6–7.1ROR 6.3 · calibrated p 0.133
5.9 EB05 5.4 · IC025 +2.4
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=218no trial arm names this drug

Clinical concept groups

MedDRA splits one clinical problem across several terms (e.g. "neutropenia", "neutrophil count decreased", "agranulocytosis"), which dilutes term-level signals. These rows count reports with any term in a concept group (an exact union, not a sum), compared with all other drugs. Groups are hand-built and listed in the methods.

ConceptReportsPRR 95% CIReading
Rhabdomyolysis / myopathy4,7475.25.1–5.4signal
Hyperglycaemia / diabetes19,0814.94.9–5.0signal
Myocardial infarction7,7953.33.3–3.4signal
Heart failure5,1242.52.4–2.6signal
Stroke7,0532.52.4–2.5signal
Gi bleeding4,8132.32.2–2.3signal
Arrhythmia / qt4,7502.12.1–2.2signal
Tendon disorder9122.11.9–2.2raised
Kidney injury10,7552.02.0–2.1raised
Hypoglycaemia2,1762.01.9–2.0raised
Fall / fracture8,6031.91.9–2.0raised
Pancreatitis1,7201.81.8–1.9raised
Anaemia6,0701.71.7–1.8raised
Liver injury5,7131.61.6–1.7raised
Hyponatraemia1,4021.51.4–1.6raised
Serious infection13,2561.51.4–1.5raised

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Atorvastatin only as a background or rescue medication (NCT01663402, NCT01492361); 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
Fatigue (tiredness)14,2521.6
1.6–1.6ROR 1.6 · calibrated p 0.713
1.6 EB05 1.5 · IC025 +0.6Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.7no trial arm names this drug
Drug ineffective (drug did not work)13,1890.9
0.8–0.9ROR 0.8 · calibrated p 0.209
0.9 EB05 0.8 · IC025 -0.3
PRR-only: not supported by EBGM or IC
Reporting / coding artifactage-adj. PRR 1.1 · serious PRR 1.0no trial arm names this drug
Nausea12,7771.4
1.4–1.4ROR 1.4 · calibrated p 0.581
1.4 EB05 1.4 · IC025 +0.4Labeled adverse reaction
exact term
age-adj. PRR 1.3 · serious PRR 1.5no trial arm names this drug
Diarrhoea (diarrhea)11,4821.5
1.5–1.6ROR 1.6 · calibrated p 0.679
1.5 EB05 1.5 · IC025 +0.6Labeled adverse reaction
exact term
age-adj. PRR 1.3 · serious PRR 1.5no trial arm names this drug
Dyspnoea (shortness of breath)11,4591.7
1.7–1.8ROR 1.8 · calibrated p 0.817
1.7 EB05 1.7 · IC025 +0.8Not in label — unassessedage-adj. PRR 1.5 · serious PRR 1.7no trial arm names this drug
Pain10,3041.4
1.4–1.5ROR 1.5 · calibrated p 0.612
1.4 EB05 1.4 · IC025 +0.5Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 1.4no trial arm names this drug
Headache10,0881.4
1.4–1.4ROR 1.4 · calibrated p 0.573
1.4 EB05 1.4 · IC025 +0.4Not in label — unassessedage-adj. PRR 1.4 · serious PRR 1.5no trial arm names this drug
Dizziness10,0301.7
1.7–1.8ROR 1.8 · calibrated p 0.808
1.7 EB05 1.7 · IC025 +0.7Labeled adverse reaction
exact term
age-adj. PRR 1.6 · serious PRR 1.8no trial arm names this drug
Myalgia (muscle pain)9,9615.3
5.1–5.4ROR 5.4 · calibrated p 0.193
5.0 EB05 4.9 · IC025 +2.3
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 4.0 · serious PRR 4.2no trial arm names this drug
Asthenia (weakness)9,0502.1
2.0–2.1ROR 2.1 · calibrated p 0.992
2.1 EB05 2.0 · IC025 +1.0
3/3 methods agree
Not in label — unassessedage-adj. PRR 1.7 · serious PRR 2.0no trial arm names this drug
Arthralgia (joint pain)8,7201.8
1.8–1.9ROR 1.8 · calibrated p 0.855
1.8 EB05 1.8 · IC025 +0.8Labeled adverse reaction
exact term
age-adj. PRR 1.6 · serious PRR 1.9no trial arm names this drug
Pain in extremity8,2992.4
2.4–2.5ROR 2.5 · calibrated p 0.818
2.4 EB05 2.4 · IC025 +1.2
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 2.0 · serious PRR 2.5no trial arm names this drug
Fall8,0462.1
2.0–2.1ROR 2.1 · calibrated p 0.988
2.1 EB05 2.0 · IC025 +1.0
3/3 methods agree
Not in label — unassessedage-adj. PRR 1.6 · serious PRR 2.0no trial arm names this drug
Death7,6340.8
0.7–0.8ROR 0.7 · calibrated p 0.154
0.8 EB05 0.7 · IC025 -0.4
PRR-only: not supported by EBGM or IC
Outcome field, not a reactionage-adj. PRR 0.7 · serious PRR 0.7no 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: Atorvastatin (statins) ↔ Type 2 diabetes mellitus.

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 Atorvastatin?

In FDA FAERS, the most frequently co-reported reaction terms for Atorvastatin are fatigue, nausea, diarrhoea, dyspnoea, type 2 diabetes mellitus, 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 Atorvastatin have an FDA boxed warning?

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

Do FAERS signals prove that Atorvastatin 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.