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Rosuvastatin side effects: what 82,998 FDA adverse event reports show

Rosuvastatin · 1,163 reaction terms · 751,519 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Who reports

82,998 reports · 77% serious · 5,613 with death outcome · 50% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Pediatric use information for patients 7 to 17 years of age is approved for AstraZeneca’s CRESTOR (rosuvastatin calcium) tablets. However, due to AstraZeneca’s marketing exclusivity rights, this drug product is not labeled with that pediatric information.

FDA label, Indications and Usage

What it is

Rosuvastatin is a dihydroxy monocarboxylic acid that is (6E)-7-{4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-(propan-2-yl)pyrimidin-5-yl} hept-6-enoic acid carrying two hydroxy substituents at positions 3 and 5 (the 3R,5S-diastereomer).

PubChem CID 446157 (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 2Labeled (related wording) 1Likely indication confounding 5Reporting / coding artifact 1Lab value / disease marker 9Not 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). 1,123 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
Spirometry abnormal13931.7
26.2–38.4ROR 31.8 · calibrated p 2e-4 ✓
24.3 EB05 21.1 · IC025 +4.2
3/3 methods agree
Lab value / disease markerserious n=137 · ♀ 0% (drug 50%)not reported in cached trials
Mite allergy13928.5
23.6–34.4ROR 28.5 · calibrated p 4e-4 ✓
22.4 EB05 19.4 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=136 · ♀ 0% (drug 50%)not reported in cached trials
Mycotic allergy15322.7
19.0–27.0ROR 22.7 · calibrated p 0.001 ✓
18.7 EB05 16.3 · IC025 +3.9
3/3 methods agree
Not in label — unassessedserious n=140 · ♀ 0% (drug 50%)not reported in cached trials
Catarrh15221.1
17.7–25.1ROR 21.1 · calibrated p 0.002 ✓
17.6 EB05 15.3 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=126 · ♀ 25% (drug 50%) · 100% cliniciannot reported in cached trials
Steroid dependence14420.9
17.4–25.0ROR 20.9 · calibrated p 0.002 ✓
17.4 EB05 15.2 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=122 · ♀ 0% (drug 50%) · 100% cliniciannot reported in cached trials
High density lipoprotein decreased54820.1
18.3–22.0ROR 20.1 · calibrated p 0.002 ✓
16.9 EB05 15.7 · IC025 +3.9
3/3 methods agree
Lab value / disease markerserious n=54not reported in cached trials
Low density lipoprotein decreased22619.4
16.8–22.4ROR 19.4 · calibrated p 0.002 ✓
16.4 EB05 14.7 · IC025 +3.8
3/3 methods agree
Lab value / disease markerserious n=51 · ♀ 0% (drug 50%)not reported in cached trials
Dust allergy14918.7
15.7–22.3ROR 18.7 · calibrated p 0.003 ✓
15.9 EB05 13.8 · IC025 +3.7
3/3 methods agree
Not in label — unassessedserious n=145 · ♀ 0% (drug 50%)not reported in cached trials
Carotid arteriosclerosis13916.1
13.4–19.2ROR 16.1 · calibrated p 0.006 ✓
13.9 EB05 12.1 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=97 · ♀ 0% (drug 50%)NCT00240331: 2/1,389 (0.1%) on Rosuvastatin (serious AE)
Obstructive sleep apnoea syndrome17414.6
12.4–17.1ROR 14.6 · calibrated p 0.008 ✓
12.8 EB05 11.3 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=97not reported in cached trials
Conjunctivitis allergic18014.3
12.3–16.8ROR 14.4 · calibrated p 0.009 ✓
12.6 EB05 11.1 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=167 · ♀ 0% (drug 50%)not reported in cached trials
Sedation complication30214.0
12.5–15.8ROR 14.1 · calibrated p 0.009 ✓
12.4 EB05 11.3 · IC025 +3.4
3/3 methods agree
Reporting / coding artifactserious n=293 · ♀ 87% (drug 50%)not reported in cached trials
Hyperparathyroidism secondary29013.2
11.7–14.9ROR 13.2 · calibrated p 0.012 ✓
11.8 EB05 10.7 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=85NCT00239681: 1/8,869 (0.0%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE)
Myoglobin blood increased16212.1
10.3–14.2ROR 12.1 · calibrated p 0.017 ✓
10.8 EB05 9.4 · IC025 +3.1
3/3 methods agree
Lab value / disease markerserious n=64 · ♀ 0% (drug 50%)not reported in cached trials
Nephrogenic anaemia48711.9
10.8–13.1ROR 11.9 · calibrated p 0.017 ✓
10.7 EB05 9.9 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=128NCT00240331: 2/1,389 (0.1%) on Rosuvastatin; 1/1,378 (0.1%) control (serious AE)
Low density lipoprotein increased79611.8
11.0–12.7ROR 11.8 · calibrated p 0.018 ✓
10.6 EB05 10.0 · IC025 +3.3
3/3 methods agree
Lab value / disease markerserious n=158not reported in cached trials
Nasal oedema18411.7
10.0–13.6ROR 11.7 · calibrated p 0.019 ✓
10.5 EB05 9.3 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=148 · ♀ 100% (drug 50%) · 100% cliniciannot reported in cached trials
Blood cholesterol decreased16910.2
8.7–11.9ROR 10.2 · calibrated p 0.031 ✓
9.2 EB05 8.1 · IC025 +2.9
3/3 methods agree
Likely indication confounding
term in indications
100% consumernot reported in cached trials
Rhabdomyolysis (muscle breakdown)3,73010.1
9.7–10.4ROR 10.2 · calibrated p 0.030 ✓
9.2 EB05 9.0 · IC025 +3.2
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 10.2 · serious PRR 9.3 · 96% clinicianNCT00240331: 1/1,378 (0.1%) control (serious AE)
Burns second degree15610.0
8.5–11.8ROR 10.0 · calibrated p 0.033 ✓
9.1 EB05 7.9 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=124 · ♀ 0% (drug 50%) · 100% cliniciannot reported in cached trials
Rebound acid hypersecretion2649.6
8.5–10.9ROR 9.6 · calibrated p 0.037 ✓
8.8 EB05 7.9 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=93not reported in cached trials
Myopathy7459.6
8.9–10.4ROR 9.6 · calibrated p 0.037 ✓
8.8 EB05 8.3 · IC025 +3.0
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 10.4NCT00239681: 2/8,869 (0.0%) on Rosuvastatin; 3/8,864 (0.0%) control (serious AE)
Blood pressure systolic abnormal2139.6
8.3–11.0ROR 9.6 · calibrated p 0.038 ✓
8.7 EB05 7.8 · IC025 +2.9
3/3 methods agree
Lab value / disease markerserious n=149not reported in cached trials
Blood cholesterol abnormal3919.4
8.5–10.5ROR 9.5 · calibrated p 0.039 ✓
8.7 EB05 8.0 · IC025 +2.9
3/3 methods agree
Likely indication confounding
term in indications
serious n=67not reported in cached trials
Creatinine renal clearance decreased3389.4
8.4–10.5ROR 9.4 · calibrated p 0.041 ✓
8.6 EB05 7.8 · IC025 +2.9
3/3 methods agree
Lab value / disease markerserious n=283 · ♀ 100% (drug 50%)not reported in cached trials
Dyslipidaemia3998.7
7.9–9.6ROR 8.7 · calibrated p 0.051
8.0 EB05 7.4 · IC025 +2.8
3/3 methods agree
Likely indication confounding
term in indications
serious n=257not reported in cached trials
Blood pressure diastolic abnormal1928.2
7.1–9.6ROR 8.3 · calibrated p 0.062
7.6 EB05 6.7 · IC025 +2.7
3/3 methods agree
Lab value / disease markerserious n=154 · 100% cliniciannot reported in cached trials
Coronary artery occlusion9437.5
7.0–8.0ROR 7.5 · calibrated p 0.080
7.0 EB05 6.7 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious PRR 3.9NCT00239681: 1/8,864 (0.0%) control (serious AE)
Blood cholesterol increased3,0297.1
6.8–7.4ROR 7.2 · calibrated p 0.091
6.7 EB05 6.5 · IC025 +2.7
3/3 methods agree
Likely indication confounding
term in indications
age-adj. PRR 3.3 · serious PRR 3.2not reported in cached trials
Bronchiectasis4317.1
6.4–7.8ROR 7.1 · calibrated p 0.096
6.6 EB05 6.1 · IC025 +2.6
3/3 methods agree
Not in label — unassessedserious n=337NCT00239681: 2/8,869 (0.0%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE)
Normochromic normocytic anaemia1947.1
6.1–8.2ROR 7.1 · calibrated p 0.098
6.6 EB05 5.8 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=159 · ♀ 0% (drug 50%)NCT00239681: 1/8,869 (0.0%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE)
Coronary artery stenosis3176.8
6.1–7.7ROR 6.9 · calibrated p 0.106
6.4 EB05 5.8 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=167 · ♀ 30% (drug 50%)NCT00239681: 1/8,869 (0.0%) on Rosuvastatin (serious AE)
Blood creatine phosphokinase increased1,8246.8
6.5–7.1ROR 6.8 · calibrated p 0.105
6.4 EB05 6.2 · IC025 +2.6
3/3 methods agree
Lab value / disease markerage-adj. PRR 5.2 · serious PRR 4.5NCT00239681: 1/8,869 (0.0%) on Rosuvastatin (serious AE)
Arterial occlusive disease4866.7
6.1–7.3ROR 6.7 · calibrated p 0.112
6.3 EB05 5.8 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious PRR 3.8NCT00239681: 1/8,864 (0.0%) control (serious AE)
Carotid artery stenosis2136.6
5.7–7.6ROR 6.6 · calibrated p 0.118
6.2 EB05 5.5 · IC025 +2.4
3/3 methods agree
Not in label — unassessedserious n=106NCT00239681: 1/8,864 (0.0%) control (serious AE)
Gastrointestinal hypomotility1346.5
5.5–7.8ROR 6.5 · calibrated p 0.122
6.1 EB05 5.3 · IC025 +2.3
3/3 methods agree
Not in label — unassessedserious n=113 · ♀ 73% (drug 50%) · 100% consumernot reported in cached trials
Euglycaemic diabetic ketoacidosis2386.5
5.7–7.4ROR 6.5 · calibrated p 0.123
6.1 EB05 5.5 · IC025 +2.4
3/3 methods agree
Not in label — unassessedserious n=200 · 100% cliniciannot reported in cached trials
Carotid artery occlusion2176.4
5.6–7.4ROR 6.4 · calibrated p 0.126
6.0 EB05 5.4 · IC025 +2.4
3/3 methods agree
Not in label — unassessedserious n=96 · ♀ 100% (drug 50%)not reported in cached trials
Essential hypertension1526.4
5.4–7.5ROR 6.4 · calibrated p 0.130
5.9 EB05 5.2 · IC025 +2.3
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
–not reported in cached trials

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 / myopathy3,0609.99.5–10.2signal
Kidney injury5,6763.23.1–3.2signal
Arrhythmia / qt2,0082.62.5–2.8signal
Tendon disorder3562.42.1–2.6signal
Heart failure1,5832.22.1–2.4signal
Myocardial infarction1,7612.22.1–2.3signal
Interstitial lung disease7862.11.9–2.2raised
Hyponatraemia6512.01.9–2.2raised
Hyperglycaemia / diabetes2,7592.01.9–2.1raised
Pancreatitis6312.01.8–2.1raised
Liver injury2,3562.01.9–2.1raised
Fall / fracture2,9382.01.9–2.0raised
Gi bleeding1,3451.91.8–2.0raised
Hypoglycaemia6811.81.7–1.9raised
Serious infection5,3151.71.7–1.8raised
Stroke1,6351.71.6–1.7raised

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Rosuvastatin 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 (12 of 40 signal terms matched).

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.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Nausea10,6041.4
1.4–1.4ROR 1.4 · calibrated p 0.583
1.4 EB05 1.4 · IC025 +0.4Labeled adverse reaction
exact term
age-adj. PRR 1.4 · serious PRR 1.7NCT00239681: 1/8,869 (0.0%) on Rosuvastatin; 2/8,864 (0.0%) control (serious AE)
Diarrhoea (diarrhea)9,7801.6
1.5–1.6ROR 1.6 · calibrated p 0.710
1.6 EB05 1.5 · IC025 +0.6Not in label — unassessedage-adj. PRR 1.5 · serious PRR 1.8NCT00239681: 5/8,869 (0.1%) on Rosuvastatin; 8/8,864 (0.1%) control (serious AE)
Drug ineffective (drug did not work)9,6620.8
0.7–0.8ROR 0.7 · calibrated p 0.152
0.8 EB05 0.7 · IC025 -0.4
PRR-only: not supported by EBGM or IC
Reporting / coding artifactage-adj. PRR 1.0 · serious PRR 1.3not reported in cached trials
Dyspnoea (shortness of breath)9,6031.8
1.7–1.8ROR 1.8 · calibrated p 0.830
1.8 EB05 1.7 · IC025 +0.8Not in label — unassessedage-adj. PRR 1.8 · serious PRR 2.0NCT00239681: 8/8,869 (0.1%) on Rosuvastatin; 6/8,864 (0.1%) control (serious AE)
Myalgia (muscle pain)9,1055.8
5.7–5.9ROR 6.0 · calibrated p 0.150
5.5 EB05 5.4 · IC025 +2.4
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 4.3 · serious PRR 5.0NCT00239681: 5/8,869 (0.1%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE)
Off label use (used outside approved label)9,0511.1
1.1–1.1ROR 1.1 · calibrated p 0.359
1.1 EB05 1.1 · IC025 +0.1Reporting / coding artifactage-adj. PRR 1.4 · serious PRR 1.6not reported in cached trials
Pain8,7721.5
1.4–1.5ROR 1.5 · calibrated p 0.640
1.5 EB05 1.4 · IC025 +0.5Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 1.6NCT00239681: 9/8,869 (0.1%) on Rosuvastatin; 7/8,864 (0.1%) control (serious AE)
Headache8,2451.4
1.3–1.4ROR 1.4 · calibrated p 0.560
1.4 EB05 1.3 · IC025 +0.4Labeled adverse reaction
exact term
age-adj. PRR 1.4 · serious PRR 1.7NCT00239681: 3/8,869 (0.0%) on Rosuvastatin; 3/8,864 (0.0%) control (serious AE)
Dizziness8,0871.7
1.6–1.7ROR 1.7 · calibrated p 0.778
1.7 EB05 1.6 · IC025 +0.7Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.8NCT00239681: 3/8,869 (0.0%) on Rosuvastatin; 7/8,864 (0.1%) control (serious AE)
Arthralgia (joint pain)7,5621.9
1.9–1.9ROR 1.9 · calibrated p 0.907
1.9 EB05 1.8 · IC025 +0.9Labeled adverse reaction
exact term
age-adj. PRR 1.8 · serious PRR 2.2NCT00239681: 7/8,869 (0.1%) on Rosuvastatin (serious AE)
Asthenia (weakness)7,5072.1
2.0–2.1ROR 2.1 · calibrated p 0.992
2.1 EB05 2.0 · IC025 +1.0
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 2.0NCT00239681: 2/8,864 (0.0%) control (serious AE)
Pain in extremity6,9802.5
2.4–2.5ROR 2.5 · calibrated p 0.802
2.4 EB05 2.4 · IC025 +1.2
3/3 methods agree
Not in label — unassessedage-adj. PRR 1.8 · serious PRR 2.4NCT00239681: 1/8,869 (0.0%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE)
Malaise (feeling unwell)6,7661.6
1.6–1.6ROR 1.6 · calibrated p 0.717
1.6 EB05 1.6 · IC025 +0.6Labeled adverse reaction
exact term
age-adj. PRR 1.4 · serious PRR 1.7NCT00239681: 1/8,864 (0.0%) control (serious AE)
Fall6,2992.0
1.9–2.0ROR 2.0 · calibrated p 0.946
2.0 EB05 1.9 · IC025 +0.9Not in label — unassessedage-adj. PRR 1.5 · serious PRR 1.7NCT00239681: 3/8,869 (0.0%) on Rosuvastatin; 3/8,864 (0.0%) control (serious AE)

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 Rosuvastatin?

In FDA FAERS, the most frequently co-reported reaction terms for Rosuvastatin are fatigue, nausea, diarrhoea, dyspnoea, myalgia, 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 Rosuvastatin have an FDA boxed warning?

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

Do FAERS signals prove that Rosuvastatin 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.