Rosuvastatin side effects: what 82,998 FDA adverse event reports show
Drug class
Not stated in label
Who reports
82,998 reports · 77% serious · 5,613 with death outcome · 50% female
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.
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).
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.
- Reporting / coding artifact An administrative, monitoring or exposure term (product issue, off-label use, 'test normal', overdose...). Not a biological reaction; a high PRR here reflects how reports are coded.
- 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). 1,123 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 |
|---|---|---|---|---|---|---|
| Spirometry abnormal | 139 | 31.7 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 marker | serious n=137 · ♀ 0% (drug 50%) | not reported in cached trials |
| Mite allergy | 139 | 28.5 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 — unassessed | serious n=136 · ♀ 0% (drug 50%) | not reported in cached trials |
| Mycotic allergy | 153 | 22.7 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 — unassessed | serious n=140 · ♀ 0% (drug 50%) | not reported in cached trials |
| Catarrh | 152 | 21.1 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 — unassessed | serious n=126 · ♀ 25% (drug 50%) · 100% clinician | not reported in cached trials |
| Steroid dependence | 144 | 20.9 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 — unassessed | serious n=122 · ♀ 0% (drug 50%) · 100% clinician | not reported in cached trials |
| High density lipoprotein decreased | 548 | 20.1 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 marker | serious n=54 | not reported in cached trials |
| Low density lipoprotein decreased | 226 | 19.4 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 marker | serious n=51 · ♀ 0% (drug 50%) | not reported in cached trials |
| Dust allergy | 149 | 18.7 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 — unassessed | serious n=145 · ♀ 0% (drug 50%) | not reported in cached trials |
| Carotid arteriosclerosis | 139 | 16.1 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 — unassessed | serious n=97 · ♀ 0% (drug 50%) | NCT00240331: 2/1,389 (0.1%) on Rosuvastatin (serious AE) |
| Obstructive sleep apnoea syndrome | 174 | 14.6 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 — unassessed | serious n=97 | not reported in cached trials |
| Conjunctivitis allergic | 180 | 14.3 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 — unassessed | serious n=167 · ♀ 0% (drug 50%) | not reported in cached trials |
| Sedation complication | 302 | 14.0 12.5–15.8ROR 14.1 · calibrated p 0.009 ✓ | 12.4 EB05 11.3 · IC025 +3.4 3/3 methods agree | Reporting / coding artifact | serious n=293 · ♀ 87% (drug 50%) | not reported in cached trials |
| Hyperparathyroidism secondary | 290 | 13.2 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 — unassessed | serious n=85 | NCT00239681: 1/8,869 (0.0%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE) |
| Myoglobin blood increased | 162 | 12.1 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 marker | serious n=64 · ♀ 0% (drug 50%) | not reported in cached trials |
| Nephrogenic anaemia | 487 | 11.9 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 — unassessed | serious n=128 | NCT00240331: 2/1,389 (0.1%) on Rosuvastatin; 1/1,378 (0.1%) control (serious AE) |
| Low density lipoprotein increased | 796 | 11.8 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 marker | serious n=158 | not reported in cached trials |
| Nasal oedema | 184 | 11.7 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 — unassessed | serious n=148 · ♀ 100% (drug 50%) · 100% clinician | not reported in cached trials |
| Blood cholesterol decreased | 169 | 10.2 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% consumer | not reported in cached trials |
| Rhabdomyolysis (muscle breakdown) | 3,730 | 10.1 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% clinician | NCT00240331: 1/1,378 (0.1%) control (serious AE) |
| Burns second degree | 156 | 10.0 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 — unassessed | serious n=124 · ♀ 0% (drug 50%) · 100% clinician | not reported in cached trials |
| Rebound acid hypersecretion | 264 | 9.6 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 — unassessed | serious n=93 | not reported in cached trials |
| Myopathy | 745 | 9.6 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 10.4 | NCT00239681: 2/8,869 (0.0%) on Rosuvastatin; 3/8,864 (0.0%) control (serious AE) |
| Blood pressure systolic abnormal | 213 | 9.6 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 marker | serious n=149 | not reported in cached trials |
| Blood cholesterol abnormal | 391 | 9.4 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=67 | not reported in cached trials |
| Creatinine renal clearance decreased | 338 | 9.4 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 marker | serious n=283 · ♀ 100% (drug 50%) | not reported in cached trials |
| Dyslipidaemia | 399 | 8.7 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=257 | not reported in cached trials |
| Blood pressure diastolic abnormal | 192 | 8.2 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 marker | serious n=154 · 100% clinician | not reported in cached trials |
| Coronary artery occlusion | 943 | 7.5 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 — unassessed | serious PRR 3.9 | NCT00239681: 1/8,864 (0.0%) control (serious AE) |
| Blood cholesterol increased | 3,029 | 7.1 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 3.2 | not reported in cached trials |
| Bronchiectasis | 431 | 7.1 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 — unassessed | serious n=337 | NCT00239681: 2/8,869 (0.0%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE) |
| Normochromic normocytic anaemia | 194 | 7.1 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 — unassessed | serious n=159 · ♀ 0% (drug 50%) | NCT00239681: 1/8,869 (0.0%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE) |
| Coronary artery stenosis | 317 | 6.8 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 — unassessed | serious n=167 · ♀ 30% (drug 50%) | NCT00239681: 1/8,869 (0.0%) on Rosuvastatin (serious AE) |
| Blood triglycerides increased | 1,112 | 6.8 6.4–7.3ROR 6.9 · calibrated p 0.104 | 6.4 EB05 6.1 · IC025 +2.6 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 3.6 · serious PRR 3.1 | not reported in cached trials |
| Blood creatine phosphokinase increased | 1,824 | 6.8 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 marker | age-adj. PRR 5.2 · serious PRR 4.5 | NCT00239681: 1/8,869 (0.0%) on Rosuvastatin (serious AE) |
| Arterial occlusive disease | 486 | 6.7 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 — unassessed | serious PRR 3.8 | NCT00239681: 1/8,864 (0.0%) control (serious AE) |
| Carotid artery stenosis | 213 | 6.6 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 — unassessed | serious n=106 | NCT00239681: 1/8,864 (0.0%) control (serious AE) |
| Gastrointestinal hypomotility | 134 | 6.5 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 — unassessed | serious n=113 · ♀ 73% (drug 50%) · 100% consumer | not reported in cached trials |
| Euglycaemic diabetic ketoacidosis | 238 | 6.5 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 — unassessed | serious n=200 · 100% clinician | not reported in cached trials |
| Carotid artery occlusion | 217 | 6.4 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 — unassessed | serious n=96 · ♀ 100% (drug 50%) | not reported in cached trials |
| Essential hypertension | 152 | 6.4 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.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Rhabdomyolysis / myopathy | 3,060 | 9.99.5–10.2 | signal |
| Kidney injury | 5,676 | 3.23.1–3.2 | signal |
| Arrhythmia / qt | 2,008 | 2.62.5–2.8 | signal |
| Tendon disorder | 356 | 2.42.1–2.6 | signal |
| Heart failure | 1,583 | 2.22.1–2.4 | signal |
| Myocardial infarction | 1,761 | 2.22.1–2.3 | signal |
| Interstitial lung disease | 786 | 2.11.9–2.2 | raised |
| Hyponatraemia | 651 | 2.01.9–2.2 | raised |
| Hyperglycaemia / diabetes | 2,759 | 2.01.9–2.1 | raised |
| Pancreatitis | 631 | 2.01.8–2.1 | raised |
| Liver injury | 2,356 | 2.01.9–2.1 | raised |
| Fall / fracture | 2,938 | 2.01.9–2.0 | raised |
| Gi bleeding | 1,345 | 1.91.8–2.0 | raised |
| Hypoglycaemia | 681 | 1.81.7–1.9 | raised |
| Serious infection | 5,315 | 1.71.7–1.8 | raised |
| Stroke | 1,635 | 1.71.6–1.7 | raised |
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).
- NCT00239681 — JUPITER - Crestor 20mg Versus Placebo in Prevention of Cardiovascular (CV) Events (N=17802, PHASE3; 894 AE terms posted; arms: PLACEBO; ROSUVASTATIN 20 MG)
- NCT00240331 — AURORA: Crestor 10mg Versus Placebo in Subjects With End-stage Renal Disease (ESRD) (N=2776, PHASE3; 939 AE terms posted; arms: Rosuvastatin 10mg; Placebo)
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 |
|---|---|---|---|---|---|---|
| Fatigue (tiredness) | 12,362 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.765 | 1.6 EB05 1.6 · IC025 +0.7 | Labeled (related wording) related wording | age-adj. PRR 1.7 · serious PRR 2.0 | NCT00239681: 1/8,864 (0.0%) control (serious AE) |
| Nausea | 10,604 | 1.4 1.4–1.4ROR 1.4 · calibrated p 0.583 | 1.4 EB05 1.4 · IC025 +0.4 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.7 | NCT00239681: 1/8,869 (0.0%) on Rosuvastatin; 2/8,864 (0.0%) control (serious AE) |
| Diarrhoea (diarrhea) | 9,780 | 1.6 1.5–1.6ROR 1.6 · calibrated p 0.710 | 1.6 EB05 1.5 · IC025 +0.6 | Not in label — unassessed | age-adj. PRR 1.5 · serious PRR 1.8 | NCT00239681: 5/8,869 (0.1%) on Rosuvastatin; 8/8,864 (0.1%) control (serious AE) |
| Drug ineffective (drug did not work) | 9,662 | 0.8 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 artifact | age-adj. PRR 1.0 · serious PRR 1.3 | not reported in cached trials |
| Dyspnoea (shortness of breath) | 9,603 | 1.8 1.7–1.8ROR 1.8 · calibrated p 0.830 | 1.8 EB05 1.7 · IC025 +0.8 | Not in label — unassessed | age-adj. PRR 1.8 · serious PRR 2.0 | NCT00239681: 8/8,869 (0.1%) on Rosuvastatin; 6/8,864 (0.1%) control (serious AE) |
| Myalgia (muscle pain) | 9,105 | 5.8 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 5.0 | NCT00239681: 5/8,869 (0.1%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE) |
| Off label use (used outside approved label) | 9,051 | 1.1 1.1–1.1ROR 1.1 · calibrated p 0.359 | 1.1 EB05 1.1 · IC025 +0.1 | Reporting / coding artifact | age-adj. PRR 1.4 · serious PRR 1.6 | not reported in cached trials |
| Pain | 8,772 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.640 | 1.5 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | age-adj. PRR 1.7 · serious PRR 1.6 | NCT00239681: 9/8,869 (0.1%) on Rosuvastatin; 7/8,864 (0.1%) control (serious AE) |
| Headache | 8,245 | 1.4 1.3–1.4ROR 1.4 · calibrated p 0.560 | 1.4 EB05 1.3 · IC025 +0.4 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.7 | NCT00239681: 3/8,869 (0.0%) on Rosuvastatin; 3/8,864 (0.0%) control (serious AE) |
| Dizziness | 8,087 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.778 | 1.7 EB05 1.6 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.8 | NCT00239681: 3/8,869 (0.0%) on Rosuvastatin; 7/8,864 (0.1%) control (serious AE) |
| Arthralgia (joint pain) | 7,562 | 1.9 1.9–1.9ROR 1.9 · calibrated p 0.907 | 1.9 EB05 1.8 · IC025 +0.9 | Labeled adverse reaction exact term | age-adj. PRR 1.8 · serious PRR 2.2 | NCT00239681: 7/8,869 (0.1%) on Rosuvastatin (serious AE) |
| Asthenia (weakness) | 7,507 | 2.1 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 2.0 | NCT00239681: 2/8,864 (0.0%) control (serious AE) |
| Pain in extremity | 6,980 | 2.5 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 — unassessed | age-adj. PRR 1.8 · serious PRR 2.4 | NCT00239681: 1/8,869 (0.0%) on Rosuvastatin; 1/8,864 (0.0%) control (serious AE) |
| Malaise (feeling unwell) | 6,766 | 1.6 1.6–1.6ROR 1.6 · calibrated p 0.717 | 1.6 EB05 1.6 · IC025 +0.6 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.7 | NCT00239681: 1/8,864 (0.0%) control (serious AE) |
| Fall | 6,299 | 2.0 1.9–2.0ROR 2.0 · calibrated p 0.946 | 2.0 EB05 1.9 · IC025 +0.9 | Not in label — unassessed | age-adj. PRR 1.5 · serious PRR 1.7 | NCT00239681: 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.
- Mite allergy — n=139, PRR 28.5
- Mycotic allergy — n=153, PRR 22.7
- Catarrh — n=152, PRR 21.1
- Steroid dependence — n=144, PRR 20.9
- Dust allergy — n=149, PRR 18.7
- Carotid arteriosclerosis — n=139, PRR 16.1 (also seen in trial arm)
- Obstructive sleep apnoea syndrome — n=174, PRR 14.6
- Conjunctivitis allergic — n=180, PRR 14.3
- Hyperparathyroidism secondary — n=290, PRR 13.2 (also seen in trial arm)
- Nephrogenic anaemia — n=487, PRR 11.9 (also seen in trial arm)
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
- FDA label via openFDA (set ID 0ad5b7de-e97d-4989-91e4-edae73543896, effective 20241030; matched on
openfda.generic_name.exact:"ROSUVASTATIN" AND openfda.product_type:"HUMAN PRESCRIPTION DRUG") - PubChem CID 446157 description (ChEBI)
- 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, 1,163 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
ROSUVASTATIN, 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.