Atorvastatin Calcium, Film Coated side effects: what 69,645 FDA adverse event reports show
Drug class
Not stated in label
Label matched
Atorvastatin Calcium, Film Coated (Atorvastatin Calcium)
Who reports
69,645 reports · 63% serious · 5,103 with death outcome · 52% female
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.
What it is
Atorvastatin is a synthetic lipid-lowering agent. Atorvastatin is an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase. This enzyme catalyzes the conversion of HMG-CoA to mevalonate, an early and rate-limiting step in cholesterol biosynthesis.
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). 1,151 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 |
|---|---|---|---|---|---|---|
| Vaginal flatulence | 163 | 346.7 276.5–434.7ROR 347.5 · calibrated p 4e-12 ✓ | 157.2 EB05 138.0 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=163 · ♀ 100% (drug 52%) | no trial arm names this drug |
| Immune-mediated necrotising myopathy | 136 | 99.3 81.8–120.5ROR 99.5 · calibrated p 2e-7 ✓ | 73.8 EB05 64.0 · IC025 +5.6 3/3 methods agree | Labeled (related wording) related wording | serious n=136 · 100% clinician | no trial arm names this drug |
| Type iia hyperlipidaemia | 48 | 80.6 58.6–110.9ROR 80.7 · calibrated p 1e-6 ✓ | 62.1 EB05 48.7 · IC025 +4.8 3/3 methods agree | Likely indication confounding term in indications | serious n=47 · 100% clinician | no trial arm names this drug |
| Amaurosis fugax | 157 | 51.6 43.6–61.2ROR 51.7 · calibrated p 1e-5 ✓ | 43.9 EB05 38.4 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious n=157 · 100% clinician | no trial arm names this drug |
| Immune-mediated myositis | 337 | 44.0 39.2–49.3ROR 44.2 · calibrated p 3e-5 ✓ | 38.3 EB05 35.0 · IC025 +5.0 3/3 methods agree | Labeled (related wording) related wording | serious n=337 · 100% clinician | no trial arm names this drug |
| Autoimmune myositis | 57 | 42.7 32.3–56.3ROR 42.7 · calibrated p 5e-5 ✓ | 37.0 EB05 29.6 · IC025 +4.4 3/3 methods agree | Labeled (related wording) related wording | serious n=57 · 100% clinician | no trial arm names this drug |
| Necrotising myositis | 93 | 36.1 29.1–44.8ROR 36.2 · calibrated p 1e-4 ✓ | 32.1 EB05 27.0 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=93 · 100% clinician | no trial arm names this drug |
| Urinary tract discomfort | 46 | 33.9 25.0–46.0ROR 33.9 · calibrated p 2e-4 ✓ | 30.2 EB05 23.6 · IC025 +4.0 3/3 methods agree | Labeled (related wording) related wording | serious n=45 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Alveolar osteitis | 43 | 33.6 24.5–46.1ROR 33.7 · calibrated p 2e-4 ✓ | 29.9 EB05 23.2 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=43 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Catarrh | 89 | 33.3 26.8–41.5ROR 33.4 · calibrated p 2e-4 ✓ | 29.9 EB05 25.0 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious n=88 · ♀ 0% (drug 52%) · 100% clinician | no trial arm names this drug |
| Female genital tract fistula | 171 | 33.1 28.3–38.7ROR 33.2 · calibrated p 2e-4 ✓ | 29.8 EB05 26.2 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=171 · ♀ 100% (drug 52%) | no trial arm names this drug |
| Steroid dependence | 80 | 31.2 24.8–39.2ROR 31.2 · calibrated p 3e-4 ✓ | 28.1 EB05 23.3 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=80 · ♀ 0% (drug 52%) · 100% clinician | no trial arm names this drug |
| Periorbital pain | 56 | 22.5 17.1–29.5ROR 22.5 · calibrated p 0.001 ✓ | 20.8 EB05 16.6 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | 100% consumer | no trial arm names this drug |
| Radiculopathy | 177 | 21.6 18.5–25.1ROR 21.6 · calibrated p 0.001 ✓ | 20.1 EB05 17.8 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=176 · ♀ 100% (drug 52%) | no trial arm names this drug |
| Chronic sinusitis | 238 | 20.3 17.8–23.2ROR 20.4 · calibrated p 0.002 ✓ | 19.1 EB05 17.1 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=237 · ♀ 100% (drug 52%) | no trial arm names this drug |
| Macular degeneration | 717 | 19.2 17.8–20.7ROR 19.4 · calibrated p 0.002 ✓ | 18.1 EB05 17.0 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious PRR 17.9 · ♀ 97% (drug 52%) | no trial arm names this drug |
| Proctitis | 167 | 19.0 16.2–22.2ROR 19.0 · calibrated p 0.003 ✓ | 17.9 EB05 15.7 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=167 · ♀ 100% (drug 52%) | no trial arm names this drug |
| Burns second degree | 90 | 16.3 13.1–20.1ROR 16.3 · calibrated p 0.005 ✓ | 15.4 EB05 12.9 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=89 · ♀ 0% (drug 52%) · 100% clinician | no trial arm names this drug |
| Eyelid pain | 99 | 16.1 13.2–19.7ROR 16.1 · calibrated p 0.006 ✓ | 15.3 EB05 12.9 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | 100% consumer | no trial arm names this drug |
| Myopathy | 416 | 15.1 13.7–16.7ROR 15.2 · calibrated p 0.007 ✓ | 14.4 EB05 13.3 · IC025 +3.7 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 12.4 | no trial arm names this drug |
| Bronchopulmonary aspergillosis allergic | 44 | 15.1 11.2–20.5ROR 15.1 · calibrated p 0.008 ✓ | 14.2 EB05 10.9 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious n=44 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Animal scratch | 46 | 14.9 11.1–20.1ROR 14.9 · calibrated p 0.008 ✓ | 14.1 EB05 10.9 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=45 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Blood pressure systolic abnormal | 113 | 14.2 11.8–17.2ROR 14.3 · calibrated p 0.009 ✓ | 13.6 EB05 11.6 · IC025 +3.4 3/3 methods agree | Lab value / disease marker | serious n=113 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Infusion site discharge | 73 | 13.4 10.6–16.9ROR 13.4 · calibrated p 0.012 ✓ | 12.7 EB05 10.4 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=50 · ♀ 100% (drug 52%) · 100% consumer | no trial arm names this drug |
| Blood pressure diastolic abnormal | 104 | 12.6 10.4–15.4ROR 12.7 · calibrated p 0.015 ✓ | 12.0 EB05 10.2 · IC025 +3.2 3/3 methods agree | Lab value / disease marker | serious n=104 · ♀ 100% (drug 52%) | no trial arm names this drug |
| Polymyositis | 70 | 12.4 9.7–15.7ROR 12.4 · calibrated p 0.016 ✓ | 11.7 EB05 9.5 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious n=69 · 100% clinician | no trial arm names this drug |
| Infusion site haemorrhage | 117 | 11.2 9.3–13.5ROR 11.2 · calibrated p 0.022 ✓ | 10.7 EB05 9.1 · IC025 +3.1 3/3 methods agree | Labeled (related wording) related wording | serious n=64 · 100% consumer | no trial arm names this drug |
| Urinary tract disorder | 151 | 10.4 8.9–12.2ROR 10.4 · calibrated p 0.029 ✓ | 10.0 EB05 8.7 · IC025 +3.0 3/3 methods agree | Labeled (related wording) related wording | serious n=142 | no trial arm names this drug |
| Device infusion issue | 76 | 9.6 7.6–12.1ROR 9.6 · calibrated p 0.039 ✓ | 9.1 EB05 7.4 · IC025 +2.8 3/3 methods agree | Reporting / coding artifact | serious n=37 · 100% consumer | no trial arm names this drug |
| Alcohol poisoning | 82 | 9.6 7.7–11.9ROR 9.6 · calibrated p 0.040 ✓ | 9.0 EB05 7.5 · IC025 +2.8 3/3 methods agree | Not in label — unassessed | serious n=82 · ♀ 0% (drug 52%) · 100% clinician | no trial arm names this drug |
| Seasonal allergy | 430 | 9.4 8.6–10.4ROR 9.5 · calibrated p 0.039 ✓ | 9.1 EB05 8.4 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious n=203 · ♀ 72% (drug 52%) · 79% consumer | no trial arm names this drug |
| Bronchiectasis | 201 | 9.3 8.1–10.7ROR 9.3 · calibrated p 0.041 ✓ | 9.0 EB05 8.0 · IC025 +2.9 3/3 methods agree | Not in label — unassessed | serious n=201 | no trial arm names this drug |
| Type 2 diabetes mellitus | 1,019 | 9.3 8.8–9.9ROR 9.4 · calibrated p 0.039 ✓ | 9.0 EB05 8.6 · IC025 +3.1 3/3 methods agree | Labeled (related wording) related wording | serious PRR 8.8 · ♀ 90% (drug 52%) | no trial arm names this drug |
| Haemorrhagic stroke | 235 | 9.2 8.1–10.5ROR 9.3 · calibrated p 0.043 ✓ | 8.9 EB05 8.0 · IC025 +2.9 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 8.3 · ♀ 0% (drug 52%) | no trial arm names this drug |
| N-terminal prohormone brain natriuretic peptide increased | 41 | 9.0 6.6–12.3ROR 9.0 · calibrated p 0.050 | 8.3 EB05 6.3 · IC025 +2.5 3/3 methods agree | Lab value / disease marker | serious n=40 · ♀ 0% (drug 52%) · 100% clinician | no trial arm names this drug |
| Hypopnoea | 101 | 9.0 7.4–11.0ROR 9.0 · calibrated p 0.048 ✓ | 8.6 EB05 7.2 · IC025 +2.7 3/3 methods agree | Not in label — unassessed | serious n=95 · ♀ 0% (drug 52%) · 100% clinician | no trial arm names this drug |
| Infusion site infection | 65 | 8.8 6.9–11.3ROR 8.9 · calibrated p 0.052 | 8.3 EB05 6.7 · IC025 +2.6 3/3 methods agree | Labeled (related wording) related wording | serious n=34 · ♀ 100% (drug 52%) · 100% consumer | no trial arm names this drug |
| Rales | 162 | 8.6 7.4–10.1ROR 8.6 · calibrated p 0.054 | 8.3 EB05 7.2 · IC025 +2.8 3/3 methods agree | Not in label — unassessed | serious n=156 | no trial arm names this drug |
| Nasal obstruction | 51 | 8.5 6.4–11.2ROR 8.5 · calibrated p 0.059 | 7.9 EB05 6.2 · IC025 +2.5 3/3 methods agree | Not in label — unassessed | serious n=49 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Sinus pain | 61 | 8.1 6.3–10.5ROR 8.1 · calibrated p 0.067 | 7.6 EB05 6.1 · IC025 +2.5 3/3 methods agree | Not in label — unassessed | serious n=55 · ♀ 100% (drug 52%) | no 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.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Rhabdomyolysis / myopathy | 1,764 | 6.76.4–7.0 | signal |
| Gi bleeding | 1,508 | 2.52.4–2.6 | signal |
| Hyperglycaemia / diabetes | 2,388 | 2.12.0–2.2 | signal |
| Heart failure | 1,209 | 2.01.9–2.2 | raised |
| Fall / fracture | 2,568 | 2.02.0–2.1 | raised |
| Arrhythmia / qt | 1,259 | 2.01.9–2.1 | raised |
| Myocardial infarction | 1,315 | 1.91.8–2.0 | raised |
| Anaemia | 1,883 | 1.91.8–2.0 | raised |
| Kidney injury | 2,815 | 1.91.8–1.9 | raised |
| Stroke | 1,531 | 1.91.8–1.9 | raised |
| Liver injury | 1,818 | 1.81.7–1.9 | raised |
| Hyponatraemia | 463 | 1.71.6–1.9 | raised |
| Tendon disorder | 210 | 1.71.4–1.9 | raised |
| Serious infection | 4,190 | 1.61.6–1.7 | raised |
| Hypoglycaemia | 487 | 1.51.4–1.7 | raised |
| Interstitial lung disease | 481 | 1.51.4–1.7 | raised |
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 |
|---|---|---|---|---|---|---|
| Fatigue (tiredness) | 4,648 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.866 | 1.8 EB05 1.8 · IC025 +0.8 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.8 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 4,374 | 1.0 1.0–1.0ROR 1.0 · calibrated p 0.306 | 1.0 EB05 1.0 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | age-adj. PRR 1.2 · serious PRR 1.4 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 4,101 | 1.9 1.9–2.0ROR 2.0 · calibrated p 0.933 | 1.9 EB05 1.9 · IC025 +0.9 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.8 | no trial arm names this drug |
| Nausea | 3,790 | 1.4 1.4–1.5ROR 1.5 · calibrated p 0.623 | 1.4 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | age-adj. PRR 1.3 · serious PRR 1.7 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 3,772 | 2.0 2.0–2.1ROR 2.1 · calibrated p 0.982 | 2.0 EB05 2.0 · IC025 +0.9 | Not in label — unassessed | age-adj. PRR 1.6 · serious PRR 2.0 | no trial arm names this drug |
| Headache | 3,432 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.760 | 1.6 EB05 1.6 · IC025 +0.7 | Not in label — unassessed | age-adj. PRR 1.5 · serious PRR 1.9 | no trial arm names this drug |
| Dizziness | 3,038 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.875 | 1.8 EB05 1.8 · IC025 +0.8 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 2.0 | no trial arm names this drug |
| Pain | 2,887 | 1.4 1.4–1.5ROR 1.4 · calibrated p 0.596 | 1.4 EB05 1.4 · IC025 +0.4 | Labeled adverse reaction exact term | age-adj. PRR 1.6 · serious PRR 1.3 | no trial arm names this drug |
| Off label use (used outside approved label) | 2,834 | 1.0 0.9–1.0ROR 1.0 · calibrated p 0.294 | 1.0 EB05 1.0 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | age-adj. PRR 1.0 · serious PRR 1.2 | no trial arm names this drug |
| Cough | 2,638 | 2.9 2.7–3.0ROR 2.9 · calibrated p 0.651 | 2.8 EB05 2.7 · IC025 +1.4 3/3 methods agree | Not in label — unassessed | age-adj. PRR 2.1 · serious PRR 2.7 | no trial arm names this drug |
| Asthenia (weakness) | 2,557 | 2.1 2.0–2.1ROR 2.1 · calibrated p 0.993 | 2.0 EB05 2.0 · IC025 +1.0 | Not in label — unassessed | age-adj. PRR 1.6 · serious PRR 2.0 | no trial arm names this drug |
| Arthralgia (joint pain) | 2,528 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.871 | 1.8 EB05 1.8 · IC025 +0.8 | Labeled adverse reaction exact term | age-adj. PRR 1.7 · serious PRR 1.9 | no trial arm names this drug |
| Myalgia (muscle pain) | 2,522 | 4.5 4.3–4.7ROR 4.6 · calibrated p 0.277 | 4.5 EB05 4.3 · IC025 +2.1 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 4.1 · serious PRR 3.8 | no trial arm names this drug |
| Fall | 2,467 | 2.2 2.2–2.3ROR 2.3 · calibrated p 0.910 | 2.2 EB05 2.2 · IC025 +1.1 3/3 methods agree | Not in label — unassessed | age-adj. PRR 1.6 · serious PRR 2.2 | no trial arm names this drug |
| Malaise (feeling unwell) | 2,367 | 1.6 1.6–1.7ROR 1.6 · calibrated p 0.734 | 1.6 EB05 1.6 · IC025 +0.6 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.8 | 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.
- Vaginal flatulence — n=163, PRR 346.7
- Amaurosis fugax — n=157, PRR 51.6
- Necrotising myositis — n=93, PRR 36.1
- Alveolar osteitis — n=43, PRR 33.6
- Catarrh — n=89, PRR 33.3
- Female genital tract fistula — n=171, PRR 33.1
- Steroid dependence — n=80, PRR 31.2
- Periorbital pain — n=56, PRR 22.5
- Radiculopathy — n=177, PRR 21.6
- Chronic sinusitis — n=238, PRR 20.3
✓ 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 Calcium, Film Coated?
In FDA FAERS, the most frequently co-reported reaction terms for Atorvastatin Calcium, Film Coated are fatigue, diarrhoea, nausea, dyspnoea, headache, dizziness. 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 Calcium, Film Coated have an FDA boxed warning?
No. The FDA label retrieved for Atorvastatin Calcium, Film Coated has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Atorvastatin Calcium, Film Coated 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 0a9d4e36-305a-2120-e063-6294a90a01bd, effective 20250203; matched on
openfda.generic_name.exact:"ATORVASTATIN CALCIUM, FILM COATED") - 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, 1,191 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
ATORVASTATIN, 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.