Atorvastatin side effects: what 245,741 FDA adverse event reports show
Drug class
Not stated in label
Label matched
Atorvastatin Calcium (Atorvastatin Calcium)
Who reports
245,741 reports · 65% serious · 18,671 with death outcome · 54% 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 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.
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.
- 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). 1,134 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 | 97.5 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 — unassessed | serious n=163 · ♀ 100% (drug 54%) · 100% clinician | no trial arm names this drug |
| Neurologic neglect syndrome | 253 | 70.1 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 — unassessed | serious n=253 · ♀ 100% (drug 54%) · 100% clinician | no trial arm names this drug |
| Type 2 diabetes mellitus | 11,260 | 42.4 41.5–43.4ROR 44.4 · calibrated p 3e-5 ✓ | 28.4 EB05 28.0 · IC025 +4.8 3/3 methods agree | Labeled (related wording) related wording | serious PRR 26.3 · ♀ 93% (drug 54%) | no trial arm names this drug |
| Carotid artery thrombosis | 255 | 36.1 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 — unassessed | serious n=255 · ♀ 100% (drug 54%) · 100% clinician | no trial arm names this drug |
| Immune-mediated necrotising myopathy | 149 | 31.6 26.2–38.2ROR 31.6 · calibrated p 2e-4 ✓ | 23.1 EB05 20.2 · IC025 +4.2 3/3 methods agree | Labeled (related wording) related wording | serious n=149 · ♀ 0% (drug 54%) · 100% clinician | no trial arm names this drug |
| Adjustment disorder | 261 | 21.1 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 — unassessed | serious n=258 · ♀ 100% (drug 54%) · 100% clinician | no trial arm names this drug |
| Amaurosis fugax | 173 | 16.3 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 — unassessed | serious n=173 · 100% clinician | no trial arm names this drug |
| Chronic kidney disease-mineral and bone disorder | 143 | 12.9 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 — unassessed | serious n=143 · ♀ 0% (drug 54%) | no trial arm names this drug |
| Immune-mediated myositis | 348 | 12.8 11.5–14.4ROR 12.8 · calibrated p 0.013 ✓ | 11.2 EB05 10.2 · IC025 +3.3 3/3 methods agree | Labeled (related wording) related wording | serious n=348 · 100% clinician | no trial arm names this drug |
| Nephrogenic anaemia | 569 | 11.7 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 — unassessed | serious n=568 | no trial arm names this drug |
| High density lipoprotein decreased | 397 | 11.4 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 marker | serious n=277 | no trial arm names this drug |
| Hyperparathyroidism secondary | 292 | 11.0 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 — unassessed | serious n=289 | no trial arm names this drug |
| Personality disorder | 293 | 10.6 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 — unassessed | serious n=289 · ♀ 100% (drug 54%) · 100% clinician | no trial arm names this drug |
| Diabetic neuropathy | 509 | 9.6 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=485 | no trial arm names this drug |
| Female genital tract fistula | 175 | 9.5 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 — unassessed | serious n=175 · ♀ 100% (drug 54%) · 100% clinician | no trial arm names this drug |
| Radiculopathy | 263 | 9.3 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 — unassessed | serious n=257 · ♀ 100% (drug 54%) | no trial arm names this drug |
| Myocardial necrosis marker increased | 157 | 9.0 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 marker | serious n=155 · ♀ 0% (drug 54%) · 100% clinician | no trial arm names this drug |
| Blood cholesterol decreased | 175 | 8.8 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% consumer | no trial arm names this drug |
| Ischaemic cardiomyopathy | 289 | 8.7 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 abnormal | 232 | 8.7 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 marker | serious n=230 · ♀ 100% (drug 54%) · 100% clinician | no trial arm names this drug |
| Myopathy | 791 | 8.5 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 6.5 | no trial arm names this drug |
| Muscle disorder | 733 | 8.4 7.7–9.0ROR 8.4 · calibrated p 0.058 | 7.7 EB05 7.2 · IC025 +2.8 3/3 methods agree | Labeled (related wording) related wording | serious n=451 · 76% consumer | no trial arm names this drug |
| Difficulty in walking | 306 | 8.1 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 — unassessed | serious n=271 | no trial arm names this drug |
| Arterial occlusive disease | 685 | 8.0 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 — unassessed | serious PRR 6.7 | no trial arm names this drug |
| Chronic sinusitis | 321 | 7.9 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 — unassessed | serious n=315 · ♀ 100% (drug 54%) | no trial arm names this drug |
| Polymyositis | 148 | 7.7 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 — unassessed | serious n=144 · 100% clinician | no trial arm names this drug |
| Blood pressure diastolic abnormal | 213 | 7.6 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 marker | serious n=212 · ♀ 100% (drug 54%) · 100% clinician | no trial arm names this drug |
| Low density lipoprotein increased | 635 | 7.6 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 marker | serious n=436 | no trial arm names this drug |
| Macular degeneration | 981 | 7.6 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 — unassessed | serious PRR 6.6 · ♀ 89% (drug 54%) | no trial arm names this drug |
| Multi-organ disorder | 160 | 7.4 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 — unassessed | serious n=157 · ♀ 100% (drug 54%) | no trial arm names this drug |
| Coronary artery occlusion | 1,105 | 7.4 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 6.1 | no trial arm names this drug |
| Angina unstable | 524 | 7.3 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 — unassessed | serious n=522 | no trial arm names this drug |
| Carotid artery stenosis | 277 | 7.2 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 — unassessed | serious n=274 | no trial arm names this drug |
| Rebound acid hypersecretion | 242 | 7.2 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 — unassessed | serious n=242 | no trial arm names this drug |
| Coronary artery stenosis | 391 | 7.1 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 hypertension | 199 | 7.0 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=178 | no trial arm names this drug |
| Hyperlipidaemia | 870 | 6.6 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 5.6 | no trial arm names this drug |
| Carotid artery occlusion | 260 | 6.5 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 — unassessed | serious n=256 | no trial arm names this drug |
| Proctitis | 196 | 6.3 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 — unassessed | serious n=195 · ♀ 100% (drug 54%) · 100% clinician | no trial arm names this drug |
| Blood cholesterol abnormal | 321 | 6.3 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=218 | 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 | 4,747 | 5.25.1–5.4 | signal |
| Hyperglycaemia / diabetes | 19,081 | 4.94.9–5.0 | signal |
| Myocardial infarction | 7,795 | 3.33.3–3.4 | signal |
| Heart failure | 5,124 | 2.52.4–2.6 | signal |
| Stroke | 7,053 | 2.52.4–2.5 | signal |
| Gi bleeding | 4,813 | 2.32.2–2.3 | signal |
| Arrhythmia / qt | 4,750 | 2.12.1–2.2 | signal |
| Tendon disorder | 912 | 2.11.9–2.2 | raised |
| Kidney injury | 10,755 | 2.02.0–2.1 | raised |
| Hypoglycaemia | 2,176 | 2.01.9–2.0 | raised |
| Fall / fracture | 8,603 | 1.91.9–2.0 | raised |
| Pancreatitis | 1,720 | 1.81.8–1.9 | raised |
| Anaemia | 6,070 | 1.71.7–1.8 | raised |
| Liver injury | 5,713 | 1.61.6–1.7 | raised |
| Hyponatraemia | 1,402 | 1.51.4–1.6 | raised |
| Serious infection | 13,256 | 1.51.4–1.5 | 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) | 14,252 | 1.6 1.6–1.6ROR 1.6 · calibrated p 0.713 | 1.6 EB05 1.5 · IC025 +0.6 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.7 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 13,189 | 0.9 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 artifact | age-adj. PRR 1.1 · serious PRR 1.0 | no trial arm names this drug |
| Nausea | 12,777 | 1.4 1.4–1.4ROR 1.4 · calibrated p 0.581 | 1.4 EB05 1.4 · IC025 +0.4 | Labeled adverse reaction exact term | age-adj. PRR 1.3 · serious PRR 1.5 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 11,482 | 1.5 1.5–1.6ROR 1.6 · calibrated p 0.679 | 1.5 EB05 1.5 · IC025 +0.6 | Labeled adverse reaction exact term | age-adj. PRR 1.3 · serious PRR 1.5 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 11,459 | 1.7 1.7–1.8ROR 1.8 · calibrated p 0.817 | 1.7 EB05 1.7 · IC025 +0.8 | Not in label — unassessed | age-adj. PRR 1.5 · serious PRR 1.7 | no trial arm names this drug |
| Type 2 diabetes mellitus | 11,260 | 42.4 41.5–43.4ROR 44.4 · calibrated p 3e-5 ✓ | 28.4 EB05 28.0 · IC025 +4.8 3/3 methods agree | Labeled (related wording) related wording | serious PRR 26.3 · ♀ 93% (drug 54%) | no trial arm names this drug |
| Pain | 10,304 | 1.4 1.4–1.5ROR 1.5 · calibrated p 0.612 | 1.4 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | age-adj. PRR 1.7 · serious PRR 1.4 | no trial arm names this drug |
| Headache | 10,088 | 1.4 1.4–1.4ROR 1.4 · calibrated p 0.573 | 1.4 EB05 1.4 · IC025 +0.4 | Not in label — unassessed | age-adj. PRR 1.4 · serious PRR 1.5 | no trial arm names this drug |
| Dizziness | 10,030 | 1.7 1.7–1.8ROR 1.8 · calibrated p 0.808 | 1.7 EB05 1.7 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.6 · serious PRR 1.8 | no trial arm names this drug |
| Myalgia (muscle pain) | 9,961 | 5.3 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 4.2 | no trial arm names this drug |
| Asthenia (weakness) | 9,050 | 2.1 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 — unassessed | age-adj. PRR 1.7 · serious PRR 2.0 | no trial arm names this drug |
| Arthralgia (joint pain) | 8,720 | 1.8 1.8–1.9ROR 1.8 · calibrated p 0.855 | 1.8 EB05 1.8 · IC025 +0.8 | Labeled adverse reaction exact term | age-adj. PRR 1.6 · serious PRR 1.9 | no trial arm names this drug |
| Pain in extremity | 8,299 | 2.4 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 2.5 | no trial arm names this drug |
| Fall | 8,046 | 2.1 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 — unassessed | age-adj. PRR 1.6 · serious PRR 2.0 | no trial arm names this drug |
| Death | 7,634 | 0.8 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 reaction | age-adj. PRR 0.7 · serious PRR 0.7 | 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 97.5
- Neurologic neglect syndrome — n=253, PRR 70.1
- Carotid artery thrombosis — n=255, PRR 36.1
- Adjustment disorder — n=261, PRR 21.1
- Amaurosis fugax — n=173, PRR 16.3
- Chronic kidney disease-mineral and bone disorder — n=143, PRR 12.9
- Nephrogenic anaemia — n=569, PRR 11.7
- Hyperparathyroidism secondary — n=292, PRR 11.0
- Personality disorder — n=293, PRR 10.6
- Female genital tract fistula — n=175, PRR 9.5
✓ 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
- FDA label via openFDA (set ID 01eadde8-37f3-4474-995f-22c1a65adf12, effective 20230407; matched on
openfda.generic_name.exact:"ATORVASTATIN CALCIUM") - PubChem CID 60823 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, 1,174 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.