Diphenhydramine and Liquid Filled side effects: what 21,221 FDA adverse event reports show
Drug class
Not stated in label
Label matched
Diphenhydramine (Nightime Sleep Aid)
Who reports
21,221 reports · 85% serious · 3,664 with death outcome · 71% female
Used for
For relief of occasional sleeplessness.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- 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.
- No label text to screen No validated FDA label was retrievable for this product, so the screen could not run. Disproportionality only.
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). 1,197 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 |
|---|---|---|---|---|---|---|
| Anti-cyclic citrullinated peptide antibody | 228 | 514.8 438.7–604.1ROR 520.4 · calibrated p 5e-14 ✓ | 327.8 EB05 293.6 · IC025 +7.4 3/3 methods agree | Lab value / disease marker | serious n=228 · ♀ 100% (drug 71%) · 93% clinician | no trial arm names this drug |
| Allergy to immunoglobulin therapy | 33 | 465.4 307.5–704.6ROR 466.2 · calibrated p 1e-12 ✓ | 266.6 EB05 198.6 · IC025 +5.2 3/3 methods agree | Reporting / coding artifact | serious n=28 · ♀ 100% (drug 71%) · 100% consumer | no trial arm names this drug |
| Vaginal flatulence | 94 | 439.8 344.9–560.9ROR 441.8 · calibrated p 4e-13 ✓ | 285.6 EB05 240.3 · IC025 +6.5 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=94 · ♀ 100% (drug 71%) | no trial arm names this drug |
| Blood pressure diastolic abnormal | 601 | 302.1 276.0–330.7ROR 310.9 · calibrated p 7e-12 ✓ | 229.1 EB05 214.1 · IC025 +7.5 3/3 methods agree | Lab value / disease marker | serious n=585 · 91% clinician | no trial arm names this drug |
| Neurologic neglect syndrome | 131 | 302.1 248.4–367.4ROR 304.0 · calibrated p 1e-11 ✓ | 223.3 EB05 193.0 · IC025 +6.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=131 · ♀ 100% (drug 71%) · 92% clinician | no trial arm names this drug |
| Swollen joint count | 57 | 298.2 221.7–401.1ROR 299.0 · calibrated p 3e-11 ✓ | 212.3 EB05 170.0 · IC025 +5.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=57 · ♀ 100% (drug 71%) · 100% clinician | no trial arm names this drug |
| Blood pressure systolic abnormal | 573 | 295.8 269.7–324.5ROR 304.0 · calibrated p 9e-12 ✓ | 225.4 EB05 210.3 · IC025 +7.4 3/3 methods agree | Lab value / disease marker | serious n=553 | no trial arm names this drug |
| Lupus vulgaris | 254 | 268.4 233.7–308.2ROR 271.6 · calibrated p 3e-11 ✓ | 207.3 EB05 186.8 · IC025 +7.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=254 · ♀ 100% (drug 71%) · 95% clinician | no trial arm names this drug |
| Grip strength | 49 | 264.9 193.2–363.2ROR 265.5 · calibrated p 8e-11 ✓ | 192.9 EB05 151.7 · IC025 +5.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=49 · ♀ 100% (drug 71%) · 100% clinician | no trial arm names this drug |
| Infusion site discharge | 293 | 204.4 180.3–231.7ROR 207.2 · calibrated p 3e-10 ✓ | 167.3 EB05 151.8 · IC025 +6.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=269 · 88% consumer | no trial arm names this drug |
| Retinitis | 285 | 203.5 179.2–231.0ROR 206.2 · calibrated p 3e-10 ✓ | 166.6 EB05 151.0 · IC025 +6.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=285 · ♀ 100% (drug 71%) · 96% clinician | no trial arm names this drug |
| Carotid artery thrombosis | 127 | 172.6 143.0–208.4ROR 173.7 · calibrated p 2e-9 ✓ | 143.6 EB05 123.9 · IC025 +6.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=127 · ♀ 100% (drug 71%) · 92% clinician | no trial arm names this drug |
| Post cholecystectomy syndrome | 41 | 168.4 120.9–234.5ROR 168.7 · calibrated p 4e-9 ✓ | 134.8 EB05 103.6 · IC025 +5.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=41 · ♀ 100% (drug 71%) | no trial arm names this drug |
| Seronegative arthritis | 144 | 145.4 122.1–173.1ROR 146.4 · calibrated p 7e-9 ✓ | 124.6 EB05 108.4 · IC025 +6.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=144 · ♀ 100% (drug 71%) · 100% clinician | no trial arm names this drug |
| Red blood cell sedimentation rate | 35 | 140.2 98.4–199.7ROR 140.4 · calibrated p 2e-8 ✓ | 115.1 EB05 86.5 · IC025 +4.9 3/3 methods agree | Lab value / disease marker | serious n=35 · 100% clinician | no trial arm names this drug |
| Granulocyte count increased | 48 | 132.7 98.2–179.4ROR 133.0 · calibrated p 2e-8 ✓ | 111.8 EB05 87.7 · IC025 +5.3 3/3 methods agree | Lab value / disease marker | serious n=48 · ♀ 100% (drug 71%) | no trial arm names this drug |
| Adjustment disorder with depressed mood | 231 | 127.8 111.5–146.5ROR 129.2 · calibrated p 2e-8 ✓ | 112.1 EB05 100.4 · IC025 +6.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=230 · ♀ 100% (drug 71%) · 96% clinician | no trial arm names this drug |
| Electric shock | 94 | 123.1 99.4–152.5ROR 123.7 · calibrated p 3e-8 ✓ | 107.1 EB05 90.1 · IC025 +5.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=94 · ♀ 100% (drug 71%) | no trial arm names this drug |
| Dislocation of vertebra | 243 | 121.1 106.0–138.3ROR 122.5 · calibrated p 3e-8 ✓ | 106.9 EB05 96.1 · IC025 +6.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=243 · ♀ 100% (drug 71%) · 95% clinician | no trial arm names this drug |
| Deep vein thrombosis postoperative | 200 | 112.1 96.9–129.7ROR 113.2 · calibrated p 5e-8 ✓ | 99.7 EB05 88.6 · IC025 +6.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=200 · ♀ 100% (drug 71%) · 95% clinician | no trial arm names this drug |
| Infusion site mass | 108 | 111.1 91.1–135.5ROR 111.7 · calibrated p 6e-8 ✓ | 98.1 EB05 83.6 · IC025 +5.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=106 · 73% consumer | no trial arm names this drug |
| Adjustment disorder | 124 | 103.7 86.2–124.7ROR 104.3 · calibrated p 1e-7 ✓ | 92.5 EB05 79.6 · IC025 +5.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=124 · ♀ 100% (drug 71%) · 91% clinician | no trial arm names this drug |
| Allergy to plants | 43 | 102.8 75.1–140.7ROR 103.0 · calibrated p 2e-7 ✓ | 89.5 EB05 69.2 · IC025 +5.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=42 · ♀ 100% (drug 71%) | no trial arm names this drug |
| Infusion site bruising | 190 | 96.9 83.5–112.4ROR 97.7 · calibrated p 2e-7 ✓ | 87.4 EB05 77.5 · IC025 +5.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=178 · 75% consumer | no trial arm names this drug |
| Temperature regulation disorder | 188 | 92.9 80.1–107.9ROR 93.7 · calibrated p 2e-7 ✓ | 84.2 EB05 74.6 · IC025 +5.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=188 · ♀ 100% (drug 71%) | no trial arm names this drug |
| X-ray abnormal | 152 | 91.9 77.8–108.4ROR 92.5 · calibrated p 2e-7 ✓ | 83.2 EB05 72.7 · IC025 +5.8 3/3 methods agree | Lab value / disease marker | serious n=152 · ♀ 100% (drug 71%) · 100% clinician | no trial arm names this drug |
| Infusion site pruritus | 263 | 91.0 80.2–103.1ROR 92.1 · calibrated p 2e-7 ✓ | 82.8 EB05 74.7 · IC025 +6.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=244 · 76% consumer | no trial arm names this drug |
| Rheumatic fever | 353 | 86.8 77.9–96.7ROR 88.2 · calibrated p 3e-7 ✓ | 79.4 EB05 72.7 · IC025 +6.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=353 · ♀ 100% (drug 71%) · 94% clinician | no trial arm names this drug |
| Swollen joint count increased | 249 | 85.6 75.3–97.4ROR 86.6 · calibrated p 4e-7 ✓ | 78.3 EB05 70.5 · IC025 +5.9 3/3 methods agree | Lab value / disease marker | serious n=248 · ♀ 100% (drug 71%) · 95% clinician | no trial arm names this drug |
| Granulomatosis with polyangiitis | 95 | 85.6 69.4–105.5ROR 86.0 · calibrated p 5e-7 ✓ | 77.6 EB05 65.3 · IC025 +5.5 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=95 | no trial arm names this drug |
| Blood immunoglobulin a increased | 40 | 79.6 57.7–109.9ROR 79.8 · calibrated p 1e-6 ✓ | 71.3 EB05 54.6 · IC025 +4.8 3/3 methods agree | Lab value / disease marker | serious n=40 · ♀ 100% (drug 71%) | no trial arm names this drug |
| Bone erosion | 261 | 78.5 69.2–89.0ROR 79.5 · calibrated p 7e-7 ✓ | 72.3 EB05 65.3 · IC025 +5.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=261 · ♀ 100% (drug 71%) · 94% clinician | no trial arm names this drug |
| Infusion site haemorrhage | 234 | 76.8 67.3–87.7ROR 77.6 · calibrated p 8e-7 ✓ | 70.9 EB05 63.6 · IC025 +5.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=222 · 78% consumer | no trial arm names this drug |
| Postmortem blood drug level increased | 26 | 76.2 51.1–113.6ROR 76.3 · calibrated p 2e-6 ✓ | 67.4 EB05 48.3 · IC025 +4.3 3/3 methods agree | Lab value / disease marker | serious n=26 · 100% clinician | no trial arm names this drug |
| Death neonatal | 97 | 74.7 60.8–91.8ROR 75.1 · calibrated p 1e-6 ✓ | 68.6 EB05 57.9 · IC025 +5.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=97 | no trial arm names this drug |
| Porphyria acute | 97 | 74.6 60.7–91.6ROR 74.9 · calibrated p 1e-6 ✓ | 68.4 EB05 57.7 · IC025 +5.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=97 · ♀ 100% (drug 71%) · 100% clinician | no trial arm names this drug |
| Infusion site urticaria | 46 | 74.1 54.9–100.0ROR 74.3 · calibrated p 2e-6 ✓ | 67.1 EB05 52.4 · IC025 +4.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=41 · ♀ 100% (drug 71%) · 100% consumer | no trial arm names this drug |
| Infusion site scar | 30 | 72.4 50.0–105.0ROR 72.5 · calibrated p 2e-6 ✓ | 64.8 EB05 47.6 · IC025 +4.4 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=30 · ♀ 100% (drug 71%) · 100% consumer | no trial arm names this drug |
| Rheumatoid factor positive | 388 | 71.2 64.2–78.8ROR 72.5 · calibrated p 1e-6 ✓ | 66.2 EB05 60.8 · IC025 +5.8 3/3 methods agree | Lab value / disease marker | serious n=388 · ♀ 100% (drug 71%) · 94% clinician | no trial arm names this drug |
| Blood pressure diastolic decreased | 494 | 70.4 64.4–77.1ROR 72.1 · calibrated p 1e-6 ✓ | 65.6 EB05 60.9 · IC025 +5.8 3/3 methods agree | Lab value / disease marker | serious PRR 46.7 | 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 |
|---|---|---|---|
| Opportunistic infection | 895 | 6.56.1–7.0 | signal |
| Serious infection | 4,413 | 5.75.5–5.8 | signal |
| Interstitial lung disease | 506 | 5.24.8–5.7 | signal |
| Liver injury | 1,375 | 4.54.3–4.8 | signal |
| Fall / fracture | 1,632 | 4.24.1–4.5 | signal |
| Tendon disorder | 136 | 3.53.0–4.2 | signal |
| Hyperglycaemia / diabetes | 1,012 | 2.92.7–3.1 | signal |
| Depression | 777 | 2.72.5–2.9 | signal |
| Suicidality | 630 | 2.52.3–2.7 | signal |
| Anaemia | 746 | 2.52.3–2.6 | signal |
| Arrhythmia / qt | 445 | 2.32.1–2.5 | signal |
| Anaphylaxis / angioedema | 287 | 2.32.0–2.5 | signal |
| Gi bleeding | 366 | 2.01.8–2.2 | raised |
| Venous thromboembolism | 431 | 2.01.8–2.2 | raised |
| Neutropenia / agranulocytosis | 460 | 1.81.7–2.0 | raised |
| Hypoglycaemia | 178 | 1.81.6–2.1 | 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) | 3,537 | 4.5 4.4–4.6ROR 5.2 · calibrated p 0.213 | 4.5 EB05 4.4 · IC025 +2.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 4.5 · serious PRR 5.4 | no trial arm names this drug |
| Off label use (used outside approved label) | 3,191 | 3.6 3.5–3.8ROR 4.1 · calibrated p 0.358 | 3.6 EB05 3.5 · IC025 +1.8 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 3.1 · serious PRR 4.4 | no trial arm names this drug |
| Headache | 3,168 | 5.0 4.9–5.2ROR 5.7 · calibrated p 0.170 | 5.0 EB05 4.8 · IC025 +2.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 4.7 · serious PRR 6.5 | no trial arm names this drug |
| Pain | 3,157 | 5.1 4.9–5.3ROR 5.8 · calibrated p 0.164 | 5.1 EB05 4.9 · IC025 +2.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 5.6 · serious PRR 5.2 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 2,844 | 2.1 2.1–2.2ROR 2.3 · calibrated p 0.898 | 2.1 EB05 2.1 · IC025 +1.0 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 2.4 · serious PRR 3.8 | no trial arm names this drug |
| Infusion related reaction (reaction during infusion) | 2,800 | 43.7 42.2–45.3ROR 50.2 · calibrated p 1e-5 ✓ | 41.8 EB05 40.5 · IC025 +5.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 37.1 · serious PRR 34.8 | no trial arm names this drug |
| Nausea | 2,742 | 3.4 3.3–3.6ROR 3.8 · calibrated p 0.417 | 3.4 EB05 3.3 · IC025 +1.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 3.4 · serious PRR 4.2 | no trial arm names this drug |
| Arthralgia (joint pain) | 2,738 | 6.6 6.3–6.8ROR 7.4 · calibrated p 0.085 | 6.5 EB05 6.3 · IC025 +2.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 5.7 · serious PRR 7.8 | no trial arm names this drug |
| Nasopharyngitis (common cold) | 2,435 | 13.2 12.7–13.7ROR 14.8 · calibrated p 0.007 ✓ | 13.0 EB05 12.6 · IC025 +3.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 11.9 · serious PRR 18.5 | no trial arm names this drug |
| Pneumonia (lung infection) | 2,361 | 7.3 7.0–7.5ROR 8.0 · calibrated p 0.066 | 7.2 EB05 7.0 · IC025 +2.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 6.7 · serious PRR 5.1 | no trial arm names this drug |
| Sinusitis | 2,314 | 22.7 21.9–23.6ROR 25.4 · calibrated p 6e-4 ✓ | 22.2 EB05 21.5 · IC025 +4.4 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 20.9 · serious PRR 28.2 | no trial arm names this drug |
| Rheumatoid arthritis | 2,184 | 19.4 18.7–20.2ROR 21.5 · calibrated p 0.001 ✓ | 19.1 EB05 18.4 · IC025 +4.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 19.1 · serious PRR 15.8 | no trial arm names this drug |
| Malaise (feeling unwell) | 1,949 | 4.4 4.2–4.6ROR 4.7 · calibrated p 0.265 | 4.4 EB05 4.2 · IC025 +2.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 5.0 · serious PRR 4.8 | no trial arm names this drug |
| Weight decreased (weight loss) | 1,945 | 6.9 6.6–7.2ROR 7.5 · calibrated p 0.080 | 6.9 EB05 6.6 · IC025 +2.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 6.5 · serious PRR 6.9 | no trial arm names this drug |
| Cough | 1,896 | 6.7 6.4–7.0ROR 7.3 · calibrated p 0.088 | 6.7 EB05 6.4 · IC025 +2.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 6.4 · serious PRR 7.4 | no trial arm names this drug |
Unlabeled candidate signals
Every screened signal with n ≥ 20 was either labeled, an indication term, or an artifact pattern — no unlabeled candidate stood out in the top signals.
✓ A hand-written Bradford Hill causality assessment exists for this drug: Oxycodone Hydrochloride ↔ Drug Dependence.
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 Diphenhydramine and Liquid Filled?
In FDA FAERS, the most frequently co-reported reaction terms for Diphenhydramine and Liquid Filled are fatigue, headache, pain, infusion related reaction, nausea, arthralgia. 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 Diphenhydramine and Liquid Filled have an FDA boxed warning?
No. The FDA label retrieved for Diphenhydramine and Liquid Filled has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Diphenhydramine and Liquid Filled 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 9c44e54f-d8bc-4451-8382-40d2e8e03b42, effective 20180521; matched on
openfda.generic_name.exact:"DIPHENHYDRAMINE") - 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, 1,237 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
DIPHENHYDRAMINE, 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.