Diphenhydramine Hydrochloride side effects: what 164,753 FDA adverse event reports show
Drug class
Not stated in label
Brand names
Nightime Sleep Aid
Who reports
164,753 reports · 71% serious · 22,785 with death outcome · 66% female
Used for
For relief of occasional sleeplessness.
What it is
Diphenhydramine is an ether that is the benzhydryl ether of 2-(dimethylamino)ethanol. It is a H1-receptor antagonist used as a antipruritic and antitussive drug.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- 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). 1,160 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 |
|---|---|---|---|---|---|---|
| Blood pressure diastolic abnormal | 1,766 | 285.3 262.2–310.4ROR 288.3 · calibrated p 1e-11 ✓ | 87.3 EB05 83.9 · IC025 +6.3 3/3 methods agree | Lab value / disease marker | serious n=1,674 · 91% clinician | no trial arm names this drug |
| Vaginal flatulence | 200 | 244.2 192.4–309.9ROR 244.5 · calibrated p 1e-10 ✓ | 82.5 EB05 73.3 · IC025 +5.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=200 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Blood pressure systolic abnormal | 1,571 | 220.6 203.2–239.5ROR 222.7 · calibrated p 2e-10 ✓ | 80.2 EB05 76.9 · IC025 +6.2 3/3 methods agree | Lab value / disease marker | serious n=1,490 · 92% clinician | no trial arm names this drug |
| Anti-cyclic citrullinated peptide antibody | 246 | 74.2 63.4–86.9ROR 74.3 · calibrated p 1e-6 ✓ | 46.7 EB05 42.0 · IC025 +5.2 3/3 methods agree | Lab value / disease marker | serious n=246 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Neurologic neglect syndrome | 172 | 56.2 47.0–67.3ROR 56.3 · calibrated p 7e-6 ✓ | 38.9 EB05 34.3 · IC025 +4.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=172 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Lupus vulgaris | 359 | 54.8 48.4–62.0ROR 54.9 · calibrated p 8e-6 ✓ | 38.3 EB05 35.1 · IC025 +5.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=359 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Infusion site urticaria | 161 | 41.0 34.3–49.0ROR 41.0 · calibrated p 5e-5 ✓ | 31.0 EB05 27.2 · IC025 +4.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | ♀ 100% (drug 66%) | no trial arm names this drug |
| Urine leukocyte esterase positive | 173 | 41.0 34.5–48.6ROR 41.0 · calibrated p 5e-5 ✓ | 31.0 EB05 27.3 · IC025 +4.6 3/3 methods agree | Lab value / disease marker | serious n=170 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Retinitis | 384 | 37.8 33.8–42.4ROR 37.9 · calibrated p 7e-5 ✓ | 29.2 EB05 26.8 · IC025 +4.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=384 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Temperature regulation disorder | 482 | 35.8 32.4–39.7ROR 35.9 · calibrated p 1e-4 ✓ | 28.0 EB05 26.0 · IC025 +4.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=482 · ♀ 100% (drug 66%) | no trial arm names this drug |
| Infusion site discharge | 366 | 34.5 30.7–38.7ROR 34.6 · calibrated p 1e-4 ✓ | 27.2 EB05 24.9 · IC025 +4.5 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=318 · 100% consumer | no trial arm names this drug |
| Pharyngeal paraesthesia | 330 | 34.0 30.1–38.4ROR 34.0 · calibrated p 1e-4 ✓ | 26.9 EB05 24.5 · IC025 +4.5 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=314 · 100% clinician | no trial arm names this drug |
| Infusion site pruritus | 641 | 32.8 30.0–35.7ROR 32.9 · calibrated p 2e-4 ✓ | 26.1 EB05 24.5 · IC025 +4.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=377 | no trial arm names this drug |
| Carotid artery thrombosis | 171 | 31.7 26.8–37.5ROR 31.7 · calibrated p 2e-4 ✓ | 25.4 EB05 22.4 · IC025 +4.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=171 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Infusion site mass | 208 | 30.6 26.3–35.6ROR 30.7 · calibrated p 3e-4 ✓ | 24.7 EB05 22.0 · IC025 +4.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=161 | no trial arm names this drug |
| Blood pressure diastolic decreased | 1,442 | 30.6 28.9–32.4ROR 30.8 · calibrated p 2e-4 ✓ | 24.7 EB05 23.7 · IC025 +4.5 3/3 methods agree | Lab value / disease marker | serious PRR 20.6 | no trial arm names this drug |
| Infusion site bruising | 391 | 28.5 25.5–31.8ROR 28.6 · calibrated p 4e-4 ✓ | 23.4 EB05 21.5 · IC025 +4.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=296 | no trial arm names this drug |
| Infusion site rash | 246 | 27.9 24.3–32.0ROR 27.9 · calibrated p 4e-4 ✓ | 22.9 EB05 20.6 · IC025 +4.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=141 | no trial arm names this drug |
| Granulomatosis with polyangiitis | 211 | 27.3 23.5–31.6ROR 27.3 · calibrated p 5e-4 ✓ | 22.5 EB05 20.1 · IC025 +4.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=208 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Ear pruritus | 596 | 26.1 23.9–28.5ROR 26.2 · calibrated p 5e-4 ✓ | 21.8 EB05 20.3 · IC025 +4.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=521 · ♀ 88% (drug 66%) | no trial arm names this drug |
| Blood pressure systolic increased | 3,279 | 25.4 24.5–26.4ROR 25.9 · calibrated p 6e-4 ✓ | 21.3 EB05 20.7 · IC025 +4.3 3/3 methods agree | Lab value / disease marker | serious PRR 18.1 | no trial arm names this drug |
| Adjustment disorder with depressed mood | 335 | 25.2 22.4–28.3ROR 25.3 · calibrated p 7e-4 ✓ | 21.1 EB05 19.3 · IC025 +4.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=334 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Deep vein thrombosis postoperative | 318 | 24.5 21.7–27.6ROR 24.5 · calibrated p 8e-4 ✓ | 20.6 EB05 18.8 · IC025 +4.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=318 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Dislocation of vertebra | 352 | 23.8 21.2–26.6ROR 23.8 · calibrated p 9e-4 ✓ | 20.1 EB05 18.4 · IC025 +4.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=352 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Infusion site discomfort | 158 | 23.1 19.5–27.4ROR 23.1 · calibrated p 0.001 ✓ | 19.6 EB05 17.2 · IC025 +4.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=113 | no trial arm names this drug |
| Blood pressure diastolic increased | 714 | 23.0 21.3–24.9ROR 23.1 · calibrated p 0.001 ✓ | 19.6 EB05 18.4 · IC025 +4.1 3/3 methods agree | Lab value / disease marker | serious n=674 | no trial arm names this drug |
| Blood pressure fluctuation | 3,660 | 22.7 21.9–23.5ROR 23.2 · calibrated p 1e-3 ✓ | 19.3 EB05 18.8 · IC025 +4.2 3/3 methods agree | Lab value / disease marker | serious PRR 19.3 | no trial arm names this drug |
| Infusion related reaction (reaction during infusion) | 9,942 | 22.4 22.0–22.9ROR 23.8 · calibrated p 9e-4 ✓ | 19.1 EB05 18.8 · IC025 +4.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 18.8 · serious PRR 16.4 | no trial arm names this drug |
| Porphyria acute | 202 | 21.7 18.7–25.2ROR 21.7 · calibrated p 0.001 ✓ | 18.6 EB05 16.5 · IC025 +3.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=202 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Infusion site swelling | 897 | 21.6 20.1–23.1ROR 21.7 · calibrated p 0.001 ✓ | 18.5 EB05 17.5 · IC025 +4.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=543 | no trial arm names this drug |
| Seronegative arthritis | 163 | 21.5 18.2–25.4ROR 21.5 · calibrated p 0.002 ✓ | 18.4 EB05 16.2 · IC025 +3.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=163 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Red blood cells urine positive | 135 | 20.5 17.1–24.5ROR 20.5 · calibrated p 0.002 ✓ | 17.7 EB05 15.3 · IC025 +3.8 3/3 methods agree | Lab value / disease marker | serious n=132 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Anticholinergic syndrome | 217 | 19.9 17.3–23.0ROR 20.0 · calibrated p 0.002 ✓ | 17.3 EB05 15.4 · IC025 +3.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=215 · 100% clinician | no trial arm names this drug |
| Infusion site haemorrhage | 438 | 19.8 17.9–21.8ROR 19.8 · calibrated p 0.002 ✓ | 17.2 EB05 15.9 · IC025 +3.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=332 | no trial arm names this drug |
| Adjustment disorder | 176 | 19.7 16.8–23.1ROR 19.7 · calibrated p 0.002 ✓ | 17.1 EB05 15.1 · IC025 +3.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=176 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Female genital tract fistula | 232 | 19.7 17.1–22.6ROR 19.7 · calibrated p 0.002 ✓ | 17.1 EB05 15.3 · IC025 +3.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=232 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| X-ray abnormal | 235 | 19.2 16.7–22.0ROR 19.2 · calibrated p 0.002 ✓ | 16.7 EB05 15.0 · IC025 +3.8 3/3 methods agree | Lab value / disease marker | serious n=235 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Enthesopathy | 205 | 18.9 16.3–21.9ROR 18.9 · calibrated p 0.003 ✓ | 16.5 EB05 14.7 · IC025 +3.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=204 · 100% clinician | no trial arm names this drug |
| White blood cells urine positive | 239 | 18.5 16.2–21.2ROR 18.6 · calibrated p 0.003 ✓ | 16.2 EB05 14.6 · IC025 +3.8 3/3 methods agree | Lab value / disease marker | serious n=236 · ♀ 100% (drug 66%) | no trial arm names this drug |
| Soft tissue disorder | 141 | 18.2 15.3–21.8ROR 18.2 · calibrated p 0.003 ✓ | 16.0 EB05 13.9 · IC025 +3.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=139 · ♀ 100% (drug 66%) · 100% clinician | 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 |
|---|---|---|---|
| Anaphylaxis / angioedema | 3,414 | 3.53.4–3.7 | signal |
| Suicidality | 5,528 | 2.92.8–3.0 | signal |
| Opportunistic infection | 2,860 | 2.72.6–2.8 | signal |
| Serious infection | 16,110 | 2.72.6–2.7 | signal |
| Neutropenia / agranulocytosis | 3,942 | 2.02.0–2.1 | raised |
| Interstitial lung disease | 1,511 | 2.01.9–2.1 | raised |
| Anaemia | 4,665 | 2.01.9–2.1 | raised |
| Tendon disorder | 580 | 2.01.8–2.1 | raised |
| Fall / fracture | 5,674 | 1.91.9–2.0 | raised |
| Liver injury | 4,277 | 1.81.8–1.9 | raised |
| Thrombocytopenia | 2,927 | 1.71.6–1.8 | raised |
| Arrhythmia / qt | 2,486 | 1.61.6–1.7 | raised |
| Depression | 3,483 | 1.61.5–1.6 | raised |
| Seizure | 2,418 | 1.61.5–1.6 | raised |
| Venous thromboembolism | 2,526 | 1.51.4–1.5 | raised |
| Kidney injury | 5,050 | 1.41.4–1.5 | 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 |
|---|---|---|---|---|---|---|
| Off label use (used outside approved label) | 17,967 | 2.7 2.6–2.7ROR 2.9 · calibrated p 0.669 | 2.6 EB05 2.6 · IC025 +1.4 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 2.2 · serious PRR 3.4 | no trial arm names this drug |
| Fatigue (tiredness) | 15,901 | 2.6 2.6–2.7ROR 2.8 · calibrated p 0.690 | 2.6 EB05 2.6 · IC025 +1.4 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.5 · serious PRR 3.1 | no trial arm names this drug |
| Nausea | 14,215 | 2.3 2.3–2.4ROR 2.4 · calibrated p 0.839 | 2.3 EB05 2.3 · IC025 +1.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.2 · serious PRR 2.8 | no trial arm names this drug |
| Headache | 13,709 | 2.8 2.8–2.9ROR 3.0 · calibrated p 0.629 | 2.8 EB05 2.7 · IC025 +1.4 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.5 · serious PRR 3.5 | no trial arm names this drug |
| Pain | 11,686 | 2.4 2.4–2.5ROR 2.6 · calibrated p 0.790 | 2.4 EB05 2.4 · IC025 +1.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.7 · serious PRR 2.6 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 11,412 | 1.1 1.1–1.1ROR 1.1 · calibrated p 0.380 | 1.1 EB05 1.1 · IC025 +0.1 | Reporting / coding artifact | age-adj. PRR 1.3 · serious PRR 1.9 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 10,851 | 2.5 2.4–2.5ROR 2.6 · calibrated p 0.783 | 2.4 EB05 2.4 · IC025 +1.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.4 · serious PRR 2.3 | no trial arm names this drug |
| Pruritus (itching) | 10,347 | 3.6 3.5–3.6ROR 3.7 · calibrated p 0.433 | 3.5 EB05 3.4 · IC025 +1.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 3.4 · serious PRR 4.5 | no trial arm names this drug |
| Infusion related reaction (reaction during infusion) | 9,942 | 22.4 22.0–22.9ROR 23.8 · calibrated p 9e-4 ✓ | 19.1 EB05 18.8 · IC025 +4.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 18.8 · serious PRR 16.4 | no trial arm names this drug |
| Arthralgia (joint pain) | 9,146 | 2.8 2.8–2.9ROR 3.0 · calibrated p 0.640 | 2.8 EB05 2.8 · IC025 +1.5 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.5 · serious PRR 3.6 | no trial arm names this drug |
| Rash | 9,109 | 2.7 2.7–2.8ROR 2.8 · calibrated p 0.692 | 2.7 EB05 2.6 · IC025 +1.4 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.7 · serious PRR 3.3 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 8,782 | 1.7 1.7–1.8ROR 1.8 · calibrated p 0.823 | 1.7 EB05 1.7 · IC025 +0.8 | No label text to screen label has no adverse-reaction text | age-adj. PRR 1.7 · serious PRR 1.9 | no trial arm names this drug |
| Pyrexia (fever) | 8,350 | 3.1 3.1–3.2ROR 3.2 · calibrated p 0.555 | 3.1 EB05 3.0 · IC025 +1.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.7 · serious PRR 2.6 | no trial arm names this drug |
| Vomiting | 7,911 | 2.2 2.1–2.2ROR 2.2 · calibrated p 0.939 | 2.1 EB05 2.1 · IC025 +1.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 1.9 · serious PRR 2.1 | no trial arm names this drug |
| Dizziness | 7,595 | 2.0 1.9–2.0ROR 2.0 · calibrated p 0.945 | 1.9 EB05 1.9 · IC025 +0.9 | No label text to screen label has no adverse-reaction text | age-adj. PRR 1.9 · serious PRR 2.2 | 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?
In FDA FAERS, the most frequently co-reported reaction terms for Diphenhydramine are fatigue, nausea, headache, pain, dyspnoea, pruritus. 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 have an FDA boxed warning?
No. The FDA label retrieved for Diphenhydramine has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Diphenhydramine 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") - PubChem CID 3100 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, 1,200 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.