Antacid side effects: what 47,212 FDA adverse event reports show
Drug class
Not stated in label
Who reports
47,212 reports · 84% serious · 7,180 with death outcome · 68% female
Used for
relieves: heartburn acid indigestion sour stomach upset stomach associated with these symptoms
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). 1,200 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 |
|---|---|---|---|---|---|---|
| Milk-alkali syndrome | 316 | 673.8 565.4–803.1ROR 678.4 · calibrated p 3e-15 ✓ | 261.5 EB05 238.2 · IC025 +7.4 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=314 · 95% clinician | no trial arm names this drug |
| Fractional exhaled nitric oxide increased | 99 | 601.1 443.8–814.2ROR 602.3 · calibrated p 3e-14 ✓ | 241.8 EB05 204.4 · IC025 +6.5 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=99 · ♀ 0% (drug 68%) | no trial arm names this drug |
| Vaginal flatulence | 168 | 548.1 436.8–687.6ROR 550.0 · calibrated p 4e-14 ✓ | 237.2 EB05 208.6 · IC025 +6.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=168 · ♀ 100% (drug 68%) | no trial arm names this drug |
| Lupus vulgaris | 464 | 285.3 253.9–320.6ROR 288.1 · calibrated p 2e-11 ✓ | 171.8 EB05 159.1 · IC025 +7.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=464 · ♀ 100% (drug 68%) · 95% clinician | no trial arm names this drug |
| Pulmonary vasculitis | 206 | 285.0 239.2–339.6ROR 286.2 · calibrated p 2e-11 ✓ | 170.2 EB05 151.6 · IC025 +6.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=206 · ♀ 0% (drug 68%) | no trial arm names this drug |
| Anti-cyclic citrullinated peptide antibody | 251 | 268.9 229.9–314.6ROR 270.4 · calibrated p 3e-11 ✓ | 164.8 EB05 148.4 · IC025 +6.8 3/3 methods agree | Lab value / disease marker | serious n=251 · ♀ 100% (drug 68%) · 94% clinician | no trial arm names this drug |
| Deep vein thrombosis postoperative | 732 | 265.8 242.6–291.2ROR 269.9 · calibrated p 3e-11 ✓ | 165.0 EB05 155.2 · IC025 +7.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=732 · ♀ 100% (drug 68%) · 96% clinician | no trial arm names this drug |
| Total lung capacity increased | 100 | 257.1 200.9–329.1ROR 257.7 · calibrated p 7e-11 ✓ | 157.4 EB05 133.2 · IC025 +6.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=100 · ♀ 100% (drug 68%) · 100% clinician | no trial arm names this drug |
| C-reactive protein | 318 | 240.5 209.8–275.7ROR 242.1 · calibrated p 8e-11 ✓ | 154.1 EB05 140.4 · IC025 +6.8 3/3 methods agree | Lab value / disease marker | serious n=318 · ♀ 100% (drug 68%) · 97% clinician | no trial arm names this drug |
| Grip strength | 79 | 230.2 175.3–302.3ROR 230.6 · calibrated p 2e-10 ✓ | 145.9 EB05 120.8 · IC025 +5.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=79 · ♀ 100% (drug 68%) · 100% clinician | no trial arm names this drug |
| Swollen joint count increased | 1,041 | 223.3 207.3–240.5ROR 228.3 · calibrated p 1e-10 ✓ | 147.7 EB05 140.4 · IC025 +7.0 3/3 methods agree | Lab value / disease marker | serious n=1,041 · ♀ 100% (drug 68%) · 97% clinician | no trial arm names this drug |
| Total lung capacity abnormal | 125 | 217.7 175.7–269.8ROR 218.3 · calibrated p 3e-10 ✓ | 142.5 EB05 122.8 · IC025 +6.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=125 · ♀ 0% (drug 68%) | no trial arm names this drug |
| Rheumatic fever | 1,377 | 205.1 192.5–218.5ROR 211.2 · calibrated p 2e-10 ✓ | 139.7 EB05 133.6 · IC025 +7.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=1,376 · ♀ 100% (drug 68%) · 96% clinician | no trial arm names this drug |
| Sleep disorder therapy | 57 | 196.2 143.6–268.1ROR 196.4 · calibrated p 1e-9 ✓ | 129.9 EB05 104.0 · IC025 +5.5 3/3 methods agree | Reporting / coding artifact | serious n=57 · ♀ 0% (drug 68%) · 100% clinician | no trial arm names this drug |
| Swollen joint count | 75 | 195.2 148.7–256.2ROR 195.5 · calibrated p 9e-10 ✓ | 130.8 EB05 107.8 · IC025 +5.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=75 · ♀ 100% (drug 68%) · 100% clinician | no trial arm names this drug |
| Adjustment disorder with depressed mood | 599 | 188.2 171.1–207.1ROR 190.7 · calibrated p 6e-10 ✓ | 131.3 EB05 122.7 · IC025 +6.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=599 · ♀ 100% (drug 68%) · 97% clinician | no trial arm names this drug |
| Facet joint syndrome | 909 | 180.4 167.1–194.8ROR 183.9 · calibrated p 8e-10 ✓ | 127.6 EB05 120.8 · IC025 +6.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=909 · ♀ 100% (drug 68%) · 96% clinician | no trial arm names this drug |
| Neurologic neglect syndrome | 158 | 174.9 145.4–210.2ROR 175.4 · calibrated p 2e-9 ✓ | 123.3 EB05 108.0 · IC025 +6.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=158 · ♀ 100% (drug 68%) · 100% clinician | no trial arm names this drug |
| Dislocation of vertebra | 579 | 156.5 142.4–172.0ROR 158.5 · calibrated p 3e-9 ✓ | 115.1 EB05 107.4 · IC025 +6.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=579 · ♀ 100% (drug 68%) · 96% clinician | no trial arm names this drug |
| Subcutaneous drug absorption impaired | 135 | 146.4 120.5–177.9ROR 146.9 · calibrated p 7e-9 ✓ | 108.3 EB05 93.8 · IC025 +6.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=135 · ♀ 100% (drug 68%) · 100% clinician | no trial arm names this drug |
| X-ray abnormal | 424 | 138.5 124.2–154.5ROR 139.8 · calibrated p 9e-9 ✓ | 104.9 EB05 96.8 · IC025 +6.4 3/3 methods agree | Lab value / disease marker | serious n=424 · ♀ 100% (drug 68%) · 96% clinician | no trial arm names this drug |
| Spirometry abnormal | 139 | 137.8 113.9–166.7ROR 138.2 · calibrated p 1e-8 ✓ | 103.5 EB05 89.9 · IC025 +6.0 3/3 methods agree | Lab value / disease marker | serious n=139 · ♀ 0% (drug 68%) | no trial arm names this drug |
| Capillaritis | 60 | 127.9 96.0–170.6ROR 128.1 · calibrated p 3e-8 ✓ | 96.2 EB05 77.5 · IC025 +5.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=60 · ♀ 0% (drug 68%) | no trial arm names this drug |
| Mite allergy | 134 | 118.1 97.6–142.9ROR 118.4 · calibrated p 4e-8 ✓ | 92.0 EB05 79.7 · IC025 +5.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=134 · ♀ 0% (drug 68%) | no trial arm names this drug |
| Retinitis | 348 | 117.0 104.0–131.7ROR 117.9 · calibrated p 3e-8 ✓ | 92.1 EB05 84.2 · IC025 +6.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=348 · ♀ 100% (drug 68%) · 95% clinician | no trial arm names this drug |
| Duodenal ulcer perforation | 1,517 | 115.8 109.5–122.4ROR 119.6 · calibrated p 3e-8 ✓ | 91.6 EB05 87.8 · IC025 +6.4 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious PRR 63.0 · ♀ 100% (drug 68%) · 96% clinician | no trial arm names this drug |
| Antineutrophil cytoplasmic antibody positive | 143 | 108.5 90.4–130.3ROR 108.9 · calibrated p 7e-8 ✓ | 86.2 EB05 75.0 · IC025 +5.8 3/3 methods agree | Lab value / disease marker | serious n=143 · ♀ 0% (drug 68%) | no trial arm names this drug |
| Rheumatoid factor positive | 1,131 | 108.3 101.6–115.5ROR 111.0 · calibrated p 5e-8 ✓ | 86.9 EB05 82.7 · IC025 +6.3 3/3 methods agree | Lab value / disease marker | serious n=1,131 · ♀ 100% (drug 68%) · 97% clinician | no trial arm names this drug |
| Asthma-chronic obstructive pulmonary disease overlap syndrome | 101 | 106.9 86.0–132.9ROR 107.1 · calibrated p 9e-8 ✓ | 84.8 EB05 71.8 · IC025 +5.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=101 · ♀ 100% (drug 68%) · 100% clinician | no trial arm names this drug |
| Carotid artery thrombosis | 160 | 102.4 86.2–121.6ROR 102.8 · calibrated p 1e-7 ✓ | 82.4 EB05 72.2 · IC025 +5.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=160 · ♀ 100% (drug 68%) · 100% clinician | no trial arm names this drug |
| Shunt stenosis | 51 | 98.6 72.8–133.7ROR 98.8 · calibrated p 2e-7 ✓ | 78.4 EB05 61.9 · IC025 +5.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=52 · ♀ 0% (drug 68%) · 100% clinician | no trial arm names this drug |
| Peripheral venous disease | 698 | 94.1 86.7–102.0ROR 95.5 · calibrated p 2e-7 ✓ | 77.4 EB05 72.7 · IC025 +6.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=698 · ♀ 100% (drug 68%) · 97% clinician | no trial arm names this drug |
| Analgesic therapy | 52 | 90.6 67.2–122.1ROR 90.7 · calibrated p 4e-7 ✓ | 73.2 EB05 58.0 · IC025 +5.0 3/3 methods agree | Reporting / coding artifact | serious n=52 · ♀ 0% (drug 68%) · 100% clinician | no trial arm names this drug |
| Anti-cyclic citrullinated peptide antibody positive | 1,185 | 88.9 83.5–94.5ROR 91.1 · calibrated p 2e-7 ✓ | 73.9 EB05 70.5 · IC025 +6.1 3/3 methods agree | Lab value / disease marker | serious PRR 51.1 · ♀ 100% (drug 68%) · 96% clinician | no trial arm names this drug |
| Seronegative arthritis | 187 | 88.8 75.9–103.8ROR 89.1 · calibrated p 3e-7 ✓ | 73.4 EB05 65.0 · IC025 +5.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=187 · ♀ 100% (drug 68%) · 100% clinician | no trial arm names this drug |
| Mycotic allergy | 138 | 86.9 72.4–104.3ROR 87.2 · calibrated p 4e-7 ✓ | 72.0 EB05 62.4 · IC025 +5.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=136 · ♀ 0% (drug 68%) | no trial arm names this drug |
| Appendicolith | 62 | 86.6 65.9–113.7ROR 86.7 · calibrated p 5e-7 ✓ | 70.9 EB05 57.3 · IC025 +5.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=62 · ♀ 0% (drug 68%) · 100% clinician | no trial arm names this drug |
| Hypocholesterolaemia | 49 | 84.0 61.9–114.0ROR 84.1 · calibrated p 7e-7 ✓ | 68.8 EB05 54.1 · IC025 +4.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=49 · ♀ 100% (drug 68%) · 100% clinician | no trial arm names this drug |
| Helicobacter infection | 1,560 | 80.2 76.1–84.6ROR 82.9 · calibrated p 5e-7 ✓ | 67.9 EB05 65.1 · IC025 +6.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious PRR 49.4 · ♀ 100% (drug 68%) · 95% clinician | no trial arm names this drug |
| Dust allergy | 135 | 72.2 60.2–86.6ROR 72.4 · calibrated p 1e-6 ✓ | 61.6 EB05 53.4 · IC025 +5.4 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=135 · ♀ 0% (drug 68%) | 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 |
|---|---|---|---|
| Interstitial lung disease | 1,419 | 6.76.3–7.0 | signal |
| Liver injury | 3,344 | 5.04.8–5.1 | signal |
| Serious infection | 5,900 | 3.43.3–3.5 | signal |
| Hyponatraemia | 569 | 3.22.9–3.4 | signal |
| Anaemia | 2,046 | 3.02.9–3.2 | signal |
| Gi bleeding | 1,244 | 3.02.9–3.2 | signal |
| Hyperglycaemia / diabetes | 2,338 | 3.02.9–3.1 | signal |
| Fall / fracture | 2,522 | 3.02.8–3.1 | signal |
| Rhabdomyolysis / myopathy | 517 | 2.82.6–3.1 | signal |
| Kidney injury | 2,714 | 2.62.6–2.7 | signal |
| Depression | 1,576 | 2.52.4–2.6 | signal |
| Venous thromboembolism | 1,170 | 2.42.3–2.5 | signal |
| Neutropenia / agranulocytosis | 1,282 | 2.32.2–2.4 | signal |
| Arrhythmia / qt | 996 | 2.32.2–2.4 | signal |
| Osteonecrosis | 289 | 2.22.0–2.5 | raised |
| Thrombocytopenia | 1,078 | 2.22.1–2.3 | signal |
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) | 4,896 | 2.8 2.7–2.9ROR 3.0 · calibrated p 0.620 | 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 2.4 · serious PRR 3.1 | no trial arm names this drug |
| Nausea | 4,316 | 2.4 2.4–2.5ROR 2.6 · calibrated p 0.779 | 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 2.2 · serious PRR 2.8 | no trial arm names this drug |
| Off label use (used outside approved label) | 4,258 | 2.2 2.1–2.2ROR 2.3 · calibrated p 0.902 | 2.2 EB05 2.1 · IC025 +1.1 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 2.1 · serious PRR 2.6 | no trial arm names this drug |
| Pain | 4,083 | 3.0 2.9–3.0ROR 3.1 · calibrated p 0.581 | 2.9 EB05 2.9 · IC025 +1.5 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 3.1 · serious PRR 3.0 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 3,900 | 3.1 3.0–3.2ROR 3.3 · calibrated p 0.547 | 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 2.8 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 3,816 | 1.3 1.2–1.3ROR 1.3 · calibrated p 0.517 | 1.3 EB05 1.3 · IC025 +0.3 | Reporting / coding artifact | age-adj. PRR 1.5 · serious PRR 2.2 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 3,764 | 2.6 2.5–2.7ROR 2.7 · calibrated p 0.714 | 2.6 EB05 2.5 · IC025 +1.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.2 · serious PRR 2.6 | no trial arm names this drug |
| Vomiting | 3,664 | 3.5 3.4–3.6ROR 3.7 · calibrated p 0.438 | 3.5 EB05 3.4 · IC025 +1.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 3.3 · serious PRR 3.4 | no trial arm names this drug |
| Pneumonia (lung infection) | 3,275 | 4.5 4.4–4.7ROR 4.8 · calibrated p 0.257 | 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 3.8 · serious PRR 3.2 | no trial arm names this drug |
| Headache | 3,230 | 2.3 2.2–2.4ROR 2.4 · calibrated p 0.860 | 2.3 EB05 2.2 · IC025 +1.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.1 · serious PRR 2.9 | no trial arm names this drug |
| Arthralgia (joint pain) | 3,099 | 3.3 3.2–3.5ROR 3.5 · calibrated p 0.484 | 3.3 EB05 3.2 · IC025 +1.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.8 · serious PRR 3.8 | no trial arm names this drug |
| Pyrexia (fever) | 3,039 | 3.9 3.8–4.1ROR 4.1 · calibrated p 0.355 | 3.9 EB05 3.8 · IC025 +1.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 3.4 · serious PRR 3.3 | no trial arm names this drug |
| Malaise (feeling unwell) | 2,911 | 3.0 2.9–3.1ROR 3.1 · calibrated p 0.600 | 2.9 EB05 2.9 · IC025 +1.5 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.9 · serious PRR 3.2 | no trial arm names this drug |
| Rash | 2,700 | 2.8 2.7–2.9ROR 2.9 · calibrated p 0.665 | 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 2.7 · serious PRR 3.8 | no trial arm names this drug |
| Condition aggravated | 2,686 | 4.0 3.8–4.1ROR 4.2 · calibrated p 0.350 | 3.9 EB05 3.8 · IC025 +1.9 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 3.7 · serious PRR 4.0 | 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.
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 Antacid?
In FDA FAERS, the most frequently co-reported reaction terms for Antacid are fatigue, nausea, pain, dyspnoea, diarrhoea, vomiting. 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 Antacid have an FDA boxed warning?
No. The FDA label retrieved for Antacid has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Antacid 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 2981c5f7-121a-4030-86b1-559061030e7a, effective 20251125; matched on
openfda.generic_name.exact:"ANTACID") - 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, 1,240 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
ANTACID, 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.