Glatiramer Acetate side effects: what 59,363 FDA adverse event reports show
Drug class
Not stated in label
Brand names
Glatiramer Acetate
Who reports
59,363 reports · 46% serious · 1,250 with death outcome · 80% female
Used for
Glatiramer acetate injection is indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. Glatiramer acetate inj.
What it is
Glatiramer acetate, the active ingredient of glatiramer acetate injection, consists of the acetate salts of synthetic polypeptides, containing four naturally occurring amino acids: L-glutamic acid, L-alanine, L-tyrosine, and L-lysine with an average molar fraction of 0.141, 0.427, 0.095, and 0.338, respectively.
Boxed warning
ANAPHYLACTIC REACTIONS Cases of life-threatening and fatal anaphylaxis have been reported with glatiramer acetate injection. Anaphylaxis can occur at any time following initiation of therapy, from as early as after the first dose, up to years following initiation of therapy.
Causality screen of the 40 strongest signals
What the badges mean
- Labeled — boxed warning The term (or its clinical synonym) appears in the FDA boxed warning: causality is regulator-recognised and considered serious.
- 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). 1,129 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 |
|---|---|---|---|---|---|---|
| Immediate post-injection reaction | 826 | 1,086.8 946.4–1,248.0ROR 1,102.1 · calibrated p 1e-17 ✓ | 262.4 EB05 247.7 · IC025 +7.7 3/3 methods agree | Labeled — boxed warning exact term | serious n=511 | NCT01067521: 1/943 (0.1%) on Glatiramer (serious AE) |
| Multiple sclerosis plaque | 17 | 393.7 196.6–788.2ROR 393.8 · calibrated p 1e-10 ✓ | 153.5 EB05 101.5 · IC025 +4.1 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=17 | not reported in cached trials |
| Lipoatrophy | 238 | 118.4 102.3–137.2ROR 118.9 · calibrated p 3e-8 ✓ | 88.0 EB05 79.0 · IC025 +6.0 3/3 methods agree | Labeled — boxed warning exact term | serious n=38 | not reported in cached trials |
| Needle fatigue | 90 | 86.4 68.6–108.8ROR 86.5 · calibrated p 5e-7 ✓ | 68.4 EB05 57.3 · IC025 +5.3 3/3 methods agree | Not in label — unassessed | serious n=19 | not reported in cached trials |
| Injection site atrophy | 323 | 85.9 76.1–97.0ROR 86.4 · calibrated p 4e-7 ✓ | 68.8 EB05 62.7 · IC025 +5.8 3/3 methods agree | Labeled adverse reaction exact term | serious n=129 · 72% consumer | not reported in cached trials |
| Injection site necrosis | 384 | 81.5 72.9–91.0ROR 82.0 · calibrated p 5e-7 ✓ | 66.0 EB05 60.6 · IC025 +5.8 3/3 methods agree | Labeled (related wording) related wording | serious n=377 | not reported in cached trials |
| Progressive relapsing multiple sclerosis | 16 | 52.4 31.0–88.7ROR 52.4 · calibrated p 3e-5 ✓ | 43.5 EB05 28.4 · IC025 +3.4 3/3 methods agree | Likely indication confounding term in indications | serious n=11 | not reported in cached trials |
| Primary progressive multiple sclerosis | 61 | 50.8 38.8–66.5ROR 50.9 · calibrated p 2e-5 ✓ | 43.9 EB05 35.4 · IC025 +4.6 3/3 methods agree | Likely indication confounding term in indications | serious n=56 · 85% consumer | not reported in cached trials |
| Embolia cutis medicamentosa | 87 | 42.9 34.4–53.6ROR 43.0 · calibrated p 4e-5 ✓ | 38.0 EB05 31.8 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=86 | not reported in cached trials |
| Secondary progressive multiple sclerosis | 196 | 40.6 35.1–47.1ROR 40.8 · calibrated p 5e-5 ✓ | 36.4 EB05 32.3 · IC025 +4.8 3/3 methods agree | Likely indication confounding term in indications | serious n=183 · 72% consumer | not reported in cached trials |
| Wrong device used | 62 | 37.3 28.7–48.4ROR 37.3 · calibrated p 1e-4 ✓ | 33.4 EB05 27.0 · IC025 +4.3 3/3 methods agree | Reporting / coding artifact | serious n=27 · 84% consumer | not reported in cached trials |
| Progressive multiple sclerosis | 102 | 33.6 27.4–41.2ROR 33.7 · calibrated p 2e-4 ✓ | 30.6 EB05 25.9 · IC025 +4.4 3/3 methods agree | Likely indication confounding term in indications | serious n=92 · 73% consumer | not reported in cached trials |
| Injection site scar | 237 | 32.4 28.3–37.0ROR 32.5 · calibrated p 2e-4 ✓ | 29.6 EB05 26.6 · IC025 +4.6 3/3 methods agree | Labeled (related wording) related wording | serious n=75 · 71% consumer | not reported in cached trials |
| Relapsing-remitting multiple sclerosis | 69 | 30.6 23.9–39.1ROR 30.6 · calibrated p 3e-4 ✓ | 28.0 EB05 22.9 · IC025 +4.2 3/3 methods agree | Likely indication confounding term in indications | serious n=66 | not reported in cached trials |
| Multiple sclerosis relapse | 5,164 | 28.4 27.7–29.2ROR 31.1 · calibrated p 2e-4 ✓ | 26.4 EB05 25.8 · IC025 +4.7 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious PRR 41.4 | NCT00451451: 36/351 (10.3%) on Glatiramer; 51/363 (14.0%) control (serious AE) |
| Nuclear magnetic resonance imaging abnormal | 245 | 27.7 24.3–31.5ROR 27.8 · calibrated p 4e-4 ✓ | 25.7 EB05 23.1 · IC025 +4.4 3/3 methods agree | Reporting / coding artifact | serious n=107 | not reported in cached trials |
| Relapsing multiple sclerosis | 22 | 27.3 17.7–42.1ROR 27.3 · calibrated p 8e-4 ✓ | 24.9 EB05 17.3 · IC025 +3.3 3/3 methods agree | Likely indication confounding term in indications | serious n=20 | not reported in cached trials |
| Injection site scab | 66 | 26.0 20.3–33.4ROR 26.0 · calibrated p 7e-4 ✓ | 24.1 EB05 19.6 · IC025 +4.0 3/3 methods agree | Labeled (related wording) related wording | serious n=34 | not reported in cached trials |
| Skin indentation | 32 | 25.8 18.0–36.9ROR 25.8 · calibrated p 8e-4 ✓ | 23.8 EB05 17.6 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | 75% consumer | not reported in cached trials |
| Injection related reaction | 109 | 25.6 21.1–31.1ROR 25.6 · calibrated p 7e-4 ✓ | 23.8 EB05 20.3 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=49 | not reported in cached trials |
| Injection site indentation | 136 | 25.2 21.2–30.0ROR 25.2 · calibrated p 7e-4 ✓ | 23.5 EB05 20.3 · IC025 +4.2 3/3 methods agree | Labeled (related wording) related wording | serious n=44 · 81% consumer | not reported in cached trials |
| Injection site erosion | 23 | 24.7 16.2–37.8ROR 24.7 · calibrated p 0.001 ✓ | 22.8 EB05 15.9 · IC025 +3.3 3/3 methods agree | Labeled (related wording) related wording | 100% consumer | NCT01067521: 1/943 (0.1%) on Glatiramer (serious AE) |
| Hemiparaesthesia | 25 | 24.4 16.3–36.6ROR 24.4 · calibrated p 0.001 ✓ | 22.5 EB05 16.0 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=25 · 100% consumer | not reported in cached trials |
| Magnetic resonance imaging abnormal | 76 | 24.3 19.3–30.7ROR 24.3 · calibrated p 9e-4 ✓ | 22.7 EB05 18.7 · IC025 +3.9 3/3 methods agree | Reporting / coding artifact | serious n=59 · 80% consumer | not reported in cached trials |
| Multiple sclerosis | 3,084 | 24.2 23.3–25.0ROR 25.4 · calibrated p 6e-4 ✓ | 22.6 EB05 22.0 · IC025 +4.4 3/3 methods agree | Likely indication confounding term in indications | serious PRR 37.7 · 71% consumer | NCT00451451: 36/351 (10.3%) on Glatiramer; 51/363 (14.0%) control (serious AE) |
| Injection site mass | 2,072 | 21.0 20.1–21.9ROR 21.7 · calibrated p 0.001 ✓ | 19.8 EB05 19.1 · IC025 +4.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 29.4 · 72% consumer | not reported in cached trials |
| Jc virus test positive | 44 | 19.2 14.1–25.9ROR 19.2 · calibrated p 0.003 ✓ | 18.1 EB05 14.0 · IC025 +3.4 3/3 methods agree | Lab value / disease marker | serious n=27 · 100% consumer | not reported in cached trials |
| Injection site reaction | 3,501 | 18.9 18.3–19.6ROR 20.1 · calibrated p 0.002 ✓ | 18.0 EB05 17.5 · IC025 +4.1 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 21.2 | not reported in cached trials |
| Expanded disability status scale score increased | 62 | 18.5 14.3–23.8ROR 18.5 · calibrated p 0.003 ✓ | 17.5 EB05 14.1 · IC025 +3.5 3/3 methods agree | Lab value / disease marker | serious n=62 · ♀ 59% (drug 80%) | not reported in cached trials |
| Gait spastic | 17 | 18.1 11.1–29.5ROR 18.1 · calibrated p 0.005 ✓ | 16.7 EB05 10.6 · IC025 +2.7 3/3 methods agree | Not in label — unassessed | – | not reported in cached trials |
| Jc polyomavirus test positive | 55 | 17.3 13.2–22.6ROR 17.3 · calibrated p 0.004 ✓ | 16.4 EB05 13.0 · IC025 +3.4 3/3 methods agree | Lab value / disease marker | serious n=36 | not reported in cached trials |
| Central nervous system lesion | 638 | 17.0 15.7–18.4ROR 17.2 · calibrated p 0.004 ✓ | 16.3 EB05 15.2 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious PRR 15.5 · 73% consumer | not reported in cached trials |
| Band sensation | 57 | 16.4 12.6–21.4ROR 16.5 · calibrated p 0.005 ✓ | 15.6 EB05 12.5 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=35 · 72% consumer | not reported in cached trials |
| Lipodystrophy acquired | 95 | 16.4 13.4–20.2ROR 16.4 · calibrated p 0.005 ✓ | 15.6 EB05 13.2 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=87 | not reported in cached trials |
| Injection site urticaria | 1,058 | 16.1 15.1–17.1ROR 16.3 · calibrated p 0.005 ✓ | 15.4 EB05 14.6 · IC025 +3.8 3/3 methods agree | Labeled (related wording) related wording | serious n=209 | NCT01067521: 1/419 (0.2%) on Glatiramer; 1/461 (0.2%) control (serious AE) |
| Injection site ulcer | 37 | 14.4 10.3–20.0ROR 14.4 · calibrated p 0.010 ✓ | 13.6 EB05 10.1 · IC025 +3.0 3/3 methods agree | Labeled (related wording) related wording | serious n=28 | NCT01067521: 1/419 (0.2%) on Glatiramer (serious AE) |
| Jc virus infection | 58 | 13.3 10.2–17.2ROR 13.3 · calibrated p 0.013 ✓ | 12.6 EB05 10.0 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious n=55 | not reported in cached trials |
| Injection site infection | 114 | 12.7 10.5–15.3ROR 12.7 · calibrated p 0.014 ✓ | 12.2 EB05 10.4 · IC025 +3.2 3/3 methods agree | Labeled (related wording) related wording | serious n=87 | NCT00451451: 1/359 (0.3%) on Glatiramer (serious AE) |
| Circumstance or information capable of leading to device use error | 78 | 12.1 9.6–15.1ROR 12.1 · calibrated p 0.018 ✓ | 11.5 EB05 9.5 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | 82% consumer | not reported in cached trials |
| Optic neuritis | 291 | 11.6 10.3–13.0ROR 11.7 · calibrated p 0.019 ✓ | 11.2 EB05 10.2 · IC025 +3.3 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 14.8 | NCT01067521: 1/943 (0.1%) on Glatiramer (serious AE) |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Glatiramer as a study intervention. The right-hand column of the signal table shows whether each FAERS term was also recorded in these trials, with a real denominator (8 of 40 signal terms matched).
- NCT00451451 — Efficacy and Safety Study of Oral BG00012 With Active Reference in Relapsing-Remitting Multiple Sclerosis (N=1417, PHASE3; 157 AE terms posted; arms: Placebo; BG00012 240 mg Twice Daily (BID); BG00012 240 mg 3 Times Daily (TID); Total BG00012)
- NCT01067521 — A Study in Subjects With Relapsing-Remitting Multiple Sclerosis (RRMS) to Assess the Efficacy, Safety and Tole (N=1404, PHASE3; 238 AE terms posted; arms: Delayed Start: GA 40 mg; Delayed Start: Placebo; Early Start: GA 40 mg / GA 40 mg)
Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.
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 |
|---|---|---|---|---|---|---|
| Multiple sclerosis relapse | 5,164 | 28.4 27.7–29.2ROR 31.1 · calibrated p 2e-4 ✓ | 26.4 EB05 25.8 · IC025 +4.7 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious PRR 41.4 | NCT00451451: 36/351 (10.3%) on Glatiramer; 51/363 (14.0%) control (serious AE) |
| Injection site pain (pain where injected) | 4,944 | 5.8 5.7–6.0ROR 6.3 · calibrated p 0.134 | 5.7 EB05 5.6 · IC025 +2.5 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 10.5 · 72% consumer | NCT00451451: 1/363 (0.3%) control (serious AE) |
| Drug ineffective (drug did not work) | 3,882 | 1.0 1.0–1.1ROR 1.0 · calibrated p 0.335 | 1.0 EB05 1.0 · IC025 +0.0 | Reporting / coding artifact | serious PRR 1.3 · 73% consumer | not reported in cached trials |
| Injection site reaction | 3,501 | 18.9 18.3–19.6ROR 20.1 · calibrated p 0.002 ✓ | 18.0 EB05 17.5 · IC025 +4.1 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 21.2 | not reported in cached trials |
| Fatigue (tiredness) | 3,267 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.651 | 1.5 EB05 1.4 · IC025 +0.5 | Labeled (related wording) related wording | serious PRR 1.6 | NCT00451451: 30/351 (8.5%) on Glatiramer; 33/363 (9.1%) control |
| Multiple sclerosis | 3,084 | 24.2 23.3–25.0ROR 25.4 · calibrated p 6e-4 ✓ | 22.6 EB05 22.0 · IC025 +4.4 3/3 methods agree | Likely indication confounding term in indications | serious PRR 37.7 · 71% consumer | NCT00451451: 36/351 (10.3%) on Glatiramer; 51/363 (14.0%) control (serious AE) |
| Dyspnoea (shortness of breath) | 2,907 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.866 | 1.8 EB05 1.8 · IC025 +0.8 | Labeled — boxed warning exact term | serious PRR 2.1 | NCT01067521: 2/419 (0.5%) on Glatiramer (serious AE) |
| Fall | 2,498 | 2.7 2.6–2.8ROR 2.7 · calibrated p 0.718 | 2.7 EB05 2.6 · IC025 +1.3 3/3 methods agree | Not in label — unassessed | serious PRR 2.2 | NCT00451451: 1/359 (0.3%) on Glatiramer (serious AE) |
| Injection site erythema (redness where injected) | 2,463 | 7.2 6.9–7.5ROR 7.4 · calibrated p 0.083 | 7.0 EB05 6.8 · IC025 +2.7 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 15.5 | NCT00451451: 6/351 (1.7%) on Glatiramer; 5/363 (1.4%) control |
| Gait disturbance | 2,118 | 3.9 3.8–4.1ROR 4.0 · calibrated p 0.371 | 3.9 EB05 3.8 · IC025 +1.9 3/3 methods agree | Not in label — unassessed | serious PRR 3.8 · 73% consumer | not reported in cached trials |
| Injection site mass | 2,072 | 21.0 20.1–21.9ROR 21.7 · calibrated p 0.001 ✓ | 19.8 EB05 19.1 · IC025 +4.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 29.4 · 72% consumer | not reported in cached trials |
| Pain | 2,031 | 1.2 1.1–1.2ROR 1.2 · calibrated p 0.421 | 1.2 EB05 1.1 · IC025 +0.1 | Labeled — boxed warning exact term | serious PRR 1.1 | NCT00451451: 1/363 (0.3%) control (serious AE) |
| Nausea | 1,924 | 0.9 0.8–0.9ROR 0.9 · calibrated p 0.216 | 0.9 EB05 0.8 · IC025 -0.3 PRR-only: not supported by EBGM or IC | Labeled adverse reaction exact term | serious PRR 1.1 | NCT00451451: 1/359 (0.3%) on Glatiramer; 1/363 (0.3%) control (serious AE) |
| Dizziness | 1,870 | 1.3 1.3–1.4ROR 1.3 · calibrated p 0.534 | 1.3 EB05 1.3 · IC025 +0.3 | Not in label — unassessed | serious PRR 1.5 | not reported in cached trials |
| Headache | 1,791 | 1.0 1.0–1.1ROR 1.0 · calibrated p 0.313 | 1.0 EB05 1.0 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Not in label — unassessed | serious PRR 1.3 | NCT00451451: 1/344 (0.3%) on Glatiramer (serious AE) |
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.
- Needle fatigue — n=90, PRR 86.4
- Embolia cutis medicamentosa — n=87, PRR 42.9
- Skin indentation — n=32, PRR 25.8
- Injection related reaction — n=109, PRR 25.6
- Hemiparaesthesia — n=25, PRR 24.4
- Central nervous system lesion — n=638, PRR 17.0
- Band sensation — n=57, PRR 16.4
- Lipodystrophy acquired — n=95, PRR 16.4
- Jc virus infection — n=58, PRR 13.3
- Circumstance or information capable of leading to device use error — n=78, PRR 12.1
✓ A hand-written Bradford Hill causality assessment exists for this drug: Medroxyprogesterone acetate ↔ Meningioma.
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 Glatiramer?
In FDA FAERS, the most frequently co-reported reaction terms for Glatiramer are multiple sclerosis relapse, injection site pain, injection site reaction, fatigue, multiple sclerosis, dyspnoea. 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 Glatiramer have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: ANAPHYLACTIC REACTIONS Cases of life-threatening and fatal anaphylaxis have been reported with glatiramer acetate injection. Anaphylaxis can occur at any time following initiation of therapy, from as early as after the first dose, up to years following initiation of therapy.
Do FAERS signals prove that Glatiramer 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 456a34c7-8511-4000-99a7-ad8f8de6d35e, effective 20250207; matched on
openfda.generic_name.exact:"GLATIRAMER") - 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, 1,169 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
GLATIRAMER, 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.