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Glatiramer Acetate side effects: what 59,363 FDA adverse event reports show

Glatiramer Acetate · Glatiramer Acetate · 1,169 reaction terms · 169,801 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Brand names

Glatiramer Acetate

openFDA label

Who reports

59,363 reports · 46% serious · 1,250 with death outcome · 80% female

openFDA FAERS counts, all years, deduplication not applied

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.

FDA label, Indications and Usage

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.

FDA label, Description section

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.

FDA label
How to read this page. FAERS is a spontaneous-reporting system: counts are not incidence rates and a signal is not proof of causation. Each reaction below is run through an automated screen — is the term in the FDA label (known), in the indications (the disease being treated), an administrative/coding term, or none of these (unlabeled)? That screen is mechanical text matching, not a causality assessment. The 30 hand-written Bradford Hill assessments are on the causality assessment page. Not medical advice.

Causality screen of the 40 strongest signals

Labeled — boxed warning 3Labeled adverse reaction 3Labeled (related wording) 8Likely indication confounding 9Reporting / coding artifact 3Lab value / disease marker 3Not in label — unassessed 11
What the badges mean

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.

Show:
ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Immediate post-injection reaction8261,086.8
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=511NCT01067521: 1/943 (0.1%) on Glatiramer (serious AE)
Multiple sclerosis plaque17393.7
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=17not reported in cached trials
Lipoatrophy238118.4
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=38not reported in cached trials
Needle fatigue9086.4
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 — unassessedserious n=19not reported in cached trials
Injection site atrophy32385.9
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% consumernot reported in cached trials
Progressive relapsing multiple sclerosis1652.4
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=11not reported in cached trials
Primary progressive multiple sclerosis6150.8
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% consumernot reported in cached trials
Embolia cutis medicamentosa8742.9
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 — unassessedserious n=86not reported in cached trials
Secondary progressive multiple sclerosis19640.6
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% consumernot reported in cached trials
Wrong device used6237.3
28.7–48.4ROR 37.3 · calibrated p 1e-4 ✓
33.4 EB05 27.0 · IC025 +4.3
3/3 methods agree
Reporting / coding artifactserious n=27 · 84% consumernot reported in cached trials
Progressive multiple sclerosis10233.6
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% consumernot reported in cached trials
Relapsing-remitting multiple sclerosis6930.6
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=66not reported in cached trials
Multiple sclerosis relapse5,16428.4
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 41.4NCT00451451: 36/351 (10.3%) on Glatiramer; 51/363 (14.0%) control (serious AE)
Nuclear magnetic resonance imaging abnormal24527.7
24.3–31.5ROR 27.8 · calibrated p 4e-4 ✓
25.7 EB05 23.1 · IC025 +4.4
3/3 methods agree
Reporting / coding artifactserious n=107not reported in cached trials
Relapsing multiple sclerosis2227.3
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=20not reported in cached trials
Skin indentation3225.8
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 — unassessed75% consumernot reported in cached trials
Injection related reaction10925.6
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 — unassessedserious n=49not reported in cached trials
Hemiparaesthesia2524.4
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 — unassessedserious n=25 · 100% consumernot reported in cached trials
Magnetic resonance imaging abnormal7624.3
19.3–30.7ROR 24.3 · calibrated p 9e-4 ✓
22.7 EB05 18.7 · IC025 +3.9
3/3 methods agree
Reporting / coding artifactserious n=59 · 80% consumernot reported in cached trials
Multiple sclerosis3,08424.2
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% consumerNCT00451451: 36/351 (10.3%) on Glatiramer; 51/363 (14.0%) control (serious AE)
Injection site mass2,07221.0
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% consumernot reported in cached trials
Jc virus test positive4419.2
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 markerserious n=27 · 100% consumernot reported in cached trials
Injection site reaction3,50118.9
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 21.2not reported in cached trials
Expanded disability status scale score increased6218.5
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 markerserious n=62 · ♀ 59% (drug 80%)not reported in cached trials
Gait spastic1718.1
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 positive5517.3
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 markerserious n=36not reported in cached trials
Central nervous system lesion63817.0
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 — unassessedserious PRR 15.5 · 73% consumernot reported in cached trials
Band sensation5716.4
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 — unassessedserious n=35 · 72% consumernot reported in cached trials
Lipodystrophy acquired9516.4
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 — unassessedserious n=87not reported in cached trials
Jc virus infection5813.3
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 — unassessedserious n=55not reported in cached trials
Circumstance or information capable of leading to device use error7812.1
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 — unassessed82% consumernot reported in cached trials
Optic neuritis29111.6
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 14.8NCT01067521: 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).

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.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Multiple sclerosis relapse5,16428.4
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 41.4NCT00451451: 36/351 (10.3%) on Glatiramer; 51/363 (14.0%) control (serious AE)
Injection site pain (pain where injected)4,9445.8
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% consumerNCT00451451: 1/363 (0.3%) control (serious AE)
Drug ineffective (drug did not work)3,8821.0
1.0–1.1ROR 1.0 · calibrated p 0.335
1.0 EB05 1.0 · IC025 +0.0Reporting / coding artifactserious PRR 1.3 · 73% consumernot reported in cached trials
Injection site reaction3,50118.9
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 21.2not reported in cached trials
Multiple sclerosis3,08424.2
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% consumerNCT00451451: 36/351 (10.3%) on Glatiramer; 51/363 (14.0%) control (serious AE)
Dyspnoea (shortness of breath)2,9071.8
1.8–1.9ROR 1.9 · calibrated p 0.866
1.8 EB05 1.8 · IC025 +0.8Labeled — boxed warning
exact term
serious PRR 2.1NCT01067521: 2/419 (0.5%) on Glatiramer (serious AE)
Fall2,4982.7
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 — unassessedserious PRR 2.2NCT00451451: 1/359 (0.3%) on Glatiramer (serious AE)
Injection site erythema (redness where injected)2,4637.2
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 15.5NCT00451451: 6/351 (1.7%) on Glatiramer; 5/363 (1.4%) control
Gait disturbance2,1183.9
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 — unassessedserious PRR 3.8 · 73% consumernot reported in cached trials
Injection site mass2,07221.0
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% consumernot reported in cached trials
Pain2,0311.2
1.1–1.2ROR 1.2 · calibrated p 0.421
1.2 EB05 1.1 · IC025 +0.1Labeled — boxed warning
exact term
serious PRR 1.1NCT00451451: 1/363 (0.3%) control (serious AE)
Nausea1,9240.9
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 1.1NCT00451451: 1/359 (0.3%) on Glatiramer; 1/363 (0.3%) control (serious AE)
Dizziness1,8701.3
1.3–1.4ROR 1.3 · calibrated p 0.534
1.3 EB05 1.3 · IC025 +0.3Not in label — unassessedserious PRR 1.5not reported in cached trials
Headache1,7911.0
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 — unassessedserious PRR 1.3NCT00451451: 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.

✓ 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

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.