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Drug · FAERS side-effect profile with label screen

Copper side effects: what 42,854 FDA adverse event reports show

Copper · Miudella · 999 reaction terms · 151,174 drug–reaction co-reports · data 2026-09-14
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Drug class

Copper-containing Intrauterine Device

FDA label (Established Pharmacologic Class)

Brand names

Miudella

openFDA label

Who reports

42,854 reports · 45% serious · 56 with death outcome · 99% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Miudella is indicated for prevention of pregnancy in females of reproductive potential for up to 3 years. Miudella is a copper-containing intrauterine system (IUS) indicated for prevention of pregnancy in females of reproductive potential for up to 3 years.( 1 )

FDA label, Indications and Usage

What it is

11.1 Miudella Miudella (copper intrauterine system) contains 99.99% pure copper for use as a contraceptive. Copper (Cu) has a molecular weight of 63.546 g/mol. Miudella consists of ten copper .

FDA label, Description section

Boxed warning

RISK OF COMPLICATIONS DUE TO IMPROPER INSERTION Improper insertion of intrauterine systems, including Miudella, increases the risk of complications [see Warnings and Precautions (5.1) ] . Proper training prior to first use of Miudella can minimize the risk of improper Miudella insertion [see Warnings and Precautions (5.1) ].

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 adverse reaction 5Labeled (related wording) 16Likely indication confounding 2Reporting / coding artifact 6Not 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). 959 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
Foreign body in reproductive tract8,69389,124.5
66,921.7–118,693.5ROR 111,803.9 · calibrated p 1e-48 ✓
479.8 EB05 471.4 · IC025 +8.8
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious PRR 608.2not reported in cached trials
Foreign body in urogenital tract73139,138.1
20,283.8–75,518.1ROR 39,817.3 · calibrated p 1e-34 ✓
471.1 EB05 443.1 · IC025 +8.4
3/3 methods agree
Not in label — unassessedserious n=691 · 77% consumernot reported in cached trials
Cervix scarring204,818.6
1,126.3–20,615.4ROR 4,820.9 · calibrated p 1e-13 ✓
309.1 EB05 211.3 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=20not reported in cached trials
Fallopian tube adhesion10602.3
237.7–1,526.1ROR 602.5 · calibrated p 7e-11 ✓
177.9 EB05 103.3 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=10not reported in cached trials
Intentional device use issue418496.1
432.9–568.5ROR 501.0 · calibrated p 7e-14 ✓
242.2 EB05 223.4 · IC025 +7.4
3/3 methods agree
Not in label — unassessedserious n=365not reported in cached trials
Embedded device4,644440.9
424.2–458.3ROR 494.4 · calibrated p 6e-14 ✓
230.5 EB05 225.0 · IC025 +7.8
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 284.0not reported in cached trials
Device toxicity18361.4
196.2–665.8ROR 361.6 · calibrated p 8e-11 ✓
169.9 EB05 113.7 · IC025 +4.2
3/3 methods agree
Reporting / coding artifactserious n=17not reported in cached trials
Device placement issue1,300352.9
328.8–378.9ROR 363.9 · calibrated p 2e-12 ✓
203.5 EB05 194.4 · IC025 +7.5
3/3 methods agree
Reporting / coding artifactserious n=355 · 91% cliniciannot reported in cached trials
Device material issue770301.9
276.0–330.2ROR 307.4 · calibrated p 8e-12 ✓
185.1 EB05 174.4 · IC025 +7.3
3/3 methods agree
Reporting / coding artifactserious n=529not reported in cached trials
Device breakage11,144194.4
190.6–198.3ROR 262.3 · calibrated p 3e-11 ✓
138.8 EB05 136.6 · IC025 +7.1
3/3 methods agree
Reporting / coding artifactserious PRR 329.8not reported in cached trials
Salpingectomy154180.6
150.1–217.2ROR 181.2 · calibrated p 1e-9 ✓
129.5 EB05 113.2 · IC025 +6.3
3/3 methods agree
Not in label — unassessedserious n=154 · 94% consumernot reported in cached trials
Cervix inflammation34167.2
113.2–246.9ROR 167.3 · calibrated p 7e-9 ✓
116.4 EB05 87.1 · IC025 +4.9
3/3 methods agree
Not in label — unassessedserious n=27not reported in cached trials
Dyspareunia1,064147.9
138.2–158.3ROR 151.7 · calibrated p 4e-9 ✓
113.2 EB05 107.6 · IC025 +6.7
3/3 methods agree
Labeled adverse reaction
exact term
serious n=731not reported in cached trials
Coital bleeding315127.9
113.0–144.7ROR 128.8 · calibrated p 2e-8 ✓
100.7 EB05 91.7 · IC025 +6.3
3/3 methods agree
Labeled adverse reaction
exact term
serious n=196not reported in cached trials
Uterine tenderness16115.1
66.7–198.5ROR 115.1 · calibrated p 3e-7 ✓
84.0 EB05 54.9 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=12not reported in cached trials
Heavy menstrual bleeding1,471111.2
105.1–117.6ROR 115.1 · calibrated p 4e-8 ✓
90.4 EB05 86.6 · IC025 +6.4
3/3 methods agree
Labeled adverse reaction
exact term
serious n=1,184 · 70% consumernot reported in cached trials
Cervical cyst44111.0
80.0–154.0ROR 111.1 · calibrated p 1e-7 ✓
87.1 EB05 67.6 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=39not reported in cached trials
Administration site indentation10102.5
51.8–202.9ROR 102.5 · calibrated p 1e-6 ✓
73.3 EB05 42.6 · IC025 +3.0
3/3 methods agree
Not in label — unassessedserious n=9not reported in cached trials
Bacterial vaginosis266101.4
88.9–115.7ROR 102.0 · calibrated p 1e-7 ✓
83.5 EB05 75.4 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious n=184not reported in cached trials
Device expulsion11,180101.3
99.5–103.2ROR 136.7 · calibrated p 1e-8 ✓
83.9 EB05 82.6 · IC025 +6.4
3/3 methods agree
Reporting / coding artifactserious PRR 159.5not reported in cached trials
Device dislocation7,25898.3
96.0–100.6ROR 118.2 · calibrated p 3e-8 ✓
81.8 EB05 80.2 · IC025 +6.3
3/3 methods agree
Reporting / coding artifactserious PRR 98.5not reported in cached trials
Laparoscopy4090.9
64.9–127.4ROR 91.0 · calibrated p 5e-7 ✓
74.0 EB05 56.7 · IC025 +4.8
3/3 methods agree
Labeled adverse reaction
exact term
serious n=40 · 100% consumernot reported in cached trials
Blood copper increased2686.4
56.9–131.2ROR 86.5 · calibrated p 1e-6 ✓
69.8 EB05 50.1 · IC025 +4.3
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=18not reported in cached trials
Deformity1,33981.5
77.0–86.3ROR 84.1 · calibrated p 4e-7 ✓
69.8 EB05 66.7 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious PRR 101.4not reported in cached trials

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Copper 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 (0 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
Device expulsion11,180101.3
99.5–103.2ROR 136.7 · calibrated p 1e-8 ✓
83.9 EB05 82.6 · IC025 +6.4
3/3 methods agree
Reporting / coding artifactserious PRR 159.5not reported in cached trials
Device breakage11,144194.4
190.6–198.3ROR 262.3 · calibrated p 3e-11 ✓
138.8 EB05 136.6 · IC025 +7.1
3/3 methods agree
Reporting / coding artifactserious PRR 329.8not reported in cached trials
Foreign body in reproductive tract8,69389,124.5
66,921.7–118,693.5ROR 111,803.9 · calibrated p 1e-48 ✓
479.8 EB05 471.4 · IC025 +8.8
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious PRR 608.2not reported in cached trials
Device dislocation7,25898.3
96.0–100.6ROR 118.2 · calibrated p 3e-8 ✓
81.8 EB05 80.2 · IC025 +6.3
3/3 methods agree
Reporting / coding artifactserious PRR 98.5not reported in cached trials
Pain5,8204.7
4.6–4.8ROR 5.2 · calibrated p 0.210
4.6 EB05 4.5 · IC025 +2.2
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 7.9not reported in cached trials
Embedded device4,644440.9
424.2–458.3ROR 494.4 · calibrated p 6e-14 ✓
230.5 EB05 225.0 · IC025 +7.8
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 284.0not reported in cached trials
Anxiety2,9305.1
4.9–5.2ROR 5.4 · calibrated p 0.198
5.0 EB05 4.9 · IC025 +2.3
3/3 methods agree
Not in label — unassessedserious PRR 9.0 · 80% consumernot reported in cached trials
Emotional distress2,89611.9
11.5–12.4ROR 12.7 · calibrated p 0.013 ✓
11.7 EB05 11.3 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious PRR 16.5 · 91% consumernot reported in cached trials
Off label use (used outside approved label)2,7711.6
1.5–1.6ROR 1.6 · calibrated p 0.708
1.6 EB05 1.5 · IC025 +0.6Reporting / coding artifactserious PRR 2.4not reported in cached trials
Pelvic pain2,59581.4
78.2–84.8ROR 86.6 · calibrated p 3e-7 ✓
69.8 EB05 67.5 · IC025 +6.0
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 103.9not reported in cached trials
Procedural pain2,57150.1
48.2–52.1ROR 53.2 · calibrated p 9e-6 ✓
45.5 EB05 44.0 · IC025 +5.4
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 48.9not reported in cached trials

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: Copper intrauterine device ↔ Foreign body in reproductive tract.

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 Copper?

In FDA FAERS, the most frequently co-reported reaction terms for Copper are complication of device removal, foreign body in reproductive tract, complication of device insertion, pain, embedded device, reproductive complication associated with device. 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 Copper have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: RISK OF COMPLICATIONS DUE TO IMPROPER INSERTION Improper insertion of intrauterine systems, including Miudella, increases the risk of complications [see Warnings and Precautions (5.1) ] . Proper training prior to first use of Miudella can minimize the risk of improper Miudella insertion [see Warnings and Precautions (5.1) ].

Do FAERS signals prove that Copper 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.