MedDRA preferred term

Complication of device insertion: adverse event reports recording this term

18,298 reports to FDA record it, 2005–2026; 0.1% of the database.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "There is no certainty that the reported event (adverse event or medication error) was actually due to the product. FDA does not require that a causal relationship between a product and event be proven, and reports do not always contain enough detail to properly evaluate an event." The information in these reports "cannot be used to estimate the incidence of these events."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

18,298
reports recording the term: 0.1% of all reports; 2,605
reports, 12 months to June 2026: 762 in the 12 months before; 20.6%
marked serious by the reporter: 57.4% across all reports; 0.1%
record death among outcomes, as reported: 9.1% across all reports

"Complication of device insertion" is a MedDRA preferred term recorded in 18,298 adverse event reports received by FDA, 0.1% of the database, from June 2005 to June 2026. The term is chosen by whoever codes the report to match what the reporter described.

2,605 reports recorded it in the 12 months to June 2026, up 242% from 762 in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Of reports recording this term, 20.6% are marked serious, 0.1% include death among the outcomes and 1.4% include hospitalisation, as reported.

The drugs listed most often as suspect products in those reports are ParaGard T 380A, Mirena and Nexplanon. That order mostly follows how many reports each drug has overall; the table also gives the term's share within each drug's own reports. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."

Reports by month, five years

FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.

Drugs listed as suspect products in these reports

Drug	Class	Reports with this term	Share of the drug's own reports
ParaGard T 380A	Copper-containing intrauterine device	8,348	19.9%
Mirena	Progestin	4,725	3.6%
Nexplanon	Progestin	3,192	7.3%
Kyleena	Progestin	649	8%
Skyla	Progestin	243	4.6%
Implanon	—	232	2.5%
Ozurdex	Corticosteroid	194	7.7%
Paragard 380a	—	99	1.6%
Liletta	Progestin	66	0.6%
Chloraprep	—	49	1.2%
Etonogestrel	Progestin	42	2%
Chloraprep with Tint	—	41	3.1%
Duodopa	—	33	0.2%
Durysta	Prostaglandin analog	32	6.8%
Yutiq	Corticosteroid	25	3.4%
Lidocaine	Amide local anesthetic	17	0.1%
Nuvaring	Estrogen	14	0.1%
Jaydess	—	13	1.8%
Carbidopa levodopa	Aromatic amino acid	12	0.1%
Paragard T380a	—	11	0.7%
Remodulin	Prostacycline vasodilator	10	0%
Levonorgestrel	Progestin	9	0.3%
Actemra	Interleukin-6 receptor antagonist	7	0%
Baclofen	gamma-Aminobutyric acid-ergic agonist	6	0%
Bupivacaine	Amide local anesthetic	5	0.1%

Drugs with a page on this site, ordered by the number of their reports recording this term. The last column is the term's share within that drug's own reports, against 0.1% across the whole database. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."

By pharmacologic class

Class	Reports with this term	Share of class reports	Median drug in class
Progestin	8,926	3%	0%
Copper-containing intrauterine device	8,348	19.3%	10%
Corticosteroid	226	0%	0%
Amide local anesthetic	22	0.1%	0%
Estrogen	17	0%	0%
Aromatic amino acid	16	0%	0%
Interleukin-6 receptor antagonist	10	0%	0%
Prostacycline vasodilator	10	0%	0%
gamma-Aminobutyric acid-ergic agonist	8	0%	0%
Tumor necrosis factor blocker	6	0%	0%

Classes ordered by count. Class shares follow the class's overall report volume as much as anything else.

Patients in these reports

Patient age

Under 20%6

2 to 110%5

12 to 173.6%656

18 to 4465.7%12,015

45 to 645.7%1,034

65 to 740.4%79

75 and over0.3%57

Age not given24.3%4,446

Patient sex

Female92.2%16,869

Male1.1%195

Not given6.7%1,234

Grey bar: all 20,646,523 reports in the database. 95.1% of these reports give the United States as the country.

Questions about "Complication of device insertion"

What does "Complication of device insertion" mean in an adverse event report?

It is a MedDRA preferred term, the dictionary FDA uses to code what a reporter described. The report's own description is not published by openFDA and is not shown here.

How many reports record complication of device insertion?

18,298 reports through June 2026 (0.1% of all reports), 2,605 of them in the latest 12 months.

Which drugs appear most often in these reports?

ParaGard T 380A (8,348), Mirena (4,725), Nexplanon (3,192), Kyleena (649) and Skyla (243). Drugs with many reports overall lead almost every term's list. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."

Does a drug appearing here mean it was responsible for this reaction?

No. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."

I have this symptom. What should I do?

This site cannot assess anyone. A pharmacist or clinician can; for an emergency, call the local emergency number. Nothing on this page is medical advice.

Where this comes from. Counts are built from the openFDA Drug Adverse Event (FAERS) bulk export released 28 Sep 2026, which holds reports FDA received through 30 Jun 2026. Drug names are as reported, resolved to the brand or generic name on the FDA label where openFDA's harmonisation matched them; classes are the pharmacologic class (EPC) from the label and the National Drug Code Directory of 17 Sep 2026. Terms are pooled across spelling and capitalisation variants of one MedDRA preferred term. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.