MedDRA preferred term

Intentional dose omission: adverse event reports recording this term

26,988 reports to FDA record it, 2012–2026; 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.

26,988
reports recording the term: 0.1% of all reports; 5,023
reports, 12 months to June 2026: 5,045 in the 12 months before; 48.5%
marked serious by the reporter: 57.4% across all reports; 1.5%
record death among outcomes, as reported: 9.1% across all reports

"Intentional dose omission" is a MedDRA preferred term recorded in 26,988 adverse event reports received by FDA, 0.1% of the database, from May 2012 to June 2026. The term is chosen by whoever codes the report to match what the reporter described.

5,023 reports recorded it in the 12 months to June 2026, close to the 5,045 of 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, 48.5% are marked serious, 1.5% include death among the outcomes and 22.2% include hospitalisation, as reported.

The drugs listed most often as suspect products in those reports are Dupixent, Xeljanz and Infliximab. 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
Dupixent	Interleukin-4 receptor alpha antagonist	2,851	0.6%
Xeljanz	Janus kinase inhibitor	879	0.6%
Infliximab	Tumor necrosis factor blocker	848	1.6%
Humira	—	756	0.1%
Certolizumab pegol	Tumor necrosis factor blocker	730	2.7%
Tymlos	—	693	2.5%
Enbrel	Tumor necrosis factor blocker	665	0.1%
Cimzia	Tumor necrosis factor blocker	586	0.7%
Infliximab-dyyb	Tumor necrosis factor blocker	584	28.8%
Ambrisentan	Endothelin receptor antagonist	582	1.1%
Xywav	Central nervous system depressant	571	6.8%
Daybue	—	463	7.1%
Adalimumab-aaty	—	399	29.2%
Eligard	Gonadotropin releasing hormone receptor agonist	378	0.9%
Nuplazid	Atypical antipsychotic	373	0.7%
Arikayce	Aminoglycoside antibacterial	337	5.2%
Lumryz	Central nervous system depressant	324	9.3%
Yuflyma	—	301	18.1%
Exondys 51	Antisense oligonucleotide	279	12.5%
Orencia	Selective T cell costimulation modulator	252	0.2%
Xyrem	Central nervous system depressant	246	0.4%
Rinvoq	Janus kinase inhibitor	244	0.3%
Truxima	CD20-directed cytolytic antibody	223	4.8%
Epclusa	Hepatitis C virus NS5A inhibitor	215	1.8%
Sofosbuvir Velpatasvir	—	207	6.1%

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
Tumor necrosis factor blocker	3,894	0.4%	0.3%
Interleukin-4 receptor alpha antagonist	2,946	0.6%	0.6%
Janus kinase inhibitor	1,203	0.4%	0%
Central nervous system depressant	1,183	1.6%	5.2%
Kinase inhibitor	723	0.1%	0%
Endothelin receptor antagonist	646	0.3%	0.1%
Atypical antipsychotic	537	0.1%	0%
Corticosteroid	401	0%	0%
Gonadotropin releasing hormone receptor agonist	387	0.6%	0%
Antisense oligonucleotide	353	3.4%	9.7%

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 20.2%64

2 to 112.2%584

12 to 172%533

18 to 4413.1%3,548

45 to 6420.5%5,526

65 to 7411.1%2,991

75 and over8.6%2,324

Age not given42.3%11,418

Patient sex

Female52.5%14,181

Male28.7%7,750

Not given18.7%5,057

Grey bar: all 20,646,523 reports in the database. 79.4% of these reports give the United States as the country.

Questions about "Intentional dose omission"

What does "Intentional dose omission" 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 intentional dose omission?

26,988 reports through June 2026 (0.1% of all reports), 5,023 of them in the latest 12 months.

Which drugs appear most often in these reports?

Dupixent (2,851), Xeljanz (879), Infliximab (848), Humira (756) and Certolizumab pegol (730). 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.