MedDRA preferred term

Drug dose omission by device: adverse event reports recording this term

75,594 reports to FDA record it, 2014–2026; 0.4% 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.

75,594
reports recording the term: 0.4% of all reports; 9,868
reports, 12 months to June 2026: 15,663 in the 12 months before; 5.7%
marked serious by the reporter: 57.4% across all reports; 0.1%
record death among outcomes, as reported: 9.1% across all reports

"Drug dose omission by device" is a MedDRA preferred term recorded in 75,594 adverse event reports received by FDA, 0.4% of the database, from May 2014 to June 2026. The term is chosen by whoever codes the report to match what the reporter described.

9,868 reports recorded it in the 12 months to June 2026, down 37% from 15,663 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, 5.7% are marked serious, 0.1% include death among the outcomes and 1.7% include hospitalisation, as reported.

The drugs listed most often as suspect products in those reports are Repatha, Genotropin and Albuterol sulfate. 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
Repatha	PCSK9 inhibitor	24,623	15.8%
Genotropin	—	17,497	38.9%
Albuterol sulfate	beta2-Adrenergic agonist	7,640	17.1%
Aimovig	—	6,654	12.8%
Enbrel	Tumor necrosis factor blocker	2,967	0.5%
Neulasta	Leukocyte growth factor	2,007	2.5%
Albuterol	beta2-Adrenergic agonist	1,853	10.4%
Bydureon Bcise	—	906	7%
Cosentyx	Interleukin-17A antagonist	866	0.6%
Omnitrope	Recombinant human growth hormone	582	5.2%
Ryaltris	Corticosteroid	517	29.8%
Breztri	Corticosteroid	458	6.4%
Levalbuterol tartrate	beta2-Adrenergic agonist	457	62.1%
Symbicort	Corticosteroid	453	1.2%
Emgality	—	432	1.5%
Ajovy	—	410	4.1%
Kesimpta	CD20-directed cytolytic antibody	367	1.3%
Dupixent	Interleukin-4 receptor alpha antagonist	301	0.1%
Prolia	RANK ligand inhibitor	271	0.2%
Arikayce	Aminoglycoside antibacterial	243	3.8%
Amjevita	Tumor necrosis factor blocker	237	16.7%
Praluent	PCSK9 inhibitor	222	1%
Lantus Solostar	Insulin analog	219	0.5%
Depo-Provera	Progestin	215	1.2%
Somatropin	Recombinant human growth hormone	215	3.9%

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 0.4% 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
PCSK9 inhibitor	24,865	13.8%	1.6%
beta2-Adrenergic agonist	9,950	10.8%	0%
Tumor necrosis factor blocker	3,588	0.3%	0%
Leukocyte growth factor	2,142	2%	0.2%
Corticosteroid	1,808	0.2%	0%
Interleukin-17A antagonist	898	0.5%	0.1%
Recombinant human growth hormone	839	3.9%	2.9%
Progestin	455	0.2%	0%
Insulin analog	433	0.1%	0%
CD20-directed cytolytic antibody	369	0.1%	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 20.3%212

2 to 118%6,080

12 to 1710.6%8,032

18 to 447%5,259

45 to 6418.4%13,936

65 to 7416.6%12,544

75 and over13.9%10,475

Age not given25.2%19,056

Patient sex

Female48.6%36,754

Male33.4%25,260

Not given18%13,580

Grey bar: all 20,646,523 reports in the database. 89% of these reports give the United States as the country.

Questions about "Drug dose omission by device"

What does "Drug dose omission by device" 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 drug dose omission by device?

75,594 reports through June 2026 (0.4% of all reports), 9,868 of them in the latest 12 months.

Which drugs appear most often in these reports?

Repatha (24,623), Genotropin (17,497), Albuterol sulfate (7,640), Aimovig (6,654) and Enbrel (2,967). 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.