MedDRA preferred term

Deformity: adverse event reports recording this term

9,247 reports to FDA record it, 2004–2026; 0% 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.

9,247
reports recording the term: 0% of all reports; 130
reports, 12 months to June 2026: 329 in the 12 months before; 87.1%
marked serious by the reporter: 57.4% across all reports; 5.5%
record death among outcomes, as reported: 9.1% across all reports

"Deformity" is a MedDRA preferred term recorded in 9,247 adverse event reports received by FDA, 0% of the database, from March 2004 to June 2026. The term is chosen by whoever codes the report to match what the reporter described.

130 reports recorded it in the 12 months to June 2026, down 60% from 329 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, 87.1% are marked serious, 5.5% include death among the outcomes and 16.1% include hospitalisation, as reported.

The drugs listed most often as suspect products in those reports are Metoclopramide, ParaGard T 380A and Docetaxel. 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
Metoclopramide	Dopamine-2 receptor antagonist	2,309	10.4%
ParaGard T 380A	Copper-containing intrauterine device	1,339	3.2%
Docetaxel	Microtubule inhibitor	912	1.5%
Taxotere	—	843	2.8%
Enbrel	Tumor necrosis factor blocker	662	0.1%
Methotrexate	Folate analog metabolic inhibitor	598	0.3%
Humira	—	565	0.1%
Depakote	Anti-epileptic agent	547	3.8%
Orencia	Selective T cell costimulation modulator	538	0.5%
Actemra	Interleukin-6 receptor antagonist	523	0.7%
Zantac	—	504	0.2%
Arava	Antirheumatic agent	376	1.1%
Sulfasalazine	Aminosalicylate	357	0.9%
Rituximab	CD20-directed cytolytic antibody	352	0.2%
Zometa	—	311	1.3%
Docetaxel Hospira	—	297	26.1%
Hydroxychloroquine sulfate	Antimalarial	289	1.2%
Docetaxel Accord	—	285	12.2%
Leflunomide	Antirheumatic agent	251	0.7%
Remicade	Tumor necrosis factor blocker	251	0.2%
Plaquenil	Antimalarial	244	1.1%
Ranitidine	Histamine-2 receptor antagonist	244	0.1%
Docetaxel Sun	—	241	35.3%
Xeljanz	Janus kinase inhibitor	212	0.1%
Ranitidine hydrochloride	Histamine-2 receptor antagonist	210	0.3%

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% 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
Dopamine-2 receptor antagonist	2,408	6%	0.2%
Tumor necrosis factor blocker	1,737	0.2%	0.1%
Copper-containing intrauterine device	1,339	3.1%	1.6%
Microtubule inhibitor	912	0.6%	0%
Antimalarial	730	0.8%	0%
Folate analog metabolic inhibitor	697	0.2%	0%
Antirheumatic agent	627	0.9%	0.9%
Interleukin-6 receptor antagonist	622	0.5%	0%
Selective T cell costimulation modulator	613	0.5%	0.4%
Anti-epileptic agent	607	0.2%	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 20.1%13

2 to 110.5%43

12 to 170.5%46

18 to 446.4%593

45 to 648.8%815

65 to 743.3%305

75 and over2.2%205

Age not given78.2%7,227

Patient sex

Female63%5,828

Male19.8%1,833

Not given17.2%1,586

Grey bar: all 20,646,523 reports in the database. 85.4% of these reports give the United States as the country.

Questions about "Deformity"

What does "Deformity" 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 deformity?

9,247 reports through June 2026 (0% of all reports), 130 of them in the latest 12 months.

Which drugs appear most often in these reports?

Metoclopramide (2,309), ParaGard T 380A (1,339), Docetaxel (912), Taxotere (843) and Enbrel (662). 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.