MedDRA preferred term

Hand fracture: adverse event reports recording this term

6,976 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.

6,976
reports recording the term: 0% of all reports; 347
reports, 12 months to June 2026: 398 in the 12 months before; 83.6%
marked serious by the reporter: 57.4% across all reports; 1.9%
record death among outcomes, as reported: 9.1% across all reports

6,976 reports in FDA's adverse event database record the MedDRA term "Hand fracture": 0% of all reports received between January 2004 and June 2026. Coders pick the term that best matches the reporter's description.

347 reports recorded it in the 12 months to June 2026, down 13% from 398 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, 83.6% are marked serious, 1.9% include death among the outcomes and 34.4% include hospitalisation, as reported.

The drugs listed most often as suspect products in those reports are Humira, Truvada and Atripla. 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
Humira	—	399	0.1%
Truvada	Human immunodeficiency virus nucleoside analog reverse transcriptase inhibitor	362	0.9%
Atripla	—	261	1.4%
Fosamax	Bisphosphonate	258	0.7%
Enbrel	Tumor necrosis factor blocker	257	0%
Forteo	Parathyroid hormone analog	233	0.2%
Viread	Hepatitis B virus nucleoside analog reverse transcriptase inhibitor	209	0.9%
Nexium	Proton pump inhibitor	146	0.2%
Stribild	Cytochrome P450 3A inhibitor	135	1.5%
Prolia	RANK ligand inhibitor	115	0.1%
Dupixent	Interleukin-4 receptor alpha antagonist	113	0%
Alendronate sodium	Bisphosphonate	106	0.6%
Complera	Human immunodeficiency virus nucleoside analog reverse transcriptase inhibitor	106	1.6%
Aclasta	—	99	0.6%
Remicade	Tumor necrosis factor blocker	95	0.1%
Tysabri	Integrin receptor antagonist	95	0.1%
Skyrizi	Interleukin-23 antagonist	92	0.1%
Avonex	Interferon beta	91	0.1%
Xeljanz	Janus kinase inhibitor	87	0.1%
Actemra	Interleukin-6 receptor antagonist	85	0.1%
Methotrexate	Folate analog metabolic inhibitor	85	0%
Cosentyx	Interleukin-17A antagonist	76	0.1%
Prednisone	Corticosteroid	73	0%
Xyrem	Central nervous system depressant	64	0.1%
Lyrica	—	58	0%

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
Tumor necrosis factor blocker	488	0%	0%
Human immunodeficiency virus nucleoside analog reverse transcriptase inhibitor	472	0.6%	0%
Bisphosphonate	408	0.4%	0%
Proton pump inhibitor	256	0.1%	0%
Parathyroid hormone analog	240	0.2%	0.2%
Hepatitis B virus nucleoside analog reverse transcriptase inhibitor	213	0.3%	0%
Janus kinase inhibitor	156	0%	0%
Integrin receptor antagonist	150	0.1%	0.1%
Corticosteroid	142	0%	0%
Cytochrome P450 3A inhibitor	139	0.3%	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

2 to 111.1%76

12 to 171.9%134

18 to 4411.7%818

45 to 6426.6%1,854

65 to 7412.4%862

75 and over10.5%729

Age not given35.8%2,500

Patient sex

Female62.1%4,335

Male31.9%2,222

Not given6%419

Grey bar: all 20,646,523 reports in the database. 68.4% of these reports give the United States as the country.

Questions about "Hand fracture"

What does "Hand fracture" 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 hand fracture?

6,976 reports through June 2026 (0% of all reports), 347 of them in the latest 12 months.

Which drugs appear most often in these reports?

Humira (399), Truvada (362), Atripla (261), Fosamax (258) and Enbrel (257). 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.