MedDRA preferred term · swelling of the face

Face oedema: adverse event reports recording this term

16,630 reports to FDA record it, 2004–2026; 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.

16,630
reports recording the term: 0.1% of all reports; 720
reports, 12 months to June 2026: 830 in the 12 months before; 89.3%
marked serious by the reporter: 57.4% across all reports; 4.2%
record death among outcomes, as reported: 9.1% across all reports

"Face oedema" (in plain words, swelling of the face) is a MedDRA preferred term recorded in 16,630 adverse event reports received by FDA, 0.1% of the database, from January 2004 to June 2026. The term is chosen by whoever codes the report to match what the reporter described.

720 reports recorded it in the 12 months to June 2026, down 13% from 830 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, 89.3% are marked serious, 4.2% include death among the outcomes and 41% include hospitalisation, as reported.

The drugs listed most often as suspect products in those reports are Ibuprofen, Amoxicillin and Lamictal. 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
Ibuprofen	Nonsteroidal anti-inflammatory drug	481	0.6%
Amoxicillin	Penicillin-class antibacterial	391	1.2%
Lamictal	Anti-epileptic agent	202	0.6%
Allopurinol	Xanthine oxidase inhibitor	192	0.9%
Lamotrigine	Anti-epileptic agent	192	0.4%
Lyrica	—	189	0.2%
Remicade	Tumor necrosis factor blocker	186	0.1%
Humira	—	181	0%
Acetaminophen	Nonsteroidal anti-inflammatory drug	172	0.2%
Bactrim	Dihydrofolate reductase inhibitor antibacterial	170	1%
Methotrexate	Folate analog metabolic inhibitor	142	0.1%
Vancomycin	Glycopeptide antibacterial	141	0.5%
Ayvakit	Kinase inhibitor	137	1.2%
Carboplatin	Platinum-based drug	136	0.1%
Diclofenac	Nonsteroidal anti-inflammatory drug	132	0.5%
Gleevec	Kinase inhibitor	129	0.6%
Ultravist	Radiographic contrast agent	127	1.8%
Revlimid	Thalidomide analog	124	0%
Carbamazepine	Mood stabilizer	116	0.5%
Lisinopril	Angiotensin converting enzyme inhibitor	116	0.3%
Prednisone	Corticosteroid	115	0.1%
Diclofenac sodium	Nonsteroidal anti-inflammatory drug	113	0.2%
Levofloxacin	Fluoroquinolone antibacterial	113	0.4%
Omeprazole	Proton pump inhibitor	112	0.2%
Xolair	Anti-IgE	111	0.2%

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
Nonsteroidal anti-inflammatory drug	1,284	0.2%	0%
Kinase inhibitor	966	0.1%	0%
Corticosteroid	593	0.1%	0%
Anti-epileptic agent	581	0.2%	0%
Penicillin-class antibacterial	521	0.8%	0%
Tumor necrosis factor blocker	407	0%	0%
Proton pump inhibitor	395	0.1%	0%
Atypical antipsychotic	315	0%	0%
Angiotensin converting enzyme inhibitor	275	0.3%	0.3%
Radiographic contrast agent	258	1%	0.5%

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%94

2 to 113.5%577

12 to 172.6%436

18 to 4420.1%3,348

45 to 6428.6%4,761

65 to 7412.7%2,114

75 and over10%1,660

Age not given21.9%3,640

Patient sex

Female60.5%10,057

Male32.4%5,386

Not given7.1%1,187

Grey bar: all 20,646,523 reports in the database. 20.6% of these reports give the United States as the country.

Questions about "Face oedema"

What does "Face oedema" mean in an adverse event report?

In plain language: swelling of the face. 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 face oedema?

16,630 reports through June 2026 (0.1% of all reports), 720 of them in the latest 12 months.

Which drugs appear most often in these reports?

Ibuprofen (481), Amoxicillin (391), Lamictal (202), Allopurinol (192) and Lamotrigine (192). 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.