LumaSon: adverse event reports filed with FDA

1,539

reports as suspect product

0% of all reports · about 148 a year

408

reports, 12 months to June 2026

206 in the 12 months before

65.2%

marked serious by the reporter

38.6% across the class

4.2%

record death among outcomes, as reported

64 reports · not verified by FDA

Reports by month, five years

Reports by the month FDA received them. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.

By year received

2026 covers reports received through June 2026 only.

Reactions recorded in the reports

share of LumaSon reports recording the termmedian drug in contrast agent for ultrasound imaging

1. Dyspnoeashortness of breath17.8%274
2. Nauseafeeling sick14.9%229
3. Anaphylactic reactiona severe, sudden allergic reaction13.5%208
4. Hyperhidrosisexcessive sweating12.7%195
5. Flushingsudden reddening or warmth of the skin10.3%159
6. Dizzinesslight-headedness or unsteadiness8.8%136
7. Feeling hotfeeling hot7.9%122
8. Hypersensitivityan allergic-type reaction7.7%119
9. Hypotensionlow blood pressure7.5%115
10. Erythemaskin redness7.1%109
11. Paraesthesiatingling or pins and needles6.8%104
12. Blood pressure decreaseda low blood pressure reading6.6%102
13. Pruritusitching6.6%101
14. Unresponsive to stimuli6.4%99
15. Cardiac arrestthe heart stopped6.1%94
16. Chest painchest pain5.5%85
17. Vomitingbeing sick5.5%85
18. Oxygen saturation decreased5.1%78
19. Drug ineffectivethe medicine did not work as expected4.5%69
20. Loss of consciousnesspassing out4.4%67
21. Headachehead pain4.3%66
22. Heart rate increaseda fast heart rate reading4.1%63
23. Cardio-respiratory arrestthe heart and breathing stopped3.6%56
24. Malaisegeneral feeling of being unwell3.6%56
25. Seizurea fit or convulsion3.5%54
26. Contrast media reaction3.4%53
27. Coughcough3.1%48
28. Presyncope3.1%47
29. Feeling abnormalfeeling odd or not right3%46
30. Back painback pain2.9%45

Top 30 of 167 MedDRA preferred terms recorded across these reports, with a plain-language gloss where one is available. One report can record several terms. The hollow bar is the median share across the 2 drugs in the contrast agent for ultrasound imaging class; it describes the reports, not the patients. 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."

Outcomes recorded

Outcome flags as the reporter set them; a report can carry several, and "other serious" is FDA's own category for serious reports outside the named outcomes. Grey bar: all 6,955 reports in the class. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."

Patients and reporters

Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 100% of reports give the United States as the country of the event or reporter.

Reason for use recorded

The indication field is filled in by the reporter and is often blank; shares are of all 1,539 reports.

Drugs most often listed in the same reports

Other products listed in reports where LumaSon is a suspect product, whatever their own role. Co-listing means the two were recorded together; it says nothing about either product's part in the event. Only the 2,500 most-reported names are counted here.

In context

Shares are of reports, not of patients treated. The number of people taking a product is not in the data, so none of these figures is a rate, and differences between columns reflect who takes a product, who reports and how long it has been sold. 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."

Other drugs in the contrast agent for ultrasound imaging class

Ordered by report count for navigation only. 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." A brand and its generic are separate rows because reporters name them separately.

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. A report counts here when it lists LumaSon as a suspect or interacting product; reports listing it only as a concomitant medication (24) are excluded. 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.