Product name as reported
Xantofyl Palmitate: adverse event reports filed with FDA
601 reports list it as a suspect or interacting product, 2019–2026.
- 601
- reports as suspect product
- 0% of all reports · about 82 a year
- 48
- reports, 12 months to June 2026
- 50 in the 12 months before
- 100%
- marked serious by the reporter
- 57.4% across all reports
- 28.6%
- record death among outcomes, as reported
- 172 reports · not verified by FDA
601 adverse event reports received by FDA list the product name "Xantofyl Palmitate" as reporters wrote it as a suspect or interacting product, from March 2019 to June 2026. A further 164 reports list it only as a concomitant medication, and those are not counted in the figures on this page.
In the 12 months to June 2026, 48 reports listed it, close to the 50 of the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Over its reporting history that is about 82 reports a year and 0% of the 20,646,523 reports in the database. How many people take it is not in the data, so a count is not a rate of occurrence.
The reactions recorded most often are drug ineffective (77.2%), macular degeneration (67.9%) and nausea (48.1%). A report can list several reactions, so shares add to more than 100%; 144 different terms appear across these reports. Drug ineffective is recorded in 77.2% of these reports, against 6.3% of all reports in the database.
100% of the reports are marked serious by the reporter; 28.6% record death among the outcomes and 54.1% record hospitalisation, as reported. 80.5% of the reports came from other health professionals, and the largest patient age group is 75 and over (26.8%). 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
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 Xantofyl Palmitate reports recording the termall reports in the database
- Drug ineffectivethe medicine did not work as expected77.2%464
- Macular degenerationa disease of the central retina67.9%408
- Nauseafeeling sick48.1%289
- Off label useused for a purpose or in a way not on the label47.4%285
- Abdominal painstomach or belly pain42.1%253
- Constipationconstipation42.1%253
- Anaemialow red blood cells36.8%221
- Painpain, site not specified30.4%183
- Pyrexiafever30.4%183
- Chronic sinusitis27.6%166
- Infusion related reactiona reaction during or soon after an infusion27.6%166
- Malaisegeneral feeling of being unwell27.6%166
- Paraesthesia oral27.5%165
- Weight decreasedweight loss27.5%165
- Dyspepsiaindigestion26.6%160
- Procedural painpain from a procedure26.3%158
- Abdominal distensiona bloated abdomen23.3%140
- General physical health deteriorationgeneral decline in health23.1%139
- Appendicitis22.6%136
- Ascitesfluid in the abdomen22.6%136
- Headachehead pain22.5%135
- Appendicolith22.3%134
- Cardiogenic shockshock from the heart failing to pump22%132
- Multiple organ dysfunction syndromeseveral organs failing21.1%127
- Condition aggravatedthe condition being treated got worse21%126
- Hyponatraemialow blood sodium21%126
- Sepsisa severe body-wide response to infection20.8%125
- Stressstress20.8%125
- Vomitingbeing sick20.6%124
Top 30 of 144 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 share of all reports in the database; 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 20,646,523 reports. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."
Patients and reporters
Patient age
Patient sex
Who reported
Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 0.3% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Nutritional supplementation | 106 | 17.6% |
| Off label use | 6 | 1% |
| Intentional product misuse | 2 | 0.3% |
The indication field is filled in by the reporter and is often blank; shares are of all 601 reports.
In context
| Measure | Xantofyl Palmitate | All reports |
|---|---|---|
| Reports as suspect product | 601 | 20,646,523 |
| Share of that pool | — | 0% |
| Reports, latest 12 months | 48 | 1,332,454 |
| Marked serious | 100% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 286 | 91 |
| Hospitalisation recorded, per 1,000 reports | 541 | 213 |
| Consumer-filed share | 12.6% | 45.8% |
| Top term, share of reports | Drug ineffective 77.2% | 6.3% |
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."
Questions about Xantofyl Palmitate reports
How many adverse event reports has FDA received for Xantofyl Palmitate?
601 reports list Xantofyl Palmitate as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 48 of them arrived in the latest 12 months. Another 164 list it only as a concomitant medication.
What reactions are recorded in Xantofyl Palmitate reports?
drug ineffective (77.2%), macular degeneration (67.9%), nausea (48.1%), off label use (47.4%) and abdominal pain (42.1%). These are MedDRA preferred terms coded from what the reporter described; a report can list several, and a term's presence is not a finding that Xantofyl Palmitate was responsible.
How serious are the reports?
100% are marked serious by the reporter. Among the outcomes recorded, 28.6% of reports include death and 54.1% include hospitalisation. FDA has not verified these outcomes and states that the reports "cannot be used to estimate the incidence" of the events.
Who files these reports?
other health professional (80.5%), consumer or non-health professional (12.6%) and physician (6.3%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Xantofyl Palmitate rising?
48 reports in the 12 months to June 2026, close to the 50 of the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Counts also move with how many people take a product, its time on the market and publicity.
Do these reports show that Xantofyl Palmitate was responsible for these reactions?
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." The reaction may relate to the condition being treated, to other medicines, or to something else.
Is this a list of the side effects of Xantofyl Palmitate?
No. It is a count of what was reported to FDA. The adverse reactions observed in clinical studies are printed on the FDA-approved label, which a pharmacist or clinician can go through with you.
How do I report an adverse event?
Consumers and health professionals can report to FDA through MedWatch (Form FDA 3500 online, or 1-800-FDA-1088), or to the manufacturer, which must pass reports on. See the guide on how to report.
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 Xantofyl Palmitate as a suspect or interacting product; reports listing it only as a concomitant medication (164) 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.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.