Brand name · Lutetium lu 177 dotatate
Lutathera: adverse event reports filed with FDA
5,624 reports list it as a suspect or interacting product, 2018–2026.
- 5,624
- reports as suspect product
- 0% of all reports · about 662 a year
- 671
- reports, 12 months to June 2026
- 960 in the 12 months before
- 40.7%
- marked serious by the reporter
- 57.4% across all reports
- 12.4%
- record death among outcomes, as reported
- 697 reports · not verified by FDA
Between January 2018 and June 2026, 5,624 adverse event reports received by FDA list the brand name Lutathera (lutetium lu 177 dotatate) as a suspect or interacting product. Reports that mention it only as a concomitant medication (57) are left out of every figure here.
In the 12 months to June 2026, 671 reports listed it, down 30% from 960 in 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 662 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.
Reporters most often recorded ill-defined disorder (27.4%), general physical health deterioration (21.3%) and death (7.8%). A report can list several reactions, so shares add to more than 100%; 534 different terms appear across these reports. Ill-defined disorder is recorded in 27.4% of these reports, against 0.3% of all reports in the database.
40.7% of the reports are marked serious by the reporter; 12.4% record death among the outcomes and 11.9% record hospitalisation, as reported. 53.5% of the reports came from other health professionals, and the largest patient age group is 45 to 64 (7%). 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 Lutathera reports recording the termall reports in the database
- Ill-defined disordera condition that was not clearly described27.4%1,539
- General physical health deteriorationgeneral decline in health21.3%1,199
- Deaththe patient died; cause not stated by this term7.8%439
- Platelet count decreasedlow platelet count4.1%229
- Nauseafeeling sick3.9%221
- Covid-19COVID-19 infection3.5%195
- Fatiguetiredness3.2%179
- Laboratory test abnormal3.1%172
- Diarrhoealoose or frequent stools3%171
- Disease progressionthe disease advanced3%166
- Illness2.9%163
- Malaisegeneral feeling of being unwell2.5%139
- Abdominal painstomach or belly pain2.3%130
- Vomitingbeing sick2.3%128
- Thrombocytopenialow platelets2.2%125
- Off label useused for a purpose or in a way not on the label2.1%120
- Decreased appetitereduced appetite2%113
- Metastases to liver1.8%100
- Neuroendocrine tumour1.7%98
- Anaemialow red blood cells1.7%97
- Weight decreasedweight loss1.4%79
- Pancreatic neuroendocrine tumour1.4%76
- Painpain, site not specified1.3%72
- Astheniaweakness or lack of energy1.2%68
- Dyspnoeashortness of breath1.2%66
- Pyrexiafever1.2%66
- SARS-CoV-2 test positive1.1%63
- White blood cell count decreasedlow white cell count1.1%60
- Inappropriate schedule of product administrationthe product was taken at the wrong times1%58
Top 30 of 534 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. 78.4% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Neuroendocrine tumour | 470 | 8.4% |
| Gastroenteropancreatic neuroendocrine tumour disease | 204 | 3.6% |
| Pancreatic neuroendocrine tumour | 164 | 2.9% |
| Small intestine neuroendocrine tumour | 64 | 1.1% |
| Pancreatic neuroendocrine tumour metastatic | 39 | 0.7% |
| Neuroendocrine carcinoma | 32 | 0.6% |
The indication field is filled in by the reporter and is often blank; shares are of all 5,624 reports.
Drugs most often listed in the same reports
| Drug (any role in the report) | Reports | Share of Lutathera reports |
|---|---|---|
| Octreotide | 132 | 2.3% |
| Sandostatin LAR Depot | 89 | 1.6% |
| Everolimus | 75 | 1.3% |
| Lanreotide acetate | 74 | 1.3% |
| Ondansetron | 67 | 1.2% |
| Sandostatin | 64 | 1.1% |
| Dexamethasone | 55 | 1% |
| Capecitabine | 54 | 1% |
| Creon | 42 | 0.7% |
| Afinitor | 41 | 0.7% |
Other products listed in reports where Lutathera 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
| Measure | Lutathera | All reports |
|---|---|---|
| Reports as suspect product | 5,624 | 20,646,523 |
| Share of that pool | — | 0% |
| Reports, latest 12 months | 671 | 1,332,454 |
| Marked serious | 40.7% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 124 | 91 |
| Hospitalisation recorded, per 1,000 reports | 119 | 213 |
| Consumer-filed share | 10.1% | 45.8% |
| Top term, share of reports | Ill-defined disorder 27.4% | 0.3% |
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 Lutathera reports
How many adverse event reports has FDA received for Lutathera?
5,624 reports list Lutathera as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 671 of them arrived in the latest 12 months. Another 57 list it only as a concomitant medication.
What reactions are recorded in Lutathera reports?
ill-defined disorder (27.4%), general physical health deterioration (21.3%), death (7.8%), malignant neoplasm progression (6.2%) and platelet count decreased (4.1%). 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 Lutathera was responsible.
How serious are the reports?
40.7% are marked serious by the reporter. Among the outcomes recorded, 12.4% of reports include death and 11.9% 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 (53.5%), physician (34.1%) and consumer or non-health professional (10.1%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Lutathera rising?
671 reports in the 12 months to June 2026, down 30% from 960 in 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 Lutathera 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 Lutathera?
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 Lutathera as a suspect or interacting product; reports listing it only as a concomitant medication (57) 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.