Sarclisa: adverse event reports filed with FDA

737

reports as suspect product

0% of all reports · about 118 a year

144

reports, 12 months to June 2026

150 in the 12 months before

69.2%

marked serious by the reporter

89.1% across the class

12.3%

record death among outcomes, as reported

91 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 Sarclisa reports recording the termmedian drug in cd38-directed cytolytic antibody

1. Infusion related reactiona reaction during or soon after an infusion7.2%53
2. Dyspnoeashortness of breath6.5%48
3. Off label useused for a purpose or in a way not on the label6%44
4. Neutropenialow neutrophils, a type of white blood cell4.3%32
5. Pyrexiafever4.2%31
6. Pneumonialung infection3.5%26
7. Diarrhoealoose or frequent stools3.4%25
8. Thrombocytopenialow platelets3.4%25
9. Anaemialow red blood cells3.3%24
10. Disease progressionthe disease advanced3.1%23
11. Deaththe patient died; cause not stated by this term3%22
12. Coughcough2.8%21
13. Plasma cell myeloma2.6%19
14. Weight increasedweight gain2.6%19
15. Chillschills or shivering2.4%18
16. Hypertensionhigh blood pressure2.4%18
17. Weight decreasedweight loss2.3%17
18. Acute kidney injurysudden loss of kidney function2.2%16
19. Nauseafeeling sick2.2%16
20. Renal impairmentreduced kidney function2.2%16
21. Chest discomfortchest discomfort2%15
22. Neutrophil count decreased1.8%13
23. Vomitingbeing sick1.8%13
24. Deep vein thrombosisa blood clot in a deep vein1.6%12
25. Fatiguetiredness1.6%12
26. Polyneuropathy1.6%12
27. Tachycardiafast heart rate1.6%12
28. Cardiac failureheart failure1.5%11
29. Neuropathy peripheralnerve damage in hands or feet1.5%11
30. Rashskin rash1.5%11

Top 30 of 180 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 5 drugs in the cd38-directed cytolytic antibody 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 37,241 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. 42.9% 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 737 reports.

Drugs most often listed in the same reports

Other products listed in reports where Sarclisa 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 cd38-directed cytolytic antibody 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 Sarclisa as a suspect or interacting product; reports listing it only as a concomitant medication (99) 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.