Durvalumab: adverse event reports filed with FDA

7,629

reports as suspect product

0% of all reports · about 770 a year

2,245

reports, 12 months to June 2026

1,983 in the 12 months before

98.5%

marked serious by the reporter

94.8% across the class

30.3%

record death among outcomes, as reported

2,311 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 Durvalumab reports recording the termmedian drug in programmed death ligand-1 blocker

1. Deaththe patient died; cause not stated by this term14.8%1,128
2. Malignant neoplasm progression6.4%486
3. Pneumonitis4.3%328
4. Pyrexiafever4%308
5. Diarrhoealoose or frequent stools3.7%283
6. Off label useused for a purpose or in a way not on the label3.4%259
7. Astheniaweakness or lack of energy3.1%237
8. Fatiguetiredness2.9%223
9. Pneumonialung infection2.8%211
10. Anaemialow red blood cells2.7%205
11. Colitisinflamed bowel2.7%204
12. Dyspnoeashortness of breath2.6%202
13. Thrombocytopenialow platelets2.5%189
14. Disease progressionthe disease advanced2.4%181
15. Vomitingbeing sick2.2%171
16. Rashskin rash2.2%167
17. Nauseafeeling sick2.2%165
18. Neutropenialow neutrophils, a type of white blood cell2%155
19. Platelet count decreasedlow platelet count1.9%148
20. Febrile neutropeniafever with low white blood cells1.9%147
21. Hypothyroidismunderactive thyroid1.9%144
22. Drug ineffectivethe medicine did not work as expected1.9%143
23. Myocarditisinflammation of the heart muscle1.8%139
24. Sepsisa severe body-wide response to infection1.8%136
25. Hepatitis1.7%131
26. Myelosuppression1.7%130
27. Decreased appetitereduced appetite1.6%121
28. Interstitial lung diseasescarring or inflammation of lung tissue1.5%117
29. Neuropathy peripheralnerve damage in hands or feet1.5%112
30. Pleural effusionfluid around the lung1.3%101

Top 30 of 903 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 4 drugs in the programmed death ligand-1 blocker 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 23,488 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. 15.5% 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 7,629 reports.

Drugs most often listed in the same reports

Other products listed in reports where Durvalumab 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 programmed death ligand-1 blocker 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 Durvalumab as a suspect or interacting product; reports listing it only as a concomitant medication (438) 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.