Brand name · Fluticasone propionate
Flovent: adverse event reports filed with FDA
10,772 reports list it as a suspect or interacting product, 2004–2026. Class: Corticosteroid. Also reported as Flovent Hfa, Flovent Inhaler.
- 10,772
- reports as suspect product
- 0.1% of all reports · about 479 a year
- 171
- reports, 12 months to June 2026
- 322 in the 12 months before
- 42.1%
- marked serious by the reporter
- 77.7% across the class
- 3.9%
- record death among outcomes, as reported
- 424 reports · not verified by FDA
Between January 2004 and June 2026, 10,772 adverse event reports received by FDA list the brand name Flovent (fluticasone propionate) as a suspect or interacting product. Reports that mention it only as a concomitant medication (18,921) are left out of every figure here.
In the 12 months to June 2026, 171 reports listed it, down 47% from 322 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 479 reports a year and 0.1% of the 20,646,523 reports in the database, and 1.3% of the reports for the corticosteroid class. 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 (19.3%), asthma (16.4%) and dyspnoea (15.3%). A report can list several reactions, so shares add to more than 100%; 878 different terms appear across these reports. Drug ineffective is recorded in 19.3% of these reports, a larger share than in the median corticosteroid drug (13.4%).
42.1% of the reports are marked serious by the reporter (77.7% across the class); 3.9% record death among the outcomes and 14.8% record hospitalisation, as reported. 78.2% of the reports came from consumers, and the largest patient age group is 45 to 64 (14.6%). 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 Flovent reports recording the termmedian drug in corticosteroid
- Drug ineffectivethe medicine did not work as expected19.3%2,074
- Asthmaasthma16.4%1,763
- Dyspnoeashortness of breath15.3%1,649
- Coughcough9.1%982
- Wheezingwheezing8.2%882
- Wrong technique in product usage processthe product was used in the wrong way8.1%877
- Off label useused for a purpose or in a way not on the label7.8%842
- Malaisegeneral feeling of being unwell6.5%699
- Painpain, site not specified6.1%652
- Headachehead pain6%648
- Pyrexiafever5.8%628
- Product quality issuea problem with the product itself5.6%598
- Macular degenerationa disease of the central retina5.1%548
- Product use issuea problem in how the product was used5%543
- Chest discomfortchest discomfort5%541
- Rashskin rash4.8%517
- Product complaint4.6%497
- Exposure during pregnancythe medicine was taken during pregnancy4.5%487
- Hypersensitivityan allergic-type reaction4.4%475
- Fatiguetiredness4.3%468
- Overdosea dose above the recommended amount4.3%466
- Infusion related reactiona reaction during or soon after an infusion4.1%444
- Pneumonialung infection4%433
- Hyperhidrosisexcessive sweating3.8%406
- Dysphoniaa hoarse voice3.7%398
- Nauseafeeling sick3.7%398
Top 30 of 878 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 74 drugs in the corticosteroid 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 808,789 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
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. 72.3% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Asthma | 2,905 | 27% |
| Chronic obstructive pulmonary disease | 478 | 4.4% |
| Eosinophilic oesophagitis | 104 | 1% |
| Dyspnoea | 98 | 0.9% |
| Cough | 75 | 0.7% |
| Emphysema | 72 | 0.7% |
The indication field is filled in by the reporter and is often blank; shares are of all 10,772 reports.
Drugs most often listed in the same reports
| Drug (any role in the report) | Reports | Share of Flovent reports |
|---|---|---|
| Albuterol | 1,477 | 13.7% |
| Prednisone | 1,374 | 12.8% |
| Albuterol sulfate | 1,302 | 12.1% |
| Singulair | 1,238 | 11.5% |
| Advair Hfa | 1,113 | 10.3% |
| Acetaminophen | 994 | 9.2% |
| Humira | 957 | 8.9% |
| Cetirizine hydrochloride | 826 | 7.7% |
| Morphine sulfate | 763 | 7.1% |
| Diphenhydramine | 755 | 7% |
Other products listed in reports where Flovent 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 | Flovent | Corticosteroid | All reports |
|---|---|---|---|
| Reports as suspect product | 10,772 | 808,789 | 20,646,523 |
| Share of that pool | — | 1.3% | 0.1% |
| Reports, latest 12 months | 171 | — | 1,332,454 |
| Marked serious | 42.1% | 77.7% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 39 | 146 | 91 |
| Hospitalisation recorded, per 1,000 reports | 148 | 336 | 213 |
| Consumer-filed share | 78.2% | 29.1% | 45.8% |
| Top term, share of reports | Drug ineffective 19.3% | median 13.4% | 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."
Other drugs in the corticosteroid class
| Drug | Name type | Reports | Latest 12 months | Marked serious |
|---|---|---|---|---|
| Prednisone | generic | 183,867 | 15,614 | 91.4% |
| Dexamethasone | generic | 129,677 | 9,216 | 95.1% |
| Prednisolone | generic | 87,806 | 6,624 | 97.6% |
| Methylprednisolone | generic | 49,537 | 4,430 | 95.2% |
| Symbicort | brand | 39,119 | 1,177 | 50.6% |
| Breo Ellipta | brand | 22,220 | 628 | 31.7% |
| Hydrocortisone | generic | 21,263 | 2,386 | 89.5% |
| Advair Diskus | brand | 20,518 | 120 | 29% |
| Advair Hfa | brand | 19,622 | 589 | 54.9% |
| Budesonide | generic | 14,714 | 1,083 | 82.2% |
| Desoximetasone | generic | 12,209 | 1,525 | 99.2% |
| Methylprednisolone sodium succinate | generic | 10,772 | 1,630 | 97.8% |
| Solu-medrol | generic | 10,288 | 432 | 88.8% |
| Cipro | brand | 9,791 | 108 | 57.3% |
| Triamcinolone acetonide | generic | 9,651 | 1,424 | 73.5% |
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.
Questions about Flovent reports
How many adverse event reports has FDA received for Flovent?
10,772 reports list Flovent as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 171 of them arrived in the latest 12 months. Another 18,921 list it only as a concomitant medication.
What reactions are recorded in Flovent reports?
drug ineffective (19.3%), asthma (16.4%), dyspnoea (15.3%), cough (9.1%) and wheezing (8.2%). 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 Flovent was responsible.
How serious are the reports?
42.1% are marked serious by the reporter. Among the outcomes recorded, 3.9% of reports include death and 14.8% 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?
consumer or non-health professional (78.2%), other health professional (12.9%) and physician (5.4%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Flovent rising?
171 reports in the 12 months to June 2026, down 47% from 322 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 Flovent 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 Flovent?
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 Flovent as a suspect or interacting product; reports listing it only as a concomitant medication (18,921) 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.