What to know
Summary
Viruses
Illness
All data are preliminary and may change as more reports are received.
Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.
A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.1
Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.
U.S. virologic surveillance
Nationally and in HHS regions 1, 2, 3, 5, 6, 7, 8, and 10, the percentage of respiratory specimens testing positive for influenza virus in clinical laboratories increased (change of ≥0.5 percentage points) compared to the previous week. In HHS regions 4 and 9, the percentage of specimens testing positive have been increasing over the past several weeks but were stable (change of <0.5 percentage points) this week compared to the previous. Influenza A(H1N1)pdm09, A(H3N2), and B(Vic) viruses are co-circulating. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses.
Clinical Laboratories
The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
| Week 49 | Data Cumulative since September 29, 2024 (Week 40) |
|
|---|---|---|
| No. of specimens tested | 81,992 | 746,191 |
| No. of positive specimens (%) | 4,151 (5.1%) | 15,408 (2.1%) |
| Positive specimens by type | ||
| Influenza A | 3,924 (94.5%) | 14,321 (92.9%) |
| Influenza B | 227 (5.5%) | 1,087 (7.1%) |
Public Health Laboratories
The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
| Week 49 |
Data Cumulative since September 29, 2024 (Week 40) |
|
|---|---|---|
| No. of specimens tested | 1,363 | 14,991 |
| No. of positive specimens | 621 | 4,372 |
| Positive specimens by type/subtype | ||
| Influenza A | 603 (97.1%) | 4,155 (95.0%) |
| Subtyping Performed | 429 (71.1%) | 3,474 (83.6%) |
| (H1N1)pdm09 | 168 (39.2%) | 1,538 (44.3%) |
| H3N2 | 261 (60.8%) | 1,869 (53.8%) |
| H3N2v | 0 | 0 |
| H5* | 0 | 67* (1.9%) |
| Subtyping not performed | 174 (28.9%) | 681 (16.7%) |
| Influenza B | 18 (2.9%) | 217 (5.0%) |
| Lineage testing performed | 1 (5.6%) | 105 (48.4%) |
| Yamagata lineage | 0 | 0 |
| Victoria lineage | 1 (100%) | 105 (100.0%) |
| Lineage not performed | 17 (94.4%) | 112 (51.6%) |
*This data reflects specimens tested and the number determined to be positive for influenza viruses at the public health labs (specimens tested is not the same as cases). It does not reflect specimens tested only at CDC and could include more than one specimen tested per person. The guidance for influenza A/H5 testing recommends testing both a conjunctival and respiratory swab for people with conjunctivitis which has resulted in more specimens testing positive for influenza A/H5 than the number of human H5 cases. For more information on the number of people infected with A/H5, please visit the "How CDC is monitoring influenza data among people to better understand the current avian influenza A (H5N1) situation"
†When an influenza virus that normally circulates in swine (but not people) is detected in a person, it is called a "variant" influenza virus. Most human infections with variant influenza viruses occur following exposure to swine, but human-to-human transmission can occur. It is important to note that in most cases, variant influenza viruses have not shown the ability to spread easily and sustainably from human-to-human.
This graph reflects the number of specimens tested and the number determined to be positive for influenza viruses at the public health lab (specimens tested is not the same as cases). It does not reflect specimens tested only at CDC and could include more than one specimen tested per person. Specimens tested as part of routine influenza surveillance as well as those tested as part of targeted testing for people exposed to influenza A(H5) are included.
Novel Influenza A Virus
Two probable cases of influenza A(H5) virus infection were reported to CDC this week by the Arizona Department of Health Services. To date, human-to-human transmission of influenza A(H5) virus has not been identified in the United States.
These cases occurred among two adult workers, ≥ 18 years of age, performing depopulation activities at a commercial poultry facility where highly pathogenic avian influenza (HPAI) A(H5N1) virus had been detected. While being monitored by local public health, these patients developed illness during the weeks ending November 23 and November 30, respectively. Both patients reported respiratory symptoms. One patient also reported conjunctivitis.
Specimens were collected from the patients and initially tested positive with high CT values at public health laboratories using the CDC influenza A(H5) assay. The specimens were negative for influenza A(H5) virus using diagnostic RT-PCR at CDC. These two probable cases are the first reported human influenza A(H5) cases reported in Arizona.
No additional notification to WHO of these probable cases is required per International Health Regulations (IHR). More information regarding IHR can be found at http://www.who.int/topics/international_health_regulations/en/.
The CSTE position statement, which includes updated case definitions for confirmed, probable, and suspected cases is available at http://www.cste.org/resource/resmgr/position_statements_files_2023/24-ID-09_Novel_Influenza_A.pdf
An up-to-date human case summary during the 2024 outbreak by state and exposure source is available at www.cdc.gov/bird-flu/situation-summary/index.html
Information about avian influenza is available at https://www.cdc.gov/flu/avianflu/index.htm.
Interim recommendations for Prevention, Monitoring, and Public Health Investigations are available at https://www.cdc.gov/bird-flu/prevention/hpai-interim-recommendations.html.
The latest case reports on avian influenza outbreaks in wild birds, commercial poultry, backyard or hobbyist flocks, and mammals in the United States are available from the USDA at https://www.aphis.usda.gov/aphis/ourfocus/animalhealth/animal-disease-information/avian/avian-influenza/2022-hpai.
Influenza Virus Characterization
CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are relative to the reference viruses representing the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the polymerase acidic protein (PA) endonuclease inhibitor baloxavir. The HA clade and subclades were assigned using Nextclade (https://clades.nextstrain.org).
CDC has genetically characterized 234 influenza viruses collected since September 29, 2024
| Virus Subtype or Lineage | Genetic Characterization | ||||
|---|---|---|---|---|---|
| Total No. of Subtype/Lineage Tested |
HA Clade |
Number (% of subtype/lineage tested) |
HA Subclade |
Number (% of subtype/lineage tested) |
|
| A/H1 | 101 | ||||
| 5a.2a | 45 (44.6%) | C.1.9 | 45 (44.6%) | ||
| 5a.2a.1 | 56 (55.4%) | D | 1 (1.0%) | ||
| D.3 | 1 (1.0%) | ||||
| D.5 | 54 (53.5%) | ||||
| A/H3 | 117 | ||||
| 2a.3a | 4 (3.4%) | G.1.3.1 | 4 (3.4%) | ||
| 2a.3a.1 | 113 (96.6%) | J.1.1 | 1 (0.9%) | ||
| J.2 | 102 (87.2%) | ||||
| J.2.1 | 1 (0.9%) | ||||
| J.2.2 | 9 (7.7%) | ||||
| B/Victoria | 16 | ||||
| V1A | 16 (100%) | C.5 | 3 (18.8%) | ||
| C.5.1 | 8 (50.0%) | ||||
| C.5.6 | 5 (31.3%) | ||||
| B/Yamagata | 0 | ||||
| Y3 | 0 | Y3 | 0 | ||
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) assay (H1N1pdm09, H3N2, and B/Victoria viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2024-2025 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset of the recent genetically characterized viruses and are chosen based on the genetic changes in their surface proteins and may not be proportional to the number of such viruses circulating in the United States.
Influenza A Viruses
- A (H1N1)pdm09: 14 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
- A (H3N2): 15 A(H3N2) viruses were antigenically characterized by HI or HINT, and 6 (40.0%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Massachusetts/18/2022-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines
Influenza B Viruses
- B/Victoria: No influenza B/Victoria-lineage virus were antigenically characterized by HI yet.
- B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications
CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.
Viruses collected in the U.S. since September 29, 2024, were tested for antiviral susceptibility as follows:
| Antiviral Medication | Total Viruses | A/H1 | A/H3 | B/Victoria | ||
|---|---|---|---|---|---|---|
| Neuraminidase Inhibitors | Oseltamivir | Viruses Tested | 345 | 140 | 180 | 25 |
| Reduced Inhibition | 1 (0.3%) | 1 (0.7%) | 0 | 0 | ||
| Highly Reduced Inhibition | 0 | 0 | 0 | 0 | ||
| Peramivir | Viruses Tested | 345 | 140 | 180 | 25 | |
| Reduced Inhibition | 0 | 0 | 0 | 0 | ||
| Highly Reduced Inhibition | 0 | 0 | 0 | 0 | ||
| Zanamivir | Viruses Tested | 345 | 140 | 180 | 25 | |
| Reduced Inhibition | 0 | 0 | 0 | 0 | ||
| Highly Reduced Inhibition | 0 | 0 | 0 | 0 | ||
| PA Cap-Dependent Endonuclease Inhibitor | Baloxavir | Viruses Tested | 311 | 121 | 169 | 21 |
| Decreased Susceptibility | 0 | 0 | 0 | 0 | ||
One A(H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir.
High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented.
Outpatient and Emergency Department Illness Surveillance
Outpatient respiratory illness visits
The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza, and will therefore capture respiratory illness visits due to infection with any pathogen that can present with similar symptoms, including influenza virus, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity.
Nationally, during Week 49, 3.4% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This week's percentage increased (change of > 0.1 percentage points) compared to Week 48 and is above the national baseline of 3.0% for the second consecutive week. The percentage of visits for ILI increased (change of > 0.1 percentage points) in HHS regions 2, 7, 8, 9, and 10. Regions 1, 3, 4, 5, and 6 have remained stable (change of ≤0.1 percentage points) compared to Week 48 but have been increasing over the past several weeks. HHS regions 1, 2, 3, 4, 7, 9, and 10 are above their respective baselines and regions 5 and 6 are at their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infections to ILI varies by location.
Outpatient respiratory illness visits by age group
About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Based on these data, the percentage of visits for respiratory illness increased (change of > 0.1 percentage point) in the 25-49 years, 50-64 years, and 65+ years age groups and decreased slightly (change of > 0.1 percentage point) in the 0-4 years and 5-24 years age groups in Week 49 compared to Week 48.
Outpatient respiratory illness activity map
Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
| Activity Level | Number of Jurisdictions | Number of CBSAs | ||
|---|---|---|---|---|
| Week 49 (Week ending Dec. 7, 2024) |
Week 48 (Week ending Nov. 30, 2024) |
Week 49 (Week ending Dec. 7, 2024) |
Week 48 (Week ending Nov. 30, 2024) |
|
| Very High | 0 | 1 | 2 | 2 |
| High | 6 | 2 | 39 | 23 |
| Moderate | 13 | 10 | 64 | 67 |
| Low | 17 | 16 | 190 | 160 |
| Minimal | 19 | 26 | 410 | 448 |
| Insufficient Data | 0 | 0 | 224 | 229 |
*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
National Syndromic Surveillance System (NSSP)
The overall percentage of emergency department (ED) visits with a discharge diagnosis of influenza reported in NSSP was 1.0% during Week 49. This percentage has remained stable from the previous week. In HHS regions 2, 3, 5, 8, 9, and 10 the percentage of ED visits increased (change of > 0.1 percentage points) in Week 49 compared to the previous week. In regions 1, 4, 6, and 7, the percentage of ED visits for influenza remained stable (change of ≤ 0.1 percentage point) compared to the previous week but have been increasing slowly over the past several weeks. The percentage of visits for influenza increased (change of > 0.1 percentage points) among the 0-4 years, 18-64 years, and 65+ years age groups and remained stable (change of ≤ 0.1 percentage points) among the 5-17 years age group.
Hospitalization surveillance
FluSurv-Net
The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.
A total of 962 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2024, and December 7, 2024. The weekly hospitalization rate observed in Week 49 was 0.9 per 100,000 population. The cumulative hospitalization rate observed in Week 49 was 3.1 per 100,000 population.
When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (9.9), followed by adults aged 50-64 years (3.2) and children aged 0-4 years (2.6).
When examining age-adjusted rates by race and ethnicity, the highest cumulative hospitalization rate per 100,000 population was among non-Hispanic Black persons (4.3) followed by Hispanic persons (2.9), non-Hispanic White persons (2.5), American Indian/Alaska Native persons (2.4), and Asian/Pacific Islander persons (2.3).
**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
National healthcare safety network (NHSN) hospitalization surveillance
Effective November 1, 2024, all acute care and critical access hospitals are required to report the number of patients admitted with laboratory-confirmed influenza to NHSN. These data will be updated weekly in FluView and on FluView Interactive once sufficient data has been collected. Public datasets, including data reported on a voluntary basis prior to November 1, 2024 can be found here: https://data.cdc.gov/Public-Health-Surveillance/Weekly-United-States-Hospitalization-Metrics-by-Ju/aemt-mg7g/about_data.
Mortality surveillance
Based on NCHS mortality surveillance data available on December 12, 2024, 0.1% of the deaths that occurred during the week ending December 7, 2024 (Week 49), were due to influenza. This percentage remained stable (≤ 0.1 percentage point change) compared to Week 48. The data presented are preliminary and may change as more data are received and processed.
Influenza-Associated Pediatric Mortality
No influenza-associated pediatric deaths were reported to CDC during Week 49.
A total of two influenza-associated pediatric deaths occurring during the 2024-2025 season have been reported to CDC.
Additional National and International Influenza Surveillance Information
Increasing: 
Decreasing: 
Stable: 
Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week.
FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.
National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
U.S. State and local influenza surveillance: Select a jurisdiction below to access the latest local influenza information.
World Health Organization:
Additional influenza surveillance information from participating WHO member nations is available through FluNet and the Global Epidemiology Reports.
WHO Collaborating Centers for Influenza:
Australia, China, Japan, the United Kingdom, and the United States (CDC in Atlanta, Georgia)
Europe:
The most up-to-date influenza information from Europe is available from WHO/Europe and the European Centre for Disease Prevention and Control.
Public Health Agency of Canada:
The most up-to-date influenza information from Canada is available in Canada's weekly FluWatch report.
Public Health England:
The most up-to-date influenza information from the United Kingdom is available from Public Health England.
Any links provided to non-Federal organizations are provided solely as a service to our users. These links do not constitute an endorsement of these organizations or their programs by CDC or the Federal Government, and none should be inferred. CDC is not responsible for the content of the individual organization web pages found at these links.
A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.