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The CPT® Code 90653 refers to an inactivated influenza vaccine (IIV) that is subunit and adjuvanted, specifically designed for intramuscular use. Vaccines, unlike immune globulins that provide short-term, passive immunity, are intended to provide active, long-term immunity. This is achieved by exposing the recipient's immune system to modified versions of specific viruses or bacteria, prompting the immune system to produce its own antibodies against these pathogens. The body retains a memory of how to produce these antibodies, enabling a quicker and more effective response upon subsequent exposures to the same antigens. The influenza vaccine is typically developed using embryonated chicken eggs, where the virus is cultivated, harvested, and then inactivated using formaldehyde to ensure it cannot cause disease. Subunit vaccines, such as this one, contain only the essential antigens that are most effective in stimulating the immune response. These antigens are identified and isolated through laboratory processes, which may involve growing the virus and using chemical methods to extract the necessary components. Alternatively, recombinant DNA technology can be employed to produce these antigens. After the subunit vaccine is created, an adjuvant is incorporated to enhance the immune response further. The inactivated influenza vaccine (IIV) is administered via intramuscular injection, and this method of administration is reported separately in medical coding.
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The inactivated influenza vaccine (IIV), as represented by CPT® Code 90653, is indicated for the prevention of influenza virus infection. It is particularly recommended for individuals who are at higher risk of developing complications from influenza, including but not limited to:
The administration of the inactivated influenza vaccine (IIV) involves several key procedural steps to ensure safety and efficacy:
Post-procedure care for the inactivated influenza vaccine (IIV) includes monitoring the patient for any immediate adverse reactions, such as allergic responses or injection site reactions. Patients are typically advised to rest and can resume normal activities unless otherwise directed. Common side effects may include soreness at the injection site, mild fever, or fatigue, which usually resolve within a few days. It is important for patients to be informed about the signs of more serious reactions and to seek medical attention if they experience difficulty breathing, swelling of the face or throat, or a rapid heartbeat. Additionally, patients should be encouraged to keep track of their vaccination history for future reference and to ensure they receive the vaccine annually, as influenza viruses can change from year to year.
| Short Descr | IIV ADJUVANT VACCINE IM | Medium Descr | IIV ADJUVANTED VACCINE FOR INTRAMUSCULAR USE | Long Descr | Influenza vaccine, inactivated (IIV), subunit, adjuvanted, for intramuscular use | Related Drugs | FLUAD | Status Code | Statutory Exclusion (from MPFS, may be paid under other methodologies) | Global Days | XXX - Global Concept Does Not Apply | PC/TC Indicator (26, TC) | 9 - Not Applicable | Multiple Procedures (51) | 9 - Concept does not apply. | Bilateral Surgery (50) | 9 - Concept does not apply. | Physician Supervisions | 09 - Concept does not apply. | Assistant Surgeon (80, 82) | 9 - Concept does not apply. | Co-Surgeons (62) | 9 - Concept does not apply. | Team Surgery (66) | 9 - Concept does not apply. | Diagnostic Imaging Family | 99 - Concept Does Not Apply | APC Status Indicator | Influenza, Pneumococcal Pneumonia, Hepatitis B, and Covid-19 Vaccines; Monoclonal Antibody Therapy Product | ASC Payment Indicator | Influenza vaccine; pneumococcal vaccine. | Berenson-Eggers TOS (BETOS) | O1G - Immunizations/Vaccinations | MUE | 1 | CCS Clinical Classification | 228 - Prophylactic vaccinations and inoculations |
| 59 | Distinct procedural service: under certain circumstances, it may be necessary to indicate that a procedure or service was distinct or independent from other non-e/m services performed on the same day. modifier 59 is used to identify procedures/services, other than e/m services, that are not normally reported together, but are appropriate under the circumstances. documentation must support a different session, different procedure or surgery, different site or organ system, separate incision/excision, separate lesion, or separate injury (or area of injury in extensive injuries) not ordinarily encountered or performed on the same day by the same individual. however, when another already established modifier is appropriate it should be used rather than modifier 59. only if no more descriptive modifier is available, and the use of modifier 59 best explains the circumstances, should modifier 59 be used. note: modifier 59 should not be appended to an e/m service. to report a separate and distinct e/m service with a non-e/m service performed on the same date, see modifier 25. | GW | Service not related to the hospice patient's terminal condition | JZ | Zero drug amount discarded/not administered to any patient | PD | Diagnostic or related non diagnostic item or service provided in a wholly owned or operated entity to a patient who is admitted as an inpatient within 3 days | SL | State supplied vaccine | SQ | Item ordered by home health |
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Action
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Notes
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| 2016-01-01 | Changed | First appearance of change in codebook. |
| 2015-11-24 | Changed | FDA Approval |
| 2015-07-01 | Changed | Description Changed. FDA Approval Pending. |
| 2013-01-01 | Added | Added |
| 1991-12-31 | Deleted | Code deleted. |
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