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Official Description

Rabies immune globulin, heat- and solvent/detergent-treated (RIg-HT S/D), human, for intramuscular and/or subcutaneous use

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

Rabies immune globulin (RIg-HT S/D) is a specialized immunizing agent designed to provide immediate, short-term immunity against the rabies virus. This preparation consists of a concentrated solution of antibodies derived from pooled human plasma collected from donors who have been sensitized with the rabies vaccine. Unlike active immunization, where the body’s immune system is stimulated to produce its own antibodies, the administration of rabies immune globulin offers passive protection. This means that the antibodies present in the immune globulin circulate in the recipient's body, providing immediate defense against the rabies virus without requiring the recipient's immune system to respond. The manufacturing process of RIg-HT S/D includes critical safety measures to ensure the product is free from viral contaminants. Initially, the plasma undergoes solvent/detergent treatment, utilizing a mixture such as tri-(n-butyl) phosphate (TnBP) and Octynoxol 9. This step is essential for inactivating enveloped viruses that may be transmitted through human blood, including HIV and hepatitis B and C. Following this, the product is subjected to heat treatment through pasteurization, which further inactivates any remaining viruses. Some formulations may also incorporate a third step of nanofiltration, which effectively removes additional viral particles based on size. RIg-HT S/D is specifically indicated for administration after exposure to rabies, such as following a bite from a rabid or potentially rabid animal. It is crucial that this immune globulin is administered either intramuscularly or subcutaneously, and it is typically given in conjunction with the rabies vaccine to ensure comprehensive protection. It is important to note that the CPT® Code 90377 specifically reports the rabies immune globulin product itself and does not encompass the administration of the immune globulin or the rabies vaccine.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

Rabies immune globulin (RIg-HT S/D) is indicated for use in the following situations:

  • Post-Exposure Prophylaxis Following a bite or scratch from an animal that is rabid or suspected to be rabid, RIg-HT S/D is administered to neutralize the rabies virus and provide immediate passive immunity.
  • Immediate Protection It is utilized to confer short-term immunity until the recipient's immune system can respond to the rabies vaccine and produce its own antibodies.

2. Procedure

The procedure for administering rabies immune globulin (RIg-HT S/D) involves several critical steps to ensure safety and efficacy:

  • Step 1: Preparation Prior to administration, the healthcare provider must ensure that the RIg-HT S/D is properly prepared and stored according to the manufacturer's guidelines. This includes checking the expiration date and ensuring that the solution is clear and free from particulate matter.
  • Step 2: Administration Site Selection The provider should select an appropriate site for intramuscular or subcutaneous injection. Common sites for intramuscular injection include the deltoid muscle in the upper arm or the anterolateral thigh muscle, while subcutaneous injections may be administered in the fatty tissue of the abdomen or thigh.
  • Step 3: Injection Technique Using aseptic technique, the provider will clean the injection site with an alcohol swab. For intramuscular injections, a suitable needle size is selected, and the needle is inserted at a 90-degree angle to the skin. For subcutaneous injections, a smaller needle is used, and the needle is inserted at a 45-degree angle. The appropriate dose of RIg-HT S/D is then drawn into the syringe and injected into the selected site.
  • Step 4: Post-Injection Care After the injection, the provider should apply gentle pressure to the injection site with a cotton ball or gauze to minimize bleeding. The site may be bandaged if necessary. The patient should be monitored for any immediate adverse reactions following the administration.

3. Post-Procedure

Post-procedure care for patients receiving rabies immune globulin (RIg-HT S/D) includes monitoring for any potential side effects or allergic reactions. Patients should be advised to report any unusual symptoms, such as swelling, redness, or pain at the injection site, as well as systemic reactions like fever or rash. It is also essential to ensure that the patient receives the rabies vaccine as part of the post-exposure prophylaxis protocol, as the immune globulin provides immediate but temporary protection. Follow-up appointments may be necessary to assess the patient's response to the rabies vaccine and to ensure that the immunization series is completed appropriately.

Short Descr RABIES IG HT&SOL HUMAN IM/SC
Medium Descr RABIES IG HEAT&SOLVENT/DETERGENT HUMAN IM&/SUBQ
Long Descr Rabies immune globulin, heat- and solvent/detergent-treated (RIg-HT S/D), human, for intramuscular and/or subcutaneous use
Related Drugs KEDRAB
Status Code Excluded from Physician Fee Schedule by Regulation
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 Nonpass-Through Drugs and Nonimplantable Biologicals, Including Therapeutic Radiopharmaceuticals
ASC Payment Indicator Drugs and biologicals paid separately when provided integral to a surgical procedure on ASC list; payment based on OPPS rate.
Type of Service (TOS) 1 - Medical Care
Berenson-Eggers TOS (BETOS) none
MUE 20
JZ Zero drug amount discarded/not administered to any patient
95 Synchronous telemedicine service rendered via a real-time interactive audio and video telecommunications system: synchronous telemedicine service is defined as a real-time interaction between a physician or other qualified health care professional and a patient who is located at a distant site from the physician or other qualified health care professional. the totality of the communication of information exchanged between the physician or other qualified health care professional and the patient during the course of the synchronous telemedicine service must be of an amount and nature that would be sufficient to meet the key components and/or requirements of the same service when rendered via a face-to-face interaction. modifier 95 may only be appended to the services listed in appendix p. appendix p is the list of cpt codes for services that are typically performed face-to-face, but may be rendered via a real-time (synchronous) interactive audio and video telecommunications system.
JW Drug amount discarded/not administered to any patient
Date
Action
Notes
2021-01-01 Added Code added.
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