2026 ICD-10-CM Diagnosis Code T36.5X6AUnderdosing of aminoglycosides, initial encounter

ICD-10-CM CodesS00–T88T36-T50T36

ICD-10-CM T36.5X6A
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

T36.5X6A is a billable ICD-10-CM diagnosis code for underdosing of aminoglycosides, initial encounter. The 7th character A marks it as an initial encounter code, used while the patient is receiving active treatment. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). The code is not accepted as a principal diagnosis by the Medicare Code Editor. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Underdosing of drugs and medicaments, initial encounter.

Code Identity

ICD-10-CM Code
T36.5X6A
Billable Status
Yes — Valid for Submission
Code Describes
Underdosing of aminoglycosides, initial encounter
Short Description
Underdosing of aminoglycosides, initial encounter
Same as the full description in the CMS dataset.
Parent Code
Underdosing of aminoglycosides

Code Classification

ChapterS00–T88Injury, poisoning and certain other consequences of external causes
SectionT36-T50Poisoning by, adverse effect of and underdosing of drugs, medicaments and biological substances
CategoryT36Poisoning by, adverse effect of and underdosing of systemic antibiotics
This CodeT36.5X6AUnderdosing of aminoglycosides, initial encounter

Code EditsBilling

Medicare Code Editor checks that affect claim validity for T36.5X6A.

There are selected codes that describe a circumstance which influences an individual's health status but not a current illness or injury, or codes that are not specific manifestations but may be due to an underlying cause. These codes are considered unacceptable as a principal diagnosis.

Coding GuidelinesGuidance

Underdosing refers to taking less of a medication than is prescribed by a provider or a manufacturer's instruction. Codes for underdosing should never be assigned as principal or first-listed codes. If a patient has a relapse or exacerbation of the medical condition for which the drug is prescribed because of the reduction in dose, then the medical condition itself should be coded.

The appropriate 7th character is to be added to each code from block Poisoning by, adverse effect of and underdosing of systemic antibiotics (T36). Use the following options for the applicable episode of care:

  • A - initial encounter
  • D - subsequent encounter
  • S - sequela

Source: ICD-10-CM Official Guidelines for Coding and Reporting, FY 2026, published by CMS and the National Center for Health Statistics.

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR INJ029
Underdosing of drugs and medicaments, initial encounter
Default principal diagnosis: inpatient No · outpatient No

Clinical InformationClinical

  • Amikacin

    a broad-spectrum antibiotic derived from kanamycin. it is reno- and oto-toxic like the other aminoglycoside antibiotics.
  • Kanamycin Kinase

    a class of enzymes that inactivate aminocyclitol-aminoglycoside antibiotics (aminoglycosides) by regiospecific phosphorylation of the 3' and/or 5' hydroxyl.
  • Dibekacin

    analog of kanamycin with antitubercular as well as broad-spectrum antimicrobial properties.
  • Framycetin

    a component of neomycin that is produced by streptomyces fradiae. on hydrolysis it yields neamine and neobiosamine b. (from merck index, 11th ed)
  • Kanamycin

    antibiotic complex produced by streptomyces kanamyceticus from japanese soil. comprises 3 components: kanamycin a, the major component, and kanamycins b and c, the minor components.
  • Kanamycin Resistance

    nonsusceptibility of bacteria to the antibiotic kanamycin, which can bind to their 70s ribosomes and cause misreading of messenger rna.
  • Netilmicin

    semisynthetic 1-n-ethyl derivative of sisomycin, an aminoglycoside antibiotic with action similar to gentamicin, but less ear and kidney toxicity.
  • Novobiocin

    an antibiotic compound derived from streptomyces niveus. it has a chemical structure similar to coumarin. novobiocin binds to dna gyrase, and blocks adenosine triphosphatase (atpase) activity. (from reynolds, martindale the extra pharmacopoeia, 30th ed, p189)
  • Paromomycin

    an aminoglycoside antibacterial and antiprotozoal agent produced by species of streptomyces.
  • Ribostamycin

    a broad-spectrum antimicrobial isolated from streptomyces ribosifidicus.
  • Sisomicin

    antibiotic produced by micromonospora inyoensis. it is closely related to gentamicin c1a, one of the components of the gentamicin complex (gentamicins).
  • Spectinomycin

    an antibiotic produced by streptomyces spectabilis. it is active against gram-negative bacteria and used for the treatment of gonorrhea.
  • Tobramycin

    an aminoglycoside, broad-spectrum antibiotic produced by streptomyces tenebrarius. it is effective against gram-negative bacteria, especially the pseudomonas species. it is a 10% component of the antibiotic complex, nebramycin, produced by the same species.
  • Tobramycin, Dexamethasone Drug Combination

    a topical preparation of tobramycin and dexamethasone that is used for treating or preventing superficial bacterial infections of the eye.

Table of Drugs and ChemicalsClinical

Substances in the Table of Drugs and Chemicals that reference this code family. Always confirm in the Tabular List before coding.

SubstanceAccidentalSelf-harmAssaultUndeter­minedAdverse
Effect
Under­dosing
AmikacinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
AstromicinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
BekanamycinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
DibekacinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
DihydrostreptomycinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
FramycetinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
GaramycinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Garamycin::ophthalmic preparationT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Garamycin::topical NECT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
GentamicinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Gentamicin::ophthalmic preparationT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Gentamicin::topical NECT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
IsepamicinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
KanamycinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
KantrexT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
MicronomicinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
MycifradinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Mycifradin::topicalT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Neomycin (derivatives)T36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Neomycin (derivatives)::withT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Neomycin (derivatives)::with::bacitracinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Neomycin (derivatives)::with::neostigmineT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Neomycin (derivatives)::ENT agentT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Neomycin (derivatives)::ophthalmic preparationT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Neomycin (derivatives)::topical NECT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
NetilmicinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
NovobiocinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
ParomomycinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
RibostamycinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
SisomicinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
SpectinomycinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
StreptoduocinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
Streptomycin (derivative)T36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
StreptonivicinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
StreptovarycinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6
TobramycinT36.5X1T36.5X2T36.5X3T36.5X4T36.5X5T36.5X6

Patient EducationClinical

Antibiotics

Antibiotics are medicines that fight bacterial infections in people and animals. They work by killing the bacteria or by making it hard for the bacteria to grow and multiply.

The full article covers:

  • What are antibiotics?
  • What do antibiotics treat?
  • Do antibiotics treat viral infections?
  • What are the side effects of antibiotics?
  • Why is it important to take antibiotics only when they're needed?
  • How do I use antibiotics correctly?

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert T36.5X6A to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
No Map There is no ICD-9 equivalent for this code.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About T36.5X6AOverview

Is T36.5X6A (Underdosing of aminoglycosides) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report underdosing of aminoglycosides, initial encounter on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What does the 7th character A in T36.5X6A mean?

The final character A marks the initial encounter: use it while the patient is receiving active treatment for underdosing of aminoglycosides, such as an emergency visit or first evaluation.

Can T36.5X6A be a principal diagnosis?

No. The Medicare Code Editor rejects this code as a principal diagnosis because underdosing of aminoglycosides, initial encounter describes a circumstance that influences health status rather than a current illness. Report it as a secondary diagnosis.

Footnotes

[1] Not chronic - A diagnosis code that does not fit the criteria for chronic condition (duration, ongoing medical treatment, and limitations) is considered not chronic. Some codes designated as not chronic are acute conditions. Other diagnosis codes that indicate a possible chronic condition, but for which the duration of the illness is not specified in the code description (i.e., we do not know the condition has lasted 12 months or longer) also are considered not chronic.