2026 ICD-10-CM Diagnosis Code T36.5X5AAdverse effect of aminoglycosides, initial encounter

ICD-10-CM CodesS00–T88T36-T50T36

ICD-10-CM T36.5X5A
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

T36.5X5A is a billable ICD-10-CM diagnosis code for adverse effect 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) and groups to MS-DRG 917 through 918. 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 Adverse effects of drugs and medicaments, initial encounter.

Code Identity

ICD-10-CM Code
T36.5X5A
Billable Status
Yes — Valid for Submission
Code Describes
Adverse effect of aminoglycosides, initial encounter
Short Description
Adverse effect of aminoglycosides, initial encounter
Same as the full description in the CMS dataset.
Parent Code
Adverse effect 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 CodeT36.5X5AAdverse effect of aminoglycosides, initial encounter

Code EditsBilling

Medicare Code Editor checks that affect claim validity for T36.5X5A.

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.

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Adverse reaction to chlorhexidine and/or neomycin
  • Amikacin adverse reaction
  • Aminoglycosides adverse reaction
  • Antituberculous drug adverse reaction
  • Gentamicin adverse reaction
  • Kanamycin adverse reaction
  • Neomycin adverse reaction
  • Nephropathy induced by aminoglycoside
  • Netilmicin adverse reaction
  • Spectinomycin adverse reaction
  • Streptomycin adverse reaction
  • Tobramycin adverse reaction

Coding GuidelinesGuidance

When coding an adverse effect of a drug that has been correctly prescribed and properly administered, assign the appropriate code for the nature of the adverse effect followed by the appropriate code for the adverse effect of the drug.

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 INJ028
Adverse effects of drugs and medicaments, initial encounter
Default principal diagnosis: inpatient No · outpatient Yes

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

Drug Reactions

Most of the time, medicines make our lives better. They reduce aches and pains, fight infections, and control problems such as high blood pressure or diabetes. But medicines can also cause unwanted reactions, such as drug interactions, side effects, and allergies.

The full article covers:

  • What is a drug interaction?
  • What are side effects?
  • What are drug allergies?
  • How can I stay safe when taking medicines?

Read the full article at MedlinePlus

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

Convert T36.5X5A to ICD-9-CMHistory

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

ICD-9-CM
995.29 Adv eff med/biol NEC/NOS
ApproximateCombination The match is approximate, and more than one code can be needed to describe the source diagnosis. Confirm with contextual judgment.
ICD-9-CM
E930.8 Adv eff antibiotics NEC
ApproximateCombination The match is approximate, and more than one code can be needed to describe the source diagnosis. Confirm with contextual judgment.

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 T36.5X5AOverview

Is T36.5X5A (Adverse effect of aminoglycosides) a billable code?

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

What does the 7th character A in T36.5X5A mean?

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

What MS-DRG does T36.5X5A group to?

On inpatient claims, adverse effect of aminoglycosides, initial encounter maps to MS-DRG 917, 918, with relative weights from 0.8571 to 1.5684 depending on complications. Higher weights mean higher Medicare reimbursement.

Can T36.5X5A be a principal diagnosis?

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

What is the ICD-9 equivalent of T36.5X5A?

Under the General Equivalence Mappings, adverse effect of aminoglycosides, initial encounter converts to ICD-9-CM 995.29 (adv eff med/biol NEC/NOS) and E930.8 (adv eff antibiotics NEC). The mapping is approximate, so confirm the match fits the documentation.

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.