2026 ICD-10-CM Diagnosis Code T42.8X6AUnderdosing of antiparkinsonism drugs and other central muscle-tone depressants, initial encounter

ICD-10-CM CodesS00–T88T36-T50T42

ICD-10-CM T42.8X6A
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

T42.8X6A is a billable ICD-10-CM diagnosis code for underdosing of antiparkinsonism drugs and other central muscle-tone depressants, 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
T42.8X6A
Billable Status
Yes — Valid for Submission
Code Describes
Underdosing of antiparkinsonism drugs and other central muscle-tone depressants, initial encounter
Short Description
Underdosing of antiparkns drug/centr muscle-tone depr, init
Parent Code
Underdosing of antiparkinsonism drugs and other central muscle-tone depressants

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
CategoryT42Poisoning by, adverse effect of and underdosing of antiepileptic, sedative- hypnotic and antiparkinsonism drugs
This CodeT42.8X6AUnderdosing of antiparkinsonism drugs and other central muscle-tone depressants, initial encounter

Code EditsBilling

Medicare Code Editor checks that affect claim validity for T42.8X6A.

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 antiepileptic, sedative- hypnotic and antiparkinsonism drugs (T42). 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

  • Amantadine

    an antiviral that is used in the prophylactic or symptomatic treatment of influenza a. it is also used as an antiparkinsonian agent, to treat extrapyramidal reactions, and for postherpetic neuralgia. the mechanisms of its effects in movement disorders are not well understood but probably reflect an increase in synthesis and release of dopamine, with perhaps some inhibition of dopamine uptake.
  • Baclofen

    a gamma-aminobutyric acid derivative that is a specific agonist of gaba-b receptors. it is used in the treatment of muscle spasticity, especially that due to spinal cord injuries. its therapeutic effects result from actions at spinal and supraspinal sites, generally the reduction of excitatory transmission.
  • Receptors, GABA-B

    a subset of gaba receptors that signal through their interaction with heterotrimeric g-proteins.
  • Benserazide

    an inhibitor of dopa decarboxylase that does not enter the central nervous system. it is often given with levodopa in the treatment of parkinsonism to prevent the conversion of levodopa to dopamine in the periphery, thereby increasing the amount that reaches the central nervous system and reducing the required dose. it has no antiparkinson actions when given alone.
  • Bromocriptine

    a semisynthetic ergotamine alkaloid that is a dopamine d2 agonist. it suppresses prolactin secretion.
  • Cabergoline

    an ergoline derivative and dopamine d2-agonist that inhibits prolactin secretion. it is used in the management of hyperprolactinemia, and to suppress lactation following childbirth for medical reasons. cabergoline is also used in the management of parkinson disease.
  • Carisoprodol

    a centrally acting skeletal muscle relaxant whose mechanism of action is not completely understood but may be related to its sedative actions. it is used as an adjunct in the symptomatic treatment of musculoskeletal conditions associated with painful muscle spasm. (from martindale, the extra pharmacopoeia, 30th ed, p1202)
  • Chlorphenesin

    a centrally acting muscle relaxant. its mode of action is unknown. (from martindale, the extra pharmacopoeia, 30th ed, p1203)
  • Chlorzoxazone

    a centrally acting central muscle relaxant with sedative properties. it is claimed to inhibit muscle spasm by exerting an effect primarily at the level of the spinal cord and subcortical areas of the brain. (from martindale, the extra pharmacopoea, 30th ed, p1202)
  • Dantrolene

    skeletal muscle relaxant that acts by interfering with excitation-contraction coupling in the muscle fiber. it is used in spasticity and other neuromuscular abnormalities. although the mechanism of action is probably not central, dantrolene is usually grouped with the central muscle relaxants.
  • Levodopa

    the naturally occurring form of dihydroxyphenylalanine and the immediate precursor of dopamine. unlike dopamine itself, it can be taken orally and crosses the blood-brain barrier. it is rapidly taken up by dopaminergic neurons and converted to dopamine. it is used for the treatment of parkinsonian disorders and is usually given with agents that inhibit its conversion to dopamine outside of the central nervous system.
  • Lisuride

    an ergot derivative that acts as an agonist at dopamine d2 receptors (dopamine agonists). it may also act as an antagonist at dopamine d1 receptors, and as an agonist at some serotonin receptors (serotonin receptor agonists).
  • Mephenesin

    a centrally acting muscle relaxant with a short duration of action.
  • Metergoline

    a dopamine agonist and serotonin antagonist. it has been used similarly to bromocriptine as a dopamine agonist and also for migraine disorders therapy.
  • Methocarbamol

    a centrally acting muscle relaxant whose mode of action has not been established. it is used as an adjunct in the symptomatic treatment of musculoskeletal conditions associated with painful muscle spasm. (from martindale, the extra pharmacopoeia, 30th ed, p1206)
  • Pergolide

    a long-acting dopamine agonist which has been used to treat parkinson disease and hyperprolactinemia but withdrawn from some markets due to potential for heart valve diseases.
  • Piribedil

    a dopamine d2 agonist. it is used in the treatment of parkinson disease, particularly for alleviation of tremor. it has also been used for circulatory disorders and in other applications as a d2 agonist.
  • Selegiline

    a selective, irreversible inhibitor of type b monoamine oxidase that is used for the treatment of newly diagnosed patients with parkinson disease, and for the treatment of depressive disorders. the compound without isomeric designation is deprenyl.
  • Zoxazolamine

    a uricosuric and muscle relaxant. zoxazolamine acts centrally as a muscle relaxant, but the mechanism of its action is not understood.

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
AfloqualoneT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
AmantadineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Antiparkinsonism drug NECT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Antirigidity drug NECT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
BaclofenT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
BenserazideT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
BenzatropineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
BromocriptineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
CabergolineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Carbidopa (with levodopa)T42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
CarisoprodolT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
ChlorphenesinT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Chlorphenesin::topical (antifungal)T42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
ChlorzoxazoneT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
DantroleneT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
DeprenalinT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
DeprenylT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
DiethazineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
DifluoromethyldopaT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
DisipalT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
DopaT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
IdrocilamideT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
L-dopaT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
LevodopaT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Levodopa::with carbidopaT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
LisurideT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Mephenamin (e)T42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
MephenesinT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
MephenoxaloneT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
MesulergineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
MetaxaloneT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
MetergolineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
MethocarbamolT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Methocarbamol::skeletal muscle relaxantT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Muscle-tone depressant, central NECT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Muscle-tone depressant, central NEC::specified NECT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
Orphenadrine (hydrochloride)T42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
PergolideT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
PhenprobamateT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
PiribedilT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
RelaT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
SelegilineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
SomaT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
StyramateT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
TizanidineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
TolserolT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6
ZoxazolamineT42.8X1T42.8X2T42.8X3T42.8X4T42.8X5T42.8X6

Patient EducationClinical

Medication Errors

Medicines treat infectious diseases, prevent problems from chronic diseases, and ease pain. But medicines can also cause harmful reactions if not used correctly. Errors can happen in the hospital, at the health care provider's office, at the pharmacy, or at home. You can help prevent errors by:

Read the full article at MedlinePlus

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

Convert T42.8X6A 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 T42.8X6AOverview

Is T42.8X6A a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report underdosing of antiparkinsonism drugs and other central muscle-tone depressants, initial encounter on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What does the 7th character A in T42.8X6A mean?

The final character A marks the initial encounter: use it while the patient is receiving active treatment for underdosing of antiparkinsonism drugs and other central muscle-tone depressants, such as an emergency visit or first evaluation.

Can T42.8X6A be a principal diagnosis?

No. The Medicare Code Editor rejects this code as a principal diagnosis because underdosing of antiparkinsonism drugs and other central muscle-tone depressants, 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.