2026 ICD-10-CM Diagnosis Code T43.505SAdverse effect of unspecified antipsychotics and neuroleptics, sequela
T43.505S is a billable ICD-10-CM diagnosis code for adverse effect of unspecified antipsychotics and neuroleptics, sequela. The 7th character S marks it as a sequela code, which reports a problem that remains after the original condition has resolved. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 922 through 923. The code is not accepted as a principal diagnosis by the Medicare Code Editor and exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Poisoning/toxic effect/adverse effects/underdosing, sequela.
Code Identity
Code Classification
Code EditsBilling
Medicare Code Editor checks that affect claim validity for T43.505S.
Present on Admission (POA)Billing
T43.505S is exempt from POA reporting on inpatient claims to general acute care hospitals. Review other POA exempt codes.
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Acute akathisia caused by drug
- Acute akathisia caused by neuroleptic
- Akathisia
- Akathisia caused by drug
- Drug-induced dyskinesia
- Neuroleptic adverse reaction
- Neuroleptic malignant syndrome
- Neuroleptic-induced parkinsonism
- Neuroleptic-induced tardive dyskinesia
- Parkinsonism caused by drug
- Post-injection delirium sedation syndrome
- Restlessness
- Subacute dyskinesia caused by drug
- Tardive dyskinesia
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 psychotropic drugs, not elsewhere classified (T43). 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.
Clinical InformationClinical
Tardive Dyskinesia
drug-related movement disorder characterized by uncontrollable movements in certain muscles. it is associated with a long-term exposure to certain neuroleptic medications (e.g., metoclopramide).Neuroleptic Malignant Syndrome
a potentially fatal syndrome associated primarily with the use of neuroleptic agents (see antipsychotic agents) which are in turn associated with dopaminergic receptor blockade (see receptors, dopamine) in the basal ganglia and hypothalamus, and sympathetic dysregulation. clinical features include diffuse muscle rigidity; tremor; high fever; diaphoresis; labile blood pressure; cognitive dysfunction; and autonomic disturbances. serum cpk level elevation and a leukocytosis may also be present. (from adams et al., principles of neurology, 6th ed, p1199; psychiatr serv 1998 sep;49(9):1163-72)Metoclopramide
a dopamine d2 antagonist that is used as an antiemetic.Grade 2 Akathisia, CTCAE|Grade 2 Akathisia
moderate restlessness or increased motor activity; limiting instrumental adl or mild/moderate impact on age-appropriate normal daily activity (pediatric)Grade 3 Akathisia, CTCAE|Grade 3 Akathisia
severe restlessness or increased motor activity; limiting self-care adl or severe impact on age-appropriate normal daily activity (pediatric)Akathisia
an uncomfortable feeling of inner restlessness and inability to stay still. it can be a side effect of psychotropic medications.Akathisia, CTCAE|Akathisia|Akathisia
a disorder characterized by an uncomfortable feeling of inner restlessness and inability to stay still; this is a side effect of some psychotropic drugs.Barnes Akathisia Rating Scale Clinical Classification|BARS|BARS|BARS01
a standardized rating scale developed by thomas r. e. barnes in 1989 to diagnose akathisia associated with use of antipsychotic agents. this instrument contains objective and subjective sections, as well as a global clinical assessment of akathisia. the first two sections contain a total of 3 items which are rated on a scale of 0 to 3 with 0 being none or normal and 3 being severe. the third section is rated on a 0 to 5 scale with 0 being none and 5 being severe.CDISC Clinical Classification BARS Test Code Terminology|BARS01TC|Barnes Akathisia Rating Scale Clinical Classification Test Code|QS-BARS TESTCD
test codes of clinical classification questions associated with the barnes akathisia rating scale (bars) for the clinical data interchange standards consortium (cdisc) standard data tabulation model (sdtm).CDISC Clinical Classification BARS Test Name Terminology|BARS01TN|Barnes Akathisia Rating Scale Clinical Classification Test Name|QS-BARS TEST
test names of clinical classification questions associated with the barnes akathisia rating scale (bars) for the clinical data interchange standards consortium (cdisc) standard data tabulation model (sdtm).Drug-Induced Akathisia|Drug induced akathisia
evidence of drug-induced akathisia.ESRS-A - Akathisia: Objective|ESRSA1-Akathisia: Objective|ESRSA1-Akathisia: Objective|ESRSA124
extrapyramidal symptom rating scale-abbreviated (esrs-a) akathisia: objective.ESRS-A - Akathisia: Subjective|ESRSA1-Akathisia: Subjective|ESRSA1-Akathisia: Subjective|ESRSA123
extrapyramidal symptom rating scale-abbreviated (esrs-a) akathisia: subjective.ESRS-A - CGI-S Akathisia|ESRSA1-CGI-S Akathisia|ESRSA1-CGI-S Akathisia|ESRSA128
extrapyramidal symptom rating scale-abbreviated (esrs-a) clinical global impression (cgi-s): akathisia.Grade 1 Akathisia, CTCAE|Grade 1 Akathisia
mild restlessness or increased motor activityGrade 2 Akathisia, CTCAE|Grade 2 Akathisia
moderate restlessness or increased motor activity; limiting instrumental adlGrade 3 Akathisia, CTCAE|Grade 3 Akathisia
severe restlessness or increased motor activity; limiting self care adl
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.
| Substance | Accidental | Self-harm | Assault | Undetermined | Adverse Effect | Underdosing |
|---|---|---|---|---|---|---|
| Antianxiety drug NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Antihallucinogen | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Antipsychotic drug | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Antipsychotic drug::specified NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Ataractic drug NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Neuroleptic drug NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::with hypnotic or sedative | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::benzodiazepine NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::butyrophenone NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::carbamate | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::dimethylamine | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::ethylamine | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::hydroxyzine | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::major NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::penothiazine NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::phenothiazine-based | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::piperazine NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::piperidine | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::propylamine | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::specified NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
| Tranquilizer NEC::thioxanthene NEC | T43.501 | T43.502 | T43.503 | T43.504 | T43.505 | T43.506 |
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 T43.505S to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About T43.505SOverview
Is T43.505S a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report adverse effect of unspecified antipsychotics and neuroleptics, sequela on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What does the 7th character S in T43.505S mean?
The final character S makes this a sequela code: it reports a lingering problem that remains after the adverse effect of unspecified antipsychotics and neuroleptics itself has resolved, not the original event.
What MS-DRG does T43.505S group to?
On inpatient claims, adverse effect of unspecified antipsychotics and neuroleptics, sequela maps to MS-DRG 922, 923, with relative weights from 1.0177 to 1.7494 depending on complications. Higher weights mean higher Medicare reimbursement.
Can T43.505S be a principal diagnosis?
No. The Medicare Code Editor rejects this code as a principal diagnosis because adverse effect of unspecified antipsychotics and neuroleptics, sequela describes a circumstance that influences health status rather than a current illness. Report it as a secondary diagnosis.
Is T43.505S exempt from POA reporting?
Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for adverse effect of unspecified antipsychotics and neuroleptics, sequela on inpatient claims.
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.
