2026 ICD-10-CM Diagnosis Code T46.7X3APoisoning by peripheral vasodilators, assault, initial encounter
T46.7X3A is a billable ICD-10-CM diagnosis code for poisoning by peripheral vasodilators, assault, 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. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under External cause codes: intent of injury, assault; External cause codes: poisoning by drug; and Poisoning by drugs, initial encounter.
Code Identity
Code Classification
Coding GuidelinesGuidance
When coding a poisoning or reaction to the improper use of a medication (e.g., overdose, wrong substance given or taken in error, wrong route of administration), first assign the appropriate code from categories T36-T50. The poisoning codes have an associated intent as their 5th or 6th character (accidental, intentional self-harm, assault and undetermined). If the intent of the poisoning is unknown or unspecified, code the intent as accidental intent. The undetermined intent is only for use if the documentation in the record specifies that the intent cannot be determined. Use additional code(s) for all manifestations of poisonings.
The appropriate 7th character is to be added to each code from block Poisoning by, adverse effect of and underdosing of agents primarily affecting the cardiovascular system (T46). 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
Alprostadil
a potent vasodilator agent that increases peripheral blood flow.Bencyclane
a vasodilator agent found to be effective in a variety of peripheral circulation disorders. it has various other potentially useful pharmacological effects. its mechanism may involve block of calcium channels.Betahistine
a histamine analog and h1 receptor agonist that serves as a vasodilator. it is used in meniere disease and in vascular headaches but may exacerbate bronchial asthma and peptic ulcers.Cyclandelate
a direct-acting smooth muscle relaxant used to dilate blood vessels.Dihydroergocornine
a 9,10alpha-dihydro derivative of ergotamine that contains isopropyl sidechains at the 2' and 5' positions of the molecule.Dihydroergotoxine
a mixture of three different hydrogenated derivatives of ergotamine: dihydroergocornine; dihydroergocristine; and dihydroergocryptine. dihydroergotoxine has been proposed to be a neuroprotective agent and a nootropic agent. the mechanism of its therapeutic actions is not clear, but it can act as an alpha-adrenergic antagonist and a dopamine agonist. the methanesulfonate salts of this mixture of alkaloids are called ergoloid mesylates.Ergoloid Mesylates
a mixture of the mesylates (methane sulfonates) of dihydroergocornine; dihydroergocristine; and the alpha- and beta-isomers of dihydroergocryptine. the substance produces a generalized peripheral vasodilation and a fall in arterial pressure and has been used to treat symptoms of mild to moderate impairment of mental function in the elderly.Flunarizine
flunarizine is a selective calcium entry blocker with calmodulin binding properties and histamine h1 blocking activity. it is effective in the prophylaxis of migraine, occlusive peripheral vascular disease, vertigo of central and peripheral origin, and as an adjuvant in the therapy of epilepsy.Iloprost
a stable analog of epoprostenol that is a platelet aggregation inhibitor; vasodilator, and has cytoprotective properties.Isoxsuprine
a beta-adrenergic agonist that causes direct relaxation of uterine and vascular smooth muscle. its vasodilating actions are greater on the arteries supplying skeletal muscle than on those supplying skin. it is used in the treatment of peripheral vascular disease and in premature labor.Minoxidil
a potent direct-acting peripheral vasodilator (vasodilator agents) that reduces peripheral resistance and produces a fall in blood pressure. (from martindale, the extra pharmacopoeia, 30th ed, p371)Moxisylyte
an alpha-adrenergic blocking agent that is used in raynaud's disease. it is also used locally in the eye to reverse the mydriasis caused by phenylephrine and other sympathomimetic agents. (from martindale, the extra pharmacopoeia, 30th ed, p1312)Niacin
a water-soluble vitamin of the b complex occurring in various animal and plant tissues. it is required by the body for the formation of coenzymes nad and nadp. it has pellagra-curative, vasodilating, and antilipemic properties.Niacinamide
an important compound functioning as a component of the coenzyme nad. its primary significance is in the prevention and/or cure of blacktongue and pellagra. most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.Xanthinol Niacinate
a vasodilator used in peripheral vascular disorders and insufficiency. it may cause gastric discomfort and hypotension.Nicergoline
an ergot derivative that has been used as a cerebral vasodilator and in peripheral vascular disease. it may ameliorate cognitive deficits in cerebrovascular disorders.Nicotinyl Alcohol
alcohol analog of nicotinic acid which is a direct-acting peripheral vasodilator that causes flushing and may decrease blood pressure. it is used in vasospasm and threatened gangrene.Nylidrin
a beta-adrenergic agonist. nylidrin causes peripheral vasodilation, a positive inotropic effect, and increased gastric volume of gastric juice. it is used in the treatment of peripheral vascular disorders and premature labor.Pentoxifylline
a methylxanthine derivative that inhibits phosphodiesterase and affects blood rheology. it improves blood flow by increasing erythrocyte and leukocyte flexibility. it also inhibits platelet aggregation. pentoxifylline modulates immunologic activity by stimulating cytokine production.Phenoxybenzamine
an alpha-adrenergic antagonist with long duration of action. it has been used to treat hypertension and as a peripheral vasodilator.Phentolamine
a nonselective alpha-adrenergic antagonist. it is used in the treatment of hypertension and hypertensive emergencies, pheochromocytoma, vasospasm of raynaud disease and frostbite, clonidine withdrawal syndrome, impotence, and peripheral vascular disease.Suloctidil
a peripheral vasodilator that was formerly used in the management of peripheral and cerebral vascular disorders. it is hepatotoxic and fatalities have occurred. (from martindale, the extra pharmacopoeia, 30th ed, p1312)Tadalafil
a carboline derivative and phosphodiesterase 5 inhibitor that is used primarily to treat erectile dysfunction; benign prostatic hyperplasia and primary pulmonary hypertension.Tolazoline
a vasodilator that apparently has direct actions on blood vessels and also increases cardiac output. tolazoline can interact to some degree with histamine, adrenergic, and cholinergic receptors, but the mechanisms of its therapeutic effects are not clear. it is used in treatment of persistent pulmonary hypertension of the newborn.Trimetazidine
a vasodilator used in angina of effort or ischemic heart disease.
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.
Patient EducationClinical
Poisoning
A poison is any substance that is harmful to your body. You might swallow it, inhale it, inject it, or absorb it through your skin. Any substance can be poisonous if too much is taken. Poisons can include:
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert T46.7X3A to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About T46.7X3AOverview
Is T46.7X3A (Poisoning by peripheral vasodilators, assault) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report poisoning by peripheral vasodilators, assault, initial encounter on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What does the 7th character A in T46.7X3A mean?
The final character A marks the initial encounter: use it while the patient is receiving active treatment for poisoning by peripheral vasodilators, assault, such as an emergency visit or first evaluation.
What MS-DRG does T46.7X3A group to?
When poisoning by peripheral vasodilators, assault, initial encounter is the principal diagnosis on an inpatient stay, it groups to MS-DRG 917, 918, with relative weights from 0.8571 to 1.5684 depending on complications. Higher weights mean higher Medicare reimbursement.
What is the ICD-9 equivalent of T46.7X3A?
Under the General Equivalence Mappings, poisoning by peripheral vasodilators, assault, initial encounter converts to ICD-9-CM 972.5 (poison-vasodilator NEC) and E962.0 (assault-pois w medic agt). 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.
