Poisoning by, adverse effect of and underdosing of primarily systemic and hematological agents, not elsewhere classified (T45)

Browse all the diagnosis codes used for poisoning by, adverse effect of and underdosing of primarily systemic and hematological agents, not elsewhere classified (t45). For easy navigation, the diagnosis codes are sorted in alphabetical order and grouped by sections. Each section is clearly marked with its description, and the corresponding three-digit code range. This format makes it simple to browse diagnosis codes in this chapter or section and find what you're looking for. We've also added green checkmark icons to label billable codes, and red warning icons for non-billable ones. This makes it easy to identify which codes can be billed.

Clinical Information

Acatalasia - A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and gangrene may be present.

Acenocoumarol - A coumarin that is used as an anticoagulant. Its actions and uses are similar to those of WARFARIN. (From Martindale, The Extra Pharmacopoeia, 30th ed, p233)

Aclarubicin - An anthracycline produced by Streptomyces galilaeus. It has potent antineoplastic activity.

Adenine - A purine base and a fundamental unit of ADENINE NUCLEOTIDES.

Adenine Nucleotide Translocator 1 - A subtype of mitochondrial ADP, ATP translocase found primarily in heart muscle (MYOCARDIUM) and skeletal muscle (MUSCLE, SKELETAL).

Adenine Nucleotide Translocator 2 - A subtype of mitochondrial ADP, ATP translocase found primarily in FIBROBLASTS.

Adenine Nucleotide Translocator 3 - A subtype of mitochondrial ADP, ATP translocase found primarily in the LIVER.

Adenine Nucleotides - A class of nucleotide translocases found abundantly in mitochondria that function as integral components of the inner mitochondrial membrane. They facilitate the exchange of ADP and ATP between the cytosol and the mitochondria, thereby linking the subcellular compartments of ATP production to those of ATP utilization.

Adenine Phosphoribosyltransferase - An enzyme catalyzing the formation of AMP from adenine and phosphoribosylpyrophosphate. It can act as a salvage enzyme for recycling of adenine into nucleic acids. EC 2.4.2.7.

Agranulocytosis - A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS).

alpha 1-Antitrypsin - Plasma glycoprotein member of the serpin superfamily which inhibits TRYPSIN; NEUTROPHIL ELASTASE; and other PROTEOLYTIC ENZYMES.

Altretamine - A hexamethyl-2,4,6-triamine derivative of 1,3,5-triazine.

Aminocaproates - Amino derivatives of caproic acid. Included under this heading are a broad variety of acid forms, salts, esters, and amides that contain the amino caproic acid structure.

Aminocaproic Acid - An antifibrinolytic agent that acts by inhibiting plasminogen activators which have fibrinolytic properties.

Aminoglutethimide - An aromatase inhibitor that is used in the treatment of advanced BREAST CANCER.

Amsacrine - An aminoacridine derivative that intercalates into DNA and is used as an antineoplastic agent.

Ancrod - An enzyme fraction from the venom of the Malayan pit viper, Agkistrodon rhodostoma. It catalyzes the hydrolysis of a number of amino acid esters and a limited proteolysis of fibrinogen. It is used clinically to produce controlled defibrination in patients requiring anticoagulant therapy. EC 3.4.21.-.

Anistreplase - An acylated inactive complex of streptokinase and human lysine-plasminogen. After injection, the acyl group is slowly hydrolyzed, producing an activator that converts plasminogen to plasmin, thereby initiating fibrinolysis. Its half-life is about 90 minutes compared to 5 minutes for TPA; (TISSUE PLASMINOGEN ACTIVATOR); 16 minutes for UROKINASE-TYPE PLASMINOGEN ACTIVATOR and 23 minutes for STREPTOKINASE. If treatment is initiated within 3 hours of onset of symptoms for acute myocardial infarction, the drug preserves myocardial tissue and left ventricular function and increases coronary artery patency. Bleeding complications are similar to other thrombolytic agents.

Anthramycin - A broad-spectrum spectrum antineoplastic antibiotic isolated from Streptomyces refuineus var. thermotolerans. It has low toxicity, some activity against Trichomonas and Endamoeba, and inhibits RNA and DNA synthesis. It binds irreversibly to DNA.

Anticoagulants - Agents that prevent BLOOD CLOTTING.

Antigens, Differentiation, B-Lymphocyte - Membrane antigens associated with maturation stages of B-lymphocytes, often expressed in tumors of B-cell origin.

Antithrombins - Endogenous factors and drugs that directly inhibit the action of THROMBIN, usually by blocking its enzymatic activity. They are distinguished from INDIRECT THROMBIN INHIBITORS, such as HEPARIN, which act by enhancing the inhibitory effects of antithrombins.

Aprotinin - A single-chain polypeptide derived from bovine tissues consisting of 58 amino-acid residues. It is an inhibitor of proteolytic enzymes including CHYMOTRYPSIN; KALLIKREIN; PLASMIN; and TRYPSIN. It is used in the treatment of HEMORRHAGE associated with raised plasma concentrations of plasmin. It is also used to reduce blood loss and transfusion requirements in patients at high risk of major blood loss during and following open heart surgery with EXTRACORPOREAL CIRCULATION. (Reynolds JEF(Ed): Martindale: The Extra Pharmacopoeia (electronic version). Micromedex, Inc, Englewood, CO, 1995)

Arabinofuranosylcytosine Triphosphate - A triphosphate nucleotide analog which is the biologically active form of CYTARABINE. It inhibits nuclear DNA synthesis.

Argon Plasma Coagulation - A method of tissue ablation and bleeding control that uses ARGON plasma (ionized argon gas) to deliver a current of thermocoagulating energy to the area of tissue to be coagulated.

Ascorbic Acid - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.

Ascorbic Acid Deficiency - A condition due to a dietary deficiency of ascorbic acid (vitamin C), characterized by malaise, lethargy, and weakness. As the disease progresses, joints, muscles, and subcutaneous tissues may become the sites of hemorrhage. Ascorbic acid deficiency frequently develops into SCURVY in young children fed unsupplemented cow's milk exclusively during their first year. It develops also commonly in chronic alcoholism. (Cecil Textbook of Medicine, 19th ed, p1177)

Asparaginase - A hydrolase enzyme that converts L-asparagine and water to L-aspartate and NH3. EC 3.5.1.1.

Astemizole - Antihistamine drug now withdrawn from the market in many countries because of rare but potentially fatal side effects.

Azacitidine - A pyrimidine analogue that inhibits DNA methyltransferase, impairing DNA methylation. It is also an antimetabolite of cytidine, incorporated primarily into RNA. Azacytidine has been used as an antineoplastic agent.

Azaserine - Antibiotic substance produced by various Streptomyces species. It is an inhibitor of enzymatic activities that involve glutamine and is used as an antineoplastic and immunosuppressive agent.

Azathioprine - An immunosuppressive agent used in combination with cyclophosphamide and hydroxychloroquine in the treatment of rheumatoid arthritis. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), this substance has been listed as a known carcinogen. (Merck Index, 11th ed)

Biotin - A water-soluble, enzyme co-factor present in minute amounts in every living cell. It occurs mainly bound to proteins or polypeptides and is abundant in liver, kidney, pancreas, yeast, and milk.

Biotinidase - An enzyme which catalyzes the release of BIOTIN from biocytin. In human, defects in the enzyme are the cause of the organic acidemia MULTIPLE CARBOXYLASE DEFICIENCY or BIOTINIDASE DEFICIENCY.

Biotinidase Deficiency - The late onset form of MULTIPLE CARBOXYLASE DEFICIENCY (deficiency of the activities of biotin-dependent enzymes propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to a defect or deficiency in biotinidase which is essential for recycling BIOTIN.

Biotinylation - Incorporation of biotinyl groups into molecules.

Bleomycin - A complex of related glycopeptide antibiotics from Streptomyces verticillus consisting of bleomycin A2 and B2. It inhibits DNA metabolism and is used as an antineoplastic, especially for solid tumors.

Blood Donation - Voluntary giving of BLOOD.

Blood Proteins - Proteins that are present in blood serum, including SERUM ALBUMIN; BLOOD COAGULATION FACTORS; and many other types of proteins.

Bromelains - Protein-digesting and milk-clotting enzymes found in PINEAPPLE fruit juice and stem tissue. Enzymes from the two sources are distinguished as fruit bromelain and stem bromelain. This enzyme was formerly listed as EC 3.4.22.4.

Brompheniramine - Histamine H1 antagonist used in treatment of allergies, rhinitis, and urticaria.

Calcifediol - The major circulating metabolite of VITAMIN D3. It is produced in the LIVER and is the best indicator of the body's vitamin D stores. It is effective in the treatment of RICKETS and OSTEOMALACIA, both in azotemic and non-azotemic patients. Calcifediol also has mineralizing properties.

Calcitriol - The physiologically active form of vitamin D. It is formed primarily in the kidney by enzymatic hydroxylation of 25-hydroxycholecalciferol (CALCIFEDIOL). Its production is stimulated by low blood calcium levels and parathyroid hormone. Calcitriol increases intestinal absorption of calcium and phosphorus, and in concert with parathyroid hormone increases bone resorption.

Carbonyl Reductase (NADPH) - NADPH-dependent reductase that catalyzes the reduction of many carbonyl compounds including QUINONES; PROSTAGLANDINS; and XENOBIOTICS.

Carboplatin - An organoplatinum compound that possesses antineoplastic activity.

Carboxypeptidase B2 - A carboxypeptidase that removes C-terminal lysine or arginine from peptides and proteins. Carboxypeptidase B2 (CPB2) is released into the circulation as a proenzyme which is activated by the THROMBIN-THROMBOMODULIN complex. Activated CPB2 is involved in modulating a variety of processes by cleaving and inactivating various circulating proteins and peptides that are its substrates including FIBRIN; KININS; and ANAPHYLATOXINS.

Carmustine - A cell-cycle phase nonspecific alkylating antineoplastic agent. It is used in the treatment of brain tumors and various other malignant neoplasms. (From Martindale, The Extra Pharmacopoeia, 30th ed, p462) This substance may reasonably be anticipated to be a carcinogen according to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985). (From Merck Index, 11th ed)

Catalase - An oxidoreductase that catalyzes the conversion of HYDROGEN PEROXIDE to water and oxygen. It is present in many animal cells. A deficiency of this enzyme results in ACATALASIA.

Cell Membrane - The lipid- and protein-containing, selectively permeable membrane that surrounds the cytoplasm in prokaryotic and eukaryotic cells.

Cetirizine - A potent second-generation histamine H1 antagonist that is effective in the treatment of allergic rhinitis, chronic urticaria, and pollen-induced asthma. Unlike many traditional antihistamines, it does not cause drowsiness or anticholinergic side effects.

Chlorambucil - A nitrogen mustard alkylating agent used as antineoplastic for chronic lymphocytic leukemia, Hodgkin's disease, and others. Although it is less toxic than most other nitrogen mustards, it has been listed as a known carcinogen in the Fourth Annual Report on Carcinogens (NTP 85-002, 1985). (Merck Index, 11th ed)

Chlorpheniramine - A histamine H1 antagonist used in allergic reactions, hay fever, rhinitis, urticaria, and asthma. It has also been used in veterinary applications. One of the most widely used of the classical antihistaminics, it generally causes less drowsiness and sedation than PROMETHAZINE.

Cholecalciferol - Derivative of 7-dehydroxycholesterol formed by ULTRAVIOLET RAYS breaking of the C9-C10 bond. It differs from ERGOCALCIFEROL in having a single bond between C22 and C23 and lacking a methyl group at C24.

Chromomycin A3 - Glycosidic antibiotic from Streptomyces griseus used as a fluorescent stain of DNA and as an antineoplastic agent.

Chymases - A family of neutral serine proteases with CHYMOTRYPSIN-like activity. Chymases are primarily found in the SECRETORY GRANULES of MAST CELLS and are released during mast cell degranulation.

Chymopapain - A cysteine endopeptidase isolated from papaya latex. Preferential cleavage at glutamic and aspartic acid residues. EC 3.4.22.6.

Chymotrypsin - A serine endopeptidase secreted by the pancreas as its zymogen, CHYMOTRYPSINOGEN and carried in the pancreatic juice to the duodenum where it is activated by TRYPSIN. It selectively cleaves aromatic amino acids on the carboxyl side.

Chymotrypsinogen - A serine endopeptidase secreted by the pancreas as its zymogen, CHYMOTRYPSINOGEN and carried in the pancreatic juice to the duodenum where it is activated by TRYPSIN. It selectively cleaves aromatic amino acids on the carboxyl side.

Cinnarizine - A piperazine derivative having histamine H1-receptor and calcium-channel blocking activity with vasodilating and antiemetic properties but it induces PARKINSONIAN DISORDERS.

Cisplatin - An inorganic and water-soluble platinum complex. After undergoing hydrolysis, it reacts with DNA to produce both intra and interstrand crosslinks. These crosslinks appear to impair replication and transcription of DNA. The cytotoxicity of cisplatin correlates with cellular arrest in the G2 phase of the cell cycle.

Clemastine - A histamine H1 antagonist used as the hydrogen fumarate in hay fever, rhinitis, allergic skin conditions, and pruritus. It causes drowsiness.

Complement C1 Inhibitor Protein - An endogenous 105-kDa plasma glycoprotein produced primarily by the LIVER and MONOCYTES. It inhibits a broad spectrum of proteases, including the COMPLEMENT C1R and the COMPLEMENT C1S proteases of the CLASSICAL COMPLEMENT PATHWAY, and the MANNOSE-BINDING PROTEIN-ASSOCIATED SERINE PROTEASES. C1-INH-deficient individuals suffer from HEREDITARY ANGIOEDEMA TYPES I AND II.

Coronavirus 3C Proteases - 3C proteases that occur in species of CORONAVIRIDAE.

Curing Lights, Dental - Light sources used to activate polymerization of light-cured DENTAL CEMENTS and DENTAL RESINS. Degree of cure and bond strength depends on exposure time, wavelength, and intensity of the curing light.

Cyclizine - A histamine H1 antagonist given by mouth or parenterally for the control of postoperative and drug-induced vomiting and in motion sickness. (From Martindale, The Extra Pharmacopoeia, 30th ed, p935)

Cyclophosphamide - Precursor of an alkylating nitrogen mustard antineoplastic and immunosuppressive agent that must be activated in the LIVER to form the active aldophosphamide. It has been used in the treatment of LYMPHOMA and LEUKEMIA. Its side effect, ALOPECIA, has been used for defleecing sheep. Cyclophosphamide may also cause sterility, birth defects, mutations, and cancer.

Cyproheptadine - A serotonin antagonist and a histamine H1 blocker used as antipruritic, appetite stimulant, antiallergic, and for the post-gastrectomy dumping syndrome, etc.

Cytarabine - A pyrimidine nucleoside analog that is used mainly in the treatment of leukemia, especially acute non-lymphoblastic leukemia. Cytarabine is an antimetabolite antineoplastic agent that inhibits the synthesis of DNA. Its actions are specific for the S phase of the cell cycle. It also has antiviral and immunosuppressant properties. (From Martindale, The Extra Pharmacopoeia, 30th ed, p472)

Dacarbazine - An antineoplastic agent. It has significant activity against melanomas. (from Martindale, The Extra Pharmacopoeia, 31st ed, p564)

Dactinomycin - A compound composed of a two CYCLIC PEPTIDES attached to a phenoxazine that is derived from STREPTOMYCES parvullus. It binds to DNA and inhibits RNA synthesis (transcription), with chain elongation more sensitive than initiation, termination, or release. As a result of impaired mRNA production, protein synthesis also declines after dactinomycin therapy. (From AMA Drug Evaluations Annual, 1993, p2015)

Daunorubicin - A very toxic anthracycline aminoglycoside antineoplastic isolated from Streptomyces peucetius and others, used in treatment of LEUKEMIA and other NEOPLASMS.

Deferoxamine - Natural product isolated from Streptomyces pilosus. It forms iron complexes and is used as a chelating agent, particularly in the mesylate form.

Demecolcine - An alkaloid isolated from Colchicum autumnale L. and used as an antineoplastic.

Dendritic Cells - Specialized cells of the hematopoietic system that have branch-like extensions. They are found throughout the lymphatic system, and in non-lymphoid tissues such as SKIN and the epithelia of the intestinal, respiratory, and reproductive tracts. They trap and process ANTIGENS, and present them to T-CELLS, thereby stimulating CELL-MEDIATED IMMUNITY. They are different from the non-hematopoietic FOLLICULAR DENDRITIC CELLS, which have a similar morphology and immune system function, but with respect to humoral immunity (ANTIBODY PRODUCTION).

Deoxyadenosines - Adenosine molecules which can be substituted in any position, but are lacking one hydroxyl group in the ribose part of the molecule.

Dexrazoxane - The (+)-enantiomorph of razoxane.

Diabetes Mellitus, Experimental - Diabetes mellitus induced experimentally by administration of various diabetogenic agents or by PANCREATECTOMY.

Dihydrotachysterol - A VITAMIN D that can be regarded as a reduction product of vitamin D2.

Dimenhydrinate - A drug combination that contains diphenhydramine and theophylline. It is used for treating VERTIGO, MOTION SICKNESS, and NAUSEA associated with PREGNANCY.

Dimethindene - A histamine H1 antagonist. It is used in hypersensitivity reactions, in rhinitis, for pruritus, and in some common cold remedies.

Diphenhydramine - A histamine H1 antagonist used as an antiemetic, antitussive, for dermatoses and pruritus, for hypersensitivity reactions, as a hypnotic, an antiparkinson, and as an ingredient in common cold preparations. It has some undesired antimuscarinic and sedative effects.

Domperidone - A specific blocker of dopamine receptors. It speeds gastrointestinal peristalsis, causes prolactin release, and is used as antiemetic and tool in the study of dopaminergic mechanisms.

Doxorubicin - Antineoplastic antibiotic obtained from Streptomyces peucetius. It is a hydroxy derivative of DAUNORUBICIN.

Doxylamine - Histamine H1 antagonist with pronounced sedative properties. It is used in allergies and as an antitussive, antiemetic, and hypnotic. Doxylamine has also been administered in veterinary applications and was formerly used in PARKINSONISM.

Epirubicin - An anthracycline which is the 4'-epi-isomer of doxorubicin. The compound exerts its antitumor effects by interference with the synthesis and function of DNA.

Epoprostenol - A prostaglandin that is a powerful vasodilator and inhibits platelet aggregation. It is biosynthesized enzymatically from PROSTAGLANDIN ENDOPEROXIDES in human vascular tissue. The sodium salt has been also used to treat primary pulmonary hypertension (HYPERTENSION, PULMONARY).

Erythropoietin - Glycoprotein hormone, secreted chiefly by the KIDNEY in the adult and the LIVER in the FETUS, that acts on erythroid stem cells of the BONE MARROW to stimulate proliferation and differentiation.

Esculin - A derivative of COUMARIN with molecular formula C15H16O9.

Estramustine - A nitrogen mustard linked to estradiol, usually as phosphate; used to treat prostatic neoplasms; also has radiation protective properties.

Ethamsylate - Benzenesulfonate derivative used as a systemic hemostatic.

Etoposide - A semisynthetic derivative of PODOPHYLLOTOXIN that exhibits antitumor activity. Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA. This complex induces breaks in double stranded DNA and prevents repair by topoisomerase II binding. Accumulated breaks in DNA prevent entry into the mitotic phase of cell division, and lead to cell death. Etoposide acts primarily in the G2 and S phases of the cell cycle.

Factor IX - Storage-stable blood coagulation factor acting in the intrinsic pathway of blood coagulation. Its activated form, IXa, forms a complex with factor VIII and calcium on platelet factor 3 to activate factor X to Xa. Deficiency of factor IX results in HEMOPHILIA B (Christmas Disease).

Factor VIII - Factor VIII of blood coagulation. Antihemophilic factor that is part of the factor VIII/von Willebrand factor complex. Factor VIII is produced in the liver and acts in the intrinsic pathway of blood coagulation. It serves as a cofactor in factor X activation and this action is markedly enhanced by small amounts of thrombin.

Factor VIIIa - Activated form of factor VIII. The B-domain of factor VIII is proteolytically cleaved by thrombin to form factor VIIIa. Factor VIIIa exists as a non-covalent dimer in a metal-linked (probably calcium) complex and functions as a cofactor in the enzymatic activation of factor X by factor IXa. Factor VIIIa is similar in structure and generation to factor Va.

Factor Xa - Activated form of factor X that participates in both the intrinsic and extrinsic pathways of blood coagulation. It catalyzes the conversion of prothrombin to thrombin in conjunction with other cofactors.

Factor Xa Inhibitors - Endogenous factors and drugs that inhibit or block the activity of FACTOR XA.

Factor XI - Stable blood coagulation factor involved in the intrinsic pathway. The activated form XIa activates factor IX to IXa. Deficiency of factor XI is often called hemophilia C.

Factor XI Deficiency - A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia.

Factor XIIIa - Activated form of FACTOR XIII, a transglutaminase, which stabilizes the formation of the fibrin polymer (clot) culminating the blood coagulation cascade.

Fatty Acid-Binding Proteins - Intracellular proteins that reversibly bind hydrophobic ligands including: saturated and unsaturated FATTY ACIDS; EICOSANOIDS; and RETINOIDS. They are considered a highly conserved and ubiquitously expressed family of proteins that may play a role in the metabolism of LIPIDS.

Feline Panleukopenia - A highly contagious DNA virus infection of the cat family, characterized by fever, enteritis and bone marrow changes. It is also called feline ataxia, feline agranulocytosis, feline infectious enteritis, cat fever, cat plague, and show fever. It is caused by FELINE PANLEUKOPENIA VIRUS or the closely related MINK ENTERITIS VIRUS or CANINE PARVOVIRUS.

Fibrin Clot Lysis Time - A measurement of the time needed for FIBRINOLYSIS to occur.

Fibrinolysis - The natural enzymatic dissolution of FIBRIN.

Flavin Mononucleotide - A coenzyme for a number of oxidative enzymes including NADH DEHYDROGENASE. It is the principal form in which RIBOFLAVIN is found in cells and tissues.

Floxuridine - An antineoplastic antimetabolite that is metabolized to fluorouracil when administered by rapid injection; when administered by slow, continuous, intra-arterial infusion, it is converted to floxuridine monophosphate. It has been used to treat hepatic metastases of gastrointestinal adenocarcinomas and for palliation in malignant neoplasms of the liver and gastrointestinal tract.

Fluorouracil - A pyrimidine analog that is an antineoplastic antimetabolite. It interferes with DNA synthesis by blocking the THYMIDYLATE SYNTHETASE conversion of deoxyuridylic acid to thymidylic acid.

Folate Receptor 2 - A subtype of GPI-anchored folate receptors that is expressed in PLACENTA and hematopoietic cells.

Folic Acid - A member of the vitamin B family that stimulates the hematopoietic system. It is present in the liver and kidney and is found in mushrooms, spinach, yeast, green leaves, and grasses (POACEAE). Folic acid is used in the treatment and prevention of folate deficiencies and megaloblastic anemia.

Folic Acid Antagonists - Inhibitors of the enzyme, dihydrofolate reductase (TETRAHYDROFOLATE DEHYDROGENASE), which converts dihydrofolate (FH2) to tetrahydrofolate (FH4). They are frequently used in cancer chemotherapy. (From AMA, Drug Evaluations Annual, 1994, p2033)

Folic Acid Deficiency - A nutritional condition produced by a deficiency of FOLIC ACID in the diet. Many plant and animal tissues contain folic acid, abundant in green leafy vegetables, yeast, liver, and mushrooms but destroyed by long-term cooking. Alcohol interferes with its intermediate metabolism and absorption. Folic acid deficiency may develop in long-term anticonvulsant therapy or with use of oral contraceptives. This deficiency causes anemia, macrocytic anemia, and megaloblastic anemia. It is indistinguishable from vitamin B 12 deficiency in peripheral blood and bone marrow findings, but the neurologic lesions seen in B 12 deficiency do not occur. (Merck Manual, 16th ed)

Folic Acid Transporters - Proteins involved in the transport of FOLIC ACID and folate derivatives across the CELLULAR MEMBRANE.

Fursultiamin - Compound used for therapy of thiamine deficiency. It has also been suggested for several non-deficiency disorders but has not yet proven useful.

Goserelin - A synthetic long-acting agonist of GONADOTROPIN-RELEASING HORMONE. Goserelin is used in treatments of malignant NEOPLASMS of the prostate, uterine fibromas, and metastatic breast cancer.

Granisetron - A serotonin receptor (5HT-3 selective) antagonist that has been used as an antiemetic for cancer chemotherapy patients.

Granuloma, Plasma Cell - A slow-growing benign pseudotumor in which plasma cells greatly outnumber the inflammatory cells.

Hemophilia B - A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008)

Hydroxocobalamin - Injectable form of VITAMIN B 12 that has been used therapeutically to treat VITAMIN B 12 DEFICIENCY.

Hydroxyethyl Starch Derivatives - Starches that have been chemically modified so that a percentage of OH groups are substituted with 2-hydroxyethyl ether groups.

Hydroxyurea - An antineoplastic agent that inhibits DNA synthesis through the inhibition of ribonucleoside diphosphate reductase.

Hypoprothrombinemias - Absence or reduced levels of PROTHROMBIN in the blood.

Idarubicin - An orally administered anthracycline antineoplastic. The compound has shown activity against BREAST NEOPLASMS; LYMPHOMA; and LEUKEMIA.

Ifosfamide - Positional isomer of CYCLOPHOSPHAMIDE which is active as an alkylating agent and an immunosuppressive agent.

Interleukin-6 - A cytokine that stimulates the growth and differentiation of B-LYMPHOCYTES and is also a growth factor for HYBRIDOMAS and plasmacytomas. It is produced by many different cells including T-LYMPHOCYTES; MONOCYTES; and FIBROBLASTS.

Ketotifen - A cycloheptathiophene blocker of histamine H1 receptors and release of inflammatory mediators. It has been proposed for the treatment of asthma, rhinitis, skin allergies, and anaphylaxis.

Leukemia, Plasma Cell - A rare, aggressive variant of MULTIPLE MYELOMA characterized by the circulation of excessive PLASMA CELLS in the peripheral blood. It can be a primary manifestation of multiple myeloma or develop as a terminal complication during the disease.

Lomustine - An alkylating agent of value against both hematologic malignancies and solid tumors.

Mannomustine - Nitrogen mustard derivative alkylating agent used as antineoplastic. It causes severe bone marrow depression and is a powerful vesicant.

Maple Syrup Urine Disease - An autosomal recessive inherited disorder with multiple forms of phenotypic expression, caused by a defect in the oxidative decarboxylation of branched-chain amino acids (AMINO ACIDS, BRANCHED-CHAIN). These metabolites accumulate in body fluids and render a maple syrup odor. The disease is divided into classic, intermediate, intermittent, and thiamine responsive subtypes. The classic form presents in the first week of life with ketoacidosis, hypoglycemia, emesis, neonatal seizures, and hypertonia. The intermediate and intermittent forms present in childhood or later with acute episodes of ataxia and vomiting. (From Adams et al., Principles of Neurology, 6th ed, p936)

Mechlorethamine - A biologic alkylating agent that exerts its cytotoxic effects by forming DNA ADDUCTS and DNA interstrand crosslinks, thereby inhibiting rapidly proliferating cells. The hydrochloride is an antineoplastic agent used to treat HODGKIN DISEASE and LYMPHOMA.

Melphalan - An alkylating nitrogen mustard that is used as an antineoplastic in the form of the levo isomer - MELPHALAN, the racemic mixture - MERPHALAN, and the dextro isomer - MEDPHALAN; toxic to bone marrow, but little vesicant action; potential carcinogen.

Mercaptopurine - An antimetabolite antineoplastic agent with immunosuppressant properties. It interferes with nucleic acid synthesis by inhibiting purine metabolism and is used, usually in combination with other drugs, in the treatment of or in remission maintenance programs for leukemia.

Methapyrilene - Histamine H1 antagonist with sedative action used as a hypnotic and in allergies.

Methotrexate - An antineoplastic antimetabolite with immunosuppressant properties. It is an inhibitor of TETRAHYDROFOLATE DEHYDROGENASE and prevents the formation of tetrahydrofolate, necessary for synthesis of thymidylate, an essential component of DNA.

Metoclopramide - A dopamine D2 antagonist that is used as an antiemetic.

Mitobronitol - Brominated analog of MANNITOL which is an antineoplastic agent appearing to act as an alkylating agent.

Mitochondrial ADP, ATP Translocases - A class of nucleotide translocases found abundantly in mitochondria that function as integral components of the inner mitochondrial membrane. They facilitate the exchange of ADP and ATP between the cytosol and the mitochondria, thereby linking the subcellular compartments of ATP production to those of ATP utilization.

Mitoguazone - Antineoplastic agent effective against myelogenous leukemia in experimental animals. Also acts as an inhibitor of animal S-adenosylmethionine decarboxylase.

Mitolactol - Alkylating antineoplastic toxic to bone marrow; used in breast cancer, also in combination with other drugs.

Mitomycin - An antineoplastic antibiotic produced by Streptomyces caespitosus. It is one of the bi- or tri-functional ALKYLATING AGENTS causing cross-linking of DNA and inhibition of DNA synthesis.

Mitomycins - A group of methylazirinopyrroloindolediones obtained from certain Streptomyces strains. They are very toxic antibiotics used as ANTINEOPLASTIC AGENTS in some solid tumors. PORFIROMYCIN and MITOMYCIN are the most useful members of the group.

Mitotane - A derivative of the insecticide DICHLORODIPHENYLDICHLOROETHANE that specifically inhibits cells of the adrenal cortex and their production of hormones. It is used to treat adrenocortical tumors and causes CNS damage, but no bone marrow depression.

Mitoxantrone - An anthracenedione-derived antineoplastic agent.

Mopidamol - A phosphodiesterase inhibitor which inhibits platelet aggregation. Formerly used as an antineoplastic.

Multiple Myeloma - A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY.

Myoclonic Epilepsies, Progressive - A heterogeneous group of primarily familial EPILEPSY disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME.

NAD - A coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. It is found widely in nature and is involved in numerous enzymatic reactions in which it serves as an electron carrier by being alternately oxidized (NAD+) and reduced (NADH). (Dorland, 27th ed)

Neoplasms, Plasma Cell - Neoplasms associated with a proliferation of a single clone of PLASMA CELLS and characterized by the secretion of PARAPROTEINS.

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.

Nimustine - Antineoplastic agent especially effective against malignant brain tumors. The resistance which brain tumor cells acquire to the initial effectiveness of this drug can be partially overcome by the simultaneous use of membrane-modifying agents such as reserpine, calcium antagonists such as nicardipine or verapamil, or the calmodulin inhibitor, trifluoperazine. The drug has also been used in combination with other antineoplastic agents or with radiotherapy for the treatment of various neoplasms.

Ondansetron - A competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties.

Orbital Pseudotumor - A nonspecific tumor-like inflammatory lesion in the ORBIT of the eye. It is usually composed of mature LYMPHOCYTES; PLASMA CELLS; MACROPHAGES; LEUKOCYTES with varying degrees of FIBROSIS. Orbital pseudotumors are often associated with inflammation of the extraocular muscles (ORBITAL MYOSITIS) or inflammation of the lacrimal glands (DACRYOADENITIS).

Pantothenic Acid - A butyryl-beta-alanine that can also be viewed as pantoic acid complexed with BETA ALANINE. It is incorporated into COENZYME A and protects cells against peroxidative damage by increasing the level of GLUTATHIONE.

Paraproteinemias - A group of related diseases characterized by an unbalanced or disproportionate proliferation of immunoglobulin-producing cells, usually from a single clone. These cells frequently secrete a structurally homogeneous immunoglobulin (M-component) and/or an abnormal immunoglobulin.

Partial Thromboplastin Time - The time required for the appearance of FIBRIN strands following the mixing of PLASMA with phospholipid platelet substitute (e.g., crude cephalins, soybean phosphatides). It is a test of the intrinsic pathway (factors VIII, IX, XI, and XII) and the common pathway (fibrinogen, prothrombin, factors V and X) of BLOOD COAGULATION. It is used as a screening test and to monitor HEPARIN therapy.

Penicillinase - A beta-lactamase preferentially cleaving penicillins. (Dorland, 28th ed) EC 3.5.2.-.

Pentostatin - A potent inhibitor of ADENOSINE DEAMINASE. The drug induces APOPTOSIS of LYMPHOCYTES, and is used in the treatment of many lymphoproliferative malignancies, particularly HAIRY CELL LEUKEMIA. It is also synergistic with some other antineoplastic agents and has immunosuppressive activity.

Peplomycin - An antineoplastic agent derived from BLEOMYCIN.

Phenindione - An indandione that has been used as an anticoagulant. Phenindione has actions similar to WARFARIN, but it is now rarely employed because of its higher incidence of severe adverse effects. (From Martindale, The Extra Pharmacopoeia, 30th ed, p234)

Pheniramine - One of the HISTAMINE H1 ANTAGONISTS with little sedative action. It is used in treatment of hay fever, rhinitis, allergic dermatoses, and pruritus.

Phenprocoumon - Coumarin derivative that acts as a long acting oral anticoagulant.

Pipobroman - An antineoplastic agent that acts by alkylation.

Plasma - The residual portion of BLOOD that is left after removal of BLOOD CELLS by CENTRIFUGATION without prior BLOOD COAGULATION.

Plasma Cell Granuloma, Pulmonary - A tumor-like inflammatory lesion of the lung that is composed of PLASMA CELLS and fibrous tissue. It is also known as an inflammatory pseudotumor, often with calcification and measuring between 2 and 5 cm in diameter.

Plasma Cells - Specialized forms of antibody-producing B-LYMPHOCYTES. They synthesize and secrete immunoglobulin. They are found only in lymphoid organs and at sites of immune responses and normally do not circulate in the blood or lymph. (Rosen et al., Dictionary of Immunology, 1989, p169 & Abbas et al., Cellular and Molecular Immunology, 2d ed, p20)

Plasma Exchange - Removal of plasma and replacement with various fluids, e.g., fresh frozen plasma, plasma protein fractions (PPF), albumin preparations, dextran solutions, saline. Used in treatment of autoimmune diseases, immune complex diseases, diseases of excess plasma factors, and other conditions.

Plasma Gases - Ionized gases, consisting of free electrons and ionized atoms or molecules which collectively behave differently than gas, solid, or liquid. Plasma gases are used in biomedical fields in surface modification; biological decontamination; dentistry (e.g., PLASMA ARC DENTAL CURING LIGHTS); and in other treatments (e.g., ARGON PLASMA COAGULATION).

Plasma Kallikrein - A peptidohydrolytic enzyme that is formed from PREKALLIKREIN by FACTOR XIIA. It activates FACTOR XII; FACTOR VII; and PLASMINOGEN. It is selective for both ARGININE and to a lesser extent LYSINE bonds. EC 3.4.21.34.

Plasma Membrane Calcium-Transporting ATPases - Calcium-transporting ATPases found on the PLASMA MEMBRANE that catalyze the active transport of CALCIUM from the CYTOPLASM into the extracellular space. They play a role in maintaining a CALCIUM gradient across plasma membrane.

Plasma Membrane Neurotransmitter Transport Proteins - A family of neurotransmitter transporter proteins that facilitate NEUROTRANSMITTER reuptake into PRESYNAPTIC TERMINALS. They may play a role in regulating the intensity and duration of neurotransmission.

Plasma Skin Regeneration - A cosmetic technique that uses PLASMA GASES in therapeutic treatment to help achieve skin REJUVENATION or REGENERATION and delay SKIN AGING.

Plasma Substitutes - Any liquid used to replace blood plasma, usually a saline solution, often with serum albumins, dextrans or other preparations. These substances do not enhance the oxygen- carrying capacity of blood, but merely replace the volume. They are also used to treat dehydration.

Plasma Volume - Volume of PLASMA in the circulation. It is usually measured by INDICATOR DILUTION TECHNIQUES.

Plasmablastic Lymphoma - Malignant lymphoma composed of large B lymphoid cells which have the immunophenotype of plasma cells and a predilection for the ORAL CAVITY.

Plasmacytoma - Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites.

Plasmalogens - GLYCEROPHOSPHOLIPIDS in which one of the two acyl chains is attached to glycerol with an ether alkenyl linkage instead of an ester as with the other glycerophospholipids.

Plasmapheresis - Procedure whereby plasma is separated and extracted from anticoagulated whole blood and the red cells retransfused to the donor. Plasmapheresis is also employed for therapeutic use.

Platelet Membrane Glycoprotein IIb - Platelet membrane glycoprotein IIb is an integrin alpha subunit that heterodimerizes with INTEGRIN BETA3 to form PLATELET GLYCOPROTEIN GPIIB-IIIA COMPLEX. It is synthesized as a single polypeptide chain which is then postranslationally cleaved and processed into two disulfide-linked subunits of approximately 18 and 110 kDa in size.

Platelet-Rich Plasma - A preparation consisting of PLATELETS concentrated in a limited volume of PLASMA. This is used in various surgical tissue regeneration procedures where the GROWTH FACTORS in the platelets enhance wound healing and regeneration.

Plicamycin - A tricyclic pentaglycosidic antibiotic from Streptomyces strains that inhibits RNA and protein synthesis by adhering to DNA. It is used as a fluorescent dye and as an antineoplastic agent, especially in bone and testicular tumors. Plicamycin is also used to reduce hypercalcemia, especially that due to malignancies.

Poly A - A group of adenine ribonucleotides in which the phosphate residues of each adenine ribonucleotide act as bridges in forming diester linkages between the ribose moieties.

Polygeline - A 3.5 per cent colloidal solution containing urea-cross-linked polymerized peptides. It has a molecular weight of approximately 35,000 and is prepared from gelatin and electrolytes. The polymeric solution is used as a plasma expander.

Porfiromycin - Toxic antibiotic of the mitomycin group, obtained from MITOMYCIN and also from Streptomyces ardus and other species. It is proposed as an antineoplastic agent, with some antibiotic properties.

Povidone - A polyvinyl polymer of variable molecular weight; used as suspending and dispersing agent and vehicle for pharmaceuticals; also used as blood volume expander.

Povidone-Iodine - An iodinated polyvinyl polymer used as topical antiseptic in surgery and for skin and mucous membrane infections, also as aerosol. The iodine may be radiolabeled for research purposes.

Prednimustine - Ester of CHLORAMBUCIL and PREDNISOLONE used as a combination alkylating agent and synthetic steroid to treat various leukemias and other neoplasms. It causes gastrointestinal and bone marrow toxicity.

Prekallikrein - A plasma protein which is the precursor of kallikrein. Plasma that is deficient in prekallikrein has been found to be abnormal in thromboplastin formation, kinin generation, evolution of a permeability globulin, and plasmin formation. The absence of prekallikrein in plasma leads to Fletcher factor deficiency, a congenital disease.

Procarbazine - An antineoplastic agent used primarily in combination with mechlorethamine, vincristine, and prednisone (the MOPP protocol) in the treatment of Hodgkin's disease.

Pronase - A proteolytic enzyme obtained from Streptomyces griseus.

Protein Binding - The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments.

Prothrombin - A plasma protein that is the inactive precursor of thrombin. It is converted to thrombin by a prothrombin activator complex consisting of factor Xa, factor V, phospholipid, and calcium ions. Deficiency of prothrombin leads to hypoprothrombinemia.

Prothrombin Time - Clotting time of PLASMA recalcified in the presence of excess TISSUE THROMBOPLASTIN. Factors measured are FIBRINOGEN; PROTHROMBIN; FACTOR V; FACTOR VII; and FACTOR X. It is used for monitoring anticoagulant therapy with COUMARINS.

Pyridoxal Kinase - An enzyme that catalyzes reversibly the phosphorylation of pyridoxal in the presence of ATP with the formation of pyridoxal 5-phosphate and ADP. Pyridoxine, pyridoxamine and various derivatives can also act as acceptors. EC 2.7.1.35.

Pyridoxal Phosphate - This is the active form of VITAMIN B 6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (PYRIDOXAMINE).

Pyridoxaminephosphate Oxidase - An enzyme catalyzing the deamination of pyridoxaminephosphate to pyridoxal phosphate. It is a flavoprotein that also oxidizes pyridoxine-5-phosphate and pyridoxine. EC 1.4.3.5.

Pyridoxic Acid - The catabolic product of most of VITAMIN B 6; (PYRIDOXINE; PYRIDOXAL; and PYRIDOXAMINE) which is excreted in the urine.

Pyridoxine - The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).

Pyrilamine - A histamine H1 antagonist. It has mild hypnotic properties and some local anesthetic action and is used for allergies (including skin eruptions) both parenterally and locally. It is a common ingredient of cold remedies.

Pyrithioxin - A neurotropic agent which reduces permeability of blood-brain barrier to phosphate. It has no vitamin B6 activity.

Razoxane - An antimitotic agent with immunosuppressive properties.

Receptor, PAR-2 - A G-protein-coupled, proteinase-activated receptor that is expressed in a variety of tissues including ENDOTHELIUM; LEUKOCYTES; and the GASTROINTESTINAL TRACT. The receptor is activated by TRYPSIN, which cleaves off the N-terminal peptide from the receptor. The new N-terminal peptide is a cryptic ligand for the receptor. The uncleaved receptor can also be activated by the N-terminal peptide present on the activated THROMBIN RECEPTOR and by small synthetic peptides that contain the unmasked N-terminal sequence.

Receptors, Calcitriol - Proteins, usually found in the cytoplasm, that specifically bind calcitriol, migrate to the nucleus, and regulate transcription of specific segments of DNA with the participation of D receptor interacting proteins (called DRIP). Vitamin D is converted in the liver and kidney to calcitriol and ultimately acts through these receptors.

Receptors, Epoprostenol - Cell surface receptors for EPOPROSTENOL. They are coupled to HETEROTRIMERIC G-PROTEINS.

Receptors, Erythropoietin - Cell surface proteins that bind erythropoietin with high affinity and trigger intracellular changes influencing the behavior of cells.

Receptors, Thrombin - A family of proteinase-activated receptors that are specific for THROMBIN. They are found primarily on PLATELETS and on ENDOTHELIAL CELLS. Activation of thrombin receptors occurs through the proteolytic action of THROMBIN, which cleaves the N-terminal peptide from the receptor to reveal a new N-terminal peptide that is a cryptic ligand for the receptor. The receptors signal through HETEROTRIMERIC GTP-BINDING PROTEINS. Small synthetic peptides that contain the unmasked N-terminal peptide sequence can also activate the receptor in the absence of proteolytic activity.

Renal Plasma Flow - The amount of PLASMA that perfuses the KIDNEYS per unit time, approximately 10% greater than effective renal plasma flow (RENAL PLASMA FLOW, EFFECTIVE). It should be differentiated from the RENAL BLOOD FLOW; (RBF), which refers to the total volume of BLOOD flowing through the renal vasculature, while the renal plasma flow refers to the rate of plasma flow (RPF).

Renal Plasma Flow, Effective - The amount of PLASMA flowing to the parts of the KIDNEY that function in the production of urine. It is the amount of plasma perfusing the KIDNEY TUBULES per unit time, generally measured by P-AMINOHIPPURATE clearance. It should be differentiated from RENAL PLASMA FLOW which is approximately 10% greater than the effective renal plasma flow.

Reticulocytosis - An increase in circulating RETICULOCYTES, which is among the simplest and most reliable signs of accelerated ERYTHROCYTE production. Reticulocytosis occurs during active BLOOD regeneration (stimulation of red bone marrow) and in certain types of ANEMIA, particularly CONGENITAL HEMOLYTIC ANEMIA.

Retinol-Binding Proteins, Plasma - Retinol binding proteins that circulate in the PLASMA. They are members of the lipocalin family of proteins and play a role in the transport of RETINOL from the LIVER to the peripheral tissues. The proteins are usually found in association with TRANSTHYRETIN.

Riboflavin - Nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source is yeast. It occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as FLAVIN MONONUCLEOTIDE and FLAVIN-ADENINE DINUCLEOTIDE.

Riboflavin Deficiency - A dietary deficiency of riboflavin causing a syndrome chiefly marked by cheilitis, angular stomatitis, glossitis associated with a purplish red or magenta-colored tongue that may show fissures, corneal vascularization, dyssebacia, and anemia. (Dorland, 27th ed)

Riboflavin Synthase - An enzyme that catalyzes the formation of riboflavin from two molecules of 6,7-dimethyl-8-ribityllumazine, utilizing a four-carbon fragment from one molecule which is transferred to the second molecule. EC 2.5.1.9.

Semen - The thick, yellowish-white, viscid fluid secretion of male reproductive organs discharged upon ejaculation. In addition to reproductive organ secretions, it contains SPERMATOZOA and their nutrient plasma.

Semustine - 4-Methyl derivative of LOMUSTINE; (CCNU). An antineoplastic agent which functions as an alkylating agent.

Serum Albumin - A major protein in the BLOOD. It is important in maintaining the colloidal osmotic pressure and transporting large organic molecules.

Streptodornase and Streptokinase - A mixture of the enzymes (streptokinase and streptodornase) produced by hemolytic streptococci. It is used topically on surface lesions and by instillation in closed body cavities to remove clotted blood or fibrinous or purulent accumulations. It is also used as a skin test antigen in evaluating generalized cell-mediated immunodeficiency. (Dorland, 27th ed) EC 3.-.

Streptokinase - Streptococcal fibrinolysin . An enzyme produced by hemolytic streptococci. It hydrolyzes amide linkages and serves as an activator of plasminogen. It is used in thrombolytic therapy and is used also in mixtures with streptodornase (STREPTODORNASE AND STREPTOKINASE). EC 3.4.-.

Streptozocin - An antibiotic that is produced by Stretomyces achromogenes. It is used as an antineoplastic agent and to induce diabetes in experimental animals.

Tegafur - Congener of FLUOROURACIL with comparable antineoplastic action. It has been suggested especially for the treatment of breast neoplasms.

Teniposide - A semisynthetic derivative of PODOPHYLLOTOXIN that exhibits antitumor activity. Teniposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA. This complex induces breaks in double stranded DNA and prevents repair by topoisomerase II binding. Accumulated breaks in DNA prevent cells from entering into the mitotic phase of the cell cycle, and lead to cell death. Teniposide acts primarily in the G2 and S phases of the cycle.

Terfenadine - A selective histamine H1-receptor antagonist devoid of central nervous system depressant activity. The drug was used for ALLERGY but withdrawn due to causing LONG QT SYNDROME.

Tetrahydrofolate Dehydrogenase - An enzyme of the oxidoreductase class that catalyzes the reaction 7,8-dihyrofolate and NADPH to yield 5,6,7,8-tetrahydrofolate and NADPH+, producing reduced folate for amino acid metabolism, purine ring synthesis, and the formation of deoxythymidine monophosphate. Methotrexate and other folic acid antagonists used as chemotherapeutic drugs act by inhibiting this enzyme. (Dorland, 27th ed) EC 1.5.1.3.

Thalidomide - A piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn from the market due to teratogenic effects. It has been reintroduced and used for a number of immunological and inflammatory disorders. Thalidomide displays immunosuppressive and anti-angiogenic activity. It inhibits release of TUMOR NECROSIS FACTOR-ALPHA from monocytes, and modulates other cytokine action.

Thiamin Pyrophosphokinase - An enzyme that catalyzes the formation of thiamine pyrophosphate from ATP and thiamine. EC 2.7.6.2.

Thiamine - 3-((4-Amino-2-methyl-5-pyrimidinyl)methyl)-5-(2- hydroxyethyl)-4-methylthiazolium chloride.

Thiamine Deficiency - A nutritional condition produced by a deficiency of THIAMINE in the diet, characterized by anorexia, irritability, and weight loss. Later, patients experience weakness, peripheral neuropathy, headache, and tachycardia. In addition to being caused by a poor diet, thiamine deficiency in the United States most commonly occurs as a result of alcoholism, since ethanol interferes with thiamine absorption. In countries relying on polished rice as a dietary staple, BERIBERI prevalence is very high. (From Cecil Textbook of Medicine, 19th ed, p1171)

Thiamine Monophosphate - Thiamine dihydrogen phosphate ester. The monophosphate ester of thiamine. Synonyms: monophosphothiamine; vitamin B1 monophosphate.

Thiamine Pyrophosphatase - An enzyme that hydrolyzes thiamine pyrophosphate to thiamine monophosphate plus inorganic phosphate. EC 3.6.1.-.

Thiamine Pyrophosphate - The coenzyme form of Vitamin B1 present in many animal tissues. It is a required intermediate in the PYRUVATE DEHYDROGENASE COMPLEX and the KETOGLUTARATE DEHYDROGENASE COMPLEX.

Thiamine Triphosphate - 3-((4-Amino-2-methyl-5-pyrimidinyl)methyl)-4-methyl-5-(4,6,8,8-tetrahydroxy-3,5,7-trioxa-4,6,8-triphosphaoct-1-yl)thiazolium hydroxide, inner salt, P,P',P''-trioxide. The triphosphate ester of thiamine. In Leigh's disease, this compound is present in decreased amounts in the brain due to a metabolic block in its formation.

Thiamin-Triphosphatase - An enzyme present in nerve tissue. It catalyzes reversibly the formation of thiamine diphosphate and orthophosphate from thiamine triphosphate. EC 3.6.1.28.

Thioguanine - An antineoplastic compound which also has antimetabolite action. The drug is used in the therapy of acute leukemia.

Thiotepa - A very toxic alkylating antineoplastic agent also used as an insect sterilant. It causes skin, gastrointestinal, CNS, and bone marrow damage. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), thiotepa may reasonably be anticipated to be a carcinogen (Merck Index, 11th ed).

Thrombin - An enzyme formed from PROTHROMBIN that converts FIBRINOGEN to FIBRIN.

Thrombin Time - Clotting time of PLASMA mixed with a THROMBIN solution. It is a measure of the conversion of FIBRINOGEN to FIBRIN, which is prolonged by AFIBRINOGENEMIA, abnormal fibrinogen, or the presence of inhibitory substances, e.g., fibrin-fibrinogen degradation products, or HEPARIN. BATROXOBIN, a thrombin-like enzyme unaffected by the presence of heparin, may be used in place of thrombin.

Thromboplastin - Constituent composed of protein and phospholipid that is widely distributed in many tissues. It serves as a cofactor with factor VIIa to activate factor X in the extrinsic pathway of blood coagulation.

Ticlopidine - An effective inhibitor of platelet aggregation commonly used in the placement of STENTS in CORONARY ARTERIES.

Tranexamic Acid - Antifibrinolytic hemostatic used in severe hemorrhage.

Triaziquone - Alkylating antineoplastic agent used mainly for ovarian tumors. It is toxic to skin, gastrointestinal tract, bone marrow and kidneys.

Trientine - An ethylenediamine derivative used as stabilizer for EPOXY RESINS, as ampholyte for ISOELECTRIC FOCUSING and as chelating agent for copper in HEPATOLENTICULAR DEGENERATION.

Triethylenemelamine - Toxic alkylating agent used in industry; also as antineoplastic and research tool to produce chromosome aberrations and cancers.

Triethylenephosphoramide - An insect chemosterilant and an antineoplastic agent.

Trimetrexate - A nonclassical folic acid inhibitor through its inhibition of the enzyme dihydrofolate reductase. It is being tested for efficacy as an antineoplastic agent and as an antiparasitic agent against PNEUMOCYSTIS PNEUMONIA in AIDS patients. Myelosuppression is its dose-limiting toxic effect.

Tripelennamine - A histamine H1 antagonist with low sedative action but frequent gastrointestinal irritation. It is used to treat ASTHMA; HAY FEVER; URTICARIA; and RHINITIS; and also in veterinary applications. Tripelennamine is administered by various routes, including topically.

Triprolidine - Histamine H1 antagonist used in allergic rhinitis; ASTHMA; and URTICARIA. It is a component of COUGH and COLD medicines. It may cause drowsiness.

Trypsin - A serine endopeptidase that is formed from TRYPSINOGEN in the pancreas. It is converted into its active form by ENTEROPEPTIDASE in the small intestine. It catalyzes hydrolysis of the carboxyl group of either arginine or lysine. EC 3.4.21.4.

Trypsin Inhibitor, Bowman-Birk Soybean - A low-molecular-weight protein (minimum molecular weight 8000) which has the ability to inhibit trypsin as well as chymotrypsin at independent binding sites. It is characterized by a high cystine content and the absence of glycine.

Trypsin Inhibitor, Kazal Pancreatic - A secreted KAZAL MOTIF-containing serine peptidase inhibitor that inhibits TRYPSIN. It is a protein composed of 56 amino acid residues and is different in amino acid composition and physiological activity from the Kunitz bovine pancreatic trypsin inhibitor (APROTININ). It protects against the trypsin-mediated premature activation of ENZYME PRECURSORS in the PANCREAS. Mutations in the SPINK1 gene are associated with CHRONIC PANCREATITIS.

Trypsin Inhibitor, Kunitz Soybean - A high-molecular-weight protein (approximately 22,500) containing 198 amino acid residues. It is a strong inhibitor of trypsin and human plasmin.

Trypsin Inhibitors - Serine proteinase inhibitors which inhibit trypsin. They may be endogenous or exogenous compounds.

Trypsinogen - The inactive proenzyme of trypsin secreted by the pancreas, activated in the duodenum via cleavage by enteropeptidase. (Stedman, 25th ed)

Uracil Mustard - Nitrogen mustard derivative of URACIL. It is a alkylating antineoplastic agent that is used in lymphatic malignancies, and causes mainly gastrointestinal and bone marrow damage.

Urethane - Antineoplastic agent that is also used as a veterinary anesthetic. It has also been used as an intermediate in organic synthesis. Urethane is suspected to be a carcinogen.

Vidarabine - A nucleoside antibiotic isolated from Streptomyces antibioticus. It has some antineoplastic properties and has broad spectrum activity against DNA viruses in cell cultures and significant antiviral activity against infections caused by a variety of viruses such as the herpes viruses, the VACCINIA VIRUS and varicella zoster virus.

Vidarabine Phosphate - An adenosine monophosphate analog in which ribose is replaced by an arabinose moiety. It is the monophosphate ester of VIDARABINE with antiviral and possibly antineoplastic properties.

Vinblastine - Antitumor alkaloid isolated from Vinca rosea. (Merck, 11th ed.)

Vincamine - A major alkaloid of Vinca minor L., Apocynaceae. It has been used therapeutically as a vasodilator and antihypertensive agent, particularly in cerebrovascular disorders.

Vincristine - An antitumor alkaloid isolated from VINCA ROSEA. (Merck, 11th ed.)

Vindesine - Vinblastine derivative with antineoplastic activity against CANCER. Major side effects are myelosuppression and neurotoxicity. Vindesine is used extensively in chemotherapy protocols (ANTINEOPLASTIC COMBINED CHEMOTHERAPY PROTOCOLS).

Vitamin B 6 Deficiency - A nutritional condition produced by a deficiency of VITAMIN B 6 in the diet, characterized by dermatitis, glossitis, cheilosis, and stomatitis. Marked deficiency causes irritability, weakness, depression, dizziness, peripheral neuropathy, and seizures. In infants and children typical manifestations are diarrhea, anemia, and seizures. Deficiency can be caused by certain medications, such as isoniazid.

Vitamin D3 24-Hydroxylase - A cytochrome P-450 enzyme that has specificity for CHOLECALCIFEROL (Vitamin D3). It hydroxylates the molecule at carbon position 24.

von Willebrand Factor - A high-molecular-weight plasma protein, produced by endothelial cells and megakaryocytes, that is part of the factor VIII/von Willebrand factor complex. The von Willebrand factor has receptors for collagen, platelets, and ristocetin activity as well as the immunologically distinct antigenic determinants. It functions in adhesion of platelets to collagen and hemostatic plug formation. The prolonged bleeding time in VON WILLEBRAND DISEASES is due to the deficiency of this factor.

Warfarin - An anticoagulant that acts by inhibiting the synthesis of vitamin K-dependent coagulation factors. Warfarin is indicated for the prophylaxis and/or treatment of venous thrombosis and its extension, pulmonary embolism, and atrial fibrillation with embolization. It is also used as an adjunct in the prophylaxis of systemic embolism after myocardial infarction. Warfarin is also used as a rodenticide.

Zinostatin - An enediyne that alkylates DNA and RNA like MITOMYCIN does, so it is cytotoxic.

Instructional Notations

7th Character Note

Certain ICD-10-CM categories have applicable 7th characters. The applicable 7th character is required for all codes within the category, or as the notes in the Tabular List instruct. The 7th character must always be the 7th character in the data field. If a code that requires a 7th character is not 6 characters, a placeholder X must be used to fill in the empty characters.

  • The appropriate 7th character is to be added to each code from category T45

7th Character

Indicates that a seventh character is to be assigned to codes in a subcategory.

  • A - initial encounter
  • D - subsequent encounter
  • S - sequela
  • Injury, poisoning and certain other consequences of external causes (S00–T88)

    • Poisoning by, adverse effect of and underdosing of drugs, medicaments and biological substances (T36-T50)

        • Poisoning by, adverse effect of and underdosing of primarily systemic and hematological agents, not elsewhere classified (T45)

        • T45 Poisoning by, adverse effect of and underdosing of primarily systemic and hematological agents, not elsewhere classified
        • T45.0 Poisoning by, adverse effect of and underdosing of antiallergic and antiemetic drugs
        • T45.0X Poisoning by, adverse effect of and underdosing of antiallergic and antiemetic drugs
        • T45.0X1 Poisoning by antiallergic and antiemetic drugs, accidental (unintentional)
        • T45.0X1A Poisoning by antiallergic and antiemetic drugs, accidental (unintentional), initial encounter
        • T45.0X1D Poisoning by antiallergic and antiemetic drugs, accidental (unintentional), subsequent encounter
        • T45.0X1S Poisoning by antiallergic and antiemetic drugs, accidental (unintentional), sequela
        • T45.0X2 Poisoning by antiallergic and antiemetic drugs, intentional self-harm
        • T45.0X2A Poisoning by antiallergic and antiemetic drugs, intentional self-harm, initial encounter
        • T45.0X2D Poisoning by antiallergic and antiemetic drugs, intentional self-harm, subsequent encounter
        • T45.0X2S Poisoning by antiallergic and antiemetic drugs, intentional self-harm, sequela
        • T45.0X3 Poisoning by antiallergic and antiemetic drugs, assault
        • T45.0X3A Poisoning by antiallergic and antiemetic drugs, assault, initial encounter
        • T45.0X3D Poisoning by antiallergic and antiemetic drugs, assault, subsequent encounter
        • T45.0X3S Poisoning by antiallergic and antiemetic drugs, assault, sequela
        • T45.0X4 Poisoning by antiallergic and antiemetic drugs, undetermined
        • T45.0X4A Poisoning by antiallergic and antiemetic drugs, undetermined, initial encounter
        • T45.0X4D Poisoning by antiallergic and antiemetic drugs, undetermined, subsequent encounter
        • T45.0X4S Poisoning by antiallergic and antiemetic drugs, undetermined, sequela
        • T45.0X5 Adverse effect of antiallergic and antiemetic drugs
        • T45.0X5A Adverse effect of antiallergic and antiemetic drugs, initial encounter
        • T45.0X5D Adverse effect of antiallergic and antiemetic drugs, subsequent encounter
        • T45.0X5S Adverse effect of antiallergic and antiemetic drugs, sequela
        • T45.0X6 Underdosing of antiallergic and antiemetic drugs
        • T45.0X6A Underdosing of antiallergic and antiemetic drugs, initial encounter
        • T45.0X6D Underdosing of antiallergic and antiemetic drugs, subsequent encounter
        • T45.0X6S Underdosing of antiallergic and antiemetic drugs, sequela
        • T45.1 Poisoning by, adverse effect of and underdosing of antineoplastic and immunosuppressive drugs
        • T45.1X Poisoning by, adverse effect of and underdosing of antineoplastic and immunosuppressive drugs
        • T45.1X1 Poisoning by antineoplastic and immunosuppressive drugs, accidental (unintentional)
        • T45.1X1A Poisoning by antineoplastic and immunosuppressive drugs, accidental (unintentional), initial encounter
        • T45.1X1D Poisoning by antineoplastic and immunosuppressive drugs, accidental (unintentional), subsequent encounter
        • T45.1X1S Poisoning by antineoplastic and immunosuppressive drugs, accidental (unintentional), sequela
        • T45.1X2 Poisoning by antineoplastic and immunosuppressive drugs, intentional self-harm
        • T45.1X2A Poisoning by antineoplastic and immunosuppressive drugs, intentional self-harm, initial encounter
        • T45.1X2D Poisoning by antineoplastic and immunosuppressive drugs, intentional self-harm, subsequent encounter
        • T45.1X2S Poisoning by antineoplastic and immunosuppressive drugs, intentional self-harm, sequela
        • T45.1X3 Poisoning by antineoplastic and immunosuppressive drugs, assault
        • T45.1X3A Poisoning by antineoplastic and immunosuppressive drugs, assault, initial encounter
        • T45.1X3D Poisoning by antineoplastic and immunosuppressive drugs, assault, subsequent encounter
        • T45.1X3S Poisoning by antineoplastic and immunosuppressive drugs, assault, sequela
        • T45.1X4 Poisoning by antineoplastic and immunosuppressive drugs, undetermined
        • T45.1X4A Poisoning by antineoplastic and immunosuppressive drugs, undetermined, initial encounter
        • T45.1X4D Poisoning by antineoplastic and immunosuppressive drugs, undetermined, subsequent encounter
        • T45.1X4S Poisoning by antineoplastic and immunosuppressive drugs, undetermined, sequela
        • T45.1X5 Adverse effect of antineoplastic and immunosuppressive drugs
        • T45.1X5A Adverse effect of antineoplastic and immunosuppressive drugs, initial encounter
        • T45.1X5D Adverse effect of antineoplastic and immunosuppressive drugs, subsequent encounter
        • T45.1X5S Adverse effect of antineoplastic and immunosuppressive drugs, sequela
        • T45.1X6 Underdosing of antineoplastic and immunosuppressive drugs
        • T45.1X6A Underdosing of antineoplastic and immunosuppressive drugs, initial encounter
        • T45.1X6D Underdosing of antineoplastic and immunosuppressive drugs, subsequent encounter
        • T45.1X6S Underdosing of antineoplastic and immunosuppressive drugs, sequela
        • T45.2 Poisoning by, adverse effect of and underdosing of vitamins
        • T45.2X Poisoning by, adverse effect of and underdosing of vitamins
        • T45.2X1 Poisoning by vitamins, accidental (unintentional)
        • T45.2X1A Poisoning by vitamins, accidental (unintentional), initial encounter
        • T45.2X1D Poisoning by vitamins, accidental (unintentional), subsequent encounter
        • T45.2X1S Poisoning by vitamins, accidental (unintentional), sequela
        • T45.2X2 Poisoning by vitamins, intentional self-harm
        • T45.2X2A Poisoning by vitamins, intentional self-harm, initial encounter
        • T45.2X2D Poisoning by vitamins, intentional self-harm, subsequent encounter
        • T45.2X2S Poisoning by vitamins, intentional self-harm, sequela
        • T45.2X3 Poisoning by vitamins, assault
        • T45.2X3A Poisoning by vitamins, assault, initial encounter
        • T45.2X3D Poisoning by vitamins, assault, subsequent encounter
        • T45.2X3S Poisoning by vitamins, assault, sequela
        • T45.2X4 Poisoning by vitamins, undetermined
        • T45.2X4A Poisoning by vitamins, undetermined, initial encounter
        • T45.2X4D Poisoning by vitamins, undetermined, subsequent encounter
        • T45.2X4S Poisoning by vitamins, undetermined, sequela
        • T45.2X5 Adverse effect of vitamins
        • T45.2X5A Adverse effect of vitamins, initial encounter
        • T45.2X5D Adverse effect of vitamins, subsequent encounter
        • T45.2X5S Adverse effect of vitamins, sequela
        • T45.2X6 Underdosing of vitamins
        • T45.2X6A Underdosing of vitamins, initial encounter
        • T45.2X6D Underdosing of vitamins, subsequent encounter
        • T45.2X6S Underdosing of vitamins, sequela
        • T45.3 Poisoning by, adverse effect of and underdosing of enzymes
        • T45.3X Poisoning by, adverse effect of and underdosing of enzymes
        • T45.3X1 Poisoning by enzymes, accidental (unintentional)
        • T45.3X1A Poisoning by enzymes, accidental (unintentional), initial encounter
        • T45.3X1D Poisoning by enzymes, accidental (unintentional), subsequent encounter
        • T45.3X1S Poisoning by enzymes, accidental (unintentional), sequela
        • T45.3X2 Poisoning by enzymes, intentional self-harm
        • T45.3X2A Poisoning by enzymes, intentional self-harm, initial encounter
        • T45.3X2D Poisoning by enzymes, intentional self-harm, subsequent encounter
        • T45.3X2S Poisoning by enzymes, intentional self-harm, sequela
        • T45.3X3 Poisoning by enzymes, assault
        • T45.3X3A Poisoning by enzymes, assault, initial encounter
        • T45.3X3D Poisoning by enzymes, assault, subsequent encounter
        • T45.3X3S Poisoning by enzymes, assault, sequela
        • T45.3X4 Poisoning by enzymes, undetermined
        • T45.3X4A Poisoning by enzymes, undetermined, initial encounter
        • T45.3X4D Poisoning by enzymes, undetermined, subsequent encounter
        • T45.3X4S Poisoning by enzymes, undetermined, sequela
        • T45.3X5 Adverse effect of enzymes
        • T45.3X5A Adverse effect of enzymes, initial encounter
        • T45.3X5D Adverse effect of enzymes, subsequent encounter
        • T45.3X5S Adverse effect of enzymes, sequela
        • T45.3X6 Underdosing of enzymes
        • T45.3X6A Underdosing of enzymes, initial encounter
        • T45.3X6D Underdosing of enzymes, subsequent encounter
        • T45.3X6S Underdosing of enzymes, sequela
        • T45.4 Poisoning by, adverse effect of and underdosing of iron and its compounds
        • T45.4X Poisoning by, adverse effect of and underdosing of iron and its compounds
        • T45.4X1 Poisoning by iron and its compounds, accidental (unintentional)
        • T45.4X1A Poisoning by iron and its compounds, accidental (unintentional), initial encounter
        • T45.4X1D Poisoning by iron and its compounds, accidental (unintentional), subsequent encounter
        • T45.4X1S Poisoning by iron and its compounds, accidental (unintentional), sequela
        • T45.4X2 Poisoning by iron and its compounds, intentional self-harm
        • T45.4X2A Poisoning by iron and its compounds, intentional self-harm, initial encounter
        • T45.4X2D Poisoning by iron and its compounds, intentional self-harm, subsequent encounter
        • T45.4X2S Poisoning by iron and its compounds, intentional self-harm, sequela
        • T45.4X3 Poisoning by iron and its compounds, assault
        • T45.4X3A Poisoning by iron and its compounds, assault, initial encounter
        • T45.4X3D Poisoning by iron and its compounds, assault, subsequent encounter
        • T45.4X3S Poisoning by iron and its compounds, assault, sequela
        • T45.4X4 Poisoning by iron and its compounds, undetermined
        • T45.4X4A Poisoning by iron and its compounds, undetermined, initial encounter
        • T45.4X4D Poisoning by iron and its compounds, undetermined, subsequent encounter
        • T45.4X4S Poisoning by iron and its compounds, undetermined, sequela
        • T45.4X5 Adverse effect of iron and its compounds
        • T45.4X5A Adverse effect of iron and its compounds, initial encounter
        • T45.4X5D Adverse effect of iron and its compounds, subsequent encounter
        • T45.4X5S Adverse effect of iron and its compounds, sequela
        • T45.4X6 Underdosing of iron and its compounds
        • T45.4X6A Underdosing of iron and its compounds, initial encounter
        • T45.4X6D Underdosing of iron and its compounds, subsequent encounter
        • T45.4X6S Underdosing of iron and its compounds, sequela
        • T45.5 Poisoning by, adverse effect of and underdosing of anticoagulants and antithrombotic drugs
        • T45.51 Poisoning by, adverse effect of and underdosing of anticoagulants
        • T45.511 Poisoning by anticoagulants, accidental (unintentional)
        • T45.511A Poisoning by anticoagulants, accidental (unintentional), initial encounter
        • T45.511D Poisoning by anticoagulants, accidental (unintentional), subsequent encounter
        • T45.511S Poisoning by anticoagulants, accidental (unintentional), sequela
        • T45.512 Poisoning by anticoagulants, intentional self-harm
        • T45.512A Poisoning by anticoagulants, intentional self-harm, initial encounter
        • T45.512D Poisoning by anticoagulants, intentional self-harm, subsequent encounter
        • T45.512S Poisoning by anticoagulants, intentional self-harm, sequela
        • T45.513 Poisoning by anticoagulants, assault
        • T45.513A Poisoning by anticoagulants, assault, initial encounter
        • T45.513D Poisoning by anticoagulants, assault, subsequent encounter
        • T45.513S Poisoning by anticoagulants, assault, sequela
        • T45.514 Poisoning by anticoagulants, undetermined
        • T45.514A Poisoning by anticoagulants, undetermined, initial encounter
        • T45.514D Poisoning by anticoagulants, undetermined, subsequent encounter
        • T45.514S Poisoning by anticoagulants, undetermined, sequela
        • T45.515 Adverse effect of anticoagulants
        • T45.515A Adverse effect of anticoagulants, initial encounter
        • T45.515D Adverse effect of anticoagulants, subsequent encounter
        • T45.515S Adverse effect of anticoagulants, sequela
        • T45.516 Underdosing of anticoagulants
        • T45.516A Underdosing of anticoagulants, initial encounter
        • T45.516D Underdosing of anticoagulants, subsequent encounter
        • T45.516S Underdosing of anticoagulants, sequela
        • T45.52 Poisoning by, adverse effect of and underdosing of antithrombotic drugs
        • T45.521 Poisoning by antithrombotic drugs, accidental (unintentional)
        • T45.521A Poisoning by antithrombotic drugs, accidental (unintentional), initial encounter
        • T45.521D Poisoning by antithrombotic drugs, accidental (unintentional), subsequent encounter
        • T45.521S Poisoning by antithrombotic drugs, accidental (unintentional), sequela
        • T45.522 Poisoning by antithrombotic drugs, intentional self-harm
        • T45.522A Poisoning by antithrombotic drugs, intentional self-harm, initial encounter
        • T45.522D Poisoning by antithrombotic drugs, intentional self-harm, subsequent encounter
        • T45.522S Poisoning by antithrombotic drugs, intentional self-harm, sequela
        • T45.523 Poisoning by antithrombotic drugs, assault
        • T45.523A Poisoning by antithrombotic drugs, assault, initial encounter
        • T45.523D Poisoning by antithrombotic drugs, assault, subsequent encounter
        • T45.523S Poisoning by antithrombotic drugs, assault, sequela
        • T45.524 Poisoning by antithrombotic drugs, undetermined
        • T45.524A Poisoning by antithrombotic drugs, undetermined, initial encounter
        • T45.524D Poisoning by antithrombotic drugs, undetermined, subsequent encounter
        • T45.524S Poisoning by antithrombotic drugs, undetermined, sequela
        • T45.525 Adverse effect of antithrombotic drugs
        • T45.525A Adverse effect of antithrombotic drugs, initial encounter
        • T45.525D Adverse effect of antithrombotic drugs, subsequent encounter
        • T45.525S Adverse effect of antithrombotic drugs, sequela
        • T45.526 Underdosing of antithrombotic drugs
        • T45.526A Underdosing of antithrombotic drugs, initial encounter
        • T45.526D Underdosing of antithrombotic drugs, subsequent encounter
        • T45.526S Underdosing of antithrombotic drugs, sequela
        • T45.6 Poisoning by, adverse effect of and underdosing of fibrinolysis-affecting drugs
        • T45.60 Poisoning by, adverse effect of and underdosing of unspecified fibrinolysis-affecting drugs
        • T45.601 Poisoning by unspecified fibrinolysis-affecting drugs, accidental (unintentional)
        • T45.601A Poisoning by unspecified fibrinolysis-affecting drugs, accidental (unintentional), initial encounter
        • T45.601D Poisoning by unspecified fibrinolysis-affecting drugs, accidental (unintentional), subsequent encounter
        • T45.601S Poisoning by unspecified fibrinolysis-affecting drugs, accidental (unintentional), sequela
        • T45.602 Poisoning by unspecified fibrinolysis-affecting drugs, intentional self-harm
        • T45.602A Poisoning by unspecified fibrinolysis-affecting drugs, intentional self-harm, initial encounter
        • T45.602D Poisoning by unspecified fibrinolysis-affecting drugs, intentional self-harm, subsequent encounter
        • T45.602S Poisoning by unspecified fibrinolysis-affecting drugs, intentional self-harm, sequela
        • T45.603 Poisoning by unspecified fibrinolysis-affecting drugs, assault
        • T45.603A Poisoning by unspecified fibrinolysis-affecting drugs, assault, initial encounter
        • T45.603D Poisoning by unspecified fibrinolysis-affecting drugs, assault, subsequent encounter
        • T45.603S Poisoning by unspecified fibrinolysis-affecting drugs, assault, sequela
        • T45.604 Poisoning by unspecified fibrinolysis-affecting drugs, undetermined
        • T45.604A Poisoning by unspecified fibrinolysis-affecting drugs, undetermined, initial encounter
        • T45.604D Poisoning by unspecified fibrinolysis-affecting drugs, undetermined, subsequent encounter
        • T45.604S Poisoning by unspecified fibrinolysis-affecting drugs, undetermined, sequela
        • T45.605 Adverse effect of unspecified fibrinolysis-affecting drugs
        • T45.605A Adverse effect of unspecified fibrinolysis-affecting drugs, initial encounter
        • T45.605D Adverse effect of unspecified fibrinolysis-affecting drugs, subsequent encounter
        • T45.605S Adverse effect of unspecified fibrinolysis-affecting drugs, sequela
        • T45.606 Underdosing of unspecified fibrinolysis-affecting drugs
        • T45.606A Underdosing of unspecified fibrinolysis-affecting drugs, initial encounter
        • T45.606D Underdosing of unspecified fibrinolysis-affecting drugs, subsequent encounter
        • T45.606S Underdosing of unspecified fibrinolysis-affecting drugs, sequela
        • T45.61 Poisoning by, adverse effect of and underdosing of thrombolytic drugs
        • T45.611 Poisoning by thrombolytic drug, accidental (unintentional)
        • T45.611A Poisoning by thrombolytic drug, accidental (unintentional), initial encounter
        • T45.611D Poisoning by thrombolytic drug, accidental (unintentional), subsequent encounter
        • T45.611S Poisoning by thrombolytic drug, accidental (unintentional), sequela
        • T45.612 Poisoning by thrombolytic drug, intentional self-harm
        • T45.612A Poisoning by thrombolytic drug, intentional self-harm, initial encounter
        • T45.612D Poisoning by thrombolytic drug, intentional self-harm, subsequent encounter
        • T45.612S Poisoning by thrombolytic drug, intentional self-harm, sequela
        • T45.613 Poisoning by thrombolytic drug, assault
        • T45.613A Poisoning by thrombolytic drug, assault, initial encounter
        • T45.613D Poisoning by thrombolytic drug, assault, subsequent encounter
        • T45.613S Poisoning by thrombolytic drug, assault, sequela
        • T45.614 Poisoning by thrombolytic drug, undetermined
        • T45.614A Poisoning by thrombolytic drug, undetermined, initial encounter
        • T45.614D Poisoning by thrombolytic drug, undetermined, subsequent encounter
        • T45.614S Poisoning by thrombolytic drug, undetermined, sequela
        • T45.615 Adverse effect of thrombolytic drugs
        • T45.615A Adverse effect of thrombolytic drugs, initial encounter
        • T45.615D Adverse effect of thrombolytic drugs, subsequent encounter
        • T45.615S Adverse effect of thrombolytic drugs, sequela
        • T45.616 Underdosing of thrombolytic drugs
        • T45.616A Underdosing of thrombolytic drugs, initial encounter
        • T45.616D Underdosing of thrombolytic drugs, subsequent encounter
        • T45.616S Underdosing of thrombolytic drugs, sequela
        • T45.62 Poisoning by, adverse effect of and underdosing of hemostatic drugs
        • T45.621 Poisoning by hemostatic drug, accidental (unintentional)
        • T45.621A Poisoning by hemostatic drug, accidental (unintentional), initial encounter
        • T45.621D Poisoning by hemostatic drug, accidental (unintentional), subsequent encounter
        • T45.621S Poisoning by hemostatic drug, accidental (unintentional), sequela
        • T45.622 Poisoning by hemostatic drug, intentional self-harm
        • T45.622A Poisoning by hemostatic drug, intentional self-harm, initial encounter
        • T45.622D Poisoning by hemostatic drug, intentional self-harm, subsequent encounter
        • T45.622S Poisoning by hemostatic drug, intentional self-harm, sequela
        • T45.623 Poisoning by hemostatic drug, assault
        • T45.623A Poisoning by hemostatic drug, assault, initial encounter
        • T45.623D Poisoning by hemostatic drug, assault, subsequent encounter
        • T45.623S Poisoning by hemostatic drug, assault, sequela
        • T45.624 Poisoning by hemostatic drug, undetermined
        • T45.624A Poisoning by hemostatic drug, undetermined, initial encounter
        • T45.624D Poisoning by hemostatic drug, undetermined, subsequent encounter
        • T45.624S Poisoning by hemostatic drug, undetermined, sequela
        • T45.625 Adverse effect of hemostatic drug
        • T45.625A Adverse effect of hemostatic drug, initial encounter
        • T45.625D Adverse effect of hemostatic drug, subsequent encounter
        • T45.625S Adverse effect of hemostatic drug, sequela
        • T45.626 Underdosing of hemostatic drugs
        • T45.626A Underdosing of hemostatic drugs, initial encounter
        • T45.626D Underdosing of hemostatic drugs, subsequent encounter
        • T45.626S Underdosing of hemostatic drugs, sequela
        • T45.69 Poisoning by, adverse effect of and underdosing of other fibrinolysis-affecting drugs
        • T45.691 Poisoning by other fibrinolysis-affecting drugs, accidental (unintentional)
        • T45.691A Poisoning by other fibrinolysis-affecting drugs, accidental (unintentional), initial encounter
        • T45.691D Poisoning by other fibrinolysis-affecting drugs, accidental (unintentional), subsequent encounter
        • T45.691S Poisoning by other fibrinolysis-affecting drugs, accidental (unintentional), sequela
        • T45.692 Poisoning by other fibrinolysis-affecting drugs, intentional self-harm
        • T45.692A Poisoning by other fibrinolysis-affecting drugs, intentional self-harm, initial encounter
        • T45.692D Poisoning by other fibrinolysis-affecting drugs, intentional self-harm, subsequent encounter
        • T45.692S Poisoning by other fibrinolysis-affecting drugs, intentional self-harm, sequela
        • T45.693 Poisoning by other fibrinolysis-affecting drugs, assault
        • T45.693A Poisoning by other fibrinolysis-affecting drugs, assault, initial encounter
        • T45.693D Poisoning by other fibrinolysis-affecting drugs, assault, subsequent encounter
        • T45.693S Poisoning by other fibrinolysis-affecting drugs, assault, sequela
        • T45.694 Poisoning by other fibrinolysis-affecting drugs, undetermined
        • T45.694A Poisoning by other fibrinolysis-affecting drugs, undetermined, initial encounter
        • T45.694D Poisoning by other fibrinolysis-affecting drugs, undetermined, subsequent encounter
        • T45.694S Poisoning by other fibrinolysis-affecting drugs, undetermined, sequela
        • T45.695 Adverse effect of other fibrinolysis-affecting drugs
        • T45.695A Adverse effect of other fibrinolysis-affecting drugs, initial encounter
        • T45.695D Adverse effect of other fibrinolysis-affecting drugs, subsequent encounter
        • T45.695S Adverse effect of other fibrinolysis-affecting drugs, sequela
        • T45.696 Underdosing of other fibrinolysis-affecting drugs
        • T45.696A Underdosing of other fibrinolysis-affecting drugs, initial encounter
        • T45.696D Underdosing of other fibrinolysis-affecting drugs, subsequent encounter
        • T45.696S Underdosing of other fibrinolysis-affecting drugs, sequela
        • T45.7 Poisoning by, adverse effect of and underdosing of anticoagulant antagonists, vitamin K and other coagulants
        • T45.7X Poisoning by, adverse effect of and underdosing of anticoagulant antagonists, vitamin K and other coagulants
        • T45.7X1 Poisoning by anticoagulant antagonists, vitamin K and other coagulants, accidental (unintentional)
        • T45.7X1A Poisoning by anticoagulant antagonists, vitamin K and other coagulants, accidental (unintentional), initial encounter
        • T45.7X1D Poisoning by anticoagulant antagonists, vitamin K and other coagulants, accidental (unintentional), subsequent encounter
        • T45.7X1S Poisoning by anticoagulant antagonists, vitamin K and other coagulants, accidental (unintentional), sequela
        • T45.7X2 Poisoning by anticoagulant antagonists, vitamin K and other coagulants, intentional self-harm
        • T45.7X2A Poisoning by anticoagulant antagonists, vitamin K and other coagulants, intentional self-harm, initial encounter
        • T45.7X2D Poisoning by anticoagulant antagonists, vitamin K and other coagulants, intentional self-harm, subsequent encounter
        • T45.7X2S Poisoning by anticoagulant antagonists, vitamin K and other coagulants, intentional self-harm, sequela
        • T45.7X3 Poisoning by anticoagulant antagonists, vitamin K and other coagulants, assault
        • T45.7X3A Poisoning by anticoagulant antagonists, vitamin K and other coagulants, assault, initial encounter
        • T45.7X3D Poisoning by anticoagulant antagonists, vitamin K and other coagulants, assault, subsequent encounter
        • T45.7X3S Poisoning by anticoagulant antagonists, vitamin K and other coagulants, assault, sequela
        • T45.7X4 Poisoning by anticoagulant antagonists, vitamin K and other coagulants, undetermined
        • T45.7X4A Poisoning by anticoagulant antagonists, vitamin K and other coagulants, undetermined, initial encounter
        • T45.7X4D Poisoning by anticoagulant antagonists, vitamin K and other coagulants, undetermined, subsequent encounter
        • T45.7X4S Poisoning by anticoagulant antagonists, vitamin K and other coagulants, undetermined, sequela
        • T45.7X5 Adverse effect of anticoagulant antagonists, vitamin K and other coagulants
        • T45.7X5A Adverse effect of anticoagulant antagonists, vitamin K and other coagulants, initial encounter
        • T45.7X5D Adverse effect of anticoagulant antagonists, vitamin K and other coagulants, subsequent encounter
        • T45.7X5S Adverse effect of anticoagulant antagonists, vitamin K and other coagulants, sequela
        • T45.7X6 Underdosing of anticoagulant antagonist, vitamin K and other coagulants
        • T45.7X6A Underdosing of anticoagulant antagonist, vitamin K and other coagulants, initial encounter
        • T45.7X6D Underdosing of anticoagulant antagonist, vitamin K and other coagulants, subsequent encounter
        • T45.7X6S Underdosing of anticoagulant antagonist, vitamin K and other coagulants, sequela
        • T45.8 Poisoning by, adverse effect of and underdosing of other primarily systemic and hematological agents
        • T45.8X Poisoning by, adverse effect of and underdosing of other primarily systemic and hematological agents
        • T45.8X1 Poisoning by other primarily systemic and hematological agents, accidental (unintentional)
        • T45.8X1A Poisoning by other primarily systemic and hematological agents, accidental (unintentional), initial encounter
        • T45.8X1D Poisoning by other primarily systemic and hematological agents, accidental (unintentional), subsequent encounter
        • T45.8X1S Poisoning by other primarily systemic and hematological agents, accidental (unintentional), sequela
        • T45.8X2 Poisoning by other primarily systemic and hematological agents, intentional self-harm
        • T45.8X2A Poisoning by other primarily systemic and hematological agents, intentional self-harm, initial encounter
        • T45.8X2D Poisoning by other primarily systemic and hematological agents, intentional self-harm, subsequent encounter
        • T45.8X2S Poisoning by other primarily systemic and hematological agents, intentional self-harm, sequela
        • T45.8X3 Poisoning by other primarily systemic and hematological agents, assault
        • T45.8X3A Poisoning by other primarily systemic and hematological agents, assault, initial encounter
        • T45.8X3D Poisoning by other primarily systemic and hematological agents, assault, subsequent encounter
        • T45.8X3S Poisoning by other primarily systemic and hematological agents, assault, sequela
        • T45.8X4 Poisoning by other primarily systemic and hematological agents, undetermined
        • T45.8X4A Poisoning by other primarily systemic and hematological agents, undetermined, initial encounter
        • T45.8X4D Poisoning by other primarily systemic and hematological agents, undetermined, subsequent encounter
        • T45.8X4S Poisoning by other primarily systemic and hematological agents, undetermined, sequela
        • T45.8X5 Adverse effect of other primarily systemic and hematological agents
        • T45.8X5A Adverse effect of other primarily systemic and hematological agents, initial encounter
        • T45.8X5D Adverse effect of other primarily systemic and hematological agents, subsequent encounter
        • T45.8X5S Adverse effect of other primarily systemic and hematological agents, sequela
        • T45.8X6 Underdosing of other primarily systemic and hematological agents
        • T45.8X6A Underdosing of other primarily systemic and hematological agents, initial encounter
        • T45.8X6D Underdosing of other primarily systemic and hematological agents, subsequent encounter
        • T45.8X6S Underdosing of other primarily systemic and hematological agents, sequela
        • T45.9 Poisoning by, adverse effect of and underdosing of unspecified primarily systemic and hematological agent
        • T45.91 Poisoning by unspecified primarily systemic and hematological agent, accidental (unintentional)
        • T45.91XA Poisoning by unspecified primarily systemic and hematological agent, accidental (unintentional), initial encounter
        • T45.91XD Poisoning by unspecified primarily systemic and hematological agent, accidental (unintentional), subsequent encounter
        • T45.91XS Poisoning by unspecified primarily systemic and hematological agent, accidental (unintentional), sequela
        • T45.92 Poisoning by unspecified primarily systemic and hematological agent, intentional self-harm
        • T45.92XA Poisoning by unspecified primarily systemic and hematological agent, intentional self-harm, initial encounter
        • T45.92XD Poisoning by unspecified primarily systemic and hematological agent, intentional self-harm, subsequent encounter
        • T45.92XS Poisoning by unspecified primarily systemic and hematological agent, intentional self-harm, sequela
        • T45.93 Poisoning by unspecified primarily systemic and hematological agent, assault
        • T45.93XA Poisoning by unspecified primarily systemic and hematological agent, assault, initial encounter
        • T45.93XD Poisoning by unspecified primarily systemic and hematological agent, assault, subsequent encounter
        • T45.93XS Poisoning by unspecified primarily systemic and hematological agent, assault, sequela
        • T45.94 Poisoning by unspecified primarily systemic and hematological agent, undetermined
        • T45.94XA Poisoning by unspecified primarily systemic and hematological agent, undetermined, initial encounter
        • T45.94XD Poisoning by unspecified primarily systemic and hematological agent, undetermined, subsequent encounter
        • T45.94XS Poisoning by unspecified primarily systemic and hematological agent, undetermined, sequela
        • T45.95 Adverse effect of unspecified primarily systemic and hematological agent
        • T45.95XA Adverse effect of unspecified primarily systemic and hematological agent, initial encounter
        • T45.95XD Adverse effect of unspecified primarily systemic and hematological agent, subsequent encounter
        • T45.95XS Adverse effect of unspecified primarily systemic and hematological agent, sequela
        • T45.96 Underdosing of unspecified primarily systemic and hematological agent
        • T45.96XA Underdosing of unspecified primarily systemic and hematological agent, initial encounter
        • T45.96XD Underdosing of unspecified primarily systemic and hematological agent, subsequent encounter
        • T45.96XS Underdosing of unspecified primarily systemic and hematological agent, sequela
        • T45.A Poisoning by, adverse effect of and underdosing of immune checkpoint inhibitors and immunostimulant drugs
        • T45.AX Poisoning by, adverse effect of and underdosing of immune checkpoint inhibitors and immunostimulant drugs
        • T45.AX1 Poisoning by immune checkpoint inhibitors and immunostimulant drugs, accidental (unintentional) NEW CODE
        • T45.AX1A Poisoning by immune checkpoint inhibitors and immunostimulant drugs, accidental (unintentional), initial encounter
        • T45.AX1D Poisoning by immune checkpoint inhibitors and immunostimulant drugs, accidental (unintentional), subsequent encounter
        • T45.AX1S Poisoning by immune checkpoint inhibitors and immunostimulant drugs, accidental (unintentional), sequela
        • T45.AX2 Poisoning by immune checkpoint inhibitors and immunostimulant drugs, intentional self-harm NEW CODE
        • T45.AX2A Poisoning by immune checkpoint inhibitors and immunostimulant drugs, intentional self-harm, initial encounter
        • T45.AX2D Poisoning by immune checkpoint inhibitors and immunostimulant drugs, intentional self-harm, subsequent encounter
        • T45.AX2S Poisoning by immune checkpoint inhibitors and immunostimulant drugs, intentional self-harm, sequela
        • T45.AX3 Poisoning by immune checkpoint inhibitors and immunostimulant drugs, assault NEW CODE
        • T45.AX3A Poisoning by immune checkpoint inhibitors and immunostimulant drugs, assault, initial encounter
        • T45.AX3D Poisoning by immune checkpoint inhibitors and immunostimulant drugs, assault, subsequent encounter
        • T45.AX3S Poisoning by immune checkpoint inhibitors and immunostimulant drugs, assault, sequela
        • T45.AX4 Poisoning by immune checkpoint inhibitors and immunostimulant drugs, undetermined NEW CODE
        • T45.AX4A Poisoning by immune checkpoint inhibitors and immunostimulant drugs, undetermined, initial encounter
        • T45.AX4D Poisoning by immune checkpoint inhibitors and immunostimulant drugs, undetermined, subsequent encounter
        • T45.AX4S Poisoning by immune checkpoint inhibitors and immunostimulant drugs, undetermined, sequela
        • T45.AX5 Adverse effect of immune checkpoint inhibitors and immunostimulant drugs NEW CODE
        • T45.AX5A Adverse effect of immune checkpoint inhibitors and immunostimulant drugs, initial encounter
        • T45.AX5D Adverse effect of immune checkpoint inhibitors and immunostimulant drugs, subsequent encounter
        • T45.AX5S Adverse effect of immune checkpoint inhibitors and immunostimulant drugs, sequela
        • T45.AX6 Underdosing of immune checkpoint inhibitors and immunostimulant drugs NEW CODE
        • T45.AX6A Underdosing of immune checkpoint inhibitors and immunostimulant drugs, initial encounter
        • T45.AX6D Underdosing of immune checkpoint inhibitors and immunostimulant drugs, subsequent encounter
        • T45.AX6S Underdosing of immune checkpoint inhibitors and immunostimulant drugs, sequela