Poisoning by, adverse effect of and underdosing of other systemic anti-infectives and antiparasitics (T37)

Browse all the diagnosis codes used for poisoning by, adverse effect of and underdosing of other systemic anti-infectives and antiparasitics (t37). 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

2,6-Dichloroindophenol - A dye used as a reagent in the determination of vitamin C.

Acamprosate - Structural analog of taurine that is used for the prevention of relapse in individuals with ALCOHOLISM.

Acedapsone - Acetylated sulfone that is slowly metabolized to give long-term, low blood levels of DAPSONE. It has antimicrobial and antimalarial action, but is mainly used as a depot leprostatic agent.

Acetrizoic Acid - An iodinated radiographic contrast medium used as acetrizoate sodium in HYSTEROSALPINGOGRAPHY.

Acetylcysteine - The N-acetyl derivative of CYSTEINE. It is used as a mucolytic agent to reduce the viscosity of mucous secretions. It has also been shown to have antiviral effects in patients with HIV due to inhibition of viral stimulation by reactive oxygen intermediates.

Acid Sensing Ion Channels - A family of proton-gated sodium channels that are primarily expressed in neuronal tissue. They are AMILORIDE-sensitive and are implicated in the signaling of a variety of neurological stimuli, most notably that of pain in response to acidic conditions.

Acriflavine - 3,6-Diamino-10-methylacridinium chloride mixt. with 3,6-acridinediamine. Fluorescent dye used as a local antiseptic and also as a biological stain. It intercalates into nucleic acids thereby inhibiting bacterial and viral replication.

Acyclovir - A GUANOSINE analog that acts as an antimetabolite. Viruses are especially susceptible. Used especially against herpes.

Albendazole - A benzimidazole broad-spectrum anthelmintic structurally related to MEBENDAZOLE that is effective against many diseases. (From Martindale, The Extra Pharmacopoeia, 30th ed, p38)

Alginates - Salts and esters of ALGINIC ACID that are used as HYDROGELS; DENTAL IMPRESSION MATERIALS, and as absorbent materials for surgical dressings (BANDAGES, HYDROCOLLOID). They are also used to manufacture MICROSPHERES and NANOPARTICLES for DIAGNOSTIC REAGENT KITS and DRUG DELIVERY SYSTEMS.

Amino Acid Transport Systems, Neutral - Amino acid transporter systems capable of transporting neutral amino acids (AMINO ACIDS, NEUTRAL).

Aminopterin - A folic acid derivative used as a rodenticide that has been shown to be teratogenic.

Aminosalicylic Acid - An antitubercular agent often administered in association with ISONIAZID. The sodium salt of the drug is better tolerated than the free acid.

Aminosalicylic Acids - A group of 2-hydroxybenzoic acids that can be substituted by amino groups at any of the 3-, 4-, 5-, or 6-positions.

Amobarbital - A barbiturate with hypnotic and sedative properties (but not antianxiety). Adverse effects are mainly a consequence of dose-related CNS depression and the risk of dependence with continued use is high. (From Martindale, The Extra Pharmacopoeia, 30th ed, p565)

Amodiaquine - A 4-aminoquinoline compound with anti-inflammatory properties.

Ampicillin - Semi-synthetic derivative of penicillin that functions as an orally active broad-spectrum antibiotic.

Antimony Sodium Gluconate - Antimony complex where the metal may exist in either the pentavalent or trivalent states. The pentavalent gluconate is used in leishmaniasis. The trivalent gluconate is most frequently used in schistosomiasis.

Arachidonic Acid - An unsaturated, essential fatty acid. It is found in animal and human fat as well as in the liver, brain, and glandular organs, and is a constituent of animal phosphatides. It is formed by the synthesis from dietary linoleic acid and is a precursor in the biosynthesis of prostaglandins, thromboxanes, and leukotrienes.

Arsanilic Acid - An arsenical which has been used as a feed additive for enteric conditions in pigs and poultry. It causes blindness and is ototoxic and nephrotoxic in animals.

Arsphenamine - An organoarsenic compound that was commonly used for treating SYPHILIS and other diseases.

Artesunate - A water-soluble, semi-synthetic derivative of the sesquiterpene lactone artemisinin with anti-malarial, anti-schistosomiasis, antiviral, and potential anti-neoplastic activities

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.

Aspartic Acid - One of the non-essential amino acids commonly occurring in the L-form. It is found in animals and plants, especially in sugar cane and sugar beets. It may be a neurotransmitter.

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)

Azlocillin - A semisynthetic ampicillin-derived acylureido penicillin.

Bithionol - Halogenated anti-infective agent that is used against trematode and cestode infestations.

Bucladesine - A cyclic nucleotide derivative that mimics the action of endogenous CYCLIC AMP and is capable of permeating the cell membrane. It has vasodilator properties and is used as a cardiac stimulant. (From Merck Index, 11th ed)

Butyric Acid - A four carbon acid, CH3CH2CH2COOH, with an unpleasant odor that occurs in butter and animal fat as the glycerol ester.

Carboxymethylcellulose Sodium - A cellulose derivative which is a beta-(1,4)-D-glucopyranose polymer. It is used as a bulk laxative and as an emulsifier and thickener in cosmetics and pharmaceuticals and as a stabilizer for reagents.

Carfecillin - The phenyl ester of CARBENICILLIN that, upon oral administration, is broken down in the intestinal mucosa to the active antibacterial. It is used for urinary tract infections.

Caseins - A mixture of related phosphoproteins occurring in milk and cheese. The group is characterized as one of the most nutritive milk proteins, containing all of the common amino acids and rich in the essential ones.

Cefazolin - A semisynthetic cephalosporin analog with broad-spectrum antibiotic action due to inhibition of bacterial cell wall synthesis. It attains high serum levels and is excreted quickly via the urine.

Cefmetazole - A semisynthetic cephamycin antibiotic with a broad spectrum of activity against both gram-positive and gram-negative microorganisms. It has a high rate of efficacy in many types of infection and to date no severe side effects have been noted.

Cefonicid - A second-generation cephalosporin administered intravenously or intramuscularly. Its bactericidal action results from inhibition of cell wall synthesis. It is used for urinary tract infections, lower respiratory tract infections, and soft tissue and bone infections.

Cefoperazone - Semisynthetic broad-spectrum cephalosporin with a tetrazolyl moiety that is resistant to beta-lactamase. It may be used to treat Pseudomonas infections.

Cefotaxime - Semisynthetic broad-spectrum cephalosporin.

Cefoxitin - A semisynthetic cephamycin antibiotic resistant to beta-lactamase.

Cefpodoxime - A third-generation cephalosporin antibiotic. Cefpodoxime contains a methoxy group at C-3 of its cephalosporin core.

Cefsulodin - A pyridinium-substituted semisynthetic, broad-spectrum antibacterial used especially for Pseudomonas infections in debilitated patients.

Ceftizoxime - A semisynthetic cephalosporin antibiotic which can be administered intravenously or by suppository. The drug is highly resistant to a broad spectrum of beta-lactamases and is active against a wide range of both aerobic and anaerobic gram-positive and gram-negative organisms. It has few side effects and is reported to be safe and effective in aged patients and in patients with hematologic disorders.

Cephacetrile - A derivative of 7-aminocephalosporanic acid.

Cephalothin - A cephalosporin antibiotic.

Cephapirin - Cephalosporin antibiotic, partly plasma-bound, that is effective against gram-negative and gram-positive organisms.

Chenodeoxycholic Acid - A bile acid, usually conjugated with either glycine or taurine. It acts as a detergent to solubilize fats for intestinal absorption and is reabsorbed by the small intestine. It is used as cholagogue, a choleretic laxative, and to prevent or dissolve gallstones.

Chenopodium - A plant genus in the CHENOPODIACEAE family.

Chenopodium album - A plant species in the CHENOPODIUM genus known for edible greens.

Chenopodium ambrosioides - A plant species of the genus Chenopodium known for toxicity to intestinal worms and other simple organisms.

Chenopodium quinoa - A species of the Chenopodium genus which is the source of edible seed called quinoa. It contains makisterone A and other STEROIDS, some having ECDYSTEROID activity on insects.

Chloride-Bicarbonate Antiporters - Electroneutral chloride bicarbonate exchangers that allow the exchange of BICARBONATE IONS exchange for CHLORIDE IONS across the cellular membrane. The action of specific antiporters in this class serve important functions such as allowing the efficient exchange of bicarbonate across red blood cell membranes as they passage through capillaries and the reabsorption of bicarbonate ions by the kidney.

Chloroquine - The prototypical antimalarial agent with a mechanism that is not well understood. It has also been used to treat rheumatoid arthritis, systemic lupus erythematosus, and in the systemic therapy of amebic liver abscesses.

Chondroitin Sulfates - Derivatives of chondroitin which have a sulfate moiety esterified to the galactosamine moiety of chondroitin. Chondroitin sulfate A, or chondroitin 4-sulfate, and chondroitin sulfate C, or chondroitin 6-sulfate, have the sulfate esterified in the 4- and 6-positions, respectively. Chondroitin sulfate B (beta heparin; DERMATAN SULFATE) is a misnomer and this compound is not a true chondroitin sulfate.

Cilastatin - A renal dehydropeptidase-I and leukotriene D4 dipeptidase inhibitor. Since the antibiotic, IMIPENEM, is hydrolyzed by dehydropeptidase-I, which resides in the brush border of the renal tubule, cilastatin is administered with imipenem to increase its effectiveness. The drug also inhibits the metabolism of leukotriene D4 to leukotriene E4.

Cinchona - A genus of rubiaceous South American trees that yields the toxic CINCHONA ALKALOIDS from their bark; QUININE; QUINIDINE; chinconine, cinchonidine and others are used to treat MALARIA and CARDIAC ARRHYTHMIAS.

Cinchona Alkaloids - Alkaloids extracted from various species of Cinchona.

Cinoxacin - Synthetic antimicrobial related to OXOLINIC ACID and NALIDIXIC ACID and used in URINARY TRACT INFECTIONS.

Clavulanic Acid - A beta-lactam antibiotic produced by the actinobacterium Streptomyces clavuligerus. It is a suicide inhibitor of bacterial beta-lactamase enzymes. Administered alone, it has only weak antibacterial activity against most organisms, but given in combination with other beta-lactam antibiotics it prevents antibiotic inactivation by microbial lactamase.

Clioquinol - A potentially neurotoxic 8-hydroxyquinoline derivative long used as a topical anti-infective, intestinal antiamebic, and vaginal trichomonacide. The oral preparation has been shown to cause subacute myelo-optic neuropathy and has been banned worldwide.

Clodronic Acid - A diphosphonate which affects calcium metabolism. It inhibits bone resorption and soft tissue calcification.

Clofazimine - A fat-soluble riminophenazine dye used for the treatment of leprosy. It has been used investigationally in combination with other antimycobacterial drugs to treat Mycobacterium avium infections in AIDS patients. Clofazimine also has a marked anti-inflammatory effect and is given to control the leprosy reaction, erythema nodosum leprosum. (From AMA Drug Evaluations Annual, 1993, p1619)

Cloprostenol - A synthetic prostaglandin F2alpha analog. The compound has luteolytic effects and is used for the synchronization of estrus in cattle.

Cloxacillin - A semi-synthetic antibiotic that is a chlorinated derivative of OXACILLIN.

Cromolyn Sodium - A chromone complex that acts by inhibiting the release of chemical mediators from sensitized MAST CELLS. It is used in the prophylactic treatment of both allergic and exercise-induced asthma, but does not affect an established asthmatic attack.

Cyclamates - Salts and esters of cyclamic acid.

Cycloserine - Antibiotic substance produced by Streptomyces garyphalus.

Cystaphos - Proposed as an adjuvant to cancer chemotherapy; may have radiation protective properties.

Dalteparin - A low-molecular-weight fragment of heparin, prepared by nitrous acid depolymerization of porcine mucosal heparin. The mean molecular weight is 4000-6000 daltons. It is used therapeutically as an antithrombotic agent. (From Merck Index, 11th ed)

Dantrolene - Skeletal muscle relaxant that acts by interfering with excitation-contraction coupling in the muscle fiber. It is used in spasticity and other neuromuscular abnormalities. Although the mechanism of action is probably not central, dantrolene is usually grouped with the central muscle relaxants.

Dapsone - A sulfone active against a wide range of bacteria but mainly employed for its actions against MYCOBACTERIUM LEPRAE. Its mechanism of action is probably similar to that of the SULFONAMIDES which involves inhibition of folic acid synthesis in susceptible organisms. It is also used with PYRIMETHAMINE in the treatment of malaria. (From Martindale, The Extra Pharmacopoeia, 30th ed, p157-8)

Degenerin Sodium Channels - A family of mechanosensitive sodium channels found primarily in NEMATODES where they play a role in CELLULAR MECHANOTRANSDUCTION. Degenerin sodium channels are structurally-related to EPITHELIAL SODIUM CHANNELS and are named after the fact that loss of their activity results in cellular degeneration.

Dehydrocholic Acid - A semisynthetic bile acid made from cholic acid. It is used as a cholagogue, hydrocholeretic, diuretic, and as a diagnostic aid.

Deoxycholic Acid - A bile acid formed by bacterial action from cholate. It is usually conjugated with glycine or taurine. Deoxycholic acid acts as a detergent to solubilize fats for intestinal absorption, is reabsorbed itself, and is used as a choleretic and detergent.

Dextran Sulfate - Long-chain polymer of glucose containing 17-20% sulfur. It has been used as an anticoagulant and also has been shown to inhibit the binding of HIV-1 to CD4-POSITIVE T-LYMPHOCYTES. It is commonly used as both an experimental and clinical laboratory reagent and has been investigated for use as an antiviral agent, in the treatment of hypolipidemia, and for the prevention of free radical damage, among other applications.

Dextrothyroxine - The dextrorotary isomer of the synthetic THYROXINE.

Diatrizoate - A commonly used x-ray contrast medium. As DIATRIZOATE MEGLUMINE and as Diatrizoate sodium, it is used for gastrointestinal studies, angiography, and urography.

Diatrizoate Meglumine - A versatile contrast medium used for DIAGNOSTIC X-RAY RADIOLOGY.

Dichloroacetic Acid - A derivative of ACETIC ACID that contains two CHLORINE atoms attached to its methyl group.

Dichlorophen - Nontoxic laxative vermicide effective for taenia infestation. It tends to produce colic and nausea. It is also used as a veterinary fungicide, anthelmintic, and antiprotozoan. (From Merck, 11th ed.)

Diclofenac - A non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt.

Dicloxacillin - One of the PENICILLINS which is resistant to PENICILLINASE.

Diet, Sodium-Restricted - A diet which contains very little sodium chloride. It is prescribed by some for hypertension and for edematous states. (Dorland, 27th ed)

Diethylcarbamazine - An anthelmintic used primarily as the citrate in the treatment of filariasis, particularly infestations with Wucheria bancrofti or Loa loa.

Diketopiperazines - Piperazines with two keto oxygens.

Dioctyl Sulfosuccinic Acid - All-purpose surfactant, wetting agent, and solubilizer used in the drug, cosmetics, and food industries. It has also been used in laxatives and as cerumenolytics. It is usually administered as either the calcium, potassium, or sodium salt.

Dithionite - Dithionite. The dithionous acid ion and its salts.

Ditiocarb - A chelating agent that has been used to mobilize toxic metals from the tissues of humans and experimental animals. It is the main metabolite of DISULFIRAM.

Eflornithine - An inhibitor of ORNITHINE DECARBOXYLASE, the rate limiting enzyme of the polyamine biosynthetic pathway.

Electrophoresis, Polyacrylamide Gel - Electrophoresis in which a polyacrylamide gel is used as the diffusion medium.

Emetine - The principal alkaloid of ipecac, from the ground roots of Uragoga (or Cephaelis) ipecacuanha or U. acuminata, of the Rubiaceae. It is used as an amebicide in many different preparations and may cause serious cardiac, hepatic, or renal damage and violent diarrhea and vomiting. Emetine inhibits protein synthesis in EUKARYOTIC CELLS but not PROKARYOTIC CELLS.

Epithelial Sodium Channels - Sodium channels found on salt-reabsorbing EPITHELIAL CELLS that line the distal NEPHRON; the distal COLON; SALIVARY DUCTS; SWEAT GLANDS; and the LUNG. They are AMILORIDE-sensitive and play a critical role in the control of sodium balance, BLOOD VOLUME, and BLOOD PRESSURE.

Ethacrynic Acid - A compound that inhibits symport of sodium, potassium, and chloride primarily in the ascending limb of Henle, but also in the proximal and distal tubules. This pharmacological action results in excretion of these ions, increased urinary output, and reduction in extracellular fluid. This compound has been classified as a loop or high ceiling diuretic.

Ethambutol - An antitubercular agent that inhibits the transfer of mycolic acids into the cell wall of the tubercle bacillus. It may also inhibit the synthesis of spermidine in mycobacteria. The action is usually bactericidal, and the drug can penetrate human cell membranes to exert its lethal effect. (From Smith and Reynard, Textbook of Pharmacology, 1992, p863)

Ethionamide - A second-line antitubercular agent that inhibits mycolic acid synthesis.

Etidronic Acid - A diphosphonate which affects calcium metabolism. It inhibits ectopic calcification and slows down bone resorption and bone turnover.

Fenbendazole - Antinematodal benzimidazole used in veterinary medicine.

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.

Fluconazole - Triazole antifungal agent that is used to treat oropharyngeal CANDIDIASIS and cryptococcal MENINGITIS in AIDS.

Flucytosine - A fluorinated cytosine analog that is used as an antifungal agent.

Fluorescein - A phthalic indicator dye that appears yellow-green in normal tear film and bright green in a more alkaline medium such as the aqueous humor.

Fluorocarbons - Liquid perfluorinated carbon compounds which may or may not contain a hetero atom such as nitrogen, oxygen or sulfur, but do not contain another halogen or hydrogen atom. This concept includes fluorocarbon emulsions, and fluorocarbon blood substitutes. Perfluorinated and related polyfluorinated chemicals are referred to as PFAS and are defined as chemicals with at least two adjacent carbon atoms, where one carbon is fully fluorinated and the other is at least partially fluorinated.

Fosinopril - A phosphinic acid-containing angiotensin-converting enzyme inhibitor that is effective in the treatment of hypertension. It is a prodrug that is converted to its active metabolite fosinoprilat.

Furazolidone - A nitrofuran derivative with antiprotozoal and antibacterial activity. Furazolidone acts by gradual inhibition of monoamine oxidase. (From Martindale, The Extra Pharmacopoeia, 30th ed, p514)

Fusidic Acid - An antibiotic isolated from the fermentation broth of Fusidium coccineum. (From Merck Index, 11th ed). It acts by inhibiting translocation during protein synthesis.

Glaucarubin - (1 beta,2 alpha,11 beta,12 alpha,15 beta(S))-11,20-Epoxy-1,2,11,12-tetrahydroxy-15-(2-hydroxy-2-methyl-1-oxobutoxy)picras-3-en-16-one. A quassinoid (Simaroubolide) from Simaruba glauca, a tropical shrub. It has been used as an antiamebic agent and is found to be cytotoxic. It may be of use in cancer chemotherapy.

Glutamate Plasma Membrane Transport Proteins - A family of plasma membrane neurotransmitter transporter proteins that couple the uptake of GLUTAMATE with the import of SODIUM ions and PROTONS and the export of POTASSIUM ions. In the CENTRAL NERVOUS SYSTEM they regulate neurotransmission through synaptic reuptake of the excitatory neurotransmitter glutamate. Outside the central nervous system they function as signal mediators and regulators of glutamate metabolism.

Gold Sodium Thiomalate - A variable mixture of the mono- and disodium salts of gold thiomalic acid used mainly for its anti-inflammatory action in the treatment of rheumatoid arthritis. It is most effective in active progressive rheumatoid arthritis and of little or no value in the presence of extensive deformities or in the treatment of other forms of arthritis.

Gold Sodium Thiosulfate - A sodium salt of gold thiosulfate. It has uses like the ORGANOGOLD COMPOUNDS.

Gossypol - A dimeric sesquiterpene found in cottonseed (GOSSYPIUM). The (-) isomer is active as a male contraceptive (CONTRACEPTIVE AGENTS, MALE) whereas toxic symptoms are associated with the (+) isomer.

Heparin - A highly acidic mucopolysaccharide formed of equal parts of sulfated D-glucosamine and D-glucuronic acid with sulfaminic bridges. The molecular weight ranges from six to twenty thousand. Heparin occurs in and is obtained from liver, lung, mast cells, etc., of vertebrates. Its function is unknown, but it is used to prevent blood clotting in vivo and vitro, in the form of many different salts.

Hexetidine - A bactericidal and fungicidal antiseptic. It is used as a 0.1% mouthwash for local infections and oral hygiene. (From Martindale, The Extra Pharmacopoeia, 30th ed, p797)

Hexobarbital - A barbiturate that is effective as a hypnotic and sedative.

Humic Substances - Organic matter in a state of advanced decay, after passing through the stages of COMPOST and PEAT and before becoming lignite (COAL). It is composed of a heterogenous mixture of compounds including phenolic radicals and acids that polymerize and are not easily separated nor analyzed. (E.A. Ghabbour & G. Davies, eds. Humic Substances, 2001).

Hyaluronic Acid - A natural high-viscosity mucopolysaccharide with alternating beta (1-3) glucuronide and beta (1-4) glucosaminidic bonds. It is found in the UMBILICAL CORD, in VITREOUS BODY and in SYNOVIAL FLUID. A high urinary level is found in PROGERIA.

Hydroxychloroquine - A chemotherapeutic agent that acts against erythrocytic forms of malarial parasites. Hydroxychloroquine appears to concentrate in food vacuoles of affected protozoa. It inhibits plasmodial heme polymerase. (From Gilman et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 9th ed, p970)

Inosine Monophosphate - Inosine 5'-Monophosphate. A purine nucleotide which has hypoxanthine as the base and one phosphate group esterified to the sugar moiety.

Inosine Pranobex - An alkylamino-alcohol complex of inosine used in the treatment of a variety of viral infections. Unlike other antiviral agents, it acts by modifying or stimulating cell-mediated immune processes rather than acting on the virus directly.

Insulin - A 51-amino acid pancreatic hormone that plays a major role in the regulation of glucose metabolism, directly by suppressing endogenous glucose production (GLYCOGENOLYSIS; GLUCONEOGENESIS) and indirectly by suppressing GLUCAGON secretion and LIPOLYSIS. Native insulin is a globular protein comprised of a zinc-coordinated hexamer. Each insulin monomer containing two chains, A (21 residues) and B (30 residues), linked by two disulfide bonds. Insulin is used as a drug to control insulin-dependent diabetes mellitus (DIABETES MELLITUS, TYPE 1).

Iodoacetic Acid - A derivative of ACETIC ACID that contains one IODINE atom attached to its methyl group.

Iodohippuric Acid - An iodine-containing compound used in pyelography as a radiopaque medium. If labeled with radioiodine, it can be used for studies of renal function.

Iodoquinol - One of the halogenated 8-quinolinols widely used as an intestinal antiseptic, especially as an antiamebic agent. It is also used topically in other infections and may cause CNS and eye damage. It is known by very many similar trade names world-wide.

Iothalamate Meglumine - A radiopaque medium used for urography, angiography, venography, and myelography. It is highly viscous and binds to plasma proteins.

Iothalamic Acid - A contrast medium in diagnostic radiology with properties similar to those of diatrizoic acid. It is used primarily as its sodium and meglumine (IOTHALAMATE MEGLUMINE) salts.

Ioxaglic Acid - A low-osmolar, ionic contrast medium used in various radiographic procedures.

Ipodate - Ionic monomeric contrast media. Usually the sodium or calcium salts are used for examination of the gall bladder and biliary tract. (From Martindale, The Extra Pharmacopoeia, 30th ed, p704)

Isethionic Acid - A colorless, syrupy, strongly acidic liquid that can form detergents with oleic acid.

Isoniazid - Antibacterial agent used primarily as a tuberculostatic. It remains the treatment of choice for tuberculosis.

Itraconazole - A triazole antifungal agent that inhibits cytochrome P-450-dependent enzymes required for ERGOSTEROL synthesis.

Ivermectin - A mixture of mostly avermectin H2B1a (RN 71827-03-7) with some avermectin H2B1b (RN 70209-81-3), which are macrolides from STREPTOMYCES avermitilis. It binds glutamate-gated chloride channel to cause increased permeability and hyperpolarization of nerve and muscle cells. It also interacts with other CHLORIDE CHANNELS. It is a broad spectrum antiparasitic that is active against microfilariae of ONCHOCERCA VOLVULUS but not the adult form.

Lansoprazole - A 2,2,2-trifluoroethoxypyridyl derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON SYNDROME. The drug inhibits H(+)-K(+)-EXCHANGING ATPASE which is found in GASTRIC PARIETAL CELLS. Lansoprazole is a racemic mixture of (R)- and (S)-isomers.

Levamisole - An antihelminthic drug that has been tried experimentally in rheumatic disorders where it apparently restores the immune response by increasing macrophage chemotaxis and T-lymphocyte function. Paradoxically, this immune enhancement appears to be beneficial in rheumatoid arthritis where dermatitis, leukopenia, and thrombocytopenia, and nausea and vomiting have been reported as side effects. (From Smith and Reynard, Textbook of Pharmacology, 1991, p435-6)

Lucanthone - One of the SCHISTOSOMICIDES, it has been replaced largely by HYCANTHONE and more recently PRAZIQUANTEL. (From Martindale The Extrapharmacopoeia, 30th ed., p46)

Malondialdehyde - The dialdehyde of malonic acid.

Mebendazole - A benzimidazole that acts by interfering with CARBOHYDRATE METABOLISM and inhibiting polymerization of MICROTUBULES.

Meclofenamic Acid - A non-steroidal anti-inflammatory agent with antipyretic and antigranulation activities. It also inhibits prostaglandin biosynthesis.

Mefloquine - A phospholipid-interacting antimalarial drug (ANTIMALARIALS). It is very effective against PLASMODIUM FALCIPARUM with very few side effects.

Meglumine - 1-Deoxy-1-(methylamino)-D-glucitol. A derivative of sorbitol in which the hydroxyl group in position 1 is replaced by a methylamino group. Often used in conjunction with iodinated organic compounds as contrast medium.

Meglumine Antimoniate - ANTIMONY salt of meglumine that is used in the treatment of LEISHMANIASIS.

Melarsoprol - Arsenical used in trypanosomiases. It may cause fatal encephalopathy and other undesirable side effects.

Mesna - A sulfhydryl compound used to prevent urothelial toxicity by inactivating metabolites from ANTINEOPLASTIC AGENTS, such as IFOSFAMIDE or CYCLOPHOSPHAMIDE.

Methanol - A colorless, flammable liquid used in the manufacture of FORMALDEHYDE and ACETIC ACID, in chemical synthesis, antifreeze, and as a solvent. Ingestion of methanol is toxic and may cause blindness.

Methisazone - An antiviral agent effective against pox viruses.

Methohexital - An intravenous anesthetic with a short duration of action that may be used for induction of anesthesia.

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.

Methylprednisolone Hemisuccinate - A water-soluble ester of METHYLPREDNISOLONE used for cardiac, allergic, and hypoxic emergencies.

Metronidazole - A nitroimidazole used to treat AMEBIASIS; VAGINITIS; TRICHOMONAS INFECTIONS; GIARDIASIS; ANAEROBIC BACTERIA; and TREPONEMAL INFECTIONS.

Mezlocillin - Semisynthetic ampicillin-derived acylureido penicillin. It has been proposed for infections with certain anaerobes and may be useful in inner ear, bile, and CNS infections.

Misonidazole - A nitroimidazole that sensitizes normally radio-resistant hypoxic cells to radiation. It may also be directly cytotoxic to hypoxic cells and has been proposed as an antineoplastic.

Mycophenolic Acid - Compound derived from Penicillium stoloniferum and related species. It blocks de novo biosynthesis of purine nucleotides by inhibition of the enzyme inosine monophosphate dehydrogenase (IMP DEHYDROGENASE). Mycophenolic acid exerts selective effects on the immune system in which it prevents the proliferation of T-CELLS, LYMPHOCYTES, and the formation of antibodies from B-CELLS. It may also inhibit recruitment of LEUKOCYTES to sites of INFLAMMATION.

Nafcillin - A semi-synthetic antibiotic related to penicillin.

Nalidixic Acid - A synthetic 1,8-naphthyridine antimicrobial agent with a limited bacteriocidal spectrum. It is an inhibitor of the A subunit of bacterial DNA GYRASE.

Naproxen - An anti-inflammatory agent with analgesic and antipyretic properties. Both the acid and its sodium salt are used in the treatment of rheumatoid arthritis and other rheumatic or musculoskeletal disorders, dysmenorrhea, and acute gout.

NAV1.1 Voltage-Gated Sodium Channel - A voltage-gated sodium channel subtype that is predominantly expressed in the CENTRAL NERVOUS SYSTEM. Defects in the SCN1A gene which codes for the alpha subunit of this sodium channel are associated with DRAVET SYNDROME, generalized epilepsy with febrile seizures plus, type 2 (GEFS+2), and familial hemiplegic migraine type 3.

NAV1.2 Voltage-Gated Sodium Channel - A voltage-gated sodium channel subtype that mediates the sodium ion permeability of excitable membranes. Defects in the SCN2A gene which codes for the alpha subunit of this sodium channel are associated with benign familial infantile seizures type 3, and early infantile epileptic encephalopathy type 11.

NAV1.4 Voltage-Gated Sodium Channel - A voltage-gated sodium channel subtype that mediates the sodium ion PERMEABILITY of SKELETAL MYOCYTES. Defects in the SCN4A gene, which codes for the alpha subunit of this sodium channel, are associated with several MYOTONIC DISORDERS.

NAV1.5 Voltage-Gated Sodium Channel - A voltage-gated sodium channel subtype that mediates the sodium ion PERMEABILITY of CARDIOMYOCYTES. Defects in the SCN5A gene, which codes for the alpha subunit of this sodium channel, are associated with a variety of CARDIAC DISEASES that result from loss of sodium channel function.

NAV1.8 Voltage-Gated Sodium Channel - A voltage-gated sodium channel subtype that is expressed in nociceptors, including spinal and trigeminal sensory neurons. It plays a role in the transmission of pain signals induced by cold, heat, and mechanical stimuli.

NAV1.9 Voltage-Gated Sodium Channel - A voltage-gated sodium channel subtype found in the neurons of the NERVOUS SYSTEM and DORSAL ROOT GANGLIA. It may play a role in the generation of heat and mechanical pain hypersensitivity.

Nedocromil - A pyranoquinolone derivative that inhibits activation of inflammatory cells which are associated with ASTHMA, including EOSINOPHILS; NEUTROPHILS; MACROPHAGES; MAST CELLS; MONOCYTES; AND PLATELETS.

Niacin - A water-soluble vitamin of the B complex occurring in various animal and plant tissues. It is required by the body for the formation of coenzymes NAD and NADP. It has PELLAGRA-curative, vasodilating, and antilipemic properties.

Niclosamide - An antihelmintic that is active against most tapeworms. (From Martindale, The Extra Pharmacopoeia, 30th ed, p48)

Nifuratel - Local antiprotozoal and antifungal agent that may also be given orally.

Nifurtimox - A nitrofuran thiazine that has been used against TRYPANOSOMIASIS.

Nimorazole - An antitrichomonal agent which is effective either topically or orally and whose urinary metabolites are also trichomonicidal.

Niridazole - An antischistosomal agent that has become obsolete.

Nitrofurantoin - A urinary anti-infective agent effective against most gram-positive and gram-negative organisms. Although sulfonamides and antibiotics are usually the agents of choice for urinary tract infections, nitrofurantoin is widely used for prophylaxis and long-term suppression.

Nitroprusside - A powerful vasodilator used in emergencies to lower blood pressure or to improve cardiac function. It is also an indicator for free sulfhydryl groups in proteins.

Norepinephrine Plasma Membrane Transport Proteins - Sodium chloride-dependent neurotransmitter symporters located primarily on the PLASMA MEMBRANE of noradrenergic neurons. They remove NOREPINEPHRINE from the EXTRACELLULAR SPACE by high affinity reuptake into PRESYNAPTIC TERMINALS. The norepinephrine transporter regulates signal amplitude and duration at noradrenergic synapses and is the target of ADRENERGIC UPTAKE INHIBITORS.

Novobiocin - An antibiotic compound derived from Streptomyces niveus. It has a chemical structure similar to coumarin. Novobiocin binds to DNA gyrase, and blocks adenosine triphosphatase (ATPase) activity. (From Reynolds, Martindale The Extra Pharmacopoeia, 30th ed, p189)

Omeprazole - A 4-methoxy-3,5-dimethylpyridyl, 5-methoxybenzimidazole derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON SYNDROME. The drug inhibits an H(+)-K(+)-EXCHANGING ATPASE which is found in GASTRIC PARIETAL CELLS.

Organic Anion Transporters, Sodium-Independent - A subclass of ORGANIC ANION TRANSPORTERS that do not rely directly or indirectly upon sodium ion gradients for the transport of organic ions.

Ornidazole - A nitroimidazole antiprotozoal agent used in ameba and trichomonas infections. It is partially plasma-bound and also has radiation-sensitizing action.

Orotic Acid - An intermediate product in PYRIMIDINE synthesis which plays a role in chemical conversions between DIHYDROFOLATE and TETRAHYDROFOLATE.

Orphenadrine - A muscarinic antagonist used to treat drug-induced parkinsonism and to relieve pain from muscle spasm.

Oxacillin - An antibiotic similar to FLUCLOXACILLIN used in resistant staphylococci infections.

Oxalic Acid - A strong dicarboxylic acid occurring in many plants and vegetables. It is produced in the body by metabolism of glyoxylic acid or ascorbic acid. It is not metabolized but excreted in the urine. It is used as an analytical reagent and general reducing agent.

Oxamniquine - An anthelmintic with schistosomicidal activity against Schistosoma mansoni, but not against other Schistosoma spp. Oxamniquine causes worms to shift from the mesenteric veins to the liver where the male worms are retained; the female worms return to the mesentery, but can no longer release eggs. (From Martindale, The Extra Pharmacopoeia, 31st ed, p121)

Oxolinic Acid - Synthetic antimicrobial related to NALIDIXIC ACID and used in URINARY TRACT INFECTIONS.

Palmitic Acid - A common saturated fatty acid found in fats and waxes including olive oil, palm oil, and body lipids.

p-Aminohippuric Acid - The glycine amide of 4-aminobenzoic acid. Its sodium salt is used as a diagnostic aid to measure effective renal plasma flow (ERPF) and excretory capacity.

Paralysis, Hyperkalemic Periodic - An autosomal dominant familial disorder which presents in infancy or childhood and is characterized by episodes of weakness associated with hyperkalemia. During attacks, muscles of the lower extremities are initially affected, followed by the lower trunk and arms. Episodes last from 15-60 minutes and typically occur after a period of rest following exercise. A defect in skeletal muscle sodium channels has been identified as the cause of this condition. Normokalemic periodic paralysis is a closely related disorder marked by a lack of alterations in potassium levels during attacks of weakness. (Adams et al., Principles of Neurology, 6th ed, p1481)

Pefloxacin - A synthetic broad-spectrum fluoroquinolone antibacterial agent active against most gram-negative and gram-positive bacteria.

Penicillin G - A penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on GAMMA-AMINOBUTYRIC ACID mediated synaptic transmission.

Penicillin V - A broad-spectrum penicillin antibiotic used orally in the treatment of mild to moderate infections by susceptible gram-positive organisms.

Pentachlorophenol - An insecticide and herbicide that has also been used as a wood preservative. Pentachlorphenol is a widespread environmental pollutant. Both chronic and acute pentachlorophenol poisoning are medical concerns. The range of its biological actions is still being actively explored, but it is clearly a potent enzyme inhibitor and has been used as such as an experimental tool.

Pentamidine - Antiprotozoal agent effective in trypanosomiasis, leishmaniasis, and some fungal infections; used in treatment of PNEUMOCYSTIS pneumonia in HIV-infected patients. It may cause diabetes mellitus, central nervous system damage, and other toxic effects.

Pentosan Sulfuric Polyester - A sulfated pentosyl polysaccharide with heparin-like properties.

Peracetic Acid - A liquid that functions as a strong oxidizing agent. It has an acrid odor and is used as a disinfectant.

Phenobarbital - A barbituric acid derivative that acts as a nonselective central nervous system depressant. It potentiates GAMMA-AMINOBUTYRIC ACID action on GABA-A RECEPTORS, and modulates chloride currents through receptor channels. It also inhibits glutamate induced depolarizations.

Phenol - An antiseptic and disinfectant aromatic alcohol.

Phenytoin - An anticonvulsant that is used to treat a wide variety of seizures. It is also an anti-arrhythmic and a muscle relaxant. The mechanism of therapeutic action is not clear, although several cellular actions have been described including effects on ion channels, active transport, and general membrane stabilization. The mechanism of its muscle relaxant effect appears to involve a reduction in the sensitivity of muscle spindles to stretch. Phenytoin has been proposed for several other therapeutic uses, but its use has been limited by its many adverse effects and interactions with other drugs.

Phytic Acid - Complexing agent for removal of traces of heavy metal ions. It acts also as a hypocalcemic agent.

Pipemidic Acid - Antimicrobial against Gram negative and some Gram positive bacteria. It is protein bound and concentrated in bile and urine and used for gastrointestinal, biliary, and urinary infections.

Piperacillin - Semisynthetic, broad-spectrum, AMPICILLIN derived ureidopenicillin antibiotic proposed for PSEUDOMONAS infections. It is also used in combination with other antibiotics.

Piperazine - An anti-nematodal agent effective against the intestinal nematodes ASCARIS LUMBRICOIDES (roundworm) and ENTEROBIUS VERMICULARIS (pinworm, threadworm). It produces a neuromuscular block leading to flaccid muscle paralysis in susceptible worms, which are then dislodged from the gut and expelled in feces.

Piperazines - Compounds that are derived from PIPERAZINE.

Piromidic Acid - Antibacterial against mainly gram negative organisms. It is used for urinary tract and intestinal infections.

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.

Polyanetholesulfonate - A compound originally developed as an anticoagulant, but possessing anticomplement action and lowering the bactericidal action of blood. It is used in vitro to inhibit blood coagulation and as a diagnostic reagent to encourage the growth of pathogens in the blood. It is also used to stabilize colloidal solutions such as milk and gelatin. (From Merck Index, 11th ed)

Potassium Channels, Sodium-Activated - Potassium channels whose activation is dependent on intracellular sodium concentrations.

Pravastatin - An antilipemic fungal metabolite isolated from cultures of Nocardia autotrophica. It acts as a competitive inhibitor of HMG CoA reductase (HYDROXYMETHYLGLUTARYL COA REDUCTASES).

Praziquantel - An anthelmintic used in most schistosome and many cestode infestations.

Primaquine - An aminoquinoline that is given by mouth to produce a radical cure and prevent relapse of vivax and ovale malarias following treatment with a blood schizontocide. It has also been used to prevent transmission of falciparum malaria by those returning to areas where there is a potential for re-introduction of malaria. Adverse effects include anemias and GI disturbances. (From Martindale, The Extra Pharmacopeia, 30th ed, p404)

Proguanil - A biguanide compound which metabolizes in the body to form cycloguanil, an anti-malaria agent.

Prothionamide - Antitubercular agent similar in action and side effects to ETHIONAMIDE. It is used mostly in combination with other agents.

Pyrantel - A depolarizing neuromuscular-blocking agent, that causes persistent nicotinic activation resulting in spastic paralysis of susceptible nematodes. It is a drug of second-choice after benzimidazoles for treatment of ascariasis, hookworm, and pinworm infections, being effective after a single dose. (From Smith and Reynard, Textbook of Pharmacology, 1992, p920)

Pyrantel Pamoate - Broad spectrum antinematodal anthelmintic used also in veterinary medicine.

Pyrantel Tartrate - Broad spectrum anthelmintic for livestock.

Pyrazinamide - A pyrazine that is used therapeutically as an antitubercular agent.

Pyrimethamine - One of the FOLIC ACID ANTAGONISTS that is used as an antimalarial or with a sulfonamide to treat toxoplasmosis.

Quinacrine - An acridine derivative formerly widely used as an antimalarial but superseded by chloroquine in recent years. It has also been used as an anthelmintic and in the treatment of giardiasis and malignant effusions. It is used in cell biological experiments as an inhibitor of phospholipase A2.

Quinacrine Mustard - Nitrogen mustard analog of quinacrine used primarily as a stain in the studies of chromosomes and chromatin. Fluoresces by reaction with nucleic acids in chromosomes.

Quinine - An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood.

Rabeprazole - A 4-(3-methoxypropoxy)-3-methylpyridinyl derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON SYNDROME. The drug inhibits H(+)-K(+)-EXCHANGING ATPASE which is found in GASTRIC PARIETAL CELLS.

Ribavirin - A nucleoside antimetabolite antiviral agent that blocks nucleic acid synthesis and is used against both RNA and DNA viruses.

Rimantadine - An RNA synthesis inhibitor that is used as an antiviral agent in the prophylaxis and treatment of influenza.

Risedronic Acid - A pyridine and diphosphonic acid derivative that acts as a CALCIUM CHANNEL BLOCKER and inhibits BONE RESORPTION.

Saline Solution, Hypertonic - Hypertonic sodium chloride solution. A solution having an osmotic pressure greater than that of physiologic salt solution (0.9 g NaCl in 100 ml purified water).

Santonin - Anthelmintic isolated from the dried unexpanded flower heads of Artemisia maritima and other species of Artemisia found principally in Russian and Chinese Turkestan and the Southern Ural region. (From Merck, 11th ed.)

Sarcosine - An amino acid intermediate in the metabolism of choline.

Secobarbital - A barbiturate that is used as a sedative. Secobarbital is reported to have no anti-anxiety activity.

Selenic Acid - A strong dibasic acid with the molecular formula H2SeO4. Included under this heading is the acid form, and inorganic salts of dihydrogen selenium tetraoxide.

Serotonin Plasma Membrane Transport Proteins - Sodium chloride-dependent neurotransmitter symporters located primarily on the PLASMA MEMBRANE of serotonergic neurons. They are different than SEROTONIN RECEPTORS, which signal cellular responses to SEROTONIN. They remove SEROTONIN from the EXTRACELLULAR SPACE by high affinity reuptake into PRESYNAPTIC TERMINALS. Regulates signal amplitude and duration at serotonergic synapses and is the site of action of the SELECTIVE SEROTONIN REUPTAKE INHIBITORS.

Silver Sulfadiazine - Antibacterial used topically in burn therapy.

SLC4A Proteins - Bicarbonate transporters that move BICARBONATE IONS in exchange of CHLORIDE IONS or SODIUM IONS across membranes. They regulate acid-base HOMEOSTASIS, cell volume and intracellular pH. Members include CHLORIDE-BICARBONATE ANTIPORTERS (SLC4A1, 2, 3, and 9); SODIUM-COUPLED BICARBONATE TRANSPORTERS (SLC4A4 and 5, 7, 8 and 10); and a sodium borate cotransporter (SLC4A11 protein).

Sodium - A member of the alkali group of metals. It has the atomic symbol Na, atomic number 11, and atomic weight 23.

Sodium Acetate - The trihydrate sodium salt of acetic acid, which is used as a source of sodium ions in solutions for dialysis and as a systemic and urinary alkalizer, diuretic, and expectorant.

Sodium Azide - A cytochrome oxidase inhibitor which is a nitridizing agent and an inhibitor of terminal oxidation. (From Merck Index, 12th ed)

Sodium Benzoate - The sodium salt of BENZOIC ACID. It is used as an antifungal preservative in pharmaceutical preparations and foods. It may also be used as a test for liver function.

Sodium Bicarbonate - A white, crystalline powder that is commonly used as a pH buffering agent, an electrolyte replenisher, systemic alkalizer and in topical cleansing solutions.

Sodium Channel Agonists - A class of drugs that stimulate sodium influx through cell membrane channels.

Sodium Channel Blockers - A class of drugs that act by inhibition of sodium influx through cell membranes. Blockade of sodium channels slows the rate and amplitude of initial rapid depolarization, reduces cell excitability, and reduces conduction velocity.

Sodium Channels - Ion channels that specifically allow the passage of SODIUM ions. A variety of specific sodium channel subtypes are involved in serving specialized functions such as neuronal signaling, CARDIAC MUSCLE contraction, and KIDNEY function.

Sodium Chloride - A ubiquitous sodium salt that is commonly used to season food.

Sodium Chloride Symporter Inhibitors - Agents that inhibit SODIUM CHLORIDE SYMPORTERS. They act as DIURETICS. Excess use is associated with HYPOKALEMIA.

Sodium Chloride Symporters - A subclass of symporters found in KIDNEY TUBULES, DISTAL that are the major pathway for salt resorption. Inhibition of these symporters by BENZOTHIADIAZINES is the basis of action of some DIURETICS.

Sodium Chloride, Dietary - Sodium chloride used in foods.

Sodium Cholate - A trihydroxy bile salt that is used as a digestive aid in dietary supplements. It is used in culture media and in conjunction with PAPAIN and PANCREATIN.

Sodium Citrate - Sodium salts of citric acid that are used as buffers and food preservatives. They are used medically as anticoagulants in stored blood, and for urine alkalization in the prevention of KIDNEY STONES.

Sodium Compounds - Inorganic compounds that contain sodium as an integral part of the molecule.

Sodium Cyanide - A highly poisonous compound that is an inhibitor of many metabolic processes and is used as a test reagent for the function of chemoreceptors. It is also used in many industrial processes.

Sodium Dodecyl Sulfate - An anionic surfactant, usually a mixture of sodium alkyl sulfates, mainly the lauryl; lowers surface tension of aqueous solutions; used as fat emulsifier, wetting agent, detergent in cosmetics, pharmaceuticals and toothpastes; also as research tool in protein biochemistry.

Sodium Fluoride - A source of inorganic fluoride which is used topically to prevent dental caries.

Sodium Glutamate - One of the FLAVORING AGENTS used to impart a meat-like flavor.

Sodium Hydroxide - A highly caustic substance that is used to neutralize acids and make sodium salts. (From Merck Index, 11th ed)

Sodium Hypochlorite - It is used as an oxidizing and bleaching agent and as a disinfectant. (From Grant & Hackh's Chemical Dictionary, 5th ed)

Sodium Iodide - A compound forming white, odorless deliquescent crystals and used as iodine supplement, expectorant or in its radioactive (I-131) form as an diagnostic aid, particularly for thyroid function tests.

Sodium Ionophores - Chemical agents that increase the permeability of CELL MEMBRANES to SODIUM ions.

Sodium Isotopes - Stable sodium atoms that have the same atomic number as the element sodium, but differ in atomic weight. Na-23 is a stable sodium isotope.

Sodium Lactate - The sodium salt of racemic or inactive lactic acid. It is a hygroscopic agent used intravenously as a systemic and urinary alkalizer.

Sodium Morrhuate - The sodium salts of the fatty acids in cod liver oil; an irritant and sclerosing agent used to treat varicose veins and arthritic joints.

Sodium Nitrite - Nitrous acid sodium salt. Used in many industrial processes, in meat curing, coloring, and preserving, and as a reagent in ANALYTICAL CHEMISTRY TECHNIQUES. It is used therapeutically as an antidote in cyanide poisoning. The compound is toxic and mutagenic and will react in vivo with secondary or tertiary amines thereby producing highly carcinogenic nitrosamines.

Sodium Oxybate - The sodium salt of 4-hydroxybutyric acid. It is used for both induction and maintenance of ANESTHESIA.

Sodium Pertechnetate Tc 99m - A gamma-emitting radionuclide imaging agent used for the diagnosis of diseases in many tissues, particularly in the gastrointestinal system, cardiovascular and cerebral circulation, brain, thyroid, and joints.

Sodium Potassium Chloride Symporter Inhibitors - Agents that inhibit SODIUM-POTASSIUM-CHLORIDE SYMPORTERS which are concentrated in the thick ascending limb at the junction of the LOOP OF HENLE and KIDNEY TUBULES, DISTAL. They act as DIURETICS. Excess use is associated with HYPOKALEMIA and HYPERGLYCEMIA.

Sodium Radioisotopes - Unstable isotopes of sodium that decay or disintegrate emitting radiation. Na atoms with atomic weights 20-22 and 24-26 are radioactive sodium isotopes.

Sodium Salicylate - A non-steroidal anti-inflammatory agent that is less effective than equal doses of ASPIRIN in relieving pain and reducing fever. However, individuals who are hypersensitive to ASPIRIN may tolerate sodium salicylate. In general, this salicylate produces the same adverse reactions as ASPIRIN, but there is less occult gastrointestinal bleeding. (From AMA Drug Evaluations Annual, 1992, p120)

Sodium Selenite - The disodium salt of selenious acid. It is used therapeutically to supply the trace element selenium and is prepared by the reaction of SELENIUM DIOXIDE with SODIUM HYDROXIDE.

Sodium Sulfate Cotransporter - A multi-pass protein that consists of 13 transmembrane helices. It is expressed primarily by renal epithelial cells and functions as a co-transporter of sodium and sulfate, to mediate sulfate reabsorption in the kidney.

Sodium Tetradecyl Sulfate - An anionic surface-active agent used for its wetting properties in industry and used in medicine as an irritant and sclerosing agent for hemorrhoids and varicose veins.

Sodium, Dietary - Sodium or sodium compounds used in foods or as a food. The most frequently used compounds are sodium chloride or sodium glutamate.

Sodium-Bicarbonate Symporters - Proteins that cotransport sodium ions and bicarbonate ions across cellular membranes.

Sodium-Calcium Exchanger - An electrogenic ion exchange protein that maintains a steady level of calcium by removing an amount of calcium equal to that which enters the cells. It is widely distributed in most excitable membranes, including the brain and heart.

Sodium-Coupled Vitamin C Transporters - Membrane transport proteins that actively co-transport ASCORBIC ACID and sodium ions across the CELL MEMBRANE. Dietary absorption of VITAMIN C is highly dependent upon this class of transporters and a subset of SODIUM GLUCOSE TRANSPORTERS which transport the oxidized form of vitamin C, DEHYDROASCORBIC ACID.

Sodium-Glucose Transport Proteins - Monosaccharide transport proteins that function as active symporters. They utilize SODIUM or HYDROGEN IONS to transport GLUCOSE across CELL MEMBRANES.

Sodium-Glucose Transporter 1 - The founding member of the sodium glucose transport proteins. It is predominately expressed in the INTESTINAL MUCOSA of the SMALL INTESTINE.

Sodium-Glucose Transporter 2 - A sodium-glucose transporter that is expressed in the luminal membrane of the PROXIMAL KIDNEY TUBULES.

Sodium-Glucose Transporter 2 Inhibitors - Compounds that inhibit SODIUM-GLUCOSE TRANSPORTER 2. They lower blood sugar by preventing the reabsorption of glucose by the kidney and are used in the treatment of TYPE 2 DIABETES MELLITUS.

Sodium-Hydrogen Exchanger 1 - A sodium-hydrogen antiporter expressed by many cell types, especially on the basolateral surfaces of EPITHELIAL CELLS. It functions through an inward sodium ion chemical gradient to eliminate acids (protons) generated by metabolism and regulate intracellular pH. It is highly sensitive to AMILORIDE.

Sodium-Hydrogen Exchanger 3 - A sodium-hydrogen antiporter expressed primarily by EPITHELIAL CELLS in the kidneys, it localizes to the apical membrane of the PROXIMAL KIDNEY TUBULE, where it functions in sodium and water reabsorption and possibly calcium homeostasis. It also is expressed in heart, brain, and lung tissues and is resistant to AMILORIDE inhibition.

Sodium-Hydrogen Exchangers - A family of plasma membrane exchange glycoprotein antiporters that transport sodium ions and protons across lipid bilayers. They have critical functions in intracellular pH regulation, cell volume regulation, and cellular response to many different hormones and mitogens.

Sodium-Phosphate Cotransporter Proteins - A family of symporters that facilitate sodium-dependent membrane transport of phosphate.

Sodium-Phosphate Cotransporter Proteins, Type I - A family of sodium-phosphate cotransporter proteins that also transport organic ANIONS. They are low affinity phosphate transporters.

Sodium-Phosphate Cotransporter Proteins, Type II - A family of sodium-phosphate cotransporter proteins with eight transmembrane domains. They are present primarily in the KIDNEY and SMALL INTESTINE and are responsible for renal and small intestinal epithelial transport of phosphates.

Sodium-Phosphate Cotransporter Proteins, Type IIa - An electrogenic sodium-dependent phosphate transporter. It is present primarily in BRUSH BORDER membranes of PROXIMAL RENAL TUBULES.

Sodium-Phosphate Cotransporter Proteins, Type IIb - A sodium-dependent phosphate transporter present primarily at apical sites of EPITHELIAL CELLS in the SMALL INTESTINE.

Sodium-Phosphate Cotransporter Proteins, Type IIc - A non-electrogenic sodium-dependent phosphate transporter. It is found primarily in apical membranes of PROXIMAL RENAL TUBULES.

Sodium-Phosphate Cotransporter Proteins, Type III - A family of highly conserved and widely expressed sodium-phosphate cotransporter proteins. They are electrogenic sodium-dependent transporters of phosphate that were originally identified as retroviral receptors in HUMANS and have been described in yeast and many other organisms.

Sodium-Potassium-Chloride Symporters - A subclass of symporters that specifically transport SODIUM; POTASSIUM and CHLORIDE ions across cellular membranes in a tightly coupled electroneutrality process.

Sodium-Potassium-Exchanging ATPase - An enzyme that catalyzes the active transport system of sodium and potassium ions across the cell wall. Sodium and potassium ions are closely coupled with membrane ATPase which undergoes phosphorylation and dephosphorylation, thereby providing energy for transport of these ions against concentration gradients.

Solute Carrier Family 12, Member 2 - Na-K-Cl transporter ubiquitously expressed. It plays a key role in salt secretion in epithelial cells and cell volume regulation in nonepithelial cells.

Solute Carrier Family 12, Member 3 - Na-Cl cotransporter in the convoluted segments of the DISTAL KIDNEY TUBULE. It mediates active reabsorption of sodium and chloride and is inhibited by THIAZIDE DIURETICS.

Solute Carrier Family 22 Member 5 - A high-affinity, ATP-binding, co-transporter for CARNITINE that is highly expressed in kidney, skeletal muscle, heart, and placental tissues. It transports one sodium ion with one carnitine molecule. It has a lower affinity for other organic cations and transports them independently of sodium. Mutations in the SLC22A5 gene are associated with systemic carnitine deficiency.

Sorbic Acid - Mold and yeast inhibitor. Used as a fungistatic agent for foods, especially cheeses.

Sulbactam - A beta-lactamase inhibitor with very weak antibacterial action. The compound prevents antibiotic destruction of beta-lactam antibiotics by inhibiting beta-lactamases, thus extending their spectrum activity. Combinations of sulbactam with beta-lactam antibiotics have been used successfully for the therapy of infections caused by organisms resistant to the antibiotic alone.

Sulfacetamide - An anti-bacterial agent that is used topically to treat skin infections and orally for urinary tract infections.

Sulfachlorpyridazine - A sulfonamide antimicrobial used for urinary tract infections and in veterinary medicine.

Sulfadiazine - One of the short-acting SULFONAMIDES used in combination with PYRIMETHAMINE to treat toxoplasmosis in patients with acquired immunodeficiency syndrome and in newborns with congenital infections.

Sulfadimethoxine - A sulfanilamide that is used as an anti-infective agent.

Sulfadoxine - A long acting sulfonamide that is used, usually in combination with other drugs, for respiratory, urinary tract, and malarial infections.

Sulfaguanidine - A sulfanilamide antimicrobial agent that is used to treat enteric infections.

Sulfalene - Long-acting plasma-bound sulfonamide used for respiratory and urinary tract infections and also for malaria.

Sulfamerazine - A sulfanilamide that is used as an antibacterial agent.

Sulfameter - Long acting sulfonamide used in leprosy, urinary, and respiratory tract infections.

Sulfamethazine - A sulfanilamide anti-infective agent. It has a spectrum of antimicrobial action similar to other sulfonamides.

Sulfamethizole - A sulfathiazole antibacterial agent.

Sulfamethoxazole - A bacteriostatic antibacterial agent that interferes with folic acid synthesis in susceptible bacteria. Its broad spectrum of activity has been limited by the development of resistance. (From Martindale, The Extra Pharmacopoeia, 30th ed, p208)

Sulfamethoxypyridazine - A sulfanilamide antibacterial agent.

Sulfamonomethoxine - Long acting sulfonamide antibacterial agent.

Sulfamoxole - A sulfanilamide antibacterial agent.

Sulfanilamide - A short-acting sulfonamide used as an anti-infective agent. It has lower anti-bacterial activity than SULFAMETHOXAZOLE.

Sulfanilamides - Compounds based on 4-aminobenzenesulfonamide. The '-anil-' part of the name refers to aniline.

Sulfaphenazole - A sulfonilamide anti-infective agent.

Sulfapyridine - Antibacterial, potentially toxic, used to treat certain skin diseases.

Sulfasalazine - A drug that is used in the management of inflammatory bowel diseases. Its activity is generally considered to lie in its metabolic breakdown product, 5-aminosalicylic acid (see MESALAMINE) released in the colon. (From Martindale, The Extra Pharmacopoeia, 30th ed, p907)

Sulfathiazole - A sulfathiazole compound that is used as a short-acting anti-infective agent. It is no longer commonly used systemically due to its toxicity, but may still be applied topically in combination with other drugs for the treatment of vaginal and skin infections, and is still used in veterinary medicine.

Sulfathiazoles - Sulfanilamides consisting of a 4-aminobenzenesulfonamido group at the 2-position of 1,3-thiazole. They are often used as ANTI-INFECTIVE AGENTS.

Sulfisomidine - A sulfanilamide antibacterial agent.

Sulfisoxazole - A short-acting sulfonamide antibacterial with activity against a wide range of gram- negative and gram-positive organisms.

Sulfobromophthalein - A phenolphthalein that is used as a diagnostic aid in hepatic function determination.

Sulfonamides - A group of compounds that contain the structure SO2NH2.

Sulfones - A group of compounds that contain the structure SO2NH2.

Suramin - A polyanionic compound with an unknown mechanism of action. It is used parenterally in the treatment of African trypanosomiasis and it has been used clinically with diethylcarbamazine to kill the adult Onchocerca. (From AMA Drug Evaluations Annual, 1992, p1643) It has also been shown to have potent antineoplastic properties.

Taurocholic Acid - The product of conjugation of cholic acid with taurine. Its sodium salt is the chief ingredient of the bile of carnivorous animals. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is used as a cholagogue and cholerectic.

Taurodeoxycholic Acid - A bile salt formed in the liver by conjugation of deoxycholate with taurine, usually as the sodium salt. It is used as a cholagogue and choleretic, also industrially as a fat emulsifier.

Tetramisole - Used in the form of the hydrochloride as a reagent in ANALYTICAL CHEMISTRY TECHNIQUES.

Tetraphenylborate - An anionic compound that is used as a reagent for determination of potassium, ammonium, rubidium, and cesium ions. It also uncouples oxidative phosphorylation and forms complexes with biological materials, and is used in biological assays.

Tetrathionic Acid - A sulfuric acid dimer, formed by disulfide linkage. This compound has been used to prolong coagulation time and as an antidote in cyanide poisoning.

Theophylline - A methyl xanthine derivative from tea with diuretic, smooth muscle relaxant, bronchial dilation, cardiac and central nervous system stimulant activities. Theophylline inhibits the 3',5'-CYCLIC NUCLEOTIDE PHOSPHODIESTERASE that degrades CYCLIC AMP thus potentiates the actions of agents that act through ADENYLYL CYCLASES and cyclic AMP.

Thiabendazole - 2-Substituted benzimidazole first introduced in 1962. It is active against a variety of nematodes and is the drug of choice for STRONGYLOIDIASIS. It has CENTRAL NERVOUS SYSTEM side effects and hepatototoxic potential. (From Smith and Reynard, Textbook of Pharmacology, 1992, p919)

Thiamylal - A barbiturate that is administered intravenously for the production of complete anesthesia of short duration, for the induction of general anesthesia, or for inducing a hypnotic state. (From Martindale, The Extra Pharmacopoeia, 30th ed, p919)

Thimerosal - An ethylmercury-sulfidobenzoate that has been used as a preservative in VACCINES; ANTIVENINS; and OINTMENTS. It was formerly used as a topical antiseptic. It degrades to ethylmercury and thiosalicylate.

Thioacetazone - A thiosemicarbazone that is used in association with other antimycobacterial agents in the initial and continuation phases of antituberculosis regimens. Thiacetazone containing regimens are less effective than the short-course regimen recommended by the International Union Against Tuberculosis and are used in some developing countries to reduce drug costs. (From Martindale, The Extra Pharmacopoeia, 30th ed, p217)

Thymopentin - Synthetic pentapeptide corresponding to the amino acids 32-36 of thymopoietin and exhibiting the full biological activity of the natural hormone. It is an immunomodulator which has been studied for possible use in the treatment of rheumatoid arthritis, AIDS, and other primary immunodeficiencies.

Thyroxine - The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (MONOIODOTYROSINE) and the coupling of iodotyrosines (DIIODOTYROSINE) in the THYROGLOBULIN. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form TRIIODOTHYRONINE which exerts a broad spectrum of stimulatory effects on cell metabolism.

Tinidazole - A nitroimidazole alkylating agent that is used as an antitrichomonal agent against TRICHOMONAS VAGINALIS; ENTAMOEBA HISTOLYTICA; and GIARDIA LAMBLIA infections. It also acts as an antibacterial agent for the treatment of BACTERIAL VAGINOSIS and anaerobic bacterial infections.

Tolmetin - A non-steroidal anti-inflammatory agent (ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL) similar in mode of action to INDOMETHACIN.

Tretinoin - An important regulator of GENE EXPRESSION during growth and development, and in NEOPLASMS. Tretinoin, also known as retinoic acid and derived from maternal VITAMIN A, is essential for normal GROWTH; and EMBRYONIC DEVELOPMENT. An excess of tretinoin can be teratogenic. It is used in the treatment of PSORIASIS; ACNE VULGARIS; and several other SKIN DISEASES. It has also been approved for use in promyelocytic leukemia (LEUKEMIA, PROMYELOCYTIC, ACUTE).

Trichloroacetic Acid - A strong acid used as a protein precipitant in clinical chemistry and also as a caustic for removing warts.

Trifluridine - An antiviral derivative of THYMIDINE used mainly in the treatment of primary keratoconjunctivitis and recurrent epithelial keratitis due to HERPES SIMPLEX virus. (From Martindale, The Extra Pharmacopoeia, 30th ed, p557)

Trimethoprim - A pyrimidine inhibitor of dihydrofolate reductase, it is an antibacterial related to PYRIMETHAMINE. It is potentiated by SULFONAMIDES and the TRIMETHOPRIM, SULFAMETHOXAZOLE DRUG COMBINATION is the form most often used. It is sometimes used alone as an antimalarial. TRIMETHOPRIM RESISTANCE has been reported.

Trimethoprim Resistance - Nonsusceptibility of bacteria to the action of TRIMETHOPRIM.

Trimethoprim, Sulfamethoxazole Drug Combination - A drug combination with broad-spectrum antibacterial activity against both gram-positive and gram-negative organisms. It is effective in the treatment of many infections, including PNEUMOCYSTIS PNEUMONIA in AIDS.

Tyropanoate - A diagnostic aid as a radiopaque medium in cholecystography.

Unithiol - A chelating agent used as an antidote to heavy metal poisoning.

Uric Acid - An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.

Ursodeoxycholic Acid - An epimer of chenodeoxycholic acid. It is a mammalian bile acid found first in the bear and is apparently either a precursor or a product of chenodeoxycholate. Its administration changes the composition of bile and may dissolve gallstones. It is used as a cholagogue and choleretic.

Ursolic Acid - A pentacyclic triterpene that co-occurs with its isomer OLEANOLIC ACID in several plant species, and occurs in large amounts in FRUITS (such as CRANBERRIES; PEARS; PLUMS; and OLIVES), MEDICINAL HERBS, and other plants.

Valacyclovir - A prodrug of acyclovir that is used in the treatment of HERPES ZOSTER and HERPES SIMPLEX VIRUS INFECTION of the skin and mucous membranes, including GENITAL HERPES.

Valproic Acid - A fatty acid with anticonvulsant and anti-manic properties that is used in the treatment of EPILEPSY and BIPOLAR DISORDER. The mechanisms of its therapeutic actions are not well understood. It may act by increasing GAMMA-AMINOBUTYRIC ACID levels in the brain or by altering the properties of VOLTAGE-GATED SODIUM CHANNELS.

Vanadates - Oxyvanadium ions in various states of oxidation. They act primarily as ion transport inhibitors due to their inhibition of Na(+)-, K(+)-, and Ca(+)-ATPase transport systems. They also have insulin-like action, positive inotropic action on cardiac ventricular muscle, and other metabolic effects.

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.

Vitamin K 3 - A synthetic naphthoquinone without the isoprenoid side chain and biological activity, but can be converted to active vitamin K2, menaquinone, after alkylation in vivo.

Voltage-Gated Sodium Channels - A family of membrane proteins that selectively conduct SODIUM ions due to changes in the TRANSMEMBRANE POTENTIAL DIFFERENCE. They typically have a multimeric structure with a core alpha subunit that defines the sodium channel subtype and several beta subunits that modulate sodium channel activity.

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.

Zalcitabine - A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication at low concentrations, acting as a chain-terminator of viral DNA by binding to reverse transcriptase. Its principal toxic side effect is axonal degeneration resulting in peripheral neuropathy.

Zidovudine - A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication, acting as a chain-terminator of viral DNA during reverse transcription. It improves immunologic function, partially reverses the HIV-induced neurological dysfunction, and improves certain other clinical abnormalities associated with AIDS. Its principal toxic effect is dose-dependent suppression of bone marrow, resulting in anemia and leukopenia.

Instructional Notations

Type 1 Excludes

A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

  • anti-infectives topically used for ear, nose and throat T49.6
  • anti-infectives topically used for eye T49.5
  • locally applied anti-infectives NEC T49.0

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 T37

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 other systemic anti-infectives and antiparasitics (T37)

        • T37 Poisoning by, adverse effect of and underdosing of other systemic anti-infectives and antiparasitics
        • T37.0 Poisoning by, adverse effect of and underdosing of sulfonamides
        • T37.0X Poisoning by, adverse effect of and underdosing of sulfonamides
        • T37.0X1 Poisoning by sulfonamides, accidental (unintentional)
        • T37.0X1A Poisoning by sulfonamides, accidental (unintentional), initial encounter
        • T37.0X1D Poisoning by sulfonamides, accidental (unintentional), subsequent encounter
        • T37.0X1S Poisoning by sulfonamides, accidental (unintentional), sequela
        • T37.0X2 Poisoning by sulfonamides, intentional self-harm
        • T37.0X2A Poisoning by sulfonamides, intentional self-harm, initial encounter
        • T37.0X2D Poisoning by sulfonamides, intentional self-harm, subsequent encounter
        • T37.0X2S Poisoning by sulfonamides, intentional self-harm, sequela
        • T37.0X3 Poisoning by sulfonamides, assault
        • T37.0X3A Poisoning by sulfonamides, assault, initial encounter
        • T37.0X3D Poisoning by sulfonamides, assault, subsequent encounter
        • T37.0X3S Poisoning by sulfonamides, assault, sequela
        • T37.0X4 Poisoning by sulfonamides, undetermined
        • T37.0X4A Poisoning by sulfonamides, undetermined, initial encounter
        • T37.0X4D Poisoning by sulfonamides, undetermined, subsequent encounter
        • T37.0X4S Poisoning by sulfonamides, undetermined, sequela
        • T37.0X5 Adverse effect of sulfonamides
        • T37.0X5A Adverse effect of sulfonamides, initial encounter
        • T37.0X5D Adverse effect of sulfonamides, subsequent encounter
        • T37.0X5S Adverse effect of sulfonamides, sequela
        • T37.0X6 Underdosing of sulfonamides
        • T37.0X6A Underdosing of sulfonamides, initial encounter
        • T37.0X6D Underdosing of sulfonamides, subsequent encounter
        • T37.0X6S Underdosing of sulfonamides, sequela
        • T37.1 Poisoning by, adverse effect of and underdosing of antimycobacterial drugs
        • T37.1X Poisoning by, adverse effect of and underdosing of antimycobacterial drugs
        • T37.1X1 Poisoning by antimycobacterial drugs, accidental (unintentional)
        • T37.1X1A Poisoning by antimycobacterial drugs, accidental (unintentional), initial encounter
        • T37.1X1D Poisoning by antimycobacterial drugs, accidental (unintentional), subsequent encounter
        • T37.1X1S Poisoning by antimycobacterial drugs, accidental (unintentional), sequela
        • T37.1X2 Poisoning by antimycobacterial drugs, intentional self-harm
        • T37.1X2A Poisoning by antimycobacterial drugs, intentional self-harm, initial encounter
        • T37.1X2D Poisoning by antimycobacterial drugs, intentional self-harm, subsequent encounter
        • T37.1X2S Poisoning by antimycobacterial drugs, intentional self-harm, sequela
        • T37.1X3 Poisoning by antimycobacterial drugs, assault
        • T37.1X3A Poisoning by antimycobacterial drugs, assault, initial encounter
        • T37.1X3D Poisoning by antimycobacterial drugs, assault, subsequent encounter
        • T37.1X3S Poisoning by antimycobacterial drugs, assault, sequela
        • T37.1X4 Poisoning by antimycobacterial drugs, undetermined
        • T37.1X4A Poisoning by antimycobacterial drugs, undetermined, initial encounter
        • T37.1X4D Poisoning by antimycobacterial drugs, undetermined, subsequent encounter
        • T37.1X4S Poisoning by antimycobacterial drugs, undetermined, sequela
        • T37.1X5 Adverse effect of antimycobacterial drugs
        • T37.1X5A Adverse effect of antimycobacterial drugs, initial encounter
        • T37.1X5D Adverse effect of antimycobacterial drugs, subsequent encounter
        • T37.1X5S Adverse effect of antimycobacterial drugs, sequela
        • T37.1X6 Underdosing of antimycobacterial drugs
        • T37.1X6A Underdosing of antimycobacterial drugs, initial encounter
        • T37.1X6D Underdosing of antimycobacterial drugs, subsequent encounter
        • T37.1X6S Underdosing of antimycobacterial drugs, sequela
        • T37.2 Poisoning by, adverse effect of and underdosing of antimalarials and drugs acting on other blood protozoa
        • T37.2X Poisoning by, adverse effect of and underdosing of antimalarials and drugs acting on other blood protozoa
        • T37.2X1 Poisoning by antimalarials and drugs acting on other blood protozoa, accidental (unintentional)
        • T37.2X1A Poisoning by antimalarials and drugs acting on other blood protozoa, accidental (unintentional), initial encounter
        • T37.2X1D Poisoning by antimalarials and drugs acting on other blood protozoa, accidental (unintentional), subsequent encounter
        • T37.2X1S Poisoning by antimalarials and drugs acting on other blood protozoa, accidental (unintentional), sequela
        • T37.2X2 Poisoning by antimalarials and drugs acting on other blood protozoa, intentional self-harm
        • T37.2X2A Poisoning by antimalarials and drugs acting on other blood protozoa, intentional self-harm, initial encounter
        • T37.2X2D Poisoning by antimalarials and drugs acting on other blood protozoa, intentional self-harm, subsequent encounter
        • T37.2X2S Poisoning by antimalarials and drugs acting on other blood protozoa, intentional self-harm, sequela
        • T37.2X3 Poisoning by antimalarials and drugs acting on other blood protozoa, assault
        • T37.2X3A Poisoning by antimalarials and drugs acting on other blood protozoa, assault, initial encounter
        • T37.2X3D Poisoning by antimalarials and drugs acting on other blood protozoa, assault, subsequent encounter
        • T37.2X3S Poisoning by antimalarials and drugs acting on other blood protozoa, assault, sequela
        • T37.2X4 Poisoning by antimalarials and drugs acting on other blood protozoa, undetermined
        • T37.2X4A Poisoning by antimalarials and drugs acting on other blood protozoa, undetermined, initial encounter
        • T37.2X4D Poisoning by antimalarials and drugs acting on other blood protozoa, undetermined, subsequent encounter
        • T37.2X4S Poisoning by antimalarials and drugs acting on other blood protozoa, undetermined, sequela
        • T37.2X5 Adverse effect of antimalarials and drugs acting on other blood protozoa
        • T37.2X5A Adverse effect of antimalarials and drugs acting on other blood protozoa, initial encounter
        • T37.2X5D Adverse effect of antimalarials and drugs acting on other blood protozoa, subsequent encounter
        • T37.2X5S Adverse effect of antimalarials and drugs acting on other blood protozoa, sequela
        • T37.2X6 Underdosing of antimalarials and drugs acting on other blood protozoa
        • T37.2X6A Underdosing of antimalarials and drugs acting on other blood protozoa, initial encounter
        • T37.2X6D Underdosing of antimalarials and drugs acting on other blood protozoa, subsequent encounter
        • T37.2X6S Underdosing of antimalarials and drugs acting on other blood protozoa, sequela
        • T37.3 Poisoning by, adverse effect of and underdosing of other antiprotozoal drugs
        • T37.3X Poisoning by, adverse effect of and underdosing of other antiprotozoal drugs
        • T37.3X1 Poisoning by other antiprotozoal drugs, accidental (unintentional)
        • T37.3X1A Poisoning by other antiprotozoal drugs, accidental (unintentional), initial encounter
        • T37.3X1D Poisoning by other antiprotozoal drugs, accidental (unintentional), subsequent encounter
        • T37.3X1S Poisoning by other antiprotozoal drugs, accidental (unintentional), sequela
        • T37.3X2 Poisoning by other antiprotozoal drugs, intentional self-harm
        • T37.3X2A Poisoning by other antiprotozoal drugs, intentional self-harm, initial encounter
        • T37.3X2D Poisoning by other antiprotozoal drugs, intentional self-harm, subsequent encounter
        • T37.3X2S Poisoning by other antiprotozoal drugs, intentional self-harm, sequela
        • T37.3X3 Poisoning by other antiprotozoal drugs, assault
        • T37.3X3A Poisoning by other antiprotozoal drugs, assault, initial encounter
        • T37.3X3D Poisoning by other antiprotozoal drugs, assault, subsequent encounter
        • T37.3X3S Poisoning by other antiprotozoal drugs, assault, sequela
        • T37.3X4 Poisoning by other antiprotozoal drugs, undetermined
        • T37.3X4A Poisoning by other antiprotozoal drugs, undetermined, initial encounter
        • T37.3X4D Poisoning by other antiprotozoal drugs, undetermined, subsequent encounter
        • T37.3X4S Poisoning by other antiprotozoal drugs, undetermined, sequela
        • T37.3X5 Adverse effect of other antiprotozoal drugs
        • T37.3X5A Adverse effect of other antiprotozoal drugs, initial encounter
        • T37.3X5D Adverse effect of other antiprotozoal drugs, subsequent encounter
        • T37.3X5S Adverse effect of other antiprotozoal drugs, sequela
        • T37.3X6 Underdosing of other antiprotozoal drugs
        • T37.3X6A Underdosing of other antiprotozoal drugs, initial encounter
        • T37.3X6D Underdosing of other antiprotozoal drugs, subsequent encounter
        • T37.3X6S Underdosing of other antiprotozoal drugs, sequela
        • T37.4 Poisoning by, adverse effect of and underdosing of anthelminthics
        • T37.4X Poisoning by, adverse effect of and underdosing of anthelminthics
        • T37.4X1 Poisoning by anthelminthics, accidental (unintentional)
        • T37.4X1A Poisoning by anthelminthics, accidental (unintentional), initial encounter
        • T37.4X1D Poisoning by anthelminthics, accidental (unintentional), subsequent encounter
        • T37.4X1S Poisoning by anthelminthics, accidental (unintentional), sequela
        • T37.4X2 Poisoning by anthelminthics, intentional self-harm
        • T37.4X2A Poisoning by anthelminthics, intentional self-harm, initial encounter
        • T37.4X2D Poisoning by anthelminthics, intentional self-harm, subsequent encounter
        • T37.4X2S Poisoning by anthelminthics, intentional self-harm, sequela
        • T37.4X3 Poisoning by anthelminthics, assault
        • T37.4X3A Poisoning by anthelminthics, assault, initial encounter
        • T37.4X3D Poisoning by anthelminthics, assault, subsequent encounter
        • T37.4X3S Poisoning by anthelminthics, assault, sequela
        • T37.4X4 Poisoning by anthelminthics, undetermined
        • T37.4X4A Poisoning by anthelminthics, undetermined, initial encounter
        • T37.4X4D Poisoning by anthelminthics, undetermined, subsequent encounter
        • T37.4X4S Poisoning by anthelminthics, undetermined, sequela
        • T37.4X5 Adverse effect of anthelminthics
        • T37.4X5A Adverse effect of anthelminthics, initial encounter
        • T37.4X5D Adverse effect of anthelminthics, subsequent encounter
        • T37.4X5S Adverse effect of anthelminthics, sequela
        • T37.4X6 Underdosing of anthelminthics
        • T37.4X6A Underdosing of anthelminthics, initial encounter
        • T37.4X6D Underdosing of anthelminthics, subsequent encounter
        • T37.4X6S Underdosing of anthelminthics, sequela
        • T37.5 Poisoning by, adverse effect of and underdosing of antiviral drugs
        • T37.5X Poisoning by, adverse effect of and underdosing of antiviral drugs
        • T37.5X1 Poisoning by antiviral drugs, accidental (unintentional)
        • T37.5X1A Poisoning by antiviral drugs, accidental (unintentional), initial encounter
        • T37.5X1D Poisoning by antiviral drugs, accidental (unintentional), subsequent encounter
        • T37.5X1S Poisoning by antiviral drugs, accidental (unintentional), sequela
        • T37.5X2 Poisoning by antiviral drugs, intentional self-harm
        • T37.5X2A Poisoning by antiviral drugs, intentional self-harm, initial encounter
        • T37.5X2D Poisoning by antiviral drugs, intentional self-harm, subsequent encounter
        • T37.5X2S Poisoning by antiviral drugs, intentional self-harm, sequela
        • T37.5X3 Poisoning by antiviral drugs, assault
        • T37.5X3A Poisoning by antiviral drugs, assault, initial encounter
        • T37.5X3D Poisoning by antiviral drugs, assault, subsequent encounter
        • T37.5X3S Poisoning by antiviral drugs, assault, sequela
        • T37.5X4 Poisoning by antiviral drugs, undetermined
        • T37.5X4A Poisoning by antiviral drugs, undetermined, initial encounter
        • T37.5X4D Poisoning by antiviral drugs, undetermined, subsequent encounter
        • T37.5X4S Poisoning by antiviral drugs, undetermined, sequela
        • T37.5X5 Adverse effect of antiviral drugs
        • T37.5X5A Adverse effect of antiviral drugs, initial encounter
        • T37.5X5D Adverse effect of antiviral drugs, subsequent encounter
        • T37.5X5S Adverse effect of antiviral drugs, sequela
        • T37.5X6 Underdosing of antiviral drugs
        • T37.5X6A Underdosing of antiviral drugs, initial encounter
        • T37.5X6D Underdosing of antiviral drugs, subsequent encounter
        • T37.5X6S Underdosing of antiviral drugs, sequela
        • T37.8 Poisoning by, adverse effect of and underdosing of other specified systemic anti-infectives and antiparasitics
        • T37.8X Poisoning by, adverse effect of and underdosing of other specified systemic anti-infectives and antiparasitics
        • T37.8X1 Poisoning by other specified systemic anti-infectives and antiparasitics, accidental (unintentional)
        • T37.8X1A Poisoning by other specified systemic anti-infectives and antiparasitics, accidental (unintentional), initial encounter
        • T37.8X1D Poisoning by other specified systemic anti-infectives and antiparasitics, accidental (unintentional), subsequent encounter
        • T37.8X1S Poisoning by other specified systemic anti-infectives and antiparasitics, accidental (unintentional), sequela
        • T37.8X2 Poisoning by other specified systemic anti-infectives and antiparasitics, intentional self-harm
        • T37.8X2A Poisoning by other specified systemic anti-infectives and antiparasitics, intentional self-harm, initial encounter
        • T37.8X2D Poisoning by other specified systemic anti-infectives and antiparasitics, intentional self-harm, subsequent encounter
        • T37.8X2S Poisoning by other specified systemic anti-infectives and antiparasitics, intentional self-harm, sequela
        • T37.8X3 Poisoning by other specified systemic anti-infectives and antiparasitics, assault
        • T37.8X3A Poisoning by other specified systemic anti-infectives and antiparasitics, assault, initial encounter
        • T37.8X3D Poisoning by other specified systemic anti-infectives and antiparasitics, assault, subsequent encounter
        • T37.8X3S Poisoning by other specified systemic anti-infectives and antiparasitics, assault, sequela
        • T37.8X4 Poisoning by other specified systemic anti-infectives and antiparasitics, undetermined
        • T37.8X4A Poisoning by other specified systemic anti-infectives and antiparasitics, undetermined, initial encounter
        • T37.8X4D Poisoning by other specified systemic anti-infectives and antiparasitics, undetermined, subsequent encounter
        • T37.8X4S Poisoning by other specified systemic anti-infectives and antiparasitics, undetermined, sequela
        • T37.8X5 Adverse effect of other specified systemic anti-infectives and antiparasitics
        • T37.8X5A Adverse effect of other specified systemic anti-infectives and antiparasitics, initial encounter
        • T37.8X5D Adverse effect of other specified systemic anti-infectives and antiparasitics, subsequent encounter
        • T37.8X5S Adverse effect of other specified systemic anti-infectives and antiparasitics, sequela
        • T37.8X6 Underdosing of other specified systemic anti-infectives and antiparasitics
        • T37.8X6A Underdosing of other specified systemic anti-infectives and antiparasitics, initial encounter
        • T37.8X6D Underdosing of other specified systemic anti-infectives and antiparasitics, subsequent encounter
        • T37.8X6S Underdosing of other specified systemic anti-infectives and antiparasitics, sequela
        • T37.9 Poisoning by, adverse effect of and underdosing of unspecified systemic anti-infective and antiparasitics
        • T37.91 Poisoning by unspecified systemic anti-infective and antiparasitics, accidental (unintentional)
        • T37.91XA Poisoning by unspecified systemic anti-infective and antiparasitics, accidental (unintentional), initial encounter
        • T37.91XD Poisoning by unspecified systemic anti-infective and antiparasitics, accidental (unintentional), subsequent encounter
        • T37.91XS Poisoning by unspecified systemic anti-infective and antiparasitics, accidental (unintentional), sequela
        • T37.92 Poisoning by unspecified systemic anti-infective and antiparasitics, intentional self-harm
        • T37.92XA Poisoning by unspecified systemic anti-infective and antiparasitics, intentional self-harm, initial encounter
        • T37.92XD Poisoning by unspecified systemic anti-infective and antiparasitics, intentional self-harm, subsequent encounter
        • T37.92XS Poisoning by unspecified systemic anti-infective and antiparasitics, intentional self-harm, sequela
        • T37.93 Poisoning by unspecified systemic anti-infective and antiparasitics, assault
        • T37.93XA Poisoning by unspecified systemic anti-infective and antiparasitics, assault, initial encounter
        • T37.93XD Poisoning by unspecified systemic anti-infective and antiparasitics, assault, subsequent encounter
        • T37.93XS Poisoning by unspecified systemic anti-infective and antiparasitics, assault, sequela
        • T37.94 Poisoning by unspecified systemic anti-infective and antiparasitics, undetermined
        • T37.94XA Poisoning by unspecified systemic anti-infective and antiparasitics, undetermined, initial encounter
        • T37.94XD Poisoning by unspecified systemic anti-infective and antiparasitics, undetermined, subsequent encounter
        • T37.94XS Poisoning by unspecified systemic anti-infective and antiparasitics, undetermined, sequela
        • T37.95 Adverse effect of unspecified systemic anti-infective and antiparasitic
        • T37.95XA Adverse effect of unspecified systemic anti-infective and antiparasitic, initial encounter
        • T37.95XD Adverse effect of unspecified systemic anti-infective and antiparasitic, subsequent encounter
        • T37.95XS Adverse effect of unspecified systemic anti-infective and antiparasitic, sequela
        • T37.96 Underdosing of unspecified systemic anti-infectives and antiparasitics
        • T37.96XA Underdosing of unspecified systemic anti-infectives and antiparasitics, initial encounter
        • T37.96XD Underdosing of unspecified systemic anti-infectives and antiparasitics, subsequent encounter
        • T37.96XS Underdosing of unspecified systemic anti-infectives and antiparasitics, sequela