Isoniazid

Isoniazid
Names
Trade namesHydra, Hyzyd, Isovit, others
Other namesIsonicotinic acid hydrazide, isonicotinyl hydrazine, INHA
IUPAC name
  • Pyridine-4-carbohydrazide
Clinical data
Drug classAntibiotic
Main usesTuberculosis[1]
Side effectsIncreased blood levels of liver enzymes, numbness in the hands and feet[2]
WHO AWaReUnlinkedWikibase error: ⧼unlinkedwikibase-error-statements-entity-not-set⧽
Pregnancy
category
    Routes of
    use    		By mouth, intramuscular, intravenous
    Defined daily dose300 mg (by mouth)
    300 mg (parenteral)[4]
    External links
    AHFS/Drugs.comMonograph
    MedlinePlusa682401
    Legal
    License data
    Legal status
    Pharmacokinetics
    Protein bindingVery low (0–10%)
    Metabolismliver; CYP450: 2C19, 3A4 inhibitor
    Elimination half-life0.5–1.6h (fast acetylators), 2-5h (slow acetylators)
    Excretionurine (primarily), feces
    Chemical and physical data
    FormulaC6H7N3O
    Molar mass137.142 g·mol−1
    3D model (JSmol)
    SMILES
    • C1=CN=CC=C1C(=O)NN
    InChI
    • InChI=1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10) checkY
    • Key:QRXWMOHMRWLFEY-UHFFFAOYSA-N checkY

    Isoniazid, also known as isonicotinic acid hydrazide (INH), is an antibiotic used for the treatment of tuberculosis.[2] For active tuberculosis it is often used together with rifampicin, pyrazinamide, and either streptomycin or ethambutol.[5] For latent tuberculosis it is often used by itself.[2] It may also be used for atypical types of mycobacteria, such as M. avium, M. kansasii, and M. xenopi.[2] It is usually taken by mouth but may be used by injection into muscle.[2]

    Common side effect include increased blood levels of liver enzymes and numbness in the hands and feet.[2] Serious side effects may include liver inflammation and acute liver failure.[2] It is unclear if use during pregnancy is safe for the baby.[6] Use during breastfeeding is likely safe.[6] Pyridoxine may be given to reduce the risk of side effects.[7] Isoniazid works in part by disrupting the formation of the bacteria's cell wall which results in cell death.[2]

    Isoniazid was first made between 1949 and 1952.[8][9] It is on the World Health Organization's List of Essential Medicines.[10] Isoniazid is available as a generic medication.[2] The wholesale cost in the developing world is about US$0.60–4.75 per month.[11] In the United States a month of treatment costs less than $25.[7] In the UK a month's of isoniazid at a dose of 300mg/day costs the NHS around £75, as of 2021.[12]

    Medical uses

    Tuberculosis

    Isoniazid is often used to treat latent and active tuberculosis infections. In persons with isoniazid-sensitive Mycobacterium tuberculosis infection, drug regimens based on isoniazid are usually effective when persons adhere to the prescribed treatment. However, in persons with isoniazid-resistant Mycobacterium tuberculosis infection, drug regimens based on isoniazid have a high rate of failure.[13]

    Isoniazid has been approved as prophylactic therapy for the following populations:

    • People with HIV infection and a PPD (purified protein derivative) reaction of at least 5 mm induration
    • Contacts of people with tuberculosis and who have a PPD reaction at least 5 mm induration
    • People whose PPD reactions convert from negative to positive in a two-year period – at least 10 mm induration for those up to 35 years of age, and at least 15 mm induration for those at least 35 years old
    • People with pulmonary damage on their chest X-ray that is likely to be due to healed tuberculosis and also have a PPD reaction at least 5 mm induration
    • Injection drug users whose HIV status is negative who have a PPD reaction at least 10 mm induration
    • People with a PPD of greater than or equal to 10 mm induration who are foreign-born from high prevalence geographical regions, low-income populations, and patients residing in long-term facilities[14][15]

    Isoniazid can be used alone or in combination with Rifampin for treatment of latent tuberculosis, or as part of a four-drug regimen for treatment of active tuberculosis.[16] The drug regimen typically requires daily or weekly oral administration for a period of three to nine months, often under Directly Observed Therapy (DOT) supervision.[16]

    Other mycobacteria

    Isoniazid was widely used in the treatment of Mycobacterium avium complex as part of a regimen including rifampicin and ethambutol.[17] Evidence suggests that isoniazid prevents mycolic acid synthesis in M. avium complex as in M. tuberculosis[18] and although this is not bactericidal to M. avium complex, it greatly potentiates the effect of rifampicin. The introduction of macrolides led to this use greatly decreasing. However, since rifampicin is broadly underdosed in M. avium complex treatment this effect may be worth re-investigating.[19]

    Special populations

    It is recommended that women with active tuberculosis who are pregnant or breastfeeding take isoniazid. Preventive therapy should be delayed until after giving birth.[20] Nursing mothers excrete a relatively low and non-toxic concentration of INH in breast milk, and their babies are at low risk for side effects. Both pregnant women and infants being breastfed by mothers taking INH should take vitamin B6 in its pyridoxine form to minimize the risk of peripheral nerve damage.[21] Vitamin B6 is used to prevent isoniazid-induced B6 deficiency and neuropathy in people with a risk factor, such as pregnancy, lactation, HIV infection, alcoholism, diabetes, kidney failure, or malnutrition.[22]

    People with liver dysfunction are at a higher risk for hepatitis caused by INH, and may need a lower dose.[20]

    Levels of liver enzymes in the bloodstream should be frequently checked in daily alcohol drinkers, pregnant women, IV drug users, people over 35, and those who have chronic liver disease, severe kidney dysfunction, peripheral neuropathy, or HIV infection since they are more likely to develop hepatitis from INH.[20][23]

    Dosage

    The defined daily dose is 300 mg (by mouth) or 300 mg (parenteral).[4] In those over 30 kg the dose is generally 4 to 6 mg/kg once a day while in those under 30 kg the dose is 7 to 15 mg/kg once per day to a maximum of 300 mg.[1]

    Side effects

    Isoniazid induced alopecia[24]

    Up to 20% of people taking isoniazid experience peripheral neuropathy when taking doses of 6 mg/kg of weight daily or higher.[25] Gastrointestinal reactions include nausea and vomiting.[14] Aplastic anemia, thrombocytopenia, and agranulocytosis due to lack of production of red blood cells, platelets, and white blood cells by the bone marrow respectively, can also occur.[14] Hypersensitivity reactions are also common and can present with a maculopapular rash and fever.[14] Gynecomastia may occur.[16]

    Asymptomatic elevation of serum liver enzyme concentrations occurs in 10% to 20% of people taking INH, and liver enzyme concentrations usually return to normal even when treatment is continued.[26] Isoniazid has a boxed warning for severe and sometimes fatal hepatitis, which is age-dependent at a rate of 0.3% in people 21 to 35 years old and over 2% in those over age 50.[14][27] Symptoms suggestive of liver toxicity include nausea, vomiting, abdominal pain, dark urine, right upper quadrant pain, and loss of appetite.[14] Black and Hispanic women are at higher risk for isoniazid-induced hepatotoxicity.[14] When it happens, isoniazid-induced liver toxicity has been shown to occur in 50% of patients within the first 2 months of therapy.[28]

    Some recommend that liver function should be monitored carefully in all people receiving it,[20] but others recommend monitoring only in certain populations.[26][29][30]

    Headache, poor concentration, weight gain, poor memory, insomnia, and depression have all been associated with isoniazid use.[31] All patients and healthcare workers should be aware of these serious side effects, especially if suicidal ideation or behavior are suspected.[31][32][33]

    Isoniazid is associated with pyridoxine (vitamin B6) deficiency because of its similar structure. Isoniazid is also associated with increased excretion of pyridoxine. Pyridoxal phosphate (a derivative of pyridoxine) is required for δ-aminolevulinic acid synthase, the enzyme responsible for the rate-limiting step in heme synthesis. Therefore, isoniazid-induced pyridoxine deficiency causes insufficient heme formation in early red blood cells, leading to sideroblastic anemia.[22]

    Interactions

    People taking isoniazid and acetaminophen are at risk of acetaminophen toxicity. Isoniazid is thought to induce a liver enzyme which causes a larger amount of acetaminophen to be metabolized to a toxic form.[34][35]

    Isoniazid decreases the metabolism of carbamazepine, thus slowing down its clearance from the body. People taking carbamazepine should have their carbamazepine levels monitored and, if necessary, have their dose adjusted accordingly.[36]

    It is possible that isoniazid may decrease the serum levels of ketoconazole after long-term treatment. This is seen with the simultaneous use of rifampin, isoniazid, and ketoconazole.[37]

    Isoniazid may increase the amount of phenytoin in the body. The doses of phenytoin may need to be adjusted when given with isoniazid.[38][39]

    Isoniazid may increase the plasma levels of theophylline. There are some cases of theophylline slowing down isoniazid elimination. Both theophylline and isoniazid levels should be monitored.[40]

    Valproate levels may increase when taken with isoniazid. Valproate levels should be monitored and its dose adjusted if necessary.[38]

    Mechanism of action

    Isoniazid is a prodrug that inhibits the formation of the mycobacterial cell wall. Isoniazid must be activated by KatG, a bacterial catalase-peroxidase enzyme in Mycobacterium tuberculosis.[41] KatG catalyzes the formation of the isonicotinic acyl radical, which spontaneously couples with NADH to form the nicotinoyl-NAD adduct. This complex binds tightly to the enoyl-acyl carrier protein reductase InhA, thereby blocking the natural enoyl-AcpM substrate and the action of fatty acid synthase. This process inhibits the synthesis of mycolic acids, which are required components of the mycobacterial cell wall. A range of radicals are produced by KatG activation of isoniazid, including nitric oxide,[42] which has also been shown to be important in the action of another antimycobacterial prodrug pretomanid.[43]

    Isoniazid (INH) is activated by KatG to the isonicotinic acyl radical, which subsequently reacts with NAD to form the isonicotinic acyl-NADH complex.

    Isoniazid is bactericidal to rapidly dividing mycobacteria, but is bacteriostatic if the mycobacteria are slow-growing.[44] It inhibits the cytochrome P450 system and hence acts as a source of free radicals.[45]

    Isoniazid is a mild monoamine oxidase inhibitor(MAO-I).[46]

    Metabolism

    Schematic representation of isoniazid metabolism[47]

    Isoniazid reaches therapeutic concentrations in serum, cerebrospinal fluid, and within caseous granulomas. It is metabolized in the liver via acetylation into acetylhydrazine. Two forms of the enzyme are responsible for acetylation, so some patients metabolize the drug more quickly than others. Hence, the half-life is bimodal, with "slow acetylators" and "fast acetylators". A graph of number of people versus time shows peaks at one and three hours. The height of the peaks depends on the ethnicities of the people being tested. The metabolites are excreted in the urine. Doses do not usually have to be adjusted in case of renal failure.

    History

    Three pharmaceutical companies unsuccessfully attempted to patent the drug at the same time,[48] the most prominent one being Roche, which launched its version, Rimifon, in 1952.[49] With the introduction of isoniazid, a cure for tuberculosis was first considered possible.

    The drug was first tested at Many Farms, a Navajo community in Arizona, due to the Navajo reservation's tuberculosis problem and because the population had not previously been treated with streptomycin, the main tuberculosis treatment at the time.[50] The research was led by Walsh McDermott, an infectious disease researcher with an interest in public health, who had previously taken isoniazid to treat his own tuberculosis.[51]

    Isoniazid and a related drug, iproniazid, were among the first drugs to be referred to as antidepressants.[52]

    Society and culture

    Preparation

    Isoniazid is an isonicotinic acid derivative. It is manufactured using 4-cyanopyridine and hydrazine hydrate.[53] In another method, isoniazid was claimed to have been made from citric acid starting material.[54]

    Brand names

    Hydra, Hyzyd, Isovit, Laniazid, Nydrazid, Rimifon, and Stanozide.[55]

    Chromatography

    Isonicotinic acid hydrazide is also used in chromatography to differentiate between various degrees of conjugation in organic compounds barring the ketone functional group.[56] The test works by forming a hydrazone which can be detected by its bathochromic shift.

    Other animals

    Isoniazid may be used for dogs, but there have been concerns it can cause seizures.[57]

    References

    1. 1 2 "ISONIAZID = H oral - Essential drugs". medicalguidelines.msf.org. Archived from the original on 2 March 2021. Retrieved 31 August 2020.
    2. 1 2 3 4 5 6 7 8 9 10 "Isoniazid". The American Society of Health-System Pharmacists. Archived from the original on 20 December 2016. Retrieved 8 December 2016.
    3. 1 2 "Isoniazid (Nydrazid) Use During Pregnancy". Drugs.com. 7 October 2019. Archived from the original on 20 December 2016. Retrieved 24 January 2020.
    4. 1 2 "WHOCC - ATC/DDD Index". www.whocc.no. Archived from the original on 6 November 2020. Retrieved 21 September 2020.
    5. ↑ World Health Organization (2009). Stuart MC, Kouimtzi M, Hill SR (eds.). WHO Model Formulary 2008. World Health Organization. p. 136. hdl:10665/44053. ISBN 9789241547659.
    6. 1 2 "Isoniazid (Nydrazid) Use During Pregnancy". www.drugs.com. Archived from the original on 20 December 2016. Retrieved 10 December 2016.
    7. 1 2 Hamilton, Richart (2015). Tarascon Pocket Pharmacopoeia 2015 Deluxe Lab-Coat Edition. Jones & Bartlett Learning. p. 49. ISBN 9781284057560.
    8. ↑ Greenwood, David (2008). "5. The taming of tuberculosis and leprosy". Antimicrobial Drugs: Chronicle of a Twentieth Century Medical Triumph. Oxford: Oxford University Press. p. 174-176. ISBN 978-0-19-953484-5. Archived from the original on 2021-12-11. Retrieved 2021-12-03.
    9. ↑ Walker, S. R. (2012). Trends and Changes in Drug Research and Development. Springer Science & Business Media. p. 109. ISBN 9789400926592. Archived from the original on 2017-09-10.
    10. ↑ World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
    11. ↑ "Isoniazid". International Drug Price Indicator Guide. Archived from the original on 25 August 2018. Retrieved 8 December 2016.
    12. ↑ "5. Infection". British National Formulary (BNF) (82 ed.). London: BMJ Group and the Pharmaceutical Press. September 2021 – March 2022. pp. 630–631. ISBN 978-0-85711-413-6.{{cite book}}: CS1 maint: date format (link)
    13. ↑ Gegia M, Winters N, Benedetti A, van Soolingen D, Menzies D (February 2017). "Treatment of isoniazid-resistant tuberculosis with first-line drugs: a systematic review and meta-analysis". Lancet Infect Dis. 17 (2): 223–234. doi:10.1016/S1473-3099(16)30407-8. PMID 27865891.
    14. 1 2 3 4 5 6 7 "Isoniazid (package insert)". Archived from the original on 2020-06-13. Retrieved 2015-11-03.
    15. ↑ "The Use of Preventive Therapy for Tuberculosis Infection in the United States – Recommendations of the Advisory Committee for Elimination of Tuberculosis". Morbidity and Mortality Weekly Report. 39 (RR-8): 9–12. May 18, 1990. Archived from the original on 2 March 2016. Retrieved 22 February 2016.
    16. 1 2 3 Lewis, Sharon Mantik. Medical-surgical nursing : assessment and management of clinical problems. Dirksen, Shannon Ruff,, Heitkemper, Margaret M. (Margaret McLean),, Bucher, Linda,, Harding, Mariann (Ninth ed.). St. Louis, Missouri. ISBN 978-0-323-10089-2. OCLC 228373703.
    17. ↑ Research Committee of the British Thoracic Society (2001). "First randomised trial of treatments for pulmonary disease caused by M avium intracellulare, M malmoense, and M xenopi in HIV negative patients: Rifampicin, ethambutol and isoniazid versus rifampicin and ethambutol". Thorax. 56 (3): 167–72. doi:10.1136/thorax.56.3.167. PMC 1758783. PMID 11182006.
    18. ↑ Mdluli, K; Swanson, J; Fischer, E; Lee, R. E; Barry Ce, 3rd (1998). "Mechanisms involved in the intrinsic isoniazid resistance of Mycobacterium avium". Molecular Microbiology. 27 (6): 1223–33. doi:10.1046/j.1365-2958.1998.00774.x. PMID 9570407.
    19. ↑ Van Ingen, J; Egelund, E. F; Levin, A; Totten, S. E; Boeree, M. J; Mouton, J. W; Aarnoutse, R. E; Heifets, L. B; Peloquin, C. A; Daley, C. L (2012). "The pharmacokinetics and pharmacodynamics of pulmonary Mycobacterium avium complex disease treatment". American Journal of Respiratory and Critical Care Medicine. 186 (6): 559–65. doi:10.1164/rccm.201204-0682OC. PMID 22744719.
    20. 1 2 3 4 "Isoniazid tablet". DailyMed. 18 October 2018. Archived from the original on 13 March 2019. Retrieved 24 January 2020.
    21. ↑ Bothamley, G. (2001). "Drug treatment for tuberculosis during pregnancy: safety considerations". Drug Safety. 24 (7): 553–565. doi:10.2165/00002018-200124070-00006. PMID 11444726.
    22. 1 2 Steichen, O.; Martinez-Almoyna, L.; De Broucker, T. (April 2006). "Isoniazid induced neuropathy: consider prevention" (PDF). Revue des Maladies Respiratoires. 23 (2 Pt 1): 157–160. doi:10.1016/S0761-8425(06)71480-2. PMID 16788441. Archived (PDF) from the original on 2019-04-20. Retrieved 2017-12-14.
    23. ↑ Saukkonen, J.J.; Cohn, D.L.; Jasmer, R.M. (October 15, 2006). "An official ATS statement: hepatotoxicity of antituberculosis therapy". American Journal of Respiratory and Critical Care Medicine. 174 (8): 935–952. doi:10.1164/rccm.200510-1666ST. PMID 17021358. Archived from the original on August 28, 2021. Retrieved January 24, 2020.
    24. ↑ Vucinic, Violeta V. Mihailovic; Jovanovic, Dragana M. (30 September 2019). Clinical Focus Series: Tuberculosis: Selected Problems. Jaypee Brothers Medical Publishers. p. 286. ISBN 978-93-86261-35-9. Archived from the original on 30 January 2022. Retrieved 29 January 2022.
    25. ↑ Alldredge, Brian (February 12, 2013). Applied Therapeutics. ISBN 9781609137137.
    26. 1 2 "Latent Tuberculosis Infection: A Guide for Primary Health Care Providers". cdc.gov. Center for Disease Control. Archived from the original on 25 March 2016. Retrieved 25 March 2016.
    27. ↑ Trevor, A. & Katzung, B. (2013). Katzung & Trevor's Pharmacology: examination & board review (10th ed., p. 417). New York. McGraw-Hill Medical, Lange.
    28. ↑ "Isoniazid UpToDate". Archived from the original on 2015-10-25.
    29. ↑ "Treatment of Tuberculosis – Guidelines (4th ed.)" (PDF). who.int. World Health Organization. Archived (PDF) from the original on 4 April 2016. Retrieved 25 March 2016.
    30. ↑ "Chemotherapy and management of tuberculosis in the United Kingdom: recommendations 1998. Joint Tuberculosis Committee of the British Thoracic Society". Thorax. 53 (7): 536–548. July 1998. doi:10.1136/thx.53.7.536. PMC 1745276. PMID 9797751.
    31. 1 2 Alao A.O.; Yolles J.C. (September 1998). "Isoniazid-induced psychosis". Annals of Pharmacotherapy. 32 (9): 889–891. doi:10.1345/aph.17377. PMID 9762376.
    32. ↑ Iannaccone, R.; Sue, Y.J.; Avner, J.R. (2002). "Suicidal psychosis secondary to isoniazid". Pediatric Emergency Care. 18 (1): 25–27. doi:10.1097/00006565-200202000-00008. PMID 11862134.
    33. ↑ Pallone K.A.; Goldman M.P.; Fuller M.A. (February 1993). "Isoniazid-associated psychosis: case report and review of the literature". Annals of Pharmacotherapy. 27 (2): 167–170. doi:10.1177/106002809302700205. PMID 8439690.
    34. ↑ Murphy, R.; Swartz, R.; Watkins, P.B. (November 15, 1990). "Severe acetaminophen toxicity in a patient receiving isoniazid". Annals of Internal Medicine. 113 (10): 799–800. doi:10.7326/0003-4819-113-10-799. PMID 2240884.
    35. ↑ Burk, R.F.; Hill, K.E.; Hunt Jr., R.W.; Martin, A.E. (July 1990). "Isoniazid potentiation of acetaminophen hepatotoxicity in the rat and 4-methylpyrazole inhibition of it". Research Communications in Chemical Pathology and Pharmacolog. 69 (1): 115–118. PMID 2218067.
    36. ↑ Fleenor, M.E.; Harden, J.W.; Curtis, G. (June 1991). "Interaction between carbamazepine and antituberculosis agents". Chest. 99 (6): 1554. doi:10.1378/chest.99.6.1554a. PMID 2036861.
    37. ↑ Baciewicz, A.M.; Baciewicz Jr., F.A. (September 13, 1993). "Ketoconazole and fluconazole drug interactions". Archives of Internal Medicine. 153 (17): 1970–1976. doi:10.1001/archinte.153.17.1970. PMID 8357281.
    38. 1 2 Jonville, A.P.; Gauchez, A.S.; Autret, E.; Billard, C.; Barbier, P.; Nsabiyumva, F.; Breteau, M. (1991). "Interaction between isoniazid and valproate: a case of valproate overdosage". European Journal of Clinical Pharmacology. 40 (2): 197–198. doi:10.1007/BF00280078 (inactive 2020-01-24). PMID 2065702.{{cite journal}}: CS1 maint: DOI inactive as of January 2020 (link)
    39. ↑ Bass, Jr., J.B.; Farer, L.S.; Hopewell, P.C.; O'Brien, R.; Jacobs, R.F.; Ruben, F.; Snider, Jr., D.E.; Thornton, G. (May 1994). "Treatment of tuberculosis and tuberculosis infection in adults and children. American Thoracic Society and The Centers for Disease Control and Prevention". Am J Respir Crit Care Med. 149 (5): 1359–1374. doi:10.1164/ajrccm.149.5.8173779. PMID 8173779.
    40. ↑ Höglund, P.; Nilsson, L.G.; Paulsen, O. (February 1987). "Interaction between isoniazid and theophylline". European Journal of Respiratory Diseases. 70 (2): 110–116. PMID 3817069.
    41. ↑ Suarez, J.; Ranguelova, K.; Jarzecki, A.A.; et al. (March 2009). "An oxyferrous heme/protein-based radical intermediate is catalytically competent in the catalase reaction of Mycobacterium tuberculosis catalase-peroxidase (KatG)". The Journal of Biological Chemistry. 284 (11): 7017–7029. doi:10.1074/jbc.M808106200. PMC 2652337. PMID 19139099.
    42. ↑ Timmins, G.S.; Master, S; Rusnak, F.; Deretic, V. (August 2004). "Nitric oxide generated from isoniazid activation by KatG: source of nitric oxide and activity against Mycobacterium tuberculosis". Antimicrobial Agents and Chemotherapy. 48 (8): 3006–3009. doi:10.1128/AAC.48.8.3006-3009.2004. PMC 478481. PMID 15273113.
    43. ↑ Singh, R.; Manjunatha, U.; Boshoff, H.I.; et al. (November 2008). "PA-824 kills nonreplicating Mycobacterium tuberculosis by intracellular NO release". Science. 322 (5906): 1392–1395. Bibcode:2008Sci...322.1392S. doi:10.1126/science.1164571. PMC 2723733. PMID 19039139.
    44. ↑ Ahmad, Z.; Klinkenberg, L.G.; Pinn, M.L.; et al. (2009). "Biphasic Kill Curve of Isoniazid Reveals the Presence of Drug‐Tolerant, Not Drug‐Resistant, Mycobacterium tuberculosis in the Guinea Pig". The Journal of Infectious Diseases. 200 (7): 1136–1143. doi:10.1086/605605. PMID 19686043.
    45. ↑ Harvey, Richard A.; Howland, Richard D.; Mycek, Mary Julia; Champe, Pamela C. (2006). Harvey, Richard A.; Champe, Pamela C. (eds.). Pharmacology. Vol. 864 (4th ed.). Lippincott Williams & Wilkins. ISBN 9780781741187.
    46. ↑ Judd, F. K.; Mijch, A. M.; Cockram, A.; Norman, T. R. (1994). "Isoniazid and antidepressants: is there cause for concern?". International Clinical Psychopharmacology. 9 (2): 123–125. doi:10.1097/00004850-199400920-00009. ISSN 0268-1315. PMID 8056994.
    47. ↑ Wang, Pengcheng; Pradhan, Komal; Zhong, Xiao-Bo; Ma, Xiaochao (September 2016). "Isoniazid metabolism and hepatotoxicity". Acta Pharmaceutica Sinica. B. 6 (5): 384–392. doi:10.1016/j.apsb.2016.07.014. ISSN 2211-3835.
    48. ↑ Riede, Hans L. (2009). "Fourth-generation fluoroquinolones in tuberculosis". Lancet. 373 (9670): 1148–1149. doi:10.1016/S0140-6736(09)60559-6. PMID 19345815.
    49. ↑ "History". rocheusa.com. Roche USA. Archived from the original on 2007-12-12.
    50. ↑ Jones, David S. (2002). "The Health Care Experiments at Many Farms: The Navajo, Tuberculosis, and the Limits of Modern Medicine, 1952–1962". Bulletin of the History of Medicine. 76 (4): 749–790. doi:10.1353/bhm.2002.0186. PMID 12446978.
    51. ↑ Beeson, Paul B. (1990). "Walsh McDermott". Biographical Memoirs: V.59. National Academies Press. pp. 282–307. Archived from the original on 2020-08-01. Retrieved 2020-01-09.
    52. ↑ Moncrieff, Joanna (June 2008). "The creation of the concept of an antidepressant: an historical analysis". Social Science & Medicine. 66 (11): 2346–2355. doi:10.1016/j.socscimed.2008.01.047. ISSN 0277-9536. PMID 18321627.
    53. ↑ William Andrew Publishing (2008). Pharmaceutical Manufacturing Encyclopedia (3rd ed.). Norwich, NY: Elsevier Science. pp. 1968–1970. ISBN 9780815515265.
    54. ↑ Baizer, Manuel M.; Dub, Michael; Gister, Sidney; Steinberg, Nathan G. (1956). "Synthesis of Isoniazid from Citric Acid". Journal of the American Pharmaceutical Association (Scientific Ed.). 45 (7): 478–480. doi:10.1002/jps.3030450714. ISSN 0095-9553. PMID 13345683.
    55. ↑ "Drugs@FDA". fda.gov. United States Food and Drug Administration. Archived from the original on 14 August 2012. Retrieved 22 August 2016.
    56. ↑ Smith, L.L.; Foell, Theodore (1959). "Differentiation of Δ4-3-Ketosteroids and Δ1,4-3-Ketosteroids with Isonicotinic Acid Hydrazide". Analytical Chemistry. 31 (1): 102–105. doi:10.1021/ac60145a020.
    57. ↑ Sykes, Jane E. (2013). Canine and Feline Infectious Diseases (E-Book). Elsevier Health Sciences. p. 425. ISBN 978-0323241946. Archived from the original on 2018-08-10. Retrieved 2018-08-10 – via Google Books.

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