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{{Short description|Antibiotic}} | {{Short description|Antibiotic}} | ||
{{Use dmy dates|date=October 2021}} | {{Use dmy dates|date=October 2021}} | ||
{{cs1 config |name-list-style=vanc |display-authors=6}} | |||
{{Infobox drug | {{Infobox drug | ||
| Verifiedfields = changed | | Verifiedfields = changed | ||
| Watchedfields = changed | | Watchedfields = changed | ||
| verifiedrevid = 462090938 | | verifiedrevid = 462090938 | ||
| drug_name = | |||
| INN = | |||
| type = <!-- empty --> | |||
| image = Levofloxacin skeletal.svg | | image = Levofloxacin skeletal.svg | ||
| width = |
| width = 250 | ||
| alt = Skeletal formula of a levofloxacin molecule | | alt = Skeletal formula of a levofloxacin molecule | ||
| image2 = Levofloxacin ball-and-stick 3RAE.png | | image2 = Levofloxacin ball-and-stick 3RAE.png | ||
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<!-- Clinical data --> | <!-- Clinical data --> | ||
| pronounce = | | pronounce = | ||
| tradename = Levaquin |
| tradename = Levaquin, others | ||
| Drugs.com = {{drugs.com|monograph|levofloxacin}} | | Drugs.com = {{drugs.com|monograph|levofloxacin}} | ||
| MedlinePlus = a697040 | | MedlinePlus = a697040 | ||
| licence_EU = yes | |||
| DailyMedID = Levofloxacin | | DailyMedID = Levofloxacin | ||
| licence_US = Levofloxacin | |||
| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> | | pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> | ||
| pregnancy_AU_comment = | | pregnancy_AU_comment = | ||
| pregnancy_category= | | pregnancy_category= | ||
| dependency_liability = | |||
| addiction_liability = | |||
| routes_of_administration = ], ] (IV), ] | | routes_of_administration = ], ] (IV), ] | ||
| class = ] | | class = ] | ||
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| ATC_suffix = MA12 | | ATC_suffix = MA12 | ||
| ATC_supplemental = {{ATC|S01|AE05}} {{ATC|A02|BD10}} {{ATC|J01|RA05}} | | ATC_supplemental = {{ATC|S01|AE05}} {{ATC|A02|BD10}} {{ATC|J01|RA05}} | ||
<!-- Legal status --> | <!-- Legal status --> | ||
| legal_AU = <!-- S2, S3, S4, S5, S6, S7, S8, S9 or Unscheduled --> | | legal_AU = <!-- S2, S3, S4, S5, S6, S7, S8, S9 or Unscheduled --> | ||
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| legal_BR = <!-- OTC, A1, A2, A3, B1, B2, C1, C2, C3, C4, C5, D1, D2, E, F --> | | legal_BR = <!-- OTC, A1, A2, A3, B1, B2, C1, C2, C3, C4, C5, D1, D2, E, F --> | ||
| legal_BR_comment = | | legal_BR_comment = | ||
| legal_CA |
| legal_CA = Rx-only | ||
| legal_CA_comment = <ref>{{cite web | title=Product monograph brand safety updates | website=Health Canada | date=February 2024 | url=https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/drug-product-database/label-safety-assessment-update/product-monograph-brand-safety-updates.html | access-date=24 March 2024}}</ref> | |||
| legal_CA_comment = | |||
| legal_DE = <!-- Anlage I, II, III or Unscheduled --> | | legal_DE = <!-- Anlage I, II, III or Unscheduled --> | ||
| legal_DE_comment = | | legal_DE_comment = | ||
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| legal_UK_comment = | | legal_UK_comment = | ||
| legal_US = Rx-only | | legal_US = Rx-only | ||
| legal_US_comment = | | legal_US_comment = <ref name="Levaquin FDA label" /> | ||
| legal_EU = Rx-only | | legal_EU = Rx-only | ||
| legal_EU_comment = | | legal_EU_comment = | ||
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | ||
| StdInChIKey = GSDSWSVVBLHKDQ-JTQLQIEISA-N | | StdInChIKey = GSDSWSVVBLHKDQ-JTQLQIEISA-N | ||
| density=1.5±0.1<ref name="chemsrc">{{Cite web|url=https://www.chemsrc.com/en/cas/100986-85-4_345636.html|title= |
| density=1.5±0.1<ref name="chemsrc">{{Cite web |url= https://www.chemsrc.com/en/cas/100986-85-4_345636.html |title=Levofloxacin | work = Material Safety Data Sheet | publisher = ChemSrc }}</ref> | ||
| density_notes = | | density_notes = | ||
| melting_point = | | melting_point = | ||
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<!-- Definition and medical uses --> | <!-- Definition and medical uses --> | ||
'''Levofloxacin''', sold under the brand name '''Levaquin''' among others, is |
'''Levofloxacin''', sold under the brand name '''Levaquin''' among others, is a ] of the ] drug class.<ref name=Preg2011/> It is the ] of the medication ].<ref name=Preg2011>{{cite book| vauthors = Yaffe GB, Freeman RK, Sumner J |title=Drugs in pregnancy and lactation: a reference guide to fetal and neonatal risk|date=2011|publisher=Wolters Kluwer Health/Lippincott Williams & Wilkins|location=Philadelphia|isbn=978-1-60831-708-0|page=828|edition=9th|url=https://books.google.com/books?id=OIgTE4aynrMC&pg=PA828|url-status=live|archive-url=https://web.archive.org/web/20160201164544/https://books.google.com/books?id=OIgTE4aynrMC&pg=PA828|archive-date=1 February 2016}}</ref><ref name=AHFS2016>{{cite web|title=Levofloxacin|url=https://www.drugs.com/monograph/levofloxacin.html|publisher=The American Society of Health-System Pharmacists|access-date=25 August 2016|url-status=live|archive-url=https://web.archive.org/web/20160501162059/http://www.drugs.com/monograph/levofloxacin.html|archive-date=1 May 2016}}</ref> It is used to treat a number of ]s including ], ], '']'' (in combination with other medications), ]s, ], ], and some types of ].<ref name=AHFS2016/> Along with other antibiotics it may be used to treat ], ], or ].<ref name=AHFS2016/> It is available by mouth, ],<ref name=AHFS2016/> and in ] form.<ref name=MTM2017>{{cite web|title=Levofloxacin ophthalmic medical facts from Drugs.com|url=https://www.drugs.com/mtm/levofloxacin-ophthalmic.html|website=Drugs.com|access-date=23 January 2017|url-status=live|archive-url=https://web.archive.org/web/20170202062127/https://www.drugs.com/mtm/levofloxacin-ophthalmic.html|archive-date=2 February 2017}}</ref> | ||
<!-- Side effects and mechanism --> | <!-- Side effects and mechanism --> | ||
Common side effects include ], ], and trouble sleeping.<ref name=AHFS2016/> A warning concerning all fluoroquinolones was issued in 2016: "An FDA safety review has shown that fluoroquinolones when used systemically (i.e. tablets, capsules, and injectable) are associated with disabling and potentially permanent serious adverse effects that can occur together. These adverse effects can involve the tendons, muscles, joints, nerves, and central nervous system."<ref name=FDA2016 /> | |||
⚫ | |||
⚫ | Other serious side effects may include ], ], ]s, ], and potentially permanent ].<ref name=AHFS2016/> Tendon damage may appear months after treatment is completed.<ref name=AHFS2016/> People may also ].<ref name=AHFS2016/> In people with ], muscle weakness and breathing problems may worsen.<ref name=AHFS2016/> While use during pregnancy is not recommended, risk appears to be low.<ref name=Preg2011/> The use of other medications in this class appear to be safe while ]; however, the safety of levofloxacin is unclear.<ref name=Preg2011/> | ||
<!-- History, society, and culture --> | <!-- History, society, and culture --> | ||
Levofloxacin was patented in 1985 and approved for medical use in the United States in 1996.<ref name=AHFS2016/><ref name=Fis2006>{{cite book | |
Levofloxacin was patented in 1985 and approved for medical use in the United States in 1996.<ref name=AHFS2016/><ref name=Fis2006>{{cite book |vauthors = Fischer J, Ganellin CR |title=Analogue-based Drug Discovery |date=2006 |publisher=John Wiley & Sons |isbn=978-3-527-60749-5 |page=500 |url=https://books.google.com/books?id=FjKfqkaKkAAC&pg=PA500 }}</ref> It is on the ].<ref name="WHO23rd">{{cite book | vauthors = ((World Health Organization)) | title = The selection and use of essential medicines 2023: web annex A: World Health Organization model list of essential medicines: 23rd list (2023) | year = 2023 | hdl = 10665/371090 | author-link = World Health Organization | publisher = World Health Organization | location = Geneva | id = WHO/MHP/HPS/EML/2023.02 | hdl-access=free }}</ref> It is available as a ].<ref name=AHFS2016/> In 2022, it was the 251st most commonly prescribed medication in the United States, with more than 1{{nbsp}}million prescriptions.<ref>{{cite web | title=The Top 300 of 2022 | url=https://clincalc.com/DrugStats/Top300Drugs.aspx | website=ClinCalc | access-date=30 August 2024 | archive-date=30 August 2024 | archive-url=https://web.archive.org/web/20240830202410/https://clincalc.com/DrugStats/Top300Drugs.aspx | url-status=live }}</ref><ref>{{cite web | title = Levofloxacin Drug Usage Statistics, United States, 2013 - 2022 | website = ClinCalc | url = https://clincalc.com/DrugStats/Drugs/Levofloxacin | access-date = 30 August 2024 }}</ref> | ||
==Medical uses== | ==Medical uses== | ||
Levofloxacin is used to treat infections including: ], ], ]s, ], ], ], ], ], ], ], and ]<ref name=AHFS2016/><ref name= |
Levofloxacin is used to treat infections including: ], ], ]s, ], ], ], ], ], ], ], and ]<ref name=AHFS2016/><ref name="Levaquin FDA label" /> and is available by mouth, ],<ref name=AHFS2016/> and in eye drop form.<ref name=MTM2017 /> | ||
As of 2016, the US ] (FDA) recommended that "serious side effects associated with fluoroquinolone antibacterial drugs generally outweigh the benefits for patients with acute sinusitis, acute bronchitis, and uncomplicated urinary tract infections who have other treatment options. For patients with these conditions, fluoroquinolones should be reserved for those who do not have alternative treatment options."<ref name=FDA2016/> | As of 2016, the US ] (FDA) recommended that "serious side effects associated with fluoroquinolone antibacterial drugs generally outweigh the benefits for patients with acute sinusitis, acute bronchitis, and uncomplicated urinary tract infections who have other treatment options. For patients with these conditions, fluoroquinolones should be reserved for those who do not have alternative treatment options."<ref name=FDA2016/> | ||
Levofloxacin is used for the treatment of pneumonia, urinary tract infections, and abdominal infections. |
Levofloxacin is used for the treatment of pneumonia, urinary tract infections, and abdominal infections. As of 2007 the ] (IDSA) and the ] recommended levofloxacin and other respiratory fluoroquinolines as first line treatment for community acquired pneumonia when co-morbidities such as heart, lung, or liver disease are present or when in-patient treatment is required.<ref name="Mandell LA, Wunderink RG, Anzueto A, et al. 2007 S27–72">{{cite journal | vauthors = Mandell LA, Wunderink RG, Anzueto A, Bartlett JG, Campbell GD, Dean NC, Dowell SF, File TM, Musher DM, Niederman MS, Torres A, Whitney CG | title = Infectious Diseases Society of America/American Thoracic Society consensus guidelines on the management of community-acquired pneumonia in adults | journal = Clinical Infectious Diseases | volume = 44 | issue = Suppl 2 | pages = S27–S72 | date = March 2007 | pmid = 17278083 | pmc = 7107997 | doi = 10.1086/511159 | doi-access = free | title-link = doi }}</ref> Levofloxacin also plays an important role in recommended treatment regimens for ventilator-associated and healthcare-associated pneumonia.<ref>{{cite journal | vauthors = File TM | title = Recommendations for treatment of hospital-acquired and ventilator-associated pneumonia: review of recent international guidelines | journal = Clinical Infectious Diseases | volume = 51 | pages = S42–S47 | date = August 2010 | issue = Suppl 1 | pmid = 20597671 | doi = 10.1086/653048 | doi-access = free | title-link = doi }}</ref> | ||
As of 2010 it was recommended by the IDSA as a first-line treatment option for catheter-associated urinary tract infections in adults.<ref>{{cite journal |vauthors=Hooton TM, Bradley SF, Cardenas DD, |
As of 2010 it was recommended by the IDSA as a first-line treatment option for catheter-associated urinary tract infections in adults.<ref>{{cite journal | vauthors = Hooton TM, Bradley SF, Cardenas DD, Colgan R, Geerlings SE, Rice JC, Saint S, Schaeffer AJ, Tambayh PA, Tenke P, Nicolle LE | title = Diagnosis, prevention, and treatment of catheter-associated urinary tract infection in adults: 2009 International Clinical Practice Guidelines from the Infectious Diseases Society of America | journal = Clinical Infectious Diseases | volume = 50 | issue = 5 | pages = 625–663 | date = March 2010 | pmid = 20175247 | doi = 10.1086/650482 | doi-access = free | title-link = doi }}</ref> In combination with ] it is recommended as one of several first-line treatment options for adult patients with community-acquired intra-abdominal infections of mild-to-moderate severity.<ref name="Solomkin JS, Mazuski JE, Bradley JS, et al. 2010 133–64">{{cite journal | vauthors = Solomkin JS, Mazuski JE, Bradley JS, Rodvold KA, Goldstein EJ, Baron EJ, O'Neill PJ, Chow AW, Dellinger EP, Eachempati SR, Gorbach S, Hilfiker M, May AK, Nathens AB, Sawyer RG, Bartlett JG | title = Diagnosis and management of complicated intra-abdominal infection in adults and children: guidelines by the Surgical Infection Society and the Infectious Diseases Society of America | journal = Clinical Infectious Diseases | volume = 50 | issue = 2 | pages = 133–164 | date = January 2010 | pmid = 20034345 | doi = 10.1086/649554 | doi-access = free | title-link = doi }}</ref> The IDSA also recommends it in combination with rifampicin as a first-line treatment for prosthetic joint infections.<ref>{{cite journal | vauthors = Osmon DR, Berbari EF, Berendt AR, Lew D, Zimmerli W, Steckelberg JM, Rao N, Hanssen A, Wilson WR | title = Executive summary: diagnosis and management of prosthetic joint infection: clinical practice guidelines by the Infectious Diseases Society of America | journal = Clinical Infectious Diseases | volume = 56 | issue = 1 | pages = 1–10 | date = January 2013 | pmid = 23230301 | doi = 10.1093/cid/cis966 | doi-access = free | title-link = doi }}</ref> The ] recommends levofloxacin as a first-line treatment to prevent bacterial prostatitis when the prostate is biopsied.<ref>{{cite web | work = American Urological Association. | date = 2016 | url = https://www.auanet.org/common/pdf/education/clinical-guidance/AUA-PNB-White-Paper.pdf | title =The Prevention and Treatment of the More Common Complications Related to Prostate Biopsy Update | archive-url = https://web.archive.org/web/20160920061133/https://www.auanet.org/common/pdf/education/clinical-guidance/AUA-PNB-White-Paper.pdf | archive-date = 20 September 2016 }}</ref> and as of 2004 it was recommended to treat bacterial prostatitis by the NIH research network studying the condition.<ref>{{cite journal | vauthors = Schaeffer AJ | title = NIDDK-sponsored chronic prostatitis collaborative research network (CPCRN) 5-year data and treatment guidelines for bacterial prostatitis | journal = International Journal of Antimicrobial Agents | volume = 24 | pages = S49–S52 | date = September 2004 | issue = Suppl 1 | pmid = 15364307 | doi = 10.1016/j.ijantimicag.2004.02.009 }}</ref> | ||
Levofloxacin and other fluoroquinolones have also been widely used for the treatment of uncomplicated community-acquired respiratory and urinary tract infections, indications for which major medical societies generally recommend the use of older, narrower spectrum drugs to avoid fluoroquinolone resistance development. Due to its widespread use, common pathogens such as ''Escherichia coli'' and ''Klebsiella pneumoniae'' have developed resistance. In many countries as of 2013, resistance rates among healthcare-associated infections with these pathogens exceeded 20%.<ref>{{cite web| url = https://www.ecdc.europa.eu/en/publications-data/antimicrobial-resistance-surveillance-europe-2014 | title = Antimicrobial resistance surveillance in Europe 2014| author = ECDC| year = 2014| url-status = live| archive-url = https://web.archive.org/web/20160414110905/http://ecdc.europa.eu/en/publications/Publications/antimicrobial-resistance-europe-2014.pdf| archive-date = 14 April 2016}}</ref><ref>{{cite web| url = https://www.cdc.gov/drugresistance/threat-report-2013/pdf/ar-threats-2013-508.pdf | title = Antibiotic Resistance Threats in the United States, 2013| author = CDC| url-status = live| archive-url = https://web.archive.org/web/20141117113220/http://www.cdc.gov/drugresistance/threat-report-2013/pdf/ar-threats-2013-508.pdf| archive-date = 17 November 2014}}</ref> | Levofloxacin and other fluoroquinolones have also been widely used for the treatment of uncomplicated community-acquired respiratory and urinary tract infections, indications for which major medical societies generally recommend the use of older, narrower spectrum drugs to avoid fluoroquinolone resistance development. Due to its widespread use, common pathogens such as ''Escherichia coli'' and ''Klebsiella pneumoniae'' have developed resistance. In many countries as of 2013, resistance rates among healthcare-associated infections with these pathogens exceeded 20%.<ref>{{cite web| url = https://www.ecdc.europa.eu/en/publications-data/antimicrobial-resistance-surveillance-europe-2014 | title = Antimicrobial resistance surveillance in Europe 2014| author = ECDC| year = 2014| url-status = live| archive-url = https://web.archive.org/web/20160414110905/http://ecdc.europa.eu/en/publications/Publications/antimicrobial-resistance-europe-2014.pdf| archive-date = 14 April 2016}}</ref><ref>{{cite web| url = https://www.cdc.gov/drugresistance/threat-report-2013/pdf/ar-threats-2013-508.pdf | title = Antibiotic Resistance Threats in the United States, 2013| author = CDC| url-status = live| archive-url = https://web.archive.org/web/20141117113220/http://www.cdc.gov/drugresistance/threat-report-2013/pdf/ar-threats-2013-508.pdf| archive-date = 17 November 2014}}</ref> | ||
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===Pregnancy and breastfeeding=== | ===Pregnancy and breastfeeding=== | ||
According to the FDA approved prescribing information, levofloxacin is ] C.<ref name= |
According to the FDA approved prescribing information, levofloxacin is ] C.<ref name="Levaquin FDA label" /> This designation indicates that animal reproduction studies have shown adverse effects on the fetus and there are no adequate and well-controlled studies in humans, but the potential benefit to the mother may in some cases outweigh the risk to the fetus. Available data point to a low risk for the unborn child.<ref name=Preg2011/> Exposure to quinolones, including levofloxacin, during the first-trimester is not associated with an increased risk of stillbirths, premature births, birth defects, or low birth weight.<ref>{{cite journal |vauthors=Ziv A, Masarwa R, Perlman A, Ziv D, Matok I |title=Pregnancy Outcomes Following Exposure to Quinolone Antibiotics – a Systematic-Review and Meta-Analysis |journal=Pharm. Res. |volume=35 |issue=5 |pages=109 |date=March 2018 |pmid=29582196 |doi=10.1007/s11095-018-2383-8 |s2cid=4724821 }}</ref> | ||
Levofloxacin does penetrate into breastmilk, though the concentration of levofloxacin in the breastfeeding infant is expected to be low.<ref name="Lactmed">{{cite web |title=TOXNET: Levofloxacin |website=toxnet.nlm.nih.gov |url=https://toxnet.nlm.nih.gov/cgi-bin/sis/search2/f?./temp/~1YokWM:1|publisher=U.S. National Library of Medicine |access-date=16 January 2019}}</ref> Due to potential risks to the baby, the manufacturer does not recommend that nursing mothers take levofloxacin.<ref name= |
Levofloxacin does penetrate into breastmilk, though the concentration of levofloxacin in the breastfeeding infant is expected to be low.<ref name="Lactmed">{{cite web |title=TOXNET: Levofloxacin |website=toxnet.nlm.nih.gov |url=https://toxnet.nlm.nih.gov/cgi-bin/sis/search2/f?./temp/~1YokWM:1|publisher=U.S. National Library of Medicine |access-date=16 January 2019}}</ref> Due to potential risks to the baby, the manufacturer does not recommend that nursing mothers take levofloxacin.<ref name="Levaquin FDA label" /> However, the risk appears to be very low, and levofloxacin can be used in breastfeeding mothers with proper monitoring of the infant, combined with delaying breastfeeding for 4–6 hours after taking levofloxacin.<ref name="Lactmed" /> | ||
===Children=== | ===Children=== | ||
Levofloxacin is not approved in most countries for the treatment of children except in unique and life-threatening infections because it is associated with an elevated risk of musculoskeletal injury in this population, a property it shares with other fluoroquinolones. | Levofloxacin is not approved in most countries for the treatment of children except in unique and life-threatening infections because it is associated with an elevated risk of musculoskeletal injury in this population, a property it shares with other fluoroquinolones. | ||
In the United States levofloxacin is approved for the treatment of anthrax and plague in children over six months of age.<ref name= |
In the United States levofloxacin is approved for the treatment of anthrax and plague in children over six months of age.<ref name="Levaquin FDA label" /> | ||
Levofloxacin is recommended by the Pediatric Infectious Disease Society and the Infectious Disease Society of America as a first-line treatment for pediatric pneumonia caused by penicillin-resistant ''Streptococcus pneumoniae'', and as a second-line agent for the treatment of penicillin-sensitive cases.<ref>{{cite journal |vauthors=Bradley JS, Byington CL, Shah SS, Alverson B, Carter ER, Harrison C, Kaplan SL, Mace SE, McCracken GH, Moore MR, St Peter SD, Stockwell JA, Swanson JT |title=The management of community-acquired pneumonia in infants and children older than 3 months of age: clinical practice guidelines by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America |journal=Clin. Infect. Dis. |volume=53 |issue=7 |pages=e25–76 |year=2011 |pmid=21880587 |doi=10.1093/cid/cir531 |pmc=7107838 |doi-access=free }}</ref> | Levofloxacin is recommended by the Pediatric Infectious Disease Society and the Infectious Disease Society of America as a first-line treatment for pediatric pneumonia caused by penicillin-resistant ''Streptococcus pneumoniae'', and as a second-line agent for the treatment of penicillin-sensitive cases.<ref>{{cite journal |vauthors=Bradley JS, Byington CL, Shah SS, Alverson B, Carter ER, Harrison C, Kaplan SL, Mace SE, McCracken GH, Moore MR, St Peter SD, Stockwell JA, Swanson JT |title=The management of community-acquired pneumonia in infants and children older than 3 months of age: clinical practice guidelines by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America |journal=Clin. Infect. Dis. |volume=53 |issue=7 |pages=e25–76 |year=2011 |pmid=21880587 |doi=10.1093/cid/cir531 |pmc=7107838 | doi-access = free | title-link = doi }}</ref> | ||
In one study,<ref name= |
In one study,<ref name="Levaquin FDA label" /><ref name="Noel GJ, Bradley JS, Kauffman RE 2007 879–91">{{cite journal |vauthors=Noel GJ, Bradley JS, Kauffman RE |title=Comparative safety profile of levofloxacin in 2523 children with a focus on four specific musculoskeletal disorders |journal=Pediatr. Infect. Dis. J. |volume=26 |issue=10 |pages=879–91 | date=October 2007 |pmid=17901792 |doi= 10.1097/INF.0b013e3180cbd382|s2cid=26457648 }}</ref> 1534 juvenile patients (age 6 months to 16 years) treated with levofloxacin as part of three efficacy trials were followed up to assess all musculoskeletal events occurring up to 12 months post-treatment. At 12 months follow-up the cumulative incidence of musculoskeletal adverse events was 3.4%, compared to 1.8% among 893 patients treated with other antibiotics. In the levafloxacin-treated group, approximately two-thirds of these musculoskeletal adverse events occurred in the first 60 days, 86% were mild, 17% were moderate, and all resolved without long-term sequelae. | ||
===Spectrum of activity=== | ===Spectrum of activity=== | ||
Levofloxacin and later generation fluoroquinolones are collectively referred to as "respiratory quinolones" to distinguish them from earlier fluoroquinolones which exhibited modest activity toward the important respiratory pathogen ''Streptococcus pneumoniae''.<ref>{{cite journal |vauthors=Wispelwey B, Schafer KR |title=Fluoroquinolones in the management of community-acquired pneumonia in primary care |journal=Expert Rev Anti Infect Ther |volume=8 |issue=11 |pages=1259–71 | date=November 2010 |pmid=21073291 |doi=10.1586/eri.10.110 |s2cid=207217824 }}</ref> | Levofloxacin and later generation fluoroquinolones are collectively referred to as "respiratory quinolones" to distinguish them from earlier fluoroquinolones which exhibited modest activity toward the important respiratory pathogen ''Streptococcus pneumoniae''.<ref>{{cite journal |vauthors=Wispelwey B, Schafer KR |title=Fluoroquinolones in the management of community-acquired pneumonia in primary care |journal=Expert Rev Anti Infect Ther |volume=8 |issue=11 |pages=1259–71 | date=November 2010 |pmid=21073291 |doi=10.1586/eri.10.110 |s2cid=207217824 }}</ref> | ||
The drug exhibits enhanced activity against the important respiratory pathogen ''Streptococcus pneumoniae'' relative to earlier fluoroquinolone derivatives like ]. |
The drug exhibits enhanced activity against the important respiratory pathogen ''Streptococcus pneumoniae'' relative to earlier fluoroquinolone derivatives like ]. For this reason, it is considered a "respiratory fluoroquinolone" along with more recently developed fluoroquinolones such as ] and ]. It is less active than ] against Gram-negative bacteria, especially ''Pseudomonas aeruginosa'', and lacks the anti-] (MRSA) activity of ] and ].<ref name="Lafredo SC, Foleno BD, Fu KP 1993 36–9"/><ref>{{cite journal | vauthors = Fu KP, Lafredo SC, Foleno B, Isaacson DM, Barrett JF, Tobia AJ, Rosenthale ME | title = In vitro and in vivo antibacterial activities of levofloxacin (l-ofloxacin), an optically active ofloxacin | journal = Antimicrobial Agents and Chemotherapy | volume = 36 | issue = 4 | pages = 860–866 | date = April 1992 | pmid = 1503449 | pmc = 189464 | doi = 10.1128/aac.36.4.860 }}</ref><ref>{{cite journal | vauthors = Blondeau JM | title = A review of the comparative in-vitro activities of 12 antimicrobial agents, with a focus on five new respiratory quinolones' | journal = The Journal of Antimicrobial Chemotherapy | volume = 43 Suppl B | issue = 90002 | pages = 1–11 | date = May 1999 | pmid = 10382869 | doi = 10.1093/jac/43.suppl_2.1 | doi-access = free | title-link = doi }}</ref><ref>{{cite journal | vauthors = Cormican MG, Jones RN | title = Antimicrobial activity and spectrum of LB20304, a novel fluoronaphthyridone | journal = Antimicrobial Agents and Chemotherapy | volume = 41 | issue = 1 | pages = 204–211 | date = January 1997 | pmid = 8980783 | pmc = 163688 | doi = 10.1128/AAC.41.1.204 }}</ref> Levofloxacin has shown moderate activity against ]s, and is about twice as potent as ofloxacin against '']'' and other mycobacteria, including ].<ref>{{cite journal |issn= 1068-7777 |title=New and Emerging Quinolone Antibiotics | vauthors = Bosso JA |journal=Journal of Infectious Disease Pharmacotherapy |volume=2 |issue=4 |pages=61–76 |doi= 10.1300/J100v02n04_06 |year= 1998}}</ref> | ||
Its spectrum of activity includes most strains of bacterial pathogens responsible for respiratory, urinary tract, gastrointestinal, and abdominal infections, including ] ('']'','' ]'', '']'', '']'', '']'', '']'', and '']''), ] (]-sensitive but not methicillin-resistant '']'', '']'', '']'', '']'', and '']''), and atypical bacterial pathogens ('']'' and '']''). |
Its spectrum of activity includes most strains of bacterial pathogens responsible for respiratory, urinary tract, gastrointestinal, and abdominal infections, including ] ('']'','' ]'', '']'', '']'', '']'', '']'', and '']''), ] (]-sensitive but not methicillin-resistant '']'', '']'', '']'', '']'', and '']''), and atypical bacterial pathogens ('']'' and '']''). Compared to earlier antibiotics of the fluoroquinoline class such as ], levofloxacin exhibits greater activity towards Gram-positive bacteria<ref name="Lafredo SC, Foleno BD, Fu KP 1993 36–9">{{cite journal |vauthors=Lafredo SC, Foleno BD, Fu KP |title=Induction of resistance of Streptococcus pneumoniae to quinolones in vitro |journal=Chemotherapy |volume=39 |issue=1 |pages=36–9 |year=1993 |pmid=8383031 |doi= 10.1159/000238971}}</ref> but lesser activity toward Gram-negative bacteria,<ref>{{cite journal |vauthors=Yamane N, Jones RN, Frei R, Hoban DJ, Pignatari AC, Marco F |title=Levofloxacin in vitro activity: results from an international comparative study with ofloxacin and ciprofloxacin |journal=J Chemother |volume=6 |issue=2 |pages=83–91 | date=April 1994 |pmid=8077990 |doi= 10.1080/1120009X.1994.11741134}}</ref> especially ''Pseudomonas aeruginosa''. | ||
===Resistance=== | ===Resistance=== | ||
Resistance to fluoroquinolones is common in ''staphylococcus'' and ''pseudomonas''. Resistance occurs in multiple ways. One mechanism is by an alteration in topoisomerase IV enzyme. A double mutant form of S. ''pneumoniae'' Gyr A + Par C bearing Ser-81-->Phe and Ser-79-->Phe mutations were eight to sixteen times less responsive to ciprofloxacin.<ref>{{cite journal | |
Resistance to fluoroquinolones is common in ''staphylococcus'' and ''pseudomonas''. Resistance occurs in multiple ways. One mechanism is by an alteration in topoisomerase IV enzyme. A double mutant form of S. ''pneumoniae'' Gyr A + Par C bearing Ser-81-->Phe and Ser-79-->Phe mutations were eight to sixteen times less responsive to ciprofloxacin.<ref>{{cite journal | vauthors = Hawkey PM |title=Mechanisms of quinolone action and microbial response. |journal=The Journal of Antimicrobial Chemotherapy |date=May 2003 |volume=51 | issue = Suppl 1 |pages=29–35 |doi=10.1093/jac/dkg207 |pmid=12702701| doi-access = free | title-link = doi }}</ref> | ||
==Contraindications and interactions== | ==Contraindications and interactions== | ||
Package inserts mention that levofloxacin is to be avoided in patients with a known hypersensitivity to levofloxacin or other quinolone drugs.<ref name= |
Package inserts mention that levofloxacin is to be avoided in patients with a known hypersensitivity to levofloxacin or other quinolone drugs.<ref name="Levaquin FDA label" /><ref name=UKEMC>{{cite web | work = UK electronic Medicines Compendium (eMC) | url = https://www.medicines.org.uk/emc/medicine/24625 | title = Levofloxacin 250mg and 500mg Tablets | archive-url = https://web.archive.org/web/20160826141227/https://www.medicines.org.uk/emc/medicine/24625 | archive-date = 26 August 2016 }}</ref> | ||
Like all fluoroquinolines, levofloxacin is contraindicated in patients with ] or other seizure disorders, and in patients who have a history of quinolone-associated tendon rupture.<ref name= |
Like all fluoroquinolines, levofloxacin is contraindicated in patients with ] or other seizure disorders, and in patients who have a history of quinolone-associated tendon rupture.<ref name="Levaquin FDA label" /><ref name=UKEMC/> | ||
Levofloxacin may prolong the ] in some people, especially the elderly, and levofloxacin should not be used for people with a family history of ], or who have long QT, ], it should not be prescribed with other drugs that prolong the QT interval.<ref name= |
Levofloxacin may prolong the ] in some people, especially the elderly, and levofloxacin should not be used for people with a family history of ], or who have long QT, ], it should not be prescribed with other drugs that prolong the QT interval.<ref name="Levaquin FDA label" /> | ||
Unlike ciprofloxacin, levofloxacin does not appear to deactivate the drug metabolizing enzyme ]. Therefore, drugs that use that enzyme, like ], do not interact with levofloxacin. It is a weak inhibitor of ],<ref>{{cite journal |vauthors=Zhang L, Wei MJ, Zhao CY, Qi HM |title=Determination of the inhibitory potential of 6 fluoroquinolones on CYP1A2 and CYP2C9 in human liver microsomes |journal=Acta Pharmacol. Sin. |volume=29 |issue=12 |pages=1507–14 | date=December 2008 |pmid=19026171 |doi=10.1111/j.1745-7254.2008.00908.x |doi-access=free }}</ref> suggesting potential to block the breakdown of ] and ]. This can result in more action of drugs like warfarin, leading to more potential side effects, such as bleeding.<ref>{{cite journal |vauthors=Schelleman H, Bilker WB, Brensinger CM, Han X, Kimmel SE, Hennessy S |title=Warfarin with fluoroquinolones, sulfonamides, or azole antifungals: interactions and the risk of hospitalization for gastrointestinal bleeding |journal=Clin. Pharmacol. Ther. |volume=84 |issue=5 |pages=581–8 | date=November 2008 |pmid=18685566 |pmc=2574587 |doi=10.1038/clpt.2008.150 }}</ref> | Unlike ciprofloxacin, levofloxacin does not appear to deactivate the drug metabolizing enzyme ]. Therefore, drugs that use that enzyme, like ], do not interact with levofloxacin. It is a weak inhibitor of ],<ref>{{cite journal |vauthors=Zhang L, Wei MJ, Zhao CY, Qi HM |title=Determination of the inhibitory potential of 6 fluoroquinolones on CYP1A2 and CYP2C9 in human liver microsomes |journal=Acta Pharmacol. Sin. |volume=29 |issue=12 |pages=1507–14 | date=December 2008 |pmid=19026171 |doi=10.1111/j.1745-7254.2008.00908.x | doi-access = free | title-link = doi }}</ref> suggesting potential to block the breakdown of ] and ]. This can result in more action of drugs like warfarin, leading to more potential side effects, such as bleeding.<ref>{{cite journal |vauthors=Schelleman H, Bilker WB, Brensinger CM, Han X, Kimmel SE, Hennessy S |title=Warfarin with fluoroquinolones, sulfonamides, or azole antifungals: interactions and the risk of hospitalization for gastrointestinal bleeding |journal=Clin. Pharmacol. Ther. |volume=84 |issue=5 |pages=581–8 | date=November 2008 |pmid=18685566 |pmc=2574587 |doi=10.1038/clpt.2008.150 }}</ref> | ||
The use of ]s (NSAIDs) in combination with high dose fluoroquinolone therapy may lead to seizures.<ref>{{cite journal | |
The use of ]s (NSAIDs) in combination with high dose fluoroquinolone therapy may lead to seizures.<ref>{{cite journal | vauthors = Domagala JM | title = Structure-activity and structure-side-effect relationships for the quinolone antibacterials | journal = The Journal of Antimicrobial Chemotherapy | volume = 33 | issue = 4 | pages = 685–706 | date = April 1994 | pmid = 8056688 | doi = 10.1093/jac/33.4.685 }}</ref> | ||
When levofloxacin is taken with anti-acids containing magnesium hydroxide or aluminum hydroxide, the two combine to form insoluble salts that are difficult to absorb from the intestines. Peak serum concentrations of levofloxacin may be reduced by 90% or more, which can prevent the levofloxacin from working. Similar results have been reported when levofloxacin is taken with iron supplements and multi-vitamins containing zinc.<ref>{{cite journal |vauthors=Rodvold KA, Piscitelli SC |title=New oral macrolide and fluoroquinolone antibiotics: an overview of pharmacokinetics, interactions, and safety |journal=Clin. Infect. Dis. |volume=17 |
When levofloxacin is taken with anti-acids containing magnesium hydroxide or aluminum hydroxide, the two combine to form insoluble salts that are difficult to absorb from the intestines. Peak serum concentrations of levofloxacin may be reduced by 90% or more, which can prevent the levofloxacin from working. Similar results have been reported when levofloxacin is taken with iron supplements and multi-vitamins containing zinc.<ref>{{cite journal |vauthors=Rodvold KA, Piscitelli SC |title=New oral macrolide and fluoroquinolone antibiotics: an overview of pharmacokinetics, interactions, and safety |journal=Clin. Infect. Dis. |volume=17 |pages=S192–9 | date=August 1993 |issue=Suppl 1 |pmid=8399914 |doi= 10.1093/clinids/17.supplement_1.s192}}</ref><ref>{{cite journal |vauthors=Tanaka M, Kurata T, Fujisawa C, etal |title=Mechanistic study of inhibition of levofloxacin absorption by aluminum hydroxide |journal=Antimicrob. Agents Chemother. |volume=37 |issue=10 |pages=2173–8 | date=October 1993 |pmid=8257141 |pmc=192246 |doi= 10.1128/aac.37.10.2173}}</ref> | ||
A 2011 review examining musculoskeletal complications of fluoroquinolones proposed guidelines with respect to administration to athletes, that called for avoiding all use of fluoroquinolone antibiotics if possible, and if they are used: ensure there is informed consent about the musculoskeletal risks, and inform coaching staff; do not use any corticosteroids if fluoroquinolones are used; consider ]s of magnesium and antioxidants during treatment; reduce training until the course of antibiotic is finished and then carefully increase back to normal; and monitor for six months after the course is finished, and stop all athletic activity if symptoms emerge.<ref name=Hall2011>{{cite journal| |
A 2011 review examining musculoskeletal complications of fluoroquinolones proposed guidelines with respect to administration to athletes, that called for avoiding all use of fluoroquinolone antibiotics if possible, and if they are used: ensure there is informed consent about the musculoskeletal risks, and inform coaching staff; do not use any corticosteroids if fluoroquinolones are used; consider ]s of magnesium and antioxidants during treatment; reduce training until the course of antibiotic is finished and then carefully increase back to normal; and monitor for six months after the course is finished, and stop all athletic activity if symptoms emerge.<ref name=Hall2011>{{cite journal | vauthors = Hall MM, Finnoff JT, Smith J | title = Musculoskeletal complications of fluoroquinolones: guidelines and precautions for usage in the athletic population | journal = PM&R | volume = 3 | issue = 2 | pages = 132–142 | date = February 2011 | pmid = 21333952 | doi = 10.1016/j.pmrj.2010.10.003 | s2cid = 207402343 }}</ref> | ||
==Adverse effects== | ==Adverse effects== | ||
Adverse effects are typically mild to moderate. However, severe, disabling, and potentially irreversible adverse effects sometimes occur, and for this reason it is recommended that use of fluoroquinolones be limited. | Adverse effects are typically mild to moderate. However, severe, disabling, and potentially irreversible adverse effects sometimes occur, and for this reason it is recommended that use of fluoroquinolones be limited. | ||
Prominent among these are adverse effects that became the subject of a ] by the FDA in 2016.<ref name=FDA2016>{{cite web|title=FDA Drug Safety Communication: FDA advises restricting fluoroquinolone antibiotic use for certain uncomplicated infections; warns about disabling adverse effects that can occur|url=https://www.fda.gov/ |
Prominent among these are adverse effects that became the subject of a ] by the FDA in 2016.<ref name=FDA2016>{{cite web|title=FDA Drug Safety Communication: FDA advises restricting fluoroquinolone antibiotic use for certain uncomplicated infections; warns about disabling adverse effects that can occur|url=https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-fda-advises-restricting-fluoroquinolone-antibiotic-use-certain |publisher=U.S. ] (FDA)|date=25 August 2016|url-status=live|archive-url=https://web.archive.org/web/20160825175205/https://www.fda.gov/drugs/drugsafety/ucm500143.htm|archive-date=25 August 2016}}</ref> The FDA wrote: "An FDA safety review has shown that fluoroquinolones when used systemically (i.e. tablets, capsules, and injectable) are associated with disabling and potentially permanent serious adverse effects that can occur together. These adverse effects can involve the tendons, muscles, joints, nerves, and central nervous system."<ref name=FDA2016/> Rarely, tendinitis or tendon rupture may occur due to fluoroquinolone antibiotics, including levofloxacin.<ref>{{cite journal | vauthors = Stephenson AL, Wu W, Cortes D, Rochon PA | title = Tendon Injury and Fluoroquinolone Use: A Systematic Review | journal = Drug Safety | volume = 36 | issue = 9 | pages = 709–721 | date = September 2013 | pmid = 23888427 | doi = 10.1007/s40264-013-0089-8 | s2cid = 24948660 }}</ref> Such injuries, including tendon rupture, has been observed up to six months after cessation of treatment; higher doses of fluoroquinolones, being elderly, transplant patients, and those with a current or historical ] use are at elevated risk.<ref>{{cite journal | vauthors = Khaliq Y, Zhanel GG | title = Fluoroquinolone-associated tendinopathy: a critical review of the literature | journal = Clinical Infectious Diseases | volume = 36 | issue = 11 | pages = 1404–1410 | date = June 2003 | pmid = 12766835 | doi = 10.1086/375078 | s2cid = 14917687 | doi-access = free | title-link = doi }}</ref><ref>{{cite journal | vauthors = Kim GK | title = The Risk of Fluoroquinolone-induced Tendinopathy and Tendon Rupture: What Does The Clinician Need To Know? | journal = The Journal of Clinical and Aesthetic Dermatology | volume = 3 | issue = 4 | pages = 49–54 | date = April 2010 | pmid = 20725547 | pmc = 2921747 }}</ref> The U.S. label for levofloxacin also contains a black box warning for the exacerbation of the symptoms of the neurological disease ].<ref name="Levaquin FDA label" /><ref>{{cite journal | vauthors = Jones SC, Sorbello A, Boucher RM | title = Fluoroquinolone-associated myasthenia gravis exacerbation: evaluation of postmarketing reports from the US FDA adverse event reporting system and a literature review | journal = Drug Safety | volume = 34 | issue = 10 | pages = 839–847 | date = October 2011 | pmid = 21879778 | doi = 10.2165/11593110-000000000-00000 | s2cid = 7262267 }}</ref> Similarly, the UK Medicines and Healthcare Products Regulatory Agency recommendations warn of rare but disabling and potentially irreversible adverse effects, and to recommend limiting use of these drugs.<ref>{{Cite web | url=https://www.gov.uk/drug-safety-update/fluoroquinolone-antibiotics-new-restrictions-and-precautions-for-use-due-to-very-rare-reports-of-disabling-and-potentially-long-lasting-or-irreversible-side-effects |title = Fluoroquinolone antibiotics: New restrictions and precautions for use due to very rare reports of disabling and potentially long-lasting or irreversible side effects | work = Drug Safety Update | publisher = gov.uk }}</ref> Increasing age and corticosteroid use appears to increase the risk of musculoskeletal complications.<ref name=Hall2011/> | ||
A wide variety of other uncommon but serious adverse events have been associated with fluoroquinolone use, with varying degrees of evidence supporting causation. These include anaphylaxis, hepatotoxicity, central nervous system effects including seizures and psychiatric effects, prolongation of the ], blood glucose disturbances, and ], among others.<ref name= |
A wide variety of other uncommon but serious adverse events have been associated with fluoroquinolone use, with varying degrees of evidence supporting causation. These include anaphylaxis, hepatotoxicity, central nervous system effects including seizures and psychiatric effects, prolongation of the ], blood glucose disturbances, and ], among others.<ref name="Levaquin FDA label" /><ref name=UKEMC/> Levofloxacin may produce fewer of these rare serious adverse effects than other fluoroquinolones.<ref>{{cite journal | vauthors = Carbon C | title = Comparison of side effects of levofloxacin versus other fluoroquinolones | journal = Chemotherapy | volume = 47 Suppl 3 | issue = 3 | pages = 9–14; discussion 44–8 | year = 2001 | pmid = 11549784 | doi = 10.1159/000057839 | s2cid = 6139065 }}</ref> | ||
There is some disagreement in the medical literature regarding whether and to what extent levofloxacin and other fluoroquinolones produce serious adverse effects more frequently than other broad spectrum antibacterial drugs.<ref>{{cite journal | |
There is some disagreement in the medical literature regarding whether and to what extent levofloxacin and other fluoroquinolones produce serious adverse effects more frequently than other broad spectrum antibacterial drugs.<ref>{{cite journal | vauthors = Liu HH | title = Safety profile of the fluoroquinolones: focus on levofloxacin | journal = Drug Safety | volume = 33 | issue = 5 | pages = 353–369 | date = May 2010 | pmid = 20397737 | doi = 10.2165/11536360-000000000-00000 | s2cid = 9014317 }}</ref><ref>{{cite journal | vauthors = Karageorgopoulos DE, Giannopoulou KP, Grammatikos AP, Dimopoulos G, Falagas ME | title = Fluoroquinolones compared with beta-lactam antibiotics for the treatment of acute bacterial sinusitis: a meta-analysis of randomized controlled trials | journal = CMAJ | volume = 178 | issue = 7 | pages = 845–854 | date = March 2008 | pmid = 18362380 | pmc = 2267830 | doi = 10.1503/cmaj.071157 }}</ref><ref>{{cite journal | vauthors = Lipsky BA, Baker CA | title = Fluoroquinolone toxicity profiles: a review focusing on newer agents | journal = Clinical Infectious Diseases | volume = 28 | issue = 2 | pages = 352–364 | date = February 1999 | pmid = 10064255 | doi = 10.1086/515104 | doi-access = free | title-link = doi }}</ref><ref>{{cite journal | vauthors = Stahlmann R, Lode HM | title = Risks associated with the therapeutic use of fluoroquinolones | journal = Expert Opinion on Drug Safety | volume = 12 | issue = 4 | pages = 497–505 | date = July 2013 | pmid = 23651367 | doi = 10.1517/14740338.2013.796362 | s2cid = 22419225 }}</ref> | ||
⚫ | Concerning more usual adverse effects, in pooled results from 7537 patients exposed to levofloxacin in 29 clinical trials, 4.3% discontinued treatment due to adverse drug reactions. The most common adverse reactions leading to discontinuation were gastrointestinal, including nausea, vomiting, and constipation. Overall, 7% of patients experienced nausea, 6% headache, 5% diarrhea, and 4% insomnia, along with other adverse reactions experienced at lower rates.<ref name="Levaquin FDA label">{{cite web | title=Levaquin (levofloxacin) tablets, for oral use Initial U.S. Approval: 1996 | website=DailyMed | url=https://dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=550731 | access-date=6 December 2024}}</ref> | ||
There are some case reports of levofloxacin associated with ].<ref>{{Cite journal|last1=Rissardo|first1=JamirPitton|last2=Fornari Caprara|first2=AnaLetícia|date=2019|title=Intracranial hypertension secondary to levofloxacin-therapy|url=http://www.amhsjournal.org/text.asp?2019/7/2/313/273053|journal=Archives of Medicine and Health Sciences|language=en|volume=7|issue=2|pages=313|doi=10.4103/amhs.amhs_118_19|s2cid=209406252|issn=2321-4848}}</ref> | |||
⚫ | Administration of levofloxacin or other broad-spectrum antibiotics is associated with '']'' associated diarrhea which may range in severity from mild diarrhea to fatal colitis. Fluoroquinolone administration may be associated with the acquisition and outgrowth of a particularly virulent ''Clostridioides'' strain.<ref>{{cite journal |vauthors=Vardakas KZ, Konstantelias AA, Loizidis G, Rafailidis PI, Falagas ME |title=Risk factors for development of Clostridium difficile infection due to BI/NAP1/027 strain: a meta-analysis |journal=Int. J. Infect. Dis. |volume=16 |issue=11 |pages=e768–73 | date=November 2012 |pmid=22921930 |doi=10.1016/j.ijid.2012.07.010 | doi-access = free | title-link = doi }}</ref> | ||
⚫ | |||
⚫ | More research is needed to determine the best dose and length of treatment.<ref name="ReferenceA">{{cite journal | vauthors = McGregor JC, Allen GP, Bearden DT | title = Levofloxacin in the treatment of complicated urinary tract infections and acute pyelonephritis | journal = Therapeutics and Clinical Risk Management | volume = 4 | issue = 5 | pages = 843–853 | date = October 2008 | pmid = 19209267 | pmc = 2621400 | doi = 10.2147/TCRM.S3426 | doi-access = free | title-link = doi }}</ref> | ||
⚫ | Administration of levofloxacin or other broad |
||
⚫ | More research is needed to determine the best dose and length of treatment.<ref name="ReferenceA">{{cite journal | |
||
==Overdose== | ==Overdose== | ||
Overdosing experiments in animals showed loss of body control and drooping, difficulty breathing, tremors, and convulsions. Doses in excess of 1500 mg/kg orally and 250 mg/kg IV produced significant mortality in rodents.<ref name= |
Overdosing experiments in animals showed loss of body control and drooping, difficulty breathing, tremors, and convulsions. Doses in excess of 1500 mg/kg orally and 250 mg/kg IV produced significant mortality in rodents.<ref name="Levaquin FDA label" /> | ||
In the event of an acute overdosage, authorities recommend unspecific standard procedures such as emptying the stomach, observing the patient and maintaining appropriate hydration. Levofloxacin is not efficiently removed by ] or ].<ref name= |
In the event of an acute overdosage, authorities recommend unspecific standard procedures such as emptying the stomach, observing the patient and maintaining appropriate hydration. Levofloxacin is not efficiently removed by ] or ].<ref name="Levaquin FDA label" /> | ||
==Pharmacology== | ==Pharmacology== | ||
===Mechanism of action=== | ===Mechanism of action=== | ||
Levofloxacin is a ] that is active against both ] and ] bacteria. Like all quinolones, it functions by inhibiting the ] and ], two bacterial ]s.<ref>{{cite journal |vauthors=Drlica K, Zhao X |title=DNA gyrase, topoisomerase IV, and the 4-quinolones |journal=Microbiol Mol Biol Rev |volume=61 |issue=3 |pages=377–92 |date=1 September 1997|doi=10.1128/mmbr.61.3.377-392.1997 |pmid=9293187 |pmc=232616 }}</ref> Topoisomerase IV is necessary to separate ] that has been ] (doubled) prior to bacterial cell division. With the DNA not being separated, the process is stopped, and the bacterium cannot divide. DNA gyrase, on the other hand, is responsible for ] the DNA, so that it will fit in the newly formed cells. Both mechanisms amount to killing the bacterium. Levofloxacin acts as a ].<ref name="Mutschler">{{Cite book| |
Levofloxacin is a ] that is active against both ] and ] bacteria. Like all quinolones, it functions by inhibiting the ] and ], two bacterial ]s.<ref>{{cite journal |vauthors=Drlica K, Zhao X |title=DNA gyrase, topoisomerase IV, and the 4-quinolones |journal=Microbiol Mol Biol Rev |volume=61 |issue=3 |pages=377–92 |date=1 September 1997|doi=10.1128/mmbr.61.3.377-392.1997 |pmid=9293187 |pmc=232616 }}</ref> Topoisomerase IV is necessary to separate ] that has been ] (doubled) prior to bacterial cell division. With the DNA not being separated, the process is stopped, and the bacterium cannot divide. DNA gyrase, on the other hand, is responsible for ] the DNA, so that it will fit in the newly formed cells. Both mechanisms amount to killing the bacterium. Levofloxacin acts as a ].<ref name="Mutschler">{{Cite book| vauthors = Mutschler E, Schäfer-Korting M |title=Arzneimittelwirkungen |language=de |location=Stuttgart |publisher=Wissenschaftliche Verlagsgesellschaft |year=2001 |edition=8th |page=814f |isbn=978-3-8047-1763-3}}</ref> | ||
As of 2011, the mechanism of action for the drug's musculoskeletal complications were not clear.<ref name=Hall2011/> | As of 2011, the mechanism of action for the drug's musculoskeletal complications were not clear.<ref name=Hall2011/> | ||
===Pharmacokinetics=== | ===Pharmacokinetics=== | ||
Levofloxacin is rapidly and essentially completely absorbed after oral administration, with a plasma concentration profile over time that is essentially identical to that obtained from intravenous administration of the same amount over 60 minutes. |
Levofloxacin is rapidly and essentially completely absorbed after oral administration, with a plasma concentration profile over time that is essentially identical to that obtained from intravenous administration of the same amount over 60 minutes. As such, the intravenous and oral formulations of levofloxacin are considered interchangeable.<ref name="Levaquin FDA label" /> Levofloxacin's ability to bind to proteins in the body ranges from 24 to 38%.<ref name="ReferenceA"/> | ||
The drug undergoes widespread distribution into body tissues. |
The drug undergoes widespread distribution into body tissues. Peak levels in skin are achieved 3 hours after administration and exceed those in plasma by a factor of 2. Similarly, lung tissue concentrations range from two-fold to five-fold higher than plasma concentrations in the 24 hours after a single dose. | ||
The mean terminal plasma elimination half-life of levofloxacin ranges from approximately 6 to 8 hours following single or multiple doses of levofloxacin given orally or intravenously. Elimination occurs mainly via excretion of unmetabolized drug in the urine. |
The mean terminal plasma elimination half-life of levofloxacin ranges from approximately 6 to 8 hours following single or multiple doses of levofloxacin given orally or intravenously. Elimination occurs mainly via excretion of unmetabolized drug in the urine. Following oral administration, 87% of an administered dose was recovered in the urine as unchanged drug within 2 days. Less than 5% was recovered in the urine as the desmethyl and N-oxide metabolites, the only metabolites identified in humans. | ||
==Chemistry== | ==Chemistry== | ||
Like all |
Like all fluoroquinolones, levofloxacin is a ] ] ]. It is a ] molecule and the pure (−)-(''S'')-] of the ] drug ].<ref>{{cite web |url=http://www.accessdata.fda.gov/drugsatfda_docs/nda/96/020634-4.pdf |title=Statistical Review and Evaluation |publisher=FDA |location=USA |date=21 November 1996 |url-status=live |archive-url=https://web.archive.org/web/20121018202909/http://www.accessdata.fda.gov/drugsatfda_docs/nda/96/020634-4.pdf |archive-date=18 October 2012 }}</ref><ref>{{cite journal | vauthors = Morrissey I, Hoshino K, Sato K, Yoshida A, Hayakawa I, Bures MG, Shen LL | title = Mechanism of differential activities of ofloxacin enantiomers | journal = Antimicrobial Agents and Chemotherapy | volume = 40 | issue = 8 | pages = 1775–1784 | date = August 1996 | pmid = 8843280 | pmc = 163416 | doi = 10.1128/AAC.40.8.1775 }}</ref><ref>{{cite journal| vauthors = Kannappan V, Mannemala SS |title=Multiple Response Optimization of a HPLC Method for the Determination of Enantiomeric Purity of S-Ofloxacin|journal=Chromatographia|date=7 June 2014|volume=77|issue=17–18|pages=1203–1211|doi=10.1007/s10337-014-2699-4|s2cid=98491475}}</ref> This enantiomer binds more effectively to the DNA gyrase enzyme and to topoisomerase IV than its (+)-(''R'')-counterpart.<ref name="ReferenceA"/> Levofloxacin is referred to as a ]: These are ] that have already been ]ed, approved and marketed as racemates (or as mixtures of ]s<ref>{{Cite book|last=Kurt.|first=Mislow|url=http://worldcat.org/oclc/1097808137|title=Introduction to stereochemistry|date=1966|publisher=W.A. Benjamín|oclc=1097808137}}</ref> but have since been redeveloped as pure enantiomers.<ref>{{cite journal | vauthors = Agranat I, Caner H | title = Intellectual property and chirality of drugs | journal = Drug Discovery Today | volume = 4 | issue = 7 | pages = 313–321 | date = July 1999 | pmid = 10377509 | doi = 10.1016/s1359-6446(99)01363-x }}</ref> Distinct functional groups on this molecules include a hydroxyl group, carbonyl group, and an aromatic ring.<ref>{{cite journal | vauthors = Mouzam MI, Dehghan MH, Asif S, Sahuji T, Chudiwal P | title = Preparation of a novel floating ring capsule-type dosage form for stomach specific delivery | journal = Saudi Pharmaceutical Journal | volume = 19 | issue = 2 | pages = 85–93 | date = April 2011 | pmid = 23960746 | pmc = 3745050 | doi = 10.1016/j.jsps.2011.01.004 }}</ref>{{Failed verification|date=May 2021}} | ||
The substance is used as the hemi], which has the empirical formula C<sub>18</sub>H<sub>20</sub>FN<sub>3</sub>O<sub>4</sub> · {{frac|1|2}} H<sub>2</sub>O and a molecular mass of 370.38 g/mol. Levofloxacin is a light-yellowish-white to yellow-white crystal or crystalline powder.<ref name= |
The substance is used as the hemi], which has the empirical formula C<sub>18</sub>H<sub>20</sub>FN<sub>3</sub>O<sub>4</sub> · {{frac|1|2}} H<sub>2</sub>O and a molecular mass of 370.38 g/mol. Levofloxacin is a light-yellowish-white to yellow-white crystal or crystalline powder.<ref name="Levaquin FDA label" /> A major issue in the synthesis of levofloxacin is identifying correct entries into the benzoxazine core in order to produce the correct chiral form.<ref>{{cite journal | vauthors = Bower JF, Rujirawanich J, Gallagher T | title = N-heterocycle construction via cyclic sulfamidates. Applications in synthesis | journal = Organic & Biomolecular Chemistry | volume = 8 | issue = 7 | pages = 1505–1519 | date = April 2010 | pmid = 20237659 | doi = 10.1039/b921842d }}</ref> | ||
==History== | ==History== | ||
Levofloxacin is a ], being one of the isomers of ], which was a broader-spectrum conformationally locked analog of ]; both ofloxacin and levofloxaxin were synthesized and developed by scientists at ].<ref name=Sneader2005>{{cite book| |
Levofloxacin is a ], being one of the isomers of ], which was a broader-spectrum conformationally locked analog of ]; both ofloxacin and levofloxaxin were synthesized and developed by scientists at ].<ref name=Sneader2005>{{cite book| vauthors = Sneader W |title=Drug Discovery: A History|url=https://books.google.com/books?id=jglFsz5EJR8C&pg=PA395|date=31 October 2005|publisher=John Wiley & Sons|isbn=978-0-470-01552-0|pages=295|url-status=live|archive-url=https://web.archive.org/web/20170908191512/https://books.google.com/books?id=jglFsz5EJR8C&pg=PA395|archive-date=8 September 2017}}</ref> The Daiichi scientists knew that ofloxacin was racemic, but tried unsuccessfully to separate the two isomers; in 1985 they succeeded in separately synthesizing the pure levo form and showed that it was less toxic and more potent than the other form.<ref name=Fish>{{cite web | author = Staff | publisher = Fish and Richardson | url = http://www.fr.com/files/Uploads/attachments/memoranda/memorANDAQ209.pdf | title = New FDA Requirements for Post-Marketing Studies and Clinical Trials: Patent Strategy | work = memorANDA | date = 2009 | archive-url = https://web.archive.org/web/20160827002405/http://www.fr.com/files/Uploads/attachments/memoranda/memorANDAQ209.pdf | archive-date=27 August 2016 | page = VIII }} Cites {{cite patent | title = Optically active pyridobenzoxazine derivatives and anti-microbial use | assign1 = Daiichi Sankyo Co Ltd. | gdate = 1 October 1991 | url = https://www.google.com/patents/US5053407 | country = US | number = 5053407 }}</ref><ref name=Atarashi/> | ||
It was first approved for marketing in Japan in 1993, for oral administration, and Daiichi marketed it there under the brand name Cravit.<ref name=Atarashi> |
It was first approved for marketing in Japan in 1993, for oral administration, and Daiichi marketed it there under the brand name Cravit.<ref name=Atarashi>{{cite web | vauthors = Atarashi S | title = Research and Development of Quinolones in Daiichi Sankyo Co | url = http://www.infectweb.com/only/03_SpeFeature.pdf | archive-url = https://web.archive.org/web/20161012025535/http://www.infectweb.com/only/03_SpeFeature.pdf | archive-date=12 October 2016 }}</ref> Daiichi, working with ] as it had with ofloxacin, obtained FDA approval in 1996 under the brand name Levaquin<ref name=Fish/> to treat bacterial sinusitus, bacterial exacerbations of bronchitis, community-acquired pneumonia, uncomplicated skin infections, complicated urinary tract infections, and acute pyelonephritis.<ref name="Levaquin FDA label" /> | ||
⚫ | Levofloxacin is marketed by ] under a license agreement signed with Daiichi in 1993, under the brand name |
||
⚫ | ==Society and culture== | ||
=== Economics === | |||
Levofloxacin had reached blockbuster status by this time; combined worldwide sales of levofloxacin and ofloxacin for J&J alone were {{US$|1.6 billion}} in 2009.<ref name=DrugFocus2009/> | Levofloxacin had reached blockbuster status by this time; combined worldwide sales of levofloxacin and ofloxacin for J&J alone were {{US$|1.6 billion}} in 2009.<ref name=DrugFocus2009/> | ||
The term of the levofloxacin United States patent was extended by the U.S. Patent and Trademark Office 810 days under the provisions of the ] so that the patent would expire in 2010 instead of 2008.<ref name=Fish/> This extension was challenged by ] manufacturer Lupin Pharmaceuticals, which did not challenge the validity of the patent, but only the validity of the patent extension, arguing that the patent did not cover a "product" and so Hatch-Waxman was not available for extensions.<ref name=Fish/> The federal patent court ruled in favor of J&J and Daiichi, and generic versions of levofloxacin did not enter the U.S. market until 2009.<ref name=Fish/><ref name=DrugFocus2009>{{cite web |url=http://www.genericsweb.com/druginfocus/Levofloxacin |title=Drug in Focus: Levofloxacin | |
The term of the levofloxacin United States patent was extended by the U.S. Patent and Trademark Office 810 days under the provisions of the ] so that the patent would expire in 2010 instead of 2008.<ref name=Fish/> This extension was challenged by ] manufacturer Lupin Pharmaceuticals, which did not challenge the validity of the patent, but only the validity of the patent extension, arguing that the patent did not cover a "product" and so Hatch-Waxman was not available for extensions.<ref name=Fish/> The federal patent court ruled in favor of J&J and Daiichi, and generic versions of levofloxacin did not enter the U.S. market until 2009.<ref name=Fish/><ref name=DrugFocus2009>{{cite web |url=http://www.genericsweb.com/druginfocus/Levofloxacin |title=Drug in Focus: Levofloxacin | vauthors = Taylor K |work=GenericsWeb |date=October 2010 |url-status=dead |archive-url=https://web.archive.org/web/20140112065215/http://www.genericsweb.com/druginfocus/Levofloxacin |archive-date=12 January 2014 }}</ref> | ||
⚫ | ==Society and culture== | ||
===Availability=== | ===Availability=== | ||
] injection, specification is 100mL / 750mg]] | ] injection, specification is 100mL / 750mg]] | ||
Levofloxacin is available in tablet form, injection, and oral solution.<ref name= |
Levofloxacin is available in tablet form, injection, and oral solution.<ref name="Levaquin FDA label" /> | ||
===Usage=== | ===Usage=== | ||
The |
The US ] estimated that in 2011, over 23 million outpatient prescriptions for fluoroquinolones, of which levofloxacin made up 28%, were filled in the United States.<ref>{{cite web|title=FDA Drug Safety Communication: FDA requires label changes to warn of risk for possibly permanent nerve damage from antibacterial fluoroquinolone drugs taken by mouth or by injection|url=https://www.fda.gov/Drugs/DrugSafety/ucm365050.htm |publisher=US Food and Drug Administration|date=16 January 2016|archive-url=https://web.archive.org/web/20160528231716/https://www.fda.gov/Drugs/DrugSafety/ucm365050.htm#tabs-2|archive-date=28 May 2016}}</ref> | ||
===Litigation=== | ===Litigation=== | ||
As of 2012, Johnson and Johnson was facing around 3400 state and federal lawsuits filed by people who claimed tendon damage from levofloxacin; about 1900 pending in a class action at the United States District Court in Minnesota<ref name="mnd.uscourts.gov">{{Cite web | |
As of 2012, Johnson and Johnson was facing around 3400 state and federal lawsuits filed by people who claimed tendon damage from levofloxacin; about 1900 pending in a class action at the United States District Court in Minnesota<ref name="mnd.uscourts.gov">{{Cite web | vauthors = Tunheim JR |title=Levaquin MDL |url=http://www.mnd.uscourts.gov/MDL-Levaquin/index.shtml |publisher=US Courts |access-date=7 September 2009 |url-status=dead |archive-url=https://web.archive.org/web/20091124200542/http://www.mnd.uscourts.gov/MDL-Levaquin/index.shtml |archive-date=24 November 2009 }}</ref> and about 1500 pending at a district court in New Jersey.<ref>{{Cite web|url=http://www.law.com/jsp/article.jsp?id=1202431984309 |title=Litigation Over Johnson & Johnson Antibiotic Levaquin Designated N.J. Mass Tort | vauthors = Toutant C |publisher=New Jersey Law Journal |date=6 July 2009 }}</ref><ref name=Bloomberg2012>{{cite web | vauthors = Fisk MC, Hawkins B | work = Bloomberg News | date = 1 November 2012 | url = https://www.bloomberg.com/news/2012-11-01/johnson-johnson-reaches-settlement-in-845-levaquin-cases.html | title = Johnson & Johnson Settles 845 Levaquin Lawsuits | archive-url = https://web.archive.org/web/20170308063305/https://www.bloomberg.com/news/2012-11-01/johnson-johnson-reaches-settlement-in-845-levaquin-cases.html/ | archive-date = 8 March 2017 }}</ref> | ||
In October 2012, J&J settled 845 cases in the Minnesota action, after Johnson and Johnson prevailed in three of the first four cases to go to trial. |
In October 2012, J&J settled 845 cases in the Minnesota action, after Johnson and Johnson prevailed in three of the first four cases to go to trial. By May 2014, all but 363 cases had been settled or adjudicated.<ref name=Bloomberg2012/><ref>{{cite web | vauthors = Fisk MC, Hawkins B | date = 1 November 2012 |url=http://www.businessweek.com/news/2012-11-01/johnson-and-johnson-reaches-settlement-in-845-levaquin-cases|title=Johnson & Johnson Settles 845 Levaquin Lawsuits | work = Businessweek |url-status=dead |archive-url= https://web.archive.org/web/20121105073224/http://www.businessweek.com/news/2012-11-01/johnson-and-johnson-reaches-settlement-in-845-levaquin-cases |archive-date=5 November 2012}}</ref><ref>{{cite web |url=http://www.mnd.uscourts.gov/MDL-Levaquin/current-developments.shtml |title=Levaquin MDL | United States District Court – District of Minnesota, United States District Court – District of Minnesota |url-status=dead |archive-url=https://web.archive.org/web/20121026164940/http://www.mnd.uscourts.gov/MDL-Levaquin/current-developments.shtml |archive-date=26 October 2012 }}</ref> | ||
=== Brand names === | |||
⚫ | Levofloxacin is marketed by ] under a license agreement signed with Daiichi in 1993, under the brand name Tavanic.<ref name=DrugFocus2009/> | ||
{{clear}} | {{clear}} | ||
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== References == | == References == | ||
{{Reflist}} | {{Reflist}} | ||
==External links== | |||
* {{cite web | url = https://druginfo.nlm.nih.gov/drugportal/name/Levofloxacin | publisher = U.S. National Library of Medicine | work = Drug Information Portal | title = Levofloxacin }} | |||
{{QuinoloneAntiBiotics}} | {{QuinoloneAntiBiotics}} | ||
{{GABAergics}} | {{GABAergics}} | ||
{{Portal bar|Medicine}} | {{Portal bar | Medicine}} | ||
{{Authority control}} | |||
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Latest revision as of 07:27, 6 December 2024
AntibioticPharmaceutical compound
Clinical data | |
---|---|
Trade names | Levaquin, others |
AHFS/Drugs.com | Monograph |
MedlinePlus | a697040 |
License data |
|
Routes of administration | By mouth, intravenous (IV), eye drops |
Drug class | Fluoroquinolone |
ATC code | |
Legal status | |
Legal status | |
Pharmacokinetic data | |
Bioavailability | 99% |
Protein binding | 31% |
Metabolism | <5% desmethyl and N-oxide metabolites |
Elimination half-life | 6.9 hours |
Excretion | Kidney, mostly unchanged (83%) |
Identifiers | |
IUPAC name
| |
CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
NIAID ChemDB | |
PDB ligand | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.115.581 |
Chemical and physical data | |
Formula | C18H20FN3O4 |
Molar mass | 361.373 g·mol |
3D model (JSmol) | |
Density | 1.5±0.1 g/cm |
SMILES
| |
InChI
| |
(what is this?) (verify) |
Levofloxacin, sold under the brand name Levaquin among others, is a broad-spectrum antibiotic of the fluoroquinolone drug class. It is the left-handed isomer of the medication ofloxacin. It is used to treat a number of bacterial infections including acute bacterial sinusitis, pneumonia, H. pylori (in combination with other medications), urinary tract infections, Legionnaires' disease, chronic bacterial prostatitis, and some types of gastroenteritis. Along with other antibiotics it may be used to treat tuberculosis, meningitis, or pelvic inflammatory disease. It is available by mouth, intravenously, and in eye drop form.
Common side effects include nausea, diarrhea, and trouble sleeping. A warning concerning all fluoroquinolones was issued in 2016: "An FDA safety review has shown that fluoroquinolones when used systemically (i.e. tablets, capsules, and injectable) are associated with disabling and potentially permanent serious adverse effects that can occur together. These adverse effects can involve the tendons, muscles, joints, nerves, and central nervous system."
Other serious side effects may include tendon rupture, tendon inflammation, seizures, psychosis, and potentially permanent peripheral nerve damage. Tendon damage may appear months after treatment is completed. People may also sunburn more easily. In people with myasthenia gravis, muscle weakness and breathing problems may worsen. While use during pregnancy is not recommended, risk appears to be low. The use of other medications in this class appear to be safe while breastfeeding; however, the safety of levofloxacin is unclear.
Levofloxacin was patented in 1985 and approved for medical use in the United States in 1996. It is on the World Health Organization's List of Essential Medicines. It is available as a generic medication. In 2022, it was the 251st most commonly prescribed medication in the United States, with more than 1 million prescriptions.
Medical uses
Levofloxacin is used to treat infections including: respiratory tract infections, cellulitis, urinary tract infections, prostatitis, anthrax, endocarditis, meningitis, pelvic inflammatory disease, traveler's diarrhea, tuberculosis, and plague and is available by mouth, intravenously, and in eye drop form.
As of 2016, the US Food and Drug Administration (FDA) recommended that "serious side effects associated with fluoroquinolone antibacterial drugs generally outweigh the benefits for patients with acute sinusitis, acute bronchitis, and uncomplicated urinary tract infections who have other treatment options. For patients with these conditions, fluoroquinolones should be reserved for those who do not have alternative treatment options."
Levofloxacin is used for the treatment of pneumonia, urinary tract infections, and abdominal infections. As of 2007 the Infectious Disease Society of America (IDSA) and the American Thoracic Society recommended levofloxacin and other respiratory fluoroquinolines as first line treatment for community acquired pneumonia when co-morbidities such as heart, lung, or liver disease are present or when in-patient treatment is required. Levofloxacin also plays an important role in recommended treatment regimens for ventilator-associated and healthcare-associated pneumonia.
As of 2010 it was recommended by the IDSA as a first-line treatment option for catheter-associated urinary tract infections in adults. In combination with metronidazole it is recommended as one of several first-line treatment options for adult patients with community-acquired intra-abdominal infections of mild-to-moderate severity. The IDSA also recommends it in combination with rifampicin as a first-line treatment for prosthetic joint infections. The American Urological Association recommends levofloxacin as a first-line treatment to prevent bacterial prostatitis when the prostate is biopsied. and as of 2004 it was recommended to treat bacterial prostatitis by the NIH research network studying the condition.
Levofloxacin and other fluoroquinolones have also been widely used for the treatment of uncomplicated community-acquired respiratory and urinary tract infections, indications for which major medical societies generally recommend the use of older, narrower spectrum drugs to avoid fluoroquinolone resistance development. Due to its widespread use, common pathogens such as Escherichia coli and Klebsiella pneumoniae have developed resistance. In many countries as of 2013, resistance rates among healthcare-associated infections with these pathogens exceeded 20%.
Levofloxacin is also used as antibiotic eye drops to prevent bacterial infection. Usage of levofloxacin eye drops, along with an antibiotic injection of cefuroxime or penicillin during cataract surgery, has been found to lower the chance of developing endophthalmitis, compared to eye drops or injections alone.
Pregnancy and breastfeeding
According to the FDA approved prescribing information, levofloxacin is pregnancy category C. This designation indicates that animal reproduction studies have shown adverse effects on the fetus and there are no adequate and well-controlled studies in humans, but the potential benefit to the mother may in some cases outweigh the risk to the fetus. Available data point to a low risk for the unborn child. Exposure to quinolones, including levofloxacin, during the first-trimester is not associated with an increased risk of stillbirths, premature births, birth defects, or low birth weight.
Levofloxacin does penetrate into breastmilk, though the concentration of levofloxacin in the breastfeeding infant is expected to be low. Due to potential risks to the baby, the manufacturer does not recommend that nursing mothers take levofloxacin. However, the risk appears to be very low, and levofloxacin can be used in breastfeeding mothers with proper monitoring of the infant, combined with delaying breastfeeding for 4–6 hours after taking levofloxacin.
Children
Levofloxacin is not approved in most countries for the treatment of children except in unique and life-threatening infections because it is associated with an elevated risk of musculoskeletal injury in this population, a property it shares with other fluoroquinolones.
In the United States levofloxacin is approved for the treatment of anthrax and plague in children over six months of age.
Levofloxacin is recommended by the Pediatric Infectious Disease Society and the Infectious Disease Society of America as a first-line treatment for pediatric pneumonia caused by penicillin-resistant Streptococcus pneumoniae, and as a second-line agent for the treatment of penicillin-sensitive cases.
In one study, 1534 juvenile patients (age 6 months to 16 years) treated with levofloxacin as part of three efficacy trials were followed up to assess all musculoskeletal events occurring up to 12 months post-treatment. At 12 months follow-up the cumulative incidence of musculoskeletal adverse events was 3.4%, compared to 1.8% among 893 patients treated with other antibiotics. In the levafloxacin-treated group, approximately two-thirds of these musculoskeletal adverse events occurred in the first 60 days, 86% were mild, 17% were moderate, and all resolved without long-term sequelae.
Spectrum of activity
Levofloxacin and later generation fluoroquinolones are collectively referred to as "respiratory quinolones" to distinguish them from earlier fluoroquinolones which exhibited modest activity toward the important respiratory pathogen Streptococcus pneumoniae.
The drug exhibits enhanced activity against the important respiratory pathogen Streptococcus pneumoniae relative to earlier fluoroquinolone derivatives like ciprofloxacin. For this reason, it is considered a "respiratory fluoroquinolone" along with more recently developed fluoroquinolones such as moxifloxacin and gemifloxacin. It is less active than ciprofloxacin against Gram-negative bacteria, especially Pseudomonas aeruginosa, and lacks the anti-methicillin-resistant Staphylococcus aureus (MRSA) activity of moxifloxacin and gemifloxacin. Levofloxacin has shown moderate activity against anaerobes, and is about twice as potent as ofloxacin against Mycobacterium tuberculosis and other mycobacteria, including Mycobacterium avium complex.
Its spectrum of activity includes most strains of bacterial pathogens responsible for respiratory, urinary tract, gastrointestinal, and abdominal infections, including Gram negative (Escherichia coli, Haemophilus influenzae, Klebsiella pneumoniae, Legionella pneumophila, Moraxella catarrhalis, Proteus mirabilis, and Pseudomonas aeruginosa), Gram positive (methicillin-sensitive but not methicillin-resistant Staphylococcus aureus, Streptococcus pneumoniae, Staphylococcus epidermidis, Enterococcus faecalis, and Streptococcus pyogenes), and atypical bacterial pathogens (Chlamydophila pneumoniae and Mycoplasma pneumoniae). Compared to earlier antibiotics of the fluoroquinoline class such as ciprofloxacin, levofloxacin exhibits greater activity towards Gram-positive bacteria but lesser activity toward Gram-negative bacteria, especially Pseudomonas aeruginosa.
Resistance
Resistance to fluoroquinolones is common in staphylococcus and pseudomonas. Resistance occurs in multiple ways. One mechanism is by an alteration in topoisomerase IV enzyme. A double mutant form of S. pneumoniae Gyr A + Par C bearing Ser-81-->Phe and Ser-79-->Phe mutations were eight to sixteen times less responsive to ciprofloxacin.
Contraindications and interactions
Package inserts mention that levofloxacin is to be avoided in patients with a known hypersensitivity to levofloxacin or other quinolone drugs.
Like all fluoroquinolines, levofloxacin is contraindicated in patients with epilepsy or other seizure disorders, and in patients who have a history of quinolone-associated tendon rupture.
Levofloxacin may prolong the QT interval in some people, especially the elderly, and levofloxacin should not be used for people with a family history of Long QT syndrome, or who have long QT, chronic low potassium, it should not be prescribed with other drugs that prolong the QT interval.
Unlike ciprofloxacin, levofloxacin does not appear to deactivate the drug metabolizing enzyme CYP1A2. Therefore, drugs that use that enzyme, like theophylline, do not interact with levofloxacin. It is a weak inhibitor of CYP2C9, suggesting potential to block the breakdown of warfarin and phenprocoumon. This can result in more action of drugs like warfarin, leading to more potential side effects, such as bleeding.
The use of non-steroidal anti-inflammatory drugs (NSAIDs) in combination with high dose fluoroquinolone therapy may lead to seizures.
When levofloxacin is taken with anti-acids containing magnesium hydroxide or aluminum hydroxide, the two combine to form insoluble salts that are difficult to absorb from the intestines. Peak serum concentrations of levofloxacin may be reduced by 90% or more, which can prevent the levofloxacin from working. Similar results have been reported when levofloxacin is taken with iron supplements and multi-vitamins containing zinc.
A 2011 review examining musculoskeletal complications of fluoroquinolones proposed guidelines with respect to administration to athletes, that called for avoiding all use of fluoroquinolone antibiotics if possible, and if they are used: ensure there is informed consent about the musculoskeletal risks, and inform coaching staff; do not use any corticosteroids if fluoroquinolones are used; consider dietary supplements of magnesium and antioxidants during treatment; reduce training until the course of antibiotic is finished and then carefully increase back to normal; and monitor for six months after the course is finished, and stop all athletic activity if symptoms emerge.
Adverse effects
Adverse effects are typically mild to moderate. However, severe, disabling, and potentially irreversible adverse effects sometimes occur, and for this reason it is recommended that use of fluoroquinolones be limited.
Prominent among these are adverse effects that became the subject of a black box warning by the FDA in 2016. The FDA wrote: "An FDA safety review has shown that fluoroquinolones when used systemically (i.e. tablets, capsules, and injectable) are associated with disabling and potentially permanent serious adverse effects that can occur together. These adverse effects can involve the tendons, muscles, joints, nerves, and central nervous system." Rarely, tendinitis or tendon rupture may occur due to fluoroquinolone antibiotics, including levofloxacin. Such injuries, including tendon rupture, has been observed up to six months after cessation of treatment; higher doses of fluoroquinolones, being elderly, transplant patients, and those with a current or historical corticosteroid use are at elevated risk. The U.S. label for levofloxacin also contains a black box warning for the exacerbation of the symptoms of the neurological disease myasthenia gravis. Similarly, the UK Medicines and Healthcare Products Regulatory Agency recommendations warn of rare but disabling and potentially irreversible adverse effects, and to recommend limiting use of these drugs. Increasing age and corticosteroid use appears to increase the risk of musculoskeletal complications.
A wide variety of other uncommon but serious adverse events have been associated with fluoroquinolone use, with varying degrees of evidence supporting causation. These include anaphylaxis, hepatotoxicity, central nervous system effects including seizures and psychiatric effects, prolongation of the QT interval, blood glucose disturbances, and photosensitivity, among others. Levofloxacin may produce fewer of these rare serious adverse effects than other fluoroquinolones.
There is some disagreement in the medical literature regarding whether and to what extent levofloxacin and other fluoroquinolones produce serious adverse effects more frequently than other broad spectrum antibacterial drugs.
Concerning more usual adverse effects, in pooled results from 7537 patients exposed to levofloxacin in 29 clinical trials, 4.3% discontinued treatment due to adverse drug reactions. The most common adverse reactions leading to discontinuation were gastrointestinal, including nausea, vomiting, and constipation. Overall, 7% of patients experienced nausea, 6% headache, 5% diarrhea, and 4% insomnia, along with other adverse reactions experienced at lower rates.
Administration of levofloxacin or other broad-spectrum antibiotics is associated with Clostridioides difficile associated diarrhea which may range in severity from mild diarrhea to fatal colitis. Fluoroquinolone administration may be associated with the acquisition and outgrowth of a particularly virulent Clostridioides strain.
More research is needed to determine the best dose and length of treatment.
Overdose
Overdosing experiments in animals showed loss of body control and drooping, difficulty breathing, tremors, and convulsions. Doses in excess of 1500 mg/kg orally and 250 mg/kg IV produced significant mortality in rodents.
In the event of an acute overdosage, authorities recommend unspecific standard procedures such as emptying the stomach, observing the patient and maintaining appropriate hydration. Levofloxacin is not efficiently removed by hemodialysis or peritoneal dialysis.
Pharmacology
Mechanism of action
Levofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. Like all quinolones, it functions by inhibiting the DNA gyrase and topoisomerase IV, two bacterial type IIA topoisomerases. Topoisomerase IV is necessary to separate DNA that has been replicated (doubled) prior to bacterial cell division. With the DNA not being separated, the process is stopped, and the bacterium cannot divide. DNA gyrase, on the other hand, is responsible for supercoiling the DNA, so that it will fit in the newly formed cells. Both mechanisms amount to killing the bacterium. Levofloxacin acts as a bactericide.
As of 2011, the mechanism of action for the drug's musculoskeletal complications were not clear.
Pharmacokinetics
Levofloxacin is rapidly and essentially completely absorbed after oral administration, with a plasma concentration profile over time that is essentially identical to that obtained from intravenous administration of the same amount over 60 minutes. As such, the intravenous and oral formulations of levofloxacin are considered interchangeable. Levofloxacin's ability to bind to proteins in the body ranges from 24 to 38%.
The drug undergoes widespread distribution into body tissues. Peak levels in skin are achieved 3 hours after administration and exceed those in plasma by a factor of 2. Similarly, lung tissue concentrations range from two-fold to five-fold higher than plasma concentrations in the 24 hours after a single dose.
The mean terminal plasma elimination half-life of levofloxacin ranges from approximately 6 to 8 hours following single or multiple doses of levofloxacin given orally or intravenously. Elimination occurs mainly via excretion of unmetabolized drug in the urine. Following oral administration, 87% of an administered dose was recovered in the urine as unchanged drug within 2 days. Less than 5% was recovered in the urine as the desmethyl and N-oxide metabolites, the only metabolites identified in humans.
Chemistry
Like all fluoroquinolones, levofloxacin is a fluorinated quinolone carboxylic acid. It is a chiral molecule and the pure (−)-(S)-enantiomer of the racemic drug ofloxacin. This enantiomer binds more effectively to the DNA gyrase enzyme and to topoisomerase IV than its (+)-(R)-counterpart. Levofloxacin is referred to as a chiral switch: These are chiral drugs that have already been patent claimed, approved and marketed as racemates (or as mixtures of diastereomers but have since been redeveloped as pure enantiomers. Distinct functional groups on this molecules include a hydroxyl group, carbonyl group, and an aromatic ring.
The substance is used as the hemihydrate, which has the empirical formula C18H20FN3O4 · 1⁄2 H2O and a molecular mass of 370.38 g/mol. Levofloxacin is a light-yellowish-white to yellow-white crystal or crystalline powder. A major issue in the synthesis of levofloxacin is identifying correct entries into the benzoxazine core in order to produce the correct chiral form.
History
Levofloxacin is a third-generation fluoroquinolone, being one of the isomers of ofloxacin, which was a broader-spectrum conformationally locked analog of norfloxacin; both ofloxacin and levofloxaxin were synthesized and developed by scientists at Daiichi Seiyaku. The Daiichi scientists knew that ofloxacin was racemic, but tried unsuccessfully to separate the two isomers; in 1985 they succeeded in separately synthesizing the pure levo form and showed that it was less toxic and more potent than the other form.
It was first approved for marketing in Japan in 1993, for oral administration, and Daiichi marketed it there under the brand name Cravit. Daiichi, working with Johnson & Johnson as it had with ofloxacin, obtained FDA approval in 1996 under the brand name Levaquin to treat bacterial sinusitus, bacterial exacerbations of bronchitis, community-acquired pneumonia, uncomplicated skin infections, complicated urinary tract infections, and acute pyelonephritis.
Society and culture
Economics
Levofloxacin had reached blockbuster status by this time; combined worldwide sales of levofloxacin and ofloxacin for J&J alone were US$1.6 billion in 2009.
The term of the levofloxacin United States patent was extended by the U.S. Patent and Trademark Office 810 days under the provisions of the Hatch Waxman Amendment so that the patent would expire in 2010 instead of 2008. This extension was challenged by generic drug manufacturer Lupin Pharmaceuticals, which did not challenge the validity of the patent, but only the validity of the patent extension, arguing that the patent did not cover a "product" and so Hatch-Waxman was not available for extensions. The federal patent court ruled in favor of J&J and Daiichi, and generic versions of levofloxacin did not enter the U.S. market until 2009.
Availability
Levofloxacin is available in tablet form, injection, and oral solution.
Usage
The US Food and Drug Administration estimated that in 2011, over 23 million outpatient prescriptions for fluoroquinolones, of which levofloxacin made up 28%, were filled in the United States.
Litigation
As of 2012, Johnson and Johnson was facing around 3400 state and federal lawsuits filed by people who claimed tendon damage from levofloxacin; about 1900 pending in a class action at the United States District Court in Minnesota and about 1500 pending at a district court in New Jersey.
In October 2012, J&J settled 845 cases in the Minnesota action, after Johnson and Johnson prevailed in three of the first four cases to go to trial. By May 2014, all but 363 cases had been settled or adjudicated.
Brand names
Levofloxacin is marketed by Sanofi-Aventis under a license agreement signed with Daiichi in 1993, under the brand name Tavanic.
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- Enantiopure drugs
- Fluoroquinolone antibiotics
- GABAA receptor negative allosteric modulators
- Janssen Pharmaceutica
- Japanese inventions
- Drugs developed by Johnson & Johnson
- Nitrogen heterocycles
- Oxygen heterocycles
- 1,4-di-hydro-7-(1-piperazinyl)-4-oxo-3-quinolinecarboxylic acids
- Sanofi
- World Health Organization essential medicines
- 4-Methylpiperazin-1-yl compounds