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Contents

   



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1 Medical uses  





2 Adverse effects  





3 History  





4 References  














Rifabutin






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Rifabutin

Clinical data

Trade names

Mycobutin[1]

AHFS/Drugs.com

Monograph

MedlinePlus

a693009

Pregnancy
category

  • AU:C
  • Routes of
    administration

    By mouth

    ATC code

    Legal status

    Legal status

  • UK: POM (Prescription only)
  • US: ℞-only
  • Pharmacokinetic data

    Bioavailability

    85%

    Protein binding

    85%

    Metabolism

    Liver

    Elimination half-life

    28 to 62 hours (mean)

    Excretion

    Kidney and fecal

    Identifiers

    • (9S,12E,14S,15R,16S,17R,18R,19R,20S,
      21S,22E,24Z)-6,16,18,20-tetrahydroxy-1'-
      isobutyl-14-methoxy-7,9,15,17,19,21,25-
      hepta-methyl-spiro[9,4-(epoxypentadeca
      [1,11,13]trienimino)-2H-furo-[2',3':7,8]-naphth
      [1,2-d]imidazol-2,4'-piperidin]-5,10,26-(3H,9H)-
      trione-16-acetate

    CAS Number

    PubChem CID

    DrugBank

    ChemSpider

    UNII

    KEGG

    ChEBI

    ChEMBL

    CompTox Dashboard (EPA)

    ECHA InfoCard

    100.133.627 Edit this at Wikidata

    Chemical and physical data

    Formula

    C46H62N4O11

    Molar mass

    847.019 g·mol−1

    3D model (JSmol)

    • C[C@H]1/C=C\C=C(/C(=O)NC2=C3C(=NC4(N3)CCN(CC4)CC(C)C)C5=C6C(=C(C(=C5C2=O)O)C)O[C@@](C6=O)(O/C=C\[C@@H]([C@H]([C@H]([C@@H]([C@@H]([C@@H]([C@H]1O)C)O)C)OC(=O)C)C)OC)C)\C

    • InChI=1S/C46H62N4O11/c1-22(2)21-50-18-16-46(17-19-50)48-34-31-32-39(54)28(8)42-33(31)43(56)45(10,61-42)59-20-15-30(58-11)25(5)41(60-29(9)51)27(7)38(53)26(6)37(52)23(3)13-12-14-24(4)44(57)47-36(40(32)55)35(34)49-46/h12-15,20,22-23,25-27,30,37-38,41,49,52-54H,16-19,21H2,1-11H3,(H,47,57)/b13-12+,20-15+,24-14-/t23-,25+,26+,27+,30-,37-,38+,41+,45-/m0/s1 checkY

  • Key:ATEBXHFBFRCZMA-VXTBVIBXSA-N checkY

  •   (verify)

    Rifabutin (Rfb) is an antibiotic used to treat tuberculosis and prevent and treat Mycobacterium avium complex.[1] It is typically only used in those who cannot tolerate rifampin such as people with HIV/AIDSonantiretrovirals.[1] For active tuberculosis it is used with other antimycobacterial medications.[1] For latent tuberculosis it may be used by itself when the exposure was with drug-resistant TB.[1]

    Rifabutin was approved for medical use in the United States in 1992.[1] It is on the World Health Organization's List of Essential Medicines.[3]

    Medical uses[edit]

    Rifabutin is now recommended as first-line treatment for tuberculosis (TB),[4] but rifampicin was used more widely because of its cheaper cost. However, due to the expiration of patents, prices are now similar.

    Adverse effects[edit]

    Common side effects include abdominal pain, nausea, rash, headache, and low blood neutrophil levels.[1] Other side effects include muscles pains and uveitis.,[1] especially when hitting Bartonella and Babesia colonies in the capillaries of the ciliary body in the eye anterior chamber. While no harms have been found during pregnancy it has not been well studied in this population.[1] Rifabutin is in the rifamycin family of medications.[1] It works by blocking RNA production in bacteria.[5]

    History[edit]

    Scientists at the Italian drug company Achifar discovered rifabutin in 1975. (Eventually Archifar became part of Farmitalia Carlo Erba, a unit of the conglomerate Montedison which was subsequently bought by Pharmacia) This company's Adria Laboratories subsidiary filed for Food and Drug Administration (FDA) approval of rifabutin under the brand name Mycobutin in the early 1990s and the drug gained FDA approval in December 1992.[citation needed]

    Rifabutin is primarily bactericidal antibiotic drug used to treat tuberculosis. Its effect on bacteria is based on the DNA-dependent RNA polymerase blocking drug rifamycin S, a semi-synthetic derivative. It is effective, for example, in highly resistant mycobacteria, Gram-positive bacteria (and some are effective against Gram-negative bacteria), but also against Mycobacterium tuberculosis, M. leprae, and M. avium intracellulare.[citation needed]

    References[edit]

    1. ^ a b c d e f g h i j "Rifabutin". The American Society of Health-System Pharmacists. Archived from the original on 20 December 2016. Retrieved 8 December 2016.
  • ^ "Product monograph brand safety updates". Health Canada. February 2024. Retrieved 24 March 2024.
  • ^ 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.
  • ^ Guidelines for the programmatic management of drug-resistant tuberculosis: emergency update 2008 (WHO/HTM/TB/2008.402). Geneva, Switzerland: World Health Organization. 2008. p. ix. ISBN 978-92-4-154758-1. Archived from the original on 2008-10-18.
  • ^ Rockwood N, Cerrone M, Barber M, Hill AM, Pozniak AL (July 2019). "Global access of rifabutin for the treatment of tuberculosis - why should we prioritize this?". Journal of the International AIDS Society. 22 (7): e25333. doi:10.1002/jia2.25333. PMC 6637439. PMID 31318176. Rifabutin is a rifamycin, which like rifampicin, works via inhibition of DNA‐dependent RNA synthesis in prokaryotes.
  • Nucleic acid inhibitor

    Rifamycins/
    RNA polymerase inhibitor

  • Rifabutin
  • Rifapentine
  • Rifalazil§
  • Antifolates/DSI

  • Acedapsone
  • Diucifon
  • Promin
  • Solasulfone
  • Sulfoxone
  • ASA

  • Sodium aminosalicylate)
  • Topoisomerase inhibitors/
    quinolones

  • Moxifloxacin
  • Protein synthesis inhibitor

    Aminoglycosides

  • Kanamycin
  • Streptomycin#
  • Oxazolidone

  • Sutezolid
  • Polypeptide antibiotics

    Cell envelope antibiotic

    Peptidoglycan layer

    Arabinogalactan layer

    Mycolic acid layer

  • Methaniazide
  • Other/unknown

  • Pyrazine (Pyrazinamide#, Morinamide)
  • Isoxazole (Terizidone)
  • Bedaquiline
  • Nitroimidazole (Delamanid, Pretomanid)
  • Combinations

  • Ethambutol/isoniazid/pyrazinamide/rifampicin#
  • Ethambutol/isoniazid/rifampicin#
  • Isoniazid/pyridoxine/sulfamethoxazole/trimethoprim#
  • Rifampicin/isoniazid/pyrazinamide
  • Withdrawn from market
  • Clinical trials:
  • §Never to phase III
  • Antifolates
    (inhibit bacterial
    purine metabolism,
    thereby inhibiting
    DNA and RNA
    synthesis)

    DHFR inhibitor

  • Iclaprim
  • Ormetoprim
  • Pyrimethamine#
  • Tetroxoprim
  • Trimethoprim#
  • Sulfonamides
    (DHPS inhibitor)

    Short-acting

  • Sulfamethizole
  • Sulfadimidine
  • Sulfapyridine (Sulfasalazine)
  • Sulfafurazole (Acetyl sulfisoxazole)
  • Sulfanilamide
  • Sulfathiazole (Phthalylsulfathiazole, Succinylsulfathiazole)
  • Sulfathiourea
  • Intermediate-acting

  • Sulfadiazine#
  • Sulfamoxole
  • Long-acting

  • Sulfadoxine
  • Sulfalene
  • Sulfametomidine
  • Sulfametoxydiazine
  • Sulfamethoxypyridazine
  • Sulfaperin
  • Sulfamerazine
  • Sulfaphenazole
  • Sulfamazone
  • Other/ungrouped

  • Sulfacetamide
  • Sulfaclozine
  • Sulfadicramide
  • Sulfaguanidine
  • Sulfametrole
  • Sulfanitran
  • Combinations

  • Ormetoprim/sulfadimethoxine
  • Pyrimethamine/dapsone
  • Pyrimethamine/sulfadoxine
  • Other DHPS inhibitors

  • Dapsone
  • Solasulfone
  • Sulfoxone
  • Quinolones
    (inhibit bacterial
    topoisomerase
    and/or DNA gyrase,
    thereby inhibiting
    DNA replication)

    1st generation

  • Flumequine
  • Nalidixic acid
  • Oxolinic acid
  • Pipemidic acid
  • Piromidic acid
  • Rosoxacin
  • Fluoroquinolones

    2nd generation

  • Ofloxacin
  • Enoxacin
  • Fleroxacin
  • Lomefloxacin
  • Nadifloxacin/Levonadifloxacin/Alalevonadifloxacin
  • Norfloxacin
  • Pefloxacin
  • Rufloxacin
  • 3rd generation

  • Balofloxacin
  • Grepafloxacin
  • Pazufloxacin
  • Sparfloxacin
  • Temafloxacin
  • Tosufloxacin
  • 4th generation

  • Delafloxacin
  • Gatifloxacin
  • Finafloxacin
  • Gemifloxacin
  • Moxifloxacin#
  • Clinafloxacin
  • Garenoxacin
  • Prulifloxacin
  • Sitafloxacin
  • Trovafloxacin/Alatrofloxacin
  • Veterinary

  • Difloxacin
  • Enrofloxacin
  • Ibafloxacin
  • Marbofloxacin
  • Orbifloxacin
  • Pradofloxacin
  • Sarafloxacin
  • Newer non-fluorinated

  • Ozenoxacin
  • Related (DG)

    Anaerobic DNA
    inhibitors

    Nitroimidazole derivatives

    RNA synthesis

    Rifamycins/
    RNA polymerase

  • Rifabutin#
  • Rifapentine#
  • Rifaximin
  • Rifalazil§
  • Lipiarmycins

  • Withdrawn from market
  • Clinical trials:
  • §Never to phase III

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Rifabutin&oldid=1225248355"

    Categories: 
    Rifamycin antibiotics
    CYP3A4 inducers
    World Health Organization essential medicines
    Anti-tuberculosis drugs
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