Benzylpenicillin

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Benzylpenicillin
Benzylpenicillin.svg
Benzylpenicillin-3D-balls.png
Clinical data
Trade names Pfizerpen, other
AHFS/Drugs.com International Drug Names
MedlinePlus a685013
Pregnancy
category
  • AU: A
  • US: B (No risk in non-human studies)
Routes of
administration
IV, IM
ATC code J01CE01 (WHO) S01AA14 (WHO) QJ51CE01 (WHO)
Legal status
Legal status
  • ℞ (Prescription only)
Pharmacokinetic data
Protein binding 60 %
Metabolism Liver
Biological half-life 30 min
Excretion Kidney
Identifiers
Synonyms penicillin G potassium,[1] penicillin G sodium
CAS Number 61-33-6 YesY (free acid)
69-57-8 (sodium salt)
PubChem (CID) 5904
IUPHAR/BPS 4796
DrugBank DB01053 YesY
ChemSpider 5693 YesY
UNII Q42T66VG0C YesY
KEGG D02336 N
ChEBI CHEBI:18208 N
ChEMBL CHEMBL29 N
E number E705 (antibiotics)
ECHA InfoCard 100.000.461
Chemical and physical data
Formula C16H18N2O4S
Molar mass 334.4 g/mol
3D model (Jmol) Interactive image
 NYesY (what is this?)  (verify)

Benzylpenicillin, also known as penicillin G, is an antibiotic used to treat a number of bacterial infections. This includes pneumonia, strep throat, syphilis, necrotizing enterocolitis, diphtheria, gas gangrene, leptospirosis, cellulitis, and tetanus. It is not a first-line agent for pneumococcal meningitis.[2] Benzylpenicillin is given by injection into a vein or muscle.[1] Two long acting forms benzathine benzylpenicillin and procaine benzylpenicillin are available for use by injection into a muscle.[2]

Side effects include diarrhea, seizures, and allergic reactions including anaphylaxis. When used to treat syphilis a reaction known as Jarisch–Herxheimer may occur. It is not recommended in those with a history of penicillin allergy.[2] Use during pregnancy is generally safe.[1] It is in the penicillin and β-lactam class of medications.[2]

Benzylpenicillin was discovered in 1929 and came into commercial use in 1942.[3] It is on the World Health Organization's List of Essential Medicines, the most effective and safe medicines needed in a health system.[4] The wholesale cost in the developing world is about 0.24 to 2.72 USD per day.[5] In the United States a course of treatment costs 100 to 200 USD.[6]

Medical uses[edit]

Antimicrobial potency[edit]

As an antibiotic, penicillin G is noted to possess effectiveness mainly against Gram-positive organisms. Some Gram-negative organisms such as Neisseria gonorrhoeae and Neisseria meningitidis are also reported to be susceptible to Penicillin G.[7]

Adverse effects[edit]

Adverse effects can include hypersensitivity reactions including urticaria, fever, joint pains, rashes, angioedema, anaphylaxis, serum sickness-like reaction. Rarely CNS toxicity including convulsions (especially with high doses or in severe renal impairment), interstitial nephritis, haemolytic anaemia, leucopenia, thrombocytopenia, and coagulation disorders. Also reported diarrhoea (including antibiotic-associated colitis).

Benzylpenicillin serum concentrations can be monitored either by traditional microbiological assay or by more modern chromatographic techniques. Such measurements can be useful to avoid central nervous system toxicity in any person receiving large doses of the drug on a chronic basis, but they are especially relevant to patients with renal failure, who may accumulate the drug due to reduced urinary excretion rates.[8][9]

References[edit]

  1. ^ a b c "Penicillin G Injection - FDA prescribing information, side effects and uses". www.drugs.com. Retrieved 10 December 2016. 
  2. ^ a b c d WHO Model Formulary 2008 (PDF). World Health Organization. 2009. pp. 98, 105. ISBN 9789241547659. Retrieved 8 December 2016. 
  3. ^ Fischer, Janos; Ganellin, C. Robin (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 490. ISBN 9783527607495. 
  4. ^ "WHO Model List of Essential Medicines (19th List)" (PDF). World Health Organization. April 2015. Retrieved 8 December 2016. 
  5. ^ "Penicillin, Benzyl". International Drug Price Indicator Guide. Retrieved 8 December 2016. 
  6. ^ Hamilton, Richart (2015). Tarascon Pocket Pharmacopoeia 2015 Deluxe Lab-Coat Edition. Jones & Bartlett Learning. p. 95. ISBN 9781284057560. 
  7. ^ "Penicillin G" (pdf). Toku-E. 2010-10-10. Retrieved 2012-06-11. 
  8. ^ Fossieck B Jr, Parker RH. Neurotoxicity during intravenous infusion of penicillin. A review. J. Clin. Pharmacol. 14: 504- 512, 1974.
  9. ^ R. Baselt, Disposition of Toxic Drugs and Chemicals in Man, 8th edition, Biomedical Publications, Foster City, CA, 2008, pp. 1195-1196.