Cefdinir Explained

Cefdinir, sold under the brand name Omnicef among others, is an antibiotic used to treat pneumonia, otitis media, strep throat, and cellulitis. It is a less preferred option for pneumonia, otitis media, and strep throat which may be used in those with a severe allergy to penicillin. It is taken by mouth.[1]

Common side effects include diarrhea, nausea, and a skin rash.[1] Serious side effects may include Clostridioides difficile infection, anaphylaxis, and Stevens–Johnson syndrome.[1] Use in pregnancy and breastfeeding is believed to be safe but has not been well studied.[2] It is a third-generation cephalosporin and works by interfering with a bacteria's ability to make a cell wall resulting in its death.[1]

It was patented in 1979 and approved for medical use in 1991.[3] It is available as a generic medication.[1] In 2021, it was the 197th most commonly prescribed medication in the United States, with more than 2million prescriptions.[4] [5]

Medical uses

Therapeutic uses of cefdinir include otitis media, soft tissue infections, and respiratory tract infections, including sinusitis, strep throat (note: no documented resistance of Group A Streptococcus to penicillin has ever been reported, and penicillin or amoxicillin is preferred except in penicillin allergic patients), community-acquired pneumonia, and acute exacerbations of bronchitis.

Susceptible organisms

Cefdinir is a bactericidal antibiotic of the cephalosporin class of antibiotics. It can be used to treat infections caused by several Gram-negative and Gram-positive bacteria.

Bacterial susceptibility and resistance

Cefdinir is a broad-spectrum antibiotic and has been used to treat infections of the respiratory tract including pneumonia, sinusitis, and bronchitis. The following represents MIC susceptibility data for a few medically significant microorganisms.[6]

Side effects

Side effects include diarrhea, vaginal infections or inflammation, nausea, headache, and abdominal pain."[7]

It is also one of the medications that can cause toxic epidermal necrolysis or Stevens–Johnson syndrome.[8]

The pediatric version of cefdinir can bind to iron in the digestive tract; in rare cases, this causes a rust or red discoloration of the stool. Blood typically appears dark brown or black in stool, and testing may confirm which is present. If the reddish stool is accompanied by abdominal pain, weight loss, diarrhea, etc., a Clostridioides difficile infection caused by the antibiotic could be signified.

Mechanism of action

See main article: Cephalosporin.

Synthesis

Acylation at the primary amine of the cephalosporin intermediate (1) with 4-bromo-3-oxobutanoyl bromide (2) gives the amide (3). The active methylene group in that compound is then nitrosated with sodium nitrite; the initial product spontaneously tautomerizes to afford the oxime (4). The bromoketone functional group reacts with thiourea in the penultimate step, forming the thiazole ring of cefdinir, which is the product after removal of the benzhydryl ester protecting group with trifluoroacetic acid.[9] [10] [11]

Society and culture

Economics

As of 2008, cefdinir was the highest-selling cephalosporin antibiotic in the United States, with more than $585 million in retail sales of its generic versions.[12]

Available forms

Cefdinir is administered orally. It is available as capsules and a suspension. Dosage, schedule, and duration of therapy varies according to the type of infection.

Warner-Lambert licensed the drug for marketing in US from Fujisawa.[13] Abbott obtained U.S. marketing rights to cefdinir in December 1998 through an agreement with Warner-Lambert Company.[14] It was approved by the FDA on 4 December 1997.[15] It is available in US as Omnicef by Abbott Laboratories and in India as Cednir by Abbott, Kefnir by Glenmark, Cefdair by Xalra Pharma and Cefdiel by Ranbaxy.

Notes and References

  1. Web site: Cefdinir Monograph for Professionals . Drugs.com . American Society of Health-System Pharmacists . 23 March 2019 . en.
  2. Web site: Cefdinir Use During Pregnancy . Drugs.com . 3 March 2019 . en.
  3. Book: Fischer J, Ganellin CR . Analogue-based Drug Discovery . 2006 . John Wiley & Sons . 9783527607495 . 49X . en.
  4. Web site: The Top 300 of 2021 . ClinCalc . 14 January 2024 . 15 January 2024 . https://web.archive.org/web/20240115223848/https://clincalc.com/DrugStats/Top300Drugs.aspx . live .
  5. Web site: Cefdinir - Drug Usage Statistics . ClinCalc . 14 January 2024.
  6. Web site: Susceptibility and Minimum Inhibitory Concentration (MIC) Data . 14 October 2015 . 1 October 2015.
  7. Web site: Omnicef capsules Patient Information . . February 2004 . 24 November 2006 . https://web.archive.org/web/20061118132152/http://www.rxabbott.com/pdf/omnicef_capsules_patient_friendly.pdf. 18 November 2006.
  8. Web site: Omnicef manufacturer's packet insert . . 11 December 2016.
  9. Inamoto Y, Chiba T, Kamimura T, Takaya T . FK 482, a new orally active cephalosporin synthesis and biological properties . The Journal of Antibiotics . 41 . 6 . 828–30 . June 1988 . 3255303 . 10.7164/antibiotics.41.828 . free .
  10. Kamachi H, Narita Y, Okita T, Abe Y, Iimura S, Tomatsu K, Yamasaki T, Okumura J, Naito T, Oki T . 6 . Synthesis and biological activity of a new cephalosporin, BMY-28232 and its prodrug-type esters for oral use . The Journal of Antibiotics . 41 . 11 . 1602–16 . November 1988 . 3198494 . 10.7164/antibiotics.41.1602 . free .
  11. González M, Rodríguez Z, Tolón B, Rodríguez JC, Velez H, Valdés B, López MA, Fini A . 6 . An alternative procedure for preparation of cefdinir . Farmaco . 58 . 6 . 409–18 . June 2003 . 12767379 . 10.1016/S0014-827X(03)00063-6 .
  12. Web site: 2008 Top 200 generic drugs by retail dollars . dead . https://web.archive.org/web/20120112121937/http://drugtopics.modernmedicine.com/drugtopics/data/articlestandard//drugtopics/252011/727243/article.pdf . 12 January 2012 .  . Drug Topics (26 May 2009). Retrieved on 24 July 2009.
  13. Web site: Document. elsevierbi.com.
  14. Web site: Medicis.com - Medicis Pharmaceutical Corporation. https://web.archive.org/web/20140714140411/http://www.globenewswire.com/newsarchive/mrx/pages/news_releases.html?d=94045. dead. 14 July 2014. globenewswire.com.
  15. Web site: Cefdinir medical facts from Drugs.com. drugs.com.