Discovering painful sores or ulcers in the genital area can be a deeply distressing and frightening experience. Chancroid is a bacterial sexually transmitted infection (STI) that causes soft, painful ulcers and often leads to swollen lymph nodes in the groin. The physical discomfort can make walking or sitting difficult, while the emotional toll of an STI diagnosis can create anxiety and embarrassment. It is important to know that chancroid is a fully curable condition, and with prompt medical attention, the infection can be resolved quickly. 

Treatment is essential not only to relieve the intense pain and heal the ulcers but also to prevent the transmission of the bacteria to sexual partners. Successful treatment also stops the formation of painful abscesses in the lymph nodes, known as buboes. Because the infection is bacterial, it does not go away on its own without specific medication. Treatment plans are generally straightforward, though doctors must consider factors such as pregnancy, allergies, and coinfection with other STIs when selecting the appropriate drug (Centers for Disease Control and Prevention, 2021). 

Overview of treatment options for Chancroid 

The primary and most effective approach to treating chancroid is the use of antibiotics. The goal is to kill the Haemophilus ducreyi bacteria responsible for the infection. Unlike viral STIs that must be managed long-term, chancroid can be cured completely. 

Medical treatment focuses on clearing the infection rapidly to allow the skin to heal. For most patients, this involves a short course or even a single dose of medication. While large, swollen lymph nodes may sometimes require a doctor to drain fluid to relieve pressure, the core of the treatment is strictly pharmacological. Lifestyle changes, primarily sexual abstinence during treatment, are necessary to prevent spreading the infection, but they do not treat the bacteria itself. 

Medications used for Chancroid 

Antibiotics are the standard of care for chancroid. There are four main antibiotics typically used, falling into three distinct drug classes. 

The first-line choices often include macrolide antibiotics, such as azithromycin. This is frequently preferred because it can often be given as a single oral dose, ensuring compliance. Another common first-line option is ceftriaxone, a cephalosporin antibiotic administered via a single injection. 

Alternative treatments include fluoroquinolones, such as ciprofloxacin, or a multi-day course of erythromycin base (another macrolide). These are effective but may require taking pills for several days. 

Patients can generally expect symptoms to improve within three days of starting treatment. Clinical experience suggests that the ulcers typically resolve completely within seven days, although large ulcers may take up to two weeks to heal. If lymph nodes are swollen, they may remain tender and swollen for weeks even after the infection is cured. Doctors typically require a follow-up visit to ensure the ulcers are healing properly (Mayo Clinic, 2022). 

How these medications work 

Each class of antibiotic attacks the Haemophilus ducreyi bacteria in a different way to stop the infection. 

Cephalosporins, like ceftriaxone, work by disrupting the construction of the bacterial cell wall. Without a strong wall, the bacteria become unstable and burst, effectively killing them. 

Macrolides (e.g., azithromycin, erythromycin) inhibit protein synthesis by binding to bacteria, preventing necessary protein production for growth and survival. 

Fluoroquinolones (e.g., ciprofloxacin) target bacterial DNA, blocking enzymes required for DNA replication and reproduction. By stopping bacterial proliferation or survival, these drugs enable the immune system to clear the infection and promote healing (National Library of Medicine, 2020). 

Side effects and safety considerations 

While these antibiotics are generally safe, they have specific profiles that patients must be aware of. Common side effects include nausea, diarrhea, and stomach upset; ceftriaxone may cause temporary injection site pain. 

Ciprofloxacin and other fluoroquinolones are generally avoided in pregnant or lactating women due to potential risk; cephalosporins or macrolides are safer alternatives. 

Patients must be aware of drug allergies, especially if they have a penicillin reaction (related to cephalosporins). Testing for other STIs (e.g., HIV, syphilis) is vital due to common coinfection. Unhealing ulcers after seven days require medical attention, suggesting resistance or an alternate diagnosis. 

Since everyone’s experience with the condition and its treatments can vary, working closely with a qualified healthcare provider helps ensure safe and effective care. 

References 

  1. Centers for Disease Control and Prevention. https://www.cdc.gov 
  1. Mayo Clinic. https://www.mayoclinic.org 
  1. National Library of Medicine. https://medlineplus.gov 
  1. World Health Organization. https://www.who.int 

Medications for Chancroid

These are drugs that have been approved by the US Food and Drug Administration (FDA), meaning they have been determined to be safe and effective for use in Chancroid.

Found 2 Approved Drugs for Chancroid

Azithromycin

Brand Names
Azasite, Zithromax

Azithromycin

Brand Names
Azasite, Zithromax
Azithromycin for oral suspension USP is a macrolide antibacterial drug indicated for the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms in the specific conditions listed below. Recommended dosages and durations of therapy in adult and pediatric patient populations vary in these indications.

Minocycline

Brand Names
ZILXI, Emrosi, Amzeeq, Arestin, Minocin

Minocycline

Brand Names
ZILXI, Emrosi, Amzeeq, Arestin, Minocin
Minocycline hydrochloride tablets, USP are indicated in the treatment of the following infections due to susceptible strains of the designated microorganisms: Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox and tick fevers caused by rickettsiae. Respiratory tract infections caused by Mycoplasma pneumoniae. Lymphogranuloma venereum caused by Chlamydia trachomatis. Psittacosis (Ornithosis) due to Chlamydophila psittaci. Trachoma caused by Chlamydia trachomatis, although the infectious agent is not always eliminated, as judged by immunofluorescence. Inclusion conjunctivitis caused by Chlamydia trachomatis. Nongonococcal urethritis, endocervical, or rectal infections in adults caused by Ureaplasma urealyticum or Chlamydia trachomatis. Relapsing fever due to Borrelia recurrentis. Chancroid caused by Haemophilus ducreyi. Plague due to Yersinia pestis. Tularemia due to Francisella tularensis. Cholera caused by Vibrio cholerae. Campylobacter fetus infections caused by Campylobacter fetus. Brucellosis due to Brucella species (in conjunction with streptomycin). Bartonellosis due to Bartonella bacilliformis. Granuloma inguinale caused by Klebsiella granulomatis. Minocycline is indicated for the treatment of infections caused by the following gram-negative microorganisms when bacteriologic testing indicates appropriate susceptibility to the drug: Escherichia coli. Klebsiella aerogenes Shigella species. Acinetobacter species. Respiratory tract infections caused by Haemophilus influenzae. Respiratory tract and urinary tract infections caused by Klebsiella species. Minocycline hydrochloride tablets, USP are indicated for the treatment of infections caused by the following gram-positive microorganisms when bacteriologic testing indicates appropriate susceptibility to the drug: Upper respiratory tract infections caused by Streptococcus pneumoniae. Skin and skin structure infections caused by Staphylococcus aureus. (NOTE: Minocycline is not the drug of choice in the treatment of any type of staphylococcal infection.) When penicillin is contraindicated, minocycline is an alternative drug in the treatment of the following infections: Uncomplicated urethritis in men due to Neisseria gonorrhoeae and for the treatment of other gonococcal infections. Infections in women caused by Neisseria gonorrhoeae. Syphilis caused by Treponema pallidum subspecies pallidum. Yaws caused by Treponema pallidum subspecies pertenue. Listeriosis due to Listeria monocytogenes. Anthrax due to Bacillus anthraci s. Vincent’s infection caused by Fusobacterium fusiforme. Actinomycosis caused by Actinomyces israelii. Infections caused by Clostridium species. In acute intestinal amebiasis, minocycline may be a useful adjunct to amebicides. In severe acne, minocycline may be useful adjunctive therapy. Oral minocycline is indicated in the treatment of asymptomatic carriers of Neisseria meningitidis to eliminate meningococci from the nasopharynx. In order to preserve the usefulness of minocycline in the treatment of asymptomatic meningococcal carriers, diagnostic laboratory procedures, including serotyping and susceptibility testing, should be performed to establish the carrier state and the correct treatment. It is recommended that the prophylactic use of minocycline be reserved for situations in which the risk of meningococcal meningitis is high. Oral minocycline is not indicated for the treatment of meningococcal infection. Although no controlled clinical efficacy studies have been conducted, limited clinical data show that oral minocycline hydrochloride has been used successfully in the treatment of infections caused by Mycobacterium marinum. To reduce the development of drug-resistant bacteria and maintain the effectiveness of minocycline hydrochloride tablets, USP and other antibacterial drugs, minocycline hydrochloride tablets, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.
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