At the core of all fluoroquinolones—including drugs like ciprofloxacin and levofloxacin—are 2 six-member carbon rings attached to a fluoride atom. These drugs work by targeting 2 bacterial enzymes responsible for notching, coiling, and sealing DNA during replication: DNA gyrase and topoisomerase IV. Because current fluoroquinolones bind to 2 separate enzymes, it’s harder for bacteria to mutate and to evade the actions of these drugs.
Uses
Here’s a list of bacteria that fluoroquinolones are active against:
Staphylococcus aureusStreptococcus pneumoniaeViridans StreptococcusChlamydia pneumoniaeEnterococcus faecalisNocardia speciesNeisseria meningitides and gonorrhoeaeHaemophilus influenzaePseudomonas aeruginosa
More specifically, fluoroquinolones are active against aerobes and facultative anaerobes. Anaerobes, however, are usually resistant to these medications.
Bacterial Infections Treated
Here’s a list of bacterial infections that fluoroquinolones like ciprofloxacin and levofloxacin treat:
Respiratory infections (pneumonia) Lower Respiratory Tract Infections (Bronchitis) Urinary Tract Infections (UTI) Sexually transmitted diseases Bone and Joint infections Typhoid Fever Anthrax Intra-abdominal infections Sinusitis
In addition to broad-spectrum bacterial coverage, fluoroquinolones also sport other properties that make them great antibiotics. First, they are taken by mouth (and not by injection). Second, they distribute well throughout various body compartments. Third, fluoroquinolones have a longer half-life which allows them to be dosed once or twice a day. Fourth, ciprofloxacin and levofloxacin are excreted mostly by the kidneys making them great at fighting urinary tract infections.
Possible Side Effects
For the most part, fluoroquinolones are very safe medication. However, they can cause certain adverse effects including:
Gastrointestinal disturbances (stomach upset)Allergic reactions (skin rash)HeadachesSeizuresHallucinationsQT prolongation (electrical disturbance of heart visible on ECG)Tendon ruptureAngioedema (skin swelling)Photosensitivity
In addition to the above adverse effects, more rarely, fluoroquinolones can also cause liver injury and increase liver enzymes. Earlier fluoroquinolones were notorious for causing liver injury (think gatifloxacin and trovafloxacin) and were subsequently withdrawn from the market.
Nowadays, the chance of any fluoroquinolone causing liver injury is 1 of 100,000 people exposed. Because levofloxacin and ciprofloxacin are the most widely prescribed fluoroquinolone antibiotics, they are the most common cause of idiosyncratic liver injury. Such liver injury typically occurs 1 to 4 weeks after fluoroquinolone administration.
Resistance
Although resistance to fluoroquinolones is less prevalent than resistance to some other antibiotics, it still happens especially among staphylococci (MRSA), Pseudomonas aeruginosa, and Serratia marcescens. And once a strain of bacteria is resistant against one fluoroquinolone then it’s resistant to them all.
If you or a loved one is prescribed a fluoroquinolone—or any antibiotic for that matter—it’s imperative that you complete your course of treatment. By abandoning treatment midway through—after you “feel” better—you contribute to the selection, survival, and spread of antibiotic-resistant bacteria which then become a serious public health concern. Remember that we’re always fighting a war against antibiotics, and we lose battles once resistance emerges.
