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Safety profile of grepafloxacin compared with other fluoroquinolones
1Institut für Klinische Pharmakologie und Toxikologie, Universitätsklinikum Benjamin Franklin Freie Universität Berlin, Germany.
Abstract:
Preclinical investigations with grepafloxacin showed that its toxicological profile is similar to that of other fluoroquinolones. The photosensitizing effect of grepafloxacin was relatively weak and similar to that of ciprofloxacin. Grepafloxacin did not cause convulsions in mice when administered in conjunction with the non-steroidal anti-inflammatory drug fenbufen. Intravenous injection of grepafloxacin caused transient dysrhythmias in rabbits at a dosage of 10 mg/kg and ventricular tachycardia at 30 mg/kg iv. Joint cartilage lesions were found in juvenile dogs after iv treatment with 100 mg/kg daily. Plasma concentrations (19-24 mg/L) under these conditions were approximately ten times above a therapeutic level. Data derived from patients who had been treated with grepafloxacin in phase II and phase III multiple-dose studies (400 mg, n = 1069; 600 mg, n = 925) were available for an analysis of the patients' tolerance of the drug. The most common adverse events observed for the 400 mg and 600 mg treatments during these studies were gastrointestinal reactions, such as nausea (11% and 15%, respectively), vomiting (1% and 6%) and diarrhoea (3% and 4%). In both groups a considerable number of patients (9% and 17%) reported an unpleasant taste; this was less common in the pooled controls (1%) after treatment with drugs such as doxycycline, ciprofloxacin, amoxycillin or cefixime. Headache occurred in 4% (400 mg) and 5% (600 mg) and insomnia in 1% (400 mg) or 2% (600 mg) of the patients. Similar incidences were found for photosensitivity (1% and 2%, respectively) and for rash (1% and 2%) in the 400 mg and 600 mg groups. So far, tolerance of the new compound seems to be similar to that of other fluoroquinolones. However, incidences of nausea, vomiting and unpleasant taste were rather high during the first clinical trials, particularly after treatment with 600 mg daily. Further data are necessary for a sound evaluation of the tolerance of grepafloxacin.
Insights
Grepafloxacin exhibits a toxicological profile similar to other fluoroquinolones, with mild photosensitivity and no convulsions when combined with fenbufen. Clinical trials indicate common side effects like nausea and unpleasant taste, requiring further evaluation for comprehensive tolerance assessment.
Area of Science:
- Pharmacology
- Toxicology
- Clinical Trials
Background:
- Grepafloxacin is a fluoroquinolone antibiotic.
- Understanding its toxicological profile and patient tolerance is crucial for its clinical application.
Purpose of the Study:
- To evaluate the preclinical toxicological profile of grepafloxacin.
- To assess the safety and tolerance of grepafloxacin in patients through phase II and III clinical trials.
Main Methods:
- Preclinical studies in mice, rabbits, and dogs to assess toxicity, including photosensitization, convulsions, cardiac effects, and cartilage lesions.
- Analysis of adverse events from phase II and III clinical trials involving 1069 patients at 400 mg and 925 patients at 600 mg of grepafloxacin.
Main Results:
- Preclinical studies showed a toxicological profile similar to other fluoroquinolones, with weak photosensitization and no convulsions with fenbufen. Adverse effects in animals included dysrhythmias, ventricular tachycardia, and joint cartilage lesions at high doses.
- Clinical trials reported common adverse events such as nausea (11-15%), unpleasant taste (9-17%), vomiting (1-6%), diarrhea (3-4%), headache (4-5%), insomnia (1-2%), photosensitivity (1-2%), and rash (1-2%).
- Incidences of nausea, vomiting, and unpleasant taste were notably high, especially at the 600 mg dosage.
Conclusions:
- Grepafloxacin's preclinical toxicological profile is comparable to other fluoroquinolones.
- Patient tolerance in early clinical trials suggests a similar safety profile to other fluoroquinolones, but with a higher incidence of gastrointestinal side effects and taste disturbances.
- Further data are required for a definitive evaluation of grepafloxacin's overall tolerance and safety in a broader patient population.
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