Tobi

Company
PathoGenesis

Approval Status
Approved December 1997

Treatment for
cystic fibrosis

Areas
Pediatrics , Respiratory

Tobi (tobramycin) has been approved as an inhaled antibiotic for the treatment of cystic fibrosis. It is indicated to treat Pseudomonas aeruginose infections, a common cause of lung infections in cystic fibrosis patients. The drug has been available intravenously since 1975.

Clinical trials demonstrated an increase in patients' lung function to be as much as 11% during six months of treatment. Of the approximate 500 patients studied, hospital admission were reduced by 26% and stays averaged 5.1 days for Tobi patients compared with 8.1 for placebo patients.

The main side effects were hoarseness and tinnitus. Eight Tobi patients had 16 episodes of tinnitus, while there were none in the placebo group. There was no evidence of hearing loss, but the FDA cautioned that tinnitus could be a preliminary indication of drug-related ototoxicity.

Tobi Drug Information

The Tobi drug information shown above is licensed from Thomson CenterWatch. The information provided here is for general educational purposes only and does not constitute medical or pharmaceutical advice which should be sought from qualified medical and pharmaceutical advisers.

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