FDA: increased risk of death with Tygacil compared to other antibiotics


The FDA ( Food and Drug Administration ) has informed healthcare professionals of an increased mortality risk associated with the use of the intravenous antibacterial Tygacil ( Tigecycline ) compared to that of other drugs used to treat a variety of serious infections. The increased risk was determined using a pooled analysis of clinical trials. The cause of the excess death in these trials is often uncertain, but it is likely that most deaths in patients with these severe infections were related to progression of the infection.

The increased risk was seen most clearly in patients treated for hospital-acquired pneumonia, especially ventilator-associated pneumonia, but was also seen in patients with complicated skin and skin structure infections, complicated intra-abdominal infections and diabetic foot infections.
Tygacil is not approved for the treatment of hospital-acquired pneumonia ( including ventilator-associated pneumonia ) or diabetic foot infection.
Tygacil is approved by FDA for the treatment of complicated skin and skin structure infections, complicated intra-abdominal infections, and community acquired pneumonia.

The pooled analysis grouped 13 trials with patients given Tygacil for both approved and unapproved indications by type of infection, comparing the overall mortality for Tygacil versus pooled control agents. Overall, in the trials, death occurred in 4.0% ( 150/3788 ) of patients receiving Tygacil and 3.0% ( 110/3646 ) of patients receiving comparator antibiotics.
An adjusted risk difference for all-cause mortality based on a random effects model stratified by trial weight was 0.6% between Tygacil and comparator treated patients.
Although for each indication, the mortality difference was not statistically significant, mortality in Tygacil treated patients was numerically greater in every infection, sometimes considerably greater, particularly in ventilator-associated pneumonia.
Tygacil is not approved for ventilator associated pneumonia because of an unacceptably low cure rate, as well as excess mortality.

Tygacil is considered bacteriostatic; however, it has demonstrated bactericidal activity against isolates of Streptococcus pneumoniae and Legionella pneumophila. One possible reason for the mortality difference is that in certain severe infections, Tygacil's bacteriostatic mechanism may put it at some disadvantage, although for approved indications, cure rates with Tygacil were generally similar to that seen with the bactericidal active control agents.

Source: FDA, 2010

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