152 153 Intestinal Disease Meeting Berlin 2006 - Dr. Falk Pharma ...
152 153 Intestinal Disease Meeting Berlin 2006 - Dr. Falk Pharma ...
152 153 Intestinal Disease Meeting Berlin 2006 - Dr. Falk Pharma ...
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Optimize clinical efficacy, minimize<br />
risks<br />
It is important to remember, said J.-F. Colombel<br />
(Lille), that therapy with immunosuppressants<br />
has specific side effects, such as a significantly<br />
increased risk of infection (figure 24). This is less<br />
pronounced with the clinically established immunosuppressants,<br />
such as azathioprine, whose<br />
side effects are well known, than with the biologics<br />
now flooding the market. “The risk of side<br />
Fig. 24<br />
Herpes simplex<br />
CMV<br />
Varicella zoster<br />
EBV<br />
HPV<br />
Congress Short Report <strong>Falk</strong> Symposium<br />
J.-F. Colombel M. Lémann<br />
M. tuberculosis<br />
M. avium sp.<br />
M. xenopi<br />
Listeria monocytogenes<br />
Staphylococcus sp.<br />
Nocardia<br />
E. coli<br />
Salmonella sp.<br />
I Infections associated with immunomodulator therapy in IBD<br />
(J.-F. Colombel, Lille)<br />
effects associated with these substances must<br />
not be underestimated. We must do all we can<br />
to optimize clinical efficacy and reduce the risks<br />
of these substances secondary to their toxicity,”<br />
J.-F. Colombel advised. Because of their clinical<br />
efficacy, immunosuppressants such as azathioprine<br />
and also methotrexate are being used<br />
earlier in the clinical course of IBD. They are indicated<br />
in chronic active disease and also for postoperative<br />
prophylaxis of disease recurrence, said<br />
Histoplasmosis<br />
Aspergillus spp.<br />
Cryptococcus spp.<br />
Candida spp.<br />
Coccidioides immitis<br />
Blastomyces<br />
Pneumocystis jiroveci<br />
Toxoplasma gondii<br />
<strong>153</strong><br />
35