Abstract | PURPOSE: METHODS: The study was an open-label, non-comparative retrospective series of 14 patients with refractory uveitis and treated with MMF for a mean of >33 months. Mycophenolate mofetil was given at a dosage of 1 g (oral) twice daily. Indications included prednisolone reduction, additive agent with cyclosporin, or replacement therapy ( azathioprine or methotrexate). The intraocular inflammatory response, side-effects, and toxicity were monitored. RESULTS: Intraocular inflammation remained under control in 10 patients, unchanged in three and deteriorated in one patient. Transient side-effects included tiredness, headache and dizziness (one patient each, lasting less than 2 weeks from the time of MMF introduction). Mycophenolate mofetil was stopped in one patient because of absence of prolonged clinical improvement. Vision improved in 25% (7 eyes), did not change in 50% (14 eyes), but was reduced in 25% (7 eyes). CONCLUSIONS:
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Authors | Chun H Lau, Marie Comer, Susan Lightman |
Journal | Clinical & experimental ophthalmology
(Clin Exp Ophthalmol)
Vol. 31
Issue 6
Pg. 487-91
(Dec 2003)
ISSN: 1442-6404 [Print] Australia |
PMID | 14641155
(Publication Type: Journal Article)
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Chemical References |
- Immunosuppressive Agents
- Mycophenolic Acid
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Topics |
- Adult
- Aged
- Female
- Follow-Up Studies
- Humans
- Immunosuppressive Agents
(adverse effects, therapeutic use)
- Male
- Middle Aged
- Mycophenolic Acid
(adverse effects, analogs & derivatives, therapeutic use)
- Retrospective Studies
- Safety
- Treatment Outcome
- Uveitis
(drug therapy, prevention & control)
- Visual Acuity
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