Bromfenac sodium
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Commercial
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Clinical
Clinical Trials
69 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Cataract | D002386 | EFO_0001059 | H26.9 | — | 1 | 5 | 1 | 1 | 8 |
| Inflammation | D007249 | MP_0001845 | — | — | — | 4 | 2 | 1 | 7 |
| Dry eye syndromes | D015352 | — | H04.12 | — | 1 | 1 | 1 | — | 3 |
| Macular edema | D008269 | — | — | 1 | — | — | 1 | — | 2 |
| Pseudophakia | D019591 | — | — | — | — | — | 1 | — | 1 |
| Retinal vein occlusion | D012170 | EFO_1001157 | H34.81 | — | — | — | 1 | — | 1 |
| Macular degeneration | D008268 | EFO_0001365 | H35.30 | — | — | — | 1 | — | 1 |
| Diabetic retinopathy | D003930 | EFO_0003770 | — | — | — | — | 1 | — | 1 |
| Choroidal neovascularization | D020256 | — | — | — | — | — | 1 | — | 1 |
| Pathologic neovascularization | D009389 | — | — | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Pain | D010146 | EFO_0003843 | R52 | — | — | 3 | — | — | 3 |
| Keratoconjunctivitis sicca | D007638 | EFO_1000906 | — | — | 1 | 1 | — | — | 2 |
| Conjunctivitis | D003231 | — | H10 | — | — | 1 | — | — | 1 |
| Allergic conjunctivitis | D003233 | EFO_0007141 | H10.44 | — | — | 1 | — | — | 1 |
| Postoperative complications | D011183 | — | — | — | — | 1 | — | — | 1 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Eye diseases | D005128 | EFO_0003966 | H44 | — | 1 | — | — | — | 1 |
| Cataract extraction | D002387 | — | — | — | 1 | — | — | — | 1 |
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Papilledema | D010211 | EFO_1001074 | H35.81 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Adverse Events
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100 adverse events reported
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