Bromfenac
Nonsteroidal Anti-inflammatory Drug — SENSORY ORGANS
Also known as: bromfenac sodium, bromfenac sodium sesquihydrate, prolensa, xibrom, yellox
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Bromfenac is an ofp drug in the Nonsteroidal Anti-inflammatory Drug class catalogued in DrugCentral. It was first approved by the FDA in 2005. Its mechanism of action is classified as Cyclooxygenase Inhibitors. DrugCentral lists 3 molecular targets, including PTGS2, PTGS1 and PTGS1|PTGS2. Recorded indications include Pain, Post-Op Ocular Inflammation and Postoperative Ocular Pain.
- Approval status: ofp (first approved 2005 by the FDA).
- Drug class: Nonsteroidal Anti-inflammatory Drug.
- Mechanism of action: Cyclooxygenase Inhibitors.
- Molecular targets: PTGS2, PTGS1 and PTGS1|PTGS2 (3 listed in DrugCentral).
- Indications: Pain, Post-Op Ocular Inflammation and Postoperative Ocular Pain.
- ATC code: S01BC11 (Antiinflammatory agents, non-steroids).
- Molecular formula: C15H12BrNO3; molecular weight 334.17 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (3)
- Pain
- Post-Op Ocular Inflammation
- Postoperative Ocular Pain
Contraindications (4)
- Diabetes mellitus
- Epithelial Keratopathy
- Red eye
- Rheumatoid arthritis
Mechanism & targets
| Mechanism of action (MoA) | Cyclooxygenase Inhibitors |
|---|---|
| Established pharmacologic class | Nonsteroidal Anti-inflammatory Drug |
Molecular targets (3)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Prostaglandin G/H synthase 2 | PTGS2 | inhibitor | IC50 8.40 |
| Prostaglandin G/H synthase 1 | PTGS1 | inhibitor | IC50 8.29 |
| Cyclooxygenase | PTGS1|PTGS2 | unknown | IC50 7.10 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2005-03-24 | FDA | — | BAUSCH AND LOMB INC |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
S01BC11 | SENSORY ORGANS › OPHTHALMOLOGICALS › ANTIINFLAMMATORY AGENTS › Antiinflammatory agents, non-steroids |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Cataract | 171.1 |
| Toxic anterior segment syndrome | 165.7 |
| Corneal oedema | 156.1 |
| Endophthalmitis | 153.4 |
| Hypopyon | 135.1 |
| Visual acuity reduced | 124.4 |
| Ulcerative keratitis | 119.8 |
| Eye pain | 110.8 |
| Eye irritation | 102.0 |
| Product packaging quantity issue | 96.4 |
| Corneal opacity | 88.2 |
| Intraocular pressure increased | 87.1 |
Chemical structure
| Molecular formula | C15H12BrNO3 |
|---|---|
| Molecular weight | 334.17 g/mol |
| CAS number | 91714-94-2 |
| InChIKey | ZBPLOVFIXSTCRZ-UHFFFAOYSA-N |
| PubChem CID | 60726 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Bromfenac used for?
DrugCentral lists the following indications for Bromfenac: Pain, Post-Op Ocular Inflammation and Postoperative Ocular Pain.
How does Bromfenac work?
Bromfenac is classified as Cyclooxygenase Inhibitors; its molecular targets in DrugCentral include PTGS2 (inhibitor), PTGS1 (inhibitor) and PTGS1|PTGS2.
When was Bromfenac first approved?
Bromfenac was first approved by the FDA in 2005.
What drug class does Bromfenac belong to?
Bromfenac is in the Nonsteroidal Anti-inflammatory Drug class.
What is the chemical formula of Bromfenac?
Bromfenac has the molecular formula C15H12BrNO3 and a molecular weight of 334.17 g/mol.
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Sources
- DrugCentral drug card 401 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1077 — compound record and bioactivity
- PubChem CID 60726 — chemical identifiers
- DrugBank DB00963 — drug record
- FDA UNII 864P0921DW — substance identity
- DailyMed: FDA labels for Bromfenac — current prescribing information (label search)
- UniProt P35354 (PTGS2) — target protein
- UniProt P23219 (PTGS1) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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