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diclofenac ophthalmic (Voltaren Ophthalmic)

 

Classes: Ophthalmic NSAIDs

Dosing and uses of Voltaren Ophthalmic (diclofenac ophthalmic)

 

Dosing Strength

ophthalmic solution

  • 0.1%

 

Cataract Surgery

1 gtt in affected eye(s) four times daily for 2 weeks, beginning 24 hours post-surgery

 

Corneal Refractive Surgery

1-2 gtt in affected eye(s) within 1 hour pre-op & 15 minutes post-op; continue 1-2 gtt four times daily for 3 days

 

Pediatric dosage forms and strengths

Safety & efficacy not established

 

Voltaren Ophthalmic (diclofenac ophthalmic) adverse (side) effects

Frequency not defined

Mild ocular stinging, irritation

May slow corneal wound healing

Lacrimation

Increased IOp

Keratitis

Dizziness

Insomnia

Pain

Fever

Chills

Nausea/vomiting

Abdominal pain

Corneal deposits

Corneal edema

Conjunctivitis

Irritation

Eyelid swelling

Corneal perforation

Corneal thinning

 

Warnings

Contraindications

Hypersensitivity to ASA, NSAIDs, or components of the formulation

 

Cautions

Contains sodium sulfite which may cause allergic reactions in susceptible individuals NSAIDs may slow or delay healing

Potential for cross-sensitivity to other NSAIDs or aspirin

Interferes with platelet aggregation and may increase bleeding of ocular tissues; use caution in patients with predisposition to bleeding

Corneal effects, including keratitis, reported

Remove contact lenses before application, may reinsert 10 minutes after instilling drops

Corneal adverse reactions may occur in patients with keratitis after continued use that may result in loss of vision; discontinue use in patients with evidence of corneal epithelial damage

Use caution in patients with diabetes (may be at risk of corneal adverse effects that may result in loss of vision)

Use caution in patients with complicated ocular surgeries, corneal denervation, repeat ocular surface disease, or corneal epithelial defects

Use caution in patients with rheumatoid arthritis

 

Pregnancy and lactation

Pregnancy category: C

Lactation: Excretion in milk significantly lower than systemic acministration of diclofenac; possibly compatible

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Voltaren Ophthalmic (diclofenac ophthalmic)

Mechanism of action

Mechanism of action Nonsteroidal anti-inflammatory agent; inhibits COX-1 and COX-2, which results in decreased formation of prostaglandin precursors

 

Pharmacokinetics

Absorption: Negligible