Guide your patients through post-cataract recovery with
NEVANAC® suspension. It offers proven performance, safety, and
tolerability.2-4 Plus the efficacy you demand:

Excellent control of inflammation3

  • Significantly more patients with resolved anterior segment inflammation vs placebo as early as Day 12
  • Unique prodrug design leads to powerful COX-2 inhibition1
  • Significantly more pain-free patients vs placebo as soon as Day 12
INDICATIONS AND USAGE:

NEVANAC® ophthalmic suspension is a nonsteroidal, anti-inflammatory prodrug indicated for the treatment of pain and inflammation associated with cataract surgery.

DOSAGE AND ADMINISTRATION:

Shake well before use. One drop of NEVANAC® ophthalmic suspension should be applied to the affected eye(s) three-times-daily beginning 1 day prior to cataract surgery, continued on the day of surgery and through the first 2 weeks of the postoperative period.

NEVANAC® ophthalmic suspension may be administered in conjunction with other topical ophthalmic medications such as beta-blockers, carbonic anhydrase inhibitors, alpha-agonists, cycloplegics, and mydriatics.

IMPORTANT SAFETY INFORMATION:

CONTRAINDICATIONS

Hypersensitivity to any of the ingredients in the formula or other NSAIDS.

WARNINGS AND PRECAUTIONS
  • Increased bleeding time due to increased thrombocyte aggregation
  • Delayed healing
  • Corneal effects including keratitis
ADVERSE REACTIONS

Most common adverse reactions (5% to 10%) are capsular opacity, decreased visual acuity, foreign body sensation, increased intraocular pressure, and sticky sensation.

References:
1. Walters T, Raizman M, Ernest P, Gayton J, Lehmann R. In vivo pharmacokinetics and in vitro pharmacodynamics of nepafenac, amfenac, ketorolac, and bromfenac. J Cataract Refract Surg. 2007;33(9):1539-1545. 2. Maxwell WA, Reiser HJ, Stewart RH, et al. Nepafenac dosing frequency for ocular pain and inflammation associated with cataract surgery. J Ocul Pharmacol Ther. 2008;24(6):593-599. 3. Lane SS, Modi SS, Lehmann RP, Holland EJ. Nepafenac ophthalmic suspension 0.1% for the prevention and treatment of ocular inflammation associated with cataract surgery. J Cataract Refract Surg. 2007;33(1):53-58. 4. NEVANAC® suspension package insert.

 

Alcon                 ©2010 Alcon, Inc.       2/10     NPF10502WB

 

 

 

 

 

 

 

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Steroids

Nonsteroidal anti-inflammatory drugs (NSAIDS)

 

 

 

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Aqueous humor drug concentration (0-4 h)

 

DOSAGE AND ADMINISTRATION:

Shake well before use. One drop of NEVANAC® ophthalmic suspension should be applied to the affected eye(s) three-times-daily beginning 1 day prior to cataract surgery, continued on the day of surgery and through the first 2 weeks of the postoperative period.

NEVANAC® ophthalmic suspension may be administered in conjunction with other topical ophthalmic medications such as beta-blockers, carbonic anhydrase inhibitors, alpha-agonists, cycloplegics, and mydriatics.

INDICATIONS AND USAGE:

NEVANAC® ophthalmic suspension is a nonsteroidal, anti-inflammatory prodrug indicated for the treatment of pain and inflammation associated with cataract surgery.

IMPORTANT SAFETY INFORMATION:

CONTRAINDICATIONS

Hypersensitivity to any of the ingredients in the formula or other NSAIDS.

WARNINGS AND PRECAUTIONS ADVERSE REACTIONS

Most common adverse reactions (5% to 10%) are capsular opacity, decreased visual acuity, foreign body sensation, increased intraocular pressure, and sticky sensation.

Reference:
1. Walters T, Raizman M, Ernest P, Gayton J, Lehmann R. In vivo pharmacokinetics and in vitro pharmacodynamics of nepafenac, amfenac, ketorolac, and bromfenac. J Cataract Refract Surg. 2007;33(9):1539-1545

 

 

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Alcon                 ©2010 Alcon, Inc.       2/10     NPF10502WB