Adult Dosing
Inflammatory ocular conditions with superficial bacterial infections
- Instill 2 gtt topically into the conjunctival sac q4 hrs while awake; max: 20 mL (initial prescription)
- Alt: Apply 0.5 inch ribbon of ointment in the conjunctival sac tid-qid and once or twice at night; max: 8 g (initial prescription)
Notes:- In chronic conditions, taper the dose gradually to discontinue the therapy
- If signs and symptoms fail to improve after two days, consider re-evaluating the patient
Pediatric Dosing
- Safety and effectiveness in pediatric patients <6 yrs of age have not been established
Inflammatory ocular conditions with superficial bacterial infections
Children >6 yrs
- Instill 2 gtt topically into the conjunctival sac q4 hrs while awake; max: 20 mL (initial prescription)
- Alt: Apply 0.5 inch ribbon of ointment in the conjunctival sac tid-qid and once or twice at night; max: 8 g (initial prescription)
Notes:- In chronic conditions, taper the dose gradually to discontinue the therapy
- If signs and symptoms fail to improve after two days, consider re-evaluating the patient
[Outline]
See Supplemental Patient Information
- Not for injection into the eye
- Ocular hypertension/glaucoma with damage to the optic nerve, defects in visual acuity and fields of vision, and posterior subcapsular cataract formation may occur with long-term use of corticosteroids. Prolonged use of this product may also suppress the host immune response and increase the hazard of secondary ocular infections
- Therapy may cause acute anterior uveitis in susceptible individuals, primarily blacks
- Various ocular diseases and long-term use of topical corticosteroids induce corneal and scleral thinning. Use of topical corticosteroids in the presence of diseases causing thinning of the cornea or sclera leads to perforation
- Acute purulent infections of the eye may be masked or activity may be enhanced by the presence of corticosteroid medication
- Routinely monitor intraocular pressure even though it may be difficult in children and uncooperative patients if this drug is used for 10 days
- Most of staphylococcal isolates are fully resistant to sulfonamides
- Increased incidence of filtering blebs and delayed healing may occur with the use of steroids after cataract surgery
- Use of ocular steroids may prolong the course and exacerbate the severity of viral infections of the eye; hence, use with extreme caution in patients with a history of herpes simplex and perform frequent slit lamp microscopy
- Do not use topical steroids for the treatment of mustard gas keratitis and Sjogren's keratoconjunctivitis as they are not effective
- Incidence of fatal reactions such as Stevens-Johnson syndrome, toxic epidermal necrolysis, fulminant hepatic necrosis, agranulocytosis, aplastic anemia, and other blood dyscrasias have been reported rarely; sensitization may recur on re-administration of the drug, irrespective of the route of administration
- Discontinue use on appearance of first sign of hypersensitivity, skin rash or other reaction
- Physician should renew medication order beyond 20 mL or 8 g only after examining the patients intraocular pressure and examination of the patient with the aid of magnification, such as slit lamp biomicroscopy and fluorescein staining
- Long-term corticosteroid use may cause fungal infections of the cornea
- The p-aminobenzoic acid present in purulent exudates competes with sulfonamides, which can reduce their effectiveness
- Ophthalmic ointments may retard corneal healing
Cautions: Use cautiously in
- Cataract surgery
- Severe dry eye
Supplemental Patient Information
- Advise patients not to touch the applicator tip to any surface, including the eye, in order to prevent contamination of the solution; inform them not to use if the solution has darkened
- Instruct patients to discontinue use of the medication and consult a physician, if inflammation or pain persists longer than 48 hours or becomes aggravated
- Inform them not to wear contact lenses during the use of this product
Pregnancy Category:C
Breastfeeding: Limited literature indicates that maternal doses of prednisolone up to 50 mg/day produce low levels in milk and is not expected to cause any adverse effects in breastfed infants. With high maternal doses, avoiding breastfeeding for 4 hrs after a dose should significantly reduce the dose received by the infant. This information is based upon LactMed database (available at http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?LACT last accessed 15 June 2011). Because there exists a potential for serious adverse reactions in nursing infants, a decision should be made whether to discontinue nursing or to discontinue the drug analyzing the importance of the drug to the mother.
US Trade Name(s)
US Availability
prednisolone/sulfacetamide (generic)
Blephamide (prednisolone/sulfacetamide)
Blephamide S.O.P. (prednisolone/sulfacetamide) (generic)
Vasocidin (prednisolone/sulfacetamide)
Canadian Trade Name(s)
- Ak Cide
- Blephamide
- Dioptimyd
Canadian Availability
Ak Cide (prednisolone/sulfacetamide)
- OPTH SOLN: [5 mg/100 mg]/mL
Blephamide (prednisolone/sulfacetamide)
- OPTH SUSP: 0.2%/10%
- OPTH OINT: 0.2%/10%
Dioptimyd (prednisolone/sulfacetamide)
- OPTH OINT: [5 mg/100 mg]/g
- OPTH SUSP: 0.5%/10%
UK Trade Name(s)
UK Availability
Australian Trade Name(s)
Australian Availability
[Outline]
Pricing data from www.DrugStore.com in U.S.A.
- Blephamide 10-0.2 % SUSP [Bottle] (ALLERGAN)
10 % = $105.99
30 % = $295.96 - Blephamide 10-0.2 % SUSP [Bottle] (ALLERGAN)
5 % = $70.99
15 % = $199.97
Warning: This pricing information is subject to change at the sole discretion of DS Pharmacy. For the most current and up-to-date pricing information, please visit drugstore.com.