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Pred Forte (Prednisolone Acetate Ophthalmic) - Side Effects and Adverse Reactions

 



ADVERSE REACTIONS

Adverse reactions include, in decreasing order of frequency, elevation of intraocular pressure (IOP) with possible development of glaucoma and infrequent optic nerve damage, posterior subcapsular cataract formation, and delayed wound healing.

Although systemic effects are extremely uncommon, there have been rare occurrences of systemic hypercorticoidism after use of topical steroids.

Corticosteroid-containing preparations have also been reported to cause acute anterior uveitis and perforation of the globe. Keratitis, conjunctivitis, corneal ulcers, mydriasis, conjunctival hyperemia, loss of accommodation and ptosis have occasionally been reported following local use of corticosteroids.

The development of secondary ocular infection (bacterial, fungal, and viral) have occurred. Fungal and viral infections of the cornea are particularly prone to develop coincidentally with long-term applications of steroids. The possibility of fungal invasion should be considered in any persistent corneal ulceration where steroid treatment has been used (see WARNINGS).

Transient burning and stinging upon instillation and other minor symptoms of ocular irritation have been reported with the use of PRED FORTE® suspension. Other adverse events reported with the use of PRED FORTE® suspension include: visual disturbance (blurry vision); foreign body sensation; and allergic reactions.



REPORTS OF SIDE EFFECTS / ADVERSE REACTIONS RELATED TO PRED FORTE

Below is a sample of reports where side effects / adverse reactions may be related to Pred Forte. The information is not vetted and should not be cosidered as verified clinical evidence.

Possible Pred Forte side effects / adverse reactions in 59 year old female

Reported by a consumer/non-health professional from United States on 2007-05-30

Patient: 59 year old female weighing 99.8 kg (219.5 pounds)

Reactions: Weight Decreased, Nausea, Injection Site Bruising, Constipation, Tremor, Blood Glucose Decreased, Feeling Jittery, Energy Increased, Blood Glucose Increased, Decreased Appetite

Suspect drug(s):
Amaryl
    Indication: Diabetes Mellitus non-Insulin-Dependent

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-01-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-01-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-01-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-01-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-06-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-07-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-09-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-06-01
    End date: 2006-08-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-08-19
    End date: 2006-09-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-09-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2007-01-01

Byetta

Byetta

Byetta

Pred Forte
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-12-20
    End date: 2007-01-18

Other drugs received by patient: Amaryl



See index of all Pred Forte side effect reports >>

Drug label data at the top of this Page last updated: 2006-07-31

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