Prescription medication · Corticosteroid (Ophthalmic)
prednisolone ophthalmic
Also sold as Pred Forte. Pred Forte treats swelling and inflammation in your eye.
Data updated 2026-05-15
- $30.57
- Brand price (NADAC)
prednisolone ophthalmic (Pred Forte) is a prescription Corticosteroid (Ophthalmic). Pred Forte treats swelling and inflammation in your eye.
Pred Forte is an eye drop medicine that helps reduce swelling and redness in your eye. It belongs to a class of drugs called corticosteroids.
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Drug Pricing (NADAC)
Brand Price
$30.57/unit
Generic Available
No
Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →
What it does
Pred Forte treats swelling and inflammation in your eye.
Common side effects
Eye pain, Feeling like something is in your eye, Headache
Key warnings
You should not take Pred Forte if you have certain types of eye infections.
The sections below are summarized in plain English from prednisolone ophthalmic's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
Pred Forte contains prednisolone acetate, which is a type of corticosteroid. Corticosteroids reduce inflammation by blocking the substances in the body that cause it. This helps to relieve symptoms like redness and swelling in the eye.
Serious Warnings
You should not take Pred Forte if you have certain types of eye infections. These include untreated bacterial infections, most viral infections of the cornea or conjunctiva (like herpes simplex), fungal infections, or tuberculosis of the eye. Also, do not use it if you are allergic to any of its ingredients or other corticosteroids.
Common Questions
Can Pred Forte cause glaucoma?
Can Pred Forte cause cataracts?
Can Pred Forte affect wound healing in my eye?
Can I get an infection from using Pred Forte?
What should I do if my symptoms don't improve after using Pred Forte for a few days?
Can I wear contact lenses while using Pred Forte?
Is it normal to have blurry vision after using Pred Forte?
Can Pred Forte cause allergic reactions?
Can Pred Forte cause my pupils to dilate?
Can Pred Forte cause the white part of my eye to become red?
What are the common side effects of prednisolone ophthalmic?
What drug class is prednisolone ophthalmic?
What pregnancy or breastfeeding source fields are listed for prednisolone ophthalmic?
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What the FDA Data Shows for prednisolone ophthalmic
The FDA label for prednisolone ophthalmic (sold under brand names such as Pred Forte) classifies it as a prescription-only medication in the Corticosteroid (Ophthalmic) class. Pred Forte treats swelling and inflammation in your eye. Official labeling lists 7 commonly reported side effects, including Eye pain, Feeling like something is in your eye, Headache.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. Voluntary reports accumulate over the lifetime of a drug and reflect wide-ranging clinical use. Interaction data is drawn directly from FDA-approved prescribing information. NADAC pricing from CMS.
Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.
Last updated: February 2, 2024
PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.
All federal data sources used on this page
- FDA Orange Book - approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed - NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) - post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm - standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files - federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database - current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages