Pred Mild

Inflammation, Conjunctivitis, Conjunctivitis + 4 more

Treatment

4 FDA approvals

20 Active Studies for Pred Mild

What is Pred Mild

Prednisolone acetate

The Generic name of this drug

Treatment Summary

Prednisolone acetate is a medication used to treat inflammation. It is a synthetic form of the steroid hormone prednisolone, and was approved by the FDA in 1955.

Blephamide

is the brand name

Pred Mild Overview & Background

Brand Name

Generic Name

First FDA Approval

How many FDA approvals?

Blephamide

Prednisolone acetate

1961

39

Approved as Treatment by the FDA

Prednisolone acetate, also known as Blephamide, is approved by the FDA for 4 uses including Inflammation and Organ Transplantation .

Inflammation

Organ Transplantation

Inflammation

Inflammatory Conditions

Helps manage Inflammatory Conditions

Effectiveness

How Pred Mild Affects Patients

Prednisolone acetate works by blocking chemicals in the body that cause inflammation. It is short-acting, as it only lasts for 2-3 hours. Patients may take larger doses of prednisolone acetate than the body naturally produces to help reduce inflammation. It is important for patients to be aware of the risk of the body's hormone system being suppressed by this drug, and the increased risk of getting infections.

How Pred Mild works in the body

Corticosteroids reduce inflammation by limiting blood vessel widening and white blood cell movement. They also change gene expression in the body, inhibiting the formation of molecules related to inflammation and activating molecules that fight it. Low doses of corticosteroids help reduce inflammation, while higher doses weaken the immune system. Extended use of high doses of these drugs can also raise sodium levels and decrease potassium levels in the body.

When to interrupt dosage

The proposed measure of Pred Mild is contingent upon the diagnosed condition, such as Ocular Infections, Irritations and Inflammations, Ocular Inflammation and Inflammatory Conditions. The amount of dosage varies as indicated by the mode of administration (e.g. Ophthalmic or Solution / drops - Ophthalmic) noted in the table beneath.

Condition

Dosage

Administration

Conjunctivitis

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops - Ophthalmic, Suspension / drops, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ophthalmic; Topical, Ointment - Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit, Kit - Ophthalmic

Conjunctivitis

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops - Ophthalmic, Suspension / drops, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ophthalmic; Topical, Ointment - Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit, Kit - Ophthalmic

Ocular Infections, Irritations and Inflammations

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops - Ophthalmic, Suspension / drops, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ophthalmic; Topical, Ointment - Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit, Kit - Ophthalmic

Organ Transplantation

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops - Ophthalmic, Suspension / drops, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ophthalmic; Topical, Ointment - Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit, Kit - Ophthalmic

Eye Infections, Bacterial

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops - Ophthalmic, Suspension / drops, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ophthalmic; Topical, Ointment - Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit, Kit - Ophthalmic

Inflammation

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops - Ophthalmic, Suspension / drops, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ophthalmic; Topical, Ointment - Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit, Kit - Ophthalmic

Inflammatory Conditions

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops - Ophthalmic, Suspension / drops, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ophthalmic; Topical, Ointment - Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit, Kit - Ophthalmic

Warnings

Pred Mild has one contraindication and therefore should not be taken with any of the conditions detailed in the table below.

Pred Mild Contraindications

Condition

Risk Level

Notes

Severe Hypersensitivity Reactions

Do Not Combine

Prednisolone Acetate may interact with Pulse Frequency

There are 20 known major drug interactions with Pred Mild.

Common Pred Mild Drug Interactions

Drug Name

Risk Level

Description

Abemaciclib

Major

The metabolism of Abemaciclib can be increased when combined with Prednisolone acetate.

Acalabrutinib

Major

The metabolism of Acalabrutinib can be increased when combined with Prednisolone acetate.

Alectinib

Major

The metabolism of Alectinib can be increased when combined with Prednisolone acetate.

Alpelisib

Major

The metabolism of Alpelisib can be increased when combined with Prednisolone acetate.

Aminophylline

Major

The metabolism of Aminophylline can be increased when combined with Prednisolone acetate.

Pred Mild Toxicity & Overdose Risk

The most toxic dose of prednisolone acetate in mice is 1680mg/kg. If someone has taken too much prednisolone acetate orally, they may experience more serious side effects than usual. To treat an overdose, the stomach can be emptied or the patient can be made to vomit if it was taken recently, and other treatments to ease the symptoms may be used. Taking too much of this drug through the eyes is not likely to cause harm.

Pred Mild Novel Uses: Which Conditions Have a Clinical Trial Featuring Pred Mild?

At present, there are 189 active trials assessing the potential of Pred Mild to reduce Inflammation, Inflammatory Conditions and Superficial Ocular Infections.

Condition

Clinical Trials

Trial Phases

Inflammation

50 Actively Recruiting

Not Applicable, Phase 1, Phase 2, Early Phase 1, Phase 3

Conjunctivitis

0 Actively Recruiting

Eye Infections, Bacterial

0 Actively Recruiting

Ocular Infections, Irritations and Inflammations

0 Actively Recruiting

Conjunctivitis

0 Actively Recruiting

Organ Transplantation

0 Actively Recruiting

Inflammatory Conditions

1 Actively Recruiting

Phase 2

Pred Mild Reviews: What are patients saying about Pred Mild?

4.7

Patient Review

1/28/2010

Pred Mild for Allergic Conjunctivitis

I was suffering for over a week with red, swollen, and itchy eyes. The doctor prescribed Patanol, which worked for maybe a day. I went back and he prescribed Pred Mild. I can't tell you how good it felt after the first treatment. It stings just a bit since it goes onto raw skin but OH how good it felt NOT to itch!
image of drug pills surrounding a glass of water symbolizing drug consumption

Patient Q&A Section about pred mild

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is pred mild eye drops used for?

"This medication is used to treat certain eye conditions caused by inflammation or injury. By relieving symptoms such as swelling, redness, and itching, Prednisolone belongs to a class of drugs known as corticosteroids."

Answered by AI

Is Pred Mild still available?

"There is not an equivalent medication to Pred Mild available in the United States at this time. Warning: There are fake online pharmacies that may try and sell a generic version of Pred Mild that is not legal. These could be counterfeit medications and could be dangerous."

Answered by AI

What is Pred good for?

"This medicine is a corticosteroid (cortisone-like medicine or steroid) that is available only with a doctor's prescription. It works by reducing swelling, redness, and itchiness caused by allergies."

Answered by AI

Is pred mild a steroid?

"Pred Mild is a steroid medicine that is used to treat eye inflammation. The conditions that it can be used for include allergies, severe acne, shingles, eye injury, and chemical burns. It can also be used for other conditions that are not listed in this guide."

Answered by AI

Clinical Trials for Pred Mild

Image of Exercise and Performance Nutrition Laboratory in Saint Charles, United States.

Multi-Strain Postbiotic for Inflammation and Gastrointestinal Symptoms

18 - 55
All Sexes
Saint Charles, MO

This study will evaluate the effects of a multi-strain postbiotic supplement on markers of inflammation, immune function, gastrointestinal symptoms, psychological well-being, and intestinal permeability in healthy adults. The primary objective is to determine whether four weeks of postbiotic supplementation alters physiological and perceptual responses to a standardized bout of moderate-to-high intensity exercise compared with placebo. Approximately 50 healthy men and women aged 18 to 55 years will be enrolled in a randomized, double-blind, placebo-controlled, parallel-group clinical trial. Participants will be randomly assigned to receive either a multi-strain postbiotic supplement or a matched placebo for 28 days. At the end of the supplementation period, participants will complete a 45-minute treadmill exercise bout at 75% of their individually determined maximum heart rate. Blood samples will be collected to assess biomarkers of inflammation, immune activity, and recovery. Gastrointestinal symptoms, intestinal permeability, anxiety, and perceived recovery will be evaluated using validated questionnaires. This study is designed to determine whether postbiotic supplementation modulates physiological stress responses and subjective well-being following prolonged exercise in healthy adults.

Waitlist Available
Paid Trial

Exercise and Performance Nutrition Laboratory

Chad M Kerksick, PhD

Image of ATX Hyperbarics in Austin, United States.

Hyperbaric Oxygen Therapy for Cardiovascular Fitness

30 - 60
All Sexes
Austin, TX

The purpose of this study is to determine whether hyperbaric oxygen therapy (HBOT) at 1.75 atmospheres of pressure (ATA) improves cardiovascular fitness (VO₂ max) and reduces inflammation in healthy adults. HBOT involves breathing pure oxygen in a pressurized chamber and is considered investigational for this use. Recent research has shown that different HBOT pressures can have different effects on inflammation. Specifically, some inflammatory cytokines (measurable markers of inflammation in the body) appear to decrease at low pressures like 1.3 ATA, while a different set of cytokines responds better at higher pressures, such as 2.0 ATA. Cytokines are small proteins that play a crucial role in cell signaling, particularly within the immune system. They help regulate inflammation, infection response, and overall immune function. While some cytokines promote inflammation to fight off threats, others help reduce inflammation when it's no longer needed. An imbalance in cytokines - especially excessive inflammatory cytokines - can contribute to chronic inflammation, cardiovascular disease, and other health issues. In this study, we are testing an intermediate pressure - 1.75 ATA - to see if we can target both sets of cytokines at once. If successful, this approach could offer broader anti-inflammatory benefits. We are also interested in how this intermediate pressure may improve VO₂ max, a key indicator of cardiovascular fitness. Since VO₂ max is strongly linked to heart health and overall longevity, finding a safe and effective way to improve it has meaningful implications not just for athletes, but for anyone looking to enhance their fitness and well-being.

Recruiting
Has No Placebo

ATX Hyperbarics (+1 Sites)

Image of University of New Brunswick in Fredericton, Canada.

Mediterranean Diet for Toddler Health

24 - 36
All Sexes
Fredericton, Canada

Toddlerhood (ages 2-3) is a critical window when the gut microbiome is still developing and eating habits are being established. Yet, many Canadian toddlers eat diets high in sugar and salt, which may affect long-term health. This study will test whether a MED diet can improve dietary inflammation, gut health, and body composition in toddlers and whether a tailored nutrition education program for parents can help families maintain healthy eating patterns. In this study, toddlers will be randomly assigned to a 3-week MED diet or their usual diet. Families in the MED diet group will receive free meal boxes for the 3 weeks, plus guidance from a nutrition researcher through a structured education program. The standard diet group will continue their regular diet with general nutrition advice. Researchers will collect dietary information, body composition assessments, and stool samples to measure gut microbiome composition and metabolites. This first study of a controlled diet intervention in toddlers, combining behavioral support, high-quality food provision, and advanced gut microbiome analysis, will help understand how early diet shapes lifelong eating habits and health, guiding public health strategies and precision nutrition approaches to prevent chronic disease from early life.

Waitlist Available
Has No Placebo

University of New Brunswick

Dr. Maryam Kebbe, PhD, CLC

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Image of UConn Health in Farmington, United States.

Cognitive Remediation for Memory and Thinking Difficulties

18+
All Sexes
Farmington, CT

The goal of this clinical trial is to determine if a neuroscience-based computerized cognitive remediation ("brain training") program can treat neurocognitive dysfunction (i.e., memory or thinking difficulties) that emerges in some older adults following a viral infection. The main questions it aims to answer are: * Does computerized cognitive remediation improve cognitive performance and day-to-day functioning in older adults with postviral neurocognitive dysfunction? * Will treatment effects be maintained over time, leading to better long term cognitive outcomes? * Does the treatment lead to reductions in blood-based markers of inflammation as a potential mechanism of cognitive symptom improvement? * Can the treatment be optimized and refined based on feedback from participants to improve user (patient) experience? Researchers will compare the computerized cognitive remediation program to an active computer-based control condition (alternative computer activities) to see if the computerized cognitive remediation program works to treat postviral neurocognitive dysfunction. Participation takes approximately 43-48 hours over 7 months, with most activities (40-46 hours) completed within the first 7-8 weeks, including: * Initial intake visit: Eligibility confirmation (\~2-3 hours) * Computer activities: About 5 hours per week for \~6 weeks (total \~30 hours) completed on a computer tablet provided by the study and loaned to participants for use during the treatment phase * Weekly remote check-in meetings: \~30 minutes each during treatment * Blood draws: Two sessions (before and after treatment), \~20-30 minutes each * Three research visits: Pre-treatment, post-treatment, and 6-month follow-up (\~2-3 hours each, including assessments of cognitive, emotional, and daily functioning)

Recruiting
Has No Placebo

UConn Health

Cutter Lindbergh, Ph.D.

Image of Department of Nutritional Sciences in Storrs, United States.

Freeze-dried Grape Powder for Healthy Aging

50 - 75
All Sexes
Storrs, CT

The purpose of this study is to investigate the effects of consuming grape powder on immune profiles in healthy middle- and older-aged individuals. Specifically, the investigators are interested in evaluating the potential effects of grapes in influencing markers of immune function, inflammation, and metabolism that are known to change with aging. Grapes contain several nutrients and antioxidant polyphenols such as resveratrol, quercetin, vitamin K and fiber, which are known to promote heart and immune health. However, the effects of grapes on altering immune profiles within the context of aging is not well understood. Therefore, this study will explore how daily grape consumption impacts certain markers of immunity in healthy middle- and older-aged adults. The main study procedures include consumption of a freeze-dried grape powder and control powder (which tastes the same but has none of the grape compounds that are being studied) mixed with water as a beverage on a daily basis for 4 weeks each. The investigators will additionally ask that participants avoid eating grapes and certain other antioxidant/grape-related foods and beverages throughout the 13-week study. Participants will additionally be asked to complete surveys about their diet, physical activity, and medical history, as well as provide blood samples and body weight measures throughout the course of the study. Participation in the study is expected to last about 6.25 hours over the course of 13 weeks and will include 7 visits.

Recruiting
Paid Trial

Department of Nutritional Sciences

Image of Abcentra Investigational Site in Los Angeles, United States.

Orticumab for Heart Attack

18+
All Sexes
Los Angeles, CA

The goal of this clinical trial is to determine the clinical effect of orticumab treatment on inflammation in study participants with prior myocardial infarction who have elevated coronary inflammation based on CCTA. The main question it aims to answer is: Clinical effects of orticumab treatment on inflammation of the coronary artery parameters measured with CCTA Researchers will compare the effects with placebo group after 6 months of treatment Participants will Keep the planned study visit appointments Provide complete information about medical and medical history Speak to the study doctor before changing any of non-study treatments, including starting new medications, receiving any vaccinations, or setting out to join any other clinical studies

Phase 2
Recruiting

Abcentra Investigational Site (+6 Sites)

Abcentra

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Image of University of California, San Diego Altman Clinical and Translational Research Institute in San Diego, United States.

Mediterranean Diet for Inflammation Post-Colonoscopy

18+
All Sexes
San Diego, CA

This study aims to investigate the impact of various healthy diets, specifically a modified plant-based Mediterranean diet, on the gut microbiome and overall well-being post-colonoscopy. The investigators hypothesize that certain diets can positively influence gut bacteria, reducing inflammation and enhancing metabolic signals. To explore this, they will utilize metagenomic testing on stool samples to analyze the DNA of gut microorganisms. Additionally, they will conduct immune profiling on serum samples and perform metabolomic analysis to comprehensively evaluate the diet-induced changes in immune response and metabolic pathways. This multi-faceted approach will help them understand how dietary changes affect the composition and function of the gut microbiome, immune function, and overall metabolism.

Waitlist Available
Has No Placebo

University of California, San Diego Altman Clinical and Translational Research Institute

Image of Montana State University in Bozeman, United States.

Haskap Berries for Gut Health

35 - 65
All Sexes
Bozeman, MT

Polyphenol-rich Haskap berries (Haskap) have untapped therapeutic potential to improve human health, and agricultural producers in northern U.S. states are poised to increase production if consumer demand increases. A critical knowledge gap is that little is known about the interactions between gut microbes and Haskap polyphenols to produce bioactive metabolites linked to downstream health impacts. Additionally, little is known about which Haskap varieties and harvest timing yield the greatest bioactive potential. This study aims to address these gaps by investigating the interaction of bioactive components in Haskap with gut microbiota and the resultant gut and serum metabolites, inflammation, and metabolic health, and then couple this with analysis of berries from different Haskap varieties and harvest times.

Recruiting
Paid Trial

Montana State University

Mary P Miles, PhD

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