Bausch Health(BHC)

Focus: Bausch Health is a $8.8B revenue public pharmaceutical company headquartered in Quebec with a portfolio spanning immunology, gastroenterology, neurology, cardiovascular, and infectious diseases. The company is heavily concentrated on small molecule assets with a concerning dependency on legacy products.

Immunology Gastroenterology Neurology Cardiovascular

Profile data last refreshed 19h ago · AI intelligence enriched 2w ago

Funding Stage

PUBLIC

Open Jobs

About Bausch Health

AI assessmentNot Hiring

No open roles listed right now. Follow Bausch Health to get notified when they start hiring — the background below is worth knowing for when they do.

Why Work Here

Data completeness

6/9 — Partial

Company HealthStrong

Pipeline

Early-stage

50 total

LOE Risk

3 in 5yr

OSMOPREP

Hiring

Stable

Revenue

$8.8B

FY2025

Key Products

XIFAXAN

Hepatic Encephalopathy, Travelers' Diarrhea

$1.1B

LOE Approaching

Backbone of Bausch Health's revenue; loss of exclusivity will trigger catastrophic revenue erosion absent pipeline success.

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Data Sources

Drug label: DailyMed / FDA
Clinical trials: ClinicalTrials.gov
Patent data: FDA Orange Book
Spending data: CMS Medicare

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.

Pipeline & Clinical Trials

REVIVE Contact Lens

Refractive Ametropia

N/A

Clinical Trials (1)

NCT060537361-Week Dispensing Evaluation of REVIVE™ Toric Soft Contact Lenses

N/A

Senofilcon C

Myopia

N/A

Clinical Trials (1)

NCT03351101Clinical Study of Approved Contact Lenses

N/A

Redesigned Purevision Contact Lens

Myopia

N/A

Clinical Trials (1)

NCT01118338Evaluation of Two Different Designs of Bausch & Lomb Contact Lenses

N/A

B&L RD2135-01 lens C

Myopia

N/A

Clinical Trials (1)

NCT01583868A Study to Evaluate the Product Feasibility of Two New Silicone Hydrogel Contact Lenses

N/A

Bausch & Lomb Multi-Purpose Solution

Contact Lens Solutions

N/A

Clinical Trials (1)

NCT00710879Evaluation of a Multi-Purpose Solution

N/A

ZenLens™

Keratoconus

N/A

Clinical Trials (1)

NCT03249233Corneal Thickness Changes With Scleral Contact Lenses

N/A

imiquimod

Mycosis Fungoides

N/A

Clinical Trials (2)

NCT03914417Genomic Markers Before and After Treatment of Actinic Keratosis With Imiquimod 3.75% Cream

Phase 2

NCT02301494Effectiveness of Imiquimod Topical Cream in Early Stage Cutaneous T-cell Lymphoma

N/A

REVIVE samfilcon B custom toric contact lenses

Astigmatism

N/A

Clinical Trials (1)

NCT06785194Revive Toric RWE Study

N/A

Bausch & Lomb Multipurpose Solution - Rub Care

Contact Lens Solutions

N/A

Clinical Trials (1)

NCT00636363Safety and Efficacy of a Bausch & Lomb Multipurpose Solution When Compared to Ciba Vision Aquify Multipurpose Solution

N/A

Technolas® TENEO 317 Model 2

Myopia

N/A

Clinical Trials (1)

NCT04111757A Study With Technolas® TENEO 317 Model 2 Excimer Laser to Treat Participants With Myopia or Myopic Astigmatism

N/A

Bausch & Lomb contact lens

Myopia

N/A

Clinical Trials (1)

NCT01130974A Study to Assess the Safety and Efficacy of a Daily Disposable Contact Lens

N/A

B&L Investigational Contact Lens

Myopia

N/A

Clinical Trials (1)

NCT01449526A Study to Evaluate the Safety and Efficacy of a New Silicone Hydrogel Contact Lens Design

N/A

BCMC lens

Myopia

N/A

Clinical Trials (1)

NCT07511387Efficacy of a Novel Myopia Defocus Spectacle Lens in School-Aged Children

N/A

Efudex

Photo-aging

N/A

Clinical Trials (1)

NCT00121511The Effect of Efudex Treatment on Photoaged Skin

N/A

Thermage FLX

Facial Skin Laxity

N/A

Clinical Trials (1)

NCT03894371Thermage FLX System to Treat the Face, Neck, and Eyelids

N/A

salix probiotic blend

Functional Gastrointestinal Disorders

N/A

Clinical Trials (1)

NCT04155801A Study to Assess the Efficacy and Safety of Salix Probiotic Blend in Participants With Functional Gastrointestinal Disturbances

N/A

Fipamezole ODT

Parkinson's Disease

N/A

Clinical Trials (1)

NCT01140841A Study of Safety and Tolerability of Fipamezole in Adult Subjects With Parkinson's Disease Who Are Receiving Levodopa

N/A

new silicone hydrogel daily disposable multifocal contact lens, the Bausch + Lomb

Myopia and Hyperopia and Presbyopia

N/A

Clinical Trials (1)

NCT05660577Evaluation of Product Performance of a New Silicone Hydrogel Multifocal Contact Lens

N/A

Comparing Two Different Ways to Take MoviPrep® Before Colonoscopy

Colonoscopy

N/A

Clinical Trials (1)

NCT00929916Comparing Two Different Ways to Take MoviPrep® Before Colonoscopy

N/A

samfilcon A Lenses with EPG01 Packaging Solution

Contact Lens Wearer

N/A

Clinical Trials (1)

NCT051269532-Hour Dispensing Evaluation of Samfilcon A Lenses With EPG01 Packaging Solution Compared to Commercially Available B+L Ultra Lenses

N/A

IC-8 Apthera IOL New Enrollment Post Approval Study

Cataract

N/A

Clinical Trials (1)

NCT06060041IC-8 Apthera IOL New Enrollment Post Approval Study

N/A

Artelac Rebalance

Dry Eye

N/A

Clinical Trials (1)

NCT01791426A Study to Evaluate the Performance and Safety of Artelac Rebalance® Versus Vismed in the Management of Dry Eye

N/A

Pimecrolimus

Atopic Dermatitis

N/A

Clinical Trials (1)

NCT0056899710 Year Registry of Children (Ages 2-17 Years) With Eczema That Have Used Pimecrolimus

N/A

pergolide

Parkinson Disease

N/A

Clinical Trials (1)

NCT00624741Compassionate Use Study of Pergolide in Patients With Parkinson's Disease

N/A

PEG-SD

Hyponatremia

N/A

Clinical Trials (1)

NCT01299779Incidence of Hyponatremia in PEG-SD Compared to PEG-ELS

N/A

LD127025 MF

Presbyopia

N/A

Clinical Trials (1)

NCT01959178A Study to Evaluate a Mid Add Multi-Focal Soft Contact Lens

N/A

dihydroergotamine mesylate

Migraine

N/A

Clinical Trials (1)

NCT00203268A Study Examining the Use of a Migraine Medicine in the Treatment of Two Migraine Attacks in Patients Who Have Increased Skin Sensitivity

N/A

BL-300-PFM04

Contact Lens Wear

N/A

Clinical Trials (1)

NCT04175340A Safety and Effectiveness Study of a New Preservative Free Rewetting Drop

N/A

Administration of Lotemax

Sjogren's Disease

N/A

Clinical Trials (1)

NCT02322528Evaluation of Ocular Surface Inflammatory Mediators Effected by Lotemax

N/A

Dental exam and periodontal cleaning if needed

Cirrhosis

N/A

Clinical Trials (1)

NCT06052150Oral Health In Cirrhosis of the Liver (ORACLE)

N/A

Xiidra

Glaucoma

N/A

Clinical Trials (1)

NCT04354545Treatment of Ocular Discomfort in Glaucoma Patients Using Multiple Topical Medications

N/A

Retisert

Uveitis, Posterior

N/A

Clinical Trials (1)

NCT03145025Corneal Endothelial Cell Density in Eyes Treated With a Fluocinolone Acetonide Intravitreal Implant

N/A

ISTA Tears

Dry Eye Disease

N/A

Clinical Trials (1)

NCT01650584Evaluation of Ocular Comfort With ISTA Tears vs Systane

N/A

clindamycin phosphate/adapalene/benzoyl peroxide

Acne Vulgaris

N/A

A Patient Reported Ocular Comfort Assessment Comparing Bepreve to Lastacaft

Allergic Conjunctivitis

N/A

Clinical Trials (1)

NCT01339507A Patient Reported Ocular Comfort Assessment Comparing Bepreve to Lastacaft

N/A

Prolensa

Cataract

N/A

Clinical Trials (1)

NCT01847638Prolensa (Bromfenac) 0.07% QD vs. Ilevro (Nepafenac) 0.3% QD for Treatment of Ocular Inflammation Post Cataract Surgery

N/A

No Intervention

Neovascular Age-Related Macular Degeneration

N/A

Clinical Trials (1)

NCT02367365Neovascular Morphology and Persistent Disease Activity Among Patients With NV AMD

N/A

ABT12 Multi-Purpose Solution

Contact Lens Wear

N/A

Clinical Trials (1)

NCT03897751A Safety and Effectiveness Study of BL-ABT12 Multi-Purpose Solution for Use by Participants With Soft Contact Lenses

N/A

Fraxel® FTX Laser System

Skin Resurfacing

N/A

Clinical Trials (1)

NCT07214272A Phase 4 Clinical Study to Investigate the Effectiveness and Safety of Skin Resurfacing

N/A

Aflibercept

Neovascular Age-related Macular Degeneration

N/A

Clinical Trials (1)

NCT02457026Adjunctive Photodynamic Therapy + Aflibercept vs. Afilbercept Alone for PDA in NV AMD

N/A

No Intervention

Neovascular Age-related Macular Degeneration

N/A

Clinical Trials (1)

NCT02452840Photodynamic Therapy for PDA in NV AMD

N/A

Once a day Trientine

Wilson Disease

N/A

Clinical Trials (1)

NCT01472874Single Daily Dosage of Trientine for Maintenance Treatment for Wilson Disease

N/A

Evaluation of the Bausch & Lomb PureVision Under Nighttime Driving Conditions

Astigmatism

N/A

Clinical Trials (1)

NCT00581659Evaluation of the Bausch & Lomb PureVision Under Nighttime Driving Conditions

N/A

kalifilcon A lenses

Habitual Soft Contact Lens Use

N/A

Clinical Trials (1)

NCT04555031Evaluation of Surface Refractive Index Shift of Kalifilcon A Lenses Compared to Dailies Total 1, Precision 1 and Biotrue ONEday Lenses

N/A

Fipamezole ODT

Parkinson's Disease

N/A

Clinical Trials (1)

NCT01149811A Study Comparing the Safety and Tolerability of Two Doses of Fipamezole in Adult Patients With Parkinson's Disease

N/A

Methylnaltrexone

Opioid-induced Constipation

N/A

Clinical Trials (1)

NCT01368562Compassionate Use Study of Methylnaltrexone

N/A

clindamycin phosphate, adapalene and benzoyl peroxide

Acne Vulgaris

N/A

Clinical Trials (1)

NCT07205107Clindamycin Phosphate, Adapalene, and Benzoyl Peroxide Triple Combination Gel in Canadian Patients With Acne Vulgaris

N/A

corneas assigned by donor age group

Corneal Disease

N/A

Clinical Trials (1)

NCT00006411Cornea Donor Study

N/A

Fluocinolone Acetonide 0.59 mg

Inflammation

N/A

Clinical Trials (1)

NCT01060787Evaluation of Corneal Endothelial Cell Density in Subjects Who Have Had a Fluocinolone Acetonide Implant

N/A

enVista MX60E

Cataract

N/A

Clinical Trials (1)

NCT03603600Evaluate the Safety and Effectiveness of the enVista® One-Piece Hydrophobic Acrylic Trifocal Intraocular Lens

N/A

CLINICAL PHARMACOLOGY Bumex is a loop diuretic with a rapid onset and short duration of action. Pharmacological and clinical studies have shown that 1 mg Bumex has a diuretic potency equivalent to approximately 40 mg furosemide. The major site of Bumex action is the ascending limb of the loop of Henle. The mode of action has been determined through various clearance studies in both humans and experimental animals. Bumex inhibits sodium reabsorption in the ascending limb of the loop of Henle, as shown by marked reduction of free-water clearance (CH 2 O) during hydration and tubular free-water reabsorption (T H 2 O) during hydropenia. Reabsorption of chloride in the ascending limb is also blocked by Bumex, and Bumex is somewhat more chloruretic than natriuretic. Potassium excretion is also increased by Bumex, in a dose-related fashion. Bumex may have an additional action in the proximal tubule. Since phosphate reabsorption takes place largely in the proximal tubule, phosphaturia during Bumex induced diuresis is indicative of this additional action. This is further supported by the reduction in the renal clearance of Bumex by probenecid, associated with diminution in the natriuretic response. This proximal tubular activity does not seem to be related to an inhibition of carbonic anhydrase. Bumex does not appear to have a noticeable action on the distal tubule. Bumex decreases uric acid excretion and increases serum uric acid. Following oral administration of Bumex the onset of diuresis occurs in 30 to 60 minutes. Peak activity is reached between 1 and 2 hours. At usual doses (1 mg to 2 mg) diuresis is largely complete within 4 hours; with higher doses, the diuretic action lasts for 4 to 6 hours. Diuresis starts within minutes following an intravenous injection and reaches maximum levels within 15 to 30 minutes. Several pharmacokinetic studies have shown that bumetanide, administered orally or parenterally, is eliminated rapidly in humans, with a half-life of between 1 and 1½ hours. Plasma protein-binding is in the range of 94% to 96%. Oral administration of carbon-14 labeled Bumex to human volunteers revealed that 81% of the administered radioactivity was excreted in the urine, 45% of it as unchanged drug. Urinary and biliary metabolites identified in this study were formed by oxidation of the N-butyl side chain. Biliary excretion of Bumex amounted to only 2% of the administered dose. Pediatric Pharmacology Elimination of bumetanide appears to be considerably slower in neonatal patients compared with adults, possibly because of immature renal and hepatobiliary function in this population. Small pharmacokinetic studies of intravenous bumetanide in preterm and full-term neonates with respiratory disorders have reported an apparent half-life of approximately 6 hours, with a range up to 15 hours and a serum clearance ranging from 0.2 mL/min/kg to 1.1 mL/min/kg. In a population of neonates receiving bumetanide for volume overload, mean serum clearance ra

Bausch Health(BHC)

About Bausch Health

Why Work Here

Key Products

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Pipeline & Clinical Trials

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Financials (FY2025)

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