Timosan: Uses, Dosage & Side Effects
A non-selective beta-blocker eye drop used to lower intraocular pressure in chronic open-angle glaucoma and ocular hypertension
Timosan (timolol maleate) is a prescription eye drop belonging to the class of non-selective beta-adrenergic receptor blocking agents (beta-blockers). It is one of the most widely prescribed first-line treatments for lowering elevated intraocular pressure (IOP) in patients with chronic open-angle glaucoma or ocular hypertension. Timosan works by reducing the production of aqueous humor in the eye. It is typically administered as one drop once daily and may be used alone or in combination with other IOP-lowering medications such as prostaglandin analogs, alpha-2 agonists, or carbonic anhydrase inhibitors.
Quick Facts: Timosan
Key Takeaways
- Timosan (timolol) is a first-line beta-blocker eye drop that lowers intraocular pressure by reducing aqueous humor production, typically achieving a 20–35% IOP reduction from baseline.
- The recommended dose is one drop once daily in the affected eye(s). Nasolacrimal occlusion (pressing the inner eye corner for 2 minutes) after application is essential to reduce systemic absorption.
- Timosan is contraindicated in patients with asthma, severe COPD, sinus bradycardia, heart block, or overt cardiac failure due to systemic beta-blockade effects.
- Common side effects include eye irritation and blurred vision. Systemic beta-blocker effects (slow heart rate, low blood pressure, bronchospasm) can occur even with topical use.
- Remove contact lenses before application and wait at least 30 minutes before reinserting due to the benzalkonium chloride preservative.
What Is Timosan and What Is It Used For?
Timosan contains the active substance timolol maleate, which belongs to a pharmacological class known as non-selective beta-adrenergic receptor blocking agents (beta-blockers). When applied topically to the eye, timolol reduces intraocular pressure (IOP) by decreasing the rate at which aqueous humor—the clear fluid that fills the anterior chamber of the eye—is produced by the ciliary body. Elevated IOP is the primary modifiable risk factor for glaucoma, a group of progressive optic neuropathies that can lead to irreversible blindness if left untreated.
Timolol was first approved for ophthalmic use in 1978 and quickly became the gold standard for medical glaucoma therapy. It remains one of the most extensively studied and widely prescribed IOP-lowering agents worldwide. The World Health Organization (WHO) includes timolol on its Model List of Essential Medicines, recognizing it as one of the most efficacious, safe, and cost-effective medicines needed in a health system. Timosan is manufactured by Santen Oy, a pharmaceutical company specializing in ophthalmic products.
The drug works through a well-characterized mechanism. By blocking beta-1 and beta-2 adrenergic receptors on the ciliary epithelium, timolol reduces the formation and secretion of aqueous humor. This typically produces a 20–35% reduction in IOP from baseline, with onset of action within approximately 30 minutes, peak effect at 1–2 hours, and a duration of approximately 24 hours. This pharmacokinetic profile allows for convenient once-daily dosing with the long-acting formulation.
Timosan is indicated for the treatment of two primary conditions:
- Chronic open-angle glaucoma — The most common form of glaucoma worldwide, affecting approximately 3.5% of people over 40 years of age. It is characterized by a gradual increase in intraocular pressure due to impaired drainage of aqueous humor through the trabecular meshwork, leading to progressive optic nerve damage and visual field loss. Open-angle glaucoma is often called the “silent thief of sight” because it typically causes no symptoms until significant irreversible damage has occurred.
- Ocular hypertension — A condition defined by an intraocular pressure consistently above 21 mmHg without detectable optic nerve damage or visual field loss. Although not all patients with ocular hypertension develop glaucoma, the condition represents a significant risk factor. The Ocular Hypertension Treatment Study (OHTS) demonstrated that reducing IOP in patients with ocular hypertension reduces the risk of developing glaucoma by approximately 50%.
Timosan may be prescribed as a first-line monotherapy or as part of a multi-drug regimen. According to the European Glaucoma Society (EGS) guidelines and the American Academy of Ophthalmology (AAO) Preferred Practice Patterns, the target IOP should be individualized based on the severity of glaucoma, the rate of disease progression, risk factors, and the patient’s life expectancy. While prostaglandin analogs have largely replaced beta-blockers as the most commonly prescribed first-line agents in some markets, timolol remains an excellent choice—particularly when cost is a consideration, when prostaglandins are not tolerated, or as adjunctive therapy in combination with other drug classes.
What Should You Know Before Using Timosan?
Before starting treatment with Timosan, it is essential to have a thorough discussion with your ophthalmologist or prescribing physician about your complete medical history, current medications, and any known allergies. Although timolol is applied topically to the eye, it can be absorbed into the bloodstream through the conjunctival vasculature and nasolacrimal duct, potentially causing systemic beta-blockade effects that affect the heart, lungs, and metabolic systems.
Contraindications
- You are allergic (hypersensitive) to timolol, other beta-blockers, or any other ingredient in Timosan (see “What Does Timosan Contain?” section below)
- You have or have ever had bronchial asthma or a history of asthma
- You have severe chronic obstructive pulmonary disease (COPD) that could cause wheezing, breathing difficulties, or long-lasting cough
- You have a slow heart rate (sinus bradycardia)
- You have heart failure or heart rhythm disturbances (second or third degree atrioventricular block)
Warnings and Precautions
Talk to your doctor before using Timosan if you have or have previously had any of the following conditions, as they may require additional monitoring, dose adjustment, or consideration of an alternative therapy:
- Coronary artery disease — Symptoms such as chest pain, tightness in the chest, or shortness of breath. Timolol may reduce heart rate and cardiac output, which could exacerbate ischemic symptoms.
- Low blood pressure — Beta-blockers can cause further blood pressure reduction, particularly when combined with other antihypertensive medications.
- Heart rhythm disorders — Including slow heart rate or irregular heartbeat not severe enough to contraindicate use, but requiring monitoring.
- Respiratory problems or mild COPD — Even non-selective topical beta-blockers can cause bronchospasm in susceptible individuals. Patients with mild-to-moderate airways disease should be closely monitored.
- Peripheral circulatory disorders — Such as Raynaud’s disease or Raynaud’s syndrome. Beta-blockers can worsen peripheral vasoconstriction and reduce blood flow to the extremities.
- Diabetes mellitus — Timolol can mask the signs and symptoms of hypoglycemia (low blood sugar), particularly tachycardia, palpitations, and tremor. This is especially important for patients on insulin or oral hypoglycemic agents who may be at risk of hypoglycemic episodes.
- Overactive thyroid (hyperthyroidism) — Timolol can mask the cardiovascular signs of thyrotoxicosis, such as rapid heart rate. Abrupt withdrawal of beta-blockers may precipitate a thyroid storm.
- Atopy or history of severe allergic reactions (anaphylaxis) — Beta-blockers can increase the severity of anaphylactic reactions and reduce the effectiveness of epinephrine (adrenaline) used to treat them. This is a particularly important consideration for patients who carry epinephrine auto-injectors.
- Corneal disease — Beta-blockers may cause dry eyes. Patients with pre-existing corneal conditions should be monitored for signs of corneal deterioration.
If you are scheduled for any surgical procedure, including dental surgery, inform your anesthesiologist and surgeon that you are using Timosan. Timolol may interact with anesthetic agents, potentially causing exaggerated hypotension or bradycardia. Your doctor will advise whether to continue or temporarily discontinue Timosan before the procedure.
Use in Children
Timosan is not recommended for children due to the lack of adequate clinical experience in pediatric populations. The systemic effects of topical beta-blockers can be proportionally greater in children due to their smaller body mass, and serious adverse events including bradycardia, hypotension, and apnea have been reported with ophthalmic timolol in neonates and young children. If a child requires IOP-lowering treatment, the pediatric ophthalmologist will select an appropriate alternative.
Pregnancy and Breastfeeding
If you are pregnant, think you may be pregnant, or are planning to become pregnant, consult your doctor before using Timosan. Beta-blockers, including timolol, may cause harmful effects on the fetus when absorbed systemically, including fetal bradycardia, hypotension, and hypoglycemia. Timosan should not be used during pregnancy unless your doctor determines that the potential benefit clearly outweighs the potential risk to the fetus.
Breastfeeding: Timolol is excreted in human breast milk. Timosan should not be used while breastfeeding, as beta-blockers may cause serious adverse effects in nursing infants, including bradycardia and respiratory depression. If treatment with Timosan is necessary, breastfeeding should be discontinued. Discuss alternative feeding options with your doctor and midwife.
Driving and Operating Machinery
Timosan may cause transient blurred vision immediately after instillation. If you experience blurred vision or other visual disturbances after applying the eye drops, do not drive or operate machinery until your vision has cleared. You are responsible for assessing whether you are fit to perform activities that require sharp eyesight, concentration, and alertness.
Important Information About Contact Lenses
Timosan contains benzalkonium chloride (0.05 mg/ml) as a preservative. This compound can be absorbed by soft contact lenses and may cause lens discoloration. You should remove contact lenses before applying Timosan and wait at least 30 minutes before reinserting them. Benzalkonium chloride may also irritate the eyes, especially if you have dry eye syndrome or corneal problems. If you experience irritation, stinging, or pain after using Timosan, contact your doctor promptly.
How Does Timosan Interact with Other Drugs?
Drug interactions with Timosan can occur because timolol, despite being applied topically to the eye, is absorbed into the systemic circulation through the conjunctival blood vessels and the nasolacrimal duct. Once absorbed, it can interact with other medications that affect the cardiovascular, respiratory, and metabolic systems. The degree of systemic absorption can be reduced by applying nasolacrimal occlusion (pressing the inner corner of the eye for 2 minutes after instillation).
Always inform your doctor or pharmacist about all medications you are currently taking, have recently taken, or plan to take. This includes prescription drugs, over-the-counter medications, herbal supplements, and other eye drops.
| Interacting Drug/Class | Severity | Effect | Recommendation |
|---|---|---|---|
| Oral beta-blockers (metoprolol, atenolol, propranolol) | Major | Additive beta-blockade: excessive heart rate reduction, hypotension, and cardiac conduction abnormalities | Use with close cardiac monitoring. Monitor heart rate and blood pressure regularly. |
| Calcium channel blockers (verapamil, diltiazem) | Major | Enhanced cardiac depression: severe bradycardia, AV block, and heart failure exacerbation | Avoid combination with verapamil or diltiazem. Use dihydropyridines (amlodipine) with caution. |
| Antihypertensive agents (ACE inhibitors, ARBs, diuretics) | Moderate | Additive blood pressure reduction; increased risk of hypotension and dizziness | Monitor blood pressure. Adjust doses if necessary. |
| Quinidine | Moderate | Quinidine inhibits CYP2D6, increasing timolol plasma levels and enhancing beta-blockade | Use with caution. Monitor for increased beta-blocker side effects. |
| Fluoxetine, Paroxetine (SSRIs) | Moderate | CYP2D6 inhibition increases systemic timolol exposure, potentially enhancing cardiac and respiratory effects | Monitor heart rate and blood pressure when initiating or adjusting SSRI therapy. |
| Insulin and oral antidiabetics | Moderate | Timolol masks the warning signs of hypoglycemia (tachycardia, tremor) and may prolong hypoglycemic episodes | Diabetic patients should monitor blood glucose more frequently. Educate about non-adrenergic hypoglycemia symptoms (sweating, hunger). |
| Cardiac glycosides (digoxin) | Moderate | Additive slowing of heart rate and increased risk of AV conduction delay | Monitor heart rate and ECG. Adjust digoxin dose if needed. |
| Epinephrine (adrenaline) | Moderate | Beta-blockers can reduce the effectiveness of epinephrine used for anaphylaxis treatment | Patients at risk of anaphylaxis should discuss alternative IOP-lowering agents. |
| General anesthetics | Moderate | Enhanced cardiovascular depression during surgical procedures | Inform your anesthesiologist before any surgical procedure. |
When using Timosan together with other eye drops, allow an interval of at least 10 minutes between instillation of each medication. This prevents the second drop from washing out the first before adequate absorption has occurred. Eye drops should generally be applied before eye ointments or gels, as thicker formulations can create a barrier to absorption of subsequent drops.
What Is the Correct Dosage of Timosan?
Always use Timosan exactly as your doctor has instructed. If you are unsure about any aspect of your treatment, consult your ophthalmologist or pharmacist. Consistent adherence to the prescribed dosing schedule is essential for maintaining stable IOP control and preventing glaucoma progression. Studies have shown that non-adherence to glaucoma medications is a significant risk factor for disease progression.
Adults
Standard Adult Dosage
One drop of Timosan 0.5% (5 mg/ml) in the affected eye(s) once daily, preferably in the morning. The dose is determined by your doctor and individualized based on your IOP response and target pressure. If adequate IOP reduction is not achieved with Timosan alone, your doctor may add another IOP-lowering agent (such as a prostaglandin analog or carbonic anhydrase inhibitor) rather than increasing the timolol dose.
Children
Pediatric Use
Timosan is not recommended for children due to the lack of adequate clinical experience. The manufacturer states that clinical experience in pediatric populations is insufficient to establish dosing recommendations. Children are at higher risk for systemic beta-blocker side effects due to their lower body mass. If a child requires glaucoma treatment, a pediatric ophthalmologist will select an appropriate alternative.
Elderly Patients
Elderly (65 years and older)
No specific dose adjustment is required for elderly patients. However, older adults may be more susceptible to systemic beta-blocker effects, including bradycardia, hypotension, and bronchospasm. Particular care should be taken in elderly patients with cardiovascular disease, diabetes, or pulmonary conditions. Blood pressure and heart rate should be monitored, especially at the initiation of treatment.
How to Apply Timosan Eye Drops
Proper application technique is crucial for ensuring the medication reaches the eye effectively while minimizing systemic absorption and potential side effects. Follow these steps carefully:
- Wash your hands thoroughly before handling the eye drop bottle.
- Open the bottle carefully. Do not touch the tip of the dropper to any surface to avoid contamination.
- Tilt your head back and look upward. You may sit, lie down, or stand in front of a mirror—choose the position that is most comfortable for you.
- Gently pull down the lower eyelid to create a small pocket between the eyelid and the eye.
- Hold the bottle upside down above the eye and squeeze gently to release one drop into the pocket formed by the lower eyelid.
- Close your eye and press your finger gently against the inner corner of the eye (near the nose) for approximately 2 minutes. This technique (nasolacrimal occlusion) is critically important as it reduces the amount of timolol that enters the systemic circulation through the nasolacrimal duct, thereby minimizing cardiovascular and respiratory side effects.
- If the drop misses the eye, try again with a new drop.
- Replace and tighten the cap immediately after use. The eye drop bottle is for personal use only—do not share it with others.
If you are using other eye drops in addition to Timosan, wait at least 10 minutes between different eye drop medications to prevent one drug from washing out the other. Apply eye drops before eye ointments or gels. Store the Timosan bottle upside down for better dripping, as recommended by the manufacturer.
Missed Dose
If you forget to apply your daily dose, use it as soon as you remember. However, if it is nearly time for your next scheduled dose, skip the missed dose and continue with your regular dosing routine. Do not apply a double dose to compensate for a forgotten one. If you frequently forget doses, consider setting a daily alarm or keeping the bottle next to something you use every morning (such as a toothbrush) as a reminder.
Overdose
If you accidentally apply too many drops to your eye, rinse the eye with lukewarm tap water. Excessive topical application may enhance the known side effects of timolol, including bradycardia, hypotension, bronchospasm, and cardiac conduction abnormalities.
If someone, especially a child, accidentally swallows Timosan, seek emergency medical attention immediately. Oral ingestion of timolol can cause severe bradycardia, hypotension, bronchospasm, and cardiac arrest. Contact your doctor, hospital emergency department, or poison control center right away.
Stopping Treatment
Do not stop using Timosan without first consulting your doctor. Abrupt discontinuation of beta-blocker therapy may lead to a rebound increase in intraocular pressure, and in patients with cardiovascular conditions, sudden withdrawal of systemic beta-blockade can precipitate angina, arrhythmias, or myocardial infarction. If your doctor decides to switch you to a different IOP-lowering medication, the transition will typically be managed gradually.
What Are the Side Effects of Timosan?
Like all medicines, Timosan can cause side effects, although not everybody gets them. Because timolol is a beta-blocker that can be absorbed into the bloodstream even when applied as eye drops, side effects can occur both in the eye (local effects) and throughout the body (systemic effects). The systemic side effects are similar to those seen with oral beta-blockers, although they occur less frequently with ophthalmic administration.
Stop using Timosan and contact your doctor immediately if swelling occurs in the face, tongue, or throat, or if you develop hives, difficulty breathing, or difficulty swallowing. These symptoms may indicate a severe allergic reaction (angioedema/anaphylaxis) that requires emergency treatment.
Eye-Related Side Effects
Common
May affect up to 1 in 10 users
- Burning or stinging sensation in the eyes (eye irritation)
- Red eyes (conjunctival hyperemia)
- Blurred vision or visual disturbances
Uncommon
May affect up to 1 in 100 users
- Inflammation of the conjunctiva (conjunctivitis)
- Inflammation or damage to the cornea (keratitis)
- Dry eyes
- Foreign body sensation in the eye
Rare
May affect up to 1 in 1,000 users
- Decreased corneal sensitivity
Systemic (Whole-Body) Side Effects
Like other ophthalmic beta-blockers, timolol is absorbed into the bloodstream. The systemic side effects listed below have been reported with beta-blocker eye drops as a class. The frequency of these effects is generally lower than with oral beta-blockers, but they can be clinically significant, particularly in patients with pre-existing cardiovascular or respiratory conditions.
Uncommon
May affect up to 1 in 100 users
- Headache
- Dizziness
- Shortness of breath (dyspnea)
Reported with Ophthalmic Beta-blockers (Frequency Not Established)
Reported through post-marketing surveillance
- Immune system: Systemic allergic reactions including angioedema (swelling of face, arms, legs), urticaria (hives), localized or generalized rash, itching, anaphylaxis
- Metabolism: Low blood sugar (hypoglycemia)
- Nervous system: Insomnia, depression, nightmares, memory loss, confusion, hallucinations, fainting (syncope), stroke, worsening of myasthenia gravis, tingling or numbness (paresthesia)
- Eye: Stinging, itching, tearing, eyelid inflammation (blepharitis), detachment of the choroid after filtration surgery, drooping eyelid (ptosis), double vision, decreased tear production, corneal erosion, refractive changes
- Heart: Slow heart rate (bradycardia), chest pain, palpitations, edema, arrhythmias, congestive heart failure, heart block, cardiac arrest, heart attack
- Blood vessels: Low blood pressure (hypotension), Raynaud’s phenomenon, cold hands and feet
- Respiratory: Bronchospasm (especially in patients with pre-existing lung disease), cough, airway constriction
- Gastrointestinal: Taste disturbances, nausea, digestive problems, diarrhea, dry mouth, abdominal pain, vomiting
- Skin: Hair loss, psoriasis-like rash or worsening of psoriasis, other skin rashes
- Musculoskeletal: Muscle pain not related to exercise, muscle weakness, fatigue
- Reproductive: Sexual dysfunction, decreased libido, Peyronie’s disease
- Ear: Tinnitus (ringing in the ears)
The most effective way to reduce the risk of systemic side effects from Timosan is to perform nasolacrimal occlusion (pressing a finger on the inner corner of the eye for 2 minutes) immediately after applying the drop. This technique can reduce systemic absorption by up to 70%, significantly decreasing the likelihood of cardiovascular and respiratory side effects. Additionally, gently closing the eyes (without squeezing) for 2 minutes after instillation allows the drug more time to be absorbed locally while reducing drainage into the nasolacrimal duct.
If any side effect worsens or persists, or if you notice effects not listed above, contact your doctor or pharmacist. You can also help monitor drug safety by reporting suspected side effects to your national medicines regulatory authority.
How Should You Store Timosan?
Proper storage of Timosan is essential to maintain the medication’s potency, sterility, and effectiveness throughout its shelf life. Eye drops are particularly susceptible to microbial contamination and chemical degradation if not stored correctly, which could reduce their therapeutic effect or introduce infection risk to the eye.
- Temperature: Store at or below 25°C (77°F). Do not freeze.
- Light: Keep the bottle in its outer carton when not in use to protect from light, as timolol may be light-sensitive.
- Orientation: Store the bottle upside down for better dripping, as recommended by the manufacturer.
- Children: Store out of the sight and reach of children.
- After opening: Discard the bottle 4 weeks after first opening, even if there is solution remaining. The preservative cannot guarantee sterility indefinitely once the seal has been broken. Write the date of first opening on the bottle to help you track this.
- Expiry date: Do not use after the expiry date printed on the packaging. The expiry date refers to the last day of the stated month.
- Visual inspection: Do not use Timosan if you notice any signs of deterioration, such as discoloration, cloudiness, or particles in the solution.
Do not dispose of medicines via wastewater or household waste. Return unused or expired medication to a pharmacy for safe disposal. This helps protect the environment and prevents accidental exposure to others.
What Does Timosan Contain?
Understanding the composition of Timosan is important for identifying potential allergens and for understanding why certain precautions—such as contact lens removal—are necessary. The formulation has been designed to ensure drug stability, appropriate pH, and adequate retention on the ocular surface.
| Component | Role | Amount |
|---|---|---|
| Timolol maleate | Active ingredient (beta-blocker) | Equivalent to 5 mg/ml timolol |
| Benzalkonium chloride | Preservative (antimicrobial) | 0.05 mg/ml |
| Sorbitol | Tonicity agent (osmotic balance) | As required |
| Polyvinyl alcohol | Viscosity agent (aids retention on eye surface) | As required |
| Carbomer | Gel-forming polymer (extends contact time) | As required |
| Sodium acetate trihydrate | Buffering agent (pH stabilization) | As required |
| Lysine monohydrate | pH adjustment / stabilizer | As required |
| Water for injections | Vehicle / solvent | To volume |
Physical appearance: Timosan is a clear solution supplied in a polyethylene dropper bottle fitted with a dropper tip and screw cap. It is available in pack sizes of 1 × 5 ml and 3 × 5 ml. Not all pack sizes may be marketed in all countries.
Manufacturer: Timosan is manufactured by Santen Oy, Kelloportinkatu 1, FI-33100 Tampere, Finland. The marketing authorization is held by Santen Oy, Niittyhaankatu 20, FI-33720 Tampere, Finland. Santen is a global pharmaceutical company specializing in ophthalmology, with products available in over 60 countries.
Frequently Asked Questions About Timosan
Timosan (timolol maleate) is a prescription eye drop used to lower elevated intraocular pressure (IOP) in patients with chronic open-angle glaucoma or ocular hypertension. It belongs to the class of non-selective beta-blockers and works by reducing the production of aqueous humor in the eye. Timolol has been a mainstay of glaucoma therapy since its introduction in 1978 and is listed on the WHO Model List of Essential Medicines. It typically reduces IOP by 20–35% from baseline.
Timosan contains timolol, a non-selective beta-adrenergic receptor blocker. It lowers IOP by blocking beta-1 and beta-2 receptors on the ciliary epithelium in the eye, which reduces the production of aqueous humor (the fluid that fills the front chamber of the eye). The onset of action is approximately 30 minutes, peak IOP reduction occurs at 1–2 hours, and the effect lasts approximately 24 hours, allowing once-daily dosing with the long-acting formulation.
No. Timosan is strictly contraindicated in patients with bronchial asthma or a history of asthma, as well as in patients with severe COPD. Even though timolol is applied topically to the eye, it can be absorbed systemically and block beta-2 receptors in the airways, causing bronchospasm (narrowing of the airways) which can be life-threatening in susceptible individuals. If you have asthma or significant respiratory disease, your doctor will prescribe an alternative IOP-lowering medication that does not carry this risk.
Pressing your finger gently on the inner corner of the eye (near the nose) for 2 minutes after applying Timosan is called nasolacrimal occlusion. This technique blocks the drainage of the eye drop into the nasolacrimal duct, which connects the eye to the nose and throat. Without this step, a significant portion of the medication drains into the nasal cavity, is absorbed into the bloodstream, and can cause systemic side effects on the heart, lungs, and blood pressure. Studies show that nasolacrimal occlusion can reduce systemic absorption by up to 70%, making it one of the most important steps in safe eye drop use.
Timosan contains benzalkonium chloride (0.05 mg/ml) as a preservative, which can be absorbed by soft contact lenses and may cause lens discoloration. You should remove your contact lenses before applying Timosan and wait at least 30 minutes before reinserting them. If you experience persistent eye irritation while using Timosan with contact lenses, consult your ophthalmologist. In some cases, preservative-free timolol formulations may be available as an alternative.
An opened bottle of Timosan should be discarded 4 weeks after first opening, even if there is solution remaining in the bottle. After this period, the preservative (benzalkonium chloride) may no longer be sufficient to prevent microbial contamination, increasing the risk of eye infection. Write the date you first open the bottle on the label or carton to help you track this. Store the bottle at or below 25°C, protected from light, and keep it upside down for better dripping.
References
- European Medicines Agency (EMA). Timolol Maleate – Summary of Product Characteristics. Last updated 2025. Available at: www.ema.europa.eu
- U.S. Food and Drug Administration (FDA). Timolol Maleate Ophthalmic Solution – Prescribing Information. Revised 2024. Available at: www.fda.gov
- American Academy of Ophthalmology (AAO). Preferred Practice Pattern: Primary Open-Angle Glaucoma. 2025. Available at: www.aao.org
- European Glaucoma Society (EGS). Terminology and Guidelines for Glaucoma, 5th Edition. 2024. Available at: www.eugs.org
- World Health Organization (WHO). Model List of Essential Medicines. 23rd List, 2023. Available at: www.who.int
- Kass MA, Heuer DK, Higginbotham EJ, et al. The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Archives of Ophthalmology. 2002;120(6):701–713. doi:10.1001/archopht.120.6.701
- Weinreb RN, Aung T, Medeiros FA. The Pathophysiology and Treatment of Glaucoma: A Review. JAMA. 2014;311(18):1901–1911. doi:10.1001/jama.2014.3192
- British National Formulary (BNF). Timolol maleate – Monograph. Updated 2025. Available at: bnf.nice.org.uk
- Tham YC, Li X, Wong TY, et al. Global prevalence of glaucoma and projections of glaucoma burden through 2040: a systematic review and meta-analysis. Ophthalmology. 2014;121(11):2081–2090. doi:10.1016/j.ophtha.2014.05.013
- National Institute for Health and Care Excellence (NICE). Glaucoma: diagnosis and management. NICE guideline [NG81]. Updated 2024. Available at: www.nice.org.uk
- Zimmerman TJ, Kooner KS, Kandarakis AS, Ziegler LP. Improving the therapeutic index of topically applied ocular drugs. Archives of Ophthalmology. 1984;102(4):551–553. doi:10.1001/archopht.1984.01040030429017
Editorial Team
Medical Content
iMedic Medical Editorial Team – Specialists in Ophthalmology and Clinical Pharmacology
Medical Review
iMedic Medical Review Board – Independent review according to international guidelines (WHO, EMA, FDA, AAO, EGS)
Evidence Framework
GRADE methodology – Evidence Level 1A based on systematic reviews and randomized controlled trials
Last Reviewed
– Content verified against current EMA SmPC and FDA label
This article was prepared based on the approved Summary of Product Characteristics (SmPC) for timolol maleate, peer-reviewed clinical literature, and international ophthalmology guidelines. All medical facts have been independently verified. iMedic receives no commercial funding and has no conflicts of interest.