DrugCite
Search

TIMOLOL MALEATE

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Timolol Maleate Adverse Events Reported to the FDA Over Time

How are Timolol Maleate adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Timolol Maleate, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Timolol Maleate is flagged as the suspect drug causing the adverse event.

Most Common Timolol Maleate Adverse Events Reported to the FDA

What are the most common Timolol Maleate adverse events reported to the FDA?

Intraocular Pressure Increased
98 (2.49%)
Eye Irritation
83 (2.1%)
Eye Pain
61 (1.55%)
Drug Ineffective
60 (1.52%)
Bradycardia
56 (1.42%)
Ocular Hyperaemia
54 (1.37%)
Visual Acuity Reduced
45 (1.14%)
Blindness
44 (1.12%)
Dizziness
44 (1.12%)
Vision Blurred
42 (1.07%)
Corneal Deposits
39 (.99%)
Show More Show More
Drug Interaction
36 (.91%)
Dyspnoea
35 (.89%)
Visual Impairment
34 (.86%)
Fatigue
33 (.84%)
Product Substitution Issue
33 (.84%)
Eye Pruritus
29 (.74%)
Erythema
27 (.68%)
Heart Rate Decreased
27 (.68%)
Hypotension
27 (.68%)
Anxiety
26 (.66%)
Eye Disorder
25 (.63%)
Headache
25 (.63%)
Hypersensitivity
24 (.61%)
Malaise
24 (.61%)
Cataract
23 (.58%)
Fall
23 (.58%)
Glaucoma
21 (.53%)
Skin Exfoliation
21 (.53%)
Chest Pain
20 (.51%)
Ectropion
20 (.51%)
Eyelid Oedema
20 (.51%)
Cough
19 (.48%)
Eye Swelling
19 (.48%)
Loss Of Consciousness
19 (.48%)
Arrhythmia
18 (.46%)
Asthma
18 (.46%)
Choroidal Detachment
18 (.46%)
Drug Hypersensitivity
18 (.46%)
Metabolic Acidosis
18 (.46%)
Nausea
18 (.46%)
Atrial Fibrillation
17 (.43%)
Conjunctival Oedema
17 (.43%)
Eye Inflammation
17 (.43%)
Eye Movement Disorder
17 (.43%)
Lethargy
17 (.43%)
Periorbital Oedema
17 (.43%)
Pruritus
17 (.43%)
Blood Pressure Increased
16 (.41%)
Dermatitis
16 (.41%)
Dry Eye
16 (.41%)
Pain
16 (.41%)
Syncope
16 (.41%)
Accidental Exposure
15 (.38%)
Atrioventricular Block Complete
15 (.38%)
Iris Adhesions
15 (.38%)
Miosis
15 (.38%)
Peripheral Coldness
15 (.38%)
Respiratory Rate Decreased
15 (.38%)
Atrioventricular Block
14 (.36%)
Blood Pressure Decreased
14 (.36%)
Corneal Epithelium Defect
14 (.36%)
Deafness
14 (.36%)
Hypertension
14 (.36%)
Keratopathy
14 (.36%)
Palpitations
14 (.36%)
Tinnitus
14 (.36%)
Abdominal Pain
13 (.33%)
Alopecia
13 (.33%)
Chest Discomfort
13 (.33%)
Conjunctival Hyperaemia
13 (.33%)
Corneal Disorder
13 (.33%)
Depressed Level Of Consciousness
13 (.33%)
Eye Haemorrhage
13 (.33%)
Feeling Abnormal
13 (.33%)
Hypotonia
13 (.33%)
Lacrimation Increased
13 (.33%)
Ulcerative Keratitis
13 (.33%)
Visual Field Defect
13 (.33%)
Asthenia
12 (.3%)
Blindness Transient
12 (.3%)
Condition Aggravated
12 (.3%)
Vitreous Haemorrhage
12 (.3%)
Blepharoplasty
11 (.28%)
Drug Effect Decreased
11 (.28%)
Eye Infection
11 (.28%)
Keratitis
11 (.28%)
Keratitis Herpetic
11 (.28%)
Medication Error
11 (.28%)
Wrong Drug Administered
11 (.28%)
Cardiac Arrest
10 (.25%)
Cardiotoxicity
10 (.25%)
Confusional State
10 (.25%)
Developmental Glaucoma
10 (.25%)
Diarrhoea
10 (.25%)
Hypotony Of Eye
10 (.25%)
Intraocular Pressure Test Abnormal
10 (.25%)
Nervous System Disorder
10 (.25%)
Paralysis
10 (.25%)
Pneumonia
10 (.25%)
Pulse Abnormal
10 (.25%)

ExportShare/Embed GraphExport Export Data

This graph shows the top adverse events submitted to the FDA for Timolol Maleate, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Timolol Maleate is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Adverse Event Categories for Timolol Maleate

What are the most common Timolol Maleate adverse events reported to the FDA?

Show More Show More

ExportShare/Embed Graph Export Export Data

This graph shows the top categories of adverse events submitted to the FDA for Timolol Maleate, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Timolol Maleate is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Common Uses of Timolol Maleate According to Those Reporting Adverse Events

Why are people taking Timolol Maleate, according to those reporting adverse events to the FDA?

Glaucoma
999
Drug Use For Unknown Indication
140
Product Used For Unknown Indication
138
Intraocular Pressure Increased
130
Open Angle Glaucoma
85
Ocular Hypertension
64
Show More Show More
Hypertension
21
Diabetic Retinopathy
16
Intraocular Pressure Test
15
Eye Disorder
15
Ill-defined Disorder
13
Cataract
13
Cataract Operation
12
Postoperative Care
9
Developmental Glaucoma
9
Angle Closure Glaucoma
9
Keratitis Herpetic
9
Uveitis
9
Herpes Zoster
8
Ulcerative Keratitis
7
Corneal Epithelium Defect
6
Optic Nerve Cup/disc Ratio Increase...
6
Pain
5
Accidental Exposure
5
Behcets Syndrome
5
Drug Therapy
5
Abnormal Sensation In Eye
5
Diabetes Mellitus
4
Prophylaxis
3
Endothelial Dysfunction
3
Corneal Graft Rejection
3
Macular Degeneration
3
Eye Injury
3
Prophylaxis Against Transplant Reje...
3
Hypertonia
3
Intraocular Pressure Test Abnormal
3
Keratitis
3
Glaucoma Congenital
3
Drug Exposure During Pregnancy
2
Eye Lubrication Therapy
2
Arrhythmia
2
Normal Tension Glaucoma
2
Mitral Valve Prolapse
2
Hyperthyroidism
2
Coronary Artery Disease
2
Diabetic Glaucoma
2
Dry Eye
2
Conjunctivitis
1
Ventricular Tachycardia
1
Eye Oedema
1
Atrial Tachycardia
1

Drug Labels

LabelLabelerEffective
Istalol ISTA PHARMACEUTICALS, INC.06-APR-04
Timolol MaleateMylan Pharmaceuticals Inc.17-AUG-06
Timolol GfsFALCON Pharmaceuticals, Ltd.01-DEC-08
Timolol MaleateAton Pharma, Inc.16-OCT-09
Dorzolamide Hydrochloride And Timolol MaleatePhysicians Total Care, Inc.26-FEB-10
CosoptPhysicians Total Care, Inc.05-MAY-10
Timolol MaleateAscend Laboratories, LLC17-MAR-11
Timolol MaleateApotex Corp.13-APR-11
CombiganPhysicians Total Care, Inc.15-APR-11
Timolol MaleateBausch & Lomb Incorporated21-APR-11
Timolol MaleatePacific Pharma, Inc.04-MAY-11
Timolol MaleateFalcon Pharmaceuticals, Ltd.01-AUG-11
Timolol MaleatePack Pharmaceuticals LLC16-SEP-11
Timolol MaleatePack Pharmaceuticals LLC16-SEP-11
Dorzolamide Hydrochloride-timolol MaleatePrasco Laboratories07-OCT-11
Timoptic-xeAton Pharma, Inc.27-OCT-11
TimopticAton Pharma, Inc.27-OCT-11
TimopticAton Pharma, Inc.27-OCT-11
Dorzolamide Hydrochloride And Timolol Maleate Sandoz Inc.15-NOV-11
Timolol MaleateAkorn, Inc.20-MAR-12
Dorzolamide Hydrochloride And Timolol MaleateHi-Tech Pharmacal Co., Inc.12-APR-12
Timolol MaleateHi-Tech Pharmacal Co., Inc.22-MAY-12
Cosopt PfMerck Sharp & Dohme Corp.24-MAY-12
Timolol MaleatePhysicians Total Care, Inc.29-AUG-12
Timolol MaleatePhysicians Total Care, Inc.29-AUG-12
CombiganAllergan, Inc.12-OCT-12
CosoptMerck Sharp & Dohme Corp.16-NOV-12
Dorzolamide Hcl /timolol MaleateBausch & Lomb Incorporated29-JAN-13
IstalolBausch & Lomb Incorporated22-MAR-13

Timolol Maleate Case Reports

What Timolol Maleate safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Timolol Maleate. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.

DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.

DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.

Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.

Comments

Share your experience with Timolol Maleate.