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Carteol Side Effects

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Common Carteol Side Effects


The most commonly reported Carteol side effects (click to view or check a box to report):

Bradycardia (9)
Muscular Weakness (6)
Peripheral Coldness (6)
Amyotrophy (6)
Systemic Lupus Erythematosus (5)
Atrioventricular Block (5)
Intraocular Pressure Increased (4)
Electrocardiogram Qrs Complex Prolonged (4)
Meningioma (4)
Disorientation (4)
Diarrhoea (4)
Blood Creatinine Increased (4)
Blood Potassium Increased (3)
Arthritis (3)
Dizziness (3)
Eye Pain (3)
Oropharyngeal Blistering (3)
Blood Sodium Decreased (3)
Idiopathic Thrombocytopenic Purpura (3)
Visual Acuity Reduced (3)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Carteol Side Effects Reported to FDA



Carteol Side Effect Report#9914843
Systemic Lupus Erythematosus, Muscular Weakness, Hyperhidrosis, Cardiac Disorder, Erythema, Alopecia
This is a report of a 53-year-old female patient (weight: NA) from FR, suffering from the following health symptoms/conditions: glaucoma, who was treated with Carteol Lp 2% Collyre A Liberation Prolongee En Recipient Unidose (dosage: NA, start time: 201002), combined with: NA. and developed a serious reaction and side effect(s): Systemic Lupus Erythematosus, Muscular Weakness, Hyperhidrosis, Cardiac Disorder, Erythema, Alopecia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Carteol Lp 2% Collyre A Liberation Prolongee En Recipient Unidose treatment in female patients, resulting in Systemic Lupus Erythematosus side effect.
Carteol Side Effect Report#9557254
Hyperkalaemia, Sinus Bradycardia
This report suggests a potential Carteol 1% Collyre Hyperkalaemia side effect(s) that can have serious consequences. A 90-year-old female patient (weight: NA) from FR was diagnosed with the following symptoms/conditions: NA and used Carteol 1% Collyre (dosage: NA) starting
Aug 27, 2013. After starting Carteol 1% Collyre the patient began experiencing various side effects, including: Hyperkalaemia, Sinus BradycardiaAdditional drugs used concurrently:
  • Cardensiel
  • Keppra
  • Tahor
  • Plavix
  • Azopt Collyre
  • Lumigan
  • Levemir
  • Actrapid
Although Carteol 1% Collyre demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hyperkalaemia, may still occur.
Carteol Side Effect Report#9553459
Alopecia Totalis, Anti-thyroid Antibody, Chest Pain, Hyperhidrosis, Nail Disorder, Dry Mouth, Vertigo, Abdominal Pain Upper, Asthenia
This Alopecia Totalis problem was reported by a consumer or non-health professional from FR. A 55-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: glaucoma,ulcerative keratitis. On 201304 this consumer started treatment with Carteol Lp 2% Collyre A Liberation Prolongee (dosage: NA). The following drugs were being taken at the same time:
  • Tobrex
  • Euronac
When using Carteol Lp 2% Collyre A Liberation Prolongee, the patient experienced the following unwanted symptoms/side effects: Alopecia Totalis, Anti-thyroid Antibody, Chest Pain, Hyperhidrosis, Nail Disorder, Dry Mouth, Vertigo, Abdominal Pain Upper, AstheniaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Alopecia Totalis, may become evident only after a product is in use by the general population.
Carteol Side Effect Report#9471258
Completed Suicide, Depression, Night Sweats, Insomnia, Visual Acuity Reduced
This Completed Suicide side effect was reported by a health professional from FR. A 78-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Carteol Lp 2% Collyre A Liberation Prolongee (drug dosage: NA), which was initiated on
Dec 14, 2012. Concurrently used drugs:
  • Mianserine Almus
  • Temesta
  • Ixprim (37.5/325 Mg)
  • Olmetec
  • Vastarel
  • Actonel
  • Topalgic Lp
  • Cortancyl
.After starting to take Carteol Lp 2% Collyre A Liberation Prolongee the consumer reported adverse symptoms, such as: Completed Suicide, Depression, Night Sweats, Insomnia, Visual Acuity ReducedThese side effects may potentially be related to Carteol Lp 2% Collyre A Liberation Prolongee.
Carteol Side Effect Report#9351041
Asphyxia
This is a report of a 76-year-old female patient (weight: NA) from FR, suffering from the following health symptoms/conditions: glaucoma, who was treated with Carteol (dosage: NA, start time:
May 27, 2013), combined with: NA. and developed a serious reaction and side effect(s): Asphyxia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Carteol treatment in female patients, resulting in Asphyxia side effect.
Carteol Side Effect Report#9158233
Dark Circles Under Eyes, Eye Pruritus
This report suggests a potential Carteolol Hydrochloride Dark Circles Under Eyes side effect(s) that can have serious consequences. A 71-year-old female patient (weight: NA) from US was diagnosed with the following symptoms/conditions: NA and used Carteolol Hydrochloride (dosage: 1 Drop In Each Eye Daily) starting NS. After starting Carteolol Hydrochloride the patient began experiencing various side effects, including: Dark Circles Under Eyes, Eye PruritusAdditional drugs used concurrently:
  • Latanoprost
  • Travoprost
Although Carteolol Hydrochloride demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dark Circles Under Eyes, may still occur.
Carteol Side Effect Report#9027097
Hypertrophic Cardiomyopathy
This Hypertrophic Cardiomyopathy problem was reported by a health professional from FR. A 71-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Carteol 1% Collyre (dosage: NA). The following drugs were being taken at the same time:
  • Kivexa
  • Aldactone
  • Lucentis 10 Mg/ml, Solution Injectable
  • Sustiva
  • Travatan
  • Mono-tildiem
  • Crestor 5 Mg
When using Carteol 1% Collyre, the patient experienced the following unwanted symptoms/side effects: Hypertrophic CardiomyopathyAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Hypertrophic Cardiomyopathy, may become evident only after a product is in use by the general population.
Carteol Side Effect Report#8456267-6
Caesarean Section, Visual Field Defect, Cervix Disorder, Premature Labour, Normal Newborn, Maternal Exposure During Pregnancy
This Caesarean Section side effect was reported by a consumer or non-health professional from France. A 28-year-old female patient (weight:NA) experienced the following symptoms/conditions: glaucoma.The patient was prescribed Carteol Lp 1% Collyre En Solution En Recipient Unidose (drug dosage: NA), which was initiated on
Jan 01, 2003. Concurrently used drugs: NA..After starting to take Carteol Lp 1% Collyre En Solution En Recipient Unidose the consumer reported adverse symptoms, such as: Caesarean Section, Visual Field Defect, Cervix Disorder, Premature Labour, Normal Newborn, Maternal Exposure During PregnancyThese side effects may potentially be related to Carteol Lp 1% Collyre En Solution En Recipient Unidose.
Carteol Side Effect Report#8286538-8
Foetal Distress Syndrome
This is a report of a male patient (weight: NA) from France, suffering from the following health symptoms/conditions: glaucoma, who was treated with Carteolol Hydrochloride (dosage: Unk, start time:
Apr 10, 2010), combined with:
  • Xalatan (1 Df, 1x/day)
and developed a serious reaction and side effect(s): Foetal Distress Syndrome after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Carteolol Hydrochloride treatment in male patients, resulting in Foetal Distress Syndrome side effect.
Carteol Side Effect Report#8164079-6
Loss Of Consciousness, Cardiac Disorder, Fall
This report suggests a potential Carteolol Hydrochloride Loss Of Consciousness side effect(s) that can have serious consequences. A 91-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Carteolol Hydrochloride (dosage: Unk Ukn, Unk) starting NS. After starting Carteolol Hydrochloride the patient began experiencing various side effects, including: Loss Of Consciousness, Cardiac Disorder, FallAdditional drugs used concurrently:
  • Xalatan (Unk Ukn, Unk)
Although Carteolol Hydrochloride demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Loss Of Consciousness, may still occur.
Carteol Side Effect Report#8132252-9
Intraocular Pressure Increased, Therapeutic Response Decreased, Conjunctival Hyperaemia
This Intraocular Pressure Increased problem was reported by a physician from Japan. A 77-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Oct 12, 2010 this consumer started treatment with Carteolol Hydrochloride (dosage: Unk). The following drugs were being taken at the same time:
  • Lumigan (1 Gtt, Qd)
  • Mikelan La (Unk)
  • Trusopt
  • Detantol (Unk)
  • Fluorometholone
  • Diamox Src (Unk)
  • Aspara K (Unk)
When using Carteolol Hydrochloride, the patient experienced the following unwanted symptoms/side effects: Intraocular Pressure Increased, Therapeutic Response Decreased, Conjunctival HyperaemiaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Intraocular Pressure Increased, may become evident only after a product is in use by the general population.
Carteol Side Effect Report#8110452-1
Visual Field Defect, Punctate Keratitis, Conjunctival Hyperaemia
This Visual Field Defect side effect was reported by a physician from Japan. A 65-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Carteolol Hydrochloride (drug dosage: Unk), which was initiated on
Mar 08, 2010. Concurrently used drugs:
  • Azopt (Unk)
  • Lumigan (1 Gtt, Night Time)
.After starting to take Carteolol Hydrochloride the consumer reported adverse symptoms, such as: Visual Field Defect, Punctate Keratitis, Conjunctival HyperaemiaThese side effects may potentially be related to Carteolol Hydrochloride.
Carteol Side Effect Report#8059219-3
Intraocular Pressure Increased
This is a report of a 80-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Carteolol Hydrochloride (dosage: Unk, start time:
Oct 23, 2008), combined with:
  • Lumigan (2 Gtt, Qd)
  • Livostin (Unk)
  • Trusopt (Unk)
and developed a serious reaction and side effect(s): Intraocular Pressure Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Carteolol Hydrochloride treatment in female patients, resulting in Intraocular Pressure Increased side effect. The patient was hospitalized.
Carteol Side Effect Report#7971994-2
Retinal Vascular Disorder, Visual Acuity Reduced
This report suggests a potential Carteolol Hydrochloride Retinal Vascular Disorder side effect(s) that can have serious consequences. A 82-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Carteolol Hydrochloride (dosage: Unk) starting
Apr 14, 2010. After starting Carteolol Hydrochloride the patient began experiencing various side effects, including: Retinal Vascular Disorder, Visual Acuity ReducedAdditional drugs used concurrently:
  • Lumigan (1 Gtt, Qpm)
  • Tafluprost (Unk)
  • Levofloxacin (Unk)
  • Rinderon-a (Unk)
Although Carteolol Hydrochloride demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Retinal Vascular Disorder, may still occur.
Carteol Side Effect Report#7699859-4
X-ray Abnormal, Sepsis, Ileus, Intestinal Perforation, Abdominal Pain
This X-ray Abnormal problem was reported by a health professional from Japan. A 63-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: tachycardia,blood pressure decreased,hyperphosphataemia,hyperuricaemia,osteoporosis,gastric ulcer. On
Nov 30, 2009 this consumer started treatment with Carteolol Hydrochloride (dosage: NA). The following drugs were being taken at the same time: NA. When using Carteolol Hydrochloride, the patient experienced the following unwanted symptoms/side effects: X-ray Abnormal, Sepsis, Ileus, Intestinal Perforation, Abdominal PainThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as X-ray Abnormal, may become evident only after a product is in use by the general population.
Carteol Side Effect Report#7584762-0
Syncope, Dizziness, Pneumonia
This Syncope side effect was reported by a pharmacist from Japan. A 46-year-old female patient (weight:NA) experienced the following symptoms/conditions: glaucoma.The patient was prescribed Carteolol Hydrochloride (drug dosage: Unk Ukn, Unk), which was initiated on NS. Concurrently used drugs:
  • Tafluprost (Unk Ukn, Unk)
.After starting to take Carteolol Hydrochloride the consumer reported adverse symptoms, such as: Syncope, Dizziness, PneumoniaThese side effects may potentially be related to Carteolol Hydrochloride. The patient was hospitalized.
Carteol Side Effect Report#7506264-X
Blood Pressure Systolic Increased, Nocturia, Hypertensive Encephalopathy, Discomfort
This is a report of a 72-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Carteolol Hydrochloride (dosage: 15 Mg, Unk, start time:
Apr 28, 2011), combined with:
  • Bezatol (400 Mg, Unk)
  • Ticlopidine Hcl (100 Mg, Unk)
  • Irbesartan (100 Mg, Unk)
  • Avapro (50 Mg, Unk)
  • Diazepam
  • Depas
  • Amoban (7.5 Mg, Unk)
  • Plavix (75 Mg, Unk)
and developed a serious reaction and side effect(s): Blood Pressure Systolic Increased, Nocturia, Hypertensive Encephalopathy, Discomfort after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Carteolol Hydrochloride treatment in female patients, resulting in Blood Pressure Systolic Increased side effect.
Carteol Side Effect Report#7495213-9
Pyrexia, Asthenia, Malaise, Hypophagia, International Normalised Ratio Increased, Bone Pain, Haematuria, Dry Mouth, Anaemia
This report suggests a potential Carteolol Hydrochloride Pyrexia side effect(s) that can have serious consequences. A 90-year-old male patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: NA and used Carteolol Hydrochloride (dosage: Unk Unk, Bid) starting
Mar 11, 2011. After starting Carteolol Hydrochloride the patient began experiencing various side effects, including: Pyrexia, Asthenia, Malaise, Hypophagia, International Normalised Ratio Increased, Bone Pain, Haematuria, Dry Mouth, AnaemiaAdditional drugs used concurrently:
  • Xgeva (120 Mg, Q4wk)
  • Simvastatin (20 Mg, Qd)
  • Vitamin B12 /00056201/
  • Vitamin B6
  • Folic Acid
  • Coumadin
  • Bicalutamide (50 Mg, Qd)
  • Sotalol Hcl (320 Mg, Qd)
The patient was hospitalized. Although Carteolol Hydrochloride demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Pyrexia, may still occur.
Carteol Side Effect Report#7244024-8
Tendonitis
This Tendonitis problem was reported by a health professional from France. A 71-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Oct 01, 2006 this consumer started treatment with Carteolol Hydrochloride (dosage: NA). The following drugs were being taken at the same time:
  • Isradipine
  • Zetia
  • Aspirin Lysine
When using Carteolol Hydrochloride, the patient experienced the following unwanted symptoms/side effects: TendonitisAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Tendonitis, may become evident only after a product is in use by the general population.
Carteol Side Effect Report#7232002-4
Tendonitis
This Tendonitis side effect was reported by a health professional from France. A 71-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Carteolol Hydrochloride (drug dosage: NA), which was initiated on
Jan 01, 2007. Concurrently used drugs:
  • Aspirin Lysine
  • Isradipine
  • Zetia
.After starting to take Carteolol Hydrochloride the consumer reported adverse symptoms, such as: TendonitisThese side effects may potentially be related to Carteolol Hydrochloride.
Carteol Side Effect Report#7030386-3
Dermatitis Bullous, Oropharyngeal Blistering, Pemphigus
This is a report of a 67-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: intraocular pressure increased, who was treated with Carteol Lp 2% Collyre En Sol Recipient Unidose (dosage: NA, start time:
Jan 01, 2000), combined with:
  • Pravastatin
and developed a serious reaction and side effect(s): Dermatitis Bullous, Oropharyngeal Blistering, Pemphigus after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Carteol Lp 2% Collyre En Sol Recipient Unidose treatment in female patients, resulting in Dermatitis Bullous side effect. The patient was hospitalized.
Carteol Side Effect Report#6956141-8
Dermatitis Bullous, Oropharyngeal Blistering
This report suggests a potential Carteolol Hydrochloride Dermatitis Bullous side effect(s) that can have serious consequences. A 67-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: intraocular pressure increased and used Carteolol Hydrochloride (dosage: 1 Gtt, Qd) starting
May 21, 2010. After starting Carteolol Hydrochloride the patient began experiencing various side effects, including: Dermatitis Bullous, Oropharyngeal BlisteringAdditional drugs used concurrently:
  • Pravastatin (Unk)
Although Carteolol Hydrochloride demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dermatitis Bullous, may still occur.
Carteol Side Effect Report#6921555-9
Arthritis, Joint Swelling, Rheumatoid Arthritis, Spondylitis
This Arthritis problem was reported by a physician from France. A 57-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: ocular hypertension. On
Jan 01, 2010 this consumer started treatment with Carteol Lp 2% Collyre En Solution A Liberation Prolongee (dosage: NA). The following drugs were being taken at the same time:
  • Xalatan /swe/
When using Carteol Lp 2% Collyre En Solution A Liberation Prolongee, the patient experienced the following unwanted symptoms/side effects: Arthritis, Joint Swelling, Rheumatoid Arthritis, SpondylitisAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Arthritis, may become evident only after a product is in use by the general population.
Carteol Side Effect Report#6895619-2
Dermatitis Bullous, Oropharyngeal Blistering, Pemphigus
This Dermatitis Bullous side effect was reported by a physician from France. A 67-year-old female patient (weight:NA) experienced the following symptoms/conditions: intraocular pressure increased.The patient was prescribed Carteol Lp 2% Collyre En Sol Recipient Unidose (drug dosage: NA), which was initiated on
Jan 01, 2000. Concurrently used drugs:
  • Pravastatin
.After starting to take Carteol Lp 2% Collyre En Sol Recipient Unidose the consumer reported adverse symptoms, such as: Dermatitis Bullous, Oropharyngeal Blistering, PemphigusThese side effects may potentially be related to Carteol Lp 2% Collyre En Sol Recipient Unidose. The patient was hospitalized.
Carteol Side Effect Report#6880902-7
Arthritis, Joint Swelling, Rheumatoid Arthritis, Spondylitis
This is a report of a 57-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: ocular hypertension, who was treated with Carteol Lp 2% Collyre En Solution A Liberation Prolongee (dosage: NA, start time:
Jan 01, 2010), combined with:
  • Xalatan /swe/
and developed a serious reaction and side effect(s): Arthritis, Joint Swelling, Rheumatoid Arthritis, Spondylitis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Carteol Lp 2% Collyre En Solution A Liberation Prolongee treatment in female patients, resulting in Arthritis side effect.


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The appearance of Carteol on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

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Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Carteol reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    Carteol Safety Alerts, Active Ingredients, Usage Information

    NDC24208-367
    TypeHUMAN PRESCRIPTION DRUG
    Proprietary NameCARTEOLOL HYDROCHLORIDE
    NameCARTEOLOL HYDROCHLORIDE
    Dosage FormSOLUTION/ DROPS
    RouteOPHTHALMIC
    On market since20000120
    LabelerBausch & Lomb Incorporated
    Active Ingredient(s)CARTEOLOL HYDROCHLORIDE
    Strength(s)10
    Unit(s)mg/mL
    Pharma ClassAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

    More About Carteol

    Side Effects reported to FDA: 62

    Carteol safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 16

    Latest Carteol clinical trials

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