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CABASER

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Cabaser Adverse Events Reported to the FDA Over Time

How are Cabaser adverse event reports trending over time?

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

Most Common Cabaser Adverse Events Reported to the FDA

What are the most common Cabaser adverse events reported to the FDA?

Mitral Valve Incompetence
23 (3.26%)
Aortic Valve Incompetence
21 (2.98%)
Cardiac Valve Disease
19 (2.7%)
Pleural Effusion
19 (2.7%)
Hallucination
16 (2.27%)
Pleurisy
15 (2.13%)
Neuroleptic Malignant Syndrome
13 (1.84%)
Dyspnoea
12 (1.7%)
Pneumonia
11 (1.56%)
Cardiac Failure
10 (1.42%)
Fall
10 (1.42%)
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Interstitial Lung Disease
10 (1.42%)
Delirium
9 (1.28%)
Delusion
7 (.99%)
Hypertension
7 (.99%)
Hypoglycaemia
7 (.99%)
Oedema Peripheral
7 (.99%)
Paranoia
7 (.99%)
Persecutory Delusion
7 (.99%)
Tremor
7 (.99%)
Blood Pressure Decreased
6 (.85%)
Hallucination, Auditory
6 (.85%)
Heart Valve Incompetence
6 (.85%)
Mitral Valve Disease
6 (.85%)
Agitation
5 (.71%)
Death
5 (.71%)
Fatigue
5 (.71%)
Fibrosis
5 (.71%)
Respiratory Failure
5 (.71%)
Aggression
4 (.57%)
Bradycardia
4 (.57%)
Coma
4 (.57%)
Confusional State
4 (.57%)
Erectile Dysfunction
4 (.57%)
Gait Disturbance
4 (.57%)
Impulsive Behaviour
4 (.57%)
Insomnia
4 (.57%)
Obsessive-compulsive Disorder
4 (.57%)
Pathological Gambling
4 (.57%)
Pneumonia Aspiration
4 (.57%)
Rapid Eye Movements Sleep Abnormal
4 (.57%)
Sexual Dysfunction
4 (.57%)
Sudden Onset Of Sleep
4 (.57%)
Suicide Attempt
4 (.57%)
Tricuspid Valve Incompetence
4 (.57%)
Abnormal Behaviour
3 (.43%)
Activities Of Daily Living Impaired
3 (.43%)
Aortic Valve Stenosis
3 (.43%)
Blood Albumin Decreased
3 (.43%)
Cardiac Failure Congestive
3 (.43%)
Cardiac Hypertrophy
3 (.43%)
Cardiac Valve Sclerosis
3 (.43%)
Cardiomegaly
3 (.43%)
Condition Aggravated
3 (.43%)
Depressed Level Of Consciousness
3 (.43%)
Drug Administration Error
3 (.43%)
Drug Exposure During Pregnancy
3 (.43%)
Drug Interaction
3 (.43%)
Haemolytic Anaemia
3 (.43%)
Hyponatraemia
3 (.43%)
Intentional Overdose
3 (.43%)
Oedema
3 (.43%)
Pericardial Effusion
3 (.43%)
Posture Abnormal
3 (.43%)
Productive Cough
3 (.43%)
Psychomotor Hyperactivity
3 (.43%)
Pulmonary Fibrosis
3 (.43%)
Respiratory Arrest
3 (.43%)
Respiratory Disorder
3 (.43%)
Stereotypy
3 (.43%)
Visual Impairment
3 (.43%)
Vomiting
3 (.43%)
Alanine Aminotransferase Increased
2 (.28%)
Amaurosis
2 (.28%)
Aortic Valve Replacement
2 (.28%)
Aortic Valve Sclerosis
2 (.28%)
Aplasia
2 (.28%)
Arrhythmia
2 (.28%)
Aspartate Aminotransferase Increase...
2 (.28%)
Atrial Fibrillation
2 (.28%)
Blindness Transient
2 (.28%)
Blood Cholesterol Increased
2 (.28%)
Blood Creatine Phosphokinase Increa...
2 (.28%)
Blood Urea Increased
2 (.28%)
Bradykinesia
2 (.28%)
Bronchial Disorder
2 (.28%)
Bronchitis
2 (.28%)
Caesarean Section
2 (.28%)
Cardiac Disorder
2 (.28%)
Cardiac Failure Acute
2 (.28%)
Cardio-respiratory Arrest
2 (.28%)
Cervical Vertebral Fracture
2 (.28%)
Chest Pain
2 (.28%)
Chest X-ray Abnormal
2 (.28%)
Cheyne-stokes Respiration
2 (.28%)
Compulsive Shopping
2 (.28%)
Depressive Symptom
2 (.28%)
Disease Progression
2 (.28%)
Dysarthria
2 (.28%)
Dysphonia
2 (.28%)
Dyspnoea Exertional
2 (.28%)

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This graph shows the top adverse events submitted to the FDA for Cabaser, 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 Cabaser 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 Cabaser

What are the most common Cabaser adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Cabaser, 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 Cabaser 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 Cabaser According to Those Reporting Adverse Events

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

Parkinsons Disease
234
Restless Legs Syndrome
18
Parkinsonism
8
Hyperprolactinaemia
6
Drug Use For Unknown Indication
5
Prolactinoma
2
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Polycystic Ovaries
2
Dementia
2
Muscle Spasms
2
Progressive Supranuclear Palsy
2
Acromegaly
1
Tremor
1
Hormone Therapy
1
Ovulation Induction
1
Suppressed Lactation
1
Motor Dysfunction
1
Blood Prolactin Abnormal
1
Multiple System Atrophy
1
Hyperlipidaemia
1

Cabaser Case Reports

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

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About Results

This report contains aggregated drug side effects and adverse events for Cabaser. 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.

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