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XENAZINE

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Xenazine Adverse Events Reported to the FDA Over Time

How are Xenazine adverse event reports trending over time?

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

Most Common Xenazine Adverse Events Reported to the FDA

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

Death
361 (7.82%)
Depression
179 (3.88%)
Insomnia
101 (2.19%)
Somnolence
90 (1.95%)
Condition Aggravated
84 (1.82%)
Suicidal Ideation
83 (1.8%)
Fatigue
77 (1.67%)
Anxiety
75 (1.62%)
Fall
73 (1.58%)
Agitation
57 (1.23%)
Tremor
54 (1.17%)
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Dysphagia
52 (1.13%)
Nausea
51 (1.1%)
Aggression
49 (1.06%)
Crying
46 (1%)
Drug Ineffective
46 (1%)
Dyskinesia
46 (1%)
Dizziness
44 (.95%)
Gait Disturbance
41 (.89%)
Vomiting
41 (.89%)
Feeling Abnormal
38 (.82%)
Musculoskeletal Stiffness
38 (.82%)
Weight Decreased
36 (.78%)
Movement Disorder
35 (.76%)
Confusional State
34 (.74%)
Dyspnoea
34 (.74%)
Diarrhoea
30 (.65%)
Restlessness
30 (.65%)
Anger
29 (.63%)
Pneumonia
28 (.61%)
Abnormal Behaviour
27 (.58%)
Asthenia
27 (.58%)
Balance Disorder
27 (.58%)
Cognitive Disorder
26 (.56%)
Convulsion
26 (.56%)
Muscle Spasms
26 (.56%)
Product Quality Issue
25 (.54%)
Drug Ineffective For Unapproved Ind...
24 (.52%)
Dysarthria
24 (.52%)
Dystonia
24 (.52%)
Sedation
24 (.52%)
Decreased Appetite
23 (.5%)
Headache
23 (.5%)
Disease Progression
22 (.48%)
Irritability
22 (.48%)
Malaise
22 (.48%)
Tardive Dyskinesia
22 (.48%)
Hallucination
21 (.45%)
Parkinsonism
21 (.45%)
Suicide Attempt
21 (.45%)
Activities Of Daily Living Impaired
20 (.43%)
Hyperhidrosis
20 (.43%)
Muscular Weakness
19 (.41%)
Drug Administration Error
18 (.39%)
Lethargy
18 (.39%)
Memory Impairment
18 (.39%)
Mood Swings
18 (.39%)
Speech Disorder
18 (.39%)
Cough
17 (.37%)
Disturbance In Attention
17 (.37%)
Pneumonia Aspiration
17 (.37%)
Constipation
16 (.35%)
Pain
16 (.35%)
Hypophagia
15 (.32%)
Loss Of Consciousness
15 (.32%)
Pyrexia
15 (.32%)
Tic
15 (.32%)
Amnesia
14 (.3%)
Rash
14 (.3%)
Urinary Tract Infection
14 (.3%)
Blood Pressure Increased
13 (.28%)
Chorea
13 (.28%)
Dehydration
13 (.28%)
Head Injury
13 (.28%)
Intentional Self-injury
13 (.28%)
Pain In Extremity
13 (.28%)
Unevaluable Event
13 (.28%)
Dysstasia
12 (.26%)
Hypersomnia
12 (.26%)
Nervousness
12 (.26%)
Psychotic Disorder
12 (.26%)
Sleep Disorder
12 (.26%)
Apathy
11 (.24%)
Chest Pain
11 (.24%)
Drooling
11 (.24%)
Drug Interaction
11 (.24%)
Mental Disorder
11 (.24%)
No Therapeutic Response
11 (.24%)
Palpitations
11 (.24%)
Disease Complication
10 (.22%)
Migraine
10 (.22%)
Myocardial Infarction
10 (.22%)
Syncope
10 (.22%)
Treatment Noncompliance
10 (.22%)
Arthralgia
9 (.19%)
Back Pain
9 (.19%)
Cardiac Arrest
9 (.19%)
Depressed Mood
9 (.19%)
Electrocardiogram Qt Prolonged
9 (.19%)
General Physical Health Deteriorati...
9 (.19%)
Mental Status Changes
9 (.19%)

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

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

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

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

Huntingtons Disease
508
Huntingtons Chorea
308
Tardive Dyskinesia
116
Dyskinesia
112
Product Used For Unknown Indication
90
Chorea
70
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Dystonia
68
Tourettes Disorder
58
Drug Use For Unknown Indication
42
Tic
21
Tremor
13
Torticollis
13
Movement Disorder
12
Meiges Syndrome
10
Ballismus
9
Choreoathetosis
5
Muscle Spasms
5
Extrapyramidal Disorder
5
Cerebral Palsy
5
Obsessive-compulsive Disorder
4
Parkinsons Disease
4
Cardiovascular Disorder
3
Blepharospasm
3
Muscle Twitching
3
Ushers Syndrome
2
Sydenhams Chorea
2
Charles Bonnet Syndrome
2
Essential Tremor
2
Cerebellar Ataxia
2
Peroneal Muscular Atrophy
2
Motor Neurone Disease
2
Hiccups
2
Basal Ganglion Degeneration
2
Spinocerebellar Disorder
2
Parkinsonism
2
Convulsion
1
Death
1
Inborn Error Of Metabolism
1
Athetosis
1
Stiff-man Syndrome
1
Primary Cerebellar Degeneration
1
Nervous System Disorder
1
Bipolar Disorder
1
Monoparesis
1
Mental Disorder
1
Anorexia Nervosa
1
Tooth Disorder
1
Hemiparesis
1
Neurodegenerative Disorder
1
Mitochondrial Enzyme Deficiency
1
Ill-defined Disorder
1

Drug Labels

LabelLabelerEffective
XenazineLundbeck Inc.01-MAY-11

Xenazine Case Reports

What Xenazine 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 Xenazine. 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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