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QUILONUM RETARD

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Quilonum Retard Adverse Events Reported to the FDA Over Time

How are Quilonum Retard adverse event reports trending over time?

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

Most Common Quilonum Retard Adverse Events Reported to the FDA

What are the most common Quilonum Retard adverse events reported to the FDA?

Suicide Attempt
65 (8.07%)
Intentional Overdose
37 (4.6%)
Somnolence
26 (3.23%)
Vomiting
25 (3.11%)
Nausea
22 (2.73%)
Diarrhoea
21 (2.61%)
Renal Failure
20 (2.48%)
Fatigue
19 (2.36%)
Drug Interaction
17 (2.11%)
Gait Disturbance
15 (1.86%)
Tremor
15 (1.86%)
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Confusional State
11 (1.37%)
Dehydration
11 (1.37%)
Disorientation
11 (1.37%)
Therapeutic Agent Toxicity
11 (1.37%)
Bradycardia
10 (1.24%)
Drug Level Increased
9 (1.12%)
Drug Abuser
8 (.99%)
Dysarthria
8 (.99%)
Overdose
8 (.99%)
Restlessness
7 (.87%)
Dizziness
6 (.75%)
Headache
6 (.75%)
Nystagmus
6 (.75%)
Psychotic Disorder
6 (.75%)
Accidental Overdose
5 (.62%)
Agitation
5 (.62%)
Coma
5 (.62%)
Delirium
5 (.62%)
Electrocardiogram Qt Prolonged
5 (.62%)
Fall
5 (.62%)
Hypotension
5 (.62%)
Oedema Peripheral
5 (.62%)
Convulsion
4 (.5%)
Coordination Abnormal
4 (.5%)
Eyelid Oedema
4 (.5%)
Hypertension
4 (.5%)
Multiple Drug Overdose Intentional
4 (.5%)
Myoclonus
4 (.5%)
Poisoning
4 (.5%)
Sinus Bradycardia
4 (.5%)
Sluggishness
4 (.5%)
Speech Disorder
4 (.5%)
Tachycardia
4 (.5%)
Accommodation Disorder
3 (.37%)
Alanine Aminotransferase Increased
3 (.37%)
Apathy
3 (.37%)
Atrioventricular Block First Degree
3 (.37%)
Blood Creatine Phosphokinase Mb Inc...
3 (.37%)
Chills
3 (.37%)
Diplopia
3 (.37%)
Disturbance In Attention
3 (.37%)
Drug Exposure During Pregnancy
3 (.37%)
Drug Toxicity
3 (.37%)
Dry Mouth
3 (.37%)
Extrapyramidal Disorder
3 (.37%)
Gastrointestinal Sounds Abnormal
3 (.37%)
General Physical Health Deteriorati...
3 (.37%)
Haemodialysis
3 (.37%)
Hallucination
3 (.37%)
Hepatitis
3 (.37%)
Hypokinesia
3 (.37%)
Hypothyroidism
3 (.37%)
Ill-defined Disorder
3 (.37%)
Infection
3 (.37%)
Nephropathy Toxic
3 (.37%)
Sedation
3 (.37%)
Sopor
3 (.37%)
Subileus
3 (.37%)
Tooth Disorder
3 (.37%)
Urinary Retention
3 (.37%)
Abasia
2 (.25%)
Abdominal Pain
2 (.25%)
Abortion Incomplete
2 (.25%)
Acidosis
2 (.25%)
Anticonvulsant Drug Level Below The...
2 (.25%)
Antipsychotic Drug Level Above Ther...
2 (.25%)
Antipsychotic Drug Level Below Ther...
2 (.25%)
Antipsychotic Drug Level Increased
2 (.25%)
Arrhythmia
2 (.25%)
Aspartate Aminotransferase Increase...
2 (.25%)
Atrial Fibrillation
2 (.25%)
Autoimmune Thyroiditis
2 (.25%)
Bacterial Infection
2 (.25%)
Balance Disorder
2 (.25%)
Blood Creatine Phosphokinase Increa...
2 (.25%)
Blood Creatinine Increased
2 (.25%)
Blood Potassium Increased
2 (.25%)
Blood Thyroid Stimulating Hormone I...
2 (.25%)
Body Temperature Increased
2 (.25%)
Bradyphrenia
2 (.25%)
Cardiopulmonary Failure
2 (.25%)
Cerebellar Syndrome
2 (.25%)
Cognitive Disorder
2 (.25%)
Consciousness Fluctuating
2 (.25%)
Csf Oligoclonal Band Present
2 (.25%)
Death
2 (.25%)
Depressed Level Of Consciousness
2 (.25%)
Depression
2 (.25%)
Drug Administration Error
2 (.25%)
Dyspnoea
2 (.25%)

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

What are the most common Quilonum Retard adverse events reported to the FDA?

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

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

Schizoaffective Disorder
12
Bipolar Disorder
12
Drug Use For Unknown Indication
11
Bipolar I Disorder
9
Depression
8
Product Used For Unknown Indication
3
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Mental Disorder
2
Ill-defined Disorder
2
Affective Disorder
2
Cluster Headache
1
Schizophrenia, Residual Type
1
Bipolar Ii Disorder
1
Cyclothymic Disorder
1
Major Depression
1
Mania
1
Affect Lability
1

Quilonum Retard Case Reports

What Quilonum Retard 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 Quilonum Retard. 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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