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INSIDON

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Insidon Adverse Events Reported to the FDA Over Time

How are Insidon adverse event reports trending over time?

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

Most Common Insidon Adverse Events Reported to the FDA

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

Suicide Attempt
12 (5.74%)
Cerebrovascular Accident
9 (4.31%)
Blood Pressure Increased
6 (2.87%)
Tachycardia
6 (2.87%)
Drug Interaction
5 (2.39%)
Hepatic Enzyme Increased
5 (2.39%)
Hypotension
5 (2.39%)
Intentional Overdose
5 (2.39%)
Multiple Drug Overdose Intentional
5 (2.39%)
Nausea
5 (2.39%)
Somnolence
5 (2.39%)
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Alanine Aminotransferase Increased
4 (1.91%)
Aspartate Aminotransferase Increase...
4 (1.91%)
Blood Bilirubin Increased
4 (1.91%)
Blood Pressure Systolic Increased
4 (1.91%)
Drug Eruption
4 (1.91%)
Muscle Spasms
4 (1.91%)
Overdose
4 (1.91%)
Stevens-johnson Syndrome
4 (1.91%)
Tetany
4 (1.91%)
Anxiety
3 (1.44%)
Blood Lactate Dehydrogenase Increas...
3 (1.44%)
Blood Sodium Increased
3 (1.44%)
Depression
3 (1.44%)
Hypertensive Crisis
3 (1.44%)
Arrhythmia
2 (.96%)
Atrial Fibrillation
2 (.96%)
Atrioventricular Block
2 (.96%)
Bronchitis
2 (.96%)
Cleft Palate
2 (.96%)
Drug Abuse
2 (.96%)
Dry Mouth
2 (.96%)
Erythema
2 (.96%)
Glomerulonephritis
2 (.96%)
Hypersensitivity
2 (.96%)
Hypertension
2 (.96%)
Hypertrophy
2 (.96%)
Multiple Drug Overdose
2 (.96%)
Osteoma
2 (.96%)
Ovarian Cyst
2 (.96%)
Panic Disorder
2 (.96%)
Pierre Robin Syndrome
2 (.96%)
Pruritus
2 (.96%)
Pyrexia
2 (.96%)
Rash
2 (.96%)
Skin Disorder
2 (.96%)
Syncope
2 (.96%)
Vertebral Artery Stenosis
2 (.96%)
Accidental Exposure
1 (.48%)
Agitation
1 (.48%)
Alcohol Use
1 (.48%)
Apathy
1 (.48%)
Blood Albumin Decreased
1 (.48%)
Blood Alkaline Phosphatase Increase...
1 (.48%)
Blood Bilirubin Unconjugated Increa...
1 (.48%)
Blood Cholesterol Increased
1 (.48%)
Blood Creatinine Increased
1 (.48%)
Blood Fibrinogen Decreased
1 (.48%)
Bradycardia
1 (.48%)
Caesarean Section
1 (.48%)
Cholestasis
1 (.48%)
Circulatory Collapse
1 (.48%)
Coma
1 (.48%)
Convulsion
1 (.48%)
Diplopia
1 (.48%)
Fatigue
1 (.48%)
Gamma-glutamyltransferase Increased
1 (.48%)
Gestational Diabetes
1 (.48%)
Glomerular Filtration Rate Decrease...
1 (.48%)
Heart Sounds Abnormal
1 (.48%)
Hepatic Fibrosis
1 (.48%)
Hepatic Steatosis
1 (.48%)
Hyperhidrosis
1 (.48%)
Hyperventilation
1 (.48%)
Hypokalaemia
1 (.48%)
Hyponatraemia
1 (.48%)
Hypothermia
1 (.48%)
Intentional Self-injury
1 (.48%)
Mean Cell Volume Increased
1 (.48%)
Middle Insomnia
1 (.48%)
Pain
1 (.48%)
Pre-eclampsia
1 (.48%)
Pregnancy
1 (.48%)
Premature Baby
1 (.48%)
Prothrombin Time Prolonged
1 (.48%)
Restlessness
1 (.48%)
Sopor
1 (.48%)
Systolic Hypertension
1 (.48%)
Vascular Injury
1 (.48%)
Weight Decreased
1 (.48%)
White Blood Cell Count Decreased
1 (.48%)
Yellow Skin
1 (.48%)

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

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

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

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

Depression
12
Product Used For Unknown Indication
12
Generalised Anxiety Disorder
5
Anxiety Disorder
5
Sleep Disorder
5
Drug Use For Unknown Indication
5
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Anxiety
2
Antidepressant Therapy
1
Restlessness
1
Bipolar Disorder
1
Dystonia
1

Insidon Case Reports

What Insidon 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 Insidon. 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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