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EQUANIL

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Equanil Adverse Events Reported to the FDA Over Time

How are Equanil adverse event reports trending over time?

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

Most Common Equanil Adverse Events Reported to the FDA

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

Confusional State
31 (2.83%)
Fall
30 (2.74%)
Malaise
26 (2.37%)
Somnolence
23 (2.1%)
Coma
22 (2.01%)
Eosinophilia
19 (1.74%)
Prurigo
17 (1.55%)
Eczema
16 (1.46%)
Pruritus
13 (1.19%)
Abnormal Behaviour
12 (1.1%)
Agitation
11 (1%)
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Hyponatraemia
11 (1%)
Loss Of Consciousness
11 (1%)
Pruritus Generalised
11 (1%)
Disorientation
10 (.91%)
Hypernatraemia
10 (.91%)
Miosis
10 (.91%)
Suicide Attempt
10 (.91%)
Aggression
9 (.82%)
Cardio-respiratory Arrest
9 (.82%)
Death
9 (.82%)
Vomiting
9 (.82%)
Cognitive Disorder
8 (.73%)
Leukopenia
8 (.73%)
Neutropenia
8 (.73%)
Renal Failure Acute
8 (.73%)
Sudden Death
8 (.73%)
Condition Aggravated
7 (.64%)
Dehydration
7 (.64%)
Drug Interaction
7 (.64%)
General Physical Health Deteriorati...
7 (.64%)
Grand Mal Convulsion
7 (.64%)
Hypotension
7 (.64%)
Lung Disorder
7 (.64%)
Pyrexia
7 (.64%)
Thrombocytopenia
7 (.64%)
Alanine Aminotransferase Increased
6 (.55%)
Balance Disorder
6 (.55%)
Convulsion
6 (.55%)
Eosinophil Count Increased
6 (.55%)
Face Oedema
6 (.55%)
Gamma-glutamyltransferase Increased
6 (.55%)
Head Injury
6 (.55%)
Multiple Drug Overdose Intentional
6 (.55%)
Overdose
6 (.55%)
Pulmonary Embolism
6 (.55%)
Renal Failure
6 (.55%)
Tachycardia
6 (.55%)
Urinary Retention
6 (.55%)
Altered State Of Consciousness
5 (.46%)
Aspartate Aminotransferase Increase...
5 (.46%)
Cytolytic Hepatitis
5 (.46%)
Drug Toxicity
5 (.46%)
Hypothermia
5 (.46%)
Hypothyroidism
5 (.46%)
Inflammation
5 (.46%)
Intentional Overdose
5 (.46%)
Malnutrition
5 (.46%)
Palatal Oedema
5 (.46%)
Respiratory Disorder
5 (.46%)
Rhabdomyolysis
5 (.46%)
Tremor
5 (.46%)
Urticaria
5 (.46%)
Aphasia
4 (.37%)
Blood Bilirubin Increased
4 (.37%)
Blood Creatine Phosphokinase Increa...
4 (.37%)
Bone Marrow Failure
4 (.37%)
Bradycardia
4 (.37%)
Drug Eruption
4 (.37%)
Dysphagia
4 (.37%)
Erythema
4 (.37%)
Haematoma
4 (.37%)
Hepatitis Cholestatic
4 (.37%)
Jaundice
4 (.37%)
Leukocytosis
4 (.37%)
Lip Oedema
4 (.37%)
Memory Impairment
4 (.37%)
Oedema Peripheral
4 (.37%)
Psychomotor Retardation
4 (.37%)
Respiratory Depression
4 (.37%)
Septic Shock
4 (.37%)
Wrong Drug Administered
4 (.37%)
Agranulocytosis
3 (.27%)
Alcohol Poisoning
3 (.27%)
Anorexia
3 (.27%)
Anxiety
3 (.27%)
Blood Alkaline Phosphatase Increase...
3 (.27%)
Blood Creatinine Increased
3 (.27%)
Cardiac Arrest
3 (.27%)
Cholestasis
3 (.27%)
Circulatory Collapse
3 (.27%)
Completed Suicide
3 (.27%)
Creatinine Renal Clearance Decrease...
3 (.27%)
Depressed Level Of Consciousness
3 (.27%)
Dizziness
3 (.27%)
Drug Exposure During Pregnancy
3 (.27%)
Extrapyramidal Disorder
3 (.27%)
Faecaloma
3 (.27%)
Foetal Growth Retardation
3 (.27%)
Gait Disturbance
3 (.27%)
Haematemesis
3 (.27%)

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

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

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

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

Drug Use For Unknown Indication
73
Anxiety
54
Product Used For Unknown Indication
33
Depression
24
Agitation
16
Alcoholism
8
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Unevaluable Event
7
Sleep Disorder
7
Insomnia
6
Ill-defined Disorder
5
Prophylaxis
5
Aggression
5
Delirium Tremens
3
Agoraphobia
3
Dementia
3
Abnormal Behaviour
3
Headache
2
Anxiolytic Therapy
2
Intentional Drug Misuse
2
Self-medication
2
Restlessness
2
Intentional Overdose
2
Suicide Attempt
1
Dysthymic Disorder
1
Dyspnoea
1
Confusional State
1
Psychotic Disorder
1
Alcohol Use
1
Dementia Alzheimers Type
1
Alcohol Withdrawal Syndrome
1
Drug Administration Error
1
Cognitive Disorder
1
Psychomotor Hyperactivity
1
Type 2 Diabetes Mellitus
1
Overdose
1

Equanil Case Reports

What Equanil 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 Equanil. 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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