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ESCITALOPRAM OXALATE

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Escitalopram Oxalate Adverse Events Reported to the FDA Over Time

How are Escitalopram Oxalate adverse event reports trending over time?

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

Most Common Escitalopram Oxalate Adverse Events Reported to the FDA

What are the most common Escitalopram Oxalate adverse events reported to the FDA?

Completed Suicide
155 (1.84%)
Drug Interaction
133 (1.58%)
Suicide Attempt
111 (1.32%)
Tremor
93 (1.1%)
Overdose
92 (1.09%)
Fall
90 (1.07%)
Somnolence
87 (1.03%)
Depression
79 (.94%)
Anxiety
76 (.9%)
Fatigue
76 (.9%)
Serotonin Syndrome
76 (.9%)
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Hyponatraemia
74 (.88%)
Suicidal Ideation
74 (.88%)
Confusional State
73 (.87%)
Condition Aggravated
72 (.85%)
Dizziness
72 (.85%)
Intentional Overdose
72 (.85%)
Nausea
68 (.81%)
Multiple Drug Overdose Intentional
67 (.79%)
Convulsion
65 (.77%)
Cardiac Arrest
64 (.76%)
Malaise
64 (.76%)
Vomiting
62 (.74%)
Agitation
59 (.7%)
Loss Of Consciousness
58 (.69%)
Diarrhoea
56 (.66%)
Restlessness
56 (.66%)
Maternal Drugs Affecting Foetus
54 (.64%)
Tachycardia
54 (.64%)
Multiple Drug Overdose
50 (.59%)
Respiratory Arrest
50 (.59%)
Drug Ineffective
48 (.57%)
Headache
48 (.57%)
Hypotension
47 (.56%)
Insomnia
47 (.56%)
Drug Exposure During Pregnancy
42 (.5%)
Feeling Abnormal
42 (.5%)
Aggression
39 (.46%)
Dyskinesia
39 (.46%)
Dyspnoea
39 (.46%)
Weight Increased
39 (.46%)
Alanine Aminotransferase Increased
38 (.45%)
Asthenia
37 (.44%)
Weight Decreased
37 (.44%)
Delirium
31 (.37%)
Rhabdomyolysis
31 (.37%)
Coma
30 (.36%)
Electrocardiogram Qt Prolonged
30 (.36%)
Paraesthesia
30 (.36%)
Caesarean Section
29 (.34%)
Decreased Appetite
29 (.34%)
Abdominal Pain
28 (.33%)
Renal Failure
28 (.33%)
Urinary Tract Infection
28 (.33%)
Pyrexia
27 (.32%)
Blood Creatine Phosphokinase Increa...
26 (.31%)
Drug Toxicity
26 (.31%)
Hallucination, Visual
26 (.31%)
Syncope
26 (.31%)
Dehydration
25 (.3%)
General Physical Health Deteriorati...
25 (.3%)
Grand Mal Convulsion
25 (.3%)
Hyperhidrosis
25 (.3%)
Hypertension
25 (.3%)
Abnormal Dreams
24 (.28%)
Cough
24 (.28%)
Disorientation
24 (.28%)
Dysarthria
24 (.28%)
Neck Pain
24 (.28%)
Neuroleptic Malignant Syndrome
24 (.28%)
Pregnancy
24 (.28%)
Renal Failure Acute
24 (.28%)
Self-injurious Ideation
24 (.28%)
Blood Pressure Increased
23 (.27%)
Crying
23 (.27%)
Depressed Level Of Consciousness
23 (.27%)
Oedema Peripheral
23 (.27%)
Thrombocytopenia
23 (.27%)
Abnormal Behaviour
22 (.26%)
Aspartate Aminotransferase Increase...
22 (.26%)
Irritability
22 (.26%)
Sleep Disorder
22 (.26%)
Blood Sodium Decreased
21 (.25%)
Cardio-respiratory Arrest
21 (.25%)
Disturbance In Attention
21 (.25%)
Premature Baby
20 (.24%)
Balance Disorder
19 (.23%)
Hepatic Cirrhosis
19 (.23%)
Pneumonia
19 (.23%)
Vertigo
19 (.23%)
Amnesia
18 (.21%)
Atrial Fibrillation
18 (.21%)
Blood Alkaline Phosphatase Increase...
18 (.21%)
Disease Recurrence
18 (.21%)
Dystonia
18 (.21%)
Eczema
18 (.21%)
Hyperphagia
18 (.21%)
Lethargy
18 (.21%)
Muscle Rigidity
18 (.21%)
Off Label Use
18 (.21%)
Pulmonary Embolism
18 (.21%)

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

What are the most common Escitalopram Oxalate adverse events reported to the FDA?

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

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

Depression
873
Drug Use For Unknown Indication
241
Anxiety
152
Product Used For Unknown Indication
76
Major Depression
57
Bipolar Disorder
27
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Ill-defined Disorder
20
Panic Disorder
18
Bipolar I Disorder
17
Antidepressant Therapy
15
Anxiety Disorder
15
Schizoaffective Disorder
15
Obsessive-compulsive Disorder
12
Generalised Anxiety Disorder
11
Panic Attack
10
Depressive Symptom
10
Suicide Attempt
8
Schizophrenia
8
Ankylosing Spondylitis
6
Dysthymic Disorder
6
Pain
6
Post-traumatic Stress Disorder
6
Hypokinesia
6
Affective Disorder
5
Psychotic Disorder
5
Depressed Mood
5
Social Phobia
5
Disease Recurrence
4
Urinary Tract Disorder
4
Hypertension
4
Suicidal Ideation
3
Dysphonia
3
Fibromyalgia
3
Agoraphobia
3
Mood Swings
3
Diabetic Foot
3
Alcoholic Psychosis
3
Intentional Overdose
3
Hiv Infection
3
Prophylaxis
3
Alcoholism
2
Stress
2
Borderline Personality Disorder
2
Conversion Disorder
2
Drug Exposure During Pregnancy
2
Mental Disorder
2
Burnout Syndrome
2
Acute Psychosis
2
Hormone Therapy
2
Neurosis
2
Phobia
2

Drug Labels

LabelLabelerEffective
LexaproBryant Ranch Prepack14-AUG-02
LexaproBryant Ranch Prepack14-AUG-02
Escitalopram OxalateAmneal Pharmaceuticals LLC21-FEB-11
LexaproCardinal Health29-APR-11
LexaproPD-Rx Pharmaceuticals, Inc.20-MAY-11
LexaproPD-Rx Pharmaceuticals, Inc.20-MAY-11
Escitalopram Oxalate Camber Pharmaceuticals, Inc.01-OCT-11
LexaproLake Erie Medical & Surgical Supply DBA Quality Care Products LLC16-DEC-11
Escitalopram OxalateMylan Institutional Inc.16-DEC-11
LexaproCardinal Health10-APR-12
LexaproSTAT Rx USA LLC16-JUL-12
Escitalopram OxalatePreferred Pharmaceuticals, Inc.20-SEP-12
Escitalopram Oxalate Exelan Pharmaceuticals Inc.01-OCT-12
Escitalopram OxalatePhysicians Total Care, Inc.19-OCT-12
EscitalopramAccord Healthcare Inc.01-DEC-12
Escitalopram OxalateMylan Pharmaceuticals Inc.10-DEC-12
LexaproForest Laboratories, Inc.11-DEC-12
EscitalopramAurobindo Pharma Limited07-JAN-13
Escitalopram OxalateTorrent Pharmaceuticals Limited09-JAN-13
Escitalopram Oxalate Aurobindo Pharma Limited10-JAN-13
EscitalopramPreferred Pharmaceuticals, Inc18-JAN-13
Escitalopram OxalateMacleods Pharmaceuticals Limited22-JAN-13
Escitalopram OxalateCardinal Health08-MAR-13
Escitalopram OxalateTaro Pharmaceuticals U.S.A., Inc.15-MAR-13
LexaproREMEDYREPACK INC. 18-MAR-13

Escitalopram Oxalate Case Reports

What Escitalopram Oxalate 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 Escitalopram Oxalate. 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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