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ESCITALOPRAM

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Escitalopram Adverse Events Reported to the FDA Over Time

How are Escitalopram adverse event reports trending over time?

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

Most Common Escitalopram Adverse Events Reported to the FDA

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

Completed Suicide
559 (1.83%)
Drug Interaction
473 (1.55%)
Anxiety
373 (1.22%)
Suicide Attempt
321 (1.05%)
Fall
319 (1.04%)
Hyponatraemia
311 (1.02%)
Dizziness
295 (.97%)
Nausea
294 (.96%)
Depression
286 (.94%)
Suicidal Ideation
279 (.91%)
Overdose
269 (.88%)
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Confusional State
265 (.87%)
Convulsion
263 (.86%)
Tremor
262 (.86%)
Somnolence
261 (.85%)
Loss Of Consciousness
253 (.83%)
Fatigue
238 (.78%)
Drug Exposure During Pregnancy
230 (.75%)
Condition Aggravated
226 (.74%)
Agitation
219 (.72%)
Malaise
217 (.71%)
Vomiting
210 (.69%)
Serotonin Syndrome
209 (.68%)
Intentional Overdose
202 (.66%)
Insomnia
199 (.65%)
Headache
188 (.62%)
Cardiac Arrest
185 (.61%)
Asthenia
176 (.58%)
Multiple Drug Overdose Intentional
175 (.57%)
Diarrhoea
158 (.52%)
Restlessness
144 (.47%)
Pregnancy
143 (.47%)
Aggression
138 (.45%)
Feeling Abnormal
135 (.44%)
Drug Ineffective
134 (.44%)
Dyspnoea
134 (.44%)
Maternal Drugs Affecting Foetus
134 (.44%)
Caesarean Section
133 (.44%)
Respiratory Arrest
127 (.42%)
Hypotension
126 (.41%)
Grand Mal Convulsion
121 (.4%)
Hyperhidrosis
119 (.39%)
Decreased Appetite
115 (.38%)
Dyskinesia
115 (.38%)
Tachycardia
115 (.38%)
Weight Increased
115 (.38%)
Paraesthesia
114 (.37%)
Pyrexia
113 (.37%)
Drug Toxicity
112 (.37%)
Coma
108 (.35%)
Disorientation
108 (.35%)
Rhabdomyolysis
108 (.35%)
Drug Withdrawal Syndrome
107 (.35%)
Multiple Drug Overdose
101 (.33%)
Hypertension
97 (.32%)
Syncope
97 (.32%)
Weight Decreased
96 (.31%)
Abdominal Pain
94 (.31%)
Irritability
92 (.3%)
Electrocardiogram Qt Prolonged
91 (.3%)
Disturbance In Attention
89 (.29%)
Off Label Use
88 (.29%)
Cytolytic Hepatitis
87 (.28%)
General Physical Health Deteriorati...
87 (.28%)
Speech Disorder
86 (.28%)
Aspartate Aminotransferase Increase...
85 (.28%)
Urinary Retention
83 (.27%)
Epilepsy
81 (.27%)
Renal Failure
80 (.26%)
Alanine Aminotransferase Increased
79 (.26%)
Blood Creatine Phosphokinase Increa...
78 (.26%)
Death
77 (.25%)
Dysarthria
77 (.25%)
Delirium
76 (.25%)
Panic Attack
74 (.24%)
Renal Failure Acute
74 (.24%)
Sleep Disorder
74 (.24%)
Balance Disorder
73 (.24%)
Gamma-glutamyltransferase Increased
73 (.24%)
Gait Disturbance
72 (.24%)
Amnesia
71 (.23%)
Urinary Tract Infection
71 (.23%)
International Normalised Ratio Incr...
70 (.23%)
Blood Pressure Increased
69 (.23%)
Haemoglobin Decreased
68 (.22%)
Hallucination
68 (.22%)
Abnormal Behaviour
66 (.22%)
Bradycardia
66 (.22%)
Palpitations
66 (.22%)
Anaemia
65 (.21%)
Crying
65 (.21%)
Neuroleptic Malignant Syndrome
65 (.21%)
Poisoning
65 (.21%)
Product Substitution Issue
65 (.21%)
Depressed Level Of Consciousness
64 (.21%)
Abdominal Pain Upper
62 (.2%)
Blood Sodium Decreased
61 (.2%)
Hypokalaemia
61 (.2%)
Oedema Peripheral
61 (.2%)
Vertigo
61 (.2%)
Withdrawal Syndrome
61 (.2%)

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

What are the most common Escitalopram 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, 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 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 According to Those Reporting Adverse Events

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

Depression
3089
Anxiety
509
Drug Use For Unknown Indication
465
Product Used For Unknown Indication
394
Major Depression
277
Bipolar Disorder
85
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Panic Disorder
69
Panic Attack
67
Generalised Anxiety Disorder
65
Obsessive-compulsive Disorder
53
Ill-defined Disorder
51
Schizoaffective Disorder
48
Anxiety Disorder
45
Antidepressant Therapy
40
Suicide Attempt
34
Depressed Mood
31
Bipolar I Disorder
31
Post-traumatic Stress Disorder
29
Affective Disorder
28
Depressive Symptom
28
Social Phobia
26
Dysthymic Disorder
21
Psychotic Disorder
21
Postpartum Depression
19
Schizophrenia
17
Phobia
14
Pain
14
Insomnia
13
Mental Disorder
13
Overdose
11
Prophylaxis
10
Stress
10
Suicidal Ideation
9
Intentional Overdose
9
Neurosis
8
Fibromyalgia
7
Agoraphobia
7
Hypokinesia
7
Adjustment Disorder
7
Disease Recurrence
7
Mood Swings
6
Burnout Syndrome
6
Ankylosing Spondylitis
6
Intentional Self-injury
5
Borderline Personality Disorder
5
Agitation
5
Alcoholism
5
Premenstrual Syndrome
5
Drug Exposure During Pregnancy
5
Sleep Disorder
5
Dementia Alzheimers Type
4

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
Escitalopram OxalateMylan Institutional Inc.16-DEC-11
LexaproLake Erie Medical & Surgical Supply DBA Quality Care Products LLC16-DEC-11
EscitalopramRebel Distributors Corp23-FEB-12
EscitalopramPD-Rx Pharmaceuticals, Inc.14-MAR-12
LexaproCardinal Health10-APR-12
EscitalopramSTAT Rx USA LLC12-APR-12
LexaproSTAT Rx USA LLC16-JUL-12
EscitalopramLupin Pharmaceuticals, Inc.24-JUL-12
EscitalopramUnit Dose Services17-AUG-12
EscitalopramApotex Corp.17-AUG-12
EscitalopramCamber Pharmaceuticals13-SEP-12
Escitalopram Jubilant Cadista Pharmaceuticals Inc.14-SEP-12
Escitalopram OxalatePreferred Pharmaceuticals, Inc.20-SEP-12
EscitalopramMajor Pharmaceuticals26-SEP-12
Escitalopram Oxalate Exelan Pharmaceuticals Inc.01-OCT-12
EscitalopramPD-Rx Pharmaceuticals, Inc.02-OCT-12
EscitalopramPD-Rx Pharmaceuticals, Inc.02-OCT-12
EscitalopramAmerican Health Packaging11-OCT-12
EscitalopramHikma Pharmaceutical15-OCT-12
Escitalopram OxalatePhysicians Total Care, Inc.19-OCT-12
EscitalopramBryant Ranch Prepack23-OCT-12
EscitalopramBryant Ranch Prepack23-OCT-12
EscitalopramWest-ward Pharmaceutical Corp27-NOV-12
EscitalopramAccord Healthcare Inc.01-DEC-12
Escitalopram OxalateMylan Pharmaceuticals Inc.10-DEC-12
LexaproForest Laboratories, Inc.11-DEC-12
EscitalopramRebel Distributors Corp25-DEC-12
EscitalopramTeva Pharmaceuticals USA Inc04-JAN-13
EscitalopramUnit Dose Services04-JAN-13
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
EscitalopramREMEDYREPACK INC. 13-FEB-13
EscitalopramREMEDYREPACK INC. 18-FEB-13
EscitalopramREMEDYREPACK INC. 20-FEB-13
Escitalopram OxalateCardinal Health08-MAR-13
Escitalopram OxalateTaro Pharmaceuticals U.S.A., Inc.15-MAR-13
EscitalopramLegacy Pharmaceutical Packaging18-MAR-13
LexaproREMEDYREPACK INC. 18-MAR-13
EscitalopramREMEDYREPACK INC. 08-APR-13
EscitalopramDispensing Solutions, Inc.08-APR-13
EscitalopramREMEDYREPACK INC. 02-MAY-13
EscitalopramTeva Pharmaceuticals USA Inc03-MAY-13

Escitalopram Case Reports

What Escitalopram 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. 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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