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Versed Adverse Events Reported to the FDA Over Time

How are Versed adverse event reports trending over time?

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

Most Common Versed Adverse Events Reported to the FDA

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

Hypotension
196 (2.13%)
Drug Ineffective
188 (2.04%)
Cardiac Arrest
121 (1.31%)
Oxygen Saturation Decreased
113 (1.23%)
Anaphylactic Reaction
102 (1.11%)
Drug Interaction
90 (.98%)
Agitation
89 (.97%)
Tachycardia
84 (.91%)
Bradycardia
82 (.89%)
Convulsion
81 (.88%)
Medication Error
78 (.85%)
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Loss Of Consciousness
73 (.79%)
Respiratory Arrest
71 (.77%)
Drug Rash With Eosinophilia And Sys...
67 (.73%)
Blood Pressure Decreased
64 (.69%)
Sedation
63 (.68%)
Depressed Level Of Consciousness
61 (.66%)
Rhabdomyolysis
59 (.64%)
Vomiting
59 (.64%)
Respiratory Depression
57 (.62%)
Cardio-respiratory Arrest
56 (.61%)
Nausea
56 (.61%)
Unresponsive To Stimuli
56 (.61%)
Procedural Complication
55 (.6%)
Hypoxia
54 (.59%)
Urticaria
54 (.59%)
Confusional State
53 (.58%)
Somnolence
52 (.56%)
Dyspnoea
50 (.54%)
Pyrexia
49 (.53%)
Overdose
48 (.52%)
Anaesthetic Complication
47 (.51%)
Post Procedural Complication
46 (.5%)
Anaphylactic Shock
45 (.49%)
Coma
45 (.49%)
Erythema
45 (.49%)
Circulatory Collapse
43 (.47%)
Dyskinesia
43 (.47%)
Heart Rate Increased
43 (.47%)
Hypertension
43 (.47%)
Anxiety
42 (.46%)
Respiratory Failure
42 (.46%)
Toxic Epidermal Necrolysis
42 (.46%)
Ventricular Tachycardia
42 (.46%)
Hyperhidrosis
41 (.44%)
Tremor
41 (.44%)
Drug Exposure During Pregnancy
38 (.41%)
Apnoea
37 (.4%)
Disseminated Intravascular Coagulat...
37 (.4%)
Ventricular Fibrillation
37 (.4%)
Renal Failure Acute
35 (.38%)
Depression
33 (.36%)
Drug Effect Decreased
33 (.36%)
Renal Failure
33 (.36%)
Serotonin Syndrome
33 (.36%)
Completed Suicide
32 (.35%)
Headache
32 (.35%)
Insomnia
31 (.34%)
Metabolic Acidosis
31 (.34%)
Cyanosis
30 (.33%)
Death
30 (.33%)
Aggression
29 (.31%)
Delirium
29 (.31%)
Drug Toxicity
29 (.31%)
Mental Status Changes
29 (.31%)
Pain
29 (.31%)
Alanine Aminotransferase Increased
28 (.3%)
Amnesia
28 (.3%)
Aspartate Aminotransferase Increase...
28 (.3%)
Delayed Recovery From Anaesthesia
28 (.3%)
Pneumonia
28 (.3%)
Suicide Attempt
28 (.3%)
Condition Aggravated
27 (.29%)
Drug Withdrawal Syndrome
27 (.29%)
Respiratory Distress
27 (.29%)
Shock
27 (.29%)
Dizziness
26 (.28%)
Myoclonus
26 (.28%)
Restlessness
26 (.28%)
Mydriasis
25 (.27%)
Sinus Tachycardia
25 (.27%)
Blood Creatine Phosphokinase Increa...
24 (.26%)
Blood Creatinine Increased
24 (.26%)
Blood Pressure Increased
24 (.26%)
Disorientation
24 (.26%)
Drug Hypersensitivity
24 (.26%)
Muscle Rigidity
24 (.26%)
Pulmonary Embolism
24 (.26%)
Stevens-johnson Syndrome
24 (.26%)
Acute Respiratory Distress Syndrome
23 (.25%)
Chills
23 (.25%)
Electrocardiogram Qt Prolonged
22 (.24%)
Rash
22 (.24%)
Respiratory Rate Increased
22 (.24%)
Suicidal Ideation
22 (.24%)
Thrombocytopenia
22 (.24%)
Asthenia
21 (.23%)
Bronchospasm
21 (.23%)
Grand Mal Convulsion
21 (.23%)
Haemorrhage
21 (.23%)
Intentional Drug Misuse
21 (.23%)

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

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

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

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

Sedation
894
Product Used For Unknown Indication
611
Drug Use For Unknown Indication
396
Anaesthesia
394
Sedative Therapy
191
Premedication
131
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Induction Of Anaesthesia
121
General Anaesthesia
90
Agitation
77
Colonoscopy
60
Surgery
55
Anxiety
55
Convulsion
50
Anaesthetic Premedication
44
Ill-defined Disorder
34
Insomnia
30
Pain
29
Sleep Disorder
28
Preoperative Care
25
Status Epilepticus
25
Anaesthesia Procedure
24
Endoscopy
24
Restlessness
22
Endotracheal Intubation
20
Analgesic Therapy
19
Sensory Disturbance
18
Prophylaxis
15
Convulsion Neonatal
14
Induction And Maintenance Of Anaest...
13
Catheterisation Cardiac
13
Analgesia
13
Endoscopic Retrograde Cholangiopanc...
12
Delirium
11
Bronchoscopy
11
Amnesia
11
Muscle Relaxant Therapy
10
Tooth Extraction
9
Complex Partial Seizures
9
Chronic Myeloid Leukaemia
9
Echocardiogram
8
Sleep Disorder Therapy
8
Oesophagogastroduodenoscopy
8
Epilepsy
7
Mechanical Ventilation
7
Abscess Drainage
7
Intentional Overdose
7
Maintenance Of Anaesthesia
7
Gastrostomy Tube Insertion
6
Intubation
6
Analgesic Effect
6
Suicide Attempt
6

Versed Case Reports

What Versed 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 Versed. 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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