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TRIAZOLAM

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Triazolam Adverse Events Reported to the FDA Over Time

How are Triazolam adverse event reports trending over time?

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

Most Common Triazolam Adverse Events Reported to the FDA

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

Drug Ineffective
63 (6.67%)
Somnolence
17 (1.8%)
Suicide Attempt
17 (1.8%)
Overdose
15 (1.59%)
Depression
11 (1.16%)
Insomnia
11 (1.16%)
Intentional Overdose
11 (1.16%)
Multiple Drug Overdose
11 (1.16%)
Drug Interaction
10 (1.06%)
Drug Toxicity
10 (1.06%)
Electrocardiogram Qt Prolonged
10 (1.06%)
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Sopor
10 (1.06%)
Completed Suicide
9 (.95%)
Blepharospasm
8 (.85%)
Rhabdomyolysis
8 (.85%)
Condition Aggravated
7 (.74%)
Death
7 (.74%)
Heart Rate Decreased
7 (.74%)
Incorrect Dose Administered
7 (.74%)
Suicidal Ideation
7 (.74%)
Altered State Of Consciousness
6 (.63%)
Asthenia
6 (.63%)
Depressed Level Of Consciousness
6 (.63%)
Dizziness
6 (.63%)
Dyspnoea
6 (.63%)
Headache
6 (.63%)
Loss Of Consciousness
6 (.63%)
Nausea
6 (.63%)
Pain
6 (.63%)
Rash
6 (.63%)
Syncope
6 (.63%)
Torsade De Pointes
6 (.63%)
Vomiting
6 (.63%)
White Blood Cell Count Increased
6 (.63%)
Anxiety
5 (.53%)
Blood Lactate Dehydrogenase Increas...
5 (.53%)
Blood Pressure Increased
5 (.53%)
Decreased Appetite
5 (.53%)
Fatigue
5 (.53%)
Head Injury
5 (.53%)
Abdominal Discomfort
4 (.42%)
Abnormal Behaviour
4 (.42%)
Agitation
4 (.42%)
Aspiration
4 (.42%)
Coeliac Disease
4 (.42%)
Dehydration
4 (.42%)
Delirium
4 (.42%)
Disturbance In Attention
4 (.42%)
Drug Dependence
4 (.42%)
Drug Exposure During Pregnancy
4 (.42%)
Drug Screen Negative
4 (.42%)
Erythema
4 (.42%)
Fall
4 (.42%)
Feeling Abnormal
4 (.42%)
Hallucination
4 (.42%)
Heart Rate Increased
4 (.42%)
Hypertension
4 (.42%)
Hypotension
4 (.42%)
Inflammation
4 (.42%)
Malaise
4 (.42%)
Oedema
4 (.42%)
Product Quality Issue
4 (.42%)
Pruritus
4 (.42%)
Sedation
4 (.42%)
Sinus Bradycardia
4 (.42%)
Stevens-johnson Syndrome
4 (.42%)
Thyroidectomy
4 (.42%)
Ventricular Tachycardia
4 (.42%)
Abortion Spontaneous
3 (.32%)
Amnesia
3 (.32%)
Arthritis
3 (.32%)
Blood Creatine Phosphokinase Increa...
3 (.32%)
Blood Pressure Decreased
3 (.32%)
Blood Urea Increased
3 (.32%)
Bradycardia
3 (.32%)
Bradyphrenia
3 (.32%)
C-reactive Protein Increased
3 (.32%)
Caesarean Section
3 (.32%)
Cardiac Failure Congestive
3 (.32%)
Constipation
3 (.32%)
Depressed Mood
3 (.32%)
Diabetes Mellitus
3 (.32%)
Discomfort
3 (.32%)
Drug Effect Decreased
3 (.32%)
Drug Withdrawal Syndrome
3 (.32%)
Dyskinesia
3 (.32%)
Faecal Incontinence
3 (.32%)
Hyperventilation
3 (.32%)
Hypokinesia
3 (.32%)
Impaired Driving Ability
3 (.32%)
Irritability
3 (.32%)
Memory Impairment
3 (.32%)
Multiple Drug Overdose Intentional
3 (.32%)
Po2 Decreased
3 (.32%)
Poor Quality Sleep
3 (.32%)
Pyrexia
3 (.32%)
Renal Failure
3 (.32%)
Renal Impairment
3 (.32%)
Shock
3 (.32%)
Sleep Disorder
3 (.32%)
Treatment Noncompliance
3 (.32%)

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

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

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

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

Insomnia
262
Drug Use For Unknown Indication
79
Sleep Disorder
70
Product Used For Unknown Indication
41
Ill-defined Disorder
15
Anxiety
15
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Depression
8
Schizophrenia
8
Sedation
5
Bipolar I Disorder
5
Restless Legs Syndrome
4
Alcoholism
3
Sedative Therapy
3
Hypersensitivity
3
Intentional Overdose
3
Pain
3
Intentional Self-injury
2
Premedication
2
Anxiety Disorder
2
Somnolence
2
Preoperative Care
2
Asthma
2
Hypnotherapy
1
Agitation
1
Mood Altered
1
Abdominal Pain Upper
1
Prophylaxis
1
Arthritis
1
Dental Operation
1
Anger
1
Poor Quality Sleep
1
Restlessness
1
Drug Exposure During Pregnancy
1
Stress
1
Tooth Disorder
1
Suicide Attempt
1
Initial Insomnia
1
Vertigo
1
Back Pain
1
Antidepressant Therapy
1
Bipolar Disorder
1
Abnormal Dreams
1
Fibromyalgia
1
Tooth Extraction
1
Sleep Disorder Therapy
1

Drug Labels

LabelLabelerEffective
TriazolamBryant Ranch Prepack01-JUN-94
TriazolamPD-Rx Pharmaceuticals, Inc.06-MAY-10
TriazolamSTAT RX USA LLC03-JUN-10
TriazolamUnit Dose Services18-OCT-10
TriazolamPhysicians Total Care, Inc.18-OCT-10
TriazolamRebel Distributors Corp01-DEC-10
TriazolamLake Erie Medical DBA Quality Care Products LLC28-DEC-11
TriazolamGreenstone LLC09-FEB-12
TriazolamAphena Pharma Solutions - Tennessee, Inc.20-JUN-12
TriazolamRoxane Laboratories, Inc.12-NOV-12
HalcionPharmacia and Upjohn Company20-MAR-13
TriazolamA-S Medication Solutions LLC02-MAY-13

Triazolam Case Reports

What Triazolam 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 Triazolam. 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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