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NORDIAZEPAM

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Nordiazepam Adverse Events Reported to the FDA Over Time

How are Nordiazepam adverse event reports trending over time?

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

Most Common Nordiazepam Adverse Events Reported to the FDA

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

Drug Toxicity
41 (6.79%)
Pulmonary Oedema
37 (6.13%)
Respiratory Depression
37 (6.13%)
Overdose
31 (5.13%)
Pulmonary Congestion
27 (4.47%)
Drug Interaction
25 (4.14%)
Completed Suicide
20 (3.31%)
Accidental Death
19 (3.15%)
Multiple Drug Overdose
19 (3.15%)
Accidental Overdose
15 (2.48%)
Accidental Poisoning
12 (1.99%)
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Pneumonia
10 (1.66%)
Asphyxia
9 (1.49%)
Cardiomegaly
9 (1.49%)
Brain Oedema
8 (1.32%)
Death
8 (1.32%)
Serotonin Syndrome
8 (1.32%)
Alcohol Poisoning
7 (1.16%)
Aspiration
7 (1.16%)
Snoring
7 (1.16%)
Bacterial Sepsis
6 (.99%)
Poisoning
6 (.99%)
Wrong Technique In Drug Usage Proce...
6 (.99%)
Arrhythmia
5 (.83%)
Bronchopneumonia
5 (.83%)
Hepatic Steatosis
5 (.83%)
Hepatitis C
5 (.83%)
Aggression
4 (.66%)
Cardiac Arrest
4 (.66%)
Drug Abuse
4 (.66%)
Encephalitis
4 (.66%)
Fall
4 (.66%)
Intentional Overdose
4 (.66%)
Loss Of Consciousness
4 (.66%)
Multiple Drug Overdose Accidental
4 (.66%)
Needle Track Marks
4 (.66%)
Stupor
4 (.66%)
Toxicologic Test Abnormal
4 (.66%)
Unresponsive To Stimuli
4 (.66%)
Vomiting
4 (.66%)
Cognitive Disorder
3 (.5%)
Congestive Cardiomyopathy
3 (.5%)
Contusion
3 (.5%)
Depression
3 (.5%)
Drug Screen Positive
3 (.5%)
Pneumonia Aspiration
3 (.5%)
Renal Failure
3 (.5%)
Respiratory Arrest
3 (.5%)
Sleep Paralysis
3 (.5%)
Accidental Exposure
2 (.33%)
Arteriosclerosis Coronary Artery
2 (.33%)
Blood Alcohol Increased
2 (.33%)
Cardio-respiratory Arrest
2 (.33%)
Drug Intolerance
2 (.33%)
Drug Level Increased
2 (.33%)
Excoriation
2 (.33%)
Hypothermia
2 (.33%)
Myocardial Ischaemia
2 (.33%)
Pneumoconiosis
2 (.33%)
Road Traffic Accident
2 (.33%)
Sleep Apnoea Syndrome
2 (.33%)
Somnolence
2 (.33%)
Spleen Congestion
2 (.33%)
Sudden Death
2 (.33%)
Visceral Congestion
2 (.33%)
Abnormal Behaviour
1 (.17%)
Acute Pulmonary Oedema
1 (.17%)
Agitation
1 (.17%)
Alcohol Use
1 (.17%)
Anuria
1 (.17%)
Aortic Arteriosclerosis
1 (.17%)
Aortic Valve Calcification
1 (.17%)
Aortic Valve Stenosis
1 (.17%)
Aspartate Aminotransferase Increase...
1 (.17%)
Asthma
1 (.17%)
Blood Glucose Increased
1 (.17%)
Blood Ph Increased
1 (.17%)
Blood Pressure Decreased
1 (.17%)
Blood Pressure Systolic Decreased
1 (.17%)
Bone Fissure
1 (.17%)
Brain Injury
1 (.17%)
Bronchiolitis
1 (.17%)
Cachexia
1 (.17%)
Cerebrovascular Disorder
1 (.17%)
Chest Injury
1 (.17%)
Condition Aggravated
1 (.17%)
Continuous Positive Airway Pressure
1 (.17%)
Coronary Artery Disease
1 (.17%)
Cyanosis
1 (.17%)
Dehydration
1 (.17%)
Dependence
1 (.17%)
Dialysis
1 (.17%)
Drug Dependence
1 (.17%)
Drug Effect Decreased
1 (.17%)
Drug Ineffective
1 (.17%)
Drug Level Below Therapeutic
1 (.17%)
Ecchymosis
1 (.17%)
Eschar
1 (.17%)
Exposure To Toxic Agent
1 (.17%)
Eye Haemorrhage
1 (.17%)
Foaming At Mouth
1 (.17%)

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

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

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

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

Product Used For Unknown Indication
103
Drug Use For Unknown Indication
52
Accidental Exposure
2
Accidental Poisoning
2
Overdose
2
Completed Suicide
2
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Toxicity To Various Agents
2
Drug Abuse
1

Nordiazepam Case Reports

What Nordiazepam 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 Nordiazepam. 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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