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PRAZEPAM

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Prazepam Adverse Events Reported to the FDA Over Time

How are Prazepam adverse event reports trending over time?

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

Most Common Prazepam Adverse Events Reported to the FDA

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

Drug Exposure During Pregnancy
26 (2.45%)
Suicide Attempt
21 (1.98%)
Somnolence
17 (1.6%)
Confusional State
16 (1.51%)
Fall
14 (1.32%)
Multiple Drug Overdose Intentional
14 (1.32%)
Intentional Overdose
12 (1.13%)
Cytolytic Hepatitis
11 (1.03%)
Coma
10 (.94%)
Cor Pulmonale Chronic
10 (.94%)
Depressed Level Of Consciousness
10 (.94%)
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Dyspnoea Exertional
10 (.94%)
Gamma-glutamyltransferase Increased
10 (.94%)
Pulmonary Arterial Hypertension
10 (.94%)
Transaminases Increased
10 (.94%)
Dehydration
9 (.85%)
Disorientation
9 (.85%)
Disturbance In Attention
9 (.85%)
General Physical Health Deteriorati...
9 (.85%)
Premature Baby
9 (.85%)
Pyrexia
9 (.85%)
Sopor
9 (.85%)
Sudden Death
9 (.85%)
Blood Alkaline Phosphatase Increase...
8 (.75%)
Diarrhoea
8 (.75%)
Drug Interaction
8 (.75%)
Hyponatraemia
8 (.75%)
Atrial Septal Defect
7 (.66%)
Caesarean Section
7 (.66%)
Hypothermia
7 (.66%)
Maternal Drugs Affecting Foetus
7 (.66%)
Renal Failure
7 (.66%)
Renal Failure Acute
7 (.66%)
Agitation
6 (.56%)
Anaemia
6 (.56%)
Congenital Musculoskeletal Anomaly
6 (.56%)
Convulsion
6 (.56%)
Extrapyramidal Disorder
6 (.56%)
Heart Rate Increased
6 (.56%)
Hypotension
6 (.56%)
Inflammation
6 (.56%)
Malaise
6 (.56%)
Myoclonus
6 (.56%)
Respiratory Acidosis
6 (.56%)
Death
5 (.47%)
Feeling Abnormal
5 (.47%)
Hypoproteinaemia
5 (.47%)
Intracranial Pressure Increased
5 (.47%)
Oxygen Saturation Decreased
5 (.47%)
Pregnancy
5 (.47%)
Abortion Induced
4 (.38%)
Abortion Spontaneous
4 (.38%)
Aggression
4 (.38%)
Agranulocytosis
4 (.38%)
Arnold-chiari Malformation
4 (.38%)
Balance Disorder
4 (.38%)
C-reactive Protein Increased
4 (.38%)
Cardiomegaly
4 (.38%)
Chills
4 (.38%)
Delirium
4 (.38%)
Depression
4 (.38%)
Loss Of Consciousness
4 (.38%)
Meningocele
4 (.38%)
Metabolic Acidosis
4 (.38%)
Mood Altered
4 (.38%)
Overdose
4 (.38%)
Pco2 Decreased
4 (.38%)
Polyhydramnios
4 (.38%)
Rales
4 (.38%)
Refusal Of Treatment By Patient
4 (.38%)
Social Avoidant Behaviour
4 (.38%)
Spina Bifida
4 (.38%)
Thrombocytopenia
4 (.38%)
Urinary Tract Infection
4 (.38%)
Vertigo
4 (.38%)
Visual Acuity Reduced
4 (.38%)
Vomiting
4 (.38%)
Weight Increased
4 (.38%)
Abnormal Behaviour
3 (.28%)
Anion Gap Increased
3 (.28%)
Apathy
3 (.28%)
Azotaemia
3 (.28%)
Blood Bicarbonate Decreased
3 (.28%)
Blood Creatinine Increased
3 (.28%)
Blood Glucose Increased
3 (.28%)
Blood Lactic Acid Decreased
3 (.28%)
Blood Sodium Increased
3 (.28%)
Breech Presentation
3 (.28%)
Cerebellar Syndrome
3 (.28%)
Cognitive Disorder
3 (.28%)
Completed Suicide
3 (.28%)
Congenital Diaphragmatic Hernia
3 (.28%)
Cyanosis
3 (.28%)
Cystic Lymphangioma
3 (.28%)
Disease Progression
3 (.28%)
Drug Level Increased
3 (.28%)
Drug Toxicity
3 (.28%)
Dyskinesia
3 (.28%)
Encephalopathy
3 (.28%)
Erythema
3 (.28%)
Eye Pain
3 (.28%)

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

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

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

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

Anxiety
132
Drug Use For Unknown Indication
83
Product Used For Unknown Indication
61
Depression
39
Suicide Attempt
7
Abnormal Behaviour
6
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Anxiolytic Therapy
5
Unevaluable Event
5
Nervousness
4
Drug Exposure During Pregnancy
4
Major Depression
3
Dysthymic Disorder
3
Anxiety Disorder
3
Bipolar I Disorder
3
Insomnia
3
Schizoaffective Disorder
3
Intentional Overdose
2
Ill-defined Disorder
2
Dementia
2
Pain
2
Phobia
2
Maternal Exposure During Pregnancy
2
Schizophrenia
2
Toxicity To Various Agents
2
Bipolar Disorder
1
Foetal Exposure During Pregnancy
1
Autism Spectrum Disorder
1
Sleep Disorder
1
Agitation
1
Drug Therapy
1
Maternal Exposure Timing Unspecifie...
1
Schizophrenia, Paranoid Type
1
Overdose
1
Akathisia
1
Hypomania
1
Renal Transplant
1
Osteogenesis Imperfecta
1

Prazepam Case Reports

What Prazepam 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 Prazepam. 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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