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DIPIPERON

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Dipiperon Adverse Events Reported to the FDA Over Time

How are Dipiperon adverse event reports trending over time?

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

Most Common Dipiperon Adverse Events Reported to the FDA

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

Somnolence
58 (4.79%)
Fall
41 (3.39%)
Suicide Attempt
36 (2.98%)
Drug Interaction
30 (2.48%)
Death
19 (1.57%)
Hyponatraemia
18 (1.49%)
Hypotension
18 (1.49%)
Fatigue
16 (1.32%)
Tachycardia
16 (1.32%)
Intentional Overdose
15 (1.24%)
Vomiting
14 (1.16%)
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Dehydration
13 (1.07%)
Multiple Drug Overdose Intentional
13 (1.07%)
Drug Exposure During Pregnancy
12 (.99%)
Pregnancy
12 (.99%)
Blood Creatine Phosphokinase Increa...
11 (.91%)
Circulatory Collapse
11 (.91%)
Dyspnoea
11 (.91%)
Disorientation
10 (.83%)
Drug Abuse
10 (.83%)
Respiratory Failure
10 (.83%)
Spina Bifida
10 (.83%)
Bradycardia
9 (.74%)
Convulsion
9 (.74%)
Nausea
9 (.74%)
Restlessness
9 (.74%)
Agitation
8 (.66%)
Alpha 1 Foetoprotein Amniotic Fluid...
8 (.66%)
Cardiac Arrest
8 (.66%)
Electrocardiogram Qt Prolonged
8 (.66%)
Pleurothotonus
8 (.66%)
Diarrhoea
7 (.58%)
Electroencephalogram Abnormal
7 (.58%)
Hypernatraemia
7 (.58%)
Hyperparathyroidism
7 (.58%)
Hyperthyroidism
7 (.58%)
Microcephaly
7 (.58%)
Stevens-johnson Syndrome
7 (.58%)
Syncope
7 (.58%)
Aspartate Aminotransferase Increase...
6 (.5%)
Blood Pressure Decreased
6 (.5%)
Extrapyramidal Disorder
6 (.5%)
Gammopathy
6 (.5%)
General Physical Health Deteriorati...
6 (.5%)
Hypercalcaemia
6 (.5%)
Hyperviscosity Syndrome
6 (.5%)
Malaise
6 (.5%)
Overdose
6 (.5%)
Parkinsonism
6 (.5%)
Pneumonia
6 (.5%)
Urinary Retention
6 (.5%)
Aggression
5 (.41%)
Arrhythmia
5 (.41%)
Asthenia
5 (.41%)
Caesarean Section
5 (.41%)
Coma
5 (.41%)
Delirium
5 (.41%)
Depression
5 (.41%)
Disturbance In Attention
5 (.41%)
Dizziness
5 (.41%)
Grand Mal Convulsion
5 (.41%)
Hallucination
5 (.41%)
Hypokalaemia
5 (.41%)
Hypothermia
5 (.41%)
Panic Attack
5 (.41%)
Pulmonary Embolism
5 (.41%)
Respiratory Distress
5 (.41%)
Rhabdomyolysis
5 (.41%)
Toxic Epidermal Necrolysis
5 (.41%)
Accidental Exposure
4 (.33%)
Adverse Event
4 (.33%)
Akathisia
4 (.33%)
Alanine Aminotransferase Increased
4 (.33%)
Anaemia
4 (.33%)
Angina Pectoris
4 (.33%)
Cerebrovascular Accident
4 (.33%)
Cholestasis
4 (.33%)
Completed Suicide
4 (.33%)
Condition Aggravated
4 (.33%)
Coronary Artery Disease
4 (.33%)
Cyanosis
4 (.33%)
Diet Refusal
4 (.33%)
Gamma-glutamyltransferase Increased
4 (.33%)
Hallucination, Auditory
4 (.33%)
Hallucination, Visual
4 (.33%)
Hyperventilation
4 (.33%)
Hypoglycaemia
4 (.33%)
Inappropriate Schedule Of Drug Admi...
4 (.33%)
Loss Of Consciousness
4 (.33%)
Multiple Drug Overdose
4 (.33%)
Productive Cough
4 (.33%)
Urinary Tract Infection
4 (.33%)
Abdominal Pain Upper
3 (.25%)
Alcohol Poisoning
3 (.25%)
Anxiety
3 (.25%)
Aphthous Stomatitis
3 (.25%)
Arnold-chiari Malformation
3 (.25%)
Atrial Fibrillation
3 (.25%)
Benign Prostatic Hyperplasia
3 (.25%)
Blister
3 (.25%)
C-reactive Protein Increased
3 (.25%)

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

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

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

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

Drug Use For Unknown Indication
96
Product Used For Unknown Indication
41
Restlessness
27
Sleep Disorder
21
Ill-defined Disorder
13
Agitation
9
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Cerebrovascular Accident
9
Dementia Alzheimers Type
7
Confusional State
4
Depression
4
Korsakoffs Syndrome
3
Psychotic Disorder
3
Acute Psychosis
3
Schizophrenia, Paranoid Type
3
Schizoaffective Disorder
3
Aggression
2
Anxiety
2
Korsakoffs Psychosis Non-alcoholic
2
Delirium
2
Abnormal Behaviour
2
Accidental Exposure
2
Disorientation
2
Somatisation Disorder
2
Bipolar Disorder
1
Attention Deficit/hyperactivity Dis...
1
Drug Exposure During Pregnancy
1
Drug Abuser
1
Mental Disorder
1
Intentional Overdose
1
Middle Insomnia
1
Schizophrenia, Disorganised Type
1
Vascular Dementia
1
Psychomotor Hyperactivity
1
Initial Insomnia
1
Sedation
1
Femoral Neck Fracture
1

Dipiperon Case Reports

What Dipiperon 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 Dipiperon. 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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