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AMPHETAMINE AND DEXTROAMPHETAMINE SALTS

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Amphetamine And Dextroamphetamine Salts Adverse Events Reported to the FDA Over Time

How are Amphetamine And Dextroamphetamine Salts adverse event reports trending over time?

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

Most Common Amphetamine And Dextroamphetamine Salts Adverse Events Reported to the FDA

What are the most common Amphetamine And Dextroamphetamine Salts adverse events reported to the FDA?

Drug Ineffective
41 (4.75%)
Product Substitution Issue
30 (3.47%)
Completed Suicide
26 (3.01%)
Feeling Abnormal
21 (2.43%)
Asthenia
19 (2.2%)
Fatigue
16 (1.85%)
Anxiety
14 (1.62%)
Headache
14 (1.62%)
Death
12 (1.39%)
Disturbance In Attention
12 (1.39%)
Agitation
11 (1.27%)
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Fall
11 (1.27%)
Nausea
11 (1.27%)
Pneumonia
11 (1.27%)
Blood Pressure Decreased
10 (1.16%)
Cachexia
10 (1.16%)
Cardiac Arrest
10 (1.16%)
Malaise
10 (1.16%)
Multiple Sclerosis
10 (1.16%)
Suicidal Ideation
10 (1.16%)
Drug Interaction
9 (1.04%)
Insomnia
9 (1.04%)
Depression
8 (.93%)
Dizziness
8 (.93%)
Dyspnoea
8 (.93%)
Hyperhidrosis
8 (.93%)
Irritability
8 (.93%)
Palpitations
8 (.93%)
Poisoning
8 (.93%)
Respiratory Arrest
8 (.93%)
Abnormal Behaviour
7 (.81%)
Activities Of Daily Living Impaired
7 (.81%)
Chest Pain
7 (.81%)
Crying
7 (.81%)
Mood Swings
7 (.81%)
Product Quality Issue
7 (.81%)
Tremor
7 (.81%)
Confusional State
6 (.69%)
Drug Effect Decreased
6 (.69%)
Heart Rate Increased
6 (.69%)
Loss Of Consciousness
6 (.69%)
Anger
5 (.58%)
Blood Pressure Increased
5 (.58%)
Hepatitis C
5 (.58%)
Memory Impairment
5 (.58%)
Overdose
5 (.58%)
Paraesthesia
5 (.58%)
Tension
5 (.58%)
Abdominal Pain Upper
4 (.46%)
Aggression
4 (.46%)
Cardio-respiratory Arrest
4 (.46%)
Condition Aggravated
4 (.46%)
Diarrhoea
4 (.46%)
Drug Abuse
4 (.46%)
Dry Mouth
4 (.46%)
Hypoaesthesia
4 (.46%)
Intentional Drug Misuse
4 (.46%)
Lower Limb Fracture
4 (.46%)
Nervous System Disorder
4 (.46%)
No Therapeutic Response
4 (.46%)
Pain
4 (.46%)
Somnolence
4 (.46%)
Visual Impairment
4 (.46%)
Withdrawal Syndrome
4 (.46%)
Blindness
3 (.35%)
Chest Discomfort
3 (.35%)
Depressed Mood
3 (.35%)
Drug Toxicity
3 (.35%)
Impaired Work Ability
3 (.35%)
Medication Error
3 (.35%)
Mental Impairment
3 (.35%)
Multiple Drug Overdose
3 (.35%)
Myocardial Infarction
3 (.35%)
Psychiatric Symptom
3 (.35%)
Psychotic Disorder
3 (.35%)
Pulmonary Oedema
3 (.35%)
Rash
3 (.35%)
Restlessness
3 (.35%)
Road Traffic Accident
3 (.35%)
Sedation
3 (.35%)
Serotonin Syndrome
3 (.35%)
Speech Disorder
3 (.35%)
Tachycardia
3 (.35%)
Abdominal Pain
2 (.23%)
Abscess Intestinal
2 (.23%)
Adrenocortical Insufficiency Acute
2 (.23%)
Adverse Event
2 (.23%)
Amphetamines Positive
2 (.23%)
Attention Deficit/hyperactivity Dis...
2 (.23%)
Bipolar Disorder
2 (.23%)
Blood Count Abnormal
2 (.23%)
Cardiac Failure Congestive
2 (.23%)
Catatonia
2 (.23%)
Convulsion
2 (.23%)
Cough
2 (.23%)
Decreased Appetite
2 (.23%)
Drug Detoxification
2 (.23%)
Drug Effect Increased
2 (.23%)
Dysarthria
2 (.23%)
Dyspepsia
2 (.23%)
Eating Disorder
2 (.23%)

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This graph shows the top adverse events submitted to the FDA for Amphetamine And Dextroamphetamine Salts, 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 Amphetamine And Dextroamphetamine Salts 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 Amphetamine And Dextroamphetamine Salts

What are the most common Amphetamine And Dextroamphetamine Salts adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Amphetamine And Dextroamphetamine Salts, 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 Amphetamine And Dextroamphetamine Salts 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 Amphetamine And Dextroamphetamine Salts According to Those Reporting Adverse Events

Why are people taking Amphetamine And Dextroamphetamine Salts, according to those reporting adverse events to the FDA?

Attention Deficit/hyperactivity Dis...
88
Product Used For Unknown Indication
27
Drug Use For Unknown Indication
15
Narcolepsy
7
Drug Abuse
5
Depression
3
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Completed Suicide
3
Anxiety
3
Appetite Disorder
3
Somnolence
2
Fibromyalgia
2
Disturbance In Attention
2
Lyme Disease
1
Fatigue
1
Drug Resistance
1
Memory Impairment
1
Multiple Sclerosis
1
Dysphoria
1
Central Nervous System Stimulation
1
Bipolar Disorder
1
Sleep Disorder
1
Intentional Overdose
1
Depression Suicidal
1
Off Label Use
1
Head Injury
1
Poor Quality Sleep
1

Amphetamine And Dextroamphetamine Salts Case Reports

What Amphetamine And Dextroamphetamine Salts 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 Amphetamine And Dextroamphetamine Salts. 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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