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ISOPTIN SR

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Isoptin Sr Adverse Events Reported to the FDA Over Time

How are Isoptin Sr adverse event reports trending over time?

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

Most Common Isoptin Sr Adverse Events Reported to the FDA

What are the most common Isoptin Sr adverse events reported to the FDA?

Completed Suicide
55 (5.33%)
Bradycardia
36 (3.49%)
Hypotension
32 (3.1%)
Drug Interaction
30 (2.91%)
Drug Toxicity
19 (1.84%)
Hyperkalaemia
17 (1.65%)
Dizziness
15 (1.45%)
Renal Failure
14 (1.36%)
Vomiting
13 (1.26%)
Cardiac Failure
12 (1.16%)
Dyspnoea
11 (1.07%)
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Shock
11 (1.07%)
Syncope
11 (1.07%)
Dehydration
10 (.97%)
Headache
10 (.97%)
Hypokalaemia
10 (.97%)
Intentional Overdose
10 (.97%)
Overdose
10 (.97%)
Palpitations
10 (.97%)
Pyrexia
10 (.97%)
Atrioventricular Block
9 (.87%)
Suicide Attempt
9 (.87%)
Atrial Fibrillation
8 (.78%)
Cardiac Arrest
8 (.78%)
Cardio-respiratory Arrest
8 (.78%)
Cardiogenic Shock
8 (.78%)
Nausea
8 (.78%)
Off Label Use
8 (.78%)
Arrhythmia
7 (.68%)
Asthenia
7 (.68%)
Atrioventricular Block Complete
7 (.68%)
Diarrhoea
7 (.68%)
Drug Ineffective
7 (.68%)
Fall
7 (.68%)
Hyperglycaemia
7 (.68%)
Malaise
7 (.68%)
Metabolic Acidosis
7 (.68%)
Orthostatic Hypotension
7 (.68%)
Abdominal Pain
6 (.58%)
Bundle Branch Block Left
6 (.58%)
Presyncope
6 (.58%)
Pruritus
6 (.58%)
Renal Failure Acute
6 (.58%)
Cardiomegaly
5 (.48%)
Constipation
5 (.48%)
Hyperhidrosis
5 (.48%)
Hyponatraemia
5 (.48%)
Liver Disorder
5 (.48%)
Sinus Bradycardia
5 (.48%)
Stevens-johnson Syndrome
5 (.48%)
Toxic Epidermal Necrolysis
5 (.48%)
Abdominal Pain Upper
4 (.39%)
Accidental Overdose
4 (.39%)
Anuria
4 (.39%)
Atrioventricular Block First Degree
4 (.39%)
Confusional State
4 (.39%)
Cytolytic Hepatitis
4 (.39%)
Depressed Level Of Consciousness
4 (.39%)
Drug Rash With Eosinophilia And Sys...
4 (.39%)
Heart Rate Decreased
4 (.39%)
Heart Rate Increased
4 (.39%)
Medication Error
4 (.39%)
Nephrosclerosis
4 (.39%)
Nodal Rhythm
4 (.39%)
Pneumonia
4 (.39%)
Renal Failure Chronic
4 (.39%)
Respiratory Failure
4 (.39%)
Therapeutic Response Unexpected Wit...
4 (.39%)
Vision Blurred
4 (.39%)
Angioedema
3 (.29%)
Blister
3 (.29%)
Body Temperature Decreased
3 (.29%)
Cardiac Failure Congestive
3 (.29%)
Condition Aggravated
3 (.29%)
Death
3 (.29%)
Diverticulitis
3 (.29%)
Drug Administration Error
3 (.29%)
Fatigue
3 (.29%)
Feeling Abnormal
3 (.29%)
General Physical Health Deteriorati...
3 (.29%)
Haemodialysis
3 (.29%)
Heart Rate Irregular
3 (.29%)
Hypertension
3 (.29%)
Hypoxia
3 (.29%)
Inappropriate Antidiuretic Hormone ...
3 (.29%)
Lactic Acidosis
3 (.29%)
Left Ventricular Failure
3 (.29%)
Loss Of Consciousness
3 (.29%)
Lung Disorder
3 (.29%)
Multi-organ Failure
3 (.29%)
Muscular Weakness
3 (.29%)
Neutropenia
3 (.29%)
Oedema Peripheral
3 (.29%)
Oropharyngeal Swelling
3 (.29%)
Oxygen Saturation Decreased
3 (.29%)
Pulse Absent
3 (.29%)
Rash Erythematous
3 (.29%)
Rash Generalised
3 (.29%)
Rash Maculo-papular
3 (.29%)
Reperfusion Arrhythmia
3 (.29%)
Sinus Arrest
3 (.29%)

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

What are the most common Isoptin Sr adverse events reported to the FDA?

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

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

Drug Use For Unknown Indication
115
Hypertension
46
Atrial Fibrillation
26
Product Used For Unknown Indication
11
Arrhythmia
9
Essential Hypertension
7
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Supraventricular Tachycardia
7
Suicide Attempt
6
Tachycardia
5
Migraine
5
Tachycardia Paroxysmal
5
Accidental Overdose
4
Cluster Headache
3
Hypertrophic Cardiomyopathy
3
Atrial Flutter
3
Arteriosclerosis Coronary Artery
2
Primary Amyloidosis
2
Sick Sinus Syndrome
2
Renal Failure
2
Angina Pectoris
2
Cardiac Failure
2
Palpitations
1
Hypertensive Heart Disease
1
Obstruction Gastric
1
Pain
1
Cardiac Disorder
1
Coronary Artery Disease
1
Suicidal Ideation
1
Ischaemic Cardiomyopathy
1
Malaise
1
Facial Pain
1

Isoptin Sr Case Reports

What Isoptin Sr 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 Isoptin Sr. 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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