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IOPAMIDOL

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Iopamidol Adverse Events Reported to the FDA Over Time

How are Iopamidol adverse event reports trending over time?

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

Most Common Iopamidol Adverse Events Reported to the FDA

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

Anaphylactic Shock
93 (3.17%)
Blood Pressure Decreased
62 (2.11%)
Vomiting
58 (1.98%)
Nausea
57 (1.94%)
Loss Of Consciousness
54 (1.84%)
Dyspnoea
46 (1.57%)
Shock
46 (1.57%)
Pyrexia
43 (1.47%)
Respiratory Arrest
36 (1.23%)
Cardiac Arrest
35 (1.19%)
Contrast Media Reaction
35 (1.19%)
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Anaphylactic Reaction
34 (1.16%)
Cardio-respiratory Arrest
34 (1.16%)
Feeling Abnormal
32 (1.09%)
Toxic Skin Eruption
29 (.99%)
Depressed Level Of Consciousness
28 (.95%)
Rash
26 (.89%)
Erythema
25 (.85%)
Atrial Fibrillation
24 (.82%)
Convulsion
24 (.82%)
Hypersensitivity
23 (.78%)
Nephropathy Toxic
21 (.72%)
Septic Shock
21 (.72%)
Cerebral Infarction
20 (.68%)
Oxygen Saturation Decreased
20 (.68%)
Renal Failure Acute
20 (.68%)
Cardiac Failure
19 (.65%)
Toxic Epidermal Necrolysis
19 (.65%)
Erythema Multiforme
18 (.61%)
General Physical Health Deteriorati...
18 (.61%)
Renal Impairment
18 (.61%)
Extravasation
17 (.58%)
Headache
17 (.58%)
Pruritus
17 (.58%)
Acute Generalised Exanthematous Pus...
16 (.55%)
Condition Aggravated
16 (.55%)
Contrast Media Allergy
16 (.55%)
Eosinophil Count Increased
16 (.55%)
Blood Creatinine Increased
15 (.51%)
Injection Site Extravasation
15 (.51%)
Acute Respiratory Distress Syndrome
14 (.48%)
Gastrointestinal Perforation
14 (.48%)
Hypotension
14 (.48%)
Pleural Effusion
14 (.48%)
Pulmonary Oedema
14 (.48%)
Urticaria
14 (.48%)
Blood Pressure Increased
13 (.44%)
Bradycardia
13 (.44%)
Renal Failure
13 (.44%)
Restlessness
13 (.44%)
Altered State Of Consciousness
12 (.41%)
Anaphylactoid Reaction
12 (.41%)
Cyanosis
12 (.41%)
Flushing
12 (.41%)
Myocardial Infarction
12 (.41%)
Stevens-johnson Syndrome
12 (.41%)
Anaphylactoid Shock
11 (.38%)
Blood Pressure Immeasurable
11 (.38%)
Chest Pain
11 (.38%)
Haematemesis
11 (.38%)
Haemoglobin Decreased
11 (.38%)
Hyperhidrosis
11 (.38%)
Liver Disorder
11 (.38%)
Post Procedural Complication
11 (.38%)
Ventricular Fibrillation
11 (.38%)
Amnesia
10 (.34%)
Central Nervous System Lesion
10 (.34%)
Cough
10 (.34%)
Heart Rate Increased
10 (.34%)
Nervous System Disorder
10 (.34%)
Off Label Use
10 (.34%)
Oropharyngeal Pain
10 (.34%)
Pharyngeal Oedema
10 (.34%)
Angioedema
9 (.31%)
Asthenia
9 (.31%)
C-reactive Protein Increased
9 (.31%)
Choking Sensation
9 (.31%)
Drug Hypersensitivity
9 (.31%)
Laryngeal Oedema
9 (.31%)
Malaise
9 (.31%)
Medication Error
9 (.31%)
Unresponsive To Stimuli
9 (.31%)
Vertigo
9 (.31%)
Arteriospasm Coronary
8 (.27%)
Cardiac Failure Acute
8 (.27%)
Chills
8 (.27%)
Death
8 (.27%)
Hypertension
8 (.27%)
Intestinal Mucosal Hypertrophy
8 (.27%)
Pain In Extremity
8 (.27%)
Pallor
8 (.27%)
Pharyngeal Erythema
8 (.27%)
Platelet Count Increased
8 (.27%)
Procedural Complication
8 (.27%)
Pulse Absent
8 (.27%)
Purpura
8 (.27%)
Rash Generalised
8 (.27%)
Ventricular Tachycardia
8 (.27%)
Blood Blister
7 (.24%)
Bronchospasm
7 (.24%)
Coma
7 (.24%)

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

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

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

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

Computerised Tomogram
227
Angiogram
60
Arteriogram Coronary
52
Computerised Tomogram Abdomen
31
Angina Pectoris
27
Diagnostic Procedure
27
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Catheterisation Cardiac
22
Percutaneous Coronary Intervention
21
Spinal Myelogram
20
Product Used For Unknown Indication
13
Drug Use For Unknown Indication
12
Computerised Tomogram Thorax
11
Scan With Contrast
11
Aortic Dissection
10
Musculoskeletal Pain
10
Arthrogram
9
Aortic Aneurysm
8
Coronary Artery Stenosis
8
Colon Cancer
7
Metastases To Liver
7
Bladder Cancer
7
Pulmonary Embolism
7
Urogram
7
Arteriosclerosis Obliterans
7
Computerised Tomogram Coronary Arte...
7
Acute Myocardial Infarction
7
Bile Duct Cancer
6
Back Pain
6
Stent Placement
6
Coronary Angioplasty
6
Intracranial Hypotension
6
Intracranial Aneurysm
5
Cardiac Imaging Procedure
5
Hepatic Neoplasm Malignant
5
Scan Brain
5
Pancreatic Carcinoma
5
Chest Pain
5
Aneurysm Repair
5
Coronary Artery Occlusion
5
Abdominal Pain
5
Gastric Varices
5
Arteriogram
5
Vascular Imaging
4
Coronary Arterial Stent Insertion
4
Renal Artery Dissection
4
Large Intestine Carcinoma
4
Angiogram Cerebral
4
Computerised Tomogram Head
4
Urography
4
Anaesthesia
4
Therapeutic Embolisation
4

Drug Labels

LabelLabelerEffective
Isovue200Bracco Diagnostics Inc23-JAN-12
Isovue370Bracco Diagnostics Inc23-JAN-12
Isovue300Bracco Diagnostics Inc23-JAN-12
Isovue250Bracco Diagnostics Inc23-JAN-12
Isovue250Bracco Diagnostics Inc26-JAN-12
Isovue300Bracco Diagnostics Inc26-JAN-12
Isovue370Bracco Diagnostics Inc26-JAN-12

Iopamidol Case Reports

What Iopamidol 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 Iopamidol. 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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