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ADRIACIN

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Adriacin Adverse Events Reported to the FDA Over Time

How are Adriacin adverse event reports trending over time?

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

Most Common Adriacin Adverse Events Reported to the FDA

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

Pneumonia
18 (3.25%)
Neoplasm Malignant
15 (2.71%)
Febrile Neutropenia
14 (2.53%)
Bone Marrow Failure
13 (2.35%)
Anaemia
9 (1.63%)
Herpes Zoster
9 (1.63%)
Interstitial Lung Disease
9 (1.63%)
Platelet Count Decreased
8 (1.45%)
White Blood Cell Count Decreased
8 (1.45%)
Cardiac Failure
7 (1.27%)
Death
7 (1.27%)
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Myelodysplastic Syndrome
7 (1.27%)
Pyrexia
7 (1.27%)
Vomiting
7 (1.27%)
Liver Disorder
6 (1.08%)
Metastases To Liver
6 (1.08%)
Respiratory Failure
6 (1.08%)
Tumour Lysis Syndrome
6 (1.08%)
Acute Myeloid Leukaemia
5 (.9%)
Anorexia
5 (.9%)
Cardiac Failure Acute
5 (.9%)
Cerebral Infarction
5 (.9%)
Constipation
5 (.9%)
Diarrhoea
5 (.9%)
Disseminated Intravascular Coagulat...
5 (.9%)
Liver Abscess
5 (.9%)
Loss Of Consciousness
5 (.9%)
Neutrophil Count Decreased
5 (.9%)
Sepsis
5 (.9%)
Thrombocytopenia
5 (.9%)
Allergic Cystitis
4 (.72%)
Atrial Fibrillation
4 (.72%)
Cardiomyopathy
4 (.72%)
Cystitis Haemorrhagic
4 (.72%)
Frontotemporal Dementia
4 (.72%)
Gamma-glutamyltransferase Increased
4 (.72%)
Malignant Neoplasm Progression
4 (.72%)
Pneumocystis Jiroveci Pneumonia
4 (.72%)
Pulmonary Oedema
4 (.72%)
Thrombosis
4 (.72%)
Tumour Embolism
4 (.72%)
Appendicitis
3 (.54%)
Cardiac Arrest
3 (.54%)
Convulsion
3 (.54%)
Dizziness
3 (.54%)
Melaena
3 (.54%)
Metabolic Acidosis
3 (.54%)
Monoplegia
3 (.54%)
Multi-organ Failure
3 (.54%)
Neutropenia
3 (.54%)
Olfactory Nerve Disorder
3 (.54%)
Pancytopenia
3 (.54%)
Septic Shock
3 (.54%)
Abasia
2 (.36%)
Abdominal Tenderness
2 (.36%)
Amyloidosis
2 (.36%)
Aortic Thrombosis
2 (.36%)
Asthenia
2 (.36%)
Blood Alkaline Phosphatase Increase...
2 (.36%)
Bone Sarcoma
2 (.36%)
Cardiac Failure Congestive
2 (.36%)
Cardiac Tamponade
2 (.36%)
Cerebrovascular Disorder
2 (.36%)
Clostridium Difficile Colitis
2 (.36%)
Colon Cancer
2 (.36%)
Cytomegalovirus Viraemia
2 (.36%)
Deep Vein Thrombosis
2 (.36%)
Depressed Level Of Consciousness
2 (.36%)
Disease Progression
2 (.36%)
Drug Ineffective
2 (.36%)
Empyema
2 (.36%)
Encephalopathy
2 (.36%)
Endotoxic Shock
2 (.36%)
Enterobacter Sepsis
2 (.36%)
Gastroenteritis Bacillus
2 (.36%)
Gastrointestinal Haemorrhage
2 (.36%)
Gastrointestinal Mucosal Disorder
2 (.36%)
Gingival Cancer
2 (.36%)
Grand Mal Convulsion
2 (.36%)
Hemiplegia
2 (.36%)
Hepatic Neoplasm Malignant Recurren...
2 (.36%)
Hepatitis
2 (.36%)
Hepatitis B
2 (.36%)
Hyperbilirubinaemia
2 (.36%)
Hypercholesterolaemia
2 (.36%)
Hyperphosphataemia
2 (.36%)
Hypertriglyceridaemia
2 (.36%)
Hypokalaemia
2 (.36%)
Hypoxia
2 (.36%)
Ileus Paralytic
2 (.36%)
Injection Site Pain
2 (.36%)
Intestinal Obstruction
2 (.36%)
Large Intestine Carcinoma
2 (.36%)
Lung Disorder
2 (.36%)
Metastases To Bone
2 (.36%)
Metastases To Lymph Nodes
2 (.36%)
Nasal Sinus Cancer
2 (.36%)
Oesophageal Carcinoma
2 (.36%)
Opportunistic Infection
2 (.36%)
Pancreatitis Acute
2 (.36%)
Pleural Effusion
2 (.36%)

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

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

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

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

Lymphoma
36
Breast Cancer
33
Non-hodgkins Lymphoma
31
Diffuse Large B-cell Lymphoma
23
Multiple Myeloma
18
Chemotherapy
15
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Adult T-cell Lymphoma/leukaemia
13
Hodgkins Disease
8
Acute Lymphocytic Leukaemia
7
Drug Use For Unknown Indication
7
Mantle Cell Lymphoma
7
Ewings Sarcoma
7
Neoplasm Malignant
5
Bone Sarcoma
5
Metastases To Bone
4
Hepatic Neoplasm Malignant
4
Uterine Cancer
4
Neuroblastoma
4
Bladder Cancer
4
Metastases To Liver
4
Synovial Sarcoma
3
Chronic Myeloid Leukaemia
3
Pleural Mesothelioma Malignant
3
Acute Promyelocytic Leukaemia
3
Peripheral T-cell Lymphoma Unspecif...
2
Nephroblastoma
2
Prostate Cancer Stage Iv
2
Uterine Leiomyosarcoma
2
Amyloidosis
2
Extranodal Nk/t-cell Lymphoma, Nasa...
2
Breast Cancer Recurrent
2
B-cell Small Lymphocytic Lymphoma
2
Anaplastic Large Cell Lymphoma T- A...
2
Plasmablastic Lymphoma
2
Mycosis Fungoides
2
Myelodysplastic Syndrome
2
Synovial Sarcoma Metastatic
2
Extranodal Marginal Zone B-cell Lym...
2
Pleural Effusion
1
Malignant Neoplasm Of Pleura
1
Malignant Melanoma
1
Leukaemia Plasmacytic
1
Endometrial Sarcoma
1
Therapeutic Embolisation
1
Acute Myeloid Leukaemia
1
T-cell Lymphoma
1
Small Cell Lung Cancer Stage Unspec...
1
Rhabdomyosarcoma
1
Breast Cancer Metastatic
1
Breast Cancer Stage Iv
1
Stem Cell Transplant
1

Adriacin Case Reports

What Adriacin 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 Adriacin. 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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