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RED BLOOD CELLS

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Red Blood Cells Adverse Events Reported to the FDA Over Time

How are Red Blood Cells adverse event reports trending over time?

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

Most Common Red Blood Cells Adverse Events Reported to the FDA

What are the most common Red Blood Cells adverse events reported to the FDA?

Transfusion-related Acute Lung Inju...
49 (4.84%)
Pulmonary Oedema
22 (2.17%)
Transfusion Reaction
22 (2.17%)
Hypotension
21 (2.08%)
Transmission Of An Infectious Agent...
16 (1.58%)
Dyspnoea
15 (1.48%)
Pyrexia
15 (1.48%)
Hepatitis C
14 (1.38%)
Hepatitis C Positive
14 (1.38%)
Hypoxia
14 (1.38%)
Lung Infiltration
14 (1.38%)
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Aspartate Aminotransferase Increase...
12 (1.19%)
Haemolysis
12 (1.19%)
Tachycardia
12 (1.19%)
Alanine Aminotransferase Increased
11 (1.09%)
Hepatitis B
11 (1.09%)
Medication Error
11 (1.09%)
Hepatitis C Antibody Positive
10 (.99%)
Anaemia
9 (.89%)
Anti-hbs Antibody Positive
9 (.89%)
Chills
9 (.89%)
Shock
9 (.89%)
Blood Alkaline Phosphatase Increase...
8 (.79%)
Hepatitis B Surface Antigen Positiv...
8 (.79%)
Multi-organ Failure
8 (.79%)
Nausea
8 (.79%)
Thrombocytopenia
8 (.79%)
Vomiting
8 (.79%)
Anti-hbc Antibody Positive
7 (.69%)
Haemoglobin Decreased
7 (.69%)
Haemolytic Anaemia
7 (.69%)
Renal Failure
7 (.69%)
Renal Failure Acute
7 (.69%)
Acute Respiratory Failure
6 (.59%)
Heart Rate Increased
6 (.59%)
Laboratory Test Abnormal
6 (.59%)
Respiratory Distress
6 (.59%)
Respiratory Rate Increased
6 (.59%)
Wheezing
6 (.59%)
Blood Bilirubin Increased
5 (.49%)
Blood Pressure Decreased
5 (.49%)
Bronchospasm
5 (.49%)
Haemoglobinuria
5 (.49%)
Hepatic Enzyme Increased
5 (.49%)
Hepatitis
5 (.49%)
Hepatitis B Antibody Positive
5 (.49%)
Hypertension
5 (.49%)
Infusion Related Reaction
5 (.49%)
Liver Disorder
5 (.49%)
Oxygen Saturation Decreased
5 (.49%)
Post Procedural Haemorrhage
5 (.49%)
Product Quality Issue
5 (.49%)
Acute Respiratory Distress Syndrome
4 (.4%)
Anti-erythrocyte Antibody Positive
4 (.4%)
Blood Lactate Dehydrogenase Increas...
4 (.4%)
Body Temperature Increased
4 (.4%)
Cardio-respiratory Arrest
4 (.4%)
Chest Pain
4 (.4%)
Chromaturia
4 (.4%)
Circulatory Collapse
4 (.4%)
Condition Aggravated
4 (.4%)
Creutzfeldt-jakob Disease
4 (.4%)
Febrile Neutropenia
4 (.4%)
Gastrointestinal Haemorrhage
4 (.4%)
General Physical Health Deteriorati...
4 (.4%)
Haematocrit Decreased
4 (.4%)
Haemorrhage
4 (.4%)
Oliguria
4 (.4%)
Pneumonia
4 (.4%)
Post Procedural Complication
4 (.4%)
Toxic Epidermal Necrolysis
4 (.4%)
Tremor
4 (.4%)
Anti-hbc Igm Antibody Positive
3 (.3%)
Anxiety
3 (.3%)
Atelectasis
3 (.3%)
Autoimmune Disorder
3 (.3%)
Blood Creatinine Increased
3 (.3%)
Brain Abscess
3 (.3%)
Cardiogenic Shock
3 (.3%)
Cardiomegaly
3 (.3%)
Crepitations
3 (.3%)
Cyanosis
3 (.3%)
Disease Progression
3 (.3%)
Disseminated Intravascular Coagulat...
3 (.3%)
Drug Dispensing Error
3 (.3%)
Fatigue
3 (.3%)
Hepatitis A Antibody Positive
3 (.3%)
Hepatitis B Positive
3 (.3%)
Htlv-1 Test Positive
3 (.3%)
Hyperbilirubinaemia
3 (.3%)
Hyperhidrosis
3 (.3%)
Hyperkalaemia
3 (.3%)
Incorrect Product Storage
3 (.3%)
Intravascular Haemolysis
3 (.3%)
Leukocytosis
3 (.3%)
Loss Of Consciousness
3 (.3%)
Myocardial Infarction
3 (.3%)
Myocardial Ischaemia
3 (.3%)
Pancytopenia
3 (.3%)
Pleural Effusion
3 (.3%)
Procedural Complication
3 (.3%)

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This graph shows the top adverse events submitted to the FDA for Red Blood Cells, 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 Red Blood Cells 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 Red Blood Cells

What are the most common Red Blood Cells adverse events reported to the FDA?

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

Why are people taking Red Blood Cells, according to those reporting adverse events to the FDA?

Anaemia
248
Product Used For Unknown Indication
198
Aplastic Anaemia
118
Drug Use For Unknown Indication
116
Acute Myeloid Leukaemia
36
Haemoglobin Decreased
30
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Anaemia Prophylaxis
29
Pancytopenia
26
Myelodysplastic Syndrome
23
Transfusion
22
Haemorrhage
21
Acute Lymphocytic Leukaemia
17
Coagulopathy
12
Coronary Artery Bypass
12
Operative Haemorrhage
12
Shock Haemorrhagic
11
Non-hodgkins Lymphoma
8
Haemoglobin
8
Tricuspid Valve Repair
7
Packed Red Blood Cell Transfusion
7
Red Blood Cell Count Decreased
6
Vascular Graft
6
Post Procedural Haemorrhage
6
Cerebral Haemorrhage
5
Haematocrit Decreased
5
Bone Marrow Conditioning Regimen
5
Blood Product Transfusion
5
Cardiac Operation
4
Multiple Myeloma
4
Septic Shock
4
Myelofibrosis
4
Anaemia Postoperative
4
Surgery
3
Haemochromatosis
3
Adverse Event
3
Hypotension
3
Aortic Surgery
3
Erythropenia
3
Aortic Valve Replacement
3
Neurogenic Shock
3
Haemorrhagic Disorder
3
Procedural Haemorrhage
3
Full Blood Count Decreased
3
Histiocytosis Haematophagic
3
Aortic Dissection
3
Transfusion-related Acute Lung Inju...
3
Hypovolaemia
3
Allogenic Bone Marrow Transplantati...
3
Blood Product Transfusion Dependent
3
Supportive Care
3
Renal Transplant
3

Red Blood Cells Case Reports

What Red Blood Cells 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 Red Blood Cells. 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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