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ESTRACYT

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Estracyt Adverse Events Reported to the FDA Over Time

How are Estracyt adverse event reports trending over time?

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

Most Common Estracyt Adverse Events Reported to the FDA

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

Decreased Appetite
33 (2.23%)
Malaise
31 (2.1%)
Anaemia
30 (2.03%)
Interstitial Lung Disease
29 (1.96%)
Nausea
29 (1.96%)
Dyspnoea
24 (1.62%)
Vomiting
23 (1.56%)
Pulmonary Embolism
19 (1.28%)
Asthenia
18 (1.22%)
Oedema Peripheral
18 (1.22%)
Renal Failure Acute
18 (1.22%)
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Cardiac Failure Congestive
17 (1.15%)
Cerebral Infarction
17 (1.15%)
Diarrhoea
16 (1.08%)
Hepatic Function Abnormal
16 (1.08%)
Pleural Effusion
16 (1.08%)
Thrombocytopenia
16 (1.08%)
Nicotinic Acid Deficiency
15 (1.01%)
Neutropenia
14 (.95%)
Pyrexia
14 (.95%)
Cardiac Failure
12 (.81%)
Dysgeusia
12 (.81%)
Haemoglobin Decreased
12 (.81%)
Headache
12 (.81%)
Fatigue
11 (.74%)
Prostatic Specific Antigen Increase...
11 (.74%)
White Blood Cell Count Increased
11 (.74%)
Aspartate Aminotransferase Increase...
10 (.68%)
Deep Vein Thrombosis
10 (.68%)
Feeling Abnormal
10 (.68%)
Renal Impairment
10 (.68%)
Weight Decreased
10 (.68%)
White Blood Cell Count Decreased
10 (.68%)
Alanine Aminotransferase Increased
9 (.61%)
Angioedema
9 (.61%)
Cholelithiasis
9 (.61%)
Desmoid Tumour
9 (.61%)
Oedema
9 (.61%)
Blood Alkaline Phosphatase Increase...
8 (.54%)
Cough
8 (.54%)
Death
8 (.54%)
Drug Interaction
8 (.54%)
Myocardial Infarction
8 (.54%)
Pharyngeal Oedema
8 (.54%)
Pneumonia
8 (.54%)
Tongue Neoplasm Malignant Stage Uns...
8 (.54%)
Tongue Oedema
8 (.54%)
Anorexia
7 (.47%)
Disseminated Intravascular Coagulat...
7 (.47%)
Gastrointestinal Disorder
7 (.47%)
General Physical Health Deteriorati...
7 (.47%)
Hypertension
7 (.47%)
Liver Disorder
7 (.47%)
Neoplasm Malignant
7 (.47%)
Platelet Count Decreased
7 (.47%)
Haematocrit Decreased
6 (.41%)
Hypophagia
6 (.41%)
Jaundice
6 (.41%)
Laryngeal Oedema
6 (.41%)
Leukopenia
6 (.41%)
Metastases To Bone
6 (.41%)
Obesity
6 (.41%)
Pain
6 (.41%)
Arthralgia
5 (.34%)
Blood Glucose Increased
5 (.34%)
Colitis
5 (.34%)
Coma
5 (.34%)
Confusional State
5 (.34%)
Dehydration
5 (.34%)
Disease Progression
5 (.34%)
Dizziness
5 (.34%)
Dyspnoea Exertional
5 (.34%)
Fibrin D Dimer Increased
5 (.34%)
Gait Disturbance
5 (.34%)
Hypotension
5 (.34%)
Multi-organ Failure
5 (.34%)
Prostate Cancer
5 (.34%)
Sudden Death
5 (.34%)
Urinary Tract Infection
5 (.34%)
Asphyxia
4 (.27%)
Blood Creatinine Increased
4 (.27%)
Blood Lactate Dehydrogenase Increas...
4 (.27%)
Blood Pressure Decreased
4 (.27%)
Breast Pain
4 (.27%)
C-reactive Protein Increased
4 (.27%)
Coagulation Time Prolonged
4 (.27%)
Condition Aggravated
4 (.27%)
Constipation
4 (.27%)
Drug Toxicity
4 (.27%)
Dyslalia
4 (.27%)
Fall
4 (.27%)
Febrile Neutropenia
4 (.27%)
Gastrointestinal Necrosis
4 (.27%)
Haematuria
4 (.27%)
Hepatitis Toxic
4 (.27%)
Hypoproteinaemia
4 (.27%)
Liver Function Test Abnormal
4 (.27%)
Malignant Neoplasm Progression
4 (.27%)
Micturition Frequency Decreased
4 (.27%)
Myelodysplastic Syndrome
4 (.27%)
Neutropenic Sepsis
4 (.27%)

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

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

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

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

Prostate Cancer
318
Prostate Cancer Stage Iv
198
Prostate Cancer Metastatic
35
Product Used For Unknown Indication
12
Prostate Cancer Stage Ii
9
Prostatic Specific Antigen Increase...
9
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Prostate Cancer Stage Iii
9
Drug Use For Unknown Indication
9
Ill-defined Disorder
8
Prostate Cancer Recurrent
6
Metastases To Bone
5
Hormone Therapy
4
Metastatic Neoplasm
4
Breast Cancer
4
Chemotherapy
3
Head And Neck Cancer
3
Neoplasm Prostate
3
Breast Cancer Metastatic
3
Uterine Cancer
2
Squamous Cell Carcinoma
2
Metastatic Malignant Melanoma
2
Adjuvant Therapy
2
Bladder Cancer
1
Ovarian Cancer Metastatic
1
Ovarian Cancer
1
Metastases To Prostate
1
Pulmonary Embolism
1
Rectal Cancer
1
Abdominal Neoplasm
1
Prostatic Disorder
1

Estracyt Case Reports

What Estracyt 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 Estracyt. 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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