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LUCRIN DEPOT

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Lucrin Depot Adverse Events Reported to the FDA Over Time

How are Lucrin Depot adverse event reports trending over time?

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

Most Common Lucrin Depot Adverse Events Reported to the FDA

What are the most common Lucrin Depot adverse events reported to the FDA?

Death
47 (7.44%)
Disease Progression
21 (3.32%)
Hot Flush
18 (2.85%)
Metastases To Bone
15 (2.37%)
Cardiac Failure
12 (1.9%)
Pulmonary Embolism
12 (1.9%)
Renal Failure
12 (1.9%)
Prostate Cancer
10 (1.58%)
Abdominal Pain
9 (1.42%)
Coma
9 (1.42%)
Malaise
9 (1.42%)
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Prostatic Specific Antigen Abnormal
9 (1.42%)
Enterovesical Fistula
8 (1.27%)
Injection Site Pain
8 (1.27%)
Weight Decreased
8 (1.27%)
Cerebrovascular Accident
7 (1.11%)
Fatigue
7 (1.11%)
Arrhythmia
6 (.95%)
Bone Pain
6 (.95%)
Drug Ineffective
6 (.95%)
Injection Site Reaction
6 (.95%)
Libido Decreased
6 (.95%)
Metastasis
6 (.95%)
Stress
6 (.95%)
Emphysema
5 (.79%)
Endometriosis
5 (.79%)
Hospitalisation
5 (.79%)
Hyperhidrosis
5 (.79%)
Myocardial Infarction
5 (.79%)
Urinary Tract Infection
5 (.79%)
Acute Coronary Syndrome
4 (.63%)
Acute Myocardial Infarction
4 (.63%)
Diarrhoea
4 (.63%)
Dyspnoea
4 (.63%)
Fracture
4 (.63%)
Herpes Zoster
4 (.63%)
Insomnia
4 (.63%)
Metastases To Liver
4 (.63%)
Oedema Peripheral
4 (.63%)
Pain
4 (.63%)
Pneumonia
4 (.63%)
Prostatic Specific Antigen Increase...
4 (.63%)
Staphylococcal Abscess
4 (.63%)
Therapeutic Response Decreased
4 (.63%)
Urinary Tract Obstruction
4 (.63%)
Cardiopulmonary Failure
3 (.47%)
Clavicle Fracture
3 (.47%)
Contusion
3 (.47%)
Drug Effect Decreased
3 (.47%)
Dysuria
3 (.47%)
Endocarditis Bacterial
3 (.47%)
Fall
3 (.47%)
Headache
3 (.47%)
Hypersensitivity
3 (.47%)
Ill-defined Disorder
3 (.47%)
Injection Site Abscess
3 (.47%)
Injection Site Discomfort
3 (.47%)
Metastases To Lymph Nodes
3 (.47%)
Multi-organ Failure
3 (.47%)
Night Sweats
3 (.47%)
Pemphigoid
3 (.47%)
Thrombosis
3 (.47%)
Transient Ischaemic Attack
3 (.47%)
Tumour Compression
3 (.47%)
Weight Increased
3 (.47%)
Accident
2 (.32%)
Angiopathy
2 (.32%)
Aphasia
2 (.32%)
Atrial Fibrillation
2 (.32%)
Bladder Squamous Cell Carcinoma Sta...
2 (.32%)
Blood Creatinine Increased
2 (.32%)
Blood Glucose Increased
2 (.32%)
Blood Urea Increased
2 (.32%)
Bone Neoplasm Malignant
2 (.32%)
Breast Reconstruction
2 (.32%)
Burning Sensation
2 (.32%)
Cachexia
2 (.32%)
Cardiovascular Insufficiency
2 (.32%)
Constipation
2 (.32%)
Depressed Level Of Consciousness
2 (.32%)
Diabetes Mellitus
2 (.32%)
Diabetic Complication
2 (.32%)
Diabetic Foot
2 (.32%)
Drug Administration Error
2 (.32%)
Drug Exposure During Pregnancy
2 (.32%)
Emotional Distress
2 (.32%)
Erectile Dysfunction
2 (.32%)
Eye Pain
2 (.32%)
Face Oedema
2 (.32%)
Foot Fracture
2 (.32%)
Gait Disturbance
2 (.32%)
Gastroenteritis
2 (.32%)
Haematochezia
2 (.32%)
Haemorrhagic Stroke
2 (.32%)
Hepatic Failure
2 (.32%)
Histology Abnormal
2 (.32%)
Hypoaesthesia
2 (.32%)
Impaired Driving Ability
2 (.32%)
In Vitro Fertilisation
2 (.32%)
Injection Site Ulcer
2 (.32%)
Lung Infection
2 (.32%)

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

What are the most common Lucrin Depot adverse events reported to the FDA?

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

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

Prostate Cancer
194
Drug Use For Unknown Indication
14
Product Used For Unknown Indication
13
Endometriosis
8
Prostate Cancer Metastatic
7
Breast Cancer
6
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Metastases To Bone
3
Precocious Puberty
2
Myomectomy
2
Drug Exposure During Pregnancy
2
Leiomyoma
2

Lucrin Depot Case Reports

What Lucrin Depot 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 Lucrin Depot. 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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