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TRELSTAR DEPOT

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Trelstar Depot Adverse Events Reported to the FDA Over Time

How are Trelstar Depot adverse event reports trending over time?

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

Most Common Trelstar Depot Adverse Events Reported to the FDA

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

Headache
18 (2.62%)
Ovarian Hyperstimulation Syndrome
15 (2.18%)
Pyrexia
13 (1.89%)
Depression
11 (1.6%)
Vision Blurred
10 (1.46%)
Asthenia
9 (1.31%)
Dyspnoea
9 (1.31%)
Hypertension
9 (1.31%)
Vomiting
8 (1.16%)
Anxiety
7 (1.02%)
Arthralgia
7 (1.02%)
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Chest Pain
7 (1.02%)
Sinus Bradycardia
7 (1.02%)
Diplopia
6 (.87%)
Electrocardiogram Qt Prolonged
6 (.87%)
Haemolytic Anaemia
6 (.87%)
Oedema Peripheral
6 (.87%)
Thrombocytopenia
6 (.87%)
Anaemia
5 (.73%)
Condition Aggravated
5 (.73%)
Joint Swelling
5 (.73%)
Metrorrhagia
5 (.73%)
Nausea
5 (.73%)
Neutropenia
5 (.73%)
Pleural Effusion
5 (.73%)
Pulmonary Embolism
5 (.73%)
Suicidal Ideation
5 (.73%)
Thrombosis
5 (.73%)
Abdominal Pain
4 (.58%)
Ascites
4 (.58%)
Cerebrovascular Accident
4 (.58%)
Dizziness
4 (.58%)
Dyspareunia
4 (.58%)
Generalised Oedema
4 (.58%)
Off Label Use
4 (.58%)
Pain
4 (.58%)
Palpitations
4 (.58%)
Pathological Fracture
4 (.58%)
Renal Failure Acute
4 (.58%)
Alanine Aminotransferase Increased
3 (.44%)
Bone Pain
3 (.44%)
Cerebral Infarction
3 (.44%)
Drug Exposure During Pregnancy
3 (.44%)
Drug Hypersensitivity
3 (.44%)
Face Oedema
3 (.44%)
Foot Fracture
3 (.44%)
Hot Flush
3 (.44%)
Hypersensitivity
3 (.44%)
Hypotension
3 (.44%)
Intestinal Infarction
3 (.44%)
Liver Disorder
3 (.44%)
Mood Altered
3 (.44%)
Ovarian Enlargement
3 (.44%)
Overdose
3 (.44%)
Pain In Extremity
3 (.44%)
Papilloedema
3 (.44%)
Paraesthesia
3 (.44%)
Pelvic Fluid Collection
3 (.44%)
Pruritus
3 (.44%)
Respiratory Distress
3 (.44%)
Retinal Detachment
3 (.44%)
Suicide Attempt
3 (.44%)
Tachycardia
3 (.44%)
Urticaria
3 (.44%)
Uterine Haemorrhage
3 (.44%)
Vitamin B12 Decreased
3 (.44%)
Weight Increased
3 (.44%)
White Blood Cell Count Decreased
3 (.44%)
Acute Generalised Exanthematous Pus...
2 (.29%)
Anaemia Haemolytic Autoimmune
2 (.29%)
Anaphylactic Reaction
2 (.29%)
Angioedema
2 (.29%)
Artery Dissection
2 (.29%)
Aspartate Aminotransferase Increase...
2 (.29%)
Bacterial Infection
2 (.29%)
Blood Bilirubin Increased
2 (.29%)
Blood Folate Increased
2 (.29%)
Blood Iron Decreased
2 (.29%)
Bone Sarcoma
2 (.29%)
Cachexia
2 (.29%)
Capillary Leak Syndrome
2 (.29%)
Cardiac Failure Chronic
2 (.29%)
Cardio-respiratory Arrest
2 (.29%)
Cerebral Haemorrhage
2 (.29%)
Chills
2 (.29%)
Cross Sensitivity Reaction
2 (.29%)
Diarrhoea
2 (.29%)
Disturbance In Attention
2 (.29%)
Drug Administration Error
2 (.29%)
Dysphagia
2 (.29%)
Endometrial Cancer
2 (.29%)
Endometrial Disorder
2 (.29%)
Exophthalmos
2 (.29%)
Factor V Leiden Mutation
2 (.29%)
Fatigue
2 (.29%)
Fibromyalgia
2 (.29%)
Gastric Polyps
2 (.29%)
Granuloma
2 (.29%)
Heart Rate Increased
2 (.29%)
Hepatic Enzyme Increased
2 (.29%)
Hepatitis
2 (.29%)

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

What are the most common Trelstar 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 Trelstar 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 Trelstar 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 Trelstar Depot According to Those Reporting Adverse Events

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

Breast Cancer
58
Precocious Puberty
28
Endometriosis
16
Prostate Cancer
16
Infertility
15
Uterine Leiomyoma
14
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In Vitro Fertilisation
12
Ovarian Disorder
7
Hormone Suppression Therapy
6
Breast Cancer Female
6
Ovarian Failure
4
Fibroma
3
Leiomyoma
2
Assisted Fertilisation
2
Hormone Therapy
2
Drug Use For Unknown Indication
2
Blood Luteinising Hormone Increased
1
Ovulation Induction
1
Contraception
1
Product Used For Unknown Indication
1
Hamartoma
1
Prostate Cancer Metastatic
1
Adenomyosis
1
Hypothalamo-pituitary Disorders
1
Infertility Female
1
Progesterone Receptor Assay Positiv...
1
Off Label Use
1
Uterine Polyp
1
Oestrogen Receptor Assay Positive
1
Disease Recurrence
1

Trelstar Depot Case Reports

What Trelstar 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 Trelstar 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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