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DROSPIRENONE AND EHTINYL ESTRADIOL

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Drospirenone And Ehtinyl Estradiol Adverse Events Reported to the FDA Over Time

How are Drospirenone And Ehtinyl Estradiol adverse event reports trending over time?

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

Most Common Drospirenone And Ehtinyl Estradiol Adverse Events Reported to the FDA

What are the most common Drospirenone And Ehtinyl Estradiol adverse events reported to the FDA?

Gallbladder Disorder
77 (11.24%)
Pulmonary Embolism
52 (7.59%)
Deep Vein Thrombosis
40 (5.84%)
Cholecystectomy
29 (4.23%)
Cholelithiasis
28 (4.09%)
Abdominal Pain
26 (3.8%)
Pain
24 (3.5%)
Nausea
21 (3.07%)
Gallbladder Injury
20 (2.92%)
Vomiting
19 (2.77%)
Abdominal Pain Upper
15 (2.19%)
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Cerebrovascular Accident
13 (1.9%)
Cholecystitis Chronic
13 (1.9%)
Dyspnoea
11 (1.61%)
Injury
11 (1.61%)
Diarrhoea
10 (1.46%)
Thrombosis
9 (1.31%)
Chest Pain
8 (1.17%)
Headache
7 (1.02%)
Myocardial Infarction
7 (1.02%)
Depression
6 (.88%)
Gallbladder Cholesterolosis
6 (.88%)
Oedema Peripheral
6 (.88%)
Pain In Extremity
6 (.88%)
Dyspepsia
5 (.73%)
Syncope
5 (.73%)
Abdominal Discomfort
4 (.58%)
Abdominal Distension
4 (.58%)
Abdominal Pain Lower
4 (.58%)
Anxiety
4 (.58%)
Bile Duct Stone
4 (.58%)
Biliary Colic
4 (.58%)
Chest Discomfort
4 (.58%)
Dizziness
4 (.58%)
Emotional Distress
4 (.58%)
Gallbladder Non-functioning
4 (.58%)
Hepatic Function Abnormal
4 (.58%)
Jaundice
4 (.58%)
Transient Ischaemic Attack
4 (.58%)
Back Pain
3 (.44%)
Biliary Dyskinesia
3 (.44%)
Fear Of Death
3 (.44%)
Hyperhidrosis
3 (.44%)
Nervousness
3 (.44%)
Palpitations
3 (.44%)
Pancreatitis
3 (.44%)
Tachycardia
3 (.44%)
Abdominal Tenderness
2 (.29%)
Abortion Induced
2 (.29%)
Aphagia
2 (.29%)
Arrhythmia
2 (.29%)
Asthma
2 (.29%)
Blood Copper Decreased
2 (.29%)
Brain Herniation
2 (.29%)
Brain Oedema
2 (.29%)
Cardiac Arrest
2 (.29%)
Cholecystitis Acute
2 (.29%)
Diarrhoea Haemorrhagic
2 (.29%)
Drug Exposure During Pregnancy
2 (.29%)
Fatigue
2 (.29%)
Food Intolerance
2 (.29%)
Gastric Disorder
2 (.29%)
Gastric Ph Decreased
2 (.29%)
Gastritis
2 (.29%)
Gastrointestinal Disorder
2 (.29%)
Haematemesis
2 (.29%)
Haematochezia
2 (.29%)
Hepatic Enzyme Increased
2 (.29%)
Hydrocephalus
2 (.29%)
Hypertension
2 (.29%)
Hysterectomy
2 (.29%)
Intracranial Venous Sinus Thrombosi...
2 (.29%)
Liver Injury
2 (.29%)
Malaise
2 (.29%)
Meningomyelocele
2 (.29%)
Metrorrhagia
2 (.29%)
Nephrolithiasis
2 (.29%)
Neural Tube Defect
2 (.29%)
Neurological Decompensation
2 (.29%)
No Adverse Event
2 (.29%)
Normal Newborn
2 (.29%)
Skin Discolouration
2 (.29%)
Talipes
2 (.29%)
Urine Copper Decreased
2 (.29%)
Vertigo
2 (.29%)
Weight Decreased
2 (.29%)
White Blood Cell Count Increased
2 (.29%)
Abortion Spontaneous
1 (.15%)
Acne
1 (.15%)
Adverse Event
1 (.15%)
Affect Lability
1 (.15%)
Appendicitis Perforated
1 (.15%)
Asthenia
1 (.15%)
Brain Compression
1 (.15%)
Breast Tenderness
1 (.15%)
Cerebral Infarction
1 (.15%)
Cholecystitis
1 (.15%)
Complex Partial Seizures
1 (.15%)
Constipation
1 (.15%)
Convulsion
1 (.15%)
Dyspnoea Exertional
1 (.15%)

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This graph shows the top adverse events submitted to the FDA for Drospirenone And Ehtinyl Estradiol, 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 Drospirenone And Ehtinyl Estradiol 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 Drospirenone And Ehtinyl Estradiol

What are the most common Drospirenone And Ehtinyl Estradiol adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Drospirenone And Ehtinyl Estradiol, 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 Drospirenone And Ehtinyl Estradiol 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 Drospirenone And Ehtinyl Estradiol According to Those Reporting Adverse Events

Why are people taking Drospirenone And Ehtinyl Estradiol, according to those reporting adverse events to the FDA?

Product Used For Unknown Indication
144
Drug Use For Unknown Indication
33
Contraception
28
Oral Contraception
24
Acne
3
Menstruation Irregular
2
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Polycystic Ovaries
2
Menstrual Cycle Management
1
Premenstrual Syndrome
1
Coagulation Factor Viii Level Decre...
1
Ovarian Cyst
1
Endometriosis
1
Menorrhagia
1

Drospirenone And Ehtinyl Estradiol Case Reports

What Drospirenone And Ehtinyl Estradiol 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 Drospirenone And Ehtinyl Estradiol. 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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