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DESOGESTREL AND ETHINYL ESTRADIOL

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Desogestrel And Ethinyl Estradiol Adverse Events Reported to the FDA Over Time

How are Desogestrel And Ethinyl Estradiol adverse event reports trending over time?

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

Most Common Desogestrel And Ethinyl Estradiol Adverse Events Reported to the FDA

What are the most common Desogestrel And Ethinyl Estradiol adverse events reported to the FDA?

Pulmonary Embolism
38 (2.57%)
Drug Interaction
34 (2.3%)
Headache
25 (1.69%)
Inappropriate Schedule Of Drug Admi...
25 (1.69%)
Nausea
24 (1.62%)
Vomiting
24 (1.62%)
Pregnancy On Oral Contraceptive
21 (1.42%)
Abortion Spontaneous
16 (1.08%)
Loss Of Consciousness
16 (1.08%)
Malaise
16 (1.08%)
Drug Exposure During Pregnancy
15 (1.01%)
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Deep Vein Thrombosis
14 (.95%)
Weight Increased
14 (.95%)
Abdominal Pain
13 (.88%)
Alopecia
13 (.88%)
Back Pain
13 (.88%)
Hypertension
13 (.88%)
Drug Dose Omission
12 (.81%)
Memory Impairment
12 (.81%)
Migraine
12 (.81%)
Off Label Use
12 (.81%)
Cardio-respiratory Arrest
11 (.74%)
Fatigue
11 (.74%)
Hypoaesthesia
11 (.74%)
Menstruation Irregular
11 (.74%)
Thrombosis
11 (.74%)
Cardiac Arrest
10 (.68%)
Diarrhoea
10 (.68%)
Dyspnoea
10 (.68%)
Fall
10 (.68%)
Metrorrhagia
10 (.68%)
Pain In Extremity
10 (.68%)
Vaginal Haemorrhage
10 (.68%)
Chest Pain
9 (.61%)
Condition Aggravated
9 (.61%)
Pain
9 (.61%)
Palpitations
9 (.61%)
Paraesthesia
9 (.61%)
Cerebral Haemorrhage
8 (.54%)
Dizziness
8 (.54%)
Intracranial Pressure Increased
8 (.54%)
Muscle Spasms
8 (.54%)
Ovarian Cyst Ruptured
8 (.54%)
Amenorrhoea
7 (.47%)
Asthenia
7 (.47%)
Brain Oedema
7 (.47%)
Dysmenorrhoea
7 (.47%)
Hypothyroidism
7 (.47%)
Pregnancy
7 (.47%)
Urinary Tract Infection
7 (.47%)
Brain Hypoxia
6 (.41%)
Cerebral Venous Thrombosis
6 (.41%)
Enteritis
6 (.41%)
Intracranial Venous Sinus Thrombosi...
6 (.41%)
Neck Pain
6 (.41%)
Nephrolithiasis
6 (.41%)
Oedema Peripheral
6 (.41%)
Ovarian Cyst
6 (.41%)
Peritoneal Haemorrhage
6 (.41%)
Pneumonia
6 (.41%)
Tachycardia
6 (.41%)
Thrombophlebitis
6 (.41%)
Abdominal Pain Upper
5 (.34%)
Death
5 (.34%)
Drug Hypersensitivity
5 (.34%)
Dry Mouth
5 (.34%)
Epilepsy
5 (.34%)
Gastritis
5 (.34%)
Incorrect Dose Administered
5 (.34%)
Klebsiella Infection
5 (.34%)
Liver Disorder
5 (.34%)
Menorrhagia
5 (.34%)
Product Substitution Issue
5 (.34%)
Serotonin Syndrome
5 (.34%)
Stress
5 (.34%)
Swelling
5 (.34%)
Visual Acuity Reduced
5 (.34%)
Vulvovaginal Burning Sensation
5 (.34%)
Accommodation Disorder
4 (.27%)
Alanine Aminotransferase Increased
4 (.27%)
Anaemia
4 (.27%)
Anxiety
4 (.27%)
Aspartate Aminotransferase Increase...
4 (.27%)
Bronchitis
4 (.27%)
Caesarean Section
4 (.27%)
Cholelithiasis
4 (.27%)
Depression
4 (.27%)
Drug Withdrawal Syndrome
4 (.27%)
Dyspepsia
4 (.27%)
Epistaxis
4 (.27%)
Gait Disturbance
4 (.27%)
Hypotension
4 (.27%)
Increased Appetite
4 (.27%)
Jugular Vein Thrombosis
4 (.27%)
Leiomyoma
4 (.27%)
Lung Disorder
4 (.27%)
Menstruation Delayed
4 (.27%)
Myocardial Infarction
4 (.27%)
No Adverse Event
4 (.27%)
Pulmonary Infarction
4 (.27%)
Subarachnoid Haemorrhage
4 (.27%)

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This graph shows the top adverse events submitted to the FDA for Desogestrel And Ethinyl 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 Desogestrel And Ethinyl 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 Desogestrel And Ethinyl Estradiol

What are the most common Desogestrel And Ethinyl 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 Desogestrel And Ethinyl 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 Desogestrel And Ethinyl 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 Desogestrel And Ethinyl Estradiol According to Those Reporting Adverse Events

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

Contraception
303
Product Used For Unknown Indication
40
Oral Contraception
31
Menorrhagia
13
Dysmenorrhoea
9
Menstrual Disorder
8
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Endometriosis
7
Polycystic Ovaries
7
Drug Use For Unknown Indication
7
Menstruation Irregular
6
Menstruation Delayed
5
Menstrual Cycle Management
4
Acne
4
Ovarian Cyst
3
Maternal Exposure During Pregnancy
3
Amenorrhoea
3
Migraine
2
Prophylaxis Against Transplant Reje...
2
Crohns Disease
2
Polymenorrhoea
1
Follicle-stimulating Hormone Defici...
1
Uterine Leiomyoma
1
Postmenopause
1
Blood Luteinising Hormone Decreased
1
Dysfunctional Uterine Bleeding
1
Cyst
1

Drug Labels

LabelLabelerEffective
KarivaPhysicians Total Care, Inc.16-JAN-11
ApriPhysicians Total Care, Inc.24-JAN-11
SoliaPrasco Laboratories02-FEB-11
VioreleGlenmark Generics Inc., USA17-APR-12
Velivettriphasic RegimenPhysicians Total Care, Inc.16-MAY-12
ApriBarr Laboratories Inc.06-AUG-12
CyclessaOrganon Pharmaceuticals USA16-AUG-12
EmoquetteQualitest Pharmaceuticals16-AUG-12
Velivettriphasic RegimenBarr Laboratories Inc.17-AUG-12
KarivaBarr Laboratories Inc.11-SEP-12
MircetteTeva Women's Health, Inc.14-NOV-12
ReclipsenWatson Pharma, Inc.10-DEC-12
Ortho CeptJanssen Pharmaceuticals, Inc.27-FEB-13

Desogestrel And Ethinyl Estradiol Case Reports

What Desogestrel And Ethinyl 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 Desogestrel And Ethinyl 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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