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CERAZETTE

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Cerazette Adverse Events Reported to the FDA Over Time

How are Cerazette adverse event reports trending over time?

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

Most Common Cerazette Adverse Events Reported to the FDA

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

Amenorrhoea
30 (2.87%)
Menstruation Irregular
25 (2.39%)
Drug Interaction
23 (2.2%)
Pregnancy On Oral Contraceptive
21 (2.01%)
Drug Exposure During Pregnancy
17 (1.62%)
Abortion Spontaneous
16 (1.53%)
Off Label Use
16 (1.53%)
Abdominal Pain
15 (1.43%)
Nausea
15 (1.43%)
Headache
14 (1.34%)
Hypertension
14 (1.34%)
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Inappropriate Schedule Of Drug Admi...
12 (1.15%)
Pulmonary Embolism
12 (1.15%)
Swelling
12 (1.15%)
Vaginal Haemorrhage
12 (1.15%)
Menorrhagia
11 (1.05%)
Metrorrhagia
11 (1.05%)
Asthenia
10 (.96%)
Breast Swelling
10 (.96%)
Dizziness
10 (.96%)
Hypothyroidism
10 (.96%)
Aggression
9 (.86%)
Depression
9 (.86%)
Ovarian Cyst
9 (.86%)
Vomiting
9 (.86%)
Weight Increased
9 (.86%)
Anaemia
8 (.76%)
Condition Aggravated
8 (.76%)
Drug Dose Omission
8 (.76%)
Oedema Peripheral
8 (.76%)
Weight Decreased
8 (.76%)
Nervousness
7 (.67%)
Pain In Extremity
7 (.67%)
Tinnitus
7 (.67%)
Agitation
6 (.57%)
Burning Sensation
6 (.57%)
Cerebrovascular Accident
6 (.57%)
Epilepsy
6 (.57%)
Insomnia
6 (.57%)
Menstruation Delayed
6 (.57%)
Pain
6 (.57%)
Polycystic Ovaries
6 (.57%)
Pregnancy
6 (.57%)
Tachycardia
6 (.57%)
Anger
5 (.48%)
Appetite Disorder
5 (.48%)
Balance Disorder
5 (.48%)
Breast Pain
5 (.48%)
Chest Pain
5 (.48%)
Diarrhoea
5 (.48%)
Focal Nodular Hyperplasia
5 (.48%)
Hepatic Steatosis
5 (.48%)
Hyperhidrosis
5 (.48%)
Malaise
5 (.48%)
Restlessness
5 (.48%)
Swelling Face
5 (.48%)
Tremor
5 (.48%)
Antepartum Haemorrhage
4 (.38%)
Anxiety
4 (.38%)
Back Pain
4 (.38%)
Caesarean Section
4 (.38%)
Cholelithiasis
4 (.38%)
Deep Vein Thrombosis
4 (.38%)
Drug Ineffective
4 (.38%)
Dysmenorrhoea
4 (.38%)
Eye Disorder
4 (.38%)
Haemorrhage
4 (.38%)
Hypomenorrhoea
4 (.38%)
Influenza
4 (.38%)
Intertrigo
4 (.38%)
Paraesthesia
4 (.38%)
Paralysis
4 (.38%)
Pneumonia
4 (.38%)
Pregnancy With Implant Contraceptiv...
4 (.38%)
Pruritus
4 (.38%)
Pustular Psoriasis
4 (.38%)
Stress At Work
4 (.38%)
Suicidal Ideation
4 (.38%)
Syncope
4 (.38%)
Uterine Disorder
4 (.38%)
Uterine Leiomyoma
4 (.38%)
Vulvovaginal Mycotic Infection
4 (.38%)
White Blood Cell Count Increased
4 (.38%)
Abdominal Distension
3 (.29%)
Asthma
3 (.29%)
Blood Cholesterol Increased
3 (.29%)
Carotid Artery Thrombosis
3 (.29%)
Carpal Tunnel Syndrome
3 (.29%)
Cholestasis
3 (.29%)
Delusion
3 (.29%)
Drug Exposure Via Breast Milk
3 (.29%)
Dysphagia
3 (.29%)
Ectopic Pregnancy
3 (.29%)
Fatigue
3 (.29%)
Feeling Abnormal
3 (.29%)
Hepatic Neoplasm
3 (.29%)
Hepatitis Acute
3 (.29%)
Impaired Work Ability
3 (.29%)
Irritability
3 (.29%)
Loss Of Libido
3 (.29%)
Menstrual Disorder
3 (.29%)

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

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

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

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

Contraception
208
Product Used For Unknown Indication
65
Oral Contraception
21
Endometriosis
14
Amenorrhoea
10
Uterine Leiomyoma
7
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Dysmenorrhoea
4
Drug Use For Unknown Indication
4
Menstrual Cycle Management
3
Premenstrual Syndrome
3
Ovarian Cyst
3
Drug Exposure During Pregnancy
2
Menstrual Disorder
2
Hormone Therapy
2
Drug Exposure Via Breast Milk
2
Menstruation Irregular
2
Menorrhagia
1
Oligomenorrhoea
1
Hormone Level Abnormal
1
Unevaluable Event
1
Thrombosis Prophylaxis
1
Leiomyoma
1
Breast Feeding
1
Polycystic Ovaries
1
Vaginal Haemorrhage
1
Cyst
1
Pain
1
Ill-defined Disorder
1
Drug Therapy
1
Constipation
1
Headache
1

Cerazette Case Reports

What Cerazette 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 Cerazette. 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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