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Cenestin Adverse Events Reported to the FDA Over Time

How are Cenestin adverse event reports trending over time?

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

Most Common Cenestin Adverse Events Reported to the FDA

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

Breast Cancer Female
154 (33.19%)
Breast Cancer
97 (20.91%)
Breast Cancer Metastatic
8 (1.72%)
Ovarian Cancer
8 (1.72%)
Anxiety
7 (1.51%)
Breast Disorder
6 (1.29%)
Pain
6 (1.29%)
Drug Ineffective
4 (.86%)
Marital Problem
4 (.86%)
Myocardial Infarction
4 (.86%)
Vision Blurred
4 (.86%)
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Abdominal Distension
3 (.65%)
Abdominal Pain
3 (.65%)
Cerebrovascular Accident
3 (.65%)
Confusional State
3 (.65%)
Memory Impairment
3 (.65%)
Neoplasm Malignant
3 (.65%)
Oestrogen Receptor Assay Positive
3 (.65%)
Progesterone Receptor Assay Positiv...
3 (.65%)
Abdominal Discomfort
2 (.43%)
Abdominal Tenderness
2 (.43%)
Amnesia
2 (.43%)
Anorexia
2 (.43%)
Aphasia
2 (.43%)
Balance Disorder
2 (.43%)
Breast Cancer In Situ
2 (.43%)
Breast Tenderness
2 (.43%)
Cholelithiasis
2 (.43%)
Depression
2 (.43%)
Dizziness
2 (.43%)
Dysarthria
2 (.43%)
Endometrial Cancer Metastatic
2 (.43%)
Fatigue
2 (.43%)
Fluid Retention
2 (.43%)
Grand Mal Convulsion
2 (.43%)
Hepatic Steatosis
2 (.43%)
Hyperhidrosis
2 (.43%)
Incontinence
2 (.43%)
Libido Decreased
2 (.43%)
Lipid Metabolism Disorder
2 (.43%)
Medication Error
2 (.43%)
Metastases To Liver
2 (.43%)
Metastases To Lymph Nodes
2 (.43%)
Migraine
2 (.43%)
Nervous System Disorder
2 (.43%)
Photophobia
2 (.43%)
Psychomotor Hyperactivity
2 (.43%)
Speech Disorder
2 (.43%)
Tearfulness
2 (.43%)
Venous Thrombosis
2 (.43%)
Withdrawal Syndrome
2 (.43%)
Adverse Drug Reaction
1 (.22%)
Alopecia
1 (.22%)
Angina Pectoris
1 (.22%)
Arthralgia
1 (.22%)
Asthenia
1 (.22%)
Blood Cholesterol Increased
1 (.22%)
Blood Glucose Increased
1 (.22%)
Blood Potassium Decreased
1 (.22%)
Blood Pressure Decreased
1 (.22%)
Blood Pressure Increased
1 (.22%)
Bone Pain
1 (.22%)
Calcinosis
1 (.22%)
Chest Pain
1 (.22%)
Convulsion
1 (.22%)
Cutaneous Lupus Erythematosus
1 (.22%)
Cystitis
1 (.22%)
Decreased Appetite
1 (.22%)
Deep Vein Thrombosis
1 (.22%)
Diarrhoea
1 (.22%)
Disease Recurrence
1 (.22%)
Drug Effect Decreased
1 (.22%)
Drug Interaction
1 (.22%)
Dyskinesia
1 (.22%)
Dyspnoea
1 (.22%)
Dysuria
1 (.22%)
Erythema
1 (.22%)
Excoriation
1 (.22%)
Feeling Abnormal
1 (.22%)
Feeling Cold
1 (.22%)
Flushing
1 (.22%)
Gastric Disorder
1 (.22%)
Haemangioma
1 (.22%)
Headache
1 (.22%)
Heart Rate Increased
1 (.22%)
Hepatic Enzyme Increased
1 (.22%)
Hepatitis
1 (.22%)
Hot Flush
1 (.22%)
Hypersensitivity
1 (.22%)
Hypoaesthesia
1 (.22%)
Injury
1 (.22%)
Insomnia
1 (.22%)
Irritability
1 (.22%)
Lupus-like Syndrome
1 (.22%)
Malaise
1 (.22%)
Malignant Neoplasm Progression
1 (.22%)
Mental Disorder
1 (.22%)
Metastases To Abdominal Cavity
1 (.22%)
Metastases To Bone
1 (.22%)
Muscle Spasms
1 (.22%)
Myalgia
1 (.22%)

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

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

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

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

Hormone Replacement Therapy
217
Menopausal Symptoms
36
Drug Use For Unknown Indication
12
Product Used For Unknown Indication
11
Hormone Therapy
10
Hot Flush
9
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Menopause
5
Oestrogen Therapy
4
Hysterectomy
3
Prophylaxis
3
Artificial Menopause
2
Ill-defined Disorder
2
Oestrogen Replacement Therapy
2
Oestradiol Decreased
2
Postmenopause
2
Osteoporosis Prophylaxis
1
Menopausal Disorder
1
Amnesia
1
Hyperhidrosis
1
Blood Oestrogen Abnormal
1
Headache
1

Drug Labels

LabelLabelerEffective
CenestinPhysicians Total Care, Inc.01-SEP-04
CenestinTeva Women's Health Inc.01-SEP-04

Cenestin Case Reports

What Cenestin 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 Cenestin. 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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