DrugCite
Search

ANGELIQ

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Angeliq Adverse Events Reported to the FDA Over Time

How are Angeliq adverse event reports trending over time?

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

Most Common Angeliq Adverse Events Reported to the FDA

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

Metrorrhagia
28 (3.79%)
Vaginal Haemorrhage
27 (3.65%)
Hot Flush
26 (3.52%)
Headache
20 (2.71%)
Alopecia
17 (2.3%)
Syncope
15 (2.03%)
Vertigo
13 (1.76%)
Abdominal Pain
12 (1.62%)
Chills
11 (1.49%)
Hyperhidrosis
11 (1.49%)
Postmenopausal Haemorrhage
11 (1.49%)
Show More Show More
Anxiety
10 (1.35%)
Breast Pain
10 (1.35%)
Nausea
10 (1.35%)
Dyspnoea
9 (1.22%)
Pain In Extremity
9 (1.22%)
Weight Increased
9 (1.22%)
Breast Tenderness
8 (1.08%)
Dizziness
8 (1.08%)
Fatigue
8 (1.08%)
Nervousness
8 (1.08%)
Speech Disorder
8 (1.08%)
Asthenia
7 (.95%)
Vision Blurred
7 (.95%)
Aneurysm
6 (.81%)
Blood Pressure Fluctuation
6 (.81%)
Blood Pressure Increased
6 (.81%)
Breast Swelling
6 (.81%)
Depression
6 (.81%)
Muscle Spasms
6 (.81%)
No Adverse Event
6 (.81%)
Pruritus
6 (.81%)
Pyrexia
6 (.81%)
Endometrial Cancer Stage I
5 (.68%)
Hypersensitivity
5 (.68%)
Night Sweats
5 (.68%)
Vomiting
5 (.68%)
Weight Decreased
5 (.68%)
Abdominal Distension
4 (.54%)
Blood Pressure Diastolic Decreased
4 (.54%)
Drug Ineffective
4 (.54%)
Flatulence
4 (.54%)
Fluid Retention
4 (.54%)
Generalised Erythema
4 (.54%)
Genital Haemorrhage
4 (.54%)
Hypertensive Crisis
4 (.54%)
Laryngeal Oedema
4 (.54%)
Menorrhagia
4 (.54%)
Migraine
4 (.54%)
Pain
4 (.54%)
Urticaria
4 (.54%)
Abdominal Pain Upper
3 (.41%)
Back Pain
3 (.41%)
Blood Urine Present
3 (.41%)
Body Temperature Increased
3 (.41%)
Bronchospasm
3 (.41%)
Chest Discomfort
3 (.41%)
Chest Pain
3 (.41%)
Dysaesthesia
3 (.41%)
Eye Disorder
3 (.41%)
Eye Haemorrhage
3 (.41%)
Eye Inflammation
3 (.41%)
Face Oedema
3 (.41%)
Flushing
3 (.41%)
Hepatic Steatosis
3 (.41%)
Insomnia
3 (.41%)
Libido Decreased
3 (.41%)
Menopausal Symptoms
3 (.41%)
Mood Altered
3 (.41%)
Oedema Peripheral
3 (.41%)
Osteochondrosis
3 (.41%)
Palpitations
3 (.41%)
Paraesthesia
3 (.41%)
Photopsia
3 (.41%)
Polyuria
3 (.41%)
Tunnel Vision
3 (.41%)
Uterine Enlargement
3 (.41%)
Uterine Haemorrhage
3 (.41%)
Varicose Vein
3 (.41%)
Acne
2 (.27%)
Adnexa Uteri Pain
2 (.27%)
Alanine Aminotransferase Increased
2 (.27%)
Arteriovenous Fistula
2 (.27%)
Aspartate Aminotransferase Increase...
2 (.27%)
Blindness Unilateral
2 (.27%)
Blood Corticotrophin Increased
2 (.27%)
Blood Cortisol Increased
2 (.27%)
Blood Creatinine Increased
2 (.27%)
Blood Lactate Dehydrogenase Increas...
2 (.27%)
Blood Oestrogen Decreased
2 (.27%)
Breast Cancer Stage I
2 (.27%)
Breast Enlargement
2 (.27%)
Breast Mass
2 (.27%)
Cerebral Artery Embolism
2 (.27%)
Confusional State
2 (.27%)
Constipation
2 (.27%)
Cystitis
2 (.27%)
Decreased Appetite
2 (.27%)
Deep Vein Thrombosis
2 (.27%)
Diverticulitis
2 (.27%)
Drug Dose Omission
2 (.27%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Hormone Replacement Therapy
81
Drug Use For Unknown Indication
60
Menopausal Symptoms
26
Hot Flush
22
Menopause
15
Product Used For Unknown Indication
8
Show More Show More
Menopausal Symptoms Prophylaxis
4
Hormone Therapy
4
Oral Contraception
2
Vulvovaginal Dryness
2
Contraception
2
Arthritis
2
Acne
1
Atrophic Vulvovaginitis
1
Premature Menopause
1
Anxiety
1
Skin Disorder
1
Insomnia
1
Endometriosis
1
Angina Pectoris
1
Loss Of Libido
1

Drug Labels

LabelLabelerEffective
AngeliqPhysicians Total Care, Inc.29-MAY-09
AngeliqBayer HealthCare Pharmaceuticals Inc.29-FEB-12

Angeliq Case Reports

What Angeliq safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Angeliq. 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.

Comments

Share your experience with Angeliq.