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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIZIDE

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Olmesartan Medoxomil And Hydrochlorothizide Adverse Events Reported to the FDA Over Time

How are Olmesartan Medoxomil And Hydrochlorothizide adverse event reports trending over time?

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

Most Common Olmesartan Medoxomil And Hydrochlorothizide Adverse Events Reported to the FDA

What are the most common Olmesartan Medoxomil And Hydrochlorothizide adverse events reported to the FDA?

Hypertensive Emergency
31 (4.17%)
Death
20 (2.69%)
Chest Pain
17 (2.29%)
Blood Pressure Increased
15 (2.02%)
Dyspnoea
15 (2.02%)
Drug Ineffective
13 (1.75%)
Headache
13 (1.75%)
Leukocyturia
12 (1.62%)
Obesity
12 (1.62%)
Renal Failure Chronic
12 (1.62%)
Angiopathy
11 (1.48%)
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Haematuria
11 (1.48%)
Cerebrovascular Accident
10 (1.35%)
Pain In Extremity
9 (1.21%)
Cardiac Disorder
8 (1.08%)
Completed Suicide
8 (1.08%)
Hypokalaemia
8 (1.08%)
Malaise
8 (1.08%)
Cough
7 (.94%)
Tobacco Abuse
7 (.94%)
Vomiting
7 (.94%)
Dyspnoea Exertional
6 (.81%)
Fall
6 (.81%)
Gait Disturbance
6 (.81%)
Oedema Peripheral
6 (.81%)
Palpitations
6 (.81%)
Renal Failure Acute
6 (.81%)
Acute Myocardial Infarction
5 (.67%)
Asthenia
5 (.67%)
Condition Aggravated
5 (.67%)
Diarrhoea
5 (.67%)
Exercise Lack Of
5 (.67%)
Gastritis
5 (.67%)
Urinary Tract Infection
5 (.67%)
Abdominal Pain Upper
4 (.54%)
Accident
4 (.54%)
Angina Pectoris
4 (.54%)
Dehydration
4 (.54%)
Fatigue
4 (.54%)
Glycosuria
4 (.54%)
Hypercalcaemia
4 (.54%)
Hyponatraemia
4 (.54%)
Joint Dislocation
4 (.54%)
Joint Injury
4 (.54%)
Lower Limb Fracture
4 (.54%)
Myocardial Infarction
4 (.54%)
Pain
4 (.54%)
Transaminases Abnormal
4 (.54%)
Treatment Noncompliance
4 (.54%)
Weight Increased
4 (.54%)
Anaemia
3 (.4%)
Angina Unstable
3 (.4%)
Angioplasty
3 (.4%)
Arthritis
3 (.4%)
Blood Cholesterol Increased
3 (.4%)
Blood Pressure Decreased
3 (.4%)
Blood Pressure Fluctuation
3 (.4%)
Cardiac Failure
3 (.4%)
Dizziness
3 (.4%)
Erythema
3 (.4%)
Hyperkalaemia
3 (.4%)
Hypersensitivity
3 (.4%)
Hypertension
3 (.4%)
Hypertensive Crisis
3 (.4%)
Incontinence
3 (.4%)
Influenza
3 (.4%)
Leukocytoclastic Vasculitis
3 (.4%)
Nausea
3 (.4%)
Sudden Cardiac Death
3 (.4%)
Abortion Induced
2 (.27%)
Anxiety
2 (.27%)
Back Pain
2 (.27%)
Blood Parathyroid Hormone Increased
2 (.27%)
Blood Pressure Abnormal
2 (.27%)
Blood Pressure Systolic Increased
2 (.27%)
Bradycardia
2 (.27%)
Burning Sensation
2 (.27%)
Cardiac Arrest
2 (.27%)
Cardiac Valve Disease
2 (.27%)
Colitis
2 (.27%)
Colitis Microscopic
2 (.27%)
Crystalluria
2 (.27%)
Disorientation
2 (.27%)
Drug Exposure During Pregnancy
2 (.27%)
Drug Interaction
2 (.27%)
Drug Rash With Eosinophilia And Sys...
2 (.27%)
Erysipelas
2 (.27%)
Eye Haemorrhage
2 (.27%)
Feeling Of Despair
2 (.27%)
Generalised Oedema
2 (.27%)
Haemodynamic Instability
2 (.27%)
Hypercholesterolaemia
2 (.27%)
Hyperhidrosis
2 (.27%)
Hypotension
2 (.27%)
Influenza Like Illness
2 (.27%)
Intermittent Claudication
2 (.27%)
Interstitial Lung Disease
2 (.27%)
Loss Of Consciousness
2 (.27%)
Myalgia
2 (.27%)
Neoplasm
2 (.27%)
Oedema
2 (.27%)

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This graph shows the top adverse events submitted to the FDA for Olmesartan Medoxomil And Hydrochlorothizide, 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 Olmesartan Medoxomil And Hydrochlorothizide 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 Olmesartan Medoxomil And Hydrochlorothizide

What are the most common Olmesartan Medoxomil And Hydrochlorothizide adverse events reported to the FDA?

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ExportShare/Embed Graph Export Export Data

This graph shows the top categories of adverse events submitted to the FDA for Olmesartan Medoxomil And Hydrochlorothizide, 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 Olmesartan Medoxomil And Hydrochlorothizide 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 Olmesartan Medoxomil And Hydrochlorothizide According to Those Reporting Adverse Events

Why are people taking Olmesartan Medoxomil And Hydrochlorothizide, according to those reporting adverse events to the FDA?

Hypertension
165
Product Used For Unknown Indication
12
Drug Use For Unknown Indication
10
Blood Pressure Abnormal
4
Essential Hypertension
3
Blood Pressure
2
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Fluid Retention
2
Blood Pressure Management
1
Blood Pressure Increased
1
Diabetes Mellitus
1
Tension
1
Investigation
1

Olmesartan Medoxomil And Hydrochlorothizide Case Reports

What Olmesartan Medoxomil And Hydrochlorothizide 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 Olmesartan Medoxomil And Hydrochlorothizide. 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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