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DIOVAN HCT

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Diovan Hct Adverse Events Reported to the FDA Over Time

How are Diovan Hct adverse event reports trending over time?

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

Most Common Diovan Hct Adverse Events Reported to the FDA

What are the most common Diovan Hct adverse events reported to the FDA?

Blood Pressure Increased
537 (2.44%)
Hypertension
521 (2.37%)
Death
426 (1.93%)
Dizziness
405 (1.84%)
Fall
330 (1.5%)
Headache
279 (1.27%)
Hypotension
272 (1.23%)
Dyspnoea
256 (1.16%)
Malaise
240 (1.09%)
Blood Pressure Inadequately Control...
236 (1.07%)
Cerebrovascular Accident
233 (1.06%)
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Diabetes Mellitus
223 (1.01%)
Fatigue
211 (.96%)
Oedema Peripheral
193 (.88%)
Nausea
192 (.87%)
Feeling Abnormal
184 (.84%)
Blood Pressure Decreased
179 (.81%)
Blood Pressure Fluctuation
177 (.8%)
Vomiting
171 (.78%)
Drug Ineffective
169 (.77%)
Chest Pain
156 (.71%)
Pneumonia
154 (.7%)
Myocardial Infarction
151 (.69%)
Surgery
144 (.65%)
Asthenia
143 (.65%)
Pain In Extremity
130 (.59%)
Cough
125 (.57%)
Pain
124 (.56%)
Syncope
117 (.53%)
Blood Glucose Increased
111 (.5%)
Cardiac Disorder
111 (.5%)
Diarrhoea
111 (.5%)
Gait Disturbance
110 (.5%)
Hyponatraemia
110 (.5%)
Weight Decreased
110 (.5%)
Arrhythmia
109 (.49%)
Loss Of Consciousness
103 (.47%)
Renal Failure
103 (.47%)
Renal Disorder
101 (.46%)
Pyrexia
99 (.45%)
Back Pain
98 (.44%)
Anxiety
97 (.44%)
Arthralgia
95 (.43%)
Pruritus
88 (.4%)
Wrong Technique In Drug Usage Proce...
83 (.38%)
Depression
82 (.37%)
Hypoaesthesia
82 (.37%)
Infarction
82 (.37%)
Abdominal Pain
81 (.37%)
Abdominal Pain Upper
81 (.37%)
Cardiac Failure
77 (.35%)
Erythema
77 (.35%)
Dehydration
76 (.35%)
Heart Rate Increased
76 (.35%)
Palpitations
76 (.35%)
Insomnia
74 (.34%)
Renal Failure Acute
74 (.34%)
Condition Aggravated
73 (.33%)
Blood Creatinine Increased
71 (.32%)
Angina Pectoris
70 (.32%)
Somnolence
70 (.32%)
Blood Potassium Decreased
67 (.3%)
Rash
67 (.3%)
Anaemia
66 (.3%)
Weight Increased
65 (.3%)
Breast Cancer
64 (.29%)
Cardiac Arrest
64 (.29%)
Vision Blurred
64 (.29%)
Decreased Appetite
63 (.29%)
Hypersensitivity
63 (.29%)
Memory Impairment
60 (.27%)
Muscle Spasms
60 (.27%)
Heart Rate Decreased
59 (.27%)
Tachycardia
59 (.27%)
Cerebral Infarction
58 (.26%)
Confusional State
58 (.26%)
Myalgia
58 (.26%)
Cardio-respiratory Arrest
57 (.26%)
Cataract
57 (.26%)
Blood Cholesterol Increased
56 (.25%)
Pollakiuria
56 (.25%)
Blood Urea Increased
53 (.24%)
Nervousness
53 (.24%)
Atrial Fibrillation
52 (.24%)
Paraesthesia
51 (.23%)
Influenza
50 (.23%)
Dry Mouth
49 (.22%)
Muscular Weakness
49 (.22%)
Neck Pain
48 (.22%)
Cardiac Pacemaker Insertion
47 (.21%)
Hypertensive Crisis
47 (.21%)
Respiratory Arrest
47 (.21%)
Tremor
47 (.21%)
Hyperglycaemia
46 (.21%)
Hyperhidrosis
46 (.21%)
Urinary Tract Infection
46 (.21%)
Infection
45 (.2%)
Nephrolithiasis
45 (.2%)
Renal Impairment
45 (.2%)
Blood Pressure Systolic Increased
44 (.2%)
Joint Swelling
44 (.2%)

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

What are the most common Diovan Hct adverse events reported to the FDA?

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

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

Hypertension
4318
Drug Use For Unknown Indication
352
Product Used For Unknown Indication
203
Blood Pressure
182
Blood Pressure Abnormal
38
Blood Pressure Increased
37
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Cardiac Disorder
33
Essential Hypertension
23
Blood Pressure Management
9
Cardiac Failure
7
Fluid Retention
7
Diabetes Mellitus
6
Ill-defined Disorder
6
Atrial Fibrillation
6
Diuretic Therapy
5
Arrhythmia
4
Blood Pressure Fluctuation
4
Palpitations
3
Hypotension
3
Myocardial Infarction
3
Renal Hypertension
3
Renal Disorder
3
Oedema
2
Aortic Valve Replacement
2
Prophylaxis
2
Cardiac Failure Congestive
2
Cardiopulmonary Failure
2
Cardiovascular Disorder
2
Cardiomyopathy
2
Cardiomegaly
2
Arterial Occlusive Disease
2
Cardiac Valve Disease
2
Device Related Infection
2
Blood Cholesterol Increased
2
Malignant Hypertension
2
Labile Hypertension
2
Peripheral Vascular Disorder
2
Coronary Arterial Stent Insertion
1
Dizziness
1
Cardiovascular Event Prophylaxis
1
Depression
1
Muscle Rupture
1
Automatic Bladder
1
Ventricular Hypertrophy
1
Lung Disorder
1
Heart Rate Irregular
1
Polyuria
1
Agitation
1
Swelling
1
Ejection Fraction Decreased
1
Ocular Hypertension
1

Drug Labels

LabelLabelerEffective
Diovan HctSTAT RX USA LLC28-DEC-09
Diovan Hct PD-Rx Pharmaceuticals, Inc.11-FEB-11
Diovan HctLake Erie Medical & Surgical Supply DBA Quality Care Products LLC16-NOV-11
Diovan HctPhysicians Total Care, Inc.09-JAN-12
Diovan HctPD-Rx Pharmaceuticals, Inc.22-FEB-12
Diovan HctLake Erie Medical & Surgical Supply DBA Quality Care Products LLC28-FEB-12
Diovan HctCardinal Health23-JUL-12
Diovan HctDispensing Solutions, Inc.10-OCT-12
Diovan HctNovartis Pharmaceuticals Corporation10-OCT-12
Diovan HctDispensing Solutions, Inc.10-OCT-12
Diovan HctLake Erie Medical DBA Quality Care Products LLC20-FEB-13

Diovan Hct Case Reports

What Diovan Hct 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 Diovan Hct. 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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