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ATACAND HCT

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Atacand Hct Adverse Events Reported to the FDA Over Time

How are Atacand Hct adverse event reports trending over time?

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

Most Common Atacand Hct Adverse Events Reported to the FDA

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

Drug Ineffective
204 (2.2%)
Renal Failure Acute
171 (1.84%)
Hypertension
150 (1.62%)
Blood Pressure Increased
132 (1.42%)
Dizziness
127 (1.37%)
Hypotension
118 (1.27%)
Malaise
111 (1.2%)
Blood Pressure Inadequately Control...
97 (1.04%)
Hyponatraemia
87 (.94%)
Drug Interaction
86 (.93%)
Fall
85 (.92%)
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Fatigue
82 (.88%)
Drug Dose Omission
77 (.83%)
Headache
75 (.81%)
Oedema Peripheral
74 (.8%)
Renal Failure
73 (.79%)
Interstitial Lung Disease
69 (.74%)
Hyperkalaemia
67 (.72%)
Blood Creatinine Increased
64 (.69%)
Vomiting
62 (.67%)
Loss Of Consciousness
61 (.66%)
Rhabdomyolysis
61 (.66%)
Asthenia
58 (.62%)
Dyspnoea
57 (.61%)
Blood Pressure Decreased
56 (.6%)
Bradycardia
56 (.6%)
Cerebrovascular Accident
53 (.57%)
Diabetes Mellitus
53 (.57%)
Weight Decreased
48 (.52%)
Alanine Aminotransferase Increased
45 (.48%)
Chest Pain
45 (.48%)
Myalgia
44 (.47%)
Nausea
44 (.47%)
Liver Disorder
43 (.46%)
Renal Impairment
43 (.46%)
Arrhythmia
42 (.45%)
Aspartate Aminotransferase Increase...
42 (.45%)
Diarrhoea
42 (.45%)
Oligohydramnios
42 (.45%)
Pneumonia
42 (.45%)
Dehydration
39 (.42%)
Gamma-glutamyltransferase Increased
39 (.42%)
Pyrexia
39 (.42%)
Pain In Extremity
38 (.41%)
Pleural Effusion
38 (.41%)
Depressed Level Of Consciousness
37 (.4%)
Hypokalaemia
37 (.4%)
Somnolence
37 (.4%)
Orthostatic Hypotension
35 (.38%)
Confusional State
34 (.37%)
Blood Cholesterol Increased
33 (.36%)
Blood Glucose Increased
33 (.36%)
Syncope
33 (.36%)
Anaemia
32 (.34%)
Cough
32 (.34%)
Drug Exposure During Pregnancy
32 (.34%)
Atrial Fibrillation
31 (.33%)
Blood Pressure Fluctuation
31 (.33%)
Myocardial Infarction
31 (.33%)
Arthralgia
30 (.32%)
Insomnia
30 (.32%)
Rash
30 (.32%)
Blood Alkaline Phosphatase Increase...
29 (.31%)
Cardiac Failure
29 (.31%)
Shock
29 (.31%)
Ventricular Extrasystoles
29 (.31%)
Coronary Artery Occlusion
26 (.28%)
Hypoaesthesia
26 (.28%)
Weight Increased
26 (.28%)
Pruritus
25 (.27%)
Blood Urea Increased
24 (.26%)
Tachycardia
24 (.26%)
Urinary Tract Infection
24 (.26%)
Depression
23 (.25%)
Hepatic Function Abnormal
23 (.25%)
Muscle Spasms
23 (.25%)
Paraesthesia
23 (.25%)
Blood Potassium Increased
22 (.24%)
Blood Sodium Decreased
22 (.24%)
Cardiac Arrest
22 (.24%)
Septic Shock
22 (.24%)
Swollen Tongue
22 (.24%)
Back Pain
21 (.23%)
Blood Creatine Phosphokinase Increa...
21 (.23%)
Haematuria
21 (.23%)
Osteoarthritis
21 (.23%)
Overdose
21 (.23%)
Pollakiuria
21 (.23%)
Venous Occlusion
21 (.23%)
Abdominal Pain
20 (.22%)
Abdominal Pain Upper
20 (.22%)
Gastrointestinal Disorder
20 (.22%)
Off Label Use
20 (.22%)
Skull Malformation
20 (.22%)
Suicide Attempt
20 (.22%)
Toxic Skin Eruption
20 (.22%)
Diabetes Mellitus Inadequate Contro...
19 (.2%)
Pain
19 (.2%)
Angioedema
18 (.19%)
Asthma
18 (.19%)
Dyspepsia
18 (.19%)

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

What are the most common Atacand 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 Atacand 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 Atacand 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 Atacand Hct According to Those Reporting Adverse Events

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

Hypertension
2715
Product Used For Unknown Indication
421
Drug Use For Unknown Indication
297
Essential Hypertension
102
Cardiac Failure
59
Ill-defined Disorder
56
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Blood Pressure
51
Cardiac Failure Chronic
38
Blood Pressure Increased
34
Cardiac Failure Congestive
18
Prophylaxis
17
Myocardial Infarction
11
Renal Hypertension
10
Cardiac Disorder
9
Hypertonia
8
Acute Myocardial Infarction
8
Renal Disorder
8
Metastatic Renal Cell Carcinoma
7
Angina Pectoris
7
Atrial Fibrillation
7
Migraine Prophylaxis
7
Blood Pressure Abnormal
7
Pulmonary Hypertension
6
Maternal Exposure Timing Unspecifie...
6
Blood Pressure Decreased
5
Blood Pressure Management
5
Coronary Artery Disease
5
Rheumatoid Arthritis
4
Diabetic Nephropathy
4
Myocardial Ischaemia
4
Renal Impairment
4
Cardiomyopathy
4
Poisoning
4
Hyperlipidaemia
4
Systemic Lupus Erythematosus
4
Cognitive Disorder
3
Cardiovascular Event Prophylaxis
3
Diastolic Hypertension
3
Diabetic Retinopathy
3
Arrhythmia
2
Hypotonia
2
Heart Rate Increased
2
Cardiotoxicity
2
Cerebral Infarction
2
Affect Lability
2
Cardiovascular Disorder
2
Blood Pressure Inadequately Control...
2
Cerebral Artery Embolism
2
Diabetes Mellitus Insulin-dependent
2
Pulmonary Arterial Hypertension
2
Nephropathy
2

Drug Labels

LabelLabelerEffective
Atacand HctAstraZeneca LP12-APR-11
Atacand HctPhysicians Total Care, Inc.02-FEB-12
Atacand HctBryant Ranch Prepack18-JAN-13

Atacand Hct Case Reports

What Atacand 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 Atacand 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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