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EXFORGE HCT

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Exforge Hct Adverse Events Reported to the FDA Over Time

How are Exforge Hct adverse event reports trending over time?

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

Most Common Exforge Hct Adverse Events Reported to the FDA

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

Oedema Peripheral
305 (1.93%)
Hypotension
259 (1.64%)
Dizziness
254 (1.61%)
Drug Ineffective
238 (1.51%)
Blood Pressure Increased
213 (1.35%)
Completed Suicide
194 (1.23%)
Headache
175 (1.11%)
Malaise
153 (.97%)
Hypertension
150 (.95%)
Fatigue
148 (.94%)
Renal Failure Acute
145 (.92%)
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Drug Interaction
141 (.89%)
Dyspnoea
139 (.88%)
Nausea
130 (.82%)
Fall
118 (.75%)
Overdose
118 (.75%)
Death
114 (.72%)
Feeling Abnormal
109 (.69%)
Renal Failure
109 (.69%)
Pain In Extremity
99 (.63%)
Syncope
99 (.63%)
Blood Pressure Inadequately Control...
94 (.6%)
Joint Swelling
93 (.59%)
Asthenia
92 (.58%)
Pruritus
89 (.56%)
Loss Of Consciousness
88 (.56%)
Blood Pressure Decreased
85 (.54%)
Palpitations
82 (.52%)
Arthralgia
81 (.51%)
Vomiting
81 (.51%)
Suicide Attempt
80 (.51%)
Bradycardia
79 (.5%)
Somnolence
77 (.49%)
Diarrhoea
76 (.48%)
Rash
74 (.47%)
Chest Pain
72 (.46%)
Pain
70 (.44%)
Pyrexia
70 (.44%)
Hyponatraemia
68 (.43%)
Cough
67 (.42%)
Cardiac Arrest
66 (.42%)
Muscle Spasms
64 (.41%)
Hyperkalaemia
63 (.4%)
Cerebrovascular Accident
62 (.39%)
Heart Rate Increased
61 (.39%)
Metabolic Acidosis
60 (.38%)
Blood Creatinine Increased
59 (.37%)
Abdominal Pain
58 (.37%)
Product Substitution Issue
58 (.37%)
Blood Glucose Increased
57 (.36%)
Anaemia
54 (.34%)
Back Pain
54 (.34%)
Muscular Weakness
54 (.34%)
Myalgia
53 (.34%)
Decreased Appetite
52 (.33%)
Condition Aggravated
51 (.32%)
Intentional Overdose
51 (.32%)
Vision Blurred
51 (.32%)
Renal Impairment
49 (.31%)
Weight Decreased
49 (.31%)
Dry Mouth
48 (.3%)
Insomnia
46 (.29%)
Respiratory Failure
46 (.29%)
Rhabdomyolysis
45 (.29%)
Convulsion
44 (.28%)
Paraesthesia
44 (.28%)
Shock
44 (.28%)
Confusional State
43 (.27%)
Gait Disturbance
43 (.27%)
Hypersensitivity
43 (.27%)
Pulmonary Oedema
43 (.27%)
Urticaria
43 (.27%)
Abdominal Distension
42 (.27%)
Angioedema
41 (.26%)
Oedema
41 (.26%)
Dehydration
40 (.25%)
Pneumonia
40 (.25%)
Tachycardia
40 (.25%)
Weight Increased
40 (.25%)
Abdominal Pain Upper
39 (.25%)
Blood Pressure Systolic Increased
39 (.25%)
Drug Hypersensitivity
39 (.25%)
Erythema
39 (.25%)
General Physical Health Deteriorati...
39 (.25%)
Haemoglobin Decreased
39 (.25%)
Hyperhidrosis
39 (.25%)
Swelling
39 (.25%)
Constipation
38 (.24%)
Depression
38 (.24%)
Visual Impairment
38 (.24%)
Cardiogenic Shock
37 (.23%)
Swelling Face
37 (.23%)
Hypokalaemia
36 (.23%)
Tremor
36 (.23%)
Respiratory Arrest
35 (.22%)
Blood Pressure Fluctuation
34 (.22%)
Coma
33 (.21%)
Multiple Drug Overdose
32 (.2%)
Atrial Fibrillation
31 (.2%)
Blood Urea Increased
31 (.2%)
Heart Rate Irregular
31 (.2%)

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

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

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

Hypertension
3897
Product Used For Unknown Indication
633
Drug Use For Unknown Indication
596
Blood Pressure
196
Blood Pressure Increased
135
Essential Hypertension
104
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Blood Pressure Abnormal
55
Myocardial Ischaemia
37
Angina Pectoris
32
Cardiac Disorder
19
Coronary Artery Disease
17
Pneumonia
16
Ill-defined Disorder
14
Suicide Attempt
14
Prophylaxis
12
Blood Pressure Management
10
Cardiovascular Disorder
9
Rheumatoid Arthritis
9
Myocardial Infarction
9
Hyperlipidaemia
7
Pulmonary Hypertension
6
Transient Ischaemic Attack
6
Cardiac Failure
6
Ischaemic Cardiomyopathy
6
Hypertensive Heart Disease
6
Chest Pain
6
Hypertonia
6
Atrial Fibrillation
6
Hypercholesterolaemia
5
Renal Hypertension
5
Overdose
4
Intentional Overdose
4
Coronary Artery Stenosis
4
Dyslipidaemia
4
Metastatic Renal Cell Carcinoma
4
Cardiac Failure Chronic
4
Renal Failure Chronic
3
Cerebral Artery Stenosis
3
Malignant Hypertension
3
Cerebral Infarction
3
Leukocytoclastic Vasculitis
3
Drug Therapy
3
Respiratory Tract Infection
3
Blood Pressure Inadequately Control...
3
Angiopathy
3
Oedema Peripheral
2
Type 2 Diabetes Mellitus
2
Raynauds Phenomenon
2
Palpitations
2
Blood Pressure Systolic Increased
2
Enterobacter Test Positive
2

Drug Labels

LabelLabelerEffective
Exforge HctPhysicians Total Care, Inc.19-DEC-11
Exforge HctNovartis Pharmaceuticals Corporation30-NOV-12

Exforge Hct Case Reports

What Exforge 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 Exforge 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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