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MODURETIC

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Moduretic Adverse Events Reported to the FDA Over Time

How are Moduretic adverse event reports trending over time?

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

Most Common Moduretic Adverse Events Reported to the FDA

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

Hyponatraemia
151 (5.69%)
Hyperkalaemia
95 (3.58%)
Renal Failure Acute
75 (2.83%)
Confusional State
66 (2.49%)
Fall
56 (2.11%)
Drug Interaction
45 (1.7%)
Vomiting
45 (1.7%)
Hypokalaemia
44 (1.66%)
Syncope
40 (1.51%)
Dehydration
39 (1.47%)
Hypotension
35 (1.32%)
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Dizziness
29 (1.09%)
Blood Creatinine Increased
28 (1.06%)
Renal Failure
27 (1.02%)
Asthenia
25 (.94%)
Blood Pressure Decreased
24 (.9%)
Malaise
23 (.87%)
Renal Failure Chronic
23 (.87%)
Blood Potassium Increased
22 (.83%)
Dyspnoea
20 (.75%)
Hypertension
20 (.75%)
Nausea
20 (.75%)
Cardiac Arrest
19 (.72%)
General Physical Health Deteriorati...
18 (.68%)
Headache
18 (.68%)
Loss Of Consciousness
18 (.68%)
Oedema Peripheral
18 (.68%)
Bradycardia
17 (.64%)
Inappropriate Antidiuretic Hormone ...
17 (.64%)
Atrioventricular Block Complete
16 (.6%)
Bronchopneumonia
16 (.6%)
Diarrhoea
16 (.6%)
Orthostatic Hypotension
16 (.6%)
Urinary Tract Infection
16 (.6%)
Atrial Fibrillation
15 (.57%)
Blood Pressure Increased
15 (.57%)
Blood Urea Increased
15 (.57%)
Chest Pain
15 (.57%)
Disorientation
15 (.57%)
Lactic Acidosis
15 (.57%)
Muscle Spasms
15 (.57%)
Presyncope
14 (.53%)
Somnolence
14 (.53%)
Traumatic Haematoma
14 (.53%)
Drug Ineffective
13 (.49%)
Haemodialysis
13 (.49%)
Hypertensive Crisis
13 (.49%)
Speech Disorder
13 (.49%)
Vertigo
13 (.49%)
Abscess Limb
12 (.45%)
Acute Respiratory Failure
12 (.45%)
Anaemia
12 (.45%)
Duodenal Ulcer Haemorrhage
12 (.45%)
Dysarthria
12 (.45%)
Fatigue
12 (.45%)
Gastric Ulcer Haemorrhage
12 (.45%)
Glomerular Filtration Rate Decrease...
12 (.45%)
Pleural Effusion
12 (.45%)
Therapeutic Agent Toxicity
12 (.45%)
Vision Blurred
12 (.45%)
Abdominal Distension
11 (.41%)
Gastrointestinal Haemorrhage
11 (.41%)
Medication Error
11 (.41%)
Metabolic Acidosis
11 (.41%)
Blood Glucose Increased
10 (.38%)
Blood Sodium Decreased
10 (.38%)
Bundle Branch Block Left
10 (.38%)
Coordination Abnormal
10 (.38%)
Eosinophilia
10 (.38%)
Insomnia
10 (.38%)
Aphasia
9 (.34%)
Constipation
9 (.34%)
Erythema
9 (.34%)
Gait Disturbance
9 (.34%)
Hypocalcaemia
9 (.34%)
Hypoglycaemia
9 (.34%)
Lung Disorder
9 (.34%)
Mesothelioma
9 (.34%)
Tachycardia
9 (.34%)
Abdominal Pain Upper
8 (.3%)
Acidosis
8 (.3%)
Atrioventricular Block
8 (.3%)
Blood Creatine Phosphokinase Increa...
8 (.3%)
Cerebral Ischaemia
8 (.3%)
Death
8 (.3%)
Drug Exposure During Pregnancy
8 (.3%)
Nephrogenic Anaemia
8 (.3%)
Pyrexia
8 (.3%)
Apathy
7 (.26%)
Blood Creatinine Decreased
7 (.26%)
Dyspepsia
7 (.26%)
Hyperhidrosis
7 (.26%)
Infection
7 (.26%)
Interstitial Lung Disease
7 (.26%)
Overdose
7 (.26%)
Pruritus
7 (.26%)
Subarachnoid Haemorrhage
7 (.26%)
Blood Bicarbonate Decreased
6 (.23%)
Cardiac Murmur
6 (.23%)
Decreased Appetite
6 (.23%)
Drug Abuse
6 (.23%)

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

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

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

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

Hypertension
652
Drug Use For Unknown Indication
156
Product Used For Unknown Indication
73
Diuretic Therapy
63
Essential Hypertension
45
Oedema
36
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Oedema Peripheral
32
Blood Pressure
23
Fluid Retention
22
Cardiac Failure
18
Ill-defined Disorder
17
Cardiac Failure Congestive
16
Polyuria
15
Hypokalaemia
13
Myocardial Ischaemia
13
Blood Pressure Increased
9
Prophylaxis
9
Hypertensive Heart Disease
9
Atrial Fibrillation
9
Calcium Metabolism Disorder
6
Ascites
5
Diabetes Mellitus
5
Swelling
5
Joint Swelling
4
Cardiovascular Disorder
4
Blood Pressure Abnormal
4
Nephrogenic Diabetes Insipidus
4
Urinary Retention
3
Renal Failure Chronic
3
Renal Disorder
3
Endolymphatic Hydrops
3
Cardiac Disorder
3
Diabetes Insipidus
2
Palpitations
2
Tenosynovitis
2
Medical Diet
2
Malignant Hypertension
2
Bursitis
2
Renal Impairment
2
Hydronephrosis
2
Glomerulonephritis
2
Coronary Artery Disease
2
Hyperthyroidism
1
Insulin Resistance
1
Varices Oesophageal
1
Cystic Fibrosis
1
Electrolyte Depletion
1
Fallots Tetralogy
1
Blood Potassium Decreased
1
Cardiomegaly
1
Immunisation
1

Moduretic Case Reports

What Moduretic 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 Moduretic. 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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