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HYDRODIURIL

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Hydrodiuril Adverse Events Reported to the FDA Over Time

How are Hydrodiuril adverse event reports trending over time?

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

Most Common Hydrodiuril Adverse Events Reported to the FDA

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

Renal Failure Acute
35 (3.57%)
Hyponatraemia
32 (3.27%)
Completed Suicide
25 (2.55%)
Overdose
22 (2.24%)
Drug Ineffective
15 (1.53%)
Blood Creatinine Increased
14 (1.43%)
Dehydration
14 (1.43%)
Rhabdomyolysis
14 (1.43%)
Diarrhoea
13 (1.33%)
Hypokalaemia
13 (1.33%)
Hypertension
12 (1.22%)
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Hypotension
11 (1.12%)
Lethargy
10 (1.02%)
Vomiting
10 (1.02%)
Dyspnoea
9 (.92%)
Nausea
9 (.92%)
Nephrolithiasis
9 (.92%)
Renal Failure
9 (.92%)
Asthenia
8 (.82%)
Blood Potassium Increased
8 (.82%)
Dizziness
8 (.82%)
Gastroenteritis
8 (.82%)
Urinary Tract Infection
8 (.82%)
Anaemia
7 (.71%)
Anti-ss-a Antibody Positive
7 (.71%)
Blood Potassium Decreased
7 (.71%)
Circulatory Collapse
7 (.71%)
Cutaneous Lupus Erythematosus
7 (.71%)
Drug Interaction
7 (.71%)
Fall
7 (.71%)
Headache
7 (.71%)
Hyperkalaemia
7 (.71%)
Acute Prerenal Failure
6 (.61%)
Lactic Acidosis
6 (.61%)
Syncope
6 (.61%)
Angioedema
5 (.51%)
Blood Potassium Abnormal
5 (.51%)
Cardiac Disorder
5 (.51%)
Cardiac Failure Congestive
5 (.51%)
Confusional State
5 (.51%)
Convulsion
5 (.51%)
Fatigue
5 (.51%)
Loss Of Consciousness
5 (.51%)
Malaise
5 (.51%)
Metabolic Alkalosis
5 (.51%)
Swollen Tongue
5 (.51%)
Abdominal Pain
4 (.41%)
Anorexia
4 (.41%)
Blood Glucose Increased
4 (.41%)
Blood Pressure Decreased
4 (.41%)
Blood Urea Increased
4 (.41%)
Diabetes Mellitus
4 (.41%)
Diabetic Neuropathy
4 (.41%)
Encephalopathy
4 (.41%)
Haematocrit Decreased
4 (.41%)
Haemoglobin Decreased
4 (.41%)
Hypercalcaemia
4 (.41%)
Hyperventilation
4 (.41%)
Hypochloraemia
4 (.41%)
Hypovolaemia
4 (.41%)
Inappropriate Antidiuretic Hormone ...
4 (.41%)
Intentional Overdose
4 (.41%)
Joint Swelling
4 (.41%)
Medication Error
4 (.41%)
Metabolic Acidosis
4 (.41%)
Myocardial Infarction
4 (.41%)
Myopathy
4 (.41%)
Obesity
4 (.41%)
Pancreatitis
4 (.41%)
Pseudoaldosteronism
4 (.41%)
Renal Disorder
4 (.41%)
Respiratory Failure
4 (.41%)
Thyroid Disorder
4 (.41%)
Tremor
4 (.41%)
Adverse Event
3 (.31%)
Anaphylactic Reaction
3 (.31%)
Anxiety
3 (.31%)
Ataxia
3 (.31%)
Blood Pressure Inadequately Control...
3 (.31%)
Blood Pressure Increased
3 (.31%)
Blood Urea Abnormal
3 (.31%)
Bradycardia
3 (.31%)
Cardiovascular Disorder
3 (.31%)
Cerebrovascular Accident
3 (.31%)
Chills
3 (.31%)
Coagulopathy
3 (.31%)
Colitis
3 (.31%)
Disseminated Intravascular Coagulat...
3 (.31%)
Hyperaldosteronism
3 (.31%)
Hyperparathyroidism
3 (.31%)
International Normalised Ratio Incr...
3 (.31%)
Liver Disorder
3 (.31%)
Multi-organ Failure
3 (.31%)
Multiple Congenital Abnormalities
3 (.31%)
Multiple Drug Overdose
3 (.31%)
Muscular Weakness
3 (.31%)
Nephropathy
3 (.31%)
Nodal Arrhythmia
3 (.31%)
Oedema Peripheral
3 (.31%)
Pancreatitis Acute
3 (.31%)
Pancreatitis Chronic
3 (.31%)

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

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

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

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

Hypertension
179
Product Used For Unknown Indication
18
Blood Pressure
15
Swelling
9
Polyuria
8
Oedema
6
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Cardiac Failure Chronic
5
Drug Use For Unknown Indication
5
Essential Hypertension
5
Oedema Peripheral
4
Univentricular Heart
3
Diuretic Therapy
3
Cardiac Disorder
3
Nephrogenic Diabetes Insipidus
2
Fluid Retention
2
Arteriosclerosis
2
Blood Pressure Management
2
Renal Artery Stenosis
2
Coronary Artery Disease
2
Urine Calcium
1
Hypertensive Cardiomyopathy
1
Blood Pressure Abnormal
1
Thyroid Disorder
1
Cardiac Failure
1
Nephrolithiasis
1
Diabetes Insipidus
1
Pain
1

Hydrodiuril Case Reports

What Hydrodiuril 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 Hydrodiuril. 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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