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TRIAMTERENE AND HYDROCHLOROTHIAZIDE

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Triamterene And Hydrochlorothiazide Adverse Events Reported to the FDA Over Time

How are Triamterene And Hydrochlorothiazide adverse event reports trending over time?

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

Most Common Triamterene And Hydrochlorothiazide Adverse Events Reported to the FDA

What are the most common Triamterene And Hydrochlorothiazide adverse events reported to the FDA?

Completed Suicide
52 (3.28%)
Dizziness
48 (3.02%)
Hyponatraemia
32 (2.02%)
Renal Failure Acute
32 (2.02%)
Dyspnoea
27 (1.7%)
Drug Ineffective
26 (1.64%)
Muscle Spasms
23 (1.45%)
Asthenia
21 (1.32%)
Pulmonary Embolism
20 (1.26%)
Hypotension
19 (1.2%)
Nausea
19 (1.2%)
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Diarrhoea
18 (1.13%)
Rash
18 (1.13%)
Hyperkalaemia
16 (1.01%)
Cardiac Arrest
15 (.95%)
Fatigue
14 (.88%)
Feeling Abnormal
14 (.88%)
Malaise
14 (.88%)
Pruritus
14 (.88%)
Reaction To Drug Excipients
14 (.88%)
Respiratory Arrest
14 (.88%)
Oedema Peripheral
13 (.82%)
Weight Decreased
13 (.82%)
Alopecia
12 (.76%)
Heart Rate Irregular
12 (.76%)
Hypokalaemia
12 (.76%)
Vomiting
12 (.76%)
Fall
11 (.69%)
Oedema
11 (.69%)
Blood Sodium Decreased
10 (.63%)
Condition Aggravated
10 (.63%)
Drug Interaction
10 (.63%)
Product Quality Issue
10 (.63%)
Product Substitution Issue
10 (.63%)
Urticaria
10 (.63%)
Blood Creatinine Increased
9 (.57%)
Blood Potassium Decreased
9 (.57%)
Dry Mouth
9 (.57%)
Headache
9 (.57%)
Heart Rate Increased
9 (.57%)
Muscular Weakness
9 (.57%)
Palpitations
9 (.57%)
Weight Increased
9 (.57%)
Constipation
8 (.5%)
Cough
8 (.5%)
Dehydration
8 (.5%)
Hypersensitivity
8 (.5%)
Hypovolaemia
8 (.5%)
Medication Error
8 (.5%)
Syncope
8 (.5%)
Abdominal Pain Upper
7 (.44%)
Back Pain
7 (.44%)
Burning Sensation
7 (.44%)
Cardio-respiratory Arrest
7 (.44%)
Cerebrovascular Accident
7 (.44%)
Chest Pain
7 (.44%)
Hyperhidrosis
7 (.44%)
Insomnia
7 (.44%)
Nephrolithiasis
7 (.44%)
Pain
7 (.44%)
Urine Output Decreased
7 (.44%)
Blood Pressure Decreased
6 (.38%)
Blood Urea Increased
6 (.38%)
Confusional State
6 (.38%)
Drug Dispensing Error
6 (.38%)
Drug Hypersensitivity
6 (.38%)
Dysgeusia
6 (.38%)
Erythema
6 (.38%)
Fluid Retention
6 (.38%)
Hypertension
6 (.38%)
Incorrect Dose Administered
6 (.38%)
Myalgia
6 (.38%)
Myocardial Infarction
6 (.38%)
Orthostatic Hypotension
6 (.38%)
Pneumonia
6 (.38%)
Rash Papular
6 (.38%)
Swelling
6 (.38%)
Therapeutic Response Unexpected Wit...
6 (.38%)
Abdominal Distension
5 (.32%)
Abdominal Pain
5 (.32%)
Atrial Fibrillation
5 (.32%)
Blood Pressure Increased
5 (.32%)
Cytolytic Hepatitis
5 (.32%)
Diabetes Mellitus
5 (.32%)
Disorientation
5 (.32%)
Drug Effect Decreased
5 (.32%)
Dysuria
5 (.32%)
Joint Swelling
5 (.32%)
Lethargy
5 (.32%)
Loss Of Consciousness
5 (.32%)
Mental Status Changes
5 (.32%)
Paraesthesia
5 (.32%)
Rash Pruritic
5 (.32%)
Somnolence
5 (.32%)
Swelling Face
5 (.32%)
Vision Blurred
5 (.32%)
Visual Acuity Reduced
5 (.32%)
Bowel Movement Irregularity
4 (.25%)
Bradycardia
4 (.25%)
Chills
4 (.25%)
Death
4 (.25%)

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This graph shows the top adverse events submitted to the FDA for Triamterene And Hydrochlorothiazide, 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 Triamterene And Hydrochlorothiazide 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 Triamterene And Hydrochlorothiazide

What are the most common Triamterene And Hydrochlorothiazide adverse events reported to the FDA?

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

Why are people taking Triamterene And Hydrochlorothiazide, according to those reporting adverse events to the FDA?

Hypertension
613
Product Used For Unknown Indication
185
Drug Use For Unknown Indication
166
Blood Pressure
71
Diuretic Therapy
52
Fluid Retention
48
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Oedema
38
Oedema Peripheral
35
Blood Pressure Increased
27
Swelling
24
Blood Pressure Abnormal
21
Menieres Disease
14
Polyuria
14
Joint Swelling
7
Essential Hypertension
7
Ill-defined Disorder
6
Cardiac Failure Congestive
5
Cardiac Disorder
4
Atrial Fibrillation
3
Prophylaxis
3
Dizziness
3
Weight Loss Diet
3
Hepatic Cirrhosis
2
Anticoagulant Therapy
2
Fluid Imbalance
2
Hypertonia
2
Blood Pressure Diastolic Abnormal
2
Dyspepsia
2
Vertigo
2
Suicide Attempt
2
Hypertensive Crisis
1
Oedema Due To Cardiac Disease
1
Cardiac Failure
1
Fibromyalgia
1
Arthritis
1
Coronary Artery Disease
1
Palpitations
1
Diabetes Mellitus
1
Dehydration
1
Inner Ear Disorder
1
Suicidal Ideation
1
Scleroderma
1
Incontinence
1
Gravitational Oedema
1
Pulmonary Arterial Hypertension
1
Vision Blurred
1
Overdose
1
Nephrolithiasis
1
Pulmonary Hypertension
1
Abdominal Distension
1
Blood Pressure Management
1

Drug Labels

LabelLabelerEffective
Triamterene And HydrochlorothiazideMylan Pharmaceuticals Inc.06-FEB-02
Triamterene HydrochlorothiazideKAISER FOUNDATION HOSPITALS17-FEB-10
Triamterene And HydrochlorothiazideState of Florida DOH Central Pharmacy21-MAY-10
Triamterene And HydrochlorothiazideState of Florida DOH Central Pharmacy21-MAY-10
Triamterene And HydrochlorothiazideState of Florida DOH Central Pharmacy07-JUN-10
Triamterene And Hydrochlorothiazide CapsulesUDL Laboratories, Inc.12-NOV-10
Triamterene And HydrochlorothiazideREMEDYREPACK INC. 17-NOV-10
Triamterene And HydrochlorothiazideRebel Distributors Corp01-DEC-10
Triamterene HydrochlorothiazideRebel Distributors Corp01-DEC-10
DyazideCardinal Health04-JAN-11
Triamterene And HydrochlorothiazideMylan Pharmaceuticals Inc.19-JAN-11
Triamterene And HydrochlorothiazidePD-Rx Pharmaceuticals, Inc.19-JAN-11
Triamterene And HydrochlorothiazidePD-Rx Pharmaceuticals, Inc.16-FEB-11
Triamterene And HydrochlorothiazidePD-Rx Pharmaceuticals, Inc.16-FEB-11
Triamterene And HydrochlorothiazideUDL Laboratories, Inc.10-JUN-11
Triamterene And HydrochlorothiazideApotex Corp.06-OCT-11
Triamterene And HydrochlorothiazideREMEDYREPACK INC. 24-OCT-11
Triamterene And HydrochlorothiazideREMEDYREPACK INC. 02-NOV-11
DyazideGlaxoSmithKline LLC20-JAN-12
Triamterene And HydrochlorothiazidePD-Rx Pharmaceuticals, Inc.25-JAN-12
Triamterene And HydrochlorothiazideSandoz Inc25-JAN-12
Triamterene HydrochlorothiazidePhysicians Total Care, Inc.03-FEB-12
Triamterene And HydrochlorothiazideREMEDYREPACK INC. 07-MAR-12
Triamterene HydrochlorothiazideSandoz Inc23-APR-12
Triamterene HydrochlorothiazidePD-Rx Pharmaceuticals, Inc.23-APR-12
Triamterene And HydrochlorothiazidePreferred Pharmaceuticals, Inc30-APR-12
Triamterene And HydrochlorothiazidePreferred Pharmaceuticals, Inc30-APR-12
Triamterene And HydrochlorothiazideWatson Laboratories, Inc.30-APR-12
Triamterene And HydrochlorothiazideLake Erie Medical & Surgical Supply DBA Quality Care Products LLC31-MAY-12
Triamterene And HydrochlorothiazidePhysicians Total Care, Inc.15-JUN-12
Triamterene And Hydrochlorothiazide AvKARE, Inc.03-JUL-12
Triamterene And HydrochlorothiazideLannett Company, Inc.12-JUL-12
Triamterene And HydrochlorothiazideBarr Laboratories Inc.14-SEP-12
Triamterene And HydrochlorothiazideSTAT Rx USA LLC25-SEP-12
Triamterene And HydrochlorothiazideBryant Ranch Prepack12-OCT-12
Triamterene HydrochlorothiazideNCS HealthCare of KY, Inc dba Vangard Labs15-NOV-12
Triamterene And HydrochlorothiazideNCS HealthCare of KY, Inc dba Vangard Labs15-NOV-12
Triamterene And HydrochlorothiazideKAISER FOUNDATION HOSPITALS17-JAN-13
Triamterene And HydrochlorothiazideBryant Ranch Prepack17-JAN-13
Triamterene HydrochlorothiazideBryant Ranch Prepack17-JAN-13
Triamterene And HydrochlorothiazideBryant Ranch Prepack17-JAN-13

Triamterene And Hydrochlorothiazide Case Reports

What Triamterene And Hydrochlorothiazide 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 Triamterene And Hydrochlorothiazide. 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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