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TEVETEN

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Teveten Adverse Events Reported to the FDA Over Time

How are Teveten adverse event reports trending over time?

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

Most Common Teveten Adverse Events Reported to the FDA

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

Dizziness
30 (2.84%)
Cerebrovascular Accident
28 (2.65%)
Dyspnoea
26 (2.46%)
Fall
21 (1.99%)
Hypertension
21 (1.99%)
Myocardial Infarction
18 (1.7%)
Hypotension
15 (1.42%)
Renal Failure
14 (1.33%)
Chronic Sinusitis
13 (1.23%)
Diarrhoea
13 (1.23%)
Asthenia
12 (1.14%)
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Loss Of Consciousness
12 (1.14%)
Syncope
12 (1.14%)
Drug Exposure During Pregnancy
11 (1.04%)
Malaise
11 (1.04%)
Blood Pressure Increased
10 (.95%)
Condition Aggravated
10 (.95%)
Cough
10 (.95%)
Arrhythmia
9 (.85%)
Blood Pressure Systolic Increased
9 (.85%)
Dysphonia
9 (.85%)
Intestinal Obstruction
9 (.85%)
Hypertensive Crisis
8 (.76%)
Hypoperfusion
8 (.76%)
Nausea
8 (.76%)
Bradycardia
7 (.66%)
Caudal Regression Syndrome
7 (.66%)
Drug Ineffective
7 (.66%)
Ovarian Cancer
7 (.66%)
Pain
7 (.66%)
Pulmonary Embolism
7 (.66%)
Acute Coronary Syndrome
6 (.57%)
Acute Myocardial Infarction
6 (.57%)
Cardiogenic Shock
6 (.57%)
Fatigue
6 (.57%)
Headache
6 (.57%)
Intra-uterine Death
6 (.57%)
Left Ventricular Failure
6 (.57%)
Pain In Extremity
6 (.57%)
Pharyngitis
6 (.57%)
Pneumonia
6 (.57%)
Pulmonary Hypoplasia
6 (.57%)
Road Traffic Accident
6 (.57%)
Angina Pectoris
5 (.47%)
Blood Potassium Decreased
5 (.47%)
Brain Stem Infarction
5 (.47%)
C-reactive Protein Increased
5 (.47%)
Caesarean Section
5 (.47%)
Fungal Infection
5 (.47%)
Gait Disturbance
5 (.47%)
Hyperhidrosis
5 (.47%)
Metastases To Large Intestine
5 (.47%)
Myalgia
5 (.47%)
Overdose
5 (.47%)
Refusal Of Treatment By Patient
5 (.47%)
Suicide Attempt
5 (.47%)
Tachycardia
5 (.47%)
Vision Blurred
5 (.47%)
Abdominal Adhesions
4 (.38%)
Abdominal Neoplasm
4 (.38%)
Anaemia
4 (.38%)
Angioedema
4 (.38%)
Anxiety
4 (.38%)
Blood Pressure Decreased
4 (.38%)
Bundle Branch Block Left
4 (.38%)
Cholelithiasis
4 (.38%)
Chronic Obstructive Pulmonary Disea...
4 (.38%)
Circulatory Collapse
4 (.38%)
Confusional State
4 (.38%)
Hemiplegia
4 (.38%)
Hypoaesthesia
4 (.38%)
Intraocular Pressure Test Abnormal
4 (.38%)
Lip Oedema
4 (.38%)
Metastases To Pleura
4 (.38%)
Mitral Valve Incompetence
4 (.38%)
Myocardial Ischaemia
4 (.38%)
Oral Pain
4 (.38%)
Renal Failure Acute
4 (.38%)
Respiratory Tract Infection
4 (.38%)
Sinus Bradycardia
4 (.38%)
Stillbirth
4 (.38%)
Sudden Death
4 (.38%)
Abasia
3 (.28%)
Abdominal Pain Upper
3 (.28%)
Alcoholic Seizure
3 (.28%)
Asthma
3 (.28%)
Atrial Fibrillation
3 (.28%)
Bronchospasm
3 (.28%)
Cardiomegaly
3 (.28%)
Cellulitis
3 (.28%)
Cold Sweat
3 (.28%)
Completed Suicide
3 (.28%)
Death
3 (.28%)
Depression
3 (.28%)
Drug Interaction
3 (.28%)
Dysstasia
3 (.28%)
Fear
3 (.28%)
Feeling Abnormal
3 (.28%)
Femur Fracture
3 (.28%)
Foetal Disorder
3 (.28%)
Gastrointestinal Disorder
3 (.28%)

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

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

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

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

Hypertension
337
Drug Use For Unknown Indication
38
Essential Hypertension
16
Blood Pressure
6
Product Used For Unknown Indication
6
Thrombosis Prophylaxis
6
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Cardiac Failure
5
Hypertonia
4
Blood Pressure Management
4
Ill-defined Disorder
3
Drug Exposure During Pregnancy
3
Chest Pain
2
Unevaluable Event
2
Cardiac Disorder
2
Blood Pressure Decreased
2
Prophylaxis
2
Bipolar Disorder
1
Cardiomyopathy
1
Blood Pressure Increased
1
Blood Pressure Fluctuation
1
Blood Pressure Abnormal
1

Drug Labels

LabelLabelerEffective
Teveten HctPhysicians Total Care, Inc.03-JAN-12
TevetenAbbott Laboratories20-SEP-12
Teveten HctAbbott Laboratories20-SEP-12

Teveten Case Reports

What Teveten 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 Teveten. 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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