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TERAZOSIN

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Terazosin Adverse Events Reported to the FDA Over Time

How are Terazosin adverse event reports trending over time?

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

Most Common Terazosin Adverse Events Reported to the FDA

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

Hypotension
248 (8.2%)
Dizziness
237 (7.83%)
Syncope
223 (7.37%)
Orthostatic Hypotension
89 (2.94%)
Fall
80 (2.64%)
Drug Ineffective
48 (1.59%)
Loss Of Consciousness
47 (1.55%)
Asthenia
40 (1.32%)
Headache
40 (1.32%)
Bradycardia
38 (1.26%)
Malaise
34 (1.12%)
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Nausea
31 (1.02%)
Back Pain
29 (.96%)
Fatigue
28 (.93%)
Abdominal Pain
27 (.89%)
Musculoskeletal Stiffness
26 (.86%)
Drug Interaction
25 (.83%)
Blood Pressure Decreased
24 (.79%)
Dyspnoea
24 (.79%)
Pancreatic Carcinoma
22 (.73%)
Blood Pressure Increased
21 (.69%)
Dehydration
21 (.69%)
Jaundice
21 (.69%)
Diarrhoea
20 (.66%)
Dysuria
20 (.66%)
Presyncope
19 (.63%)
Vision Blurred
18 (.59%)
Completed Suicide
17 (.56%)
Hyperhidrosis
15 (.5%)
Palpitations
15 (.5%)
Head Injury
14 (.46%)
Oedema Peripheral
13 (.43%)
Pneumonia
13 (.43%)
Pollakiuria
13 (.43%)
Rash
13 (.43%)
Renal Failure Acute
13 (.43%)
Muscle Spasms
12 (.4%)
Angina Pectoris
11 (.36%)
Blood Creatinine Increased
11 (.36%)
Chest Pain
11 (.36%)
Feeling Abnormal
11 (.36%)
Joint Swelling
11 (.36%)
Dizziness Postural
10 (.33%)
Oedema
10 (.33%)
Paraesthesia
10 (.33%)
Priapism
10 (.33%)
Treatment Noncompliance
10 (.33%)
Atrial Fibrillation
9 (.3%)
Blood Urea Increased
9 (.3%)
Insomnia
9 (.3%)
Myoclonus
9 (.3%)
Vomiting
9 (.3%)
Arthralgia
8 (.26%)
Benign Prostatic Hyperplasia
8 (.26%)
Cardiac Arrest
8 (.26%)
Chest Discomfort
8 (.26%)
Fibula Fracture
8 (.26%)
Heart Rate Decreased
8 (.26%)
Hypoaesthesia
8 (.26%)
Hypokalaemia
8 (.26%)
Incorrect Dose Administered
8 (.26%)
Medication Error
8 (.26%)
Nocturia
8 (.26%)
Pain In Extremity
8 (.26%)
Sinus Bradycardia
8 (.26%)
Therapeutic Response Unexpected Wit...
8 (.26%)
Tibia Fracture
8 (.26%)
Unevaluable Event
8 (.26%)
Unresponsive To Stimuli
8 (.26%)
Urinary Retention
8 (.26%)
Blood Pressure Diastolic Decreased
7 (.23%)
Condition Aggravated
7 (.23%)
Constipation
7 (.23%)
Drug Dose Omission
7 (.23%)
Drug Intolerance
7 (.23%)
Dysarthria
7 (.23%)
Erectile Dysfunction
7 (.23%)
Heart Rate Increased
7 (.23%)
Hypovolaemia
7 (.23%)
Suicide Attempt
7 (.23%)
Tachycardia
7 (.23%)
Vertigo
7 (.23%)
Weight Increased
7 (.23%)
Blood Pressure Systolic Increased
6 (.2%)
Cardiac Failure
6 (.2%)
Cold Sweat
6 (.2%)
Depression
6 (.2%)
Drug Effect Decreased
6 (.2%)
Drug Hypersensitivity
6 (.2%)
Faeces Discoloured
6 (.2%)
Gait Disturbance
6 (.2%)
Impaired Work Ability
6 (.2%)
Pallor
6 (.2%)
Prostatic Specific Antigen Increase...
6 (.2%)
Renal Failure
6 (.2%)
Rhabdomyolysis
6 (.2%)
Tremor
6 (.2%)
Urinary Incontinence
6 (.2%)
Alanine Aminotransferase Increased
5 (.17%)
Amnesia
5 (.17%)
Aspartate Aminotransferase Increase...
5 (.17%)

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

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

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

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

Benign Prostatic Hyperplasia
625
Hypertension
465
Drug Use For Unknown Indication
291
Product Used For Unknown Indication
237
Prostatic Disorder
135
Prostatomegaly
108
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Blood Pressure
60
Dysuria
33
Prostate Cancer
25
Prostatitis
22
Urinary Tract Disorder
21
Bladder Disorder
17
Urinary Retention
15
Pollakiuria
14
Micturition Disorder
10
Cardiac Disorder
10
Blood Pressure Increased
10
Blood Pressure Abnormal
9
Prostatism
8
Prostate Examination Abnormal
8
Drug Interaction
7
Prophylaxis
7
Hyperhidrosis
6
Renal Disorder
6
Fluid Retention
6
Diuretic Therapy
6
Hypertonic Bladder
5
Neurogenic Bladder
5
Heart Rate Irregular
5
Atonic Urinary Bladder
4
Complex Regional Pain Syndrome
4
Nocturia
4
Sleep Apnoea Syndrome
4
Insomnia
4
Urinary Tract Infection
3
Blood Pressure Management
3
Blood Urine Present
3
Ill-defined Disorder
3
Bladder Sphincter Atony
2
Urinary Incontinence
2
Hypotension
2
Urinary Tract Obstruction
2
Promotion Of Peripheral Circulation
2
Urethral Disorder
2
Nephrolithiasis
2
Coronary Artery Disease
2
Sleep Disorder
2
Benign Neoplasm Of Prostate
2
Hot Flush
1
Obstructive Uropathy
1
Bladder Cancer
1

Drug Labels

LabelLabelerEffective
Terazosin Hydrochloride AnhydrousUDL Laboratories, Inc.15-JAN-09
Terazosin HydrochlorideState of Florida DOH Central Pharmacy02-JUN-10
Terazosin Hydrochloride Bryant Ranch Prepack02-JUN-10
Terazosin HydrochlorideState of Florida DOH Central Pharmacy02-JUN-10
Terazosin HydrochlorideState of Florida DOH Central Pharmacy02-JUN-10
Terazosin HydrochlorideREMEDYREPACK INC. 10-NOV-10
Terazosin HydrochlorideRebel Distributors Corp17-JAN-11
Terazosin HydrochlorideREMEDYREPACK INC. 17-MAY-11
Terazosin HydrochlorideREMEDYREPACK INC. 09-JUN-11
Terazosin HydrochlorideREMEDYREPACK INC. 01-JUL-11
Terazosin HydrochlorideREMEDYREPACK INC. 28-JUL-11
Terazosin HydrochlorideREMEDYREPACK INC. 29-JUL-11
Terazosin HydrochlorideREMEDYREPACK INC. 16-AUG-11
Terazosin HydrochlorideSandoz Inc21-OCT-11
Terazosin HydrochlorideREMEDYREPACK INC. 10-NOV-11
Terazosin HydrochloridePreferred Pharmaceuticals, Inc28-FEB-12
TerazosinApotex Corp.06-MAR-12
Terazosin HydrochlorideSTAT Rx USA LLC21-MAR-12
Terazosin Hydrochloride AnhydrousMylan Pharmaceuticals Inc.31-MAR-12
Terazosin HydrochloridePreferred Pharmaceuticals, Inc05-APR-12
Terazosin HydrochlorideMajor Pharmaceuticals23-JUL-12
Terazosin HydrochlorideTeva Pharmaceuticals USA Inc30-JUL-12
Terazosin Jubilant Cadista Pharmaceuticals Inc.01-AUG-12
Terazosin Hydrochloride AnhydrousCardinal Health01-AUG-12
Terazosin Hydrochloride Aphena Pharma Solutions - Tennessee, Inc.15-AUG-12
Terazosin HydrochlorideCardinal Health22-AUG-12
Terazosin Hydrochloride Bryant Ranch Prepack18-JAN-13
Terazosin HydrochlorideNCS HealthCare of KY, Inc dba Vangard Labs25-FEB-13
Terazosin HydrochloridePhysicians Total Care, Inc.25-FEB-13
Terazosin REMEDYREPACK INC. 28-MAR-13

Terazosin Case Reports

What Terazosin 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 Terazosin. 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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