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TAPAZOLE

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Tapazole Adverse Events Reported to the FDA Over Time

How are Tapazole adverse event reports trending over time?

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

Most Common Tapazole Adverse Events Reported to the FDA

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

Pyrexia
18 (1.69%)
Asthenia
17 (1.6%)
Headache
17 (1.6%)
Agranulocytosis
16 (1.5%)
Drug Exposure During Pregnancy
13 (1.22%)
Arthralgia
12 (1.13%)
Hypothyroidism
12 (1.13%)
Dyspnoea
11 (1.03%)
Fatigue
11 (1.03%)
Myalgia
11 (1.03%)
Nausea
11 (1.03%)
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Thrombocytopenia
11 (1.03%)
Choanal Atresia
10 (.94%)
Jaundice
10 (.94%)
Completed Suicide
9 (.85%)
Drug Interaction
9 (.85%)
Paraesthesia
9 (.85%)
Alanine Aminotransferase Increased
8 (.75%)
Heart Rate Increased
8 (.75%)
Hypoaesthesia
8 (.75%)
Increased Upper Airway Secretion
8 (.75%)
Malaise
8 (.75%)
Product Tampering
8 (.75%)
Rash
8 (.75%)
Urticaria
8 (.75%)
Vomiting
8 (.75%)
White Blood Cell Count Decreased
8 (.75%)
Abdominal Pain Upper
7 (.66%)
Anaemia
7 (.66%)
Blood Bilirubin Increased
7 (.66%)
Blood Glucose Increased
7 (.66%)
Dysgeusia
7 (.66%)
Pain
7 (.66%)
Tri-iodothyronine Increased
7 (.66%)
Weight Decreased
7 (.66%)
Diabetes Mellitus
6 (.56%)
Dry Eye
6 (.56%)
Exomphalos
6 (.56%)
Feeling Abnormal
6 (.56%)
Haematocrit Decreased
6 (.56%)
Hepatitis Acute
6 (.56%)
Hunger
6 (.56%)
Metabolic Acidosis
6 (.56%)
Muscular Weakness
6 (.56%)
Polyuria
6 (.56%)
Pruritus
6 (.56%)
Rash Pruritic
6 (.56%)
Thirst
6 (.56%)
Weight Increased
6 (.56%)
Alopecia
5 (.47%)
Aspartate Aminotransferase Increase...
5 (.47%)
Blood Alkaline Phosphatase Increase...
5 (.47%)
Blood Thyroid Stimulating Hormone I...
5 (.47%)
Cardio-respiratory Arrest
5 (.47%)
Delayed Fontanelle Closure
5 (.47%)
Drug Ineffective
5 (.47%)
Dysphagia
5 (.47%)
Gastric Haemorrhage
5 (.47%)
Haemoglobin Decreased
5 (.47%)
Leukopenia
5 (.47%)
Neutropenia
5 (.47%)
Ocular Icterus
5 (.47%)
Pain In Extremity
5 (.47%)
Renal Failure
5 (.47%)
Renal Failure Acute
5 (.47%)
Splenic Infarction
5 (.47%)
Abdominal Pain
4 (.38%)
Ageusia
4 (.38%)
Anaphylactic Reaction
4 (.38%)
Anti-neutrophil Cytoplasmic Antibod...
4 (.38%)
Anxiety
4 (.38%)
Back Pain
4 (.38%)
Breast Cyst
4 (.38%)
Chills
4 (.38%)
Coordination Abnormal
4 (.38%)
Dental Caries
4 (.38%)
Dysmorphism
4 (.38%)
Glomerulonephritis
4 (.38%)
Haemorrhage
4 (.38%)
Hepatitis Cholestatic
4 (.38%)
International Normalised Ratio Incr...
4 (.38%)
Micturition Disorder
4 (.38%)
Musculoskeletal Chest Pain
4 (.38%)
Oropharyngeal Pain
4 (.38%)
Pharyngeal Disorder
4 (.38%)
Platelet Count Decreased
4 (.38%)
Post Procedural Haemorrhage
4 (.38%)
Product Container Seal Issue
4 (.38%)
Rhabdomyolysis
4 (.38%)
Stevens-johnson Syndrome
4 (.38%)
Tooth Disorder
4 (.38%)
Tremor
4 (.38%)
Activated Partial Thromboplastin Ti...
3 (.28%)
Acute Myeloid Leukaemia
3 (.28%)
Angioedema
3 (.28%)
Aplasia Cutis Congenita
3 (.28%)
Areflexia
3 (.28%)
Central Nervous System Lesion
3 (.28%)
Clinodactyly
3 (.28%)
Decreased Appetite
3 (.28%)
Developmental Delay
3 (.28%)

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

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

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

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

Hyperthyroidism
122
Basedows Disease
54
Thyroid Disorder
24
Product Used For Unknown Indication
14
Hypothyroidism
11
Goitre
7
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Drug Use For Unknown Indication
6
Toxic Nodular Goitre
4
Autoimmune Thyroiditis
3
Secondary Hyperthyroidism
1
Acute Myocardial Infarction
1
Drug Exposure During Pregnancy
1
Completed Suicide
1
Thyrotoxic Crisis
1
Thyroiditis
1
Psychomotor Hyperactivity
1
Thyroid Mass
1

Drug Labels

LabelLabelerEffective
TapazoleKing Pharmaceuticals, Inc.12-APR-12
TapazoleREMEDYREPACK INC. 18-FEB-13
TapazoleREMEDYREPACK INC. 13-MAR-13

Tapazole Case Reports

What Tapazole 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 Tapazole. 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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