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Bondronat Adverse Events Reported to the FDA Over Time

How are Bondronat adverse event reports trending over time?

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

Most Common Bondronat Adverse Events Reported to the FDA

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

Osteonecrosis
166 (18.89%)
Metastases To Bone
22 (2.5%)
Osteomyelitis
22 (2.5%)
Bone Disorder
17 (1.93%)
Tooth Extraction
16 (1.82%)
Metastases To Liver
14 (1.59%)
Abdominal Pain Upper
11 (1.25%)
Impaired Healing
11 (1.25%)
Abscess
9 (1.02%)
Chest Pain
9 (1.02%)
Diarrhoea
9 (1.02%)
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Dyspnoea
9 (1.02%)
Pyrexia
9 (1.02%)
Death
8 (.91%)
General Physical Health Deteriorati...
8 (.91%)
Malignant Neoplasm Progression
8 (.91%)
Pain In Jaw
8 (.91%)
Infection
7 (.8%)
Jaw Disorder
7 (.8%)
Pain
7 (.8%)
Vomiting
7 (.8%)
Blood Pressure Decreased
6 (.68%)
Chills
6 (.68%)
Disease Progression
6 (.68%)
Heart Rate Increased
6 (.68%)
Liver Disorder
6 (.68%)
Polyneuropathy
6 (.68%)
Swelling
6 (.68%)
Tachypnoea
6 (.68%)
Anaemia
5 (.57%)
Bone Pain
5 (.57%)
Breast Cancer
5 (.57%)
Deep Vein Thrombosis
5 (.57%)
Erythema
5 (.57%)
Gastric Disorder
5 (.57%)
Hypocalcaemia
5 (.57%)
Myalgia
5 (.57%)
Nausea
5 (.57%)
Oral Disorder
5 (.57%)
Paraesthesia
5 (.57%)
Tooth Disorder
5 (.57%)
Toothache
5 (.57%)
Actinomycosis
4 (.46%)
Asthenia
4 (.46%)
Blood Creatinine Increased
4 (.46%)
Colon Cancer
4 (.46%)
Epistaxis
4 (.46%)
Extravasation
4 (.46%)
Fatigue
4 (.46%)
Headache
4 (.46%)
Hypercalcaemia
4 (.46%)
Incorrect Route Of Drug Administrat...
4 (.46%)
Iridocyclitis
4 (.46%)
Macular Oedema
4 (.46%)
Oral Surgery
4 (.46%)
Osteitis
4 (.46%)
Periodontitis
4 (.46%)
Primary Sequestrum
4 (.46%)
Pulmonary Embolism
4 (.46%)
Stomatitis
4 (.46%)
Tachycardia
4 (.46%)
Visual Impairment
4 (.46%)
Arrhythmia
3 (.34%)
Arthralgia
3 (.34%)
Bacterial Infection
3 (.34%)
Biopsy Site Unspecified Abnormal
3 (.34%)
Cough
3 (.34%)
Dizziness
3 (.34%)
Drug Interaction
3 (.34%)
Dysphagia
3 (.34%)
Eye Pain
3 (.34%)
Gastrointestinal Haemorrhage
3 (.34%)
Haemoglobin Decreased
3 (.34%)
Hypertension
3 (.34%)
Hypomagnesaemia
3 (.34%)
Inflammation
3 (.34%)
Jaw Operation
3 (.34%)
Lenticular Opacities
3 (.34%)
Loose Tooth
3 (.34%)
Metabolic Acidosis
3 (.34%)
Multi-organ Failure
3 (.34%)
Neoplasm Malignant
3 (.34%)
Oral Mucosa Erosion
3 (.34%)
Osteoarthritis
3 (.34%)
Osteotomy
3 (.34%)
Pneumonia
3 (.34%)
Renal Failure
3 (.34%)
Abdominal Discomfort
2 (.23%)
Abdominal Pain
2 (.23%)
Abdominal Symptom
2 (.23%)
Abscess Jaw
2 (.23%)
Angina Pectoris
2 (.23%)
Arthritis
2 (.23%)
Body Temperature Increased
2 (.23%)
Bone Lesion
2 (.23%)
Bone Operation
2 (.23%)
Cardiotoxicity
2 (.23%)
Chest Discomfort
2 (.23%)
Condition Aggravated
2 (.23%)
Dementia
2 (.23%)
Dental Operation
2 (.23%)

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

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

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

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

Drug Use For Unknown Indication
77
Metastases To Bone
49
Breast Cancer
26
Osteoporosis
25
Breast Cancer Metastatic
24
Prophylaxis
15
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Plasmacytoma
12
Multiple Myeloma
10
Hypercalcaemia
8
Product Used For Unknown Indication
5
Osteolysis
5
Lung Cancer Metastatic
3
Breast Cancer Female
3
Bone Pain
2
Osteoporosis Prophylaxis
2
Cancer Pain
2
Breast Neoplasm
2
Breast Cancer Stage Iv
2
Colon Cancer Metastatic
2
Metastasis
1
Paraproteinaemia
1
Bone Marrow Oedema
1
Prostate Cancer Metastatic
1
Sternal Fracture
1
Bone Neoplasm
1
Metastatic Pain
1
Hypercalcaemia Of Malignancy
1
Osteoporotic Fracture
1

Bondronat Case Reports

What Bondronat 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 Bondronat. 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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