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ZOLEDRONOC ACID

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Zoledronoc Acid Adverse Events Reported to the FDA Over Time

How are Zoledronoc Acid adverse event reports trending over time?

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

Most Common Zoledronoc Acid Adverse Events Reported to the FDA

What are the most common Zoledronoc Acid adverse events reported to the FDA?

Death
1734 (7.31%)
Fall
783 (3.3%)
Pain
449 (1.89%)
Malaise
443 (1.87%)
Arthralgia
397 (1.67%)
Pyrexia
378 (1.59%)
Pain In Extremity
294 (1.24%)
Bone Pain
271 (1.14%)
Back Pain
237 (1%)
Headache
230 (.97%)
Nausea
229 (.97%)
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Pneumonia
222 (.94%)
Asthenia
208 (.88%)
Myalgia
205 (.86%)
Influenza Like Illness
187 (.79%)
Chills
186 (.78%)
Hip Fracture
180 (.76%)
Gait Disturbance
178 (.75%)
Dizziness
176 (.74%)
Dyspnoea
176 (.74%)
Fatigue
175 (.74%)
Oedema Peripheral
167 (.7%)
Vomiting
162 (.68%)
Feeling Abnormal
151 (.64%)
Cerebrovascular Accident
145 (.61%)
Chest Pain
130 (.55%)
Diarrhoea
130 (.55%)
Spinal Fracture
130 (.55%)
Femur Fracture
118 (.5%)
Fracture
111 (.47%)
Wrist Fracture
111 (.47%)
Neoplasm Malignant
110 (.46%)
Rib Fracture
110 (.46%)
Drug Ineffective
108 (.46%)
Influenza
106 (.45%)
Upper Limb Fracture
99 (.42%)
Breast Cancer
98 (.41%)
Myocardial Infarction
97 (.41%)
Foot Fracture
93 (.39%)
Syncope
90 (.38%)
Joint Swelling
87 (.37%)
Hypertension
85 (.36%)
Inappropriate Schedule Of Drug Admi...
85 (.36%)
General Physical Health Deteriorati...
84 (.35%)
Musculoskeletal Pain
84 (.35%)
Pain In Jaw
82 (.35%)
Loss Of Consciousness
81 (.34%)
Erythema
80 (.34%)
Lung Neoplasm Malignant
79 (.33%)
Blood Pressure Increased
76 (.32%)
Hypokinesia
76 (.32%)
Insomnia
76 (.32%)
Urinary Tract Infection
76 (.32%)
Weight Decreased
75 (.32%)
Blood Creatinine Increased
74 (.31%)
Cough
74 (.31%)
Nasopharyngitis
73 (.31%)
Infection
72 (.3%)
Rash
72 (.3%)
C-reactive Protein Increased
69 (.29%)
Cardiac Failure
69 (.29%)
Decreased Appetite
69 (.29%)
Renal Failure
69 (.29%)
Bronchitis
68 (.29%)
Abasia
67 (.28%)
Cardiac Disorder
66 (.28%)
Lower Respiratory Tract Infection
66 (.28%)
Abdominal Pain
65 (.27%)
Chest Discomfort
64 (.27%)
Musculoskeletal Stiffness
64 (.27%)
Atrial Fibrillation
63 (.27%)
Pelvic Fracture
62 (.26%)
Tremor
62 (.26%)
Abdominal Pain Upper
61 (.26%)
Contusion
61 (.26%)
Swelling
61 (.26%)
Tooth Disorder
61 (.26%)
Bone Density Decreased
60 (.25%)
Dehydration
59 (.25%)
Renal Impairment
59 (.25%)
Muscle Spasms
57 (.24%)
Cystitis
56 (.24%)
Dementia
56 (.24%)
Creatinine Renal Clearance Decrease...
55 (.23%)
Neck Pain
55 (.23%)
Renal Failure Chronic
55 (.23%)
Glomerular Filtration Rate Decrease...
54 (.23%)
Haemoglobin Decreased
54 (.23%)
Palpitations
54 (.23%)
Sepsis
54 (.23%)
Arthritis
53 (.22%)
Osteomyelitis
53 (.22%)
Renal Disorder
53 (.22%)
Dysstasia
52 (.22%)
Inflammation
52 (.22%)
Toothache
52 (.22%)
Bone Disorder
50 (.21%)
Road Traffic Accident
50 (.21%)
Depression
49 (.21%)
Poor Venous Access
49 (.21%)
Anaemia
48 (.2%)

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

What are the most common Zoledronoc Acid adverse events reported to the FDA?

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

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

Osteoporosis
3793
Osteoporosis Postmenopausal
79
Metastases To Bone
42
Osteoporotic Fracture
34
Osteopenia
24
Bone Disorder
22
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Product Used For Unknown Indication
18
Osteitis Deformans
18
Breast Cancer
14
Multiple Myeloma
10
Traumatic Fracture
8
Spinal Fracture
8
Bone Sarcoma
5
Osteonecrosis
5
Prophylaxis
4
Hypercalcaemia Of Malignancy
4
Hypercalcaemia
3
Bone Loss
3
Fracture
3
Bone Pain
3
Breast Cancer Metastatic
3
Lower Limb Fracture
3
Hip Fracture
3
Arthritis
2
Renal Cancer
2
Prostate Cancer
2
Spinal Compression Fracture
2
Femoral Neck Fracture
2
Osteogenesis Imperfecta
2
Renal Cancer Metastatic
1
Fibrous Dysplasia Of Bone
1
Spinal Cord Compression
1
Senile Osteoporosis
1
Renal Cell Carcinoma
1
Metastases To Spine
1
Calcium Metabolism Disorder
1
Pelvic Fracture
1
Metastasis
1
Metastatic Renal Cell Carcinoma
1
Arthralgia
1
Bone Decalcification
1
Langerhans Cell Histiocytosis
1
Humerus Fracture
1
Spinal Osteoarthritis
1
Bone Density Abnormal
1
Femur Fracture
1
Prostate Cancer Metastatic
1
Osteoporosis Prophylaxis
1

Zoledronoc Acid Case Reports

What Zoledronoc Acid 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 Zoledronoc Acid. 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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