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OXINORM

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Oxinorm Adverse Events Reported to the FDA Over Time

How are Oxinorm adverse event reports trending over time?

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

Most Common Oxinorm Adverse Events Reported to the FDA

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

Pyrexia
7 (4.09%)
Disseminated Intravascular Coagulat...
6 (3.51%)
Pneumonia Aspiration
6 (3.51%)
Interstitial Lung Disease
5 (2.92%)
Platelet Count Decreased
5 (2.92%)
Somnolence
5 (2.92%)
Altered State Of Consciousness
4 (2.34%)
Constipation
4 (2.34%)
Gastritis
4 (2.34%)
Hypotension
4 (2.34%)
Neuropathy Peripheral
4 (2.34%)
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Palmar-plantar Erythrodysaesthesia ...
4 (2.34%)
Proctalgia
4 (2.34%)
Rash
4 (2.34%)
Rectal Perforation
4 (2.34%)
Sepsis
4 (2.34%)
Urticaria
4 (2.34%)
Dermatitis Acneiform
3 (1.75%)
Gamma-glutamyltransferase Increased
3 (1.75%)
Herpes Zoster
3 (1.75%)
Ileus
3 (1.75%)
Pain
3 (1.75%)
Pruritus
3 (1.75%)
Skin Fissures
3 (1.75%)
Thrombocytopenia
3 (1.75%)
Vomiting
3 (1.75%)
Wrong Technique In Drug Usage Proce...
3 (1.75%)
Anaemia
2 (1.17%)
C-reactive Protein Increased
2 (1.17%)
Depressed Level Of Consciousness
2 (1.17%)
Dizziness
2 (1.17%)
Dyschezia
2 (1.17%)
Dysphagia
2 (1.17%)
Dyspnoea
2 (1.17%)
Faecaloma
2 (1.17%)
Febrile Neutropenia
2 (1.17%)
Haemoglobin Decreased
2 (1.17%)
Hypercapnia
2 (1.17%)
Hyperphosphataemia
2 (1.17%)
Hypoaesthesia Oral
2 (1.17%)
Multi-organ Failure
2 (1.17%)
Multiple Myeloma
2 (1.17%)
Neoplasm Malignant
2 (1.17%)
Neoplasm Progression
2 (1.17%)
Nerve Injury
2 (1.17%)
Pleural Effusion
2 (1.17%)
Spinal Compression Fracture
2 (1.17%)
Urinary Retention
2 (1.17%)
White Blood Cell Count Increased
2 (1.17%)
Abdominal Distension
1 (.58%)
Blood Alkaline Phosphatase Increase...
1 (.58%)
Death
1 (.58%)
Delirium
1 (.58%)
Diarrhoea
1 (.58%)
Enterocolitis
1 (.58%)
Extradural Abscess
1 (.58%)
Hallucination
1 (.58%)
Headache
1 (.58%)
Hypertension
1 (.58%)
Mood Swings
1 (.58%)
Movement Disorder
1 (.58%)
Musculoskeletal Pain
1 (.58%)
Nausea
1 (.58%)
Neutropenia
1 (.58%)
Ovarian Cancer
1 (.58%)
Renal Failure Acute
1 (.58%)
Respiratory Depression
1 (.58%)
Tongue Paralysis
1 (.58%)

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

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

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

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

Cancer Pain
161
Pain
76
Metastatic Renal Cell Carcinoma
24
Product Used For Unknown Indication
16
Analgesic Therapy
12
Pain Management
11
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Renal Cell Carcinoma
11
Back Pain
8
Chest Pain
7
Multiple Myeloma
6
Metastases To Bone
5
Metastatic Pain
5
Abdominal Pain
4
Prophylaxis
4
Bone Pain
4
Hepatic Neoplasm Malignant
4
Ovarian Cancer Recurrent
4
Abdominal Pain Lower
3
Drug Use For Unknown Indication
3
Anxiety
3
Breast Cancer
3
Peripheral Sensory Neuropathy
3
Headache
2
Myalgia
2
Toothache
1
Ill-defined Disorder
1
Adenocarcinoma Pancreas
1

Oxinorm Case Reports

What Oxinorm 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 Oxinorm. 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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