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DUROTEP MT

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Durotep Mt Adverse Events Reported to the FDA Over Time

How are Durotep Mt adverse event reports trending over time?

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

Most Common Durotep Mt Adverse Events Reported to the FDA

What are the most common Durotep Mt adverse events reported to the FDA?

Wrong Technique In Drug Usage Proce...
446 (11.52%)
Drug Prescribing Error
289 (7.46%)
Somnolence
140 (3.61%)
Nausea
122 (3.15%)
Delirium
113 (2.92%)
Inappropriate Schedule Of Drug Admi...
74 (1.91%)
Constipation
73 (1.88%)
Altered State Of Consciousness
72 (1.86%)
Vomiting
64 (1.65%)
Pain
60 (1.55%)
Overdose
57 (1.47%)
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Pyrexia
55 (1.42%)
Depressed Level Of Consciousness
49 (1.27%)
Respiratory Depression
49 (1.27%)
Dizziness
47 (1.21%)
Death
42 (1.08%)
Pneumonia Aspiration
42 (1.08%)
Incorrect Dose Administered
38 (.98%)
Drug Administration Error
33 (.85%)
Product Quality Issue
31 (.8%)
Inadequate Analgesia
29 (.75%)
Malaise
29 (.75%)
Malignant Neoplasm Progression
29 (.75%)
Gastric Cancer
28 (.72%)
Oxygen Saturation Decreased
28 (.72%)
Lung Neoplasm Malignant
27 (.7%)
Restlessness
27 (.7%)
Drug Administered At Inappropriate ...
26 (.67%)
Dyspnoea
26 (.67%)
Insomnia
26 (.67%)
Respiratory Failure
26 (.67%)
Feeling Abnormal
25 (.65%)
Drug Ineffective
24 (.62%)
Myocardial Infarction
23 (.59%)
Treatment Noncompliance
22 (.57%)
Condition Aggravated
21 (.54%)
Decreased Appetite
20 (.52%)
Blood Pressure Decreased
19 (.49%)
Hallucination
19 (.49%)
Eating Disorder
18 (.46%)
Pancreatic Carcinoma
18 (.46%)
Disease Progression
17 (.44%)
Drug Effect Increased
17 (.44%)
Anaemia
16 (.41%)
Application Site Pruritus
16 (.41%)
Cough
16 (.41%)
Incorrect Drug Administration Durat...
16 (.41%)
Intentional Drug Misuse
16 (.41%)
Respiratory Arrest
16 (.41%)
Fall
15 (.39%)
Aspartate Aminotransferase Increase...
14 (.36%)
Gait Disturbance
14 (.36%)
Neoplasm Malignant
14 (.36%)
Pneumonia
14 (.36%)
Pruritus
14 (.36%)
Speech Disorder
14 (.36%)
Asthenia
13 (.34%)
Discomfort
13 (.34%)
Hepatic Failure
13 (.34%)
Off Label Use
13 (.34%)
Confusional State
12 (.31%)
Dementia
12 (.31%)
Dysphagia
12 (.31%)
Hospitalisation
12 (.31%)
Hypoventilation
12 (.31%)
Intervertebral Discitis
12 (.31%)
Mental Impairment
12 (.31%)
Narcotic Intoxication
12 (.31%)
Sleep Talking
12 (.31%)
Staphylococcal Sepsis
12 (.31%)
Allodynia
11 (.28%)
Aspiration
11 (.28%)
Breast Cancer
11 (.28%)
Irritability
11 (.28%)
Loss Of Consciousness
11 (.28%)
Sepsis
11 (.28%)
Anxiety
10 (.26%)
Application Site Bleeding
10 (.26%)
Cardio-respiratory Arrest
10 (.26%)
Hyperhidrosis
10 (.26%)
Myoclonus
10 (.26%)
Oesophageal Carcinoma
10 (.26%)
Rectal Cancer
10 (.26%)
Urinary Tract Infection
10 (.26%)
Uterine Cancer
10 (.26%)
Abnormal Behaviour
9 (.23%)
Application Site Erythema
9 (.23%)
Delusion
9 (.23%)
Depressive Symptom
9 (.23%)
Drug Effect Decreased
9 (.23%)
Drug Interaction
9 (.23%)
Renal Impairment
9 (.23%)
Withdrawal Syndrome
9 (.23%)
Blood Amylase Increased
8 (.21%)
Blood Glucose Increased
8 (.21%)
Blood Lactate Dehydrogenase Increas...
8 (.21%)
Cardiac Failure Acute
8 (.21%)
Cervix Carcinoma
8 (.21%)
Circulatory Collapse
8 (.21%)
Depression
8 (.21%)
Drug Dispensing Error
8 (.21%)

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

What are the most common Durotep Mt adverse events reported to the FDA?

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

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

Cancer Pain
428
Drug Use For Unknown Indication
187
Product Used For Unknown Indication
185
Pain
111
Ill-defined Disorder
90
Back Pain
18
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Arthralgia
12
Scleroderma
10
Analgesic Therapy
10
Pain Management
8
Osteoarthritis
8
Pain In Extremity
6
Spinal Column Stenosis
6
Rheumatoid Arthritis
6
Metastases To Bone
6
Perineal Pain
4
Hepatic Neoplasm Malignant
4
Spinal Compression Fracture
4
Malignant Ascites
4
Musculoskeletal Pain
3
Osteonecrosis
3
Large Intestine Carcinoma
3
Uterine Cancer
2
Gastric Cancer
2
Sleep Disorder
2
Abdominal Pain Lower
2
Small Cell Lung Cancer Stage Unspec...
2
Emphysema
2
Adenocarcinoma
2
Bone Sarcoma
2
Prostate Cancer
2
Central Pain Syndrome
2
Decubitus Ulcer
2
Lip And/or Oral Cavity Cancer
2
Scoliosis
2
Peripheral Vascular Disorder
1
Rectal Cancer
1
Lung Neoplasm Malignant
1
Multiple Myeloma
1
Pancreatic Carcinoma
1
Intervertebral Disc Protrusion
1
Cystitis Interstitial
1
Dyspnoea
1
Cervix Carcinoma
1
Diabetic Neuropathy
1
Metastatic Pain
1
Procedural Pain
1
Compression Fracture
1
Sciatica
1
Complex Regional Pain Syndrome
1
Bladder Cancer
1

Durotep Mt Case Reports

What Durotep Mt 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 Durotep Mt. 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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