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PALLADONE

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Palladone Adverse Events Reported to the FDA Over Time

How are Palladone adverse event reports trending over time?

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

Most Common Palladone Adverse Events Reported to the FDA

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

Completed Suicide
175 (2.24%)
Drug Toxicity
123 (1.57%)
Drug Ineffective
115 (1.47%)
Unresponsive To Stimuli
104 (1.33%)
Somnolence
103 (1.32%)
Medication Error
99 (1.27%)
Pain
95 (1.21%)
Nausea
90 (1.15%)
Respiratory Arrest
88 (1.12%)
Death
84 (1.07%)
Dyspnoea
84 (1.07%)
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Overdose
77 (.98%)
Confusional State
75 (.96%)
Hypotension
75 (.96%)
Delirium
74 (.95%)
Vomiting
74 (.95%)
Sedation
68 (.87%)
Drug Withdrawal Syndrome
65 (.83%)
Loss Of Consciousness
65 (.83%)
Coma
64 (.82%)
Cardiac Arrest
62 (.79%)
Hyperaesthesia
62 (.79%)
Respiratory Depression
62 (.79%)
Cardio-respiratory Arrest
61 (.78%)
Depressed Level Of Consciousness
59 (.75%)
Dehydration
50 (.64%)
Pruritus
48 (.61%)
Drug Interaction
47 (.6%)
Back Pain
45 (.58%)
Anxiety
44 (.56%)
Constipation
44 (.56%)
Fatigue
44 (.56%)
Incorrect Dose Administered
44 (.56%)
Oxygen Saturation Decreased
44 (.56%)
Pulmonary Oedema
44 (.56%)
Fall
43 (.55%)
Agitation
42 (.54%)
Lethargy
42 (.54%)
Condition Aggravated
41 (.52%)
Accidental Death
40 (.51%)
Hyperhidrosis
40 (.51%)
Tachycardia
39 (.5%)
Convulsion
38 (.49%)
Multiple Drug Overdose
38 (.49%)
Asthenia
37 (.47%)
Respiratory Distress
37 (.47%)
Abdominal Pain
35 (.45%)
Drug Effect Decreased
35 (.45%)
Disorientation
34 (.43%)
Inadequate Analgesia
33 (.42%)
Drug Abuser
32 (.41%)
Myoclonus
32 (.41%)
Pneumonia
32 (.41%)
Respiratory Rate Decreased
32 (.41%)
Accidental Overdose
31 (.4%)
Dizziness
31 (.4%)
Hallucination
31 (.4%)
Diarrhoea
30 (.38%)
Sepsis
30 (.38%)
Faecaloma
29 (.37%)
Intentional Drug Misuse
29 (.37%)
Pneumonia Aspiration
29 (.37%)
Restlessness
29 (.37%)
Disease Progression
28 (.36%)
Heart Rate Increased
28 (.36%)
Mental Status Changes
28 (.36%)
Renal Failure Acute
28 (.36%)
Respiratory Failure
28 (.36%)
Tremor
28 (.36%)
Apnoea
27 (.35%)
Headache
27 (.35%)
Pulmonary Congestion
27 (.35%)
Alcohol Poisoning
26 (.33%)
Infection
26 (.33%)
Chest Pain
25 (.32%)
Narcotic Intoxication
25 (.32%)
Arthralgia
24 (.31%)
Blood Pressure Decreased
24 (.31%)
Drug Abuse
24 (.31%)
Insomnia
24 (.31%)
Weight Decreased
24 (.31%)
Aggression
23 (.29%)
Bradycardia
23 (.29%)
Miosis
23 (.29%)
Product Quality Issue
23 (.29%)
Suicide Attempt
23 (.29%)
Malaise
22 (.28%)
Poisoning
22 (.28%)
Hypoxia
21 (.27%)
Post Procedural Complication
21 (.27%)
Pyrexia
21 (.27%)
Blood Pressure Increased
20 (.26%)
Feeling Abnormal
20 (.26%)
Rash
20 (.26%)
Renal Impairment
20 (.26%)
Depression
19 (.24%)
Hypertension
19 (.24%)
Pulmonary Embolism
19 (.24%)
Blood Creatinine Increased
18 (.23%)
Muscular Weakness
18 (.23%)
Pulse Absent
18 (.23%)

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

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

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

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

Pain
1190
Drug Use For Unknown Indication
473
Product Used For Unknown Indication
337
Back Pain
126
Cancer Pain
81
Pain Management
56
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Breakthrough Pain
54
Procedural Pain
41
Abdominal Pain
40
Analgesia
31
Bone Pain
31
Pain In Extremity
29
Chest Pain
27
Analgesic Therapy
25
Neuralgia
18
Arthralgia
16
Ill-defined Disorder
15
Rheumatoid Arthritis
14
Constipation
14
Fibromyalgia
13
Analgesic Effect
11
Drug Abuse
10
Migraine
10
Postoperative Analgesia
10
Anaesthesia
9
Nephrolithiasis
9
Drug Abuser
7
Diabetic Neuropathy
7
Headache
7
Sedation
6
Maternal Exposure During Pregnancy
6
Respiratory Distress
6
Abdominal Pain Upper
6
Malignant Melanoma
5
Tumour Pain
5
Suicide Attempt
5
Neck Pain
5
Post Procedural Pain
5
Drug Therapy
5
Anaesthesia Procedure
4
Peripheral Sensory Neuropathy
4
Spinal Fracture
4
Debridement
4
Phantom Pain
4
Nerve Compression
4
Surgery
4
Oesophagitis
4
Completed Suicide
4
Neuropathy Peripheral
4
Spondylolisthesis
3
Endoscopy
3

Palladone Case Reports

What Palladone 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 Palladone. 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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