DrugCite
Search

PERMAX

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Permax Adverse Events Reported to the FDA Over Time

How are Permax adverse event reports trending over time?

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

Most Common Permax Adverse Events Reported to the FDA

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

Mitral Valve Incompetence
66 (2.86%)
Aortic Valve Incompetence
60 (2.6%)
Cardiac Valve Disease
46 (1.99%)
Dyspnoea
42 (1.82%)
Tricuspid Valve Incompetence
42 (1.82%)
Oedema Peripheral
32 (1.39%)
Cardiac Failure
31 (1.34%)
Pleural Effusion
31 (1.34%)
Neuroleptic Malignant Syndrome
27 (1.17%)
Pathological Gambling
27 (1.17%)
Fall
26 (1.13%)
Show More Show More
Retroperitoneal Fibrosis
26 (1.13%)
Mitral Valve Disease
22 (.95%)
Weight Increased
22 (.95%)
Condition Aggravated
20 (.87%)
Depression
19 (.82%)
C-reactive Protein Increased
18 (.78%)
Hydronephrosis
18 (.78%)
Abnormal Behaviour
17 (.74%)
Delirium
17 (.74%)
Pulmonary Hypertension
17 (.74%)
Atrial Fibrillation
16 (.69%)
Akinesia
15 (.65%)
Back Pain
15 (.65%)
Cardiac Murmur
15 (.65%)
Cardiomegaly
15 (.65%)
Dyskinesia
15 (.65%)
Hallucination
14 (.61%)
Pneumonia
14 (.61%)
Suicide Attempt
14 (.61%)
Tremor
14 (.61%)
Balance Disorder
13 (.56%)
Pericardial Effusion
13 (.56%)
Red Blood Cell Sedimentation Rate I...
13 (.56%)
Psychomotor Hyperactivity
12 (.52%)
Aortic Valve Stenosis
11 (.48%)
Compulsive Shopping
11 (.48%)
Ejection Fraction Decreased
11 (.48%)
Hepatic Function Abnormal
11 (.48%)
Hypomania
11 (.48%)
Malaise
11 (.48%)
Muscle Rigidity
11 (.48%)
Pleural Fibrosis
11 (.48%)
Pneumonia Aspiration
11 (.48%)
Renal Failure
11 (.48%)
Somnolence
11 (.48%)
Blood Creatine Phosphokinase Increa...
10 (.43%)
Cardiac Failure Congestive
10 (.43%)
Drug Ineffective
10 (.43%)
Dyspnoea Exertional
10 (.43%)
Gait Disturbance
10 (.43%)
Hallucination, Visual
10 (.43%)
Pulmonary Oedema
10 (.43%)
Suicidal Ideation
10 (.43%)
Alanine Aminotransferase Increased
9 (.39%)
Anxiety
9 (.39%)
Aortic Valve Disease
9 (.39%)
Aortic Valve Sclerosis
9 (.39%)
Aspartate Aminotransferase Increase...
9 (.39%)
Blood Lactate Dehydrogenase Increas...
9 (.39%)
Chest Pain
9 (.39%)
Confusional State
9 (.39%)
Constipation
9 (.39%)
Depressed Level Of Consciousness
9 (.39%)
Depressed Mood
9 (.39%)
Drug Effect Decreased
9 (.39%)
Dysuria
9 (.39%)
Hypersexuality
9 (.39%)
Insomnia
9 (.39%)
Loss Of Consciousness
9 (.39%)
Musculoskeletal Pain
9 (.39%)
Pneumonitis
9 (.39%)
Ventricular Hypertrophy
9 (.39%)
Chromaturia
8 (.35%)
Corneal Reflex Decreased
8 (.35%)
Dystonia
8 (.35%)
Neck Pain
8 (.35%)
Psychotic Behaviour
8 (.35%)
Pulmonary Fibrosis
8 (.35%)
Pulmonary Valve Incompetence
8 (.35%)
Pyrexia
8 (.35%)
Aggression
7 (.3%)
Agitation
7 (.3%)
Amimia
7 (.3%)
Aortic Dilatation
7 (.3%)
Asthenia
7 (.3%)
Cardiac Disorder
7 (.3%)
Cough
7 (.3%)
Fatigue
7 (.3%)
Fibrosis
7 (.3%)
Influenza
7 (.3%)
Interstitial Lung Disease
7 (.3%)
Mitral Valve Prolapse
7 (.3%)
Muscle Spasms
7 (.3%)
Nausea
7 (.3%)
Oedema
7 (.3%)
Overdose
7 (.3%)
Tachycardia
7 (.3%)
Anaemia
6 (.26%)
Benign Prostatic Hyperplasia
6 (.26%)
Blood Pressure Decreased
6 (.26%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Parkinsons Disease
533
Restless Legs Syndrome
34
Parkinsonism
10
Muscle Twitching
7
Drug Use For Unknown Indication
5
Tourettes Disorder
2
Show More Show More
Condition Aggravated
2
Pituitary Tumour Benign
1
Rheumatic Fever
1
Nervous System Disorder
1
Cerebral Disorder
1
Dyskinesia
1
Tremor
1
Movement Disorder
1
Fibromyalgia
1
Cerebrovascular Disorder
1
Dystonia
1

Permax Case Reports

What Permax safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Permax. 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.

Comments

Share your experience with Permax.