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PERPHENAZINE

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Perphenazine Adverse Events Reported to the FDA Over Time

How are Perphenazine adverse event reports trending over time?

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

Most Common Perphenazine Adverse Events Reported to the FDA

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

Completed Suicide
41 (3.63%)
Ileus Paralytic
18 (1.59%)
Drug Interaction
17 (1.5%)
Depression
16 (1.42%)
Mental Status Changes
16 (1.42%)
Asthenia
13 (1.15%)
Fatigue
13 (1.15%)
Hypotension
12 (1.06%)
Drug Ineffective
11 (.97%)
Dystonia
11 (.97%)
Agitation
10 (.88%)
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Cardiac Arrest
10 (.88%)
Death
10 (.88%)
Drug Toxicity
10 (.88%)
Anxiety
9 (.8%)
Dysarthria
9 (.8%)
Dysphagia
9 (.8%)
Feeling Abnormal
9 (.8%)
Insomnia
9 (.8%)
Neuroleptic Malignant Syndrome
9 (.8%)
Pyrexia
9 (.8%)
Renal Failure Acute
9 (.8%)
Vomiting
9 (.8%)
Confusional State
8 (.71%)
Delirium
8 (.71%)
Fall
8 (.71%)
Nausea
8 (.71%)
Pain
8 (.71%)
Tremor
8 (.71%)
Urinary Retention
8 (.71%)
Urinary Tract Infection
8 (.71%)
Disorientation
7 (.62%)
Extrapyramidal Disorder
7 (.62%)
Hallucination, Visual
7 (.62%)
Injury
7 (.62%)
Intentional Overdose
7 (.62%)
Multiple Drug Overdose
7 (.62%)
Muscle Rigidity
7 (.62%)
Respiratory Failure
7 (.62%)
Decreased Appetite
6 (.53%)
Diarrhoea
6 (.53%)
Dizziness
6 (.53%)
Dyskinesia
6 (.53%)
Facial Paresis
6 (.53%)
Loss Of Consciousness
6 (.53%)
Overdose
6 (.53%)
Parkinsonism
6 (.53%)
Psychotic Disorder
6 (.53%)
Pyuria
6 (.53%)
Respiratory Distress
6 (.53%)
Somnolence
6 (.53%)
Suicide Attempt
6 (.53%)
Tardive Dyskinesia
6 (.53%)
Urinary Incontinence
6 (.53%)
Appendicitis Perforated
5 (.44%)
Cardio-respiratory Arrest
5 (.44%)
Leukocytosis
5 (.44%)
Metabolic Acidosis
5 (.44%)
Multiple Drug Overdose Intentional
5 (.44%)
Pneumonia
5 (.44%)
Pneumonia Aspiration
5 (.44%)
Pulmonary Embolism
5 (.44%)
Serotonin Syndrome
5 (.44%)
Speech Disorder
5 (.44%)
Weight Decreased
5 (.44%)
Weight Increased
5 (.44%)
Anger
4 (.35%)
Arthralgia
4 (.35%)
Blood Creatine Phosphokinase Increa...
4 (.35%)
Cardiolipin Antibody Positive
4 (.35%)
Cerebral Atrophy
4 (.35%)
Cognitive Disorder
4 (.35%)
Drug Hypersensitivity
4 (.35%)
Dry Mouth
4 (.35%)
Hallucination
4 (.35%)
Hallucination, Auditory
4 (.35%)
Hyperhidrosis
4 (.35%)
Hypokalaemia
4 (.35%)
Intentional Self-injury
4 (.35%)
Intestinal Perforation
4 (.35%)
Irritability
4 (.35%)
Restlessness
4 (.35%)
Road Traffic Accident
4 (.35%)
Sedation
4 (.35%)
Suicidal Ideation
4 (.35%)
Treatment Noncompliance
4 (.35%)
Abdominal Distension
3 (.27%)
Abdominal Pain
3 (.27%)
Abnormal Behaviour
3 (.27%)
Acute Respiratory Distress Syndrome
3 (.27%)
Akathisia
3 (.27%)
Amnesia
3 (.27%)
Anorexia
3 (.27%)
Antiphospholipid Antibodies Positiv...
3 (.27%)
Antipsychotic Drug Level Below Ther...
3 (.27%)
Atelectasis
3 (.27%)
Blood Pressure Increased
3 (.27%)
Burnout Syndrome
3 (.27%)
Catatonia
3 (.27%)
Condition Aggravated
3 (.27%)
Constipation
3 (.27%)

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

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

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

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

Depression
38
Drug Use For Unknown Indication
35
Schizophrenia
33
Product Used For Unknown Indication
31
Psychotic Disorder
18
Anxiety
12
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Bipolar Disorder
10
Mental Disorder
9
Schizoaffective Disorder
7
Dementia
7
Insomnia
7
Nausea
6
Schizophrenia, Paranoid Type
6
Bipolar I Disorder
6
Agitation
6
Mood Altered
5
Stress
5
Prophylaxis
4
Suicide Attempt
4
Affective Disorder
3
Paranoia
3
Major Depression
3
Ill-defined Disorder
2
Panic Attack
2
Drug Exposure During Pregnancy
2
Vomiting
2
Delusion
2
Hallucination
2
Schizophrenia, Residual Type
2
Foetal Exposure During Pregnancy
1
Nervous System Disorder
1
Sleep Disorder
1
Pain
1
Personality Disorder
1
Confusional State
1
Postpartum Depression
1
Abdominal Discomfort
1
Extrapyramidal Disorder
1
Adjustment Disorder
1
Emotional Disorder
1
Senile Psychosis
1
Dementia Alzheimers Type
1
Diverticulitis
1
Fibromyalgia
1
Hypomania
1
Delusional Disorder, Persecutory Ty...
1
Thinking Abnormal
1

Drug Labels

LabelLabelerEffective
PerphenazineContract Pharmacy Services-PA07-APR-10
PerphenazineState of Florida DOH Central Pharmacy31-MAY-10
PerphenazineState of Florida DOH Central Pharmacy18-AUG-10
Perphenazine And Amitriptyline HydrochlorideMylan Pharmaceuticals Inc.15-SEP-10
PerphenazineQualitest Pharmaceuticals16-DEC-10
PerphenazineRebel Distributors Corp28-DEC-10
PerphenazineNCS HealthCare of KY, Inc dba Vangard Labs22-MAR-11
PerphenazineREMEDYREPACK INC. 19-OCT-11
PerphenazineSandoz Inc21-OCT-11
Perphenazine And Amitriptyline HydrochlorideREMEDYREPACK INC. 07-DEC-11
PerphenazineH.J. Harkins Company, Inc.20-DEC-11
PerphenazineCardinal Health27-APR-12
PerphenazineAmerican Health Packaging16-MAY-12
PerphenazineQualitest Pharmaceuticals30-AUG-12
PerphenazineREMEDYREPACK INC. 26-SEP-12
PerphenazineREMEDYREPACK INC. 19-MAR-13
PerphenazineREMEDYREPACK INC. 20-MAR-13
PerphenazineREMEDYREPACK INC. 26-MAR-13

Perphenazine Case Reports

What Perphenazine 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 Perphenazine. 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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