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ZYPREXA ZYDIS

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Zyprexa Zydis Adverse Events Reported to the FDA Over Time

How are Zyprexa Zydis adverse event reports trending over time?

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

Most Common Zyprexa Zydis Adverse Events Reported to the FDA

What are the most common Zyprexa Zydis adverse events reported to the FDA?

Weight Increased
139 (5.07%)
Overdose
103 (3.75%)
Diabetes Mellitus
98 (3.57%)
Hyperglycaemia
47 (1.71%)
Hospitalisation
46 (1.68%)
Blood Cholesterol Increased
44 (1.6%)
Off Label Use
44 (1.6%)
Type 2 Diabetes Mellitus
44 (1.6%)
Hypertension
42 (1.53%)
Blood Triglycerides Increased
34 (1.24%)
Death
34 (1.24%)
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Drug Ineffective
28 (1.02%)
Aspartate Aminotransferase Increase...
23 (.84%)
Myocardial Infarction
22 (.8%)
Neuroleptic Malignant Syndrome
22 (.8%)
Renal Failure
22 (.8%)
Alanine Aminotransferase Increased
21 (.77%)
Convulsion
21 (.77%)
Dyslipidaemia
21 (.77%)
Dyspnoea
21 (.77%)
Cerebrovascular Accident
19 (.69%)
Aggression
18 (.66%)
Blood Glucose Increased
18 (.66%)
Hepatic Steatosis
18 (.66%)
Psychotic Disorder
18 (.66%)
White Blood Cell Count Increased
17 (.62%)
Blood Pressure Increased
15 (.55%)
Oedema Peripheral
14 (.51%)
Fall
13 (.47%)
Hyperhidrosis
13 (.47%)
Somnolence
13 (.47%)
Tremor
13 (.47%)
Hyperlipidaemia
12 (.44%)
Loss Of Consciousness
12 (.44%)
Abnormal Behaviour
11 (.4%)
Cardiac Murmur
11 (.4%)
Dizziness
11 (.4%)
Drug Exposure During Pregnancy
11 (.4%)
Haematochezia
11 (.4%)
Intentional Drug Misuse
11 (.4%)
Pneumonia
11 (.4%)
Blindness
10 (.36%)
Cataract
10 (.36%)
Chest Pain
10 (.36%)
Coronary Artery Disease
10 (.36%)
Depression
10 (.36%)
Dysphagia
10 (.36%)
Hypercholesterolaemia
10 (.36%)
Skin Discolouration
10 (.36%)
Agitation
9 (.33%)
Cardiac Disorder
9 (.33%)
Coma
9 (.33%)
Confusional State
9 (.33%)
Dehydration
9 (.33%)
Feeling Abnormal
9 (.33%)
Headache
9 (.33%)
Platelet Count Decreased
9 (.33%)
Vomiting
9 (.33%)
Anaemia
8 (.29%)
Blood Creatine Phosphokinase Increa...
8 (.29%)
Fatigue
8 (.29%)
Gastrointestinal Haemorrhage
8 (.29%)
Haematuria
8 (.29%)
Hallucination
8 (.29%)
Hepatic Enzyme Increased
8 (.29%)
Hypoaesthesia
8 (.29%)
Increased Appetite
8 (.29%)
Insomnia
8 (.29%)
Neuropathy Peripheral
8 (.29%)
Palpitations
8 (.29%)
Pulmonary Embolism
8 (.29%)
Syncope
8 (.29%)
Asthenia
7 (.26%)
Caesarean Section
7 (.26%)
Constipation
7 (.26%)
Dermatitis Allergic
7 (.26%)
Extrapyramidal Disorder
7 (.26%)
Eye Operation
7 (.26%)
Haemoglobin Decreased
7 (.26%)
Hypersomnia
7 (.26%)
Hypoglycaemia
7 (.26%)
Hypotension
7 (.26%)
Lymphocyte Count Increased
7 (.26%)
Mental Disorder
7 (.26%)
Obesity
7 (.26%)
Pancreatitis
7 (.26%)
Respiratory Failure
7 (.26%)
Sedation
7 (.26%)
Urinary Tract Infection
7 (.26%)
Blood Alkaline Phosphatase Increase...
6 (.22%)
Cellulitis
6 (.22%)
Condition Aggravated
6 (.22%)
Drug Dose Omission
6 (.22%)
Gait Disturbance
6 (.22%)
Haematemesis
6 (.22%)
Hypersensitivity
6 (.22%)
Hypothyroidism
6 (.22%)
Nausea
6 (.22%)
Paranoia
6 (.22%)
Pneumonia Aspiration
6 (.22%)
Polydipsia
6 (.22%)

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

What are the most common Zyprexa Zydis adverse events reported to the FDA?

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

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

Schizophrenia
90
Bipolar Disorder
57
Schizoaffective Disorder
38
Schizophrenia, Paranoid Type
27
Psychotic Disorder
22
Depression
14
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Agitation
12
Bipolar I Disorder
10
Major Depression
9
Anxiety
8
Dementia
6
Agitated Depression
4
Mood Swings
3
Aggression
3
Hallucination
3
Bipolar Ii Disorder
3
Insomnia
3
Vascular Dementia
2
Paranoia
2
Delirium
2
Somatic Delusion
2
Post-traumatic Stress Disorder
2
Amnesia
2
Hallucination, Auditory
2
Delusion
2
Delusional Disorder, Unspecified Ty...
1
Panic Attack
1
Anorexia And Bulimia Syndrome
1
Feeling Of Relaxation
1
Obsessive-compulsive Disorder
1
Schizoaffective Disorder Bipolar Ty...
1
Thinking Abnormal
1
Stress
1
Anxiety Disorder
1
Abnormal Behaviour
1
Anorexia Nervosa
1
Schizoid Personality Disorder
1
Schizophrenia, Residual Type
1
Weight Control
1
Catatonia
1
Affective Disorder
1
Wernickes Encephalopathy
1
Acute Psychosis
1
Borderline Personality Disorder
1
Autism
1
Mood Altered
1

Drug Labels

LabelLabelerEffective
ZyprexaPhysicians Total Care, Inc.30-NOV-09
ZyprexaSTAT RX USA LLC21-JUL-10
ZyprexaRebel Distributors Corp01-DEC-10
Zyprexa PD-Rx Pharmaceuticals, Inc.21-JUN-11
ZyprexaDispensing Solutions, Inc.04-OCT-11
Zyprexa H.J. Harkins Company, Inc.25-OCT-11
Zyprexa Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC30-MAR-12
ZyprexazydisCardinal Health08-MAY-12
ZyprexaCardinal Health08-MAY-12
Zyprexa Bryant Ranch Prepack23-OCT-12
Zyprexa Eli Lilly and Company 17-DEC-12
Zyprexa Intramuscular Eli Lilly and Company 17-DEC-12
Zyprexa Zydis Eli Lilly and Company 17-DEC-12
Zyprexa REMEDYREPACK INC. 10-APR-13
Zyprexa REMEDYREPACK INC. 10-APR-13

Zyprexa Zydis Case Reports

What Zyprexa Zydis 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 Zyprexa Zydis. 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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