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AVINZA

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Avinza Adverse Events Reported to the FDA Over Time

How are Avinza adverse event reports trending over time?

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

Most Common Avinza Adverse Events Reported to the FDA

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

Somnolence
930 (1.66%)
Overdose
883 (1.57%)
Vomiting
778 (1.38%)
Nausea
761 (1.35%)
Drug Ineffective
738 (1.31%)
Death
727 (1.29%)
Completed Suicide
674 (1.2%)
Confusional State
602 (1.07%)
Drug Toxicity
559 (1%)
Pain
551 (.98%)
Respiratory Arrest
546 (.97%)
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Cardiac Arrest
544 (.97%)
Cardio-respiratory Arrest
536 (.95%)
Constipation
525 (.93%)
Hypotension
518 (.92%)
Dyspnoea
476 (.85%)
Respiratory Depression
444 (.79%)
Drug Interaction
439 (.78%)
Loss Of Consciousness
416 (.74%)
Multiple Drug Overdose
416 (.74%)
Coma
411 (.73%)
Drug Abuse
383 (.68%)
Depressed Level Of Consciousness
363 (.65%)
Product Quality Issue
362 (.64%)
Drug Hypersensitivity
350 (.62%)
Lethargy
342 (.61%)
Agitation
335 (.6%)
Unresponsive To Stimuli
335 (.6%)
Sedation
334 (.59%)
Medication Error
329 (.59%)
Fall
314 (.56%)
Diarrhoea
305 (.54%)
Asthenia
303 (.54%)
Drug Withdrawal Syndrome
299 (.53%)
Dizziness
297 (.53%)
Delirium
295 (.53%)
Headache
289 (.51%)
Pyrexia
289 (.51%)
Hyperhidrosis
276 (.49%)
Mental Status Changes
259 (.46%)
Accidental Overdose
258 (.46%)
Hallucination
250 (.45%)
Abdominal Pain
246 (.44%)
Renal Failure Acute
244 (.43%)
Insomnia
239 (.43%)
Miosis
239 (.43%)
Pneumonia
238 (.42%)
Fatigue
237 (.42%)
Dehydration
234 (.42%)
Anxiety
227 (.4%)
Oxygen Saturation Decreased
227 (.4%)
Respiratory Failure
227 (.4%)
Pruritus
221 (.39%)
Condition Aggravated
215 (.38%)
Malaise
211 (.38%)
Back Pain
209 (.37%)
Tachycardia
208 (.37%)
Weight Decreased
196 (.35%)
Convulsion
194 (.35%)
Oedema Peripheral
193 (.34%)
Drug Abuser
189 (.34%)
Drug Effect Decreased
189 (.34%)
Renal Failure
187 (.33%)
Chest Pain
185 (.33%)
Disorientation
184 (.33%)
Intentional Drug Misuse
180 (.32%)
Pain In Extremity
174 (.31%)
Pulmonary Oedema
172 (.31%)
Tremor
171 (.3%)
Heart Rate Increased
165 (.29%)
Myoclonus
165 (.29%)
Substance Abuse
163 (.29%)
Drug Exposure During Pregnancy
160 (.28%)
Feeling Abnormal
159 (.28%)
Hypertension
158 (.28%)
Rhabdomyolysis
158 (.28%)
Drug Dependence
156 (.28%)
Decreased Appetite
154 (.27%)
Depression
151 (.27%)
Respiratory Rate Decreased
151 (.27%)
Hypoaesthesia
143 (.25%)
Pneumonia Aspiration
143 (.25%)
Withdrawal Syndrome
140 (.25%)
Abdominal Pain Upper
139 (.25%)
Aggression
139 (.25%)
Alanine Aminotransferase Increased
138 (.25%)
Aspartate Aminotransferase Increase...
138 (.25%)
Hypoxia
138 (.25%)
Drug Screen Positive
135 (.24%)
Hyperaesthesia
132 (.23%)
Restlessness
131 (.23%)
Urticaria
130 (.23%)
Poisoning
129 (.23%)
Urinary Retention
128 (.23%)
Anaemia
127 (.23%)
Bradycardia
127 (.23%)
Dysarthria
125 (.22%)
General Physical Health Deteriorati...
125 (.22%)
Rash
125 (.22%)
Apnoea
122 (.22%)
Incorrect Dose Administered
122 (.22%)

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

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

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

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

Pain
5416
Drug Use For Unknown Indication
2211
Product Used For Unknown Indication
1816
Back Pain
820
Cancer Pain
735
Analgesic Therapy
295
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Breakthrough Pain
253
Procedural Pain
238
Abdominal Pain
204
Pain Management
194
Postoperative Analgesia
159
Arthralgia
146
Analgesia
145
Pain In Extremity
126
Bone Pain
125
Analgesic Effect
124
Headache
104
Neuralgia
98
Drug Abuse
96
Spinal Anaesthesia
95
Ill-defined Disorder
91
Sedation
88
Chest Pain
82
Fibromyalgia
78
Anaesthesia
72
Abdominal Pain Upper
68
Rheumatoid Arthritis
59
Arthritis
57
Musculoskeletal Pain
51
Complex Regional Pain Syndrome
49
Neck Pain
48
Drug Abuser
46
Migraine
44
Post Procedural Pain
44
Epidural Anaesthesia
44
Osteoarthritis
42
Surgery
40
Prophylaxis
37
Premedication
34
Neuropathy Peripheral
33
Dyspnoea
32
Sciatica
31
Accidental Exposure
30
Back Disorder
29
Pain Prophylaxis
28
Intervertebral Disc Degeneration
27
General Anaesthesia
27
Drug Dependence
26
Myalgia
26
Suicide Attempt
26
Palliative Care
24

Drug Labels

LabelLabelerEffective
AvinzaSTAT RX USA LLC22-SEP-11
AvinzaLake Erie Medical DBA Quality Care Products LLC16-NOV-11
AvinzaKing Pharmaceuticals, Inc.16-JUL-12
AvinzaKing Pharmaceuticals, Inc.16-JUL-12
AvinzaBryant Ranch Prepack23-OCT-12
AvinzaBryant Ranch Prepack23-OCT-12
AvinzaBryant Ranch Prepack23-OCT-12

Avinza Case Reports

What Avinza 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 Avinza. 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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