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XANAX XR

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Xanax Xr Adverse Events Reported to the FDA Over Time

How are Xanax Xr adverse event reports trending over time?

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

Most Common Xanax Xr Adverse Events Reported to the FDA

What are the most common Xanax Xr adverse events reported to the FDA?

Drug Ineffective
37 (4.08%)
Anxiety
34 (3.75%)
Malaise
28 (3.09%)
Panic Attack
23 (2.54%)
Depression
19 (2.09%)
Feeling Abnormal
18 (1.98%)
Insomnia
18 (1.98%)
Somnolence
18 (1.98%)
Fatigue
17 (1.87%)
Drug Intolerance
13 (1.43%)
Headache
13 (1.43%)
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Nausea
13 (1.43%)
Withdrawal Syndrome
13 (1.43%)
Drug Dependence
11 (1.21%)
Hypersensitivity
11 (1.21%)
Drug Effect Decreased
10 (1.1%)
Mental Disorder
10 (1.1%)
Drug Withdrawal Syndrome
9 (.99%)
Pain
9 (.99%)
Weight Decreased
9 (.99%)
Abdominal Discomfort
8 (.88%)
Diarrhoea
8 (.88%)
Dizziness
8 (.88%)
Hallucination
8 (.88%)
Sedation
8 (.88%)
Decreased Appetite
7 (.77%)
Hypertension
7 (.77%)
Stress
7 (.77%)
Suicidal Ideation
7 (.77%)
Abdominal Pain Upper
6 (.66%)
Activities Of Daily Living Impaired
6 (.66%)
Blood Cholesterol Increased
6 (.66%)
Suicide Attempt
6 (.66%)
Tremor
6 (.66%)
Arthralgia
5 (.55%)
Balance Disorder
5 (.55%)
Cold Sweat
5 (.55%)
Convulsion
5 (.55%)
Death
5 (.55%)
Disturbance In Attention
5 (.55%)
Drug Exposure During Pregnancy
5 (.55%)
Medication Residue
5 (.55%)
Nervousness
5 (.55%)
Panic Reaction
5 (.55%)
Premature Baby
5 (.55%)
Sensory Disturbance
5 (.55%)
Tachycardia
5 (.55%)
Amnesia
4 (.44%)
Back Pain
4 (.44%)
Chondrodystrophy
4 (.44%)
Coordination Abnormal
4 (.44%)
Dyskinesia
4 (.44%)
Dyspnoea
4 (.44%)
Gastric Disorder
4 (.44%)
Gastrooesophageal Reflux Disease
4 (.44%)
Hepatic Pain
4 (.44%)
Hyperhidrosis
4 (.44%)
Lower Limb Fracture
4 (.44%)
Narcolepsy
4 (.44%)
Pyrexia
4 (.44%)
Rash
4 (.44%)
Respiratory Rate Increased
4 (.44%)
Retching
4 (.44%)
Thyroid Disorder
4 (.44%)
Vision Blurred
4 (.44%)
Visual Impairment
4 (.44%)
Vomiting
4 (.44%)
Aggression
3 (.33%)
Anaphylactic Reaction
3 (.33%)
Anger
3 (.33%)
Confusional State
3 (.33%)
Discomfort
3 (.33%)
Disinhibition
3 (.33%)
Flatulence
3 (.33%)
Grand Mal Convulsion
3 (.33%)
Head Injury
3 (.33%)
Infection
3 (.33%)
Intentional Drug Misuse
3 (.33%)
Laceration
3 (.33%)
Mania
3 (.33%)
Oedema Peripheral
3 (.33%)
Pollakiuria
3 (.33%)
Speech Disorder
3 (.33%)
Abdominal Pain
2 (.22%)
Abnormal Clotting Factor
2 (.22%)
Abnormal Faeces
2 (.22%)
Agitation
2 (.22%)
Agoraphobia
2 (.22%)
Alcohol Abuse
2 (.22%)
Asthenia
2 (.22%)
Attention Deficit/hyperactivity Dis...
2 (.22%)
Bipolar Disorder
2 (.22%)
Blood Potassium Decreased
2 (.22%)
Blood Pressure Increased
2 (.22%)
Breast Cancer
2 (.22%)
Burning Sensation
2 (.22%)
Cardiac Arrest
2 (.22%)
Cardiac Disorder
2 (.22%)
Chest Crushing
2 (.22%)
Chest Discomfort
2 (.22%)
Chest Pain
2 (.22%)

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

What are the most common Xanax Xr adverse events reported to the FDA?

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

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

Anxiety
97
Panic Attack
28
Panic Disorder
24
Depression
12
Nervousness
6
Generalised Anxiety Disorder
6
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Agoraphobia
5
Nervous System Disorder
5
Product Used For Unknown Indication
4
Post-traumatic Stress Disorder
3
Drug Use For Unknown Indication
2
Bipolar Disorder
2
Stress
2
Major Depression
2
Anxiety Disorder
2
Sleep Disorder
2
Drug Exposure During Pregnancy
2
Social Phobia
1
Drug Dependence
1
Sleep Disorder Therapy
1
Irritable Bowel Syndrome
1
Relaxation Therapy
1
Blood Pressure Abnormal
1
Insomnia
1
Feeling Of Relaxation
1
Hypertension
1
Borderline Personality Disorder
1

Drug Labels

LabelLabelerEffective
Xanax XrPharmacia and Upjohn Company26-MAR-13

Xanax Xr Case Reports

What Xanax Xr 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 Xanax Xr. 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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