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REQUIP XL

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Requip Xl Adverse Events Reported to the FDA Over Time

How are Requip Xl adverse event reports trending over time?

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

Most Common Requip Xl Adverse Events Reported to the FDA

What are the most common Requip Xl adverse events reported to the FDA?

Drug Ineffective
73 (4.04%)
Somnolence
64 (3.54%)
Insomnia
49 (2.71%)
Nausea
49 (2.71%)
Hallucination
35 (1.93%)
Tremor
35 (1.93%)
Dyskinesia
32 (1.77%)
Dizziness
31 (1.71%)
Fatigue
30 (1.66%)
Oedema Peripheral
29 (1.6%)
Medication Residue
26 (1.44%)
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Asthenia
24 (1.33%)
Malaise
21 (1.16%)
Obsessive-compulsive Disorder
21 (1.16%)
Ill-defined Disorder
20 (1.11%)
Restless Legs Syndrome
20 (1.11%)
Headache
19 (1.05%)
Withdrawal Syndrome
19 (1.05%)
Fall
18 (1%)
Muscle Spasms
18 (1%)
Pain
16 (.88%)
Feeling Abnormal
15 (.83%)
Product Quality Issue
15 (.83%)
Sleep Disorder
15 (.83%)
Drug Administration Error
14 (.77%)
Aggression
13 (.72%)
Balance Disorder
13 (.72%)
Dementia
13 (.72%)
Joint Swelling
13 (.72%)
Loss Of Consciousness
13 (.72%)
Overdose
13 (.72%)
Confusional State
12 (.66%)
Psychotic Disorder
12 (.66%)
Movement Disorder
11 (.61%)
Musculoskeletal Stiffness
11 (.61%)
Paranoia
11 (.61%)
Parkinsonism
11 (.61%)
Sudden Onset Of Sleep
11 (.61%)
Abasia
10 (.55%)
Drug Effect Decreased
10 (.55%)
Gait Disturbance
10 (.55%)
Immobile
10 (.55%)
Pain In Extremity
10 (.55%)
Palpitations
10 (.55%)
Anxiety
9 (.5%)
Drug Interaction
9 (.5%)
Hallucination, Visual
9 (.5%)
Hypersexuality
9 (.5%)
Libido Increased
9 (.5%)
Muscular Weakness
9 (.5%)
Orthostatic Hypotension
9 (.5%)
Restlessness
9 (.5%)
Vomiting
9 (.5%)
Abdominal Discomfort
8 (.44%)
Abnormal Behaviour
8 (.44%)
Blood Pressure Decreased
8 (.44%)
Depression
8 (.44%)
Hyperhidrosis
8 (.44%)
Personality Change
8 (.44%)
Arthralgia
7 (.39%)
Constipation
7 (.39%)
Dependence
7 (.39%)
Diarrhoea
7 (.39%)
Disturbance In Sexual Arousal
7 (.39%)
Dysgraphia
7 (.39%)
Dyspnoea
7 (.39%)
Hypoaesthesia
7 (.39%)
Middle Insomnia
7 (.39%)
Off Label Use
7 (.39%)
Adverse Drug Reaction
6 (.33%)
Death
6 (.33%)
Drug Effect Delayed
6 (.33%)
Gambling
6 (.33%)
Impulse-control Disorder
6 (.33%)
Mental Disorder
6 (.33%)
Mobility Decreased
6 (.33%)
Myocardial Infarction
6 (.33%)
Nervousness
6 (.33%)
On And Off Phenomenon
6 (.33%)
Panic Attack
6 (.33%)
Pneumonia
6 (.33%)
Suicidal Ideation
6 (.33%)
Swelling
6 (.33%)
Therapeutic Response Decreased
6 (.33%)
Therapeutic Response Unexpected
6 (.33%)
Transient Ischaemic Attack
6 (.33%)
Back Pain
5 (.28%)
Blood Pressure Increased
5 (.28%)
Compulsive Shopping
5 (.28%)
Erythema
5 (.28%)
Excessive Sexual Fantasies
5 (.28%)
Inappropriate Schedule Of Drug Admi...
5 (.28%)
Initial Insomnia
5 (.28%)
Intentional Overdose
5 (.28%)
Mania
5 (.28%)
Pathological Gambling
5 (.28%)
Weight Decreased
5 (.28%)
Abdominal Pain Upper
4 (.22%)
Agitation
4 (.22%)
Alopecia
4 (.22%)
Arthropathy
4 (.22%)

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

What are the most common Requip Xl adverse events reported to the FDA?

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

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

Parkinsons Disease
374
Restless Legs Syndrome
71
Drug Use For Unknown Indication
32
Product Used For Unknown Indication
17
Parkinsonism
2
Tremor
1
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Dementia
1
Prophylaxis
1
Musculoskeletal Disorder
1
Muscle Spasms
1

Drug Labels

LabelLabelerEffective
RequipxlPhysicians Total Care, Inc.27-DEC-11
RequipxlGlaxoSmithKline LLC18-DEC-12

Requip Xl Case Reports

What Requip Xl 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 Requip Xl. 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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