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LEVODOPA

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Levodopa Adverse Events Reported to the FDA Over Time

How are Levodopa adverse event reports trending over time?

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

Most Common Levodopa Adverse Events Reported to the FDA

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

Dyskinesia
152 (2.38%)
Drug Ineffective
106 (1.66%)
Tremor
105 (1.65%)
Fall
89 (1.4%)
Condition Aggravated
85 (1.33%)
Gait Disturbance
78 (1.22%)
Hallucination
74 (1.16%)
Hallucination, Visual
67 (1.05%)
Dopamine Dysregulation Syndrome
65 (1.02%)
Hypersexuality
64 (1%)
Nausea
63 (.99%)
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Anxiety
62 (.97%)
Confusional State
60 (.94%)
Pathological Gambling
59 (.93%)
Drug Effect Decreased
57 (.89%)
On And Off Phenomenon
57 (.89%)
Agitation
55 (.86%)
Drug Interaction
55 (.86%)
Vomiting
53 (.83%)
Neuroleptic Malignant Syndrome
51 (.8%)
Muscle Rigidity
50 (.78%)
Somnolence
48 (.75%)
Delirium
47 (.74%)
Insomnia
44 (.69%)
Depression
42 (.66%)
Asthenia
40 (.63%)
Delusion
40 (.63%)
Fatigue
40 (.63%)
Aggression
39 (.61%)
Dizziness
39 (.61%)
Abnormal Behaviour
37 (.58%)
Weight Decreased
37 (.58%)
Dyspnoea
36 (.56%)
Muscle Spasms
36 (.56%)
Pneumonia
34 (.53%)
Dehydration
32 (.5%)
Dysphagia
32 (.5%)
Overdose
31 (.49%)
Psychotic Disorder
31 (.49%)
Hyperhidrosis
30 (.47%)
Drug Abuse
29 (.45%)
Pain
29 (.45%)
Movement Disorder
28 (.44%)
Orthostatic Hypotension
28 (.44%)
Constipation
27 (.42%)
Loss Of Consciousness
27 (.42%)
Hypotension
26 (.41%)
Rhabdomyolysis
26 (.41%)
Bradykinesia
25 (.39%)
Dystonia
25 (.39%)
Musculoskeletal Stiffness
25 (.39%)
Renal Failure Acute
24 (.38%)
Impulse-control Disorder
23 (.36%)
Jealous Delusion
23 (.36%)
Oedema Peripheral
23 (.36%)
Pneumonia Aspiration
23 (.36%)
Balance Disorder
22 (.34%)
General Physical Health Deteriorati...
22 (.34%)
Obsessive-compulsive Disorder
22 (.34%)
Compulsive Shopping
21 (.33%)
Diarrhoea
21 (.33%)
Aphasia
20 (.31%)
Feeling Abnormal
20 (.31%)
Pain In Extremity
20 (.31%)
Pyrexia
20 (.31%)
Abasia
19 (.3%)
Aspartate Aminotransferase Increase...
19 (.3%)
Blood Creatine Phosphokinase Increa...
19 (.3%)
Disorientation
19 (.3%)
Hypomania
19 (.3%)
Irritability
19 (.3%)
Motor Dysfunction
19 (.3%)
Persecutory Delusion
19 (.3%)
Cerebral Atrophy
18 (.28%)
Dysarthria
18 (.28%)
Paranoia
18 (.28%)
Sudden Onset Of Sleep
18 (.28%)
Completed Suicide
17 (.27%)
Dysphonia
17 (.27%)
Road Traffic Accident
17 (.27%)
Syncope
17 (.27%)
Hypertension
16 (.25%)
Stereotypy
16 (.25%)
Akinesia
15 (.24%)
Alanine Aminotransferase Increased
15 (.24%)
Headache
15 (.24%)
Parkinsonism
15 (.24%)
Product Substitution Issue
15 (.24%)
Cerebrovascular Accident
14 (.22%)
Chest Pain
14 (.22%)
Convulsion
14 (.22%)
Drug Withdrawal Syndrome
14 (.22%)
Erythema
14 (.22%)
Hypoaesthesia
14 (.22%)
Ileus
14 (.22%)
Malaise
14 (.22%)
Marital Problem
14 (.22%)
Paralysis
14 (.22%)
Posture Abnormal
14 (.22%)
Activities Of Daily Living Impaired
13 (.2%)
Coronary Artery Dissection
13 (.2%)

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

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

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

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

Parkinsons Disease
1752
Parkinsonism
103
Restless Legs Syndrome
78
Product Used For Unknown Indication
75
Drug Use For Unknown Indication
68
Tremor
31
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Ill-defined Disorder
16
Dystonia
15
On And Off Phenomenon
11
Multiple System Atrophy
11
Muscle Spasms
6
Parkinsonian Gait
5
Brain Neoplasm
5
Drug Level
4
Nervous System Disorder
4
Psychotic Disorder
4
Gait Disturbance
4
Pain
3
Epilepsy
3
Extrapyramidal Disorder
3
Spinocerebellar Ataxia
3
Pain In Extremity
3
Cerebrovascular Accident
2
Dementia
2
Postpartum Hypopituitarism
2
Dementia Alzheimers Type
2
Essential Tremor
2
Periodic Limb Movement Disorder
1
Heart Valve Replacement
1
Accidental Exposure
1
Neurodegenerative Disorder
1
Blood Sodium
1
Burning Sensation
1
Stent Placement
1
Diagnostic Procedure
1
Paraesthesia
1
Dyskinesia
1
Arthritis
1
Musculoskeletal Stiffness
1
Prophylaxis
1
Vascular Parkinsonism
1
Suicide Attempt
1
Intentional Drug Misuse
1
Off Label Use
1
Peripheral Coldness
1
Dementia With Lewy Bodies
1
Back Pain
1
Inflammation
1
Completed Suicide
1

Drug Labels

LabelLabelerEffective
Carbidopa And LevodopaMylan Pharmaceuticals Inc.27-AUG-08
Sinemet CrBristol-Myers Squibb Pharma Company01-JAN-09
SinemetBristol-Myers Squibb Pharma Company04-FEB-09
Carbidopa And LevodopaSun Pharmaceutical Industries Limited01-AUG-09
Carbidopa And Levodopa Apotex Corp.09-SEP-09
Carbidopa And LevodopaMylan Pharmaceuticals Inc.30-SEP-09
Carbidopa And LevodopaSUN PHARMACEUTICAL INDUSTRIES LIMITED05-DEC-09
Carbidopa And LevodopaMcKesson Packaging Services Business Unit of McKesson Corporation21-DEC-09
Carbidopa And LevodopaActavis Elizabeth LLC19-JAN-10
Carbidopa And LevodopaSun Pharmaceutical Industries Limited15-MAY-10
Carbidopa And Levodopa Unit Dose Services15-MAY-10
Carbidopa And LevodopaPhysicians Total Care, Inc.08-JUN-10
SinemetMerck Sharp & Dohme Corp.01-FEB-11
SinemetcrMerck Sharp & Dohme Corp.01-FEB-11
Carbidopa And LevodopaMajor Pharmaceuticals07-MAR-11
Carbidopa And LevodopaAmerican Health Packaging28-MAR-11
Carbidopa And Levodopa Preferred Pharmaceuticals, Inc31-MAR-11
StalevoNovartis Pharmaceuticals Corporation06-APR-11
Carbidopa And LevodopaAmerican Health Packaging12-APR-11
Carbidopa And LevodopaCardinal Health27-APR-11
Carbidopa And LevodopaCardinal Health17-JUN-11
Carbidopa And LevodopaCardinal Health10-NOV-11
Carbidopa And LevodopaMylan Institutional Inc.09-DEC-11
Carbidopa And LevodopaGlobal Pharmaceuticals, Division of Impax Laboratories Inc.19-JAN-12
Carbidopa And LevodopaMylan Insitutional Inc.20-JAN-12
Carbidopa And LevodopaPhysicians Total Care, Inc.02-FEB-12
Carbidopa And LevodopaCardinal Health03-APR-12
Carbidopa And LevodopaCardinal Health10-MAY-12
Carbidopa And LevodopaMcKesson Contract Packaging10-MAY-12
Carbidopa And LevodopaMcKesson Contract Packaging10-MAY-12
Carbidopa And LevodopaGoldline Laboratories, Inc.10-MAY-12
Carbidopa And LevodopaNCS HealthCare of KY, Inc dba Vangard Labs14-MAY-12
Carbidopa, Levodopa And EntacaponeSun Pharma Global FZE22-MAY-12
Carbidopa, Levodopa And EntacaponeWockhardt Limited28-MAY-12
Carbidopa, Levodopa And EntacaponeWockhardt USA LLC.28-MAY-12
Carbidopa And LevodopaMylan Pharmaceuticals Inc.22-JUN-12
Carbidopa And LevodopaAphena Pharma Solutions - Tennessee, Inc.17-JUL-12
Carbidopa And LevodopaMajor Pharmaceuticals19-JUL-12
Carbidopa And LevodopaCardinal Health07-AUG-12
Carbidopa And LevodopaGoldline Laboratories, Inc.08-AUG-12
Carbidopa And LevodopaTeva Pharmaceuticals USA Inc13-AUG-12
Carbidopa And LevodopaBryant Ranch Prepack12-OCT-12
Carbidopa, Levodopa And EntacaponeSun Pharma Global FZE07-DEC-12
ParcopaJazz Pharmaceuticals, Inc.28-JAN-13
Carbidopa And LevodopaNCS HealthCare of KY, Inc dba Vangard Labs19-FEB-13
Carbidopa And LevodopaREMEDYREPACK INC. 22-FEB-13
Carbidopa And LevodopaREMEDYREPACK INC. 27-FEB-13
Carbidopa And LevodopaCardinal Health05-MAR-13
Carbidopa And LevodopaCardinal Health13-MAR-13
Carbidopa And LevodopaREMEDYREPACK INC. 15-MAR-13
Carbidopa And LevodopaREMEDYREPACK INC. 25-MAR-13
Carbidopa And LevodopaREMEDYREPACK INC. 25-MAR-13
Carbidopa And LevodopaREMEDYREPACK INC. 28-MAR-13
Carbidopa And LevodopaApotex Corp.08-APR-13
Carbidopa And LevodopaCardinal Health18-APR-13
Carbidopa And LevodopaPreferred Pharmaceuticals, Inc.23-APR-13
Carbidopa And LevodopaPreferred Pharmaceuticals, Inc23-APR-13

Levodopa Case Reports

What Levodopa 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 Levodopa. 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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