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CARBIDOPA AND LEVODOPA

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Carbidopa And Levodopa Adverse Events Reported to the FDA Over Time

How are Carbidopa And Levodopa adverse event reports trending over time?

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

Most Common Carbidopa And Levodopa Adverse Events Reported to the FDA

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

Dyskinesia
102 (2.38%)
Drug Ineffective
87 (2.03%)
Tremor
73 (1.7%)
Fall
59 (1.38%)
Gait Disturbance
55 (1.28%)
Hallucination
54 (1.26%)
Nausea
54 (1.26%)
Confusional State
49 (1.14%)
Drug Effect Decreased
48 (1.12%)
Condition Aggravated
46 (1.07%)
Agitation
42 (.98%)
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Hallucination, Visual
42 (.98%)
Anxiety
39 (.91%)
On And Off Phenomenon
39 (.91%)
Vomiting
38 (.89%)
Hypersexuality
37 (.86%)
Delirium
36 (.84%)
Asthenia
33 (.77%)
Muscle Rigidity
33 (.77%)
Drug Interaction
32 (.75%)
Insomnia
32 (.75%)
Neuroleptic Malignant Syndrome
32 (.75%)
Dizziness
31 (.72%)
Pathological Gambling
31 (.72%)
Somnolence
31 (.72%)
Pneumonia
30 (.7%)
Muscle Spasms
28 (.65%)
Dopamine Dysregulation Syndrome
27 (.63%)
Fatigue
27 (.63%)
Weight Decreased
27 (.63%)
Loss Of Consciousness
26 (.61%)
Aggression
25 (.58%)
Delusion
24 (.56%)
Dysphagia
24 (.56%)
Dyspnoea
24 (.56%)
Movement Disorder
24 (.56%)
Dehydration
23 (.54%)
Bradykinesia
22 (.51%)
Hyperhidrosis
22 (.51%)
Musculoskeletal Stiffness
22 (.51%)
Pneumonia Aspiration
22 (.51%)
Constipation
21 (.49%)
Depression
20 (.47%)
Pain
20 (.47%)
Overdose
19 (.44%)
Hypotension
18 (.42%)
Oedema Peripheral
18 (.42%)
Rhabdomyolysis
18 (.42%)
Balance Disorder
17 (.4%)
Orthostatic Hypotension
17 (.4%)
Abnormal Behaviour
16 (.37%)
Disorientation
16 (.37%)
Dysarthria
16 (.37%)
Dystonia
16 (.37%)
Psychotic Disorder
16 (.37%)
Abasia
15 (.35%)
Blood Creatine Phosphokinase Increa...
15 (.35%)
Feeling Abnormal
15 (.35%)
Renal Failure Acute
15 (.35%)
Road Traffic Accident
15 (.35%)
Sudden Onset Of Sleep
15 (.35%)
Aphasia
14 (.33%)
Drug Abuse
14 (.33%)
Dysphonia
14 (.33%)
Pain In Extremity
14 (.33%)
Product Substitution Issue
14 (.33%)
Aspartate Aminotransferase Increase...
13 (.3%)
Coronary Artery Dissection
13 (.3%)
Erythema
13 (.3%)
General Physical Health Deteriorati...
13 (.3%)
Ileus Paralytic
13 (.3%)
Persecutory Delusion
13 (.3%)
Pyrexia
13 (.3%)
Abdominal Pain
12 (.28%)
Alanine Aminotransferase Increased
12 (.28%)
Completed Suicide
12 (.28%)
Diarrhoea
12 (.28%)
Impulse-control Disorder
12 (.28%)
Obsessive-compulsive Disorder
12 (.28%)
Rash
12 (.28%)
Syncope
12 (.28%)
Abdominal Discomfort
11 (.26%)
Decreased Appetite
11 (.26%)
Headache
11 (.26%)
Ileus
11 (.26%)
Incorrect Dose Administered
11 (.26%)
Irritability
11 (.26%)
Jealous Delusion
11 (.26%)
Malaise
11 (.26%)
Motor Dysfunction
11 (.26%)
Muscular Weakness
11 (.26%)
Parkinsonism
11 (.26%)
Adverse Event
10 (.23%)
Blood Urea Increased
10 (.23%)
Cerebral Atrophy
10 (.23%)
Contusion
10 (.23%)
Convulsion
10 (.23%)
Depressed Level Of Consciousness
10 (.23%)
Drug Dependence
10 (.23%)
Faecaloma
10 (.23%)
Fear
10 (.23%)

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

What are the most common Carbidopa And 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 Carbidopa And 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 Carbidopa And 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 Carbidopa And Levodopa According to Those Reporting Adverse Events

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

Parkinsons Disease
1150
Parkinsonism
58
Restless Legs Syndrome
51
Product Used For Unknown Indication
40
Drug Use For Unknown Indication
35
Tremor
28
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Dystonia
13
On And Off Phenomenon
11
Brain Neoplasm
5
Multiple System Atrophy
5
Ill-defined Disorder
5
Muscle Spasms
4
Drug Level
4
Parkinsonian Gait
4
Pain In Extremity
3
Gait Disturbance
3
Nervous System Disorder
3
Spinocerebellar Ataxia
3
Dementia Alzheimers Type
2
Dementia
2
Extrapyramidal Disorder
2
Postpartum Hypopituitarism
2
Inflammation
1
Dementia With Lewy Bodies
1
Accidental Exposure
1
Burning Sensation
1
Blood Sodium
1
Off Label Use
1
Periodic Limb Movement Disorder
1
Stent Placement
1
Paraesthesia
1
Musculoskeletal Stiffness
1
Suicide Attempt
1
Peripheral Coldness
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

Carbidopa And Levodopa Case Reports

What Carbidopa And 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 Carbidopa And 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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