DrugCite
Search

SINEMET CR

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Sinemet Cr Adverse Events Reported to the FDA Over Time

How are Sinemet Cr adverse event reports trending over time?

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

Most Common Sinemet Cr Adverse Events Reported to the FDA

What are the most common Sinemet Cr adverse events reported to the FDA?

Drug Ineffective
42 (5.01%)
Tremor
18 (2.15%)
Dyskinesia
17 (2.03%)
Overdose
17 (2.03%)
Fall
14 (1.67%)
Asthenia
12 (1.43%)
Confusional State
12 (1.43%)
Nausea
12 (1.43%)
Drug Interaction
11 (1.31%)
Adverse Event
10 (1.19%)
Drug Effect Decreased
10 (1.19%)
Show More Show More
Dysphagia
10 (1.19%)
Hallucination
10 (1.19%)
Product Quality Issue
10 (1.19%)
Back Pain
9 (1.07%)
Dizziness
9 (1.07%)
Insomnia
9 (1.07%)
Death
8 (.95%)
Malaise
8 (.95%)
Pain
8 (.95%)
Wrong Technique In Drug Usage Proce...
8 (.95%)
Balance Disorder
7 (.83%)
Medication Error
7 (.83%)
Psychotic Disorder
7 (.83%)
Aggression
6 (.72%)
Agitation
6 (.72%)
Dysarthria
6 (.72%)
Dystonia
6 (.72%)
Feeling Abnormal
6 (.72%)
Hallucination, Visual
6 (.72%)
Loss Of Consciousness
6 (.72%)
Muscle Rigidity
6 (.72%)
Restlessness
6 (.72%)
Somnolence
6 (.72%)
Speech Disorder
6 (.72%)
Syncope
6 (.72%)
Cerebrovascular Accident
5 (.6%)
Decreased Appetite
5 (.6%)
Delirium
5 (.6%)
Disease Progression
5 (.6%)
Fatigue
5 (.6%)
Gait Disturbance
5 (.6%)
Movement Disorder
5 (.6%)
Muscle Spasms
5 (.6%)
Parkinsonism
5 (.6%)
Weight Decreased
5 (.6%)
Abdominal Discomfort
4 (.48%)
Anger
4 (.48%)
Condition Aggravated
4 (.48%)
Feeling Jittery
4 (.48%)
Nervousness
4 (.48%)
Paralysis
4 (.48%)
Paranoia
4 (.48%)
Pathological Gambling
4 (.48%)
Product Substitution Issue
4 (.48%)
Rhabdomyolysis
4 (.48%)
Urinary Retention
4 (.48%)
Abdominal Pain Upper
3 (.36%)
Amnesia
3 (.36%)
Anaemia
3 (.36%)
Aphonia
3 (.36%)
Cardiac Failure
3 (.36%)
Depression
3 (.36%)
Diplopia
3 (.36%)
Dry Mouth
3 (.36%)
Dysphonia
3 (.36%)
Dysstasia
3 (.36%)
Epistaxis
3 (.36%)
Haemoglobin Decreased
3 (.36%)
Hyperhidrosis
3 (.36%)
Hypoaesthesia Facial
3 (.36%)
Hypotension
3 (.36%)
Hypotonia
3 (.36%)
Incorrect Dose Administered
3 (.36%)
International Normalised Ratio Incr...
3 (.36%)
Lethargy
3 (.36%)
Logorrhoea
3 (.36%)
Mastication Disorder
3 (.36%)
Muscular Weakness
3 (.36%)
Mydriasis
3 (.36%)
Neuroleptic Malignant Syndrome
3 (.36%)
Neutropenia
3 (.36%)
Off Label Use
3 (.36%)
Orthostatic Hypotension
3 (.36%)
Pneumonia Aspiration
3 (.36%)
Psychomotor Hyperactivity
3 (.36%)
Pulmonary Embolism
3 (.36%)
Sinus Tachycardia
3 (.36%)
Therapeutic Response Decreased
3 (.36%)
Thrombocytopenia
3 (.36%)
Vomiting
3 (.36%)
Withdrawal Syndrome
3 (.36%)
Abnormal Behaviour
2 (.24%)
Accidental Exposure
2 (.24%)
Activities Of Daily Living Impaired
2 (.24%)
Akinesia
2 (.24%)
Anaemia Haemolytic Autoimmune
2 (.24%)
Anxiety
2 (.24%)
Arthralgia
2 (.24%)
Arthritis
2 (.24%)
Aspartate Aminotransferase Increase...
2 (.24%)

ExportShare/Embed GraphExport Export Data

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

What are the most common Sinemet Cr adverse events reported to the FDA?

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Parkinsons Disease
297
Parkinsonism
17
Restless Legs Syndrome
17
Drug Use For Unknown Indication
14
Product Used For Unknown Indication
10
Tremor
5
Show More Show More
Dystonia
4
Ill-defined Disorder
3
Drug Level
2
Cerebrovascular Accident
1
Closed Head Injury
1
Dyskinesia
1
Multiple System Atrophy
1
Nervous System Disorder
1
Brain Injury
1

Drug Labels

LabelLabelerEffective
Sinemet CrBristol-Myers Squibb Pharma Company01-JAN-09
SinemetcrMerck Sharp & Dohme Corp.01-FEB-11

Sinemet Cr Case Reports

What Sinemet Cr safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Sinemet Cr. 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.

Comments

Share your experience with Sinemet Cr.