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APO GO AMPOULES

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Apo Go Ampoules Adverse Events Reported to the FDA Over Time

How are Apo Go Ampoules adverse event reports trending over time?

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

Most Common Apo Go Ampoules Adverse Events Reported to the FDA

What are the most common Apo Go Ampoules adverse events reported to the FDA?

Death
76 (10.63%)
Hallucination
18 (2.52%)
Fall
15 (2.1%)
Muscle Rigidity
15 (2.1%)
Somnolence
13 (1.82%)
Confusional State
12 (1.68%)
Psychotic Disorder
12 (1.68%)
Condition Aggravated
11 (1.54%)
Hyperkinesia
11 (1.54%)
Loss Of Consciousness
10 (1.4%)
General Physical Health Deteriorati...
9 (1.26%)
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Nodule
9 (1.26%)
Fatigue
8 (1.12%)
Malaise
8 (1.12%)
Nausea
8 (1.12%)
Drug Ineffective
7 (.98%)
Infusion Site Mass
7 (.98%)
Pneumonia
7 (.98%)
Aggression
6 (.84%)
Dyskinesia
6 (.84%)
Haemoglobin Decreased
6 (.84%)
Hallucination, Visual
6 (.84%)
Infusion Site Necrosis
6 (.84%)
Injection Site Inflammation
6 (.84%)
Abscess
5 (.7%)
Anaemia Haemolytic Autoimmune
5 (.7%)
Depression
5 (.7%)
Device Malfunction
5 (.7%)
Disease Progression
5 (.7%)
Hospitalisation
5 (.7%)
Hypertension
5 (.7%)
Incorrect Dose Administered
5 (.7%)
Inflammation
5 (.7%)
Muscle Spasms
5 (.7%)
Pain
5 (.7%)
Vomiting
5 (.7%)
Abdominal Wall Haematoma
4 (.56%)
Accidental Overdose
4 (.56%)
Agitation
4 (.56%)
Cellulitis
4 (.56%)
Diarrhoea
4 (.56%)
Injection Site Haematoma
4 (.56%)
Injection Site Nodule
4 (.56%)
Syncope
4 (.56%)
Urinary Tract Infection
4 (.56%)
Abnormal Behaviour
3 (.42%)
Anxiety
3 (.42%)
Cardiac Disorder
3 (.42%)
Cardiac Failure
3 (.42%)
Circulatory Collapse
3 (.42%)
Dementia
3 (.42%)
Dermatitis Allergic
3 (.42%)
Drug Effect Decreased
3 (.42%)
Erythema
3 (.42%)
Femoral Neck Fracture
3 (.42%)
General Physical Condition Abnormal
3 (.42%)
Headache
3 (.42%)
Hypotension
3 (.42%)
Incontinence
3 (.42%)
Infusion Site Abscess
3 (.42%)
Injection Site Erythema
3 (.42%)
Memory Impairment
3 (.42%)
Mobility Decreased
3 (.42%)
Narcolepsy
3 (.42%)
No Therapeutic Response
3 (.42%)
Oedema
3 (.42%)
Oedema Peripheral
3 (.42%)
Paranoia
3 (.42%)
Pyrexia
3 (.42%)
Respiratory Arrest
3 (.42%)
Skin Discolouration
3 (.42%)
Skin Nodule
3 (.42%)
Tremor
3 (.42%)
Accident
2 (.28%)
Altered State Of Consciousness
2 (.28%)
Apathy
2 (.28%)
Balance Disorder
2 (.28%)
Blood Pressure Decreased
2 (.28%)
Blood Pressure Fluctuation
2 (.28%)
Cerebral Infarction
2 (.28%)
Coma
2 (.28%)
Completed Suicide
2 (.28%)
Contusion
2 (.28%)
Dehydration
2 (.28%)
Delusion
2 (.28%)
Delusional Disorder, Unspecified Ty...
2 (.28%)
Dependence
2 (.28%)
Depressed Mood
2 (.28%)
Disturbance In Attention
2 (.28%)
Dizziness
2 (.28%)
Dysarthria
2 (.28%)
Dysphagia
2 (.28%)
Erection Increased
2 (.28%)
Feeling Hot
2 (.28%)
Gangrene
2 (.28%)
Haematoma
2 (.28%)
Haemolytic Anaemia
2 (.28%)
Hepatitis C
2 (.28%)
Hypokalaemia
2 (.28%)
Impulse-control Disorder
2 (.28%)
Inappropriate Schedule Of Drug Admi...
2 (.28%)

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This graph shows the top adverse events submitted to the FDA for Apo Go Ampoules, 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 Apo Go Ampoules 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 Apo Go Ampoules

What are the most common Apo Go Ampoules adverse events reported to the FDA?

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

Why are people taking Apo Go Ampoules, according to those reporting adverse events to the FDA?

Product Used For Unknown Indication
135
Parkinsons Disease
95
Drug Use For Unknown Indication
54
Parkinsonism
4
On And Off Phenomenon
3
Restless Legs Syndrome
3
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Freezing Phenomenon
1
Dystonia
1

Apo Go Ampoules Case Reports

What Apo Go Ampoules 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 Apo Go Ampoules. 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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