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PHYSIOSOL IN PLASTIC CONTAINER

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Physiosol In Plastic Container Adverse Events Reported to the FDA Over Time

How are Physiosol In Plastic Container adverse event reports trending over time?

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

Most Common Physiosol In Plastic Container Adverse Events Reported to the FDA

What are the most common Physiosol In Plastic Container adverse events reported to the FDA?

Death
139 (11.54%)
Peritonitis Bacterial
65 (5.4%)
Peritonitis
53 (4.4%)
Sepsis
38 (3.16%)
Peritoneal Dialysis Complication
25 (2.08%)
Sclerosing Encapsulating Peritoniti...
24 (1.99%)
Pyrexia
21 (1.74%)
Fungal Peritonitis
19 (1.58%)
Abdominal Pain
18 (1.5%)
Vomiting
18 (1.5%)
Peritonitis Sclerosing
17 (1.41%)
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Nausea
15 (1.25%)
Cardiac Arrest
14 (1.16%)
Catheter Site Infection
13 (1.08%)
Ileus
13 (1.08%)
Pneumonia
13 (1.08%)
Cardiac Failure
12 (1%)
Cerebrovascular Accident
12 (1%)
Ascites
11 (.91%)
General Physical Health Deteriorati...
11 (.91%)
Intestinal Obstruction
11 (.91%)
Peritoneal Cloudy Effluent
11 (.91%)
Constipation
10 (.83%)
Cardiac Disorder
9 (.75%)
Dyspnoea
9 (.75%)
Fluid Overload
9 (.75%)
Malaise
9 (.75%)
Acute Myocardial Infarction
8 (.66%)
Diarrhoea
8 (.66%)
Anuria
7 (.58%)
Multi-organ Failure
7 (.58%)
Renal Failure Chronic
7 (.58%)
Weight Decreased
7 (.58%)
Abdominal Distension
6 (.5%)
Asthenia
6 (.5%)
Cachexia
6 (.5%)
Dyspepsia
6 (.5%)
Hypertension
6 (.5%)
Hypotension
6 (.5%)
Intestinal Ischaemia
6 (.5%)
Staphylococcal Infection
6 (.5%)
Cardio-respiratory Arrest
5 (.42%)
Chills
5 (.42%)
Convulsion
5 (.42%)
Gastrointestinal Disorder
5 (.42%)
Hyperphosphataemia
5 (.42%)
Infection
5 (.42%)
Intra-abdominal Haematoma
5 (.42%)
Procedural Complication
5 (.42%)
Urinary Tract Infection
5 (.42%)
Abdominal Abscess
4 (.33%)
Abdominal Symptom
4 (.33%)
Anaemia
4 (.33%)
Dehydration
4 (.33%)
Diverticulitis
4 (.33%)
Hypokalaemia
4 (.33%)
Ischaemic Stroke
4 (.33%)
Malnutrition
4 (.33%)
Pancreatitis
4 (.33%)
Peripheral Ischaemia
4 (.33%)
Peripheral Vascular Disorder
4 (.33%)
Pleural Effusion
4 (.33%)
Pneumothorax
4 (.33%)
Post Procedural Complication
4 (.33%)
Reflux Oesophagitis
4 (.33%)
Septic Shock
4 (.33%)
Tachycardia
4 (.33%)
Therapy Cessation
4 (.33%)
Urosepsis
4 (.33%)
Abdominal Pain Upper
3 (.25%)
Abdominal Wall Infection
3 (.25%)
Abscess Intestinal
3 (.25%)
Atelectasis
3 (.25%)
Bacteraemia
3 (.25%)
Blood Pressure Increased
3 (.25%)
Body Temperature Increased
3 (.25%)
Cytomegalovirus Infection
3 (.25%)
Dementia
3 (.25%)
Depressed Level Of Consciousness
3 (.25%)
Eczema
3 (.25%)
Enterococcal Infection
3 (.25%)
Escherichia Infection
3 (.25%)
Fistula
3 (.25%)
Flank Pain
3 (.25%)
Flatulence
3 (.25%)
Gangrene
3 (.25%)
Gastrointestinal Oedema
3 (.25%)
Haematoma Infection
3 (.25%)
Haemodynamic Instability
3 (.25%)
Haemoglobin Decreased
3 (.25%)
Haemorrhagic Anaemia
3 (.25%)
Haemorrhagic Ascites
3 (.25%)
Hernia
3 (.25%)
Hypotonia
3 (.25%)
Ill-defined Disorder
3 (.25%)
Intra-abdominal Haemorrhage
3 (.25%)
Ischaemia
3 (.25%)
Oedema
3 (.25%)
Pancreatitis Acute
3 (.25%)
Peritoneal Disorder
3 (.25%)
Peritoneal Fluid Analysis Abnormal
3 (.25%)

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This graph shows the top adverse events submitted to the FDA for Physiosol In Plastic Container, 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 Physiosol In Plastic Container 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 Physiosol In Plastic Container

What are the most common Physiosol In Plastic Container adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Physiosol In Plastic Container, 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 Physiosol In Plastic Container 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 Physiosol In Plastic Container According to Those Reporting Adverse Events

Why are people taking Physiosol In Plastic Container, according to those reporting adverse events to the FDA?

Peritoneal Dialysis
463
Renal Failure Chronic
48
Renal Failure
13
Glomerulonephritis Proliferative
4
Tubulointerstitial Nephritis
4
Product Used For Unknown Indication
4
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Wegeners Granulomatosis
4
Diabetic Nephropathy
4
Kidney Transplant Rejection
3
Iga Nephropathy
3
Vascular Access Complication
3
Congenital Cystic Kidney Disease
2
Type 2 Diabetes Mellitus
2
Dialysis
2
Cardiorenal Syndrome
2
Drug Use For Unknown Indication
2
Kidney Small
1
Cardiac Failure
1
Nephrosclerosis
1
Nephroangiosclerosis
1
Refusal Of Treatment By Patient
1
Diabetes Mellitus
1
Glomerulonephritis Chronic
1

Physiosol In Plastic Container Case Reports

What Physiosol In Plastic Container 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 Physiosol In Plastic Container. 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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