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DIANEAL PD

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Dianeal Pd Adverse Events Reported to the FDA Over Time

How are Dianeal Pd adverse event reports trending over time?

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

Most Common Dianeal Pd Adverse Events Reported to the FDA

What are the most common Dianeal Pd adverse events reported to the FDA?

Death
647 (13.06%)
Peritonitis
125 (2.52%)
Sepsis
117 (2.36%)
Pneumonia
110 (2.22%)
Cardiac Arrest
102 (2.06%)
Peritonitis Bacterial
97 (1.96%)
Myocardial Infarction
95 (1.92%)
Peritoneal Dialysis Complication
85 (1.72%)
Cardiac Failure
76 (1.53%)
Vomiting
73 (1.47%)
Fungal Peritonitis
66 (1.33%)
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Infection
62 (1.25%)
Diarrhoea
57 (1.15%)
Dyspnoea
54 (1.09%)
Cerebrovascular Accident
53 (1.07%)
Hypotension
52 (1.05%)
Dehydration
50 (1.01%)
Cardiac Disorder
49 (.99%)
Asthenia
47 (.95%)
Cardio-respiratory Arrest
39 (.79%)
Nausea
39 (.79%)
Cardiac Failure Congestive
38 (.77%)
Fall
38 (.77%)
Abdominal Pain
37 (.75%)
Hypertension
35 (.71%)
Chest Pain
32 (.65%)
Hernia
32 (.65%)
Pyrexia
32 (.65%)
Convulsion
29 (.59%)
Renal Failure Chronic
28 (.57%)
Constipation
26 (.52%)
Blood Pressure Decreased
25 (.5%)
Pulmonary Oedema
25 (.5%)
Respiratory Failure
25 (.5%)
Cerebral Infarction
24 (.48%)
Fluid Overload
24 (.48%)
Malnutrition
24 (.48%)
Multi-organ Failure
24 (.48%)
Fluid Retention
23 (.46%)
Gastrointestinal Haemorrhage
23 (.46%)
Urinary Tract Infection
23 (.46%)
Wound
23 (.46%)
Wound Infection
23 (.46%)
Cardiovascular Disorder
22 (.44%)
Cerebral Haemorrhage
22 (.44%)
Pain
22 (.44%)
Azotaemia
20 (.4%)
Condition Aggravated
19 (.38%)
Peripheral Arterial Occlusive Disea...
19 (.38%)
Lung Neoplasm Malignant
18 (.36%)
Septic Shock
18 (.36%)
Anaemia
17 (.34%)
Decreased Appetite
17 (.34%)
Abdominal Distension
16 (.32%)
Renal Failure
16 (.32%)
Abscess
15 (.3%)
Hypophagia
15 (.3%)
Malaise
15 (.3%)
Oedema Peripheral
15 (.3%)
Feeling Abnormal
14 (.28%)
General Physical Health Deteriorati...
14 (.28%)
Loss Of Consciousness
14 (.28%)
Muscle Spasms
14 (.28%)
Oedema
14 (.28%)
Pancreatitis
14 (.28%)
Cellulitis
13 (.26%)
Discomfort
13 (.26%)
Haemorrhage
13 (.26%)
Procedural Complication
13 (.26%)
Blood Potassium Decreased
12 (.24%)
Dizziness
12 (.24%)
Drug Ineffective
12 (.24%)
Head Injury
12 (.24%)
Impaired Gastric Emptying
12 (.24%)
Localised Infection
12 (.24%)
Staphylococcal Infection
12 (.24%)
Marasmus
11 (.22%)
Pleural Effusion
11 (.22%)
Procedural Pain
11 (.22%)
Sudden Death
11 (.22%)
Syncope
11 (.22%)
Treatment Noncompliance
11 (.22%)
Cataract
10 (.2%)
Cholelithiasis
10 (.2%)
Depressed Level Of Consciousness
10 (.2%)
Diabetes Mellitus
10 (.2%)
Granuloma Skin
10 (.2%)
Keloid Scar
10 (.2%)
Neoplasm Malignant
10 (.2%)
Subarachnoid Haemorrhage
10 (.2%)
Upper Limb Fracture
10 (.2%)
Blood Calcium Decreased
9 (.18%)
Gangrene
9 (.18%)
Headache
9 (.18%)
Hypoglycaemia
9 (.18%)
Injection Site Nodule
9 (.18%)
Liver Disorder
9 (.18%)
Pneumonia Aspiration
9 (.18%)
Poor Peripheral Circulation
9 (.18%)
Thrombosis
9 (.18%)
Weight Decreased
9 (.18%)

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

What are the most common Dianeal Pd adverse events reported to the FDA?

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

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

Peritoneal Dialysis
1604
Renal Failure Chronic
250
Drug Use For Unknown Indication
38
Product Used For Unknown Indication
32
Diarrhoea
23
Prophylaxis
21
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Crohns Disease
17
Renal Failure
13
Diabetic Nephropathy
11
Ill-defined Disorder
10
Enterocolitis
10
Fluid Replacement
9
Osteoporosis
6
Pruritus
5
Intravenous Catheter Management
4
Glomerulonephritis Chronic
4
Gastrointestinal Disorder
4
Enteritis
4
Drug Therapy
4
Disbacteriosis
3
Surgery
3
Glomerulonephritis
3
Otitis Media Acute
3
Drug Exposure During Pregnancy
3
Adverse Event
3
Migraine
3
Renal Disorder
2
Peritoneal Lavage
2
Atypical Mycobacterial Infection
2
Hypertension
2
Gastroenteritis
2
Nephrosclerosis
2
Bronchitis Acute
2
Mineral Supplementation
2
Constipation
2
Dehydration
2
Diabetic Neuropathy
2
Prophylaxis Against Diarrhoea
2
Probiotic Therapy
2
Upper Respiratory Tract Inflammatio...
2
Dialysis
2
Perianal Abscess
2
Facial Wasting
1
Trichostasis Spinulosa
1
Urethral Disorder
1
Skin Cosmetic Procedure
1
Renal Failure Acute
1
Induction Of Anaesthesia
1
Hypotension
1
Cows Milk Intolerance
1
Cerebral Infarction
1

Drug Labels

LabelLabelerEffective
Dianeal Pd-2 With DextroseBaxter Healthcare Corporation02-FEB-02
Dianeal Pd-2 Peritoneal Dialysis Solution With DextroseBaxter Healthcare Corporation07-JUN-10

Dianeal Pd Case Reports

What Dianeal Pd 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 Dianeal Pd. 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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