Product name as reported
Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium: adverse event reports filed with FDA
1,030 reports list it as a suspect or interacting product, 2012–2014.
- 1,030
- reports as suspect product
- 0% of all reports · about 74 a year
- 0
- reports, 12 months to June 2026
- 0 in the 12 months before
- 99.4%
- marked serious by the reporter
- 57.4% across all reports
- 25%
- record death among outcomes, as reported
- 258 reports · not verified by FDA
1,030 adverse event reports received by FDA list the product name "Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium" as reporters wrote it as a suspect or interacting product, from July 2012 to June 2014. A further 0 reports list it only as a concomitant medication, and those are not counted in the figures on this page.
In the 12 months to June 2026, 0 reports listed it, and none in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Over its reporting history that is about 74 reports a year and 0% of the 20,646,523 reports in the database. How many people take it is not in the data, so a count is not a rate of occurrence.
The MedDRA terms listed most often are death (10.6%), myocardial infarction (8%) and pneumonia (6.3%). A report can list several reactions, so shares add to more than 100%; 280 different terms appear across these reports. Death is recorded in 10.6% of these reports, against 4.1% of all reports in the database.
99.4% of the reports are marked serious by the reporter; 25% record death among the outcomes and 77.6% record hospitalisation, as reported. 84.2% of the reports came from consumers, and the largest patient age group is 45 to 64 (20%). FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."
Reports by month, five years
No report listing Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium was received in the five years to June 2026; the latest was received in June 2014.
By year received
Reactions recorded in the reports
share of Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium reports recording the termall reports in the database
- Deaththe patient died; cause not stated by this term10.6%109
- Myocardial infarctionheart attack8%82
- Pneumonialung infection6.3%65
- Infectionan infection, type not specified6.2%64
- Falla fall6.1%63
- Peritonitis5.4%56
- Hypotensionlow blood pressure5.2%54
- Astheniaweakness or lack of energy4.7%48
- Pulmonary oedemafluid in the lungs4.3%44
- Cardiac disorder3.8%39
- Dehydrationdehydration3.8%39
- Fluid retentionthe body holding extra fluid3.3%34
- Renal failurekidney failure3.3%34
- General physical health deteriorationgeneral decline in health3.2%33
- Painpain, site not specified3.2%33
- Vomitingbeing sick3.2%33
- Cerebrovascular accidentstroke3.1%32
- Hernia3%31
- Localised infection2.9%30
- Hypertensionhigh blood pressure2.8%29
- Dyspnoeashortness of breath2.7%28
- Cardiac failureheart failure2.6%27
- Malaisegeneral feeling of being unwell2.6%27
- Influenzaflu2.4%25
- Peritonitis bacterial2.3%24
- Local swelling2.1%22
- Sepsisa severe body-wide response to infection2.1%22
- Diarrhoealoose or frequent stools1.7%18
Top 30 of 280 MedDRA preferred terms recorded across these reports, with a plain-language gloss where one is available. One report can record several terms. The hollow bar is the share of all reports in the database; it describes the reports, not the patients. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Outcomes recorded
Outcome flags as the reporter set them; a report can carry several, and "other serious" is FDA's own category for serious reports outside the named outcomes. Grey bar: all 20,646,523 reports. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."
Patients and reporters
Patient age
Patient sex
Who reported
Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 0.3% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Peritoneal dialysis | 769 | 74.7% |
| Renal failure | 183 | 17.8% |
| Renal disorder | 16 | 1.6% |
| Diabetic end stage renal disease | 10 | 1% |
| Nephropathy | 10 | 1% |
| Renal failure chronic | 10 | 1% |
The indication field is filled in by the reporter and is often blank; shares are of all 1,030 reports.
In context
| Measure | Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium | All reports |
|---|---|---|
| Reports as suspect product | 1,030 | 20,646,523 |
| Share of that pool | — | 0% |
| Reports, latest 12 months | 0 | 1,332,454 |
| Marked serious | 99.4% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 250 | 91 |
| Hospitalisation recorded, per 1,000 reports | 776 | 213 |
| Consumer-filed share | 84.2% | 45.8% |
| Top term, share of reports | Death 10.6% | 4.1% |
Shares are of reports, not of patients treated. The number of people taking a product is not in the data, so none of these figures is a rate, and differences between columns reflect who takes a product, who reports and how long it has been sold. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Questions about Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium reports
How many adverse event reports has FDA received for Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium?
1,030 reports list Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 0 of them arrived in the latest 12 months. Another 0 list it only as a concomitant medication.
What reactions are recorded in Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium reports?
death (10.6%), myocardial infarction (8%), pneumonia (6.3%), infection (6.2%) and fall (6.1%). These are MedDRA preferred terms coded from what the reporter described; a report can list several, and a term's presence is not a finding that Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium was responsible.
How serious are the reports?
99.4% are marked serious by the reporter. Among the outcomes recorded, 25% of reports include death and 77.6% include hospitalisation. FDA has not verified these outcomes and states that the reports "cannot be used to estimate the incidence" of the events.
Who files these reports?
consumer or non-health professional (84.2%) and other health professional (15.8%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium rising?
0 reports in the 12 months to June 2026, and none in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Counts also move with how many people take a product, its time on the market and publicity.
Do these reports show that Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium was responsible for these reactions?
No. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event." The reaction may relate to the condition being treated, to other medicines, or to something else.
Is this a list of the side effects of Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium?
No. It is a count of what was reported to FDA. The adverse reactions observed in clinical studies are printed on the FDA-approved label, which a pharmacist or clinician can go through with you.
How do I report an adverse event?
Consumers and health professionals can report to FDA through MedWatch (Form FDA 3500 online, or 1-800-FDA-1088), or to the manufacturer, which must pass reports on. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Drug Adverse Event (FAERS) bulk export released 28 Sep 2026, which holds reports FDA received through 30 Jun 2026. Drug names are as reported, resolved to the brand or generic name on the FDA label where openFDA's harmonisation matched them; classes are the pharmacologic class (EPC) from the label and the National Drug Code Directory of 17 Sep 2026. A report counts here when it lists Dianeal Pd4 Solution with 2 5% Dextrose and 2 5 Meq/L Calcium as a suspect or interacting product; reports listing it only as a concomitant medication (0) are excluded. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.