MedDRA preferred term

Blood pressure diastolic decreased: adverse event reports recording this term

7,309 reports to FDA record it, 2004–2026; 0% of the database.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "There is no certainty that the reported event (adverse event or medication error) was actually due to the product. FDA does not require that a causal relationship between a product and event be proven, and reports do not always contain enough detail to properly evaluate an event." The information in these reports "cannot be used to estimate the incidence of these events."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

7,309
reports recording the term: 0% of all reports; 258
reports, 12 months to June 2026: 344 in the 12 months before; 94.3%
marked serious by the reporter: 57.4% across all reports; 9.2%
record death among outcomes, as reported: 9.1% across all reports

7,309 reports in FDA's adverse event database record the MedDRA term "Blood pressure diastolic decreased": 0% of all reports received between January 2004 and June 2026. Coders pick the term that best matches the reporter's description.

258 reports recorded it in the 12 months to June 2026, down 25% from 344 in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Of reports recording this term, 94.3% are marked serious, 9.2% include death among the outcomes and 45.3% include hospitalisation, as reported.

The drugs listed most often as suspect products in those reports are Rituximab, Actemra and Sandostatin LAR Depot. That order mostly follows how many reports each drug has overall; the table also gives the term's share within each drug's own reports. 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

FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.

Drugs listed as suspect products in these reports

Drug	Class	Reports with this term	Share of the drug's own reports
Rituximab	CD20-directed cytolytic antibody	932	0.6%
Actemra	Interleukin-6 receptor antagonist	772	1%
Sandostatin LAR Depot	—	599	3.5%
Inflectra	Tumor necrosis factor blocker	554	2.2%
Sandostatin	Somatostatin analog	526	9.7%
Infliximab	Tumor necrosis factor blocker	450	0.9%
Methotrexate	Folate analog metabolic inhibitor	385	0.2%
Rituxan	CD20-directed cytolytic antibody	293	0.7%
Prednisone	Corticosteroid	230	0.1%
Adempas	Soluble guanylate cyclase stimulator	217	1.2%
Amlodipine	Calcium channel blocker	155	0.3%
Metformin	Biguanide	132	0.2%
Xolair	Anti-IgE	126	0.2%
Diovan	Angiotensin 2 receptor blocker	117	0.7%
Entresto	Angiotensin 2 receptor blocker	102	0.1%
Remicade	Tumor necrosis factor blocker	99	0.1%
Mycophenolate mofetil	Antimetabolite immunosuppressant	91	0.1%
Pantoprazole	Proton pump inhibitor	90	0.2%
Ramipril	Angiotensin converting enzyme inhibitor	89	0.2%
Benadryl	Histamine-1 receptor antagonist	82	0.9%
Aspirin	Nonsteroidal anti-inflammatory drug	79	0.1%
Morphine sulfate	Opioid agonist	75	0.1%
Perjeta	HER2/neu receptor antagonist	75	0.6%
Afinitor	Kinase inhibitor	74	0.2%
Cymbalta	Serotonin and norepinephrine reuptake inhibitor	74	0.1%

Drugs with a page on this site, ordered by the number of their reports recording this term. The last column is the term's share within that drug's own reports, against 0% across the whole database. 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."

By pharmacologic class

Class	Reports with this term	Share of class reports	Median drug in class
CD20-directed cytolytic antibody	1,266	0.4%	0%
Tumor necrosis factor blocker	1,229	0.1%	0%
Interleukin-6 receptor antagonist	796	0.6%	0.1%
Somatostatin analog	550	3%	0.4%
Corticosteroid	484	0.1%	0%
Folate analog metabolic inhibitor	446	0.1%	0%
Angiotensin 2 receptor blocker	403	0.2%	0.1%
Nonsteroidal anti-inflammatory drug	308	0.1%	0%
Histamine-1 receptor antagonist	269	0.2%	0%
Opioid agonist	240	0%	0%

Classes ordered by count. Class shares follow the class's overall report volume as much as anything else.

Patients in these reports

Patient age

Under 20.4%29

2 to 111%70

12 to 171.3%94

18 to 4411.9%869

45 to 6423.2%1,693

65 to 7418.7%1,364

75 and over17%1,244

Age not given26.6%1,946

Patient sex

Female52.2%3,812

Male30.3%2,214

Not given17.6%1,283

Grey bar: all 20,646,523 reports in the database. 21.2% of these reports give the United States as the country.

Questions about "Blood pressure diastolic decreased"

What does "Blood pressure diastolic decreased" mean in an adverse event report?

It is a MedDRA preferred term, the dictionary FDA uses to code what a reporter described. The report's own description is not published by openFDA and is not shown here.

How many reports record blood pressure diastolic decreased?

7,309 reports through June 2026 (0% of all reports), 258 of them in the latest 12 months.

Which drugs appear most often in these reports?

Rituximab (932), Actemra (772), Sandostatin LAR Depot (599), Inflectra (554) and Sandostatin (526). Drugs with many reports overall lead almost every term's list. 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."

Does a drug appearing here mean it was responsible for this reaction?

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."

I have this symptom. What should I do?

This site cannot assess anyone. A pharmacist or clinician can; for an emergency, call the local emergency number. Nothing on this page is medical advice.

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. Terms are pooled across spelling and capitalisation variants of one MedDRA preferred term. 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.