MedDRA preferred term

Dizziness postural: adverse event reports recording this term

9,458 reports to FDA record it, 2004–2026; 0.1% 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.

9,458
reports recording the term: 0.1% of all reports; 839
reports, 12 months to June 2026: 738 in the 12 months before; 62.4%
marked serious by the reporter: 57.4% across all reports; 3%
record death among outcomes, as reported: 9.1% across all reports

9,458 reports in FDA's adverse event database record the MedDRA term "Dizziness postural": 0.1% of all reports received between January 2004 and June 2026. Coders pick the term that best matches the reporter's description.

839 reports recorded it in the 12 months to June 2026, up 14% from 738 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, 62.4% are marked serious, 3% include death among the outcomes and 27% include hospitalisation, as reported.

The drugs listed most often as suspect products in those reports are Entresto, Adempas and Remodulin. 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
Entresto	Angiotensin 2 receptor blocker	661	0.6%
Adempas	Soluble guanylate cyclase stimulator	179	1%
Remodulin	Prostacycline vasodilator	170	0.4%
Gilenya	Sphingosine 1-phosphate receptor modulator	164	0.2%
Opsumit	Endothelin receptor antagonist	149	0.4%
Forteo	Parathyroid hormone analog	147	0.1%
Tyvaso	Prostacycline vasodilator	146	0.5%
Orenitram	Prostacycline vasodilator	132	0.8%
Ambrisentan	Endothelin receptor antagonist	129	0.2%
Humira	—	126	0%
Tymlos	—	126	0.4%
Northera	—	122	0.6%
Revlimid	Thalidomide analog	114	0%
Tyvaso DPI	Prostacycline vasodilator	112	1.2%
Filspari	Angiotensin 2 receptor blocker	106	1.9%
Orgovyx	Gonadotropin releasing hormone receptor antagonist	106	0.5%
Enbrel	Tumor necrosis factor blocker	105	0%
Uptravi	Prostacyclin receptor agonist	96	0.6%
Amlodipine	Calcium channel blocker	89	0.2%
Dupixent	Interleukin-4 receptor alpha antagonist	87	0%
Furosemide	Loop diuretic	87	0.2%
Jakafi	Janus kinase inhibitor	86	0.2%
Metoprolol	beta-Adrenergic blocker	86	0.3%
Cymbalta	Serotonin and norepinephrine reuptake inhibitor	80	0.2%
Lisinopril	Angiotensin converting enzyme inhibitor	76	0.2%

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 0.1% 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
Angiotensin 2 receptor blocker	878	0.4%	0.1%
Prostacycline vasodilator	637	0.5%	0.6%
Endothelin receptor antagonist	377	0.2%	0.2%
Atypical antipsychotic	283	0%	0%
Kinase inhibitor	270	0%	0%
beta-Adrenergic blocker	214	0.1%	0.1%
Tumor necrosis factor blocker	201	0%	0%
Serotonin reuptake inhibitor	195	0.1%	0.1%
Soluble guanylate cyclase stimulator	184	0.9%	1%
Sphingosine 1-phosphate receptor modulator	183	0.2%	0.1%

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%1

2 to 110.1%12

12 to 170.9%81

18 to 4411.6%1,097

45 to 6423.6%2,234

65 to 7416.3%1,542

75 and over15.2%1,435

Age not given32.3%3,056

Patient sex

Female49.7%4,701

Male42.8%4,050

Not given7.5%707

Grey bar: all 20,646,523 reports in the database. 67.6% of these reports give the United States as the country.

Questions about "Dizziness postural"

What does "Dizziness postural" 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 dizziness postural?

9,458 reports through June 2026 (0.1% of all reports), 839 of them in the latest 12 months.

Which drugs appear most often in these reports?

Entresto (661), Adempas (179), Remodulin (170), Gilenya (164) and Opsumit (149). 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.