Drugs › Central nervous system depressant
Brand name · Calcium, magnesium, potassium, and sodium oxybates
Xywav: adverse event reports filed with FDA
8,426 reports list it as a suspect or interacting product, 2015–2026. Class: Central nervous system depressant.
- 8,426
- reports as suspect product
- 0% of all reports · about 778 a year
- 1,317
- reports, 12 months to June 2026
- 1,923 in the 12 months before
- 82.7%
- marked serious by the reporter
- 54.4% across the class
- 1%
- record death among outcomes, as reported
- 81 reports · not verified by FDA
8,426 adverse event reports received by FDA list the brand name Xywav (calcium, magnesium, potassium, and sodium oxybates) as a suspect or interacting product, from September 2015 to June 2026. A further 135 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, 1,317 reports listed it, down 32% from 1,923 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 778 reports a year and 0% of the 20,646,523 reports in the database, and 11.3% of the reports for the central nervous system depressant class. How many people take it is not in the data, so a count is not a rate of occurrence.
The reactions recorded most often are product administration interrupted (18.1%), surgery (14.7%) and nausea (10.9%). A report can list several reactions, so shares add to more than 100%; 1,227 different terms appear across these reports. Product administration interrupted is recorded in 18.1% of these reports, a larger share than in the median central nervous system depressant drug (8%).
82.7% of the reports are marked serious by the reporter (54.4% across the class); 1% record death among the outcomes and 18.9% record hospitalisation, as reported. 61.7% of the reports came from consumers, and the largest patient age group is 18 to 44 (24.3%). 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
Reports by the month FDA received them. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.
By year received
2026 covers reports received through June 2026 only.
Reactions recorded in the reports
share of Xywav reports recording the termmedian drug in central nervous system depressant
- Product administration interrupted18.1%1,525
- Surgeryan operation14.7%1,238
- Nauseafeeling sick10.9%915
- Product dose omission issuea dose was missed10%842
- Anxietyanxiety7.8%654
- Intentional dose omission6.8%571
- Intentional product use issuedeliberate use not as intended6%505
- Dizzinesslight-headedness or unsteadiness6%503
- Headachehead pain5.9%501
- Somnolencedrowsiness5.4%457
- Vomitingbeing sick5.2%438
- Feeling abnormalfeeling odd or not right4.9%417
- Weight decreasedweight loss4.7%399
- Depressionlow mood4.7%394
- Falla fall4.6%390
- Hospitalisationadmission to hospital4.4%373
- Illness4.3%366
- Fatiguetiredness4.2%351
- Drug ineffectivethe medicine did not work as expected4.1%349
- Suicidal ideationthoughts of suicide3.9%326
- Off label useused for a purpose or in a way not on the label3.8%322
- Covid-19COVID-19 infection3.8%316
- Insomniadifficulty sleeping3.7%313
- Dyspnoeashortness of breath3.4%288
- Hyperhidrosisexcessive sweating3.1%264
- Nephrolithiasiskidney stones3.1%264
- Diarrhoealoose or frequent stools3.1%260
- Tremorshaking3%256
- Condition aggravatedthe condition being treated got worse2.8%237
- Muscle spasmsmuscle cramps2.7%226
Top 30 of 1,227 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 median share across the 4 drugs in the central nervous system depressant class; 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 74,407 reports in the class. 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. 99.8% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Narcolepsy | 5,260 | 62.4% |
| Hypersomnia | 2,012 | 23.9% |
| Cataplexy | 88 | 1% |
| Somnolence | 26 | 0.3% |
| Insomnia | 14 | 0.2% |
| Fibromyalgia | 10 | 0.1% |
The indication field is filled in by the reporter and is often blank; shares are of all 8,426 reports.
Drugs most often listed in the same reports
| Drug (any role in the report) | Reports | Share of Xywav reports |
|---|---|---|
| Adderall | 1,156 | 13.7% |
| Ergocalciferol | 890 | 10.6% |
| Sunosi | 665 | 7.9% |
| Gabapentin | 609 | 7.2% |
| Modafinil | 557 | 6.6% |
| Omeprazole | 470 | 5.6% |
| Albuterol sulfate | 455 | 5.4% |
| Aspirin | 433 | 5.1% |
| Levothyroxine | 399 | 4.7% |
| Wakix | 375 | 4.5% |
Other products listed in reports where Xywav is a suspect product, whatever their own role. Co-listing means the two were recorded together; it says nothing about either product's part in the event. Only the 2,500 most-reported names are counted here.
In context
| Measure | Xywav | Central nervous system depressant | All reports |
|---|---|---|---|
| Reports as suspect product | 8,426 | 74,407 | 20,646,523 |
| Share of that pool | — | 11.3% | 0% |
| Reports, latest 12 months | 1,317 | — | 1,332,454 |
| Marked serious | 82.7% | 54.4% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 10 | 14 | 91 |
| Hospitalisation recorded, per 1,000 reports | 189 | 129 | 213 |
| Consumer-filed share | 61.7% | 36.8% | 45.8% |
| Top term, share of reports | Product administration interrupted 18.1% | median 8% | 0% |
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."
Other drugs in the central nervous system depressant class
| Drug | Name type | Reports | Latest 12 months | Marked serious |
|---|---|---|---|---|
| Xyrem | brand | 61,308 | 218 | 52.1% |
| Lumryz | brand | 3,488 | 325 | 13.7% |
| Sodium oxybate | generic | 1,185 | 244 | 88.5% |
Ordered by report count for navigation only. 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." A brand and its generic are separate rows because reporters name them separately.
Questions about Xywav reports
How many adverse event reports has FDA received for Xywav?
8,426 reports list Xywav as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 1,317 of them arrived in the latest 12 months. Another 135 list it only as a concomitant medication.
What reactions are recorded in Xywav reports?
product administration interrupted (18.1%), surgery (14.7%), nausea (10.9%), product dose omission issue (10%) and anxiety (7.8%). 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 Xywav was responsible.
How serious are the reports?
82.7% are marked serious by the reporter. Among the outcomes recorded, 1% of reports include death and 18.9% 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 (61.7%), other health professional (19.1%) and physician (18.5%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Xywav rising?
1,317 reports in the 12 months to June 2026, down 32% from 1,923 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 Xywav 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 Xywav?
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 Xywav as a suspect or interacting product; reports listing it only as a concomitant medication (135) 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.