Brand name · Haloperidol decanoate
Haldol Decanoate: adverse event reports filed with FDA
825 reports list it as a suspect or interacting product, 2004–2026. Class: Typical antipsychotic. Also reported as Haldol Decanoate Injection.
- 825
- reports as suspect product
- 0% of all reports · about 37 a year
- 26
- reports, 12 months to June 2026
- 16 in the 12 months before
- 60%
- marked serious by the reporter
- 92.3% across the class
- 6.1%
- record death among outcomes, as reported
- 50 reports · not verified by FDA
825 adverse event reports received by FDA list the brand name Haldol Decanoate (haloperidol decanoate) as a suspect or interacting product, from April 2004 to June 2026. A further 224 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, 26 reports listed it, up 63% from 16 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 37 reports a year and 0% of the 20,646,523 reports in the database, and 5% of the reports for the typical antipsychotic class. How many people take it is not in the data, so a count is not a rate of occurrence.
Reporters most often recorded drug ineffective (8.4%), off label use (7.4%) and hospitalisation (5.8%). A report can list several reactions, so shares add to more than 100%; 239 different terms appear across these reports. Drug ineffective is recorded in 8.4% of these reports, a smaller share than in the median typical antipsychotic drug (11.2%).
60% of the reports are marked serious by the reporter (92.3% across the class); 6.1% record death among the outcomes and 28.2% record hospitalisation, as reported. 35.5% of the reports came from consumers, and the largest patient age group is 18 to 44 (24.2%). 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 Haldol Decanoate reports recording the termmedian drug in typical antipsychotic
- Drug ineffectivethe medicine did not work as expected8.4%69
- Off label useused for a purpose or in a way not on the label7.4%61
- Hospitalisationadmission to hospital5.8%48
- Drug dose omissiona dose was missed5%41
- Extrapyramidal disordermovement problems such as stiffness or tremor3.9%32
- Psychotic disordera loss of contact with reality3.9%32
- Adverse eventan unwanted medical event, type not specified3.4%28
- Tremorshaking3.4%28
- Treatment noncompliancethe treatment was not taken as directed3.3%27
- Agitationrestlessness3.2%26
- Somnolencedrowsiness3.2%26
- Weight increasedweight gain2.8%23
- Dizzinesslight-headedness or unsteadiness2.7%22
- Speech disordera speech problem2.5%21
- Feeling abnormalfeeling odd or not right2.4%20
- Malaisegeneral feeling of being unwell2.4%20
- Adverse drug reactiona harmful or unpleasant reaction reported to a medicine2.2%18
- Dyspnoeashortness of breath2.2%18
- General physical health deteriorationgeneral decline in health2.2%18
- Anxietyanxiety2.1%17
- Heart rate increaseda fast heart rate reading2.1%17
- Product quality issuea problem with the product itself2.1%17
- Product use issuea problem in how the product was used2.1%17
- Tardive dyskinesiainvoluntary repetitive movements2.1%17
- Cardiovascular disorder1.9%16
- Aggressionaggressive behaviour1.8%15
- Constipationconstipation1.8%15
- Headachehead pain1.8%15
- Performance status decreased1.8%15
- Incorrect route of drug administrationthe medicine was given by the wrong route1.7%14
Top 30 of 239 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 3 drugs in the typical antipsychotic 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 16,422 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. 64.2% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Schizophrenia | 142 | 17.2% |
| Psychotic disorder | 49 | 5.9% |
| Schizoaffective disorder | 25 | 3% |
| Bipolar disorder | 19 | 2.3% |
| Surgery | 8 | 1% |
| Schizophrenia, paranoid type | 5 | 0.6% |
The indication field is filled in by the reporter and is often blank; shares are of all 825 reports.
In context
| Measure | Haldol Decanoate | Typical antipsychotic | All reports |
|---|---|---|---|
| Reports as suspect product | 825 | 16,422 | 20,646,523 |
| Share of that pool | — | 5% | 0% |
| Reports, latest 12 months | 26 | — | 1,332,454 |
| Marked serious | 60% | 92.3% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 61 | 132 | 91 |
| Hospitalisation recorded, per 1,000 reports | 282 | 461 | 213 |
| Consumer-filed share | 35.5% | 11.4% | 45.8% |
| Top term, share of reports | Drug ineffective 8.4% | median 11.2% | 6.3% |
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 typical antipsychotic class
| Drug | Name type | Reports | Latest 12 months | Marked serious |
|---|---|---|---|---|
| Haloperidol | generic | 14,280 | 819 | 94.7% |
| Haloperidol decanoate | generic | 1,317 | 93 | 86.9% |
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 Haldol Decanoate reports
How many adverse event reports has FDA received for Haldol Decanoate?
825 reports list Haldol Decanoate as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 26 of them arrived in the latest 12 months. Another 224 list it only as a concomitant medication.
What reactions are recorded in Haldol Decanoate reports?
drug ineffective (8.4%), off label use (7.4%), hospitalisation (5.8%), drug dose omission (5%) and extrapyramidal disorder (3.9%). 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 Haldol Decanoate was responsible.
How serious are the reports?
60% are marked serious by the reporter. Among the outcomes recorded, 6.1% of reports include death and 28.2% 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 (35.5%), other health professional (29.2%) and physician (20.8%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Haldol Decanoate rising?
26 reports in the 12 months to June 2026, up 63% from 16 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 Haldol Decanoate 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 Haldol Decanoate?
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 Haldol Decanoate as a suspect or interacting product; reports listing it only as a concomitant medication (224) 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.