Drugs › Intestinal lipase inhibitor
Brand name · Orlistat
Alli: adverse event reports filed with FDA
21,224 reports list it as a suspect or interacting product, 2007–2026. Class: Intestinal lipase inhibitor.
- 21,224
- reports as suspect product
- 0.1% of all reports · about 1,112 a year
- 139
- reports, 12 months to June 2026
- 226 in the 12 months before
- 12.1%
- marked serious by the reporter
- 22.2% across the class
- 0.1%
- record death among outcomes, as reported
- 24 reports · not verified by FDA
Between June 2007 and June 2026, 21,224 adverse event reports received by FDA list the brand name Alli (orlistat) as a suspect or interacting product. Reports that mention it only as a concomitant medication (120) are left out of every figure here.
In the 12 months to June 2026, 139 reports listed it, down 38% from 226 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 1,112 reports a year and 0.1% of the 20,646,523 reports in the database, and 87% of the reports for the intestinal lipase inhibitor 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 drug ineffective (20.3%), rectal discharge (11.4%) and gastrointestinal disorder (10.1%). A report can list several reactions, so shares add to more than 100%; 768 different terms appear across these reports. Drug ineffective is recorded in 20.3% of these reports, a larger share than in the median intestinal lipase inhibitor drug (7.3%).
12.1% of the reports are marked serious by the reporter (22.2% across the class); 0.1% record death among the outcomes and 2.7% record hospitalisation, as reported. 97.1% of the reports came from consumers, and the largest patient age group is 18 to 44 (21.7%). 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 Alli reports recording the termmedian drug in intestinal lipase inhibitor
- Drug ineffectivethe medicine did not work as expected20.3%4,311
- Rectal discharge11.4%2,412
- Gastrointestinal disorder10.1%2,148
- Constipationconstipation8.9%1,886
- Weight increasedweight gain8.3%1,764
- Diarrhoealoose or frequent stools8%1,696
- Flatulencewind7.4%1,570
- Steatorrhoea7.4%1,565
- Abdominal pain upperupper stomach pain5.9%1,261
- Abdominal distensiona bloated abdomen4.5%958
- Headachehead pain4.4%926
- Treatment noncompliancethe treatment was not taken as directed3.7%792
- Nauseafeeling sick3.5%736
- Malaisegeneral feeling of being unwell3.3%692
- Frequent bowel movements2.9%623
- Product quality issuea problem with the product itself2.8%604
- Faeces discoloured2.7%574
- Abdominal painstomach or belly pain2.4%501
- Dizzinesslight-headedness or unsteadiness2.2%457
- Vomitingbeing sick1.9%409
- Muscle spasmsmuscle cramps1.9%395
- Rectal haemorrhage1.7%355
- Fatiguetiredness1.7%351
- Painpain, site not specified1.6%329
- Ill-defined disordera condition that was not clearly described1.4%292
- Haematocheziablood in the stool1.3%276
- Feeling abnormalfeeling odd or not right1.2%259
- Rashskin rash1.2%259
Top 30 of 768 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 intestinal lipase inhibitor 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 24,403 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. 97.9% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Weight loss diet | 2,734 | 12.9% |
| Weight decreased | 1,718 | 8.1% |
| Weight control | 396 | 1.9% |
| Obesity | 48 | 0.2% |
| Constipation | 21 | 0.1% |
| Overweight | 17 | 0.1% |
The indication field is filled in by the reporter and is often blank; shares are of all 21,224 reports.
Drugs most often listed in the same reports
| Drug (any role in the report) | Reports | Share of Alli reports |
|---|---|---|
| Aspirin | 70 | 0.3% |
| Synthroid | 65 | 0.3% |
| Lipitor | 43 | 0.2% |
| Fluoxetine | 39 | 0.2% |
| Lisinopril | 37 | 0.2% |
| Meloxicam | 36 | 0.2% |
| Levothyroxine sodium | 33 | 0.2% |
| Nexium | 31 | 0.1% |
| Bupropion hydrochloride | 28 | 0.1% |
| Calcium | 28 | 0.1% |
Other products listed in reports where Alli 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 | Alli | Intestinal lipase inhibitor | All reports |
|---|---|---|---|
| Reports as suspect product | 21,224 | 24,403 | 20,646,523 |
| Share of that pool | — | 87% | 0.1% |
| Reports, latest 12 months | 139 | — | 1,332,454 |
| Marked serious | 12.1% | 22.2% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 1 | 6 | 91 |
| Hospitalisation recorded, per 1,000 reports | 27 | 68 | 213 |
| Consumer-filed share | 97.1% | 92% | 45.8% |
| Top term, share of reports | Drug ineffective 20.3% | median 7.3% | 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 intestinal lipase inhibitor class
| Drug | Name type | Reports | Latest 12 months | Marked serious |
|---|---|---|---|---|
| Xenical | brand | 1,723 | 2 | 84.8% |
| Orlistat | generic | 1,456 | 64 | 95.2% |
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 Alli reports
How many adverse event reports has FDA received for Alli?
21,224 reports list Alli as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 139 of them arrived in the latest 12 months. Another 120 list it only as a concomitant medication.
What reactions are recorded in Alli reports?
drug ineffective (20.3%), rectal discharge (11.4%), gastrointestinal disorder (10.1%), constipation (8.9%) and weight increased (8.3%). 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 Alli was responsible.
How serious are the reports?
12.1% are marked serious by the reporter. Among the outcomes recorded, 0.1% of reports include death and 2.7% 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 (97.1%), pharmacist (0.8%) and physician (0.6%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Alli rising?
139 reports in the 12 months to June 2026, down 38% from 226 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 Alli 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 Alli?
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 Alli as a suspect or interacting product; reports listing it only as a concomitant medication (120) 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.