Drugs › Cholinergic muscarinic antagonist
Generic name
Solifenacin succinate: adverse event reports filed with FDA
575 reports list it as a suspect or interacting product, 2008–2026. Class: Cholinergic muscarinic antagonist.
- 575
- reports as suspect product
- 0% of all reports · about 31 a year
- 137
- reports, 12 months to June 2026
- 106 in the 12 months before
- 87.7%
- marked serious by the reporter
- 39.8% across the class
- 5.6%
- record death among outcomes, as reported
- 32 reports · not verified by FDA
575 adverse event reports received by FDA list solifenacin succinate, a generic name as a suspect or interacting product, from February 2008 to June 2026. A further 1,302 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, 137 reports listed it, up 29% from 106 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 31 reports a year and 0% of the 20,646,523 reports in the database, and 3.1% of the reports for the cholinergic muscarinic antagonist 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 hypotension (11.3%), constipation (10.6%) and cerebral hypoperfusion (8.7%). A report can list several reactions, so shares add to more than 100%; 250 different terms appear across these reports. Hypotension is recorded in 11.3% of these reports, a larger share than in the median cholinergic muscarinic antagonist drug (0.3%).
87.7% of the reports are marked serious by the reporter (39.8% across the class); 5.6% record death among the outcomes and 22.6% record hospitalisation, as reported. 35.1% of the reports came from consumers, and the largest patient age group is 75 and over (24%). 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 Solifenacin succinate reports recording the termmedian drug in cholinergic muscarinic antagonist
- Hypotensionlow blood pressure11.3%65
- Constipationconstipation10.6%61
- Cerebral hypoperfusion8.7%50
- Dizzinesslight-headedness or unsteadiness8.3%48
- Drug ineffectivethe medicine did not work as expected8.3%48
- Gait disturbancedifficulty walking8.3%48
- Speech disordera speech problem8.3%48
- Feeling coldfeeling cold8.2%47
- Falla fall7.1%41
- Dry mouthdry mouth6.8%39
- Fatiguetiredness6.1%35
- Balance disorderproblems with balance4.9%28
- Diplopiadouble vision4.5%26
- Abdominal distensiona bloated abdomen4.3%25
- Malaisegeneral feeling of being unwell4.3%25
- Nocturia4.3%25
- Depressionlow mood4.2%24
- Dysarthria4.2%24
- Micturition urgency4.2%24
- Binocular eye movement disorder4%23
- Cerebellar stroke4%23
- Dysphoniaa hoarse voice4%23
- Neuralgia4%23
- Neuropathy peripheralnerve damage in hands or feet4%23
- Presyncope4%23
- Urinary retentionbeing unable to empty the bladder4%23
- Condition aggravatedthe condition being treated got worse3.8%22
- Diarrhoealoose or frequent stools3.7%21
- Drug interactionan interaction between medicines3.3%19
Top 30 of 250 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 9 drugs in the cholinergic muscarinic antagonist 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 18,647 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. 18.4% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Hypertonic bladder | 86 | 15% |
| Urinary incontinence | 34 | 5.9% |
| Pollakiuria | 11 | 1.9% |
| Nocturia | 9 | 1.6% |
| Ill-defined disorder | 8 | 1.4% |
| Micturition urgency | 8 | 1.4% |
The indication field is filled in by the reporter and is often blank; shares are of all 575 reports.
In context
| Measure | Solifenacin succinate | Cholinergic muscarinic antagonist | All reports |
|---|---|---|---|
| Reports as suspect product | 575 | 18,647 | 20,646,523 |
| Share of that pool | — | 3.1% | 0% |
| Reports, latest 12 months | 137 | — | 1,332,454 |
| Marked serious | 87.7% | 39.8% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 56 | 42 | 91 |
| Hospitalisation recorded, per 1,000 reports | 226 | 135 | 213 |
| Consumer-filed share | 35.1% | 66.4% | 45.8% |
| Top term, share of reports | Hypotension 11.3% | median 0.3% | 1% |
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 cholinergic muscarinic antagonist class
| Drug | Name type | Reports | Latest 12 months | Marked serious |
|---|---|---|---|---|
| Oxytrol for Women | brand | 6,283 | 80 | 0.9% |
| Detrol | brand | 4,851 | 15 | 55.8% |
| Oxybutynin | generic | 2,996 | 178 | 61.8% |
| Oxybutynin chloride | generic | 1,133 | 52 | 59.9% |
| Tolterodine tartrate | generic | 942 | 7 | 63.9% |
| Oxytrol | brand | 803 | 125 | 23% |
| Tolterodine | generic | 552 | 47 | 82.2% |
| Trospium chloride | generic | 512 | 58 | 72.7% |
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 Solifenacin succinate reports
How many adverse event reports has FDA received for Solifenacin succinate?
575 reports list Solifenacin succinate as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 137 of them arrived in the latest 12 months. Another 1,302 list it only as a concomitant medication.
What reactions are recorded in Solifenacin succinate reports?
hypotension (11.3%), constipation (10.6%), cerebral hypoperfusion (8.7%), dizziness (8.3%) and drug ineffective (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 Solifenacin succinate was responsible.
How serious are the reports?
87.7% are marked serious by the reporter. Among the outcomes recorded, 5.6% of reports include death and 22.6% 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 (35.1%), other health professional (31.1%) and physician (23.5%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Solifenacin succinate rising?
137 reports in the 12 months to June 2026, up 29% from 106 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 Solifenacin succinate 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 Solifenacin succinate?
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 Solifenacin succinate as a suspect or interacting product; reports listing it only as a concomitant medication (1,302) 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.