Solifenacin Succiate
Brand Names: Solifenacin Succinate
Methodology & AI Transparency ⓘ
Solifenacin Succiate Key Takeaways
Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level
- 1 What it does: Solifenacin Succinate Tablets is a muscarinic antagonist indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency.
- 2 Real-world patient consensus: Zero-PHI community consensus: 80% favorable across 20 logged regimens (Solifenacin Succinate).
- 3 Typical cash cost range: Public pharmacy ledger: $15.85 low cash benchmark vs. $38.83 chain retail average ($0.1816/unit CMS NADAC).
- 4 Top reported side effects / signs: Primary clinical safety signals tracked in FAERS for Solifenacin Succiate include constipation (8%), dry mouth (6.9%), blurred vision (4%).
Ask our AI Specialists anything about Solifenacin Succiate
Solifenacin Succiate Mechanism, CYP450 Pathways & DailyMed Monograph
Solifenacin Succinate Tablets is a muscarinic antagonist indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency. Solifenacin Succinate Tablets is a muscarinic antagonist indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency (1)
12.1 Mechanism of Action Solifenacin is a competitive muscarinic receptor antagonist. Muscarinic receptors play an important role in several major cholinergically mediated functions, including contractions of urinary bladder smooth muscle and stimulation of salivary secretion. 12.2 Pharmacodynamics Cardiac Electrophysiology The effect of 10 mg and 30 mg solifenacin succinate on the QT interval was evaluated at the time of peak plasma concentration of solifenacin in a multi-dose, randomized, double-blind, placebo and positive-controlled (moxifloxacin 400 mg) trial.
Clinical clearance of Solifenacin Succiate (Cholinergic Muscarinic Antagonist) relies on phase i cyp3a4 hepatic clearance and subsequent renal metabolite filtration with a Steady-state plasma equilibrium reached over 3–7 hour t½ intervals for Solifenacin Succiate half-life; patients absorbing at Approximately 58% to 70% enteral uptake across labeled Solifenacin Succiate strengths bioavailability typically observe target onset around maximum serum exposure occurs 2–4 hours after solifenacin succiate dosing.
FDA clinical labeling for Solifenacin Succiate restricts administration in contraindicated in patients with prior serious allergic response to solifenacin succiate (ndc 42291-739); severe baseline organ impairment where solifenacin succiate accumulation exceeds safe therapeutic margins across 5 mg/1 Tablet, Film Coated, 5 mg, 10 mg once daily, 30 ml, with self-reported patient tracking dominated by nausea (8.3% of reports), constipation (8% of reports), headache (7% of reports).
Azole antifungals or ritonavir can markedly raise Solifenacin Succiate plasma peaks; dose reduction may be warranted.
Co-prescribing strong CYP3A4 inhibitors or inducers can modify Solifenacin Succiate metabolic elimination kinetics.
Standard Adult Titration & Dosages
Absolute & Relative Contraindications
- Contraindicated in patients with prior serious allergic response to Solifenacin Succiate (NDC 42291-739)
- Severe baseline organ impairment where Solifenacin Succiate accumulation exceeds safe therapeutic margins
Logged Side-Effect Incidence (20 Reports)
Solifenacin Succiate Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs
Peer-Reviewed Human Clinical Trials & Meta-Analyses (Solifenacin Succiate)
| Study & Plain-English Finding | Sample (N) | Rigor | Primary Source |
|---|---|---|---|
| Can This Approach Help? Inside the Latest Research on Effect of tadalafil add-on therapy in patients with persistant storage symptoms Tadalafil add-on therapy was not inferior to solifenacin add-on therapy in terms of effect and safety. Lower urinary tract symptoms • 2019-05-15 • Randomized Controlled Trial | Multi-cohort | 82/100 | PMID 30251330 ↗ |
Solifenacin Succiate Public Price Transparency Ledger
| Dispensing Channel / Benchmark | Verification Source | Reference Cost | Details |
|---|---|---|---|
| Pharmacy Acquisition Cost (CMS NADAC) | CMS Medicaid NADAC Weekly National Survey | $0.1816/unit (~$5.45/30u) | Wholesale baseline |
| Average U.S. Walk-In Retail Cash Price | Chain Pharmacy Uninsured Cash Index | $38.83 / mo | Before coupon/insurance |
| Patient-Logged Out-of-Pocket Average | 20 Anonymous DotMD Community Micro-Logs | $15.85 / mo | View logs ↓ |
Solifenacin Succiate Federal Verification & Benchmark Summary
| Metric | Verified Benchmark | Source |
|---|---|---|
| Solifenacin Succiate RxNorm Concept ID | 477372 | U.S. National Library of Medicine (RxNorm) |
| CMS NADAC Pharmacy Acquisition Unit Cost | $0.1816 / unit | CMS Medicaid NADAC Weekly Feed |
| Walk-In Chain Pharmacy Cash Average | $38.83 / mo | U.S. Uninsured Retail Cash Index |
| Public Mail-Order Wholesale Benchmark | $15.85 / mo (Patient Mean) | Public Cash Reference |
| Real-World Patient Consensus | 80.00% Worth It (20 anonymous logs) | DotMD Zero-PHI Patient Ledger |
Solifenacin Succiate Patient Community, Cohort Filters & Dosage Logs
Evidence synthesis for Solifenacin Succiate: FDA labeling (2026-01-15, NDC 42291-739), CYP/interaction screening, and public pharmacy acquisition costs.
Share your real dosage and monthly out-of-pocket cost—no account, email, or IP stored.
Filter Solifenacin Succiate community threads and patient logs by age, biological sex, dosage, and treatment duration.