Medication for Overactive Bladder
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Cigna Home Delivery Pharmacy Drug List
Exclusive Cigna Home Delivery Pharmacy drug list If your prescription drug plan includes Exclusive Cigna Home Delivery Pharmacy, you are required to fill maintenance medication prescriptions (medications taken on an regular basis) through Cigna Home Delivery PharmacySM. Depending on your benefit plan, you are typically allowed three fills before you are required to use Cigna Home Delivery Pharmacy. At that time, if you choose not use Cigna Home Delivery Pharmacy, your plan will not cover the cost of your medication. To see real-time drug pricing, visit myCigna.com and use the Prescription Drug Price Quote tool to search for medications and compare pricing for your selected medications and lower-cost alternatives. The tool provides guidance on options you can discuss with your doctor and shows annual savings when you use Cigna Home Delivery Pharmacy. In addition to cost savings, Cigna Home Delivery Pharmacy offers valuable benefits, such as: • Licensed pharmacists available 24/7 • Up to a 90-day supply of medications in one fill • Standard delivery at no additional cost • Reminders if you forget to fill your prescriptions • Specialty medications, including those that require refrigeration and overnight delivery The following is a list of medications that apply to your Exclusive Cigna Home Delivery Pharmacy plan. Refer to your enrollment materials to understand the medications covered under your plan and to see if there are any requirements such as prior authorization (PA), quantity limits (QL) or Step Therapy (ST), as well as those requiring use of Cigna Home Delivery Pharmacy. If you have questions We’re here to help. Just call us at the toll-free number on your ID card and we will be happy to answer your questions. -
The National Drugs List
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The Effects of Oral Administration of the Novel Muscarinic Receptor
Choi et al. BMC Urology (2020) 20:41 https://doi.org/10.1186/s12894-020-00611-8 RESEARCH ARTICLE Open Access The effects of oral administration of the novel muscarinic receptor antagonist DA- 8010 on overactive bladder in rat with bladder outlet obstruction Jin Bong Choi1, Seung Hwan Jeon2, Eun Bi Kwon3, Woong Jin Bae4, Hyuk Jin Cho2, U-Syn Ha2, Sung-Hoo Hong2, Ji Youl Lee2 and Sae Woong Kim4* Abstract Background: DA-8010 is a novel compound developed for the treatment of overactive bladder (OAB) and urinary incontinence. The aims of this study were to investigate the effects of DA-8010 on OAB in a rat model. Methods: Study animals were divided into the following five groups of seven animals each: a sham-operated control group, a control group with partial bladder outlet obstruction (BOO) (OAB group), and three DA-8010 (doses of 0.3 mg/kg/day, 1 mg/kg/day, and 3 mg/kg/day, respectively) with partial BOO groups. Oral administration of the drugs was continued for 14 days after 2 weeks of partial BOO. After 4 weeks of partial BOO, cystometrography was performed in all groups. Additionally, pro-inflammatory cytokines, Rho-kinases, and histology of the bladder were analyzed. Results: There was a significant increase in the contraction interval and a decrease in contraction pressure in the 3 mg/kg/day DA-8010 group versus those in the OAB group. Rho kinase was also significantly decreased in the DA- 8010 3 mg/kg/day dosage treatment group. The increased ratio of collagen to smooth muscle after partial BOO was significantly attenuated in the DA-8010 3 mg/kg/day dosage group. -
Anticholinergic Drugs Improve Symptoms but Increase Dry Mouth in Adults with Overactive Bladder Syndrome
Source of funding: Evid Based Nurs: first published as 10.1136/ebn.6.2.49 on 1 April 2003. Downloaded from Review: anticholinergic drugs improve symptoms but Health Research Council of Aotearoa increase dry mouth in adults with overactive bladder New Zealand. syndrome For correspondence: Jean Hay-Smith, Hay-Smith J, Herbison P,Ellis G, et al. Anticholinergic drugs versus placebo for overactive bladder syndrome in adults. Dunedin School of Cochrane Database Syst Rev 2002;(3):CD003781 (latest version May 29 2002). Medicine, University of Otago, Dunedin, New QUESTION: What are the effects of anticholinergic drugs in adults with overactive Zealand. jean.hay-smith@ bladder syndrome? otago.ac.nz Data sources Parallel arm studies of anticholinergic drugs v placebo for overactive bladder syndrome in Studies were identified by searching the Cochrane adults at 12 days to 12 weeks* Incontinence Group trials register (to January 2002) Weighted event rates and reference lists of relevant papers. Anticholinergic Study selection Outcomes drugs Placebo RBI (95% CI) NNT (CI) Randomised or quasi-randomised controlled trials in Self reported cure or adults with symptomatic diagnosis of overactive bladder improvement (8 studies) 63% 45% 41% (29 to 54) 6 (5 to 8) syndrome, urodynamic diagnosis of detrusor overactiv- RRI (CI) NNH (CI) ity, or both, that compared an anticholinergic drug Dry mouth (20 studies) 36% 15% 138 (70 to 232) 5 (4 to 7) (given to decrease symptoms of overactive bladder) with Outcomes Weighted mean difference (CI) placebo or no treatment. Studies of darifenacin, emepronium bromide or carrageenate, dicyclomine Number of leakage episodes in 24 hours (9 − chloride, oxybutynin chloride, propiverine, propanthe- studies) 0.56 (–0.73 to –0.39) Number of micturitions in 24 hours (8 studies) −0.59 (–0.83 to –0.36) line bromide, tolterodine, and trospium chloride were Maximum cystometric volume (ml) (12 studies) 54.3 (43.0 to 65.7) included. -
Package Leaflet
Version 4, 02/2016 Propigen 5 mg coated tablets v005common PACKAGE LEAFLET 1 PACKAGE LEAFLET: INFORMATION FOR THE USER PROPIGEN 5 MG COATED TABLETS (PROPIVERINE HYDROCHLORIDE) Read all of this leaflet carefully before you or your child start taking this medicine because it contains important information for you. - Keep this leaflet. You may need to read it again. - If you have any further questions, ask your doctor or your pharmacist. - This medicine has been prescribed for you or your child, respectively, only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours or your child’s. - If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet (see section 4). The name of your medicine is Propigen 5 mg. The active substance is propiverine hydrochloride and the other ingredients are listed at the end of the leaflet (section 6, Contents of the pack and other information). What is in this leaflet: 1. What Propigen 5 mg is and what it is used for 2. What you need to know before you or your child take Propigen 5 mg 3. How to take Propigen 5 mg 4. Possible side effects 5. How to store Propigen 5 mg 6. Contents of the pack and other information 1. WHAT PROPIGEN 5 MG IS AND WHAT IT IS USED FOR Propigen 5 mg is used for the treatment of adults and children who have difficulty in controlling their bladder due to bladder overactivity or, in some cases, problems with the spinal cord. -
Urinary Antispasmodics TCO 02.2018
Therapeutic Class Overview Urinary antispasmodics INTRODUCTION • Overactive bladder (OAB) is defined as urinary urgency, with or without urge incontinence, usually with frequency and nocturia, in the absence of a causative infection or pathological conditions. Urinary incontinence has been shown to greatly reduce quality of life in areas such as mental and general health in addition to physical and social functioning (American Urological Association 2019, Coyne et al 2008, Haab 2014, International Continence Society 2015). Children with OAB usually have detrusor overactivity as diagnosed through cystometric evaluation. Neurogenic detrusor overactivity is predominantly caused by a congenital neural tube defect in children (Austin et al 2016, Franco ○ et al 2020). • Behavioral therapies (eg, bladder training, bladder control strategies, pelvic floor muscle training and fluid management) are considered first-line treatment in all patients with OAB (American Urological Association 2019). • Urinary antispasmodics are used as first-line pharmacological therapy in OAB (American College of Obstetricians and Gynecologists 2015, American Urological Association 2019, Blok et al 2020, Burkhard et al 2018). Anticholinergic therapy has been frequently used in patients with neurogenic detrusor overactivity, but there are limited data in this specific population (Haab 2014). • The○ urinary antispasmodics used for the treatment of OAB belong to 2 classes of drugs, which include anticholinergic compounds known as muscarinic receptor antagonists, and the beta-3 adrenergic agonist (AR), mirabegron. The anticholinergic agents act as antagonists of acetylcholine at muscarinic cholinergic receptors, thereby relaxing smooth muscle in the bladder and decreasing bladder contractions. ○ . Oral immediate-release (IR) and extended-release (ER) formulations (LA, XL, and XR) are available for oxybutynin (Ditropan), tolterodine (Detrol), and trospium. -
Solifenacin Succinate Tablets PI
465mm (18.31”) 32mm (1.26”) HIGHLIGHTS OF PRESCRIBING • Gastrointestinal Disorders: Use with 3 DOSAGE FORMS AND STRENGTHS Table 1. Percentages of Patients With Identified Adverse Reactions, Derived From Multiple dose studies of solifenacin succinate in elderly volunteers (65 to 80 years) FDA Approved Patient Labeling FDA Approved Patient Labeling INFORMATION caution in patients with decreased Solifenacin succinate tablets are available as follows: All Adverse Events Exceeding Placebo Rate and Reported by 1% or More Patients showed that Cmax, AUC and t1/2 values were 20 to 25% higher as compared to the These highlights do not include gastrointestinal motility (5.3) 5 mg – white, round, standard, normal convex, film-coated, unscored tablets, debossed for Combined Pivotal Studies younger volunteers (18 to 55 years). Solifenacin Succinate Tablets Solifenacin Succinate Tablets all the information needed to • Central Nervous System Effects: with “TV” on one side of the tablet and with “2N” on the other side of the tablet. Placebo Solifenacin Succinate Solifenacin Succinate 8.6 Renal Impairment Read the Patient Information that comes with Read the Patient Information that comes with use SOLIFENACIN SUCCINATE Somnolence has been reported with 10 mg – light-pink to pink, round, standard, normal convex, film-coated, unscored (%) 5 mg (%) 10 mg (%) Solifenacin succinate should be used with caution in patients with renal impairment. TABLETS safely and effectively. solifenacin succinate tablets before you start solifenacin succinate tablets before you start solifenacin succinate. Advise patients not tablets, debossed with “TV” on one side of the tablet and with “3N” on the other side Number of Patients 1216 578 1233 There is a 2.1 fold increase in AUC and 1.6 fold increase in t1/2 of solifenacin in patients See full prescribing information for to drive or operate heavy machinery until of the tablet. -
Solifenacin-Induced Delirium and Hallucinations☆
General Hospital Psychiatry 35 (2013) 682.e3–682.e4 Contents lists available at ScienceDirect General Hospital Psychiatry journal homepage: http://www.ghpjournal.com Case Report Solifenacin-induced delirium and hallucinations☆ Matej Štuhec, Pharm.D. ⁎ Ormoz Psychiatric Hospital, Department for Clinical Pharmacy, Slovenia, Ptujska Cesta 33, Ormoz, Slovenia article info abstract Article history: Solifenacin-induced cognitive adverse effects have not been reported frequently, but solifenacin-induced Received 11 April 2013 delirium and hallucinations with successful switching to darifenacin, without additional drug, have not been Revised 5 June 2013 reported in the literature. In this case report, we present an 80-year-old Caucasian male with insomnia and Accepted 5 June 2013 anxiety symptoms and overactive bladder who developed delirium and hallucinations when treated with Keywords: solifenacin and trazodone. After solifenacin discontinuation and switching to darifenacin, symptoms significantly improved immediately. Such a case has not yet been described in literature; however, an Solifenacin Delirium adverse effect associated with solifenacin can occur, as this report clearly demonstrates. Hallucinations © 2013 Elsevier Inc. All rights reserved. Darifenacin Antimuscarinic adverse effect Case report 1. Introduction tion of Diseases, 10th Revision (ICD-10)], and depression with psychotic features was ruled out with differential diagnosis. Patient reported Solifenacin is a competitive muscarinic receptor antagonist, which insomnia, fear, fatigue, nausea, chest pain, shortness of breath and is used for overactive bladder (OAB) treatment. It acts as an headache. Solifenacin (Vesicare) 5 mg daily in morning dose was antimuscarinic agent, showing the highest affinity for the muscarinic prescribed to him 1 week earlier by his physicians because of OAB. M(3) receptor, which mediates urinary bladder contraction. -
Magellan Anticholinergic Risk Scale
Magellan Anticholinergic Risk Scale 1 POINT 2 POINTS 3 POINTS GENERIC BRAND GENERIC BRAND GENERIC BRAND Alprazolam Xanax® Amantadine Symmetrel® Amitriptyline Elavil® Aripiprazole Abilify® Baclofen Lioresal® Amoxapine Asendin® Asenapine Saphris® Carbamazepine Tegretol® Atropine -- Captopril Capoten® Carisoprodol Soma® Benztropine Cogentin® Chlordiazepoxide Librium® Cetirizine Zyrtec® Brompheniramine Respa-BR® Chlorthalidone Diuril® Cimetidine Tagamet® Carbinoxamine Arbinoxa® Clonazepam Klonopin® Clidinium & Librax® Chlorpheniramine Chlor-Trimeton® Chlordiazepoxide Clorazepate Tranxene® Cyclizine Cyclivert® Chlorpromazine Thorazine® Codeine -- Cyclobenzaprine Flexeril® Clemastine Tavist® Diazepam Valium® Cyproheptadine Periactin® Clomipramine Anafranil® Digoxin Lanoxin® Disopyramide Norpace® Clozapine Clozaril® Dipyridamole Persantine® Fluphenazine Prolixin® Darifenacin Enablex® Famotidine Pepcid® Loperamide Diamode® Desipramine Norpramin® Fentanyl Duragesic® Loratadine Claritin® Dicyclomine Bentyl® Fluoxetine Prozac® Loxapine Loxitane® Dimenhydrinate Dramamine® Flurazepam Dalmane® Meperidine Demerol® Diphenhydramine Benadryl® Fluvoxamine Luvox® Methocarbamol Robaxin® Doxepin Sinequan® Furosemide Lasix® Oxcarbazepine Trileptal® Flavoxate Urispas® Haloperidol Haldol® Pimozide Orap® Glycopyrrolate Robinul® Hydralazine Apresoline® Prochlorperazine Compazine® Hydroxyzine Atarax® Iloperidone Fanapt® Pseudoephedrine Sudafed® Hyoscyamine Anaspaz® Isosorbide Imdur® Quetiapine Seroquel® Imipramine Tofranil® Mirtazapine Remeron® Trimethobenzamide -
Guideline for Preoperative Medication Management
Guideline: Preoperative Medication Management Guideline for Preoperative Medication Management Purpose of Guideline: To provide guidance to physicians, advanced practice providers (APPs), pharmacists, and nurses regarding medication management in the preoperative setting. Background: Appropriate perioperative medication management is essential to ensure positive surgical outcomes and prevent medication misadventures.1 Results from a prospective analysis of 1,025 patients admitted to a general surgical unit concluded that patients on at least one medication for a chronic disease are 2.7 times more likely to experience surgical complications compared with those not taking any medications. As the aging population requires more medication use and the availability of various nonprescription medications continues to increase, so does the risk of polypharmacy and the need for perioperative medication guidance.2 There are no well-designed trials to support evidence-based recommendations for perioperative medication management; however, general principles and best practice approaches are available. General considerations for perioperative medication management include a thorough medication history, understanding of the medication pharmacokinetics and potential for withdrawal symptoms, understanding the risks associated with the surgical procedure and the risks of medication discontinuation based on the intended indication. Clinical judgement must be exercised, especially if medication pharmacokinetics are not predictable or there are significant risks associated with inappropriate medication withdrawal (eg, tolerance) or continuation (eg, postsurgical infection).2 Clinical Assessment: Prior to instructing the patient on preoperative medication management, completion of a thorough medication history is recommended – including all information on prescription medications, over-the-counter medications, “as needed” medications, vitamins, supplements, and herbal medications. Allergies should also be verified and documented. -
Vesicare (Solifenacin Succinate)
VESIcare® (solifenacin succinate) Tablets Description VESIcare® (solifenacin succinate) is a muscarinic receptor antagonist. Chemically, solifenacin succinate is butanedioic acid, compounded with (1S)-(3R)-1-azabicyclo[2.2.2]oct-3-yl 3,4 dihydro-1-phenyl-2(1H)-iso-quinolinecarboxylate (1:1) having an empirical formula of C23H26N2O2•C4H6O4, and a molecular weight of 480.55. The structural formula of solifenacin succinate is: Solifenacin succinate is a white to pale-yellowish-white crystal or crystalline powder. It is freely soluble at room temperature in water, glacial acetic acid, dimethyl sulfoxide, and methanol. Each VESIcare tablet contains 5 or 10 mg of solifenacin succinate and is formulated for oral administration. In addition to the active ingredient solifenacin succinate, each VESIcare tablet also contains the following inert ingredients: lactose monohydrate, corn starch, hypromellose 2910, magnesium stearate, talc, polyethylene glycol 8000 and titanium dioxide with yellow ferric oxide (5 mg VESIcare tablet) or red ferric oxide (10 mg VESIcare tablet). Clinical Pharmacology 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. Pharmacokinetics Absorption After oral administration of VESIcare to healthy volunteers, peak plasma levels (Cmax) of solifenacin are reached within 3 to 8 hours after administration, and at steady state ranged from 32.3 to 62.9 ng/mL for the 5 and 10 mg VESIcare tablets, respectively. The absolute bioavailability of solifenacin is approximately 90%, and plasma concentrations of solifenacin are proportional to the dose administered. Effect of food There is no significant effect of food on the pharmacokinetics of solifenacin. -
Solifenacin Succinate Tablets, 5 Mg and 10 Mg
Solifenacin Succinate Tablets, 5 mg and 10 mg S.No. Category Question Answer Clinical Particulars 1 Use/Indication What is the product Solifenacin succinate tablet is a muscarinic antagonist indicated for? indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency 2 Dosage What is the • 5 mg tablet taken once daily, and if well tolerated may be recommended increased to 10 mg once daily. dosage? • Do not exceed 5 mg tablet once daily in patients with: Severe renal impairment [Creatinine Clearance](CLcr <30 ml/min). Moderate hepatic impairment (Child-Pugh B). Concomitant use of potent CYP3A4 inhibitors. • Use of solifenacin succinate tablets is not recommended in patients with severe hepatic impairment (Child-Pugh C) 3 Administration What do I do if I If you miss a dose of solifenacin succinate tablets, begin miss a dose? taking solifenacin succinate tablets again the next day. Do not take 2 doses of solifenacin succinate tablets the same day. 4 Administration Use in Pediatric The safety and effectiveness of solifenacin succinate in Population pediatric patients have not been established. 5 Administration Use in Geriatric No overall differences in safety and efficacy were Population observed between these patients and younger patients. 6 Mechanism Mechanism of Solifenacin is a competitive muscarinic receptor Action 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. 7 Warning Black Box Warning No black box warning 8 Lactation Use in Lactation Solifenacin succinate should not be administered during nursing.