Page 15 - P4304.1-V92_PS-Magazine-December 2023 PRINT
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The material is intended for UK healthcare professionals only and has been co-developed by Gedeon Richter and PSUK Prescribing
             information can be found on the following page.

 Kentera® (oxybutynin)



 3.9mg/24h Transdermal Patch





 8 Patch

             Benilexa  One Handed
                                                       ®

 Kentera® (oxybutynin) 3.9mg/24h
 Product Presentation
 Transdermal patch
 Pack Size  8 Patch
 Product Format  Transdermal Patch  New MDS
 Legal Category  POM
 Pack Dimensions (HxWxD)  108mm x 25mm x 95mm  PSUK are delighted to announce a NEW and EXCLUSIVE MDS discount
 Shelf Life  36 months  BACK IN STOCK • BACK IN STOCK • BACK IN STOCK • BACK IN STOCK • BACK IN STOCK • BACK IN STOCK • BACK IN STOCK •  available to Dispensing Doctors on Benilexa 52MD.
             This new MDS ensures that dispensing practices can make a saving on the NHS
 PIP Code  315-0018  . . .
 EAN Code  5012617001962  BACK IN   cost and a increased profit vs comparable intauterine contraceptive devices.

 STOCK                                                                   Gedeon Richter offer product
 . . .        Product Description                    Benilexa
 Prescribing Information   Supplier               Gedeon Richter         demonstrations, demonstration placebo
                                                     4195178
              Pip Code
 Kentera® (oxybutynin) 3.9mg/24h Transdermal patch                       devices and support materials for both
                                  Reimbursement                          healthcare professionals and patients.
 Please refer to the Summary of Product Characteristics (SmPC) before prescribing.
              Drug Tariff Price:                      £71.00
                                                                         In addition to the discounts, Benelexa
              Clawback (at 11.18%)                    -£7.94
 Presentation:  Each transdermal patch contains 36mg of   evidence there is no need for dose adjustment in elderly patients.  When oxybutynin  is used  during breast-feeding, a small  amount is   will attract a 20% PA fee meaning
 oxybutynin.  The area of the patch is 39cm2, releasing a nominal   Psychiatric and central nervous system (CNS) anticholinergic events  excreted in the mother’s milk. Use of oxybutynin while breast-feeding   Price after Clawback:  £63.06  dispensing this product will generate
 3.9 mg of oxybutynin per 24 hours. The patch is a clear plastic with an  like sleep disorders (e.g. insomnia) and cognitive disorders have been  is therefore not recommended.
 adhesive backing, protected by a release liner that is to be removed prior  associated with oxybutynin use, especially in elderly patients. Caution   +Dispensing Fee  £2.26  a profit for the practice of £17.48
 to application.   should be exercised when oxybutynin is administrated concomitantly   Adverse Events include:  +PA Admin Fee  £12.61  once clawback has been taken into
 Indications: Symptomatic treatment of urge incontinence and/or   with other anticholinergic medicines. If patients experience such   Adverse events which could be considered serious: Urinary tract infection,   consideration.
 increased urinary frequency and urgency as may occur in adult patients   events, drug discontinuation should be considered. Other psychiatric  upper respiratory tract infection, fungal infection, delirium, hallucinations,   Total Reimbursed:  £77.93
 with unstable bladder.  events implying an anticholinergic mechanism have been reported  amnesia, rhinitis, urinary retention, tachycardia, arrhythmia, convulsion,   Cost to Surgery
 during post-marketing use. Gastrointestinal disorders: Anticholinergic  intraocular hypertension, glaucoma, erectile dysfunction.  Please contact:
 Dosage and Administration: The patch should be applied to dry,   medicinal products may decrease gastrointestinal motility and should   PSUK Member MDS Rebate  20.00%  devicesupport@gedeonrichter.com to
 intact skin on the abdomen, hip, or buttock immediately after removal   be used with caution in patients with gastrointestinal obstructive   Other Very Common adverse events: Application site pruritis.
 from the protective sachet. A new application site should be selected   disorders because of the risk of gastric retention. Also in conditions  Other Common adverse events: Headache, somnolence, blurred vision,   Nett Price (Incl. discount)  £56.80  order any of these items/services.
 with each new patch to avoid reapplication to the same site within     such as ulcerative colitis, and intestinal atony. Anticholinergic medicinal  dizziness, dry mouth, constipation, diarrhoea, nausea, abdominal pain,
 7 days. The recommended dose is one 3.9 mg transdermal patch applied   products should be used with caution in patients who have hiatus  application site erythema, application site reaction, application site rash.  +VAT (@5%)  £3.55
 twice weekly (every 3 to 4 days). Elderly: No dose adjustment required.   hernia/gastro-oesophageal reflux and/or who are concurrently taking
 Paediatric population: Safety and efficacy have not been established     medicinal products (such as bisphosphonates) that can cause or   See SmPC for details of other adverse events.  Total Cost to Practice:  £60.35
 so not recommended.  exacerbate oesophagitis. Anticholinergic medicinal products should  Presentation and Price: 8 patches £27.20  Profit to Surgery
 Contraindications: Hypersensitivity to the active substance or to any  be used with caution in patients who have autonomic neuropathy,   Legal Category: POM
 of the excipients. Contraindicated in patients with urinary retention,  cognitive impairment or Parkinson’s disease. Patients should be   Total Reimbursement:  £77.93
 severe gastro-intestinal condition, myasthenia gravis or narrow-angle  informed that heat prostration (fever and heat stroke due to decreased  Further information is available from:
 glaucoma and in patients who are at risk for these conditions.  sweating) can occur when anticholinergics such as oxybutynin are  Accord-UK Ltd, Whiddon Valley, Barnstaple, Devon, EX32 8NS.   Cost to Practice:  (£60.35)
 Warnings and Precautions: Kentera should be used with caution   used in a hot environment. Oxybutynin may exacerbate the symptoms   Marketing Authorisation Numbers: PLGB 0142/1151  Profit per dose:  £17.58
 in patients  with hepatic  or renal  impairment, and  patients with   of hyperthyroidism, coronary heart disease, congestive heart
 failure, cardiac  arrhythmias,  tachycardia,  hypertension  and  prostatic  Date of PI Preparation: February 2022
 hepatic impairment should be carefully monitored. Other causes of
 frequent urination (heart failure or renal disease) should be assessed   hypertrophy. Oxybutynin may lead to suppressed salivary secretions   Document number: UK-03757
 before treatment with Kentera. If urinary tract infection is present,   which could result in dental caries, parodontosis or oral candidiasis.
 appropriate antibacterial therapy should be started. Urinary retention:   Effects on ability to drive and use machines: Kentera may produce   Adverse events should be reported.
 Anticholinergic products should be administered with caution to   drowsiness, somnolence, or blurred vision, therefore patients should be   Reporting forms and information can be found at
 patients with clinically significant bladder outflow obstruction because   advised to exercise caution when driving or using machinery.  www.mhra.gov.uk/yellowcard
 of the risk of urinary retention. Use with caution in elderly patients, who  Fertility, Pregnancy & Lactation:  There are no adequate data
 may be more sensitive to the effects of centrally acting anticholinergics  on the use of oxybutynin transdermal patch in pregnant women.     Adverse events should also be reported to Accord-UK LTD on
 01271 385257 or email medinfo@accord-healthcare.com.
             Order now                                                           01904 558 360
 and exhibit differences in pharmacokinetics. Based on current clinical  Kentera should not be used during pregnancy unless clearly necessary.   or call:
 UK-04230     |  Date of Preparation: July 2022  online at:
              Adverse events shou ld be reported. Reporting forms and information can be fo und at
              https:ljyellowcard.mhra.gov.uk/, or you can report via t he Yellow Card app which is available to
              download from the Apple App Store or Google Play St ore. Adverse events should also be reported to   UK--2300181
              Gedeon Richter (UK) Ltd on +44 (0) 207 604 8806 or by emai l to drugsafety.uk@gedeonrichter.eu      October 2023
                                                                                                                 P4260.306-V2
                                                                                                                    15
               or call us on 01904 558 350                                    MDS Terms Information | PS Magazine   15

         P4304.1-V92_PS-Magazine-December 2023.indd   15                                                         09/11/2023   10:39:19
         P4304.1-V92_PS-Magazine-December 2023.indd   15
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