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Drugs. ;68(12) Fentanyl transdermal matrix patch (Durotep MT patch; Durogesic DTrans; Durogesic SMAT): in adults with cancer-related pain. Indications, side effects, contraindications and other prescribing information for Durogesic DTrans on MIMS. Following an abbreviated submission. transdermal fentanyl (Durogesic D Trans patches) 12 mcg/hour is accepted for restricted use within NHS.

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Therefore, they must keep all patches out of the sight and reach of children, both before and after use. Gastrointestinal tract Opioids increase the tone and decrease the propulsive contractions of the smooth muscle of the gastrointestinal tract. To help us improve GOV. Access PIL of durayesic month via our website.

transdermal fentanyl (Durogesic D Trans 12mcg/hr)

Physicochemical Principles of Pharmacy This established textbook covers every aspect of drug properties from the design of dosage forms to their delivery by all routes to sites of action in the body. Durogesic D Trans Transdermal Patch. The Durogesic DTrans patch should be replaced dursgesic 72 hours. Introduction to Renal Therapeutics Introduction to Renal Therapeutics covers all aspects of drug use in renal failure. This delay is due to the gradual increase in serum fentanyl concentration in the 24 hours following initial patch application.

The concomitant use of buprenorphine, nalbuphine or pentazocine is not recommended see also section 4. If patients with hepatic impairment receive Durogesic DTrans, they should be observed carefully for signs of fentanyl toxicity and the dose of Durogesic DTrans reduced if necessary see section 5.

This class of medicine is in the list of drugs included in regulations under 5a of the Road Traffic Act To view the changes to a medicine you must sign up and log in. Want to keep up with the latest news, comment and CPD articles in pharmacy and science? A patient who is treated with Durogesic Duragrsic should wait at least 1 week after removal of the last patch before initiating treatment with a CYP3A4 inhibitor.

Soaps, oils, lotions, or any other agent that might irritate the skin or alter its characteristics should not be used. The potential for serious or life-threatening hypoventilation exists regardless of the dose of Durogesic DTrans d-hrans system administered. The appropriate initiating dose of Durogesic DTrans should be based on the patient’s current opioid use. Hypoaesthesia, Convulsion including clonic convulsions and grand mal convulsionAmnesia, Depressed level of consciousness, Loss of consciousness.

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Durogesic DTrans 12 mcg/hr Transdermal Patch

vuragesic Introduction to Renal Therapeutics covers all aspects of drug use in renal failure. The safety of Durogesic DTrans was evaluated in 1, adult and paediatric subjects who participated in 11 clinical studies 1 double-blind, placebo-controlled; 7 open-label, active-controlled; 3 duragesi, uncontrolled used for the management of chronic malignant or non-malignant pain. To derive the Durogesic DTrans dosage corresponding to the calculated hour, equianalgesic morphine dosage, use dosage-conversion Table 2 or 3 as follows: UK uses cookies to make the site simpler.

Some patients may experience significant respiratory depression with Durogesic DTrans; patients must be observed for these effects.

Written for new pharmaceutical scientists, this book provides a background in paediatric pharmacy and a comprehensive introduction to children’s medication. The treatment of cancer pain. Pregnancy There are no adequate data from the use of Durogesic DTrans in pregnant women.

Severe and unpredictable interactions with MAOIs, involving the potentiation of opiate effects or the potentiation of serotoninergic effects, have been reported. For commenting, please login or register as a user and agree to our Community Guidelines. PIL of the month: Reporting suspected adverse reactions after authorisation of the medicinal product is important.

To calculate the appropriate starting dose of Durogesic DTrans, follow the steps below. The lowest effective dose should be used. Patients should be advised that if accidental patch transfer occurs, the transferred patch must be removed immediately from the skin of the non-patch wearer see section 4. To bookmark a medicine you must sign up and log in.

The concentration gradient existing between the system and the lower concentration in the skin drives drug release. Optimise drug ruragesic for your patients.

Durogesic DTrans 12 mcg/hr Transdermal Patch – Summary of Product Characteristics (SmPC) – (eMC)

Patients at increased risk of opioid abuse may still be appropriately treated with modified-release opioid formulations; however, these patients will require d-tranx for signs of misuse, abuse, or addiction.


Any unused durageskc product or waste material should be disposed of in accordance with local requirements. Name of the medicinal product 2. The interval between IV antagonist doses should be carefully chosen because of the possibility of re-narcotisation after the patch is removed; repeated administration or a continuous infusion of naloxone may be necessary.

Then wash hands with clean water. Tolerance, physical dependence, and psychological dependence can develop on repeated use of Durogesic DTrans see section 4. Following Durogesic DTrans application, the skin under the system absorbs fentanyl, and a depot of fentanyl concentrates in the upper skin layers. American Society of Health-System Pharmacists; The concomitant use of Durogesic DTrans with cytochrome P 3A4 CYP3A4 inhibitors may result in an increase in fentanyl plasma concentrations, which could increase or prolong both the therapeutic and adverse effects, and may cause serious respiratory depression.

It is recommended that Durogesic DTrans be used in patients who have demonstrated opioid tolerance. Durogesic DTrans should be applied to non-irritated and non-irradiated skin on a flat surface of the torso or upper arms. However, the duration of inhibition varies and for some CYP3A4 inhibitors with a long elimination half-life, such as amiodarone, or for time-dependent inhibitors such as erythromycin, idelalisib, nicardipine and ritonavir, this period may duragwsic to be longer.

It also crosses the placenta and is excreted in breast milk.

Paediatric population Interaction studies duragesif only been performed in adults. No risk was identified in the paediatric population beyond that expected with the use of opioids for the relief of pain associated with serious illness and there does not appear to be any paediatric-specific risk associated with Durogesic DTrans use in children as young as 2 years old when used as directed. The adverse reactions are presented by System Organ Class and in order of decreasing seriousness dudagesic each frequency category.


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