This information is intended for use by health professionals
Cynril 400 micrograms compressed lozenges with integral oromucosal applicator
Cynril 400 microgram compressed lozenges
One compressed lozenge contains 400 micrograms fentanyl (as citrate).
Excipients with known effect
One compressed lozenge contains 1.89g of glucose (as hydrated dextrates)
For the full list of excipients, see section 6.1.
Cynril is a white or slightly yellowish cylindrical lozenge of 17 – 20 mm of thickness and 11 – 12 mm of diameter, on which its respective dosage strength is printed, attached to a plastic handle at the opposite end also labelled with the dosage strength. The lozenges may develop brownish spots during storage.
Cynril is indicated for management of breakthrough pain in patients already receiving maintenance opioid therapy for chronic cancer pain. Breakthrough pain is a transitory exacerbation of pain that occurs on a background of persistent pain controlled by other means.
Patients receiving maintenance opioid therapy are those who are taking at least 60 mg of oral morphine daily, at least 25 micrograms of transdermal fentanyl per hour, at least 30 mg of oxycodone daily, at least 8 mg of oral hydromorphone daily or an equianalgesic dose of another opioid for a week or longer.
In order to minimise the risks of opioid-related side-effects and to identify the “successful” dose, it is imperative that patients be monitored closely by health professionals during the titration process or dose adjustment.
Cynril is not interchangeable on a mcg to mcg basis with other short-acting fentanyl products that are indicated for the use of breakthrough cancer pain, as the pharmacokinetic profiles and/or dosing schedules of these products are significantly different. Patients should be instructed not to use more than one short-acting fentanyl product concurrently for the treatment of breakthrough cancer pain, and to dispose of any fentanyl product prescribed for breakthrough pain (BTP) when switching to Cynril. The number of Cynril strengths available to the patient at any time should be minimised to prevent confusion and potential overdose.
Any unused Cynril units that the patient no longer requires must be disposed of properly. Patients must be reminded of the requirements to keep Cynril stored in a location away from children.
Dose titration and maintenance therapy
Cynril should be individually titrated to a “successful” dose that provides adequate analgesia and minimises adverse reaction. In clinical trials the successful dose of Cynril for breakthrough pain was not predicted from the daily maintenance dose of opioid.
Before patients are titrated with Cynril, it is expected that their background persistent pain will be controlled by use of opioid therapy and that they are typically experiencing no more than 4 episodes of breakthrough pain per day.
The initial dose of Cynril used should be 200 micrograms, titrating upwards as necessary through the range of available dosage strengths (200, 400, 600, 800, 1200 and 1600 micrograms). Patients should be carefully monitored until a dose is reached that provides adequate analgesia with acceptable adverse reaction using a single dosage unit per episode of breakthrough pain. This is defined as the successful dose.
During titration, if adequate analgesia is not obtained within 30 minutes after starting the first unit (i.e. 15 minutes after the patient completes consumption of a single Cynril unit), a second Cynril unit of the same strength may be consumed. No more than two Cynril units should be used to treat any individual pain episode. At 1600 micrograms, a second dose is only likely to be required by a minority of patients.
If treatment of consecutive breakthrough pain episodes requires more than one dosage unit per episode, an increase in dose to the next higher available strength should be considered.
Cynril Titration Process
*Dose concentration available are 200, 400, 600, 800, 1200 and 1600 micrograms.
Once a successful dose has been established (i.e., on average, an episode is effectively treated with a single unit), patients should be maintained on this dose and should limit consumption to a maximum of four Cynril units per day.
Patients should be monitored by a health professional to ensure that the maximum consumption of four units of Cynril per day is not exceeded.
The maintenance dose of Cynril should be increased when an episode is not effectively treated with a single unit for several consecutive BTP episodes. For dose- readjustment the same principles apply as outlined for dose titration (see above).
If more than four episodes of breakthrough pain are experienced per day the dose of the long acting opioid used for persistent pain should be re-evaluated. If the dose of the long acting opioid is increased, the dose of Cynril to treat breakthrough pain may need to be reviewed.
In absence of adequate pain control, the possibility of hyperalgesia, tolerance and progression of underlying disease should be considered (see section 4.4).
It is imperative that any dose re-titration of any analgesic is monitored by a health professional.
Discontinuation of therapy
Cynril should be discontinued immediately if the patient no longer experiences breakthrough pain episodes. The treatment for the persistent background pain should be kept as prescribed.
If discontinuation of all opioid therapy is required, the patient must be closely followed by the doctor as gradual downward opioid titration is necessary in order to avoid the possibility of abrupt withdrawal effects.
Use in the elderly
Elderly patients have been shown to be more sensitive to the effects of fentanyl when administered intravenously. Therefore dose titration needs to be approached with particular care. In the elderly, elimination of fentanyl is slower and the terminal elimination half-life is longer, which may result in accumulation of the active substance and to a greater risk of undesirable effects.
Formal clinical trials with Cynril have not been conducted in the elderly population. It has been observed, however, in clinical trials that patients over 65 years of age required lower doses of fentanyl for successful relief of breakthrough pain.
Use in patients with hepatic or renal impairment
Special care should be taken during the titration process in patients with kidney or liver dysfunction (see section 4.4).
Adolescents aged 16 years and above:
Follow adult dosage
Children aged 2 to 16 years old:
There is limited clinical trial experience of the use of Cynril in paediatric patients already receiving maintenance opioid therapy (see sections 5.1 and 5.2). Safety and efficacy in paediatric patients below the age of 16 years have not been established; use in this patient population is therefore not recommended.
Method of administration
Cynril is intended for oromucosal administration, and therefore should be placed in the mouth against the cheek and should be moved around the mouth using the applicator, with the aim of maximising the amount of mucosal exposure to the product. The Cynril unit should be sucked, not chewed, as absorption of fentanyl via the buccal mucosa is rapid in comparison with systemic absorption via the gastrointestinal tract. Water may be used to moisten the buccal mucosa in patients with a dry mouth.
The Cynril unit should be consumed over a 15- minute period. If signs of excessive opioid effects appear before the Cynril unit is fully consumed it should be immediately removed, and consideration given to decreasing future dosages.
• Hypersensitivity to fentanyl or to any of the excipients listed in section 6.1.
• Patients without maintenance opioid therapy (see section 4.4) as there is an increased risk of respiratory depression.
• Treatment of acute pain other than breakthrough pain (e.g. postoperative pain, headache, migraine).
• Simultaneous use with monoamine oxidase inhibitors (MAOIs), or within 2 weeks after cessation of the use of MAOIs inhibitors (see sections 4.4 and 4.5).
• Severe respiratory depression or severe obstructive lung conditions.
• Patients being treated with medicinal products containing sodium oxybate.
Accidental use in children
Patients and their carers must be instructed that Cynril contains an active substance in an amount that can be fatal to a child. Death has been reported in children who have accidentally ingested Cynril.
Patients and their carers must be instructed to keep all units out of the reach and sight of children and to discard open and unopened units appropriately. An evaluation of each out- patient concerning possible accidental child exposures should be undertaken.
Maintenance opioid therapy
The product should not be given to patients without maintenance opioid therapy as there is an increased risk of respiratory depression and death. It is important that the maintenance opioid therapy used to treat the patient's persistent pain has been stabilized before Cynril therapy begins and that the patient continues to be treated with the maintenance opioid therapy whilst taking Cynril.
Opioid Use Disorder (abuse and dependence)
Tolerance and physical and/or psychological dependence may develop upon repeated administration of opioids such as fentanyl. Iatrogenic addiction following therapeutic use of opioids is known to occur.
Repeated use of Cynril may lead to Opioid Use Disorder (OUD). Abuse or intentional misuse of Cynril may result in overdose and/or death. The risk of developing OUD is increased in patients with a personal or a family history (parents or siblings) of substance use disorders (including alcohol use disorder), in current tobacco users or in patients with a personal history of other mental health disorders (e.g. major depression, anxiety and personality disorders).
Patients will require monitoring for signs of drug-seeking behaviour (e.g. too early requests for refills). This includes the review of concomitant opioids and psycho-active drugs (like benzodiazepines). For patients with signs and symptoms of OUD, consultation with an addiction specialist should be considered.
Cases of adrenal insufficiency have been reported with opioid use including fentanyl lozenges, more often following greater than one month of use. Wean the patient off of the opioid to allow adrenal function to recover and continue corticosteroid treatment until adrenal function recovers (see section 4.8).
As with all opioids, there is a risk of clinically significant respiratory depression associated with the use of Cynril. Cynril patients should be monitored accordingly. Particular caution should be used when titrating Cynril in patients with non-severe chronic obstructive pulmonary disease or other medical conditions predisposing them to respiratory depression, as even normally therapeutic doses of Cynril may further decrease respiratory drive to the point of respiratory failure.
Sleep-related breathing disorders
Opioids can cause sleep-related breathing disorders including central sleep apnoea (CSA) and sleep-related hypoxemia. Opioid use increases the risk of CSA in a dose-dependent fashion. In patients who present with CSA, consider decreasing the total opioid dosage.
The concomitant use of alcohol with fentanyl can produce increased depressant effects which may result in a fatal outcome (see section 4.5).
Intracranial effects of CO2 retention, impaired consciousness, head injury
Cynril should only be administered with extreme caution in patients who may be particularly susceptible to the intracranial effects of CO2 retention, such as those with evidence of increased intracranial pressure, or impaired consciousness. Opioids may obscure the clinical course of a patient with a head injury and should be used only if clinically warranted.
Intravenous fentanyl may produce bradycardia. Therefore, Cynril should be used with caution in patients with previous or pre-existing bradyarrhythmias.
Hepatic or renal impairment
In addition, Cynril should be administered with caution to patients with liver or kidney dysfunction. The influence of liver and renal impairment on the pharmacokinetics of the medicinal product has not been evaluated; however, when administered intravenously the clearance of fentanyl has been shown to be altered in hepatic and renal disease due to alterations in metabolic clearance and plasma proteins. After administration of Cynril, impaired liver and renal function may both increase the bioavailability of swallowed fentanyl and decrease its systemic clearance, which could lead to increased and prolonged opioid effects. Therefore, special care should be taken during the titration process in patients with moderate or severe hepatic or renal disease.
Careful consideration should be given to patients with hypovolaemia and hypotension.
Diabetic patients should be advised that the medicine product contains dextrates (dextrates are composed of 93% dextrose monohydrate and 7% maltodextrin. The total glucose load per dosage unit is approximately 1.89 grams per dose).
Normal oral hygiene is recommended to reduce any potential harm to the teeth. Because Cynril contains approximately 2 grams of sugar, frequent consumption increases the risk of dental decay. The occurrence of dry mouth associated with the use of opioid medications may add to this risk. During treatment with Cynril regular dental visits are advised.
Caution is advised when Cynril is co-administered with medicinal products that affect the serotoninergic neurotransmitter systems.
The development of a potentially life-threatening serotonin syndrome may occur with the concomitant use of serotonergic medicinal products such as Selective Serotonin Re-uptake Inhibitors (SSRIs) and Serotonin Norepinephrine Re-uptake Inhibitors (SNRIs), and with medicinal products which impair metabolism of serotonin (including Monoamine Oxidase Inhibitors [MAOIs]). This may occur within the recommended dose.
Serotonin syndrome may include mental-status changes (e.g., agitation, hallucinations, coma), autonomic instability (e.g., tachycardia, labile blood pressure, hyperthermia), neuromuscular abnormalities (e.g., hyperreflexia, incoordination, rigidity), and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhoea).
If serotonin syndrome is suspected, treatment with Cynril should be discontinued.
As with other opioids, in case of insufficient pain control in response to an increased dose of fentanyl, the possibility of opioid-induced hyperalgesia should be considered. A fentanyl dose reduction or discontinuation of fentanyl treatment or treatment review may be indicated.
Anaphylaxis and hypersensitivity have been reported in association with the use of oral transmucosal fentanyl products (see section 4.8).
Concomitant use of sedative medicines
Concomitant use of Cynril and sedative medicines such as benzodiazepines or related drugs may result in sedation, respiratory depression, coma and death. Because of these risks, concomitant prescribing with these sedative medicines should be reserved for patients for whom alternative treatment options are not possible. If a decision is made to prescribe Cynril concomitantly with sedative medicines, the lowest effective dose should be used, and the duration of treatment should be as short as possible.
The patients should be followed closely for signs and symptoms of respiratory depression and sedation.
In this respect, it is strongly recommended to inform patients and their caregivers to be aware of these symptoms (see section 4.5).
Cynril is not recommended for use in children and adolescents below 16 years due to lack of data on safety and efficacy (see sections 5.1 and 5.2).
This medicine contains less than 1mmol sodium (23 mg) per compressed lozenge, that is to say essentially 'sodium-free
This medicine contains glucose (as hydrated dextrates) Patients with rare glucose-galactose malabsorption should not take this medicine. May be harmful to teeth.
Agents that affect CYP3A4 activity
Fentanyl is metabolized by the CYP3A4 isoenzyme in the liver and intestinal mucosa. Potent inhibitors of CYP3A4 such as macrolide antibiotics (e.g. erythromycin), azole antifungals (e.g. ketoconazole, itraconazole, and fluconazole) and certain protease inhibitors (e.g. ritonavir), may increase the bioavailability of swallowed fentanyl and may also decrease its systemic clearance which may result in increased or prolonged opioid effects. Similar effects could be seen after concurrent ingestion of grapefruit juice, which is known to inhibit CYP3A4. Hence caution is advised if fentanyl is given concomitantly with CYP3A4 inhibitors.
Co-administration with agents that induce 3A4 activity may reduce the efficacy of Cynril.
Agents that can increase CNS depressants effects
The concomitant use of other CNS depressants, including other opioids, sedatives or hypnotics, general anaesthetics, phenothiazines, tranquillisers, skeletal muscle relaxants, sedating antihistamines and alcohol may produce additive depressant effects which may result in a fatal outcome (see section 4.4).
Partial opioid agonists/antagonists
The concomitant use of partial opioid agonists/antagonists (e.g. buprenorphine, nalbuphine, pentazocine) is not recommended. They have high affinity to opioid receptors with relatively low intrinsic activity and therefore partially antagonise the analgesic effect of fentanyl and may induce withdrawal symptoms in opioid dependent patients.
Co-administration of fentanyl with a serotonergic agent, such as a Selective Serotonin Reuptake Inhibitor (SSRI) or a Serotonin Norepinephrine Reuptake Inhibitor (SNRI) or a Monoamine Oxidase Inhibitor (MAOI), may increase the risk of serotonin syndrome, a potentially life-threatening condition (see section 4.3).
Sedative medicines such as benzodiazepines or related drugs
The concomitant use of opioids with sedative medicines such as benzodiazepines or related drugs increases the risk of sedation, respiratory depression, coma and death because of additive CNS depressant effect. The dose and duration of concomitant use should be limited (see section 4.4).
Concomitant use of medicinal products containing sodium oxybate and fentanyl is contraindicated (see section 4.3). The treatment of sodium oxybate should be discontinued before start of treatment with Cynril.
There are limited of amount data from the use of fentanyl in pregnant women. Studies in animals have shown reproductive toxicity (see section 5.3). The potential risk for humans is unknown. Cynril should not be used in pregnancy unless clearly necessary.
With long-term use of fentanyl during pregnancy, there is a risk of neonatal opioid withdrawal syndrome which may be life-threatening if not recognized and treated and requires management according to protocols developed by neonatology experts. If opioid use is required for a prolonged period in a pregnant woman, advise the patient of the risk of neonatal opioid withdrawal syndrome and ensure that appropriate treatment will be available (see section 4.8).
It is advised not to use fentanyl during labour and delivery (including caesarean section) because fentanyl passes through the placenta and may cause respiratory depression in the foetus. If Cynril is administered, an antidote for the child should be readily available.
Fentanyl passes into breast milk and may cause sedation and respiratory depression in the breast-fed child. Fentanyl should not be used by breast-feeding women and breast-feeding should not be restarted until at least 5 days after the last administration of fentanyl.
There are no human data on fertility available. In animal studies, male fertility was impaired (see section 5.3).
No studies of the effects on the ability to drive and use machines have been performed. However, opioid analgesics may impair the mental and/or physical ability required for the performance of potentially dangerous tasks (e.g., driving a car or operating machinery). Patients should be advised not to drive or operate machinery if they experience somnolence, dizziness, blurred or double vision while taking Cynril.
Typical opioid side effects are to be expected with Cynril. Frequently, these will cease or decrease in intensity with continued use of the product, as the patient is titrated to the most appropriate dose. However, the most serious adverse events are respiratory depression (potentially leading to apnoea or respiratory arrest), circulatory depression, hypotension and shock and all patients should be closely monitored for these.
Application site reactions, including gum bleeding, irritation, pain and ulcer have been reported in post-marketing use.
Because the clinical trials of Cynril were designed to evaluate safety and efficacy in treating breakthrough pain, all patients were also taking concomitant opioids, such as sustained-release morphine or transdermal fentanyl, for their persistent pain. Thus it is not possible to definitively separate the effects of Cynril alone.
The following adverse reactions have been reported with Cynril during clinical studies and post marketing experience. Adverse reactions are listed below as MedDRA preferred term by system organ class and frequency (frequencies are defined as: very common ≥1/10, common ≥1/100 to <1/10, uncommon ≥ 1/1,000 to <1/100, not known (cannot be estimated from the available data) :
System organ class
Immune system disorders
anaphylactic reaction, tongue oedema, lip oedema
adrenal insufficiency, androgen deficiency
Metabolism and nutrition disorders
confusion, anxiety, hallucinations, depression, emotional lability
abnormal dreams, depersonalisation, abnormal thinking, euphoria
Nervous system disorders
somnolence, dizziness, headache
loss of consciousness, convulsion, vertigo, myoclonus, sedation, parathesia (including hyperaesthesia/circu moral parathesia), abnormal gait/incoordination, taste perversion
coma, slurred speech
abnormal vision (blurred, double vision)
flushing, hot flush
Respiratory, thoracic and mediastinal disorders
pharyangeal oedema, respiratory depression
nausea, vomiting, constipation, abdominal pain
dry mouth, dyspepsia, stomatitis, tongue disorder (for example, burning sensation, ulcers), flatulence, abdomen enlarged
ileus, mouth ulcers, dental caries, gingival bleeding
tooth loss, gingival recession, gingivitis, diarrhoea
Skin and subcutaneous tissue disorders
pruritis, sweating, rash
Renal and urinary disorders
General disorders and administration site conditions
application site reactions including irritation, pain and ulcer, malaise
fatigue, peripheral oedema, pyrexia, withdrawal syndrome*, neonatal withdrawal syndrome, drug dependence (addiction), drug abuse, bleeding at the site of application
Injury, poisoning and procedural complications
accidental injury (for example, falls)
*opioid withdrawal symptoms such as nausea, vomiting, diarrhoea, anxiety, chills, tremor and sweating have been observed with transmucosal fentanyl.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme. Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
The symptoms of fentanyl overdosage are expected to be similar in nature to those of intravenous fentanyl and other opioids, and are an extension of its pharmacological actions, with the most serious significant effects being altered mental status, loss of consciousness, coma, cardiorespiratory arrest, respiratory depression, respiratory distress, and respiratory failure, which have resulted in death.
Cases of Cheynes Stokes respiration have been observed in case of fentanyl overdose, particularly in patients with history of heart failure.
Immediate management of opioid overdose includes removal of the Cynril unit via the applicator, if still in the mouth, ensuring a patent airway, physical and verbal stimulation of the patient, assessment of the level of consciousness, ventilatory and circulatory status, and assisted ventilation (ventilatory support) if necessary.
Overdose (accidental ingestion) in the opioid naive person
For treatment of overdose (accidental ingestion) in the opioid naive person intravenous access should be obtained, and naloxone or other opioid antagonists should be employed as clinically indicated. The duration of respiratory depression following overdose may be longer than the effects of the opioid antagonist's action (e.g., the half-life of naloxone ranges from 30 to 81 minutes) and repeated administration may be necessary. Consult the Summary of Product Characteristics of the individual opioid antagonist for details about such use.
Overdose in opioid-maintained patients
For treatment of overdose in opioid-maintained patients, intravenous access should be obtained. The judicious use of naloxone or another opioid antagonist may be warranted in some instances, but it is associated with the risk of precipitating an acute withdrawal syndrome.
Although muscle rigidity interfering with respiration has not been seen following the use of Cynril, this is possible with fentanyl and other opioids. If it occurs, it should be managed by the use of assisted ventilation, by an opioid antagonist, and as a final alternative, by a neuromuscular blocking agent.
Pharmacotherapeutic group: Opioid analgesic, phenylpiperidine derivative. ATC code N02A BO3.
Mechanism of action
Fentanyl, a pure opioid agonist, acts primarily through interaction with mu-opioid receptors located in the brain, spinal cord and smooth muscle. The primary site of therapeutic action is the central nervous system (CNS). The most clinically useful pharmacological effect of the interaction of fentanyl with mu-opioid receptors is analgesia. The analgesic effects of fentanyl are related to the blood level of the active substance if proper allowance is made for the delay into and out of the CNS (a process with a 3-5 minute half-life). In opioid-naive individuals, analgesia occurs at blood levels of 1 to 2 ng/ml, while blood levels of 10-20 ng/ml would produce surgical anaesthesia and profound respiratory depression.
In patients with chronic cancer pain on stable doses of regularly scheduled opioids to control their persistent pain, fentanyl produced significantly more breakthrough pain relief compared with placebo at 15, 30, 45, and 60 minutes following administration.
Opioids may influence the hypothalamic-pituitary-adrenal or -gonadal axes. Some changes that can be seen include an increase in serum prolactin and decreases in plasma cortisol and testosterone. Clinical signs and symptoms may be manifest from these hormonal changes.
Other secondary actions include increase in the tone and decrease in the contractions of the gastrointestinal smooth muscle, which results in prolongation of gastrointestinal transit time and may be responsible for the constipatory effect of opioids.
While opioids generally increase the tone of urinary tract smooth muscle, the overall effect tends to vary, in some cases producing urinary urgency, in others difficulty in urination.
All opioid mu-receptor agonists, including fentanyl, produce dose dependent respiratory depression. The risk of respiratory depression is less in patients with pain and those receiving chronic opioid therapy who develop tolerance to respiratory depression and other opioid effects. In non-tolerant subjects, typically peak respiratory effects are seen 15 to 30 minutes following the administration of fentanyl and may persist for several hours.
Additional secondary pharmacological effect includes miosis.
There is limited experience of the use of Cyril in paediatric patients, below the age of 16. In a clinical study, 15 (out of 38) paediatric patients, ranging in age from 5 to 15 years, already receiving maintenance opioid therapy and with breakthrough pain were treated with a similar product. The study was too small to allow conclusions on safety and efficacy in this patient population.
Fentanyl is highly lipophilic and can be absorbed very rapidly through the oral mucosa and more slowly by the conventional gastrointestinal route. It is subject to first- pass hepatic and intestinal metabolism and the metabolites do not contribute to fentanyl's therapeutic effects.
The absorption pharmacokinetics of fentanyl from Cynril are a combination of rapid oromucosal absorption and slower gastrointestinal absorption of swallowed fentanyl.
Approximately 25% of the total dose of Cynril is rapidly absorbed from the buccal mucosa. The remaining 75% of the dose is swallowed and slowly absorbed from the gastrointestinal tract. About 1/3 of this amount (25% of the total dose) escapes hepatic and intestinal first-pass elimination and becomes systemically available. Absolute bioavailability is about 50% compared to intravenous fentanyl, divided equally between rapid oromucosal and slower gastrointestinal absorption. Cmax ranges from 0.39 to 2.51 ng/ml after consumption of Cynril (200 micrograms to 1600 micrograms). Tmax is around 20 to 40 minutes after consumption of an Cynril unit (range 20 – 480 minutes).
Animal data show that fentanyl is rapidly distributed to the brain, heart, lungs, kidneys and spleen followed by a slower redistribution to muscles and fat. The plasma protein binding of fentanyl is 80-85%. The main binding protein is alpha-1- acid glycoprotein, but both albumin and lipoproteins contribute to some extent. The free fraction of fentanyl increases with acidosis. The mean volume of distribution at steady state (Vss) is 4 l/kg.
Fentanyl is metabolised in the liver and in the intestinal mucosa to norfentanyl by CYP3A4 isoform. Norfentanyl is not pharmacologically active in animal studies. More than 90% of the administered dose of fentanyl is eliminated by biotransformation to N-dealkylated and hydroxylated inactive metabolites.
Less than 7% of the dose is excreted unchanged in the urine, and only about 1% is excreted unchanged in the faeces. The metabolites are mainly excreted in the urine, while faecal excretion is less important. The total plasma clearance of fentanyl is 0.5 l/hr/kg (range 0.3-0.7 l/hr/kg). The terminal elimination half-life after Cynril administration is about 7 hours.
Dose proportionality across the available range of dosages (200 micrograms to 1600 micrograms) of Cynril has been demonstrated.
In a clinical study, 15 paediatric patients, ranging in age from 5 to 15 years, already receiving maintenance opioid therapy and with breakthrough pain were treated with a similar product at doses ranging from 200 mcg to 600 mcg. Area under the curve values based on observed concentrations were 2-fold higher in younger children than adolescents (5.25 versus 2.65 ng.hr/mL, respectively) and 4-fold higher in the younger children as compared to adults (5.25 versus 1.20 ng.hr/mL). On a weight adjusted basis, clearance and volume of distribution values were similar across the age range.
Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicity and carcinogenicity.
Embryo-foetal developmental toxicity studies conducted in rats and rabbits revealed no compound-induced malformations or developmental variations when administered during the period of organogenesis.
In a fertility and early embryonic development study in rats, a male-mediated effect was observed at high doses (300 mcg/kg/day, s.c.) and is consistent with the sedative effects of fentanyl in animal studies.
In studies on pre and postnatal development in rats the survival rate of offspring was significantly reduced at doses causing severe maternal toxicity. Further findings at maternally toxic doses in F1 pups were delayed physical development, sensory functions, reflexes and behaviour. These effects could either be indirect effects due to altered maternal care and/or decreased lactation rate or a direct effect of fentanyl on the pups.
Carcinogenicity studies (26-week dermal alternative bioassay in Tg.AC transgenic mice; two-year subcutaneous carcinogenicity study in rats) did not induce any findings indicative of oncogenic potential. Evaluation of brain slides from carcinogenicity study in rats revealed brain lesions in animals administered high doses of fentanyl citrate. The relevance of these findings to humans is unknown.
Citric acid, anhydrous
Disodium phosphate, anhydrous
Artificial berry flavour (main components Tapioca starch, Arabic gum (E-414) and Triacetine)
Edible glue used to attach the lozenge to the handle:
Purified Shellac (E904),
FD&C Blue No.1 (E133 Brilliant Blue FCF),
Ammonium Hydroxide (E527)
Do not store about 25°C
Each Cynril dosage unit is contained in a child-resistance and opaque PVC-PCTFE- PVdC-PVC/Al blisters, supplied in cartons of 1, 3, 15 or 30 individual units.
Not all pack size may be marketed.
Lozenges with residual active substance should at no time be discarded or misplaced.
Any unused medicinal product or waste material should be disposed in accordance with local requirements.
Fontus Health Ltd
60 Lichfield Street