effects are achieved. monitor patients for respiratory depression and sedation at frequent intervals. if a cyp3a4 inhibitor is discontinued, consider increasing the oral transmucosal fentanyl citrate dosage until stable drug effects are achieved. monitor for signs of opioid withdrawal. examples: macrolide antibiotics (e.g., erythromycin), azole-antifungal agents (e.g., ketoconazole), protease inhibitors (e.g., ritonavir), grapefruit juice cyp3a4 inducers clinical impact: the concomitant use of oral transmucosal fentanyl citrate and cyp3a4 inducers can decrease the plasma concentration of fentanyl [see clinical pharmacology ( 12.3 )] , resulting in decreased efficacy or onset of a withdrawal syndrome in patients who have developed physical dependence to fentanyl [see warnings and precautions ( 5.3 )] . after stopping a cyp3a4 inducer, as the effects of the inducer decline, the fentanyl plasma concentration will increase [see clinical pharmacology ( 12.3 )] , which could increase or prolong both the therapeutic effects and adverse reactions, and may cause serious respiratory depression. intervention: if concomitant use is necessary, consider increasing the oral transmucosal fentanyl citrate dosage until stable drug effects are achieved. monitor for signs of opioid withdrawal. if a cyp3a4 inducer is discontinued, consider oral transmucosal fentanyl citrate dosage reduction and monitor for signs of respiratory depression. examples: rifampin, carbamazepine, phenytoin benzodiazepines and other central nervous system (cns) depressants clinical impact: due to additive pharmacologic effect, the concomitant use of benzodiazepines or other cns depressants including alcohol, increases the risk of respiratory depression, profound sedation, coma, and death. intervention: reserve concomitant prescribing of these drugs for use in patients for whom alternative treatment options are inadequate. limit dosages and durations to the minimum required. follow patients closely for signs of respiratory depression and sedation. if concomitant use is warranted, consider prescribing naloxone for the emergency treatment of opioid overdose [see dosage and administration ( 2.2 ), warnings and precautions ( 5.1 , 5.4 , 5.6 )] . examples: benzodiazepines and other sedatives/hypnotics, anxiolytics, tranquilizers, muscle relaxants, general anesthetics, antipsychotics, other opioids, alcohol. serotonergic drugs clinical impact: the concomitant use of opioids with other drugs that affect the serotonergic neurotransmitter system has resulted in serotonin syndrome [see warnings and precautions ( 5.10 )] . intervention: if concomitant use is warranted, carefully observe the patient, particularly during treatment initiation and dose adjustment. discontinue oral transmucosal fentanyl citrate if serotonin syndrome is suspected. examples: selective serotonin reuptake inhibitors (ssris), serotonin and norepinephrine reuptake inhibitors (snris), tricyclic antidepressants (tcas), triptans, 5-ht3 receptor antagonists, drugs that affect the serotonin neurotransmitter system (e.g., mirtazapine, trazodone, tramadol), certain muscle relaxants (i.e., cyclobenzaprine, metaxalone), monoamine oxidase (mao) inhibitors (those intended to treat psychiatric disorders and also others, such as linezolid and intravenous methylene blue). monoamine oxidase inhibitors (maois) clinical impact: maoi interactions with opioids may manifest as serotonin syndrome [see warnings and precautions ( 5.10 )] or opioid toxicity (e.g., respiratory depression, coma) [see warnings and precautions ( 5.1 )] . intervention: the use of oral transmucosal fentanyl citrate is not recommended for patients taking maois or within 14 days of stopping such treatment. examples: phenelzine, tranylcypromine, linezolid mixed agonist/antagonist and partial agonist opioid analgesics clinical impact: may reduce the analgesic effect of oral transmucosal fentanyl citrate and/or precipitate withdrawal symptoms. intervention: avoid concomitant use. examples: butorphanol, nalbuphine, pentazocine, buprenorphrine muscle relaxants clinical impact: fentanyl may enhance the neuromuscular blocking action of skeletal muscle relaxants and produce an increased degree of respiratory depression. intervention: monitor patients for signs of respiratory depression that may be greater than otherwise expected and decrease the dosage of oral transmucosal fentanyl citrate and/or the muscle relaxant as necessary. due to the risk of respiratory depression with concomitant use of skeletal muscle relaxants and opioids, consider prescribing naloxone for the emergency treatment of opioid overdose [see dosage and administration ( 2.2 ), warnings and precautions ( 5.1 , 5.4 )]. examples: cyclobenzaprine, metaxalone diuretics clinical impact: opioids can reduce the efficacy of diuretics by inducing the release of antidiuretic hormone. intervention: monitor patients for signs of diminished diuresis and/or effects on blood pressure and increase the dosage of the diuretic as needed. anticholinergic drugs clinical impact: the concomitant use of anticholinergic drugs may increase risk of urinary retention and/or severe constipation, which may lead to paralytic ileus. intervention: monitor patients for signs of urinary retention or reduced gastric motility when oral transmucosal fentanyl citrate is used concomitantly with anticholinergic drugs. mixed agonist/antagonist and partial agonist opioid analgesics : avoid the use of mixed agonist/antagonist or partial agonist analgesics in patients who are already receiving a full opioid agonist analgesic (including oral transmucosal fentanyl citrate) because they may reduce analgesic effect of oral transmucosal fentanyl citrate or precipitate withdrawal symptoms. ( 7 )

ications ( 4 )] . as a part of the tirf rems, oral transmucosal fentanyl citrate may be dispensed by outpatient pharmacies only to outpatients enrolled in the program [see warnings and precautions ( 5.7 )] . for inpatient administration of oral transmucosal fentanyl citrate, patient and prescriber enrollment are not required. oral transmucosal fentanyl citrate is an opioid agonist indicated for the management of breakthrough pain in cancer patients 16 years of age and older who are already receiving and who are tolerant to around-the-clock opioid therapy for their underlying persistent cancer pain. patients considered opioid tolerant are those who are taking, for one week or longer, around-the-clock medicine consisting of at least 60 mg of oral morphine per day, at least 25 mcg of transdermal fentanyl per hour, at least 30 mg of oral oxycodone per day, at least 8 mg of oral hydromorphone per day, at least 25 mg oral oxymorphone per day, at least 60 mg oral hydrocodone per day, or an equianalgesic dose of another opioid. patients must remain on around-the-clock opioids while taking oral transmucosal fentanyl citrate. limitations of use not for use in opioid non-tolerant patients. not for use in the management of acute or postoperative pain, including headache/migraine or dental pain. ( 4 ) as a part of the tirf rems, oral transmucosal fentanyl citrate may be dispensed by outpatient pharmacies only to outpatients enrolled in the program. ( 5.7 ) for inpatient administration of oral transmucosal fentanyl citrate, patient and prescriber enrollment are not required.

ess or coma. ( 5.13 ) 5.1 life-threatening respiratory depression serious, life-threatening, or fatal respiratory depression has been reported with the use of opioids, even when used as recommended. respiratory depression, if not immediately recognized and treated, may lead to respiratory arrest and death. management of respiratory depression may include close observation, supportive measures, and use of opioid antagonists, depending on the patient’s clinical status [see overdosage ( 10 )] . carbon dioxide (co 2 ) retention from opioid-induced respiratory depression can exacerbate the sedating effects of opioids. while serious, life-threatening, or fatal respiratory depression can occur at any time during the use of oral transmucosal fentanyl citrate, the risk is greatest during the initiation of therapy or following a dosage increase. monitor patients closely for respiratory depression, especially within the first 24 to 72 hours of initiating therapy with and following dosage increases of oral transmucosal fentanyl citrate. to reduce the risk of respiratory depression, proper dosing and titration of oral transmucosal fentanyl citrate are essential [see dosage and administration ( 2 )] . overestimating the oral transmucosal fentanyl citrate dosage can result in a fatal overdose with the first dose. the substitution of oral transmucosal fentanyl citrate for any other fentanyl product may result in fatal overdose [see warnings and precautions ( 5.5 )] . oral transmucosal fentanyl citrate could be fatal to individuals for whom it is not prescribed and for those who are not opioid-tolerant. accidental ingestion of even one dose of oral transmucosal fentanyl citrate, especially by children, can result in respiratory depression and death due to an overdose of fentanyl [see warnings and precautions ( 5.1 , 5.2 )] . educate patients and caregivers on how to recognize respiratory depression and emphasize the importance of calling 911 or getting emergency medical help right away in the event of a known or suspected overdose [see patient counseling information ( 17 )] . opioids can cause sleep-related breathing disorders including central sleep apnea (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 opioid dosage using best practices for opioid taper [see dosage and administration ( 2.7 )] . patient access to naloxone for the emergency treatment of opioid overdose discuss the availability of naloxone for the emergency treatment of opioid overdose with the patient and caregiver and assess the potential need for access to naloxone, both when initiating and renewing treatment with oral transmucosal fentanyl citrate. inform patients and caregivers about the various ways to obtain naloxone as permitted by individual state naloxone dispensing and prescribing requirements or guidelines (e.g., by prescription, directly from a pharmacist, or as part of a community-based program). educate patients and caregivers on how to recognize respiratory depression and emphasize the importance of calling 911 or getting emergency medical help, even if naloxone is administered [see patient counseling information ( 17 )]. consider prescribing naloxone, based on the patient’s risk factors for overdose, such as concomitant use of cns depressants, a history of opioid use disorder, or prior opioid overdose. the presence of risk factors for overdose should not prevent the proper management of pain in any given patient. also consider prescribing naloxone if the patient has household members (including children) or other close contacts at risk for accidental ingestion or overdose. if naloxone is prescribed, educate patients and caregivers on how to treat with naloxone [see warnings and precautions ( 5.4 , 5.6 ), patient counseling information ( 17 )] . 5.2 increased risk of overdose in children due to accidental ingestion or exposure death has been reported in children who have accidentally ingested oral transmucosal fentanyl citrate. patients and their caregivers must be informed that oral transmucosal fentanyl citrate contains a medicine in an amount which can be fatal to a child. healthcare providers and dispensing pharmacists must specifically question patients or caregivers about the presence of children in the home (on a full time or visiting basis) and counsel them regarding the dangers to children from inadvertent exposure. patients and their caregivers must be instructed to keep both used and unused dosage units out of the reach of children. while all units should be disposed of immediately after use, partially consumed units represent a special risk to children. in the event that a unit is not completely consumed it must be properly disposed as soon as possible [see patient counseling information ( 17 )] . detailed instructions for the proper storage, administration, disposal, and important instructions for managing an overdose of oral transmucosal fentanyl citrate are provided in the oral transmucosal fentanyl citrate medication guide . encourage patients to read this information in its entirety and give them an opportunity to have their questions answered. 5.3 risks of concomitant use or discontinuation of cytochrome p450 3a4 inhibitors and inducers concomitant use of oral transmucosal fentanyl citrate with a cyp3a4 inhibitor, such as macrolide antibiotics (e.g., erythromycin), azole-antifungal agents (e.g., ketoconazole), and protease inhibitors (e.g., ritonavir), may increase plasma concentrations of fentanyl and prolong opioid adverse reactions, which may cause potentially fatal respiratory depression [see warnings and precautions ( 5.1 )] , particularly when an inhibitor is added after a stable dose of oral transmucosal fentanyl citrate is achieved. similarly, discontinuation of a cyp3a4 inducer, such as rifampin, carbamazepine, and phenytoin, in oral transmucosal fentanyl citrate-treated patients may increase fentanyl plasma concentrations and prolong opioid adverse reactions. when using oral transmucosal fentanyl citrate with cyp3a4 inhibitors or discontinuing cyp3a4 inducers in oral transmucosal fentanyl citrate-treated patients, monitor patients closely at frequent intervals and consider dosage reduction of oral transmucosal fentanyl citrate until stable drug effects are achieved [see drug interactions ( 7 )] . concomitant use of oral transmucosal fentanyl citrate with cyp3a4 inducers or discontinuation of a cyp3a4 inhibitor could decrease fentanyl plasma concentrations, decrease opioid efficacy or, possibly, lead to a withdrawal syndrome in a patient who had developed physical dependence to fentanyl. when using oral transmucosal fentanyl citrate with cyp3a4 inducers or discontinuing cyp3a4 inhibitors, monitor patients closely at frequent intervals and consider increasing the opioid dosage if needed to maintain adequate analgesia or if symptoms of opioid withdrawal occur [see drug interactions ( 7 )] . 5.4 risks from concomitant use with benzodiazepines or other cns depressants (including alcohol) profound sedation, respiratory depression, coma, and death may result from the concomitant use of oral transmucosal fentanyl citrate with benzodiazepines or other cns depressants (e.g., non-benzodiazepine sedatives/hypnotics, anxiolytics, tranquilizers, muscle relaxants, general anesthetics, antipsychotics, other opioids, alcohol). because of these risks, reserve concomitant prescribing of these drugs for use in patients for whom alternative treatment options are inadequate. observational studies have demonstrated that concomitant use of opioid analgesics and benzodiazepines increases the risk of drug-related mortality compared to use of opioid analgesics alone. because of similar pharmacological properties, it is reasonable to expect similar risk with the concomitant use of other cns depressant drugs with opioid analgesics [see drug interactions ( 7 )] . if the decision is made to prescribe a benzodiazepine or other cns depressant concomitantly with an opioid analgesic, prescribe the lowest effective dosages and minimum durations of concomitant use. in patients already receiving an opioid analgesic, prescribe a lower initial dose of the benzodiazepine or other cns depressant than indicated in the absence of an opioid, and titrate based on clinical response. if an opioid analgesic is initiated in a patient already taking a benzodiazepine or other cns depressant, prescribe a lower initial dose of the opioid analgesic, and titrate based on clinical response. follow patients closely for signs and symptoms of respiratory depression and sedation. if concomitant use is warranted, consider prescribing naloxone for the emergency treatment of opioid overdose [see dosage and administration ( 2.2 ), warnings and precautions ( 5.1 )] . advise both patients and caregivers about the risks of respiratory depression and sedation when oral transmucosal fentanyl citrate is used with benzodiazepines or other cns depressants (including alcohol and illicit drugs). advise patients not to drive or operate heavy machinery until the effects of concomitant use of the benzodiazepine or other cns depressant have been determined. screen patients for risk of substance use disorders, including opioid abuse and misuse, and warn them of the risk for overdose and death associated with the use of additional cns depressants including alcohol and illicit drugs [see drug interactions (7) and patient counseling information ( 17 )] . 5.5 risk of medication errors when prescribing, do not convert a patient to oral transmucosal fentanyl citrate from any other fentanyl product on a mcg per mcg basis as oral transmucosal fentanyl citrate and other fentanyl products are not equivalent on a microgram per microgram basis. oral transmucosal fentanyl citrate is not a generic version of other transmucosal immediate release fentanyl (tirf) formulations. when dispensing, do not substitute an oral transmucosal fentanyl citrate prescription for any other tirf formulation under any circumstances. other tirf formulations and oral transmucosal fentanyl citrate are not equivalent. substantial differences exist in the pharmacokinetic profile of oral transmucosal fentanyl citrate compared to other fentanyl products including other tirf formulations that result in clinically important differences in the rate and extent of absorption of fentanyl. as a result of these differences, the substitution of oral transmucosal fentanyl citrate for any other fentanyl product may result in a fatal overdose. there are no safe conversion directions available for patients on any other fentanyl products. (note: this includes oral, transdermal, or parenteral formulations of fentanyl.) therefore, for opioid tolerant patients, the initial dose of oral transmucosal fentanyl citrate should always be 200 mcg. each patient should be individually titrated to provide adequate analgesia while minimizing side effects [see dosage and administration ( 2.4 )] . 5.6 addiction, abuse, and misuse oral transmucosal fentanyl citrate contains fentanyl, a schedule ii controlled substance. as an opioid, oral transmucosal fentanyl citrate exposes users to the risks of addiction, abuse, and misuse [see drug abuse and dependence ( 9 )] . although the risk of addiction in any individual is unknown, it can occur in patients appropriately prescribed oral transmucosal fentanyl citrate. addiction can occur at recommended dosages and if the drug is misused or abused. assess each patient’s risk for opioid addiction, abuse, or misuse prior to prescribing oral transmucosal fentanyl citrate, and monitor all patients receiving oral transmucosal fentanyl citrate for the development of these behaviors and conditions. risks are increased in patients with a personal or family history of substance abuse (including drug or alcohol abuse or addiction) or mental illness (e.g., major depression). the potential for these risks should not, however, prevent the proper management of pain in any given patient. patients at increased risk may be prescribed opioids such as oral transmucosal fentanyl citrate, but use in such patients necessitates intensive counseling about the risks and proper use of oral transmucosal fentanyl citrate along with intensive monitoring for signs of addiction, abuse, and misuse. consider prescribing naloxone for the emergency treatment of opioid overdose [see dosage and administration ( 2.2 ), warnings and precautions ( 5.1 )] . opioids are sought by drug abusers and people with addiction disorders and are subject to criminal diversion. consider these risks when prescribing or dispensing oral transmucosal fentanyl citrate. strategies to reduce these risks include prescribing the drug in the smallest appropriate quantity and advising the patient on the proper disposal of unused drug [see patient counseling information (17)] . contact local state professional licensing board or state controlled substances authority for information on how to prevent and detect abuse or diversion of this product. 5.7 transmucosal immediate release fentanyl (tirf) risk evaluation and mitigation strategy (rems) because of the risk for accidental exposure, misuse, abuse, addiction, and overdose [see warnings and precautions ( 5.6 )], oral transmucosal fentanyl citrate is available only through a restricted program called the tirf rems. under the tirf rems, healthcare professionals who prescribe to outpatients, the outpatients themselves, and pharmacies are required to enroll in the program. notable requirements of the tirf rems are: prescribers for outpatient use must be certified with the rems program by enrolling and completing training. prescribers must document opioid tolerance with every oral transmucosal fentanyl citrate prescription. outpatients must be enrolled in the rems program and must be opioid tolerant to receive oral transmucosal fentanyl citrate [see dosage and administration ( 2.1 )] . outpatient pharmacies must be certified with the rems program and verify documentation of opioid tolerance with every oral transmucosal fentanyl citrate prescription. inpatient pharmacies must be certified with the rems program and develop policies and procedures to verify opioid tolerance in inpatients who require oral transmucosal fentanyl citrate while hospitalized. wholesalers and distributors must enroll in the rems program and distribute only to certified pharmacies. further information, including a list of certified pharmacies and enrolled distributors, is available at www.tirfremsaccess.com or by calling 1-866-822-1483. 5.8 neonatal opioid withdrawal syndrome prolonged use of oral transmucosal fentanyl citrate during pregnancy can result in withdrawal in the neonate. neonatal opioid withdrawal syndrome, unlike opioid withdrawal syndrome in adults, may be life-threatening if not recognized and treated, and requires management according to protocols developed by neonatology experts. observe newborns for signs of neonatal opioid withdrawal syndrome and manage accordingly. advise pregnant women using opioids for a prolonged period of the risk of neonatal opioid withdrawal syndrome and ensure that appropriate treatment will be available [see use in specific populations ( 8.1 ), patient counseling information ( 17 )] . 5.9 life-threatening respiratory depression in patients with chronic pulmonary disease or in elderly, cachectic, or debilitated patients the use of oral transmucosal fentanyl citrate in patients with acute or severe bronchial asthma in an unmonitored setting or in the absence of resuscitative equipment is contraindicated. patients with chronic pulmonary disease : oral transmucosal fentanyl citrate-treated patients with significant chronic obstructive pulmonary disease or cor pulmonale, and those with a substantially decreased respiratory reserve, hypoxia, hypercapnia, or pre-existing respiratory depression are at increased risk of decreased respiratory drive including apnea, even at recommended dosages of oral transmucosal fentanyl citrate [see warnings and precautions ( 5.1 )] . elderly, cachectic, or debilitated patients : life-threatening respiratory depression is more likely to occur in elderly, cachectic, or debilitated patients because they may have altered pharmacokinetics or altered clearance compared to younger, healthier patients [see warnings and precautions ( 5.1 )] . monitor such patients closely, particularly when initiating and titrating oral transmucosal fentanyl citrate and when oral transmucosal fentanyl citrate is given concomitantly with other drugs that depress respiration [see warnings and precautions ( 5.1 )] . alternatively, consider the use of non-opioid analgesics in these patients. 5.10 serotonin syndrome with concomitant use of serotonergic drugs cases of serotonin syndrome, a potentially life-threatening condition, have been reported during concomitant use of oral transmucosal fentanyl citrate with serotonergic drugs. serotonergic drugs include selective serotonin reuptake inhibitors (ssris), serotonin and norepinephrine reuptake inhibitors (snris), tricyclic antidepressants (tcas), triptans, 5-ht3 receptor antagonists, drugs that affect the serotonergic neurotransmitter system (e.g., mirtazapine, trazodone, tramadol), certain muscle relaxants (i.e., cyclobenzaprine, metaxalone), and drugs that impair metabolism of serotonin (including mao inhibitors, both those intended to treat psychiatric disorders and also others, such as linezolid and intravenous methylene blue) [see drug interactions ( 7 )] . this may occur within the recommended dosage range. serotonin syndrome symptoms may include mental status changes (e.g., agitation, hallucinations, coma), autonomic instability (e.g., tachycardia, labile blood pressure, hyperthermia), neuromuscular aberrations (e.g., hyperreflexia, incoordination, rigidity), and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea). the onset of symptoms generally occurs within several hours to a few days of concomitant use, but may occur later than that. discontinue oral transmucosal fentanyl citrate if serotonin syndrome is suspected. 5.11 adrenal insufficiency cases of adrenal insufficiency have been reported with opioid use, more often following greater than one month of use. presentation of adrenal insufficiency may include non-specific symptoms and signs including nausea, vomiting, anorexia, fatigue, weakness, dizziness, and low blood pressure. if adrenal insufficiency is suspected, confirm the diagnosis with diagnostic testing as soon as possible. if adrenal insufficiency is diagnosed, treat with physiologic replacement doses of corticosteroids. wean the patient off of the opioid to allow adrenal function to recover and continue corticosteroid treatment until adrenal function recovers. other opioids may be tried as some cases reported use of a different opioid without recurrence of adrenal insufficiency. the information available does not identify any particular opioids as being more likely to be associated with adrenal insufficiency. 5.12 severe hypotension oral transmucosal fentanyl citrate may cause severe hypotension including orthostatic hypotension and syncope in ambulatory patients. there is increased risk in patients whose ability to maintain blood pressure has already been compromised by a reduced blood volume or concurrent administration of certain cns depressant drugs (e.g., phenothiazines or general anesthetics) [see drug interactions ( 7 )] . monitor these patients for signs of hypotension after initiating or titrating the dosage of oral transmucosal fentanyl citrate. in patients with circulatory shock, oral transmucosal fentanyl citrate may cause vasodilation that can further reduce cardiac output and blood pressure. avoid the use of oral transmucosal fentanyl citrate in patients with circulatory shock. 5.13 risks of use in patients with increased intracranial pressure, brain tumors, head injury, or impaired consciousness in patients who may be susceptible to the intracranial effects of co 2 retention (e.g., those with evidence of increased intracranial pressure or brain tumors), oral transmucosal fentanyl citrate may reduce respiratory drive, and the resultant co 2 retention can further increase intracranial pressure. monitor such patients for signs of sedation and respiratory depression, particularly when initiating therapy with oral transmucosal fentanyl citrate. opioids may also obscure the clinical course in a patient with a head injury. avoid the use of oral transmucosal fentanyl citrate in patients with impaired consciousness or coma. 5.14 risks of use in patients with gastrointestinal conditions oral transmucosal fentanyl citrate is contraindicated in patients with known or suspected gastrointestinal obstruction, including paralytic ileus. the fentanyl in oral transmucosal fentanyl citrate may cause spasm of the sphincter of oddi. opioids may cause increases in serum amylase. monitor patients with biliary tract disease, including acute pancreatitis for worsening symptoms. 5.15 increased risk of seizures in patients with seizure disorders the fentanyl in oral transmucosal fentanyl citrate may increase the frequency of seizures in patients with seizure disorders, and may increase the risk of seizures occurring in other clinical settings associated with seizures. monitor patients with a history of seizure disorders for worsened seizure control during oral transmucosal fentanyl citrate therapy. 5.16 risks of driving and operating machinery oral transmucosal fentanyl citrate may impair the mental or physical abilities needed to perform potentially hazardous activities such as driving a car or operating machinery. warn patients not to drive or operate dangerous machinery unless they are tolerant to the effects of oral transmucosal fentanyl citrate and know how they will react to the medication. 5.17 cardiac disease intravenous fentanyl may produce bradycardia. therefore, use oral transmucosal fentanyl citrate with caution in patients with bradyarrhythmias.

citrate dosage unit per breakthrough cancer pain episode. ( 2.4 ) no more than two doses can be taken per breakthrough pain episode. ( 2.4 , 2.5 ) wait at least 4 hours before treating another episode of breakthrough pain with oral transmucosal fentanyl citrate. ( 2.4 , 2.5 ) limit consumption to four or fewer units per day once successful dose is found. ( 2.5 ) when opioid therapy is no longer required, consider discontinuing oral transmucosal fentanyl citrate along with a gradual downward of other opioids to minimize possible withdrawal effects. ( 2.7 ) 2.1 important dosage and administration instructions healthcare professionals who prescribe oral transmucosal fentanyl citrate for outpatients must enroll in the tirf rems and comply with the requirements of the rems to ensure safe use of oral transmucosal fentanyl citrate [see warnings and precautions ( 5.7 )] . use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals [see warnings and precautions ( 5 )] . it is important to minimize the number of strengths available to patients at any time to prevent confusion and possible overdose. initiate the dosing regimen for each patient individually, taking into account the patient’s severity of pain, patient response, prior analgesic treatment experience, and risk factors for addiction, abuse, and misuse [see warnings and precautions ( 5.1 )] . monitor patients closely for respiratory depression, especially within the first 24 to 72 hours of initiating therapy and following dosage increases with oral transmucosal fentanyl citrate and adjust the dosage accordingly [see warnings and precautions ( 5.1 )] . instruct patients and caregivers to take steps to store oral transmucosal fentanyl citrate securely and to properly dispose of unused oral transmucosal fentanyl citrate as soon as no longer needed [see warnings and precautions ( 5.1 , 5.2 ), patient counseling information ( 17 )]. other tirf formulations and oral transmucosal fentanyl citrate are not equivalent. do not substitute an oral transmucosal fentanyl citrate prescription for any other tirf formulation under any circumstances. do not convert patients on a mcg per mcg basis from any other fentanyl product to oral transmucosal fentanyl citrate [see warnings and precautions ( 5.5 )] . 2.2 patient access to naloxone for the emergency treatment of opioid overdose discuss the availability of naloxone for the emergency treatment of opioid overdose with the patient and caregiver and assess the potential need for access to naloxone, both when initiating and renewing treatment with oral transmucosal fentanyl citrate [see warnings and precautions ( 5.1 ), patient counseling information ( 17 )] . inform patients and caregivers about the various ways to obtain naloxone as permitted by individual state naloxone dispensing and prescribing requirements or guidelines (e.g., by prescription, directly from a pharmacist, or as part of a community-based program). consider prescribing naloxone, based on the patient’s risk factors for overdose, such as concomitant use of cns depressants, a history of opioid use disorder, or prior opioid overdose. the presence of risk factors for overdose should not prevent the proper management of pain in any given patient [see warnings and precautions ( 5.1 , 5.4 , 5.6 )] . consider prescribing naloxone if the patient has household members (including children) or other close contacts at risk for accidental ingestion or overdose . 2.3 initial dosage individually titrate oral transmucosal fentanyl citrate to a dose that provides adequate analgesia and minimizes side effects. the initial dose of oral transmucosal fentanyl citrate to treat episodes of breakthrough cancer pain is always 200 mcg . the oral transmucosal fentanyl citrate unit should be consumed over 15 minutes. patients should be prescribed an initial titration supply of six 200 mcg oral transmucosal fentanyl citrate units, thus limiting the number of units in the home during titration. patients should use up all units before increasing to a higher dose to prevent confusion and possible overdose. repeat dosing a. in cases where the breakthrough pain episode is not relieved after 15 minutes after completion of the oral transmucosal fentanyl citrate unit (30 minutes after the start of the unit), patients may take only one additional dose using the same strength for that episode. thus patients should take a maximum of two doses of oral transmucosal fentanyl citrate for any episode of breakthrough pain. b. patients must wait at least 4 hours before treating another episode of breakthrough pain with oral transmucosal fentanyl citrate. 2.4 dose titration from an initial dose, closely follow patients and change the dosage strength until the patient reaches a dose that provides adequate analgesia using a single oral transmucosal fentanyl citrate dosage unit per breakthrough cancer pain episode. if signs of excessive opioid effects appear before the unit is consumed, the dosage unit should be removed from the patient’s mouth immediately, disposed of properly, and subsequent doses should be decreased. patients should record their use of oral transmucosal fentanyl citrate over several episodes of breakthrough cancer pain and review their experience with their physicians to determine if a dosage adjustment is warranted. in cases where the breakthrough pain episode is not relieved 15 minutes after completion of the oral transmucosal fentanyl citrate unit (30 minutes after the start of the unit), patients may take only one additional dose of the same strength for that episode. thus, patients should take a maximum of two doses of oral transmucosal fentanyl citrate for any breakthrough pain episode. patients must wait at least 4 hours before treating another episode of breakthrough pain with oral transmucosal fentanyl citrate. to reduce the risk of overdosing during titration, patients should have only one strength of oral transmucosal fentanyl citrate available at any one time. dose titration 2.5 maintenance dosing a. once titrated to an effective dose, patients should generally use only one oral transmucosal fentanyl citrate unit of the appropriate strength per breakthrough pain episode. b. on those occasions when the breakthrough pain episode is not relieved 15 minutes after completion of the oral transmucosal fentanyl citrate unit, patient may take only one additional dose using the same strength for that episode. c. patients must wait at least 4 hours before treating another episode of breakthrough pain with oral transmucosal fentanyl citrate. once a successful dose has been found (i.e., an average episode is treated with a single unit), patients should limit consumption to four or fewer units per day. d. dosage adjustment of oral transmucosal fentanyl citrate may be required in some patients in order to continue to provide adequate relief of breakthrough pain. e. generally, the oral transmucosal fentanyl citrate dose should be increased only when a single administration of the current dose fails to adequately treat the breakthrough pain episode for several consecutive episodes. f. if the patient experiences greater than four breakthrough pain episodes per day, the dose of the maintenance (around-the-clock) opioid used for persistent pain should be re-evaluated. 2.6 administration of oral transmucosal fentanyl citrate open the blister package with scissors immediately prior to product use. the patient should place the oral transmucosal fentanyl citrate unit in his or her mouth between the cheek and lower gum, occasionally moving the drug matrix from one side to the other using the handle. the oral transmucosal fentanyl citrate unit should be sucked, not chewed. a unit dose of oral transmucosal fentanyl citrate, if chewed and swallowed, might result in lower peak concentrations and lower bioavailability than when consumed as directed [see clinical pharmacology ( 12.3 )] . the oral transmucosal fentanyl citrate unit should be consumed over a 15-minute period. longer or shorter consumption times may produce less efficacy than reported in oral transmucosal fentanyl citrate clinical trials. if signs of excessive opioid effects appear before the unit is consumed, remove the drug matrix from the patient’s mouth immediately and decrease future doses. 2.7 discontinuation of oral transmucosal fentanyl citrate when opioid therapy is no longer required, consider discontinuing oral transmucosal fentanyl citrate along with a gradual downward tapering (titration) of other opioids to minimize possible withdrawal effects. in patients who continue to take their chronic opioid therapy for persistent pain but no longer require treatment for breakthrough pain, oral transmucosal fentanyl citrate therapy can usually be discontinued immediately [see drug abuse and dependence ( 9.3 )] . 2.8 disposal of oral transmucosal fentanyl citrate after consumption of the unit is complete and the matrix is totally dissolved, throw away the handle in a trash container that is out of the reach of children. if any of the drug matrix remains on the handle, place the handle under hot running tap water until all of the drug matrix is dissolved, and then dispose of the handle in a place that is out of the reach of children. dispose of handles in the child-resistant container (as described in steps 1 and 2) at least once a day. if the temporary storage bottle provided as part of the oral transmucosal fentanyl citrate child safety kit is available, partially consumed units may be stored in the specially provided child-resistant container out of the reach of children until proper disposal is possible. unopened units remaining from a prescription must be properly disposed as soon as they are no longer needed. to dispose of the unused oral transmucosal fentanyl citrate units: remove the oral transmucosal fentanyl citrate unit from its blister package using scissors, and hold oral transmucosal fentanyl citrate by its handle over the toilet bowl. using wire-cutting pliers cut off the drug matrix end so that it falls into the toilet. dispose of the handle in a place that is out of the reach of children. repeat steps 1, 2, and 3 for each oral transmucosal fentanyl citrate unit. flush the toilet twice after 5 units have been cut and deposited into the toilet. do not flush the entire oral transmucosal fentanyl citrate units, oral transmucosal fentanyl citrate handles, blister packages, or cartons down the toilet. dispose of the handle where children cannot reach it. in the event that a caregiver requires additional assistance in disposing of excess unusable units that remain in the home after a patient has expired, instruct them to call the toll-free number for specgx llc (1-800-778-7898) or seek assistance from their local dea office.

-778-7898 or fda at 1-800-fda-1088 or www.fda.gov/medwatch. 6.1 clinical studies experience because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. the safety of oral transmucosal fentanyl citrate has been evaluated in 257 opioid-tolerant chronic cancer pain patients. the duration of oral transmucosal fentanyl citrate use varied during the open-label study. some patients were followed for over 21 months. the average duration of therapy in the open-label study was 129 days. the most serious adverse reactions associated with oral transmucosal fentanyl citrate are respiratory depression (potentially leading to apnea or respiratory arrest), circulatory depression, hypotension, and shock. because the clinical trials of oral transmucosal fentanyl citrate were designed to evaluate safety and efficacy in treating breakthrough cancer pain, all patients were also taking concomitant opioids, such as sustained-release morphine or transdermal fentanyl, for their persistent cancer pain. the adverse event data presented here reflect the actual percentage of patients experiencing each adverse effect among patients who received oral transmucosal fentanyl citrate for breakthrough cancer pain along with a concomitant opioid for persistent cancer pain. there has been no attempt to correct for concomitant use of other opioids, duration of oral transmucosal fentanyl citrate therapy, or cancer-related symptoms. three short-term clinical trials with similar titration schemes were conducted in 257 patients with malignancy and breakthrough cancer pain. data are available for 254 of these patients. table 1 lists, by dose groups, adverse reactions with an overall frequency of 1% or greater that occurred during titration. the ability to assign a dose-response relationship to these adverse reactions is limited by the titration schemes used in these studies. adverse reactions are listed in descending order of frequency within each body system. table 1. percent of patients with specific adverse events commonly associated with opioid administration or of particular clinical interest which occurred during titration (events in 1% or more of patients) percentage of patients reporting event dose group 200-600 mcg (n =230) 800-1400 mcg (n =138) 1600 mcg (n =54) >1600 mcg (n =41) any dose any dose = a patient who experienced the same adverse event at multiple doses was only counted once. (n =254) body as a whole asthenia 6 4 0 7 9 headache 3 4 6 5 6 accidental injury 1 1 4 0 2 digestive nausea 14 15 11 22 23 vomiting 7 6 6 15 12 constipation 1 4 2 0 4 nervous dizziness 10 16 6 15 17 somnolence 9 9 11 20 17 confusion 1 6 2 0 4 anxiety 3 0 2 0 3 abnormal gait 0 1 4 0 2 dry mouth 1 1 2 0 2 nervousness 1 1 0 0 2 vasodilatation 2 0 2 0 2 hallucinations 0 1 2 2 1 insomnia 0 1 2 0 1 thinking abnormal 0 1 2 0 1 vertigo 1 0 0 0 1 respiratory dyspnea 2 3 6 5 4 skin pruritus 1 0 0 5 2 rash 1 1 0 2 2 sweating 1 1 2 2 2 special senses abnormal vision 1 0 2 0 2 the following adverse reactions not reflected in table 1 occurred during titration with an overall frequency of 1% or greater and are listed in descending order of frequency within each body system. body as a whole : pain, fever, abdominal pain, chills, back pain, chest pain, infection digestive : diarrhea, dyspepsia, flatulence metabolic and nutritional : peripheral edema, dehydration nervous : hypesthesia, migraine respiratory : pharyngitis, cough increased the following reactions occurred during titration with an overall frequency of less than 1% and are listed in descending order of frequency within each body system. body as a whole : bone pain cardiovascular : deep thrombophlebitis, hypertension, hypotension digestive : anorexia, eructation, fecal impaction, gum hemorrhage, mouth ulceration, oral moniliasis hemic and lymphatic : anemia, leukopenia metabolic and nutritional : edema, hypercalcemia, weight loss musculoskeletal : myalgia, pathological fracture, myasthenia nervous : abnormal dreams, urinary retention, agitation, amnesia, emotional lability, euphoria, incoordination, libido decreased, neuropathy, paresthesia, speech disorder respiratory : hemoptysis, pleural effusion, rhinitis, asthma, hiccup, pneumonia, respiratory insufficiency, sputum increased skin and appendages : alopecia, exfoliative dermatitis special senses : taste perversion urogenita l: vaginal hemorrhage, dysuria, hematuria, urinary incontinence, urinary tract infection a long-term extension study was conducted in 156 patients with malignancy and breakthrough cancer pain who were treated for an average of 129 days. data are available for 152 of these patients. table 2 lists by dose groups, adverse reactions with an overall frequency of 1% or greater that occurred during the long-term extension study. adverse reactions are listed in descending order of frequency within each body system. table 2. percent of patients with adverse events commonly associated with opioid administration or of particular clinical interest which occurred during long term treatment (events in 1% or more of patients) dose group percentage of patients reporting event 200-600 mcg (n=98) 800-1400 mcg (n=83) 1600 mcg (n=53) >1600 mcg (n=27) any dose any dose = a patient who experienced the same adverse event at multiple doses was only counted once. (n=152) body as a whole asthenia 25 30 17 15 38 headache 12 17 13 4 20 accidental injury 4 6 4 7 9 hypertonia 2 2 2 0 3 digestive nausea 31 36 25 26 45 vomiting 21 28 15 7 31 constipation 14 11 13 4 20 intestinal obstruction 0 2 4 0 3 cardiovascular hypertension 1 1 0 0 1 nervous dizziness 12 10 9 0 16 anxiety 9 8 8 7 15 somnolence 8 13 8 7 15 confusion 2 5 13 7 10 depression 9 4 2 7 9 insomnia 5 1 8 4 7 abnormal gait 5 1 0 0 4 dry mouth 3 1 2 4 4 nervousness 2 2 0 4 3 stupor 4 1 0 0 3 vasodilatation 1 1 4 0 3 thinking abnormal 2 1 0 0 2 abnormal dreams 1 1 0 0 1 convulsion 0 1 2 0 1 myoclonus 0 0 4 0 1 tremor 0 1 2 0 1 vertigo 0 0 4 0 1 respiratory dyspnea 15 16 8 7 22 skin rash 3 5 8 4 8 sweating 3 2 2 0 4 pruritus 2 0 2 0 2 special senses abnormal vision 2 2 0 0 3 urogenital urinary retention 1 2 0 0 2 the following reactions not reflected in table 2 occurred with an overall frequency of 1% or greater in the long-term extension study and are listed in descending order of frequency within each body system. body as a whole : pain, fever, back pain, abdominal pain, chest pain, flu syndrome, chills, infection, abdomen enlarged, bone pain, ascites, sepsis, neck pain, viral infection, fungal infection, cachexia, cellulitis, malaise, pelvic pain cardiovascular : deep thrombophlebitis, palpitation, vascular disorder digestive : diarrhea, anorexia, dyspepsia, dysphagia, oral moniliasis, mouth ulceration, rectal disorder, stomatitis, flatulence, gastrointestinal hemorrhage, gingivitis, jaundice, periodontal abscess, eructation, glossitis, rectal hemorrhage hemic and lymphatic : anemia, leukopenia, thrombocytopenia, ecchymosis, lymphadenopathy, lymphedema, pancytopenia metabolic and nutritional : peripheral edema, edema, dehydration, weight loss, hyperglycemia, hypokalemia, hypercalcemia, hypomagnesemia musculoskeletal : myalgia, pathological fracture, joint disorder, leg cramps, arthralgia, bone disorder nervous : hypesthesia, paresthesia, hypokinesia, neuropathy, speech disorder, migraine respiratory : cough increased, pharyngitis, pneumonia, rhinitis, sinusitis, bronchitis, epistaxis, asthma, hemoptysis, sputum increased skin and appendages : skin ulcer, alopecia special senses : tinnitus, conjunctivitis, ear disorder, taste perversion urogenital : urinary tract infection, urinary incontinence, breast pain, dysuria, hematuria, scrotal edema, hydronephrosis, kidney failure, urinary urgency, urination impaired, breast neoplasm, vaginal hemorrhage, vaginitis the following reactions occurred with a frequency of less than 1% in the long-term extension study and are listed in descending order of frequency within each body system. body as a whole : allergic reaction, cyst, face edema, flank pain, granuloma, bacterial infection, mucous membrane disorder, neck rigidity cardiovascular : angina pectoris, hemorrhage, hypotension, peripheral vascular disorder, postural hypotension, tachycardia digestive : cheilitis, esophagitis, fecal incontinence, gastroenteritis, gastrointestinal disorder, gum hemorrhage, hemorrhage of colon, hepatorenal syndrome, liver tenderness, tooth caries, tooth disorder hemic and lymphatic : bleeding time increased metabolic and nutritional : acidosis, generalized edema, hypocalcemia, hypoglycemia, hyponatremia, hypoproteinemia, thirst musculoskeletal : arthritis, muscle atrophy, myopathy, synovitis, tendon disorder nervous : acute brain syndrome, agitation, cerebral ischemia, facial paralysis, foot drop, hallucinations, hemiplegia, miosis, subdural hematoma respiratory : hiccup, hyperventilation, lung disorder, pneumothorax, respiratory failure, voice alteration skin and appendages : herpes zoster, maculopapular rash, skin discoloration, urticaria, vesiculobullous rash special senses : ear pain, eye hemorrhage, lacrimation disorder, partial permanent deafness, partial transitory deafness urogenita l: kidney pain, nocturia, oliguria, polyuria, pyelonephritis 6.2 postmarketing experience the following adverse reactions have been identified during post approval use of oral transmucosal fentanyl citrate. because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. digestive : - dental decay : dental decay, including dental caries, tooth loss, and gum line erosion. nervous system disorders : - serotonin syndrome : cases of serotonin syndrome, a potentially life-threatening condition, have been reported during concomitant use of opioids with serotonergic drugs. endocrine disorders : - adrenal insufficiency : cases of adrenal insufficiency have been reported with opioid use, more often following greater than one month of use. - androgen deficiency : cases of androgen deficiency have occurred with chronic use of opioids. immune system disorders : - anaphylaxis : anaphylaxis has been reported with ingredients contained in oral transmucosal fentanyl citrate. general disorders and administration site conditions : application site reactions including irritation, pain, and ulcer, and drug withdrawal syndrome.

effects are achieved. monitor patients for respiratory depression and sedation at frequent intervals. if a cyp3a4 inhibitor is discontinued, consider increasing the oral transmucosal fentanyl citrate dosage until stable drug effects are achieved. monitor for signs of opioid withdrawal. examples: macrolide antibiotics (e.g., erythromycin), azole-antifungal agents (e.g., ketoconazole), protease inhibitors (e.g., ritonavir), grapefruit juice cyp3a4 inducers clinical impact: the concomitant use of oral transmucosal fentanyl citrate and cyp3a4 inducers can decrease the plasma concentration of fentanyl [see clinical pharmacology ( 12.3 )] , resulting in decreased efficacy or onset of a withdrawal syndrome in patients who have developed physical dependence to fentanyl [see warnings and precautions ( 5.3 )] . after stopping a cyp3a4 inducer, as the effects of the inducer decline, the fentanyl plasma concentration will increase [see clinical pharmacology ( 12.3 )] , which could increase or prolong both the therapeutic effects and adverse reactions, and may cause serious respiratory depression. intervention: if concomitant use is necessary, consider increasing the oral transmucosal fentanyl citrate dosage until stable drug effects are achieved. monitor for signs of opioid withdrawal. if a cyp3a4 inducer is discontinued, consider oral transmucosal fentanyl citrate dosage reduction and monitor for signs of respiratory depression. examples: rifampin, carbamazepine, phenytoin benzodiazepines and other central nervous system (cns) depressants clinical impact: due to additive pharmacologic effect, the concomitant use of benzodiazepines or other cns depressants including alcohol, increases the risk of respiratory depression, profound sedation, coma, and death. intervention: reserve concomitant prescribing of these drugs for use in patients for whom alternative treatment options are inadequate. limit dosages and durations to the minimum required. follow patients closely for signs of respiratory depression and sedation. if concomitant use is warranted, consider prescribing naloxone for the emergency treatment of opioid overdose [see dosage and administration ( 2.2 ), warnings and precautions ( 5.1 , 5.4 , 5.6 )] . examples: benzodiazepines and other sedatives/hypnotics, anxiolytics, tranquilizers, muscle relaxants, general anesthetics, antipsychotics, other opioids, alcohol. serotonergic drugs clinical impact: the concomitant use of opioids with other drugs that affect the serotonergic neurotransmitter system has resulted in serotonin syndrome [see warnings and precautions ( 5.10 )] . intervention: if concomitant use is warranted, carefully observe the patient, particularly during treatment initiation and dose adjustment. discontinue oral transmucosal fentanyl citrate if serotonin syndrome is suspected. examples: selective serotonin reuptake inhibitors (ssris), serotonin and norepinephrine reuptake inhibitors (snris), tricyclic antidepressants (tcas), triptans, 5-ht3 receptor antagonists, drugs that affect the serotonin neurotransmitter system (e.g., mirtazapine, trazodone, tramadol), certain muscle relaxants (i.e., cyclobenzaprine, metaxalone), monoamine oxidase (mao) inhibitors (those intended to treat psychiatric disorders and also others, such as linezolid and intravenous methylene blue). monoamine oxidase inhibitors (maois) clinical impact: maoi interactions with opioids may manifest as serotonin syndrome [see warnings and precautions ( 5.10 )] or opioid toxicity (e.g., respiratory depression, coma) [see warnings and precautions ( 5.1 )] . intervention: the use of oral transmucosal fentanyl citrate is not recommended for patients taking maois or within 14 days of stopping such treatment. examples: phenelzine, tranylcypromine, linezolid mixed agonist/antagonist and partial agonist opioid analgesics clinical impact: may reduce the analgesic effect of oral transmucosal fentanyl citrate and/or precipitate withdrawal symptoms. intervention: avoid concomitant use. examples: butorphanol, nalbuphine, pentazocine, buprenorphrine muscle relaxants clinical impact: fentanyl may enhance the neuromuscular blocking action of skeletal muscle relaxants and produce an increased degree of respiratory depression. intervention: monitor patients for signs of respiratory depression that may be greater than otherwise expected and decrease the dosage of oral transmucosal fentanyl citrate and/or the muscle relaxant as necessary. due to the risk of respiratory depression with concomitant use of skeletal muscle relaxants and opioids, consider prescribing naloxone for the emergency treatment of opioid overdose [see dosage and administration ( 2.2 ), warnings and precautions ( 5.1 , 5.4 )]. examples: cyclobenzaprine, metaxalone diuretics clinical impact: opioids can reduce the efficacy of diuretics by inducing the release of antidiuretic hormone. intervention: monitor patients for signs of diminished diuresis and/or effects on blood pressure and increase the dosage of the diuretic as needed. anticholinergic drugs clinical impact: the concomitant use of anticholinergic drugs may increase risk of urinary retention and/or severe constipation, which may lead to paralytic ileus. intervention: monitor patients for signs of urinary retention or reduced gastric motility when oral transmucosal fentanyl citrate is used concomitantly with anticholinergic drugs. mixed agonist/antagonist and partial agonist opioid analgesics : avoid the use of mixed agonist/antagonist or partial agonist analgesics in patients who are already receiving a full opioid agonist analgesic (including oral transmucosal fentanyl citrate) because they may reduce analgesic effect of oral transmucosal fentanyl citrate or precipitate withdrawal symptoms. ( 7 )

k of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. clinical considerations fetal/neonatal adverse reactions prolonged use of opioid analgesics during pregnancy for medical or nonmedical purposes can result in physical dependence in the neonate and neonatal opioid withdrawal syndrome shortly after birth. neonatal opioid withdrawal syndrome presents as irritability, hyperactivity and abnormal sleep pattern, high pitched cry, tremor, vomiting, diarrhea and failure to gain weight. the onset of neonatal withdrawal symptoms usually occurs in the first days after birth. the duration and severity of neonatal opioid withdrawal syndrome may vary. observe newborns for symptoms of neonatal opioid withdrawal syndrome and manage accordingly [see warnings and precautions ( 5.8 )] . labor or delivery opioids cross the placenta and may produce respiratory depression and psycho-physiologic effects in neonates. an opioid antagonist, such as naloxone, must be available for reversal of opioid-induced respiratory depression in the neonate. oral transmucosal fentanyl citrate is not recommended for use in pregnant women during or immediately prior to labor, when other analgesic techniques are more appropriate. opioid analgesics, including oral transmucosal fentanyl citrate, can prolong labor through actions which temporarily reduce the strength, duration, and frequency of uterine contractions. however, this effect is not consistent and may be offset by an increased rate of cervical dilation, which tends to shorten labor. monitor neonates exposed to opioid analgesics during labor for signs of excess sedation and respiratory depression. data human data in women treated acutely with intravenous or epidural fentanyl during labor, symptoms of neonatal respiratory or neurological depression were no more frequent than would be expected in infants of untreated mothers. transient neonatal muscular rigidity has been observed in infants whose mothers were treated with intravenous fentanyl. animal data fentanyl (25, 50, or 100 mcg/kg) citrate was administered subcutaneously to pregnant rats during the period of organogenesis (gestation day, gd 6 to 17). maternal toxicity and a decrease in fetal weights were observed at 100 mcg/kg but no teratogenicity was seen in the study (the no observed effect level of 50 mcg/kg is equivalent to 0.7 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison). fentanyl (50, 100, or 250 mcg/kg) was also administered subcutaneously to pregnant rabbits during the period of organogenesis (gd 6 to 18). maternal toxicity was noted at doses >100 mcg/kg. no teratogenicity was seen in the study (250 mcg/kg dose is equivalent to 3.5 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison). fentanyl has been shown to embryocidal in pregnant rats at doses of 30 mcg/kg intravenously (0.2 times the 1600 mcg dose of oral transmucosal fentanyl citrate on a mg/m 2 basis) from gd 6 to 18 and 160 mcg/kg subcutaneously (1 times the 1600 mcg dose of oral transmucosal fentanyl citrate based on a mg/m 2 basis). no evidence of teratogenicity was reported. no evidence of malformations or adverse effects on the fetus was reported in a published study in which pregnant rats were administered fentanyl continuously via subcutaneously implanted osmotic minipumps at doses of 10, 100, or 500 mcg/kg/day starting 2-weeks prior to breeding and throughout pregnancy. the high dose was approximately 3 times the human dose of 1600 mcg oral transmucosal fentanyl citrate per pain episode on a mg/m 2 basis and produced mean steady-state plasma levels that are 3.4 times higher than the mean c max observed following administration of 1600 mcg dose of oral transmucosal fentanyl citrate in humans. in a postnatal development study, pregnant rats were treated from gd 6 through lactation day (ld) 20 with subcutaneous doses of fentanyl (25, 50, 100, and 400 mcg/kg). maternal toxicity was noted at doses >100 mcg/kg. a reduction in pup growth and delayed attainment of developmental indices were observed at >100 mcg/kg. no difference in the number of live pups/litter was seen at birth, however, pup survival at ld 4 was reduced to 48% at 400 mcg/kg and by ld 21 pup survival was reduced to 30% and 26% at 100 and 400 mcg/kg, respectively. during lactation, fentanyl-related clinical signs (decreased activity, skin cold to touch, and moribund appearance) were noted in the f1 pups, most prominently in the 400 mcg/kg group. pups from this group also had significantly reduced body weights throughout the lactation period. the dose of fentanyl administered to rats at which no developmental toxicity in the f1 generation was seen was 50 mcg/kg which is 0.6 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison. 8.2 lactation risk summary fentanyl is present in breast milk. one published lactation study reports a relative infant dose of fentanyl of 0.024%. however, there is insufficient information to determine the effects of fentanyl on the breastfed infant and the effects of fentanyl on milk production. because of the potential for serious adverse reactions, including excess sedation and respiratory depression in a breastfed infant, advise patients that breastfeeding is not recommended during treatment with oral transmucosal fentanyl citrate. clinical considerations monitor infants exposed to oral transmucosal fentanyl citrate through breast milk for excess sedation and respiratory depression. withdrawal symptoms can occur in breastfed infants when maternal administration of an opioid analgesic is stopped, or when breast-feeding is stopped. 8.3 females and males of reproductive potential infertility chronic use of opioids may cause reduced fertility in females and males of reproductive potential. it is not known whether these effects on fertility are reversible [see adverse reactions ( 6.2 ), clinical pharmacology ( 12.2 ), nonclinical toxicology ( 13.1 )] . 8.4 pediatric use safety and effectiveness in pediatric patients below 16 years of age have not been established. in a clinical study, 15 opioid-tolerant pediatric patients with breakthrough pain, ranging in age from 5 to 15 years, were treated with oral transmucosal fentanyl citrate. the study was too small to allow conclusions on safety and efficacy in this patient population. twelve of the fifteen opioid-tolerant children and adolescents aged 5 to 15 years in this study received oral transmucosal fentanyl citrate at doses ranging from 200 mcg to 600 mcg. the mean (cv%; range) dose-normalized (to 200 mcg) c max and auc 0-8 values were 0.87 ng/ml (51%; 0.42-1.30) and 4.54 ng•h/ml (42%; 2.37-6.0), respectively, for children ages 5 to <11 years old (n = 3) and 0.68 ng/ml (72%; 0.15-1.44) and 8.38 (192%; 0.84-50.78), respectively, for children ages ≥11 to <16 y (n = 9). 8.5 geriatric use of the 257 patients in clinical studies of oral transmucosal fentanyl citrate in breakthrough cancer pain, 61 (24%) were 65 years of age and older, while 15 (6%) were 75 years of age and older. those patients over the age of 65 years were titrated to a mean dose that was about 200 mcg less than the mean dose titrated to by younger patients. no difference was noted in the safety profile of the group over 65 years of age as compared to younger patients in oral transmucosal fentanyl citrate clinical trials. elderly patients have been shown to be more sensitive to the effects of fentanyl when administered intravenously, compared with the younger population. therefore, exercise caution when individually titrating oral transmucosal fentanyl citrate in elderly patients to provide adequate efficacy while minimizing risk. respiratory depression is the chief risk for elderly patients treated with opioids, and has occurred after large initial doses were administered to patients who were not opioid-tolerant or when opioids were co-administered with other agents that depress respiration. titrate the dosage of oral transmucosal fentanyl citrate slowly in geriatric patients and monitor closely for signs of central nervous system and respiratory depression [see warnings and precautions ( 5.9 )] . fentanyl is known to be substantially excreted by the kidney, and the risk of adverse reactions to this drug may be greater in patients with impaired renal function. because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function. 8.6 patients with renal or hepatic impairment insufficient information exists to make recommendations regarding the use of oral transmucosal fentanyl citrate in patients with impaired renal or hepatic function. fentanyl is metabolized primarily via human cytochrome p450 3a4 isoenzyme system and mostly eliminated in urine. if the drug is used in these patients, it should be used with caution because of the hepatic metabolism and renal excretion of fentanyl. 8.7 sex both male and female opioid-tolerant cancer patients were studied for the treatment of breakthrough cancer pain. no clinically relevant sex differences were noted either in dosage requirement or in observed adverse reactions.

n, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. clinical considerations fetal/neonatal adverse reactions prolonged use of opioid analgesics during pregnancy for medical or nonmedical purposes can result in physical dependence in the neonate and neonatal opioid withdrawal syndrome shortly after birth. neonatal opioid withdrawal syndrome presents as irritability, hyperactivity and abnormal sleep pattern, high pitched cry, tremor, vomiting, diarrhea and failure to gain weight. the onset of neonatal withdrawal symptoms usually occurs in the first days after birth. the duration and severity of neonatal opioid withdrawal syndrome may vary. observe newborns for symptoms of neonatal opioid withdrawal syndrome and manage accordingly [see warnings and precautions ( 5.8 )] . labor or delivery opioids cross the placenta and may produce respiratory depression and psycho-physiologic effects in neonates. an opioid antagonist, such as naloxone, must be available for reversal of opioid-induced respiratory depression in the neonate. oral transmucosal fentanyl citrate is not recommended for use in pregnant women during or immediately prior to labor, when other analgesic techniques are more appropriate. opioid analgesics, including oral transmucosal fentanyl citrate, can prolong labor through actions which temporarily reduce the strength, duration, and frequency of uterine contractions. however, this effect is not consistent and may be offset by an increased rate of cervical dilation, which tends to shorten labor. monitor neonates exposed to opioid analgesics during labor for signs of excess sedation and respiratory depression. data human data in women treated acutely with intravenous or epidural fentanyl during labor, symptoms of neonatal respiratory or neurological depression were no more frequent than would be expected in infants of untreated mothers. transient neonatal muscular rigidity has been observed in infants whose mothers were treated with intravenous fentanyl. animal data fentanyl (25, 50, or 100 mcg/kg) citrate was administered subcutaneously to pregnant rats during the period of organogenesis (gestation day, gd 6 to 17). maternal toxicity and a decrease in fetal weights were observed at 100 mcg/kg but no teratogenicity was seen in the study (the no observed effect level of 50 mcg/kg is equivalent to 0.7 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison). fentanyl (50, 100, or 250 mcg/kg) was also administered subcutaneously to pregnant rabbits during the period of organogenesis (gd 6 to 18). maternal toxicity was noted at doses >100 mcg/kg. no teratogenicity was seen in the study (250 mcg/kg dose is equivalent to 3.5 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison). fentanyl has been shown to embryocidal in pregnant rats at doses of 30 mcg/kg intravenously (0.2 times the 1600 mcg dose of oral transmucosal fentanyl citrate on a mg/m 2 basis) from gd 6 to 18 and 160 mcg/kg subcutaneously (1 times the 1600 mcg dose of oral transmucosal fentanyl citrate based on a mg/m 2 basis). no evidence of teratogenicity was reported. no evidence of malformations or adverse effects on the fetus was reported in a published study in which pregnant rats were administered fentanyl continuously via subcutaneously implanted osmotic minipumps at doses of 10, 100, or 500 mcg/kg/day starting 2-weeks prior to breeding and throughout pregnancy. the high dose was approximately 3 times the human dose of 1600 mcg oral transmucosal fentanyl citrate per pain episode on a mg/m 2 basis and produced mean steady-state plasma levels that are 3.4 times higher than the mean c max observed following administration of 1600 mcg dose of oral transmucosal fentanyl citrate in humans. in a postnatal development study, pregnant rats were treated from gd 6 through lactation day (ld) 20 with subcutaneous doses of fentanyl (25, 50, 100, and 400 mcg/kg). maternal toxicity was noted at doses >100 mcg/kg. a reduction in pup growth and delayed attainment of developmental indices were observed at >100 mcg/kg. no difference in the number of live pups/litter was seen at birth, however, pup survival at ld 4 was reduced to 48% at 400 mcg/kg and by ld 21 pup survival was reduced to 30% and 26% at 100 and 400 mcg/kg, respectively. during lactation, fentanyl-related clinical signs (decreased activity, skin cold to touch, and moribund appearance) were noted in the f1 pups, most prominently in the 400 mcg/kg group. pups from this group also had significantly reduced body weights throughout the lactation period. the dose of fentanyl administered to rats at which no developmental toxicity in the f1 generation was seen was 50 mcg/kg which is 0.6 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison.

een due to hypoxia in overdose situations. effects on the gastrointestinal tract and other smooth muscle fentanyl causes a reduction in motility associated with an increase in smooth muscle tone in the antrum of the stomach and in the duodenum. digestion of food in the small intestine is delayed and propulsive contractions are decreased. propulsive peristaltic waves in the colon are decreased, while tone may be increased to the point of spasm resulting in constipation. other opioid-induced effects may include a reduction in biliary and pancreatic secretions, spasm of the sphincter of oddi, and transient elevations in serum amylase. effects on the cardiovascular system fentanyl may produce release of histamine with or without associated peripheral vasodilation. fentanyl produces peripheral vasodilation which may result in orthostatic hypotension or syncope. manifestations of histamine release and/or peripheral vasodilation may include pruritus, flushing, red eyes, and sweating, and/or orthostatic hypotension. effects on the endocrine system opioids inhibit the secretion of adrenocorticotropic hormone (acth), cortisol, and luteinizing hormone (lh) in humans [see adverse reactions ( 6.2 )] . they also stimulate prolactin, growth hormone (gh) secretion, and pancreatic secretion of insulin and glucagon [see adverse reactions ( 6.2 )] . thyroid stimulating hormone (tsh) has been shown to be both inhibited and stimulated by opioids. chronic use of opioids may influence the hypothalamic-pituitary-gonadal axis, leading to androgen deficiency that may manifest as low libido, impotence, erectile dysfunction, amenorrhea, or infertility. the causal role of opioids in the clinical syndrome of hypogonadism is unknown because the various medical, physical, lifestyle, and psychological stressors that may influence gonadal hormone levels have not been adequately controlled for in studies conducted to date [see adverse reactions ( 6.2 )] . effects on the immune system opioids have been shown to have a variety of effects on components of the immune system in in vitro and animal models. the clinical significance of these findings is unknown. overall, the effects of opioids appear to be modestly immunosuppressive. concentration-efficacy relationships the analgesic effects of fentanyl are related to the blood level of the drug, if proper allowance is made for the delay into and out of the cns (a process with a 3- to 5-minute half-life). in general, the effective concentration and the concentration at which toxicity occurs increase with increasing tolerance with any and all opioids. the rate of development of tolerance varies widely among individuals. the minimum effective analgesic concentration of fentanyl for any individual patient may increase over time due to an increase in pain, the development of a new pain syndrome and/or the development of analgesic tolerance. concentration-adverse reaction relationships there is a relationship between increasing fentanyl plasma concentration and increasing frequency of dose-related opioid adverse reactions such as nausea, vomiting, cns effects, and respiratory depression. in opioid-tolerant patients, the situation may be altered by the development of tolerance to opioid-related adverse reactions [see dosage and administration ( 2.1 , 2.3 , 2.4 , 2.5 )] . respiratory system all opioid mu -receptor agonists, including fentanyl, produce dose-dependent respiratory depression. the risk of respiratory depression is less in patients receiving chronic opioid therapy who develop tolerance to respiratory depression and other opioid effects. during the titration phase of the clinical trials, somnolence, which may be a precursor to respiratory depression, did increase in patients who were treated with higher doses of oral transmucosal fentanyl citrate. peak respiratory depressive effects may be seen as early as 15 to 30 minutes from the start of oral transmucosal fentanyl citrate product administration and may persist for several hours. serious or fatal respiratory depression can occur even at recommended doses. although not observed with oral transmucosal fentanyl products in clinical trials, fentanyl given rapidly by intravenous injection in large doses may interfere with respiration by causing rigidity in the muscles of respiration [see warnings and precautions ( 5.1 , 5.2 , 5.3 , 5.4 ), adverse reactions ( 6 ), and overdosage ( 10 )] . 12.3 pharmacokinetics absorption the absorption pharmacokinetics of fentanyl from the oral transmucosal dosage form is a combination of an initial rapid absorption from the buccal mucosa and a more prolonged absorption of swallowed fentanyl from the gi tract. both the blood fentanyl profile and the bioavailability of fentanyl will vary depending on the fraction of the dose that is absorbed through the oral mucosa and the fraction swallowed. absolute bioavailability, as determined by area under the concentration-time curve, of 15 mcg/kg in 12 adult males was 50% compared to intravenous fentanyl. normally, approximately 25% of the total dose of oral transmucosal fentanyl citrate is rapidly absorbed from the buccal mucosa and becomes systemically available. the remaining 75% of the total dose is swallowed with the saliva and then is slowly absorbed from the gi tract. about 1/3 of this amount (25% of the total dose) escapes hepatic and intestinal first-pass elimination and becomes systemically available. thus, the generally observed 50% bioavailability of oral transmucosal fentanyl citrate is divided equally between rapid transmucosal and slower gi absorption. therefore, a unit dose of oral transmucosal fentanyl citrate, if chewed and swallowed, might result in lower peak concentrations and lower bioavailability than when consumed as directed. dose proportionality among four of the available strengths of oral transmucosal fentanyl citrate (200, 400, 800, and 1600 mcg) has been demonstrated in a balanced crossover design in adult subjects (n=11). mean serum fentanyl levels following these four doses of oral transmucosal fentanyl citrate are shown in figure 1. the curves for each dose level are similar in shape with increasing dose levels producing increasing serum fentanyl levels. c max and auc 0→∞ increased in a dose-dependent manner that is approximately proportional to the oral transmucosal fentanyl citrate administered. figure 1. mean serum fentanyl concentration (ng/ml) in adult subjects comparing 4 doses of oral transmucosal fentanyl citrate the pharmacokinetic parameters of the four strengths of oral transmucosal fentanyl citrate tested in the dose-proportionality study are shown in table 4. the mean c max ranged from 0.39 to 2.51 ng/ml. the median time of maximum plasma concentration (t max ) across these four doses of oral transmucosal fentanyl citrate varied from 20 to 40 minutes (range of 20 to 480 minutes) as measured after the start of administration. table 4. pharmacokinetic parameters based on arterial blood samples. in adult subjects receiving 200, 400, 800, and 1600 mcg units of oral transmucosal fentanyl citrate pharmacokinetic parameter 200 mcg 400 mcg 800 mcg 1600 mcg t max , minute median (range) 40 (20-120) 25 (20-240) 25 (20-120) 20 (20-480) c max , ng/ml mean (%cv) 0.39 (23) 0.75 (33) 1.55 (30) 2.51 (23) auc 0-1440 , ng/ml minute mean (%cv) 102 (65) 243 (67) 573 (64) 1026 (67) t 1/2 , minute mean (%cv) 193 (48) 386 (115) 381 (55) 358 (45) distribution fentanyl is highly lipophilic. animal data showed that following absorption, 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 to 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) was 4 l/kg. elimination the total plasma clearance of fentanyl was 0.5 l/hr/kg (range 0.3 to 0.7 l/hr/kg). the terminal elimination half-life after oral transmucosal fentanyl citrate administration is about 7 hours. metabolism fentanyl is metabolized in the liver and in the intestinal mucosa to norfentanyl by cytochrome p450 3a4 isoform. norfentanyl was not found to be pharmacologically active in animal studies [see drug interactions ( 7 )] . excretion fentanyl is primarily (more than 90%) 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 feces. the metabolites are mainly excreted in the urine, while fecal excretion is less important. figure 1

ally available. thus, the generally observed 50% bioavailability of oral transmucosal fentanyl citrate is divided equally between rapid transmucosal and slower gi absorption. therefore, a unit dose of oral transmucosal fentanyl citrate, if chewed and swallowed, might result in lower peak concentrations and lower bioavailability than when consumed as directed. dose proportionality among four of the available strengths of oral transmucosal fentanyl citrate (200, 400, 800, and 1600 mcg) has been demonstrated in a balanced crossover design in adult subjects (n=11). mean serum fentanyl levels following these four doses of oral transmucosal fentanyl citrate are shown in figure 1. the curves for each dose level are similar in shape with increasing dose levels producing increasing serum fentanyl levels. c max and auc 0→∞ increased in a dose-dependent manner that is approximately proportional to the oral transmucosal fentanyl citrate administered. figure 1. mean serum fentanyl concentration (ng/ml) in adult subjects comparing 4 doses of oral transmucosal fentanyl citrate the pharmacokinetic parameters of the four strengths of oral transmucosal fentanyl citrate tested in the dose-proportionality study are shown in table 4. the mean c max ranged from 0.39 to 2.51 ng/ml. the median time of maximum plasma concentration (t max ) across these four doses of oral transmucosal fentanyl citrate varied from 20 to 40 minutes (range of 20 to 480 minutes) as measured after the start of administration. table 4. pharmacokinetic parameters based on arterial blood samples. in adult subjects receiving 200, 400, 800, and 1600 mcg units of oral transmucosal fentanyl citrate pharmacokinetic parameter 200 mcg 400 mcg 800 mcg 1600 mcg t max , minute median (range) 40 (20-120) 25 (20-240) 25 (20-120) 20 (20-480) c max , ng/ml mean (%cv) 0.39 (23) 0.75 (33) 1.55 (30) 2.51 (23) auc 0-1440 , ng/ml minute mean (%cv) 102 (65) 243 (67) 573 (64) 1026 (67) t 1/2 , minute mean (%cv) 193 (48) 386 (115) 381 (55) 358 (45) distribution fentanyl is highly lipophilic. animal data showed that following absorption, 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 to 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) was 4 l/kg. elimination the total plasma clearance of fentanyl was 0.5 l/hr/kg (range 0.3 to 0.7 l/hr/kg). the terminal elimination half-life after oral transmucosal fentanyl citrate administration is about 7 hours. metabolism fentanyl is metabolized in the liver and in the intestinal mucosa to norfentanyl by cytochrome p450 3a4 isoform. norfentanyl was not found to be pharmacologically active in animal studies [see drug interactions ( 7 )] . excretion fentanyl is primarily (more than 90%) 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 feces. the metabolites are mainly excreted in the urine, while fecal excretion is less important. figure 1

neously for 14 days prior to mating with untreated males at doses up to 300 mcg/kg and no effects on female fertility were observed. the systemic exposure at the dose of 300 mcg/kg was approximately 4.0 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison. males were administered fentanyl subcutaneously for 28 days prior to mating with untreated females at doses up to 300 mcg/kg. at 300 mcg/kg, adverse effects on sperm parameters, which affected fertility, were observed. these effects included decreased percent mobile sperm, decreased sperm concentrations as well as an increase in the percent abnormal sperm. the dose in males at which no effects on fertility were observed was 100 mcg/kg, which is approximately 2.7 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison. fentanyl has been shown to impair fertility in rats at doses of 30 mcg/kg iv and 160 mcg/kg subcutaneously. conversion to the human equivalent doses indicates that this is within the range of the human recommended dosing for oral transmucosal fentanyl citrate.

to mating with untreated males at doses up to 300 mcg/kg and no effects on female fertility were observed. the systemic exposure at the dose of 300 mcg/kg was approximately 4.0 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison. males were administered fentanyl subcutaneously for 28 days prior to mating with untreated females at doses up to 300 mcg/kg. at 300 mcg/kg, adverse effects on sperm parameters, which affected fertility, were observed. these effects included decreased percent mobile sperm, decreased sperm concentrations as well as an increase in the percent abnormal sperm. the dose in males at which no effects on fertility were observed was 100 mcg/kg, which is approximately 2.7 times the exposure of a single human dose of 1600 mcg per pain episode, based on an auc comparison. fentanyl has been shown to impair fertility in rats at doses of 30 mcg/kg iv and 160 mcg/kg subcutaneously. conversion to the human equivalent doses indicates that this is within the range of the human recommended dosing for oral transmucosal fentanyl citrate.

nts were also taking concomitant opioids, such as sustained-release morphine or transdermal fentanyl, for their persistent cancer pain. the adverse event data presented here reflect the actual percentage of patients experiencing each adverse effect among patients who received oral transmucosal fentanyl citrate for breakthrough cancer pain along with a concomitant opioid for persistent cancer pain. there has been no attempt to correct for concomitant use of other opioids, duration of oral transmucosal fentanyl citrate therapy, or cancer-related symptoms. three short-term clinical trials with similar titration schemes were conducted in 257 patients with malignancy and breakthrough cancer pain. data are available for 254 of these patients. table 1 lists, by dose groups, adverse reactions with an overall frequency of 1% or greater that occurred during titration. the ability to assign a dose-response relationship to these adverse reactions is limited by the titration schemes used in these studies. adverse reactions are listed in descending order of frequency within each body system. table 1. percent of patients with specific adverse events commonly associated with opioid administration or of particular clinical interest which occurred during titration (events in 1% or more of patients) percentage of patients reporting event dose group 200-600 mcg (n =230) 800-1400 mcg (n =138) 1600 mcg (n =54) >1600 mcg (n =41) any dose any dose = a patient who experienced the same adverse event at multiple doses was only counted once. (n =254) body as a whole asthenia 6 4 0 7 9 headache 3 4 6 5 6 accidental injury 1 1 4 0 2 digestive nausea 14 15 11 22 23 vomiting 7 6 6 15 12 constipation 1 4 2 0 4 nervous dizziness 10 16 6 15 17 somnolence 9 9 11 20 17 confusion 1 6 2 0 4 anxiety 3 0 2 0 3 abnormal gait 0 1 4 0 2 dry mouth 1 1 2 0 2 nervousness 1 1 0 0 2 vasodilatation 2 0 2 0 2 hallucinations 0 1 2 2 1 insomnia 0 1 2 0 1 thinking abnormal 0 1 2 0 1 vertigo 1 0 0 0 1 respiratory dyspnea 2 3 6 5 4 skin pruritus 1 0 0 5 2 rash 1 1 0 2 2 sweating 1 1 2 2 2 special senses abnormal vision 1 0 2 0 2 the following adverse reactions not reflected in table 1 occurred during titration with an overall frequency of 1% or greater and are listed in descending order of frequency within each body system. body as a whole : pain, fever, abdominal pain, chills, back pain, chest pain, infection digestive : diarrhea, dyspepsia, flatulence metabolic and nutritional : peripheral edema, dehydration nervous : hypesthesia, migraine respiratory : pharyngitis, cough increased the following reactions occurred during titration with an overall frequency of less than 1% and are listed in descending order of frequency within each body system. body as a whole : bone pain cardiovascular : deep thrombophlebitis, hypertension, hypotension digestive : anorexia, eructation, fecal impaction, gum hemorrhage, mouth ulceration, oral moniliasis hemic and lymphatic : anemia, leukopenia metabolic and nutritional : edema, hypercalcemia, weight loss musculoskeletal : myalgia, pathological fracture, myasthenia nervous : abnormal dreams, urinary retention, agitation, amnesia, emotional lability, euphoria, incoordination, libido decreased, neuropathy, paresthesia, speech disorder respiratory : hemoptysis, pleural effusion, rhinitis, asthma, hiccup, pneumonia, respiratory insufficiency, sputum increased skin and appendages : alopecia, exfoliative dermatitis special senses : taste perversion urogenita l: vaginal hemorrhage, dysuria, hematuria, urinary incontinence, urinary tract infection a long-term extension study was conducted in 156 patients with malignancy and breakthrough cancer pain who were treated for an average of 129 days. data are available for 152 of these patients. table 2 lists by dose groups, adverse reactions with an overall frequency of 1% or greater that occurred during the long-term extension study. adverse reactions are listed in descending order of frequency within each body system. table 2. percent of patients with adverse events commonly associated with opioid administration or of particular clinical interest which occurred during long term treatment (events in 1% or more of patients) dose group percentage of patients reporting event 200-600 mcg (n=98) 800-1400 mcg (n=83) 1600 mcg (n=53) >1600 mcg (n=27) any dose any dose = a patient who experienced the same adverse event at multiple doses was only counted once. (n=152) body as a whole asthenia 25 30 17 15 38 headache 12 17 13 4 20 accidental injury 4 6 4 7 9 hypertonia 2 2 2 0 3 digestive nausea 31 36 25 26 45 vomiting 21 28 15 7 31 constipation 14 11 13 4 20 intestinal obstruction 0 2 4 0 3 cardiovascular hypertension 1 1 0 0 1 nervous dizziness 12 10 9 0 16 anxiety 9 8 8 7 15 somnolence 8 13 8 7 15 confusion 2 5 13 7 10 depression 9 4 2 7 9 insomnia 5 1 8 4 7 abnormal gait 5 1 0 0 4 dry mouth 3 1 2 4 4 nervousness 2 2 0 4 3 stupor 4 1 0 0 3 vasodilatation 1 1 4 0 3 thinking abnormal 2 1 0 0 2 abnormal dreams 1 1 0 0 1 convulsion 0 1 2 0 1 myoclonus 0 0 4 0 1 tremor 0 1 2 0 1 vertigo 0 0 4 0 1 respiratory dyspnea 15 16 8 7 22 skin rash 3 5 8 4 8 sweating 3 2 2 0 4 pruritus 2 0 2 0 2 special senses abnormal vision 2 2 0 0 3 urogenital urinary retention 1 2 0 0 2 the following reactions not reflected in table 2 occurred with an overall frequency of 1% or greater in the long-term extension study and are listed in descending order of frequency within each body system. body as a whole : pain, fever, back pain, abdominal pain, chest pain, flu syndrome, chills, infection, abdomen enlarged, bone pain, ascites, sepsis, neck pain, viral infection, fungal infection, cachexia, cellulitis, malaise, pelvic pain cardiovascular : deep thrombophlebitis, palpitation, vascular disorder digestive : diarrhea, anorexia, dyspepsia, dysphagia, oral moniliasis, mouth ulceration, rectal disorder, stomatitis, flatulence, gastrointestinal hemorrhage, gingivitis, jaundice, periodontal abscess, eructation, glossitis, rectal hemorrhage hemic and lymphatic : anemia, leukopenia, thrombocytopenia, ecchymosis, lymphadenopathy, lymphedema, pancytopenia metabolic and nutritional : peripheral edema, edema, dehydration, weight loss, hyperglycemia, hypokalemia, hypercalcemia, hypomagnesemia musculoskeletal : myalgia, pathological fracture, joint disorder, leg cramps, arthralgia, bone disorder nervous : hypesthesia, paresthesia, hypokinesia, neuropathy, speech disorder, migraine respiratory : cough increased, pharyngitis, pneumonia, rhinitis, sinusitis, bronchitis, epistaxis, asthma, hemoptysis, sputum increased skin and appendages : skin ulcer, alopecia special senses : tinnitus, conjunctivitis, ear disorder, taste perversion urogenital : urinary tract infection, urinary incontinence, breast pain, dysuria, hematuria, scrotal edema, hydronephrosis, kidney failure, urinary urgency, urination impaired, breast neoplasm, vaginal hemorrhage, vaginitis the following reactions occurred with a frequency of less than 1% in the long-term extension study and are listed in descending order of frequency within each body system. body as a whole : allergic reaction, cyst, face edema, flank pain, granuloma, bacterial infection, mucous membrane disorder, neck rigidity cardiovascular : angina pectoris, hemorrhage, hypotension, peripheral vascular disorder, postural hypotension, tachycardia digestive : cheilitis, esophagitis, fecal incontinence, gastroenteritis, gastrointestinal disorder, gum hemorrhage, hemorrhage of colon, hepatorenal syndrome, liver tenderness, tooth caries, tooth disorder hemic and lymphatic : bleeding time increased metabolic and nutritional : acidosis, generalized edema, hypocalcemia, hypoglycemia, hyponatremia, hypoproteinemia, thirst musculoskeletal : arthritis, muscle atrophy, myopathy, synovitis, tendon disorder nervous : acute brain syndrome, agitation, cerebral ischemia, facial paralysis, foot drop, hallucinations, hemiplegia, miosis, subdural hematoma respiratory : hiccup, hyperventilation, lung disorder, pneumothorax, respiratory failure, voice alteration skin and appendages : herpes zoster, maculopapular rash, skin discoloration, urticaria, vesiculobullous rash special senses : ear pain, eye hemorrhage, lacrimation disorder, partial permanent deafness, partial transitory deafness urogenita l: kidney pain, nocturia, oliguria, polyuria, pyelonephritis

e used consistently for at least two consecutive days to treat breakthrough cancer pain without unacceptable side effects. in these studies 11% of patients withdrew due to adverse reactions and 14% withdrew due to other reasons. the successful dose of oral transmucosal fentanyl citrate for breakthrough cancer pain was not predicted from the daily maintenance dose of opioid used to manage the persistent cancer pain and is thus best determined by dose titration. a double-blind placebo controlled crossover study was performed in cancer patients to evaluate the effectiveness of oral transmucosal fentanyl citrate for the treatment of breakthrough cancer pain. of 130 patients who entered the study 92 patients (71%) achieved a successful dose during the titration phase. the distribution of successful doses is shown in table 5. table 5. successful dose of oral transmucosal fentanyl citrate following initial titration oral transmucosal fentanyl citrate dose total no. (%) (n=92) 200 mcg 13 (14) 400 mcg 19 (21) 600 mcg 14 (15) 800 mcg 18 (20) 1200 mcg 13 (14) 1600 mcg 15 (16) mean +/- sd 789 +/- 468 mcg on average, patients over 65 years of age titrated to a mean dose that was about 200 mcg less than the mean dose to which younger adult patients were titrated. oral transmucosal fentanyl citrate was administered beginning at time 0 minutes and produced more pain relief compared with placebo at 15, 30, 45, and 60 minutes as measured after the start of administration (see figure 2). the differences were statistically significant. figure 2. pain relief (pr) scores (mean±sd) during the double-blind phase ─ all patients with evaluable episodes on both oral transmucosal fentanyl citrate and placebo (n=86) figure 2

ntanyl, 800 mcg 1200 mcg green ndc 0406-9212-30 fentanyl, 1200 mcg 1600 mcg burgundy ndc 0406-9216-30 fentanyl, 1600 mcg note: colors are a secondary aid in product identification. please be sure to confirm the printed dosage before dispensing. store at 20° to 25°c (68° to 77°f) with excursions permitted between 15° and 30°c (59° to 86°f) until ready to use [see usp controlled room temperature]. protect oral transmucosal fentanyl citrate from freezing and moisture. do not use if the blister package has been opened. store oral transmucosal fentanyl citrate securely and dispose of properly [see patient counseling information ( 17 )] .