tivity reactions use caution in the management of patients with known anaphylactic reactions to hydroxocobalamin or cyanocobalamin. consider alternative therapies, if available. allergic reactions may include: anaphylaxis, chest tightness, edema, urticaria, pruritus, dyspnea, and rash. allergic reactions including angioneurotic edema have also been reported in postmarketing experience. 5.3 risk of renal injury cases of acute renal failure with acute tubular necrosis, renal impairment, and urine calcium oxalate crystals have been reported. in some situations, hemodialysis was required to achieve recovery. regular monitoring of renal function, including but not limited to blood urea nitrogen (bun) and serum creatinine, should be performed for 7 days following cyanokit therapy. 5.4 risk of increased blood pressure many patients with cyanide poisoning will be hypotensive; however, elevations in blood pressure have also been observed in known or suspected cyanide poisoning victims. elevations in blood pressure (≥180 mmhg systolic or ≥110 mmhg diastolic) were observed in approximately 18% of healthy subjects (not exposed to cyanide) receiving hydroxocobalamin 5 g and 28% of subjects receiving 10 g. increases in blood pressure were noted shortly after the infusions were started; the maximal increase in blood pressure was observed toward the end of the infusion. these elevations were generally transient and returned to baseline levels within 4 hours of dosing. monitor blood pressure during treatment with cyanokit. 5.5 interference with clinical laboratory evaluations and clinical methods clinical laboratory evaluations because of its deep red color, hydroxocobalamin has been found to interfere with colorimetric determination of certain laboratory parameters (e.g., clinical chemistry, hematology, coagulation, and urine parameters). in vitro tests indicated that the extent and duration of the interference are dependent on numerous factors such as the dose of hydroxocobalamin, analyte, methodology, analyzer, hydroxocobalamin concentration, and partially on the time between sampling and measurement. the data presented in table 2 is collected from in vitro studies and pharmacokinetic data in healthy volunteers and describes laboratory interference that may be observed following a 5 g dose of hydroxocobalamin. interference following a 10 g dose can be expected to last up to an additional 24 hours. the extent and duration of interference in cyanide-poisoned patients may differ. in addition, results may vary substantially from one analyzer to another. be aware of this when reporting and interpreting laboratory results. table 2 laboratory interference observed with in vitro samples of hydroxocobalamin laboratory parameter no interference observed artificially increased * artificially decreased * un-predictable duration of interference * ≥10% interference observed on at least 1 analyzer analyzers used: acl futura (instrumentation laboratory), axsym ® /architect ™ (abbott), bm coasys 110 (boehringer mannheim), celldyn 3700 ® (abbott), clinitek ® 500 (bayer), cobas integra ® 700, 400 (roche), gen-s coultronics, hitachi 917, sta ® compact, vitros ® 950 (ortho diagnostics) clinical chemistry calcium sodium potassium chloride urea ggt creatinine bilirubin triglycerides cholesterol total protein glucose albumin alkaline phosphatase alt amylase phosphate uric acid ast ck ckmb ldh 24 hours with the exception of bilirubin (up to 4 days) hematology erythrocytes hematocrit mcv leukocytes lymphocytes monocytes eosinophils neutrophils platelets hemoglobin mch mchc basophils 12 - 16 hours coagulation aptt pt (quick or inr) 24 - 48 hours urinalysis ph (with all doses) glucose protein erythrocytes leukocytes ketones bilirubin urobilinogen nitrite ph (with equivalent doses of <5 g) 48 hours up to 8 days; color changes may persist up to 28 days clinical methods because of its deep red color, hydroxocobalamin may cause hemodialysis machines to shut down due to an erroneous detection of a “blood leak”. this should be considered before hemodialysis is initiated in patients treated with hydroxocobalamin. 5.6 photosensitivity hydroxocobalamin absorbs visible light in the uv spectrum. it therefore has potential to cause photosensitivity. while it is not known if the skin redness predisposes to photosensitivity, patients should be advised to avoid direct sun while their skin remains discolored. 5.7 use of blood cyanide assay while determination of blood cyanide concentration is not required for management of cyanide poisoning and should not delay treatment with cyanokit, collecting a pretreatment blood sample may be useful for documenting cyanide poisoning as sampling post-cyanokit use may be inaccurate.

osage and administration instructions if clinical suspicion of cyanide poisoning is high, administer cyanokit without delay. comprehensive treatment of acute cyanide intoxication requires support of vital functions. airway, ventilatory and circulatory support, oxygen administration, and management of seizures should not be delayed to administer cyanokit [see warnings and precautions ( 5.1 )] . the expert advice of a regional poison control center may be obtained by calling 1-800-222-1222. identifying patients with cyanide poisoning cyanide poisoning may result from inhalation, ingestion, or dermal exposure to various cyanide-containing compounds, including smoke from closed-space fires. sources of cyanide poisoning include hydrogen cyanide and its salts, cyanogenic plants, aliphatic nitriles, and prolonged exposure to sodium nitroprusside. the presence and extent of cyanide poisoning are often initially unknown. there is no widely available, rapid, confirmatory cyanide blood test. treatment decisions must be made on the basis of clinical history and signs and symptoms of cyanide intoxication. table 1 common signs and symptoms of cyanide poisoning symptoms headache confusion dyspnea chest tightness nausea signs altered mental status (e.g., confusion, disorientation) seizures or coma mydriasis tachypnea / hyperpnea (early) bradypnea / apnea (late) hypertension (early) / hypotension (late) cardiovascular collapse vomiting plasma lactate concentration ≥8 mmol/l in some settings, panic symptoms including tachypnea and vomiting may mimic early cyanide poisoning signs. the presence of altered mental status (e.g., confusion and disorientation) and/or mydriasis is suggestive of true cyanide poisoning although these signs can occur with other toxic exposures as well. smoke inhalation not all smoke inhalation victims will have cyanide poisoning and may present with burns, trauma, and exposure to other toxic substances making a diagnosis of cyanide poisoning particularly difficult. prior to administration of cyanokit, smoke-inhalation victims should be assessed for the following: exposure to fire or smoke in an enclosed area presence of soot around the mouth, nose or oropharynx altered mental status although hypotension is highly suggestive of cyanide poisoning, it is only present in a small percentage of cyanide-poisoned smoke inhalation victims. also indicative of cyanide poisoning is a plasma lactate concentration ≥10 mmol/l (a value higher than that typically listed in the table of signs and symptoms of isolated cyanide poisoning because carbon monoxide associated with smoke inhalation also contributes to lactic acidemia). if cyanide poisoning is suspected, treatment should not be delayed to obtain a plasma lactate concentration. use with other cyanide antidotes the safety of administering other cyanide antidotes simultaneously with cyanokit has not been established. if a decision is made to administer another cyanide antidote with cyanokit, these drugs should not be administered concurrently in the same intravenous line [see dosage and administration ( 2.4 )]. 2.2 recommended dosing the starting dose of hydroxocobalamin for adults is 5 g administered as an intravenous infusion over 15 minutes (approximately 15 ml/min). administration of the entire vial constitutes a complete starting dose. depending upon the severity of the poisoning and the clinical response, a second dose of 5 g may be administered by intravenous infusion for a total dose of 10 g. the rate of infusion for the second dose may range from 15 minutes (for patients in extremis) to two hours, as clinically indicated. 2.3 preparation of solution for infusion reconstitute the 5 g vial of hydroxocobalamin with 200 ml of diluent (not provided with cyanokit) using the supplied sterile transfer spike. the recommended diluent is 0.9% sodium chloride injection (0.9% nacl). lactated ringers injection and 5% dextrose injection (d5w) have also been found to be compatible with hydroxocobalamin and may be used if 0.9% nacl is not readily available. the line on the vial label represents 200 ml volume of diluent. following the addition of diluent to the lyophilized powder, the vial should be repeatedly inverted or rocked, not shaken, for at least 60 seconds prior to infusion. visually inspect hydroxocobalamin solutions for particulate matter and color prior to administration. if the reconstituted solution is not dark red or if particulate matter is observed after the solution has been appropriately mixed, the solution should be discarded. 2.4 incompatibility information physical incompatibility (particle formation) and chemical incompatibility were observed with the mixture of hydroxocobalamin in solution with selected drugs that are frequently used in resuscitation efforts. hydroxocobalamin is also chemically incompatible with sodium thiosulfate and sodium nitrite and has been reported to be incompatible with ascorbic acid. therefore, these and other drugs should not be administered simultaneously through the same intravenous line as hydroxocobalamin. simultaneous administration of hydroxocobalamin and blood products (whole blood, packed red cells, platelet concentrate and/or fresh frozen plasma) through the same intravenous line is not recommended. however, blood products and hydroxocobalamin can be administered simultaneously using separate intravenous lines (preferably on contralateral extremities, if peripheral lines are being used). 2.5 storage of reconstituted drug product once reconstituted, hydroxocobalamin is stable for up to 6 hours at temperatures not exceeding 40°c (104°f). do not freeze. any reconstituted product not used by 6 hours should be discarded.

. because of the dark red color of hydroxocobalamin, the two most frequently occurring adverse reactions were chromaturia (red-colored urine) which was reported in all subjects receiving a 5 g dose or greater; and erythema (skin redness), which occurred in most subjects receiving a 5 g dose or greater. adverse reactions reported in at least 5% of the 5 g dose group and corresponding rates in the 10 g and placebo groups are shown in table 3 . table 3 incidence of adverse reactions occurring in >5% of subjects in 5 g dose group and corresponding incidence in 10 g dose group and placebo * rashes were predominantly acneiform adr 5 g dose group 10 g dose group hydroxocobalamin n=66 n (%) placebo n=22 n (%) hydroxocobalamin n=18 n (%) placebo n=6 n (%) chromaturia (red colored urine) 66 (100) 0 18 (100) 0 erythema 62 (94) 0 18 (100) 0 oxalate crystals in urine 40 (61) 1 (5) 10 (56) 0 rash* 13 (20) 0 8 (44) 0 blood pressure increased 12 (18) 0 5 (28) 0 nausea 4 (6) 1 (5) 2 (11) 0 headache 4 (6) 1 (5) 6 (33) 0 lymphocyte percent decreased 5 (8) 0 3 (17) 0 infusion site reaction 4 (6) 0 7 (39) 0 in this study, the following adverse reactions were reported to have occurred in a dose-dependent fashion and with greater frequency than observed in placebo-treated cohorts: increased blood pressure (particularly diastolic blood pressure), rash, nausea, headache and infusion site reactions. all were mild to moderate in severity and resolved spontaneously when the infusion was terminated or with standard supportive therapies. other adverse reactions reported in this study and considered clinically relevant were: eye disorders: swelling, irritation, redness gastrointestinal disorders: dysphagia, abdominal discomfort, vomiting, diarrhea, dyspepsia, hematochezia general disorders and administration site conditions: peripheral edema, chest discomfort immune system disorders: allergic reaction nervous system disorders: memory impairment, dizziness psychiatric disorders: restlessness respiratory, thoracic and mediastinal disorders: dyspnea, throat tightness, dry throat skin and subcutaneous tissue disorders: urticaria, pruritus vascular disorders: hot flush experience in known or suspected cyanide poisoning victims four open-label, uncontrolled, clinical studies (one of which was prospective and three of which were retrospective) were conducted in known or suspected cyanide-poisoning victims. a total of 245 patients received hydroxocobalamin treatment in these studies. systematic collection of adverse events was not done in all of these studies and interpretation of causality is limited due to the lack of a control group and due to circumstances of administration (e.g., use in fire victims). adverse reactions reported in these studies listed by system organ class included: cardiac disorders: ventricular extrasystoles investigations: electrocardiogram repolarization abnormality, heart rate increased respiratory, thoracic, and mediastinal disorders: pleural effusion adverse reactions common to both the studies in known or suspected cyanide poisoning victims and the study in healthy volunteers are listed in the healthy volunteer section only and are not duplicated in this list. 6.2 postmarketing experience the following adverse reactions have been identified during postapproval use of cyanokit. because adverse reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency. cases of acute renal failure with acute tubular necrosis, renal impairment, and urine calcium oxalate crystals have been reported in patients treated with cyanokit.

ta ) . the estimated background risk 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 2-4% and 15-20%, respectively. clinical considerations disease-associated maternal and/or embryo/fetal risk cyanide readily crosses the placenta. cyanide poisoning is a medical emergency in pregnancy which can be fatal for the pregnant woman and fetus if left untreated. life-sustaining therapy should not be withheld due to pregnancy. data animal data in animal studies, pregnant rats and rabbits received cyanokit (75, 150, or 300 mg/kg/d) during the period of organogenesis. following intraperitoneal dosing in rats and intravenous dosing in rabbits, maternal exposures were equivalent to 0.5, 1, or 2 times the human exposure at the therapeutic dose (based on auc). in the high dose groups for both species, maternal toxicity occurred, and there was a reduced number of live fetuses due to embryofetal resorptions. in addition, decreased live fetal weight occurred in high dose rats, but not in rabbits. incomplete skeletal ossification occurred in both rats and rabbits. in rats, two fetuses of the high dose group and two fetuses of the mid dose group (each from a different litter) had short, rudimentary or small front or hind legs. rabbit litters and fetuses exhibited a dose-dependent increase in various gross soft tissue and skeletal anomalies. the main findings in rabbits were flexed, rigid flexor or medially rotated forelimbs or hindlimbs and domed heads at external examination; enlarged anterior or posterior fontanelles of the ventricles of the brain and flat, bowed or large ribs at skeletal examination; and dilated ventricles of the brain, and thick wall of the stomach at visceral examination. it is unknown if similar findings would be observed in rats and rabbits if cyanokit was administered as a single dose during any critical period of development. 8.2 lactation risk summary breastfeeding is not recommended during treatment with cyanokit. there are no data to determine when breastfeeding may be safely restarted following administration of cyanokit. hydroxocobalamin and vitamin b12 (which is formed when hydroxocobalamin combines with cyanide) are present in human milk. there are no data on the effects of hydroxocobalamin on the breastfed infant or the effects on milk production. 8.4 pediatric use safety and effectiveness of cyanokit have not been established in this population. in non-us marketing experience, a dose of 70 mg/kg has been used to treat pediatric patients. 8.5 geriatric use approximately 50 known or suspected cyanide poisoning victims aged 65 or older received hydroxocobalamin in clinical studies. in general, the safety and effectiveness of hydroxocobalamin in these patients was similar to that of younger patients. no adjustment of dose is required in elderly patients. 8.6 renal impairment the safety and effectiveness of cyanokit have not been studied in patients with renal impairment. hydroxocobalamin and cyanocobalamin are eliminated unchanged by the kidneys. 8.7 hepatic impairment the safety and effectiveness of cyanokit have not been studied in patients with hepatic impairment.

ge in clinically recognized pregnancies is 2-4% and 15-20%, respectively. clinical considerations disease-associated maternal and/or embryo/fetal risk cyanide readily crosses the placenta. cyanide poisoning is a medical emergency in pregnancy which can be fatal for the pregnant woman and fetus if left untreated. life-sustaining therapy should not be withheld due to pregnancy. data animal data in animal studies, pregnant rats and rabbits received cyanokit (75, 150, or 300 mg/kg/d) during the period of organogenesis. following intraperitoneal dosing in rats and intravenous dosing in rabbits, maternal exposures were equivalent to 0.5, 1, or 2 times the human exposure at the therapeutic dose (based on auc). in the high dose groups for both species, maternal toxicity occurred, and there was a reduced number of live fetuses due to embryofetal resorptions. in addition, decreased live fetal weight occurred in high dose rats, but not in rabbits. incomplete skeletal ossification occurred in both rats and rabbits. in rats, two fetuses of the high dose group and two fetuses of the mid dose group (each from a different litter) had short, rudimentary or small front or hind legs. rabbit litters and fetuses exhibited a dose-dependent increase in various gross soft tissue and skeletal anomalies. the main findings in rabbits were flexed, rigid flexor or medially rotated forelimbs or hindlimbs and domed heads at external examination; enlarged anterior or posterior fontanelles of the ventricles of the brain and flat, bowed or large ribs at skeletal examination; and dilated ventricles of the brain, and thick wall of the stomach at visceral examination. it is unknown if similar findings would be observed in rats and rabbits if cyanokit was administered as a single dose during any critical period of development.

by substituting it for the hydroxo ligand linked to the trivalent cobalt ion, to form cyanocobalamin, which is then excreted in the urine. 12.2 pharmacodynamics administration of cyanokit to cyanide-poisoned patients with the attendant formation of cyanocobalamin resulted in increases in blood pressure and variable changes in heart rate upon initiation of hydroxocobalamin infusions [see warnings and precautions ( 5.4 )] . 12.3 pharmacokinetics following intravenous administration of hydroxocobalamin significant binding to plasma proteins and low molecular weight physiological compounds occurs, forming various cobalamin-(iii) complexes by replacing the hydroxo ligand. the low molecular weight cobalamins-(iii) formed, including hydroxocobalamin, are termed “free cobalamins-(iii)”; the sum of free and protein-bound cobalamins is termed “total cobalamins-(iii)”. in order to reflect the exposure to the sum of all derivatives, pharmacokinetics of cobalamins-(iii) (i.e., cobalamin-(iii) entity without specific ligand) were investigated instead of hydroxocobalamin alone, using the concentration unit μg eq/ml. dose-proportional pharmacokinetics was observed following single dose intravenous administration of 2.5 to 10 g of hydroxocobalamin in healthy volunteers. mean free and total cobalamins-(iii) c max values of 113 and 579 μg eq/ml, respectively, were determined following a dose of 5 g of hydroxocobalamin. similarly, mean free and total cobalamins-(iii) c max values of 197 and 995 μg eq/ml, respectively, were determined following the dose of 10 g of hydroxocobalamin. when normalized for body weight, male and female subjects revealed no major differences in pharmacokinetic parameters of free and total cobalamins-(iii) following the administration of 5 and 10 g of hydroxocobalamin. distribution the volume of distribution at steady state (v ss ) for both free and total cobalamins-(iii) showed no apparent relationship to dose. the v ss ranged from 280.7 to 349.5 l for free cobalamins-(iii), and from 21.8 to 25.6 l for total cobalamins-(iii). the comparatively high values for v ss of free cobalamins-(iii) are due to the high protein binding of hydroxocobalamin as it reacts in the blood with plasma constituents to form cobalamins-(iii) complexes and the rapid distribution of free cobalamins-(iii) into tissues. elimination the mean total amount of cobalamins-(iii) excreted in urine during the collection period of 72 hours was about 60% of a 5 g dose and about 50% of a 10 g dose of hydroxocobalamin. overall, the total urinary excretion was calculated to be at least 60 to 70% of the administered dose. the majority of the urinary excretion occurred during the first 24 hours, but red-colored urine was observed for up to 35 days following the intravenous infusion. the mean half-life of free and total cobalamins-(iii) was found to be approximately 26 to 31 hours at both the 5 g and 10 g dose level. metabolism hydroxocobalamin does not undergo metabolism. excretion hydroxocobalamin is mainly excreted in urine. in cyanide poisoning victims, hydroxocobalamin binds to cyanide to form cyanocobalamin, which is mainly excreted in urine.

g of hydroxocobalamin. similarly, mean free and total cobalamins-(iii) c max values of 197 and 995 μg eq/ml, respectively, were determined following the dose of 10 g of hydroxocobalamin. when normalized for body weight, male and female subjects revealed no major differences in pharmacokinetic parameters of free and total cobalamins-(iii) following the administration of 5 and 10 g of hydroxocobalamin. distribution the volume of distribution at steady state (v ss ) for both free and total cobalamins-(iii) showed no apparent relationship to dose. the v ss ranged from 280.7 to 349.5 l for free cobalamins-(iii), and from 21.8 to 25.6 l for total cobalamins-(iii). the comparatively high values for v ss of free cobalamins-(iii) are due to the high protein binding of hydroxocobalamin as it reacts in the blood with plasma constituents to form cobalamins-(iii) complexes and the rapid distribution of free cobalamins-(iii) into tissues. elimination the mean total amount of cobalamins-(iii) excreted in urine during the collection period of 72 hours was about 60% of a 5 g dose and about 50% of a 10 g dose of hydroxocobalamin. overall, the total urinary excretion was calculated to be at least 60 to 70% of the administered dose. the majority of the urinary excretion occurred during the first 24 hours, but red-colored urine was observed for up to 35 days following the intravenous infusion. the mean half-life of free and total cobalamins-(iii) was found to be approximately 26 to 31 hours at both the 5 g and 10 g dose level. metabolism hydroxocobalamin does not undergo metabolism. excretion hydroxocobalamin is mainly excreted in urine. in cyanide poisoning victims, hydroxocobalamin binds to cyanide to form cyanocobalamin, which is mainly excreted in urine.

cyanide-poisoned adult dogs assigned to treatment with vehicle (0.9% saline), or 75 or 150 mg/kg hydroxocobalamin. anesthetized dogs were poisoned by intravenous administration of a lethal dose of potassium cyanide. dogs then received vehicle or 75 or 150 mg/kg hydroxocobalamin, administered intravenously over 7.5 minutes. the 75 and 150 mg/kg doses are approximately equivalent to 5 and 10 g of hydroxocobalamin (respectively) in humans based on both body weight and the c max of hydroxocobalamin (total cobalamins-(iii)). survival at 4 hours and at 14 days was significantly greater in low-and high-dose groups compared with dogs receiving vehicle alone ( table 4 ). hydroxocobalamin reduced whole blood cyanide concentrations by approximately 50% by the end of the infusion compared with vehicle. table 4 survival of cyanide-poisoned dogs parameter treatment vehicle n=17 cyanokit 75 mg/kg n=19 150 mg/kg n=18 survival at hour 4, n (%) 7 (41) 18 (95) 18 (100) survival at day 14, n (%) 3 (18) 15 (79) 18 (100) histopathology revealed brain lesions that were consistent with cyanide-induced hypoxia. the incidence of brain lesions was markedly lower in hydroxocobalamin treated animals compared to vehicle treated groups. 14.2 smoke inhalation victims a prospective, uncontrolled, open-label study was carried out in 69 subjects who had been exposed to smoke inhalation from fires. subjects had to be over 15 years of age, present with soot in the mouth and expectoration (to indicate significant smoke exposure), and have altered neurological status. the median hydroxocobalamin dose was 5 g with a range from 4 to 15 g. fifty of 69 subjects (73%) survived following treatment with hydroxocobalamin. nineteen subjects treated with hydroxocobalamin did not survive. fifteen patients treated with hydroxocobalamin were in cardiac arrest initially at the scene; 13 of these subjects died and 2 survived. of the 42 subjects with pretreatment cyanide levels considered to be potentially toxic, 28 (67%) survived. of the 19 subjects whose pretreatment cyanide levels were considered potentially lethal, 11 (58%) survived. of the 50 subjects who survived, 9 subjects (18%) had neurological sequelae at hospital discharge. these included dementia, confusion, psychomotor retardation, anterograde amnesia, intellectual deterioration moderate cerebellar syndrome, aphasia, and memory impairment. two additional retrospective, uncontrolled studies were carried out in subjects who had been exposed to cyanide from fire or smoke inhalation. subjects were treated with up to 15 g of hydroxocobalamin. survival in these two studies was 34 of 61 (56%) for one study, and 30 of 72 (42%) for the second. 14.3 cyanide poisoning by ingestion or inhalation a retrospective, uncontrolled study was carried out in 14 subjects who had been exposed to cyanide from sources other than from fire or smoke (i.e., ingestion or inhalation). subjects were treated with 5 to 20 g of hydroxocobalamin. eleven of 12 subjects whose blood cyanide concentration was known had initial blood cyanide levels considered to be above the lethal threshold. ten of 14 subjects (71%) survived, following administration of hydroxocobalamin. one of the four subjects who died had presented in cardiac arrest. of the 10 subjects who survived, only 1 subject had neurological sequelae at hospital discharge. this subject had post-anoxic encephalopathy, with memory impairment, considered to be due to cyanide poisoning. 14.4 cross-study findings experience with dosing greater than 10 g of hydroxocobalamin across all four uncontrolled studies, 10 patients who did not demonstrate a full response to 5 or 10 g-doses of hydroxocobalamin were treated with more than 10 g of hydroxocobalamin. one of these 10 patients survived with unspecified neurological sequelae. effects on blood pressure initiation of hydroxocobalamin infusion as part of the therapeutic interventions generally resulted in increases in blood pressure and variable changes in heart rate (often normalization). survival of patients presenting in cardiac arrest of the 245 patients across all four studies, 68 (28%) presented in cardiac arrest. while blood pressure and heart rate may have been restored in many of these 68 patients, only five (7%) survived.

ours.

ide poisoning. treatment for cyanide poisoning may be lifesaving for both the pregnant woman and fetus. advise females of reproductive potential to notify their provider if they were pregnant during therapy with cyanokit [see use in specific populations ( 8.1 )] . lactation advise women that breastfeeding is not recommended during treatment with cyanokit [see use in specific populations ( 8.2 )] .

er if you: have had an allergic reaction to hydroxocobalamin or cyanocobalamin are pregnant or think you may have been pregnant during treatment with cyanokit . cyanokit may harm your unborn baby. however, treatment for cyanide poisoning may save your life and the life of your unborn baby. are breastfeeding. breastfeeding is not recommended during treatment with cyanokit. talk to your healthcare provider about the best way to feed your baby during this time. tell your healthcare provider about all of the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. how is cyanokit given? your healthcare provider will give you cyanokit through a vein by intravenous (iv) infusion over 15 minutes. a second dose of cyanokit may be given to you if needed. what should i avoid after i receive cyanokit? cyanokit may cause red colored skin. skin redness is common during treatment with cyanokit and may last up to 2 weeks after treatment with cyanokit. you should avoid sunlight while your skin is red. what are the possible side effects of cyanokit? cyanokit may cause serious side effects, including: allergic reactions . signs and symptoms of a serious allergic reaction include chest tightness, trouble breathing, swelling, hives, itching, and rash. seek emergency help if you experience signs and/or symptoms of an allergic reaction. kidney problems . cyanokit can cause kidney problems, including kidney failure. tell your healthcare provider if you develop crystals in your urine. your healthcare provider will monitor your kidney function for 7 days after treatment with cyanokit, or longer if needed. increased blood pressure. increased blood pressure is a common but serious side effect during treatment with cyanokit. your healthcare provider will monitor your blood pressure during treatment with cyanokit. the most common side effects of cyanokit include: red colored urine. red colored urine redness may last up to 5 weeks after treatment with cyanokit. nausea headache reactions at the site of infusion acne-like rash. acne-like rash may appear 7 to 28 days after treatment with cyanokit. this rash usually goes away without any treatment. these are not all the side effects with cyanokit. call your doctor for medical advice about side effects. you may report side effects to fda at 1-800-fda-1088. general information about the safe and effective use of cyanokit. this patient information leaflet summarizes the most important information about cyanokit. if you would like more information, talk to your healthcare provider. you can ask your pharmacist or healthcare provider for information about cyanokit that is written for health professionals. what are the ingredients in cyanokit? active ingredient: hydroxocobalamin manufactured by: merck santé s.a.s., semoy, france distributed by meridian medical technologies®, inc. columbia, md 21046 1-800-438-1985 180_us_20181_no for more information, go to www.cyanokit.com.