EMFLAZA- deflazacort tablet EMFLAZA- deflazacort suspension

EMFLAZA by

Drug Labeling and Warnings

EMFLAZA by is a Prescription medication manufactured, distributed, or labeled by PTC Therapeutics, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    EMFLAZA is indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients 2 years of age and older.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Assessments Prior to First Dose of EMFLAZA

    Administer all immunizations according to immunization guidelines prior to starting EMFLAZA. Administer live-attenuated or live vaccines at least 4 to 6 weeks prior to starting EMFLAZA [see Warnings and Precautions (5.8)].

    2.2 Dosing Information

    The recommended oral dosage of EMFLAZA is approximately 0.9 mg/kg/day once daily.  If tablets are used, round up to the nearest possible dose.  Any combination of the four EMFLAZA tablet strengths can be used to achieve this dose.  If the oral suspension is used, round up to the nearest tenth of a milliliter (mL).

    2.3 Discontinuation

    Dosage of EMFLAZA must be decreased gradually if the drug has been administered for more than a few days [see Warnings and Precautions (5.1)].

    2.4 Important Preparation and Administration Instructions

    EMFLAZA Tablets and Oral Suspension can be taken with or without food.

    EMFLAZA Tablets
    EMFLAZA Tablets can be administered whole or crushed and taken immediately after mixing with applesauce.

    EMFLAZA Oral Suspension
    Shake EMFLAZA Oral Suspension well before administration.

    Use only the oral dispenser provided with the product.  After withdrawing the appropriate dose into the oral dispenser, slowly add the EMFLAZA Oral Suspension into 3 to 4 ounces of juice or milk and mix well.  The dose should then be administered immediately.  Do not administer EMFLAZA with grapefruit juice [see Drug Interactions (7.1)].

    Discard any unused EMFLAZA Oral Suspension remaining after 1 month of first opening the bottle.

    2.5 Dosage Modification for Use with CYP3A4 Inhibitors and Inducers

    CYP3A4 Inhibitors
    Give one third of the recommended dosage when EMFLAZA is administered with moderate or strong CYP3A4 inhibitors.  For example, a 36 mg per day dose would be reduced to a 12 mg per day dose when used with moderate or strong CYP3A4 inhibitors [see Drug Interactions (7.1) and Clinical Pharmacology (12.3)].

    CYP3A4 Inducers
    Avoid use with moderate or strong CYP3A4 inducers with EMFLAZA [see Drug Interactions (7.1) and Clinical Pharmacology (12.3)].

  • 3 DOSAGE FORMS AND STRENGTHS

    Tablets

    • 6 mg:   White and round with “6” debossed on one side
    • 18 mg: White and round with “18” debossed on one side
    • 30 mg: White and oval with “30” debossed on one side
    • 36 mg: White and oval with “36” debossed on one side

    Oral Suspension

    • 22.75 mg/mL: Whitish suspension
  • 4 CONTRAINDICATIONS

    EMFLAZA is contraindicated in patients with known hypersensitivity to deflazacort or to any of the inactive ingredients.  Instances of hypersensitivity, including anaphylaxis, have occurred in patients receiving corticosteroid therapy [see Warnings and Precautions (5.15) and Adverse Reactions (6.2)].

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Alterations in Endocrine Function

    Corticosteroids, such as EMFLAZA, can cause serious and life-threatening alterations in endocrine function, especially with chronic use.  Monitor patients receiving EMFLAZA for Cushing’s syndrome, hyperglycemia, and adrenal insufficiency after EMFLAZA withdrawal.  In addition, patients with hypopituitarism, primary adrenal insufficiency or congenital adrenal hyperplasia, altered thyroid function, or pheochromocytoma may be at increased risk for adverse endocrine events.

    Risk of Adrenal Insufficiency Following Corticosteroid Withdrawal
    Corticosteroids produce reversible hypothalamic-pituitary-adrenal (HPA) axis suppression, with the potential for the development of secondary adrenal insufficiency after withdrawal of corticosteroid treatment.  Acute adrenal insufficiency can occur if corticosteroids are withdrawn abruptly, and can be fatal.  The degree and duration of adrenocortical insufficiency produced is variable among patients and depends on the dose, frequency, and duration of corticosteroid therapy.  The risk is reduced by gradually tapering the corticosteroid dose when withdrawing treatment.  This insufficiency may persist, however, for months after discontinuation of prolonged therapy; therefore, in any situation of stress occurring during that period of discontinuation, corticosteroid therapy should be reinstituted.  For patients already taking corticosteroids during times of stress, the dosage may need to be increased.

    A steroid “withdrawal syndrome”, seemingly unrelated to adrenocortical insufficiency, may also occur following abrupt discontinuance of corticosteroids.  This syndrome includes symptoms such as anorexia, nausea, vomiting, lethargy, headache, fever, joint pain, desquamation, myalgia, and/or weight loss.  These effects are thought to be due to the sudden change in corticosteroid concentration rather than to low corticosteroid levels.

    Cushing’s Syndrome
    Cushing’s syndrome (hypercortisolism) occurs with prolonged exposure to exogenous corticosteroids, including EMFLAZA.  Symptoms include hypertension, truncal obesity and thinning of the limbs, purple striae, facial rounding, facial plethora, muscle weakness, easy and frequent bruising with thin fragile skin, posterior neck fat deposition, osteopenia, acne, amenorrhea, hirsutism and psychiatric abnormalities.

    Hyperglycemia
    Corticosteroids can increase blood glucose, worsen pre-existing diabetes, predispose those on long-term therapy to diabetes mellitus, and may reduce the effect of anti-diabetic drugs.  Monitor blood glucose at regular intervals.  For patients with hyperglycemia, anti-diabetic treatment should be initiated or adjusted accordingly.

    Considerations for Use in Patients with Altered Thyroid Function
    Metabolic clearance of corticosteroids is decreased in hypothyroid patients and increased in hyperthyroid patients.  Changes in thyroid status of the patient may necessitate a dose adjustment of the corticosteroid.  When concomitant administration of corticosteroids and levothyroxine is required, administration of corticosteroid should precede the initiation of levothyroxine therapy to reduce the risk of adrenal crisis.

    Pheochromocytoma Crisis
    There have been reports of pheochromocytoma crisis, which can be fatal, after administration of systemic corticosteroids.  In patients with suspected or identified pheochromocytoma, consider the risk of pheochromocytoma crisis prior to administering corticosteroids.

    5.2 Immunosuppression and Increased Risk of Infection

    Corticosteroids, including EMFLAZA, suppress the immune system and increase the risk of infection with any pathogen, including viral, bacterial, fungal, protozoan, or helminthic.  Corticosteroids reduce resistance to new infections, exacerbate existing infections, increase the risk of disseminated infections, increase the risk of reactivation or exacerbation of latent infections, and mask some signs of infection.  These infections can be severe, and at times fatal.  The degree to which the dose, route, and duration of corticosteroid administration correlates with the specific risks of infection is not well characterized; however, the rate of occurrence of infectious complications increases with increasing doses of corticosteroids.

    Monitor for the development of infection and consider withdrawal of corticosteroids or reduction of the dose of corticosteroids as needed.

    Varicella Zoster and Measles Viral Infections
    Chickenpox caused by Varicella Zoster virus and measles can have a serious or even fatal course in non-immune children or adults on corticosteroids, including EMFLAZA.  In children or adults who have not had these diseases, particular care should be taken to avoid exposure.  If a patient is exposed to chickenpox, prophylaxis with varicella zoster immune globulin (VZIG) may be indicated.  If a patient is exposed to measles, prophylaxis with immunoglobulin (IG) may be indicated.  If chickenpox develops, treatment with antiviral agents may be considered.

    Hepatitis B Virus Reactivation
    Hepatitis B virus reactivation can occur in patients who are hepatitis B carriers undergoing treatment with immunosuppressive drugs including corticosteroids.  Reactivation can also occur in patients who appear to have resolved hepatitis B infection.

    Fungal Infections
    Corticosteroids may exacerbate systemic fungal infections and therefore should not be used in the presence of such infections.  For patients on corticosteroids who develop systemic fungal infections, withdrawal of corticosteroids or reduction of the dose of corticosteroids is recommended.

    Amebiasis
    Corticosteroids may activate latent amebiasis.  Therefore, it is recommended that latent amebiasis or active amebiasis be ruled out before initiating corticosteroid therapy in any patient who has spent time in the tropics, or any patient with unexplained diarrhea.

    Strongyloides Infestation
    In patients with known or suspected Strongyloides (threadworm) infestation, corticosteroid-induced immunosuppression may lead to Strongyloides hyperinfection and dissemination with widespread larval migration, often accompanied by severe enterocolitis and potentially fatal gram-negative septicemia.  For patients on corticosteroids who develop known or suspected Strongyloides (threadworm) infestation, withdrawal of corticosteroids or reduction of the dose of corticosteroids is recommended.

    5.3 Alterations in Cardiovascular/Renal Function

    Corticosteroids, including EMFLAZA, can cause elevation of blood pressure, salt, and water retention, and increased excretion of potassium and calcium.  Monitor blood pressure and assess for signs and symptoms of volume overload.  Monitor serum potassium levels.  Dietary salt restriction and potassium supplementation may be necessary.  EMFLAZA should be used with caution in patients with congestive heart failure, hypertension, or renal insufficiency.

    Literature reports suggest an association between use of corticosteroids and left ventricular free wall rupture after a recent myocardial infarction; therefore, therapy with EMFLAZA should be used with great caution in these patients.

    5.4 Gastrointestinal Perforation

    There is an increased risk of gastrointestinal perforation during corticosteroid use in patients with certain gastrointestinal disorders such as active or latent peptic ulcers, diverticulitis, fresh intestinal anastomoses, and non-specific ulcerative colitis.  Signs of gastrointestinal perforation, such as peritoneal irritation, may be masked in patients receiving corticosteroids.

    Avoid corticosteroids if there is a probability of impending perforation, abscess, or other pyogenic infections; diverticulitis; fresh intestinal anastomoses; or active or latent peptic ulcer.

    5.5 Behavioral and Mood Disturbances

    Potentially severe psychiatric adverse reactions may occur with systemic corticosteroids, including EMFLAZA.  Symptoms typically emerge within a few days or weeks of starting treatment and may be dose-related.  These reactions may improve after either dose reduction or withdrawal, although pharmacologic treatment may be necessary.  Psychiatric adverse reactions usually involve hypomanic or manic symptoms (e.g., euphoria, insomnia, mood swings) during treatment and depressive episodes after discontinuation of treatment.  Inform patients or caregivers of the potential for behavioral and mood changes and encourage them to seek medical attention if psychiatric symptoms develop, especially if depressed mood or suicidal ideation is suspected.

    5.6 Effects on Bones

    Decreased Bone Mineral Density
    Corticosteroids, including EMFLAZA, decrease bone formation and increase bone resorption both through their effect on calcium regulation (i.e., decreasing absorption and increasing excretion) and inhibition of osteoblast function.  This, together with a decrease in the protein matrix of the bone secondary to an increase in protein catabolism and reduced sex hormone production, may lead to inhibition of bone growth in pediatric patients and the development of bone loss at any age.  Bone loss can predispose patients to vertebral and long bone fractures.  Consider a patient’s risk of osteoporosis before initiating corticosteroid therapy.  Monitor bone mineral density in patients on long-term treatment with EMFLAZA.

    Avascular Necrosis
    Corticosteroids, including EMFLAZA, may cause avascular necrosis.

    5.7 Ophthalmic Effects

    Use of corticosteroids, including EMFLAZA, may produce posterior subcapsular cataracts.  Corticosteroids may also cause glaucoma with possible damage to the optic nerves, and may increase the risk of secondary ocular infections caused by bacteria, fungi, or viruses.  Corticosteroids are not recommended for patients with active ocular herpes simplex.

    Intraocular pressure may become elevated in some patients taking corticosteroids.  If treatment with EMFLAZA is continued for more than 6 weeks, monitor intraocular pressure.

    5.8 Immunizations

    Administer all immunizations according to immunization guidelines prior to starting EMFLAZA. Administer live-attenuated or live vaccines at least 4 to 6 weeks prior to starting EMFLAZA. Patients on EMFLAZA may receive concurrent vaccinations, except for live-attenuated or live vaccines.

    5.9 Serious Skin Rashes

    Toxic epidermal necrolysis has been reported with the use of deflazacort with symptoms beginning within 8 weeks of starting treatment.  Discontinue at the first sign of rash, unless the rash is clearly not drug related.

    5.10 Effects on Growth and Development

    Long-term use of corticosteroids, including EMFLAZA, can have negative effects on growth and development in children.

    5.11 Myopathy

    Patients receiving corticosteroids, including EMFLAZA, and concomitant therapy with neuromuscular blocking agents (e.g., pancuronium) or patients with disorders of neuromuscular transmission (e.g., myasthenia gravis) may be at increased risk of developing acute myopathy.  This acute myopathy is generalized, may involve ocular and respiratory muscles, and may result in quadriparesis.  Elevation of creatine kinase may occur.  Clinical improvement or recovery after stopping corticosteroids may require weeks to years.

    5.12 Kaposi’s Sarcoma

    Kaposi’s sarcoma has been reported to occur in patients receiving corticosteroid therapy, most often for chronic conditions.  Discontinuation of corticosteroids may result in clinical improvement.

    5.13 Risk of Serious Adverse Reactions in Infants because of Benzyl Alcohol Preservative

    EMFLAZA Oral Suspension contains benzyl alcohol and is not approved for use in pediatric patients less than 2 years of age.  Serious and fatal adverse reactions including “gasping syndrome” can occur in neonates and low birth weight infants treated with benzyl alcohol-preserved drugs, including EMFLAZA.  The “gasping syndrome” is characterized by central nervous system depression, metabolic acidosis, and gasping respirations.
    When prescribing EMFLAZA Oral Suspension, consider the combined daily metabolic load of benzyl alcohol from all sources, including EMFLAZA Oral Suspension (EMFLAZA Oral Suspension contains 10.45 mg of benzyl alcohol per mL; EMFLAZA Tablets do not contain benzyl alcohol) and other drugs containing benzyl alcohol. The minimum amount of benzyl alcohol at which serious adverse reactions may occur is not known. At the recommended dose of 0.9 mg/kg/day of EMFLAZA Oral Suspension, patients would receive approximately 0.4 mg/kg/day of benzyl alcohol [see Use in Specific Populations (8.4)].

    5.14 Thromboembolic Events

    Observational studies have shown an increased risk of thromboembolism (including venous thromboembolism) particularly with higher cumulative doses of corticosteroids.  It is unclear if risk differs by daily dose or duration of use.  Use EMFLAZA with caution in patients who have or may be predisposed to thromboembolic disorders.

    5.15 Anaphylaxis

    Rare instances of anaphylaxis have occurred in patients receiving corticosteroid therapy, including EMFLAZA.

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions are discussed in more detail in other sections:

    • Alterations in Endocrine Function [see Warnings and Precautions (5.1)]
    • Immunosuppression and Increased Risk of Infection [see Warnings and Precautions (5.2)]
    • Alterations in Cardiovascular/Renal Function [see Warnings and Precautions (5.3)]
    • Gastrointestinal Perforation [see Warnings and Precautions (5.4)]
    • Behavioral and Mood Disturbances [see Warnings and Precautions (5.5)]
    • Effects on Bones [see Warnings and Precautions (5.6)]
    • Ophthalmic Effects [see Warnings and Precautions (5.7)]
    • Immunizations [see Warnings and Precautions (5.8)]
    • Serious Skin Rashes [see Warnings and Precautions (5.9)]
    • Effects on Growth and Development [see Warnings and Precautions (5.10)]
    • Myopathy [see Warnings and Precautions (5.11)]
    • Kaposi’s Sarcoma [see Warnings and Precautions (5.12)]
    • Risk of Serious Adverse Reactions in Infants because of Benzyl Alcohol Preservative [see Warnings and Precautions (5.13)]
    • Thromboembolic Events [see Warnings and Precautions (5.14)]
    • Anaphylaxis [see Warnings and Precautions (5.15)]

    6.1 Clinical Trials 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.

    In Study 1 [see Clinical Studies (14)], the adverse reactions that were associated with deflazacort treatment discontinuation, in decreasing order of frequency, were weight increased, obesity, cataract, and sleep disorder.

    Most Common Adverse Reactions in Clinical Studies
    Table 1 lists the adverse reactions that occurred in ≥ 5% of patients in the 0.9 mg/kg/day deflazacort-treated group and that occurred more frequently than in placebo patients in Study 1, which included patients with DMD between the ages of 5 and 15 years.

    Table 1: Adverse Reactions that Occurred in ≥ 5% of Deflazacort-Treated Patients and Occurred More Frequently than in Placebo Patients with DMD (Study 1)

    1 At 12 weeks placebo patients were re-randomized to receive either deflazacort or an active comparator.
    Adverse ReactionDeflazacort
    0.9 mg/kg/d (N=51)
    % at 12 weeks    		Placebo (N=50)
    % at 12 weeks1
    Cushingoid appearance3312
    Weight increased206
    Increased appetite142
    Upper respiratory tract infection1210
    Cough126
    Pollakiuria122
    Nasopharyngitis106
    Hirsutism102
    Central obesity104
    Erythema86
    Irritability84
    Rhinorrhea80
    Abdominal discomfort62

    Common adverse reactions (≥ 5% of deflazacort-treated patients) that occurred over 52 weeks of exposure to deflazacort 0.9 mg/kg/day in Study 1 and at a higher rate than deflazacort 0.9 mg/kg/day in the 12-week placebo-controlled phase of the trial include Cushingoid appearance (60%), hirsutism (35%), weight increased (28%), erythema (28%), central obesity (25%), abdominal pain/abdominal pain upper (18% combined), pollakiuria (15%), constipation (10%), irritability (10%), abnormal behavior (9%), pyrexia (9%), back pain (7%), rash (7%), contusion (6%), nausea (6%), psychomotor hyperactivity (6%), epistaxis (6%), and skin striae (6%).

    Study 1 also evaluated a higher dosage of deflazacort (1.2 mg/kg/day).  Compared with the 0.9 mg/kg/day dosage, deflazacort 1.2 mg/kg/day over 52 weeks was associated with a higher incidence of certain adverse reactions, including Cushingoid appearance (69%), erythema (49%), hirsutism (37%), headache (34%), weight increased (32%), constipation (15%), abdominal pain upper (14%), skin striae (11%), acne (11%), and abdominal discomfort (8%).  As there was no additional benefit with the 1.2 mg/kg/day dose of deflazacort, use of EMFLAZA 1.2 mg/kg/day is not recommended for the treatment of DMD [see Dosage and Administration (2.2)].

    In an additional clinical study of two years duration with extended follow-up (Study 2), many of the same adverse reactions were observed.  In addition, musculoskeletal events associated with long-term steroid use were also observed, including muscle weakness, tendon disorder, and osteopenia.

    Less Common Adverse Reactions Observed in Clinical Studies
    Other adverse reactions (≥ 1% frequency in any deflazacort treatment group and greater than placebo) that were observed during the 12-week placebo-controlled phase of Study 1 are shown below.

    Eye Disorders: Lacrimation increased

    Gastrointestinal Disorders: Dyspepsia, nausea, gastrointestinal disorder

    General Disorders and Administration Site Conditions: Thirst

    Infections: Hordeolum, impetigo, influenza, otitis externa, pharyngitis, tooth abscess, urinary tract infection, viral infection

    Injury, Poisoning and Procedural Complications: Back injury, contusion, face injury, fibula fracture, greenstick fracture, heat exhaustion

    Investigations: Glucose urine present, heart rate irregular

    Musculoskeletal and Connective Tissue Disorders: Back pain, muscle spasms, myalgia, neck mass, neck pain, pain in extremity

    Nervous System Disorders: Dizziness, psychomotor hyperactivity

    Psychiatric Disorders: Affect lability, aggression, depression, emotional disorder, middle insomnia, mood altered, mood swings, sleep disorder

    Renal and Urinary Disorders: Chromaturia, dysuria, hypertonic bladder

    Reproductive System and Breast Disorders: Testicular pain

    Respiratory, Thoracic, and Mediastinal Disorders: Hypoventilation, rhinorrhea

    Skin and Subcutaneous Tissue Disorders: Acne, alopecia, dermatitis acneiform

    Vascular Disorders: Hot flush

    6.2 Postmarketing Experience

    The following adverse reactions have been reported during post-approval use of deflazacort worldwide or during post-approval use of other corticosteroids.  These reactions are reported voluntarily from a population of uncertain size; therefore, it is not always possible to estimate their frequency or establish a causal relationship to drug exposure.

    Blood and Lymphatic System Disorders: Leukocytosis

    Cardiac Disorder: Heart failure

    Eye Disorders: Chorioretinopathy, corneal or scleral thinning

    Gastrointestinal Disorders: Acute pancreatitis (especially in children), hemorrhage, peptic ulceration, perforation of peptic ulcer

    General Disorders and Administration Site Conditions: Edema, impaired healing

    Immune System Disorders: Hypersensitivity including anaphylaxis

    Metabolism and Nutrition Disorders: Impaired carbohydrate tolerance with increased requirement for anti-diabetic therapy, negative protein and calcium balance, potassium loss and hypokalemic alkalosis when co-administered with beta 2-agonist and xanthines

    Musculoskeletal and Connective Tissue Disorders: Avascular necrosis, muscle wasting, negative nitrogen balance, tendonitis and tendon rupture when co-administered with quinolones, vertebral and long bone fractures

    Nervous System Disorders: Aggravation of epilepsy, increased intra-cranial pressure with papilledema in children (pseudotumor cerebri) usually after treatment withdrawal, vertigo

    Psychiatric Disorders: Anxiety, cognitive dysfunction including confusion and amnesia, delusions, hallucinations, mania, suicidal thoughts

    Skin and Subcutaneous Tissue Disorders: Toxic epidermal necrolysis

    Vascular Disorders: Thromboembolism, in particular in patients with underlying conditions associated with increased thrombotic tendency, benign intracranial hypertension

  • 7 DRUG INTERACTIONS

    7.1 CYP3A4 Inhibitors and Inducers

    Moderate or Strong CYP3A4 Inhibitors
    The active metabolite of deflazacort, 21-desDFZ, is a substrate of CYP3A4 [see Clinical Pharmacology (12.3)].  Co-administration of deflazacort with clarithromycin, a strong CYP3A4 inhibitor, increased total exposure to 21-desDFZ by about 3-fold.  Therefore, give one third the recommended dosage of EMFLAZA when moderate or strong CYP3A4 inhibitors (e.g., clarithromycin, fluconazole, diltiazem, verapamil, grapefruit juice) are used concomitantly with EMFLAZA [see Dosage and Administration (2.5) and Clinical Pharmacology (12.3)].

    Moderate or Strong CYP3A4 Inducers
    Co-administration of deflazacort with rifampin, a strong CYP3A4 inducer, significantly decreased the exposure of 21-desDFZ.  Avoid concomitant use of strong (e.g., efavirenz) or moderate (e.g., carbamazepine, phenytoin) CYP3A4 inducers with EMFLAZA [see Dosage and Administration (2.5) and Clinical Pharmacology (12.3)].

    7.2 Neuromuscular Blockers

    Patients receiving corticosteroids, including EMFLAZA, and concomitant therapy with neuromuscular blocking drugs (e.g., pancuronium) may be at increased risk of developing an acute myopathy [see Warnings and Precautions (5.11)].

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary
    Corticosteroids should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.  Infants born to mothers who have received substantial doses of corticosteroids during pregnancy should be carefully observed for signs of hypoadrenalism.  There are no adequate and well-controlled studies with EMFLAZA in pregnant women to inform drug-associated risks.

    Corticosteroids, including EMFLAZA, readily cross the placenta.  Adverse developmental outcomes, including orofacial clefts (cleft lip, with or without cleft palate) and intrauterine growth restriction, and decreased birth weight, have been reported with maternal use of corticosteroids, including EMFLAZA, during pregnancy.  Some epidemiologic studies report an increased risk of orofacial clefts from about 1 per 1000 infants to 3 to 5 per 1000 infants; however, a risk for orofacial clefts has not been observed in all studies.  Intrauterine growth restriction and decreased birth weight appear to be dose-related; however, the underlying maternal condition may also contribute to these risks (see Data).  The estimated background risk of major birth defects and miscarriage for the indicated populations is unknown.  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.

    Animal reproduction studies have not been conducted with deflazacort.  Animal reproduction studies conducted with other corticosteroids in pregnant mice, rats, hamsters, and rabbits using clinically relevant doses have shown an increased incidence of cleft palate.  An increase in embryofetal death, intrauterine growth retardation, and constriction of the ductus arteriosus were observed in some animal species.

    Data
    Human Data
    Multiple cohort and case-controlled studies in humans suggest that maternal corticosteroid use during the first trimester increases the rate of cleft lip, with or without cleft palate, from about 1/1000 infants to 3-5/1000 infants.  Two prospective case-controlled studies showed decreased birth weight in infants exposed to maternal corticosteroids in utero.

    8.2 Lactation

    Risk Summary
    Systemically administered corticosteroids appear in human milk and could suppress growth, interfere with endogenous corticosteroid production, or cause other untoward effects.  The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for EMFLAZA and any potential adverse effects on the breastfed infant from EMFLAZA.  There are no data on the effects on milk production.

    8.4 Pediatric Use

    The safety and effectiveness of EMFLAZA for the treatment of DMD have been established in patients 2 years of age and older.  Use of EMFLAZA in pediatric patients is supported by a multicenter, randomized, double-blind, placebo- and active-controlled study in 196 males 5 to 15 years of age [see Clinical Studies (14)]. Use of EMFLAZA in patients 2 years to less than 5 years of age is supported by the findings of efficacy and safety in patients 5 years and older with DMD.

    Safety and effectiveness in pediatric patients below the age of 2 years have not been established.

    EMFLAZA Oral Suspension contains benzyl alcohol and is not approved for use in pediatric patients less than 2 years of age.  Serious adverse reactions including fatal reactions and “gasping syndrome” occurred in premature neonates and low birth weight infants in the neonatal intensive care unit who received drugs containing benzyl alcohol as a preservative.  In these cases, benzyl alcohol dosages of 99 to 234 mg/kg/day produced high levels of benzyl alcohol and its metabolites in the blood and urine (blood levels of benzyl alcohol were 0.61 to 1.378 mmol/L).  Additional adverse reactions included gradual neurological deterioration, seizures, intracranial hemorrhage, hematologic abnormalities, skin breakdown, hepatic and renal failure, hypotension, bradycardia, and cardiovascular collapse.  Preterm, low-birth weight infants may be more likely to develop these reactions because they may be less able to metabolize benzyl alcohol.

    When prescribing EMFLAZA Oral Suspension consider the combined daily metabolic load of benzyl alcohol from all sources including EMFLAZA Oral Suspension (EMFLAZA Oral Suspension contains 10.45 mg of benzyl alcohol per mL; EMFLAZA Tablets do not contain benzyl alcohol) and other drugs containing benzyl alcohol. The minimum amount of benzyl alcohol at which serious adverse reactions may occur is not known. At the recommended dose of 0.9 mg/kg/day of EMFLAZA Oral Suspension, patients would receive approximately 0.4 mg/kg/day of benzyl alcohol [see Warnings and Precautions (5.13)].

    Juvenile Animal Toxicity Data
    Oral administration of deflazacort (0, 0.1, 0.3, and 1.0 mg/kg/day) to juvenile rats from postnatal day (PND) 21 to 80 resulted in decreased body weight gain and adverse effects on skeletal development (including decreased cellularity of growth plate and altered bone distribution) and on lymphoid tissue (decreased cellularity).  A no-effect dose was not identified.  In addition, neurological and neurobehavioral abnormalities were observed at the mid and/or high dose.  Plasma 21-desDFZ exposure (AUC) at the lowest dose tested (0.1 mg/kg/day) was lower than that in humans at the recommended human dose of EMFLAZA (0.9 mg/kg/day).

    8.5 Geriatric Use

    DMD is largely a disease of children and young adults; therefore, there is no geriatric experience with EMFLAZA.

    8.6 Renal Impairment

    No dose adjustment is required in patients with mild, moderate or severe renal impairment [see Clinical Pharmacology (12.3)].

    8.7 Hepatic Impairment

    No dose adjustment is required in patients with mild or moderate hepatic impairment [see Clinical Pharmacology (12.3)].  There is no clinical experience in patients with severe hepatic impairment, and a dosing recommendation can not be provided for patients with severe hepatic impairment.

  • 10 OVERDOSAGE

    Treatment of acute overdosage is by immediate gastric lavage or emesis followed by supportive and symptomatic therapy.  For chronic overdosage in the face of severe disease requiring continuous steroid therapy, the dosage of EMFLAZA may be reduced temporarily, or alternate day treatment may be introduced.

  • 11 DESCRIPTION

    The active ingredient in EMFLAZA is deflazacort (a corticosteroid).  Corticosteroids are adrenocortical steroids, both naturally occurring and synthetic.  The molecular formula for deflazacort is C25H31NO6.  The chemical name for deflazacort is (11β,16β)-21-(acetyloxy)-11-hydroxy-2'-methyl-5'H-pregna-1,4-dieno[17,16-d]oxazole-3,20-dione, and the structural formula is:

    The structural formula for EMFLAZA is deflazacort (a corticosteroid).  Corticosteroids are adrenocortical steroids, both naturally occurring and synthetic.  The molecular formula for deflazacort is C25H31NO6.  The chemical name for deflazacort is (11β,16β)-21-(acetyloxy)-11-hydroxy-2'-methyl-5'H-pregna-1,4-dieno[17,16-d]oxazole-3,20-dione.

    Deflazacort is a white to off white, odorless fine powder and has a molecular weight of 441.517.  Deflazacort is freely soluble in acetic acid and dichloromethane and soluble in methanol and acetone.

    EMFLAZA for oral administration is available as an immediate-release tablet in strengths of 6, 18, 30 and 36 mg and an immediate-release oral suspension in a strength of 22.75 mg/mL.  Each tablet contains deflazacort and the following inactive ingredients: colloidal silicon dioxide, lactose monohydrate, magnesium stearate, and pre-gelatinized corn starch.  The oral suspension contains deflazacort and the following inactive ingredients: acetic acid, aluminum magnesium silicate, benzyl alcohol, carboxymethylcellulose sodium, polysorbate 80, purified water, and sorbitol.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Deflazacort is a corticosteroid prodrug, whose active metabolite, 21-desDFZ, acts through the glucocorticoid receptor to exert anti-inflammatory and immunosuppressive effects.  The precise mechanism by which deflazacort exerts its therapeutic effects in patients with DMD is unknown.

    12.3 Pharmacokinetics

    Absorption
    After oral administration in the fasted state, the median Tmax with deflazacort tablets or suspension is about 1 hour (range 0.25 to 2 hours).

    Food Effect: Co-administration of deflazacort tablets with a high-fat meal reduced Cmax by about 30% and delayed Tmax by one hour, relative to administration under fasting conditions, but there was no effect on the overall systemic absorption as measured by AUC.  The bioavailability of deflazacort tablets was similar to that of the oral suspension.  The administration of deflazacort with food or crushed in applesauce did not affect the absorption and bioavailability of deflazacort.

    Distribution
    The protein binding of the active metabolite of deflazacort is about 40%.

    Elimination
    Metabolism
    Deflazacort is rapidly converted to the active metabolite 21-desDFZ by esterases after oral administration.  21-desDFZ is further metabolized by CYP3A4 to several other inactive metabolites.

    Excretion
    Urinary excretion is the predominant route of deflazacort elimination (about 68% of the dose), and the elimination is almost completed by 24 hours post dose.  21-desDFZ accounts for 18% of the eliminated drug in the urine.

    Specific Populations
    Pediatric Patients
    The Cmax values (Geometric mean, %CV) of 21-desDFZ in children (ages 4-11, N=16) and adolescents (ages 12-16, N=8) was 206 ng/mL (95.6%) and 381 ng/mL (37.7%), respectively, on Day 1 after administration of 0.9 mg/kg deflazacort.  The AUCinf (Geometric mean, %CV) of 21-desDFZ in children (ages 4-11, N=16) and adolescents (ages 12-16, N=8) was 400 ngh/mL (87.5%) and 655 ngh/mL (58.1%) on Day 1 after administration of 0.9 mg/kg deflazacort.

    Male and Female Patients
    There are no differences in the pharmacokinetics of 21-desDFZ between males and females.

    Racial or Ethnic Groups
    There are no differences in the pharmacokinetics of 21-desDFZ between Caucasians and non-Caucasians.

    Patients with Renal Impairment
    In a study (N=16) comparing subjects with end stage renal disease (creatinine clearance less than 15 mL/min) with healthy matched controls, 21-desDFZ exposure was similar between the groups.

    Patients with Hepatic Impairment
    In a study (N=16) comparing subjects with moderate hepatic impairment (Child-Pugh Class B) with healthy matched controls, 21-desDFZ exposure was similar between the groups.  There is no experience in patients with severe hepatic impairment.

    Drug Interaction Studies

    In Vivo Assessment of Drug Interactions

    Compared to administration of deflazacort alone, administration of deflazacort following multiple doses of a strong CYP3A4 and Pgp inhibitor (clarithromycin) resulted in markedly higher Cmax, AUClast, and AUCinf values of 21-desDFZ.  Geometric mean exposure (Cmax, AUClast, and AUCinf) of 21-desDFZ ranged from 2.3-fold to 3.4-fold higher following administration of clarithromycin [see Dosage and Administration (2.5)].

    Compared to administration of deflazacort alone, administration of deflazacort following multiple doses of a strong CYP3A4 inducer (rifampicin) resulted in markedly lower Cmax, AUClast, and AUCinf values of 21-desDFZ.  Geometric mean exposures (Cmax, AUClast, and AUCinf) of 21-desDFZ were approximately 95% lower following administration of rifampin [see Drug Interactions (7.1)].

    6β-Hydroxy-21-desacetyl deflazacort, a secondary and inactive metabolite, is not expected to cause any clinically meaningful interactions with the CYP enzymes or transporters.

    In Vitro Assessment of Drug Interactions

    Drug-Metabolizing Enzyme Inhibition
    21-desDFZ at concentrations up to 100 μM did not inhibit CYP1A2, 2C9, 2C19, 3A4, UGT1A1, UGT1A4, UGT1A6, UGT1A9, or UGT2B7 and exhibited weak and not likely clinically meaningful inhibition for 2B6, 2C8, 2D6, and 3A4, UGT1A3 and UGT2B15.

    6β-Hydroxy-21-desacetyl deflazacort exhibited modestly detectable inhibition for CYP2C19 and 3A4 (midazolam as probe substrate) with IC50 at approximately 50 and 35 μM, respectively. Weak inhibition was observed for CYP1A2, 2B6, 2C8, 2C9, 2D6 and 3A4 (testosterone as probe substrate) with IC50 greater than 50 μM.

    Drug-Metabolizing Enzyme Induction
    Deflazacort and 6β-hydroxy-21-desacetyl deflazacort at concentrations up to 10 μM caused no significant induction response for CYP1A2, 2B6, or 3A4.

    Transporters
    Both deflazacort and 21-desDFZ are substrates of Pgp.  21-desDFZ is not a substrate for BCRP.  Neither deflazacort nor 21-desDFZ inhibited Pgp or BCRP in vitro.  21-desDFZ was not a substrate for SLC transporters OATP1B1 or OATP1B3, and did not inhibit SLC transporters OATP1B1, OATP1B3, OAT1, OAT3, or OCT2.

    6β-Hydroxy-21-desacetyl deflazacort is a substrate of human OAT3 uptake transporter but not a substrate of the human BCRP, Pgp, MATE1, MATE2-K, OAT1, OATP1B1, OATP1B3, and OCT2 transporters. It did not inhibit BCRP, OAT1, OAT3 or OCT2 but slightly inhibited Pgp (IC50 19.81 μM), OATP1B1 (IC50 36.72 μM), and OATP1B3 (IC50 42.22 μM). 6β-Hydroxy-21-desacetyl deflazacort had weak inhibition on MATE1, MATE2-K, OCT1, and BSEP with IC50 greater than 50 μM.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenesis
    In a published 2-year carcinogenicity study in rats, oral administration of deflazacort (0, 0.03, 0.06, 0.12, 0.25, 0.50, or 1.0 mg/kg/day) resulted in bone tumors (osteosarcoma and osteoma) of the head at 0.25 mg/kg/day, the highest evaluable dose.  Doses higher than 0.25 mg/kg/day could not be evaluated for tumors because of a marked decrease in survival.

    Mutagenesis
    Deflazacort and 21-desDFZ were negative in in vitro (bacterial reverse mutation and human lymphocyte chromosomal aberration) assays and deflazacort was negative in an in vivo (rat micronucleus) assay.

    Impairment of Fertility
    Fertility studies in animals were not conducted with deflazacort.  No effects on the male reproductive system were observed following oral administration of deflazacort to monkeys (0, 1.0, 3.0, or 6.0 mg/kg/day) for 39 weeks or rats (0, 0.05, 0.15, or 0.5 mg/kg/day) for 26 weeks.  Plasma 21-desDFZ exposures (AUC) at the highest doses tested in monkey and rat were 4 and 2 times, respectively, that in humans at the recommended human dose of EMFLAZA (0.9 mg/kg/day).

  • 14 CLINICAL STUDIES

    The effectiveness of EMFLAZA for the treatment of DMD was established in Study 1, a multicenter, randomized, double-blind, placebo-controlled, 52-week study conducted in the US and Canada.  The study population consisted of 196 male pediatric patients 5 to 15 years of age with documented mutation of the dystrophin gene, onset of weakness before 5 years of age, and serum creatinine kinase activity at least 10 times the upper limit of normal (ULN) at some stage in their illness.  Patients were randomized to therapy with deflazacort (0.9 or 1.2 mg/kg/day), an active comparator, or placebo.  A comparison to placebo was made after 12 weeks of treatment.  After 12 weeks, placebo patients were re-randomized to receive either deflazacort or the active comparator; all patients continued treatment for an additional 40 weeks.  Baseline characteristics were comparable between the treatment arms.

    In Study 1, efficacy was evaluated by assessing the change between Baseline and Week 12 in average strength of 18 muscle groups.  Individual muscle strength was graded using a modified Medical Research Council (MRC) 11-point scale, with higher scores representing greater strength.

    The change in average muscle strength score between Baseline and Week 12 was significantly greater for the deflazacort 0.9 mg/kg/day dose group than for the placebo group (see Table 2).

    Table 2: Analysis of Change from Baseline at Week 12 in Average Muscle Strength Score (Study 1)
    TreatmentNChange from
    Baseline
    LS Mean (95% CI)    		P-value
    Deflazacort 0.9 mg/kg/day510.15 (0.01, 0.28)0.017
    Placebo50-0.10 (-0.23, 0.03)

    Compared with the deflazacort 0.9 mg/kg/day group, the deflazacort 1.2 mg/kg/day group demonstrated a small additional benefit compared to placebo at Week 12, but had a greater incidence of adverse reactions.  Therefore, use of a 1.2 mg/kg/day dosage of EMFLAZA is not recommended [see Dosage and Administration (2.2)].

    Although not a pre-specified statistical analysis, compared with placebo, the deflazacort 0.9 mg/kg/day dose group demonstrated at Week 52 the persistence of the treatment effect observed at Week 12 and the small advantage of the 1.2 mg/kg/day dose that was observed at Week 12 was no longer present.  Also not statistically controlled for multiple comparisons, results on several timed measures of patient function (i.e., time to stand from supine, time to climb 4 stairs, and time to walk or run 30 feet) numerically favored deflazacort 0.9 mg/kg/day at Week 12, in comparison with placebo.

    An additional randomized, double-blind, placebo-controlled, 104-week clinical trial evaluated deflazacort in comparison to placebo (Study 2).  The study population consisted of 29 male children 6 to 12 years of age with a DMD diagnosis confirmed by the documented presence of abnormal dystrophin or a confirmed mutation of the dystrophin gene.  The results of the analysis of the primary endpoint of average muscle strength scores in Study 2 (graded on a 0-5 scale) at 2 years were not statistically significant, possibly because of a limited number of patients remaining in the placebo arm (subjects were discontinued from the trial when they lost ambulation).  Although not statistically controlled for multiple comparisons, average muscle strength scores at Months 6 and 12, as well as the average time to loss of ambulation, numerically favored deflazacort in comparison with placebo.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    16.1 How Supplied

    EMFLAZA Tablets

    • 6 mg are white, round with “6” debossed on one side.  They are supplied as follows:
      NDC: 52856-501-01      Bottle of 100 tablets

    • 18 mg are white, round with “18” debossed on one side.  They are supplied as follows:
      NDC: 52856-502-03      Bottle of 30 tablets

    • 30 mg are white, oval with “30” debossed on one side.  They are supplied as follows:
      NDC: 52856-503-03      Bottle of 30 tablets

    • 36 mg are white, oval with “36” debossed on one side.  They are supplied as follows:
      NDC: 52856-504-03      Bottle of 30 tablets

    EMFLAZA Oral Suspension

    • 22.75 mg/mL is a whitish colored suspension. Supplied as 13 mL in a 30 mL bottle packaged with one bottle adapter and two 1 mL oral dispensers.
      NDC: 52856-505-22

    16.2 Storage and Handling

    Store at 20°C to 25°C (68°F to 77°F).  Excursion permitted between 15°C to 30°C (59°F to 86°F).  See USP controlled room temperature.

    Discard any unused EMFLAZA Oral Suspension remaining after 1 month of first opening the bottle.

  • 17 PATIENT COUNSELING INFORMATION

    Advise the patients and/or caregivers to read the FDA-approved patient labeling if EMFLAZA Oral Suspension is prescribed (Instructions for Use).

    Administration

    • Warn patients and/or caregivers to not stop taking EMFLAZA abruptly or without first checking with their healthcare providers as there may be a need for gradual dose reduction to decrease the risk of adrenal insufficiency [see Dosage and Administration (2.3) and Warnings and Precautions (5.1)].
    • EMFLAZA may be taken with or without food.

    Tablets

    • EMFLAZA Tablets may be taken whole or crushed and taken immediately after mixing with applesauce.

    Oral Suspension

    • EMFLAZA Oral Suspension must be shaken well prior to measuring out each dose with the enclosed oral dispenser.
    • The EMFLAZA Oral Suspension dose may be placed in 3-4 ounces of juice or milk, mixed thoroughly, and immediately administered.  Do not take with grapefruit juice.
    • Discard any unused EMFLAZA Oral Suspension remaining after 1 month of first opening the bottle.

    Increased Risk of Infection
    Tell patients and/or caregivers to inform their healthcare provider if the patient has had recent or ongoing infections or if they have recently received a vaccine.  Medical advice should be sought immediately if the patient develops fever or other signs of infection.  Patients and/or caregivers should be made aware that some infections can potentially be severe and fatal.

    Warn patients who are on corticosteroids to avoid exposure to chickenpox or measles and to alert their healthcare provider immediately if they are exposed [see Warnings and Precautions (5.2)].

    Alterations in Cardiovascular/Renal Function
    Inform patients and/or caregivers that EMFLAZA can cause an increase in blood pressure and water retention.  If this occurs, dietary salt restriction and potassium supplementation may be needed [see Warnings and Precautions (5.3)].

    Behavioral and Mood Disturbances
    Advise patients and/or caregivers about the potential for severe behavioral and mood changes with EMFLAZA and encourage them to seek medical attention if psychiatric symptoms develop [see Warnings and Precautions (5.5)].

    Decreases in Bone Mineral Density
    Advise patients and/or caregivers about the risk of osteoporosis with prolonged use of EMFLAZA, which can predispose the patient to vertebral and long bone fractures [see Warnings and Precautions (5.6)].

    Ophthalmic Effects
    Inform patients and/or caregivers that EMFLAZA may cause cataracts or glaucoma and advise monitoring if corticosteroid therapy is continued for more than 6 weeks [see Warnings and Precautions (5.7)].

    Vaccination
    Advise patients and/or caregivers to bring immunizations up-to-date according to immunization guidelines prior to starting therapy with EMFLAZA. Live-attenuated or live vaccines should be administered at least 4 to 6 weeks prior to starting EMFLAZA. Inform patients and/or caregivers that they may receive concurrent vaccinations with use of EMFLAZA, except for live-attenuated or live vaccines. [see Warnings and Precautions (5.8)].

    Serious Skin Rashes
    Instruct patients and/or caregivers to seek medical attention at the first sign of a rash [see Warnings and Precautions (5.9)].

    Drug Interactions
    Certain medications can cause an interaction with EMFLAZA.  Advise patients and/or caregivers to inform their healthcare provider of all the medicines the patient is taking, including over-the-counter medicines (such as insulin, aspirin or other NSAIDS), dietary supplements, and herbal products.  Inform patients and/or caregivers that alternate therapy, dosage adjustment, and/or special test(s) may be needed during the treatment.


    Manufactured for:
    PTC Therapeutics, Inc.
    South Plainfield, NJ 07080 U.S.A.

    EMFLAZA Oral Suspension made in Spain

    EMFLAZA® is a trademark of PTC Therapeutics, Inc.



  • PATIENT PACKAGE INSERT

    Instructions for Use
    EMFLAZA™ (em fla' zah)
    (deflazacort)
    oral suspension

    Read this Instructions for Use before you start using EMFLAZA oral suspension and each time you get a refill.  There may be new information.  This information does not take the place of talking to your healthcare provider about your medical condition or treatment.


    Important information before you use EMFLAZA oral suspension:

    • Only use the oral dispenser (see Figure A below) that comes in your EMFLAZA carton when using this medicine.
    • EMFLAZA oral suspension can be taken with or without food.
    • Take your dose of EMFLAZA oral suspension with juice or milk.  Do not take EMFLAZA with grapefruit juice.
    • Throw away (discard) any unused EMFLAZA oral suspension after 1 month of first opening the bottle.
    • Do not stop taking EMFLAZA oral suspension without talking to your healthcare provider first.

    Preparing for your EMFLAZA oral suspension dose:

    You will need the following supplies: See Figure A.

    • 1 EMFLAZA oral suspension bottle
    • 1 oral dispenser (2 oral dispensers are included in the EMFLAZA oral suspension carton.  1 is to be used to give (administer) the product and 1 extra oral dispenser is included as a spare, if needed.)
    • 1 household cup filled with 3 to 4 ounces of juice or milk
    • 1 spoon

    Figure A

    Figure A

    How to prepare your dose of EMFLAZA oral suspension:

    Step 1.  Remove the EMFLAZA oral suspension bottle and 1 of the oral dispensers from the carton.

    Step 2.  Make sure the bottle cap is put on tightly and shake well before each use.  See Figure B.

    Figure B

    Figure B

    Step 3.  Remove the cap from the bottle by pushing down firmly on the cap and turning the cap in a counter-clockwise direction (to the left).  See Figure C.  Place the open bottle upright on a flat surface.

    Figure C

    Figure C

    First time use of bottle only:
    Unwrap the bottle adapter.
    Place the ribbed end of the bottle adapter in the bottle top.
    Wrap both hands around the bottle.  Press down on the bottle adapter using both thumbs.  Push the ribbed end of the bottle adapter firmly into the neck of the bottle until the adapter top is even with the bottle top.  See Figure D.
    Do not remove the bottle adapter from the bottle after it is inserted.
    Write the date that you first open the bottle on the bottle label.

    Figure D

    Figure D

    Step 4.  Unwrap the oral dispenser if it is the first time you are using the oral dispenser.
    Check your dose in milliliters (mL) as prescribed by your healthcare provider.  Find this number on the barrel of the oral dispenser.  See Figure E.

    Figure E

    Figure E

    The oral dispenser only holds 1 mL of medicine at a time.  If your dose is more than 1 mL, you will need to repeat Steps 5 through 8 using the same oral dispenser until your entire dose has been drawn from the bottle.

    Step 5.  Push the plunger of the oral dispenser all the way down.  Insert the oral dispenser into the bottle adapter.  See Figure F.

    Figure F

    Figure F

    Step 6.  With the oral dispenser in the bottle adapter, carefully turn the bottle upside down.  Slowly pull back on the plunger until the widest part of the plunger is at the line marking on the oral dispenser of the number of mL needed for your dose.  See Figure G.  Do not use the narrow tip on the end of the plunger to measure the dose.

    If you see air bubbles in the oral suspension, fully push in the plunger so the oral suspension flows back into the bottle.  Then withdraw the dose of oral suspension that you need.

    Figure G

    Figure G

    Step 7.  Leave the oral dispenser in the bottle adapter and turn the bottle to an upright position.  Place the bottle onto a flat surface.  Remove the oral dispenser from the bottle adapter by gently twisting the oral dispenser while pulling it straight up.  See Figure H.

    Figure H

    Figure H

    Step 8.  Slowly push all the way down on the plunger of the oral dispenser to add the EMFLAZA oral suspension dose to a household cup filled with 3 to 4 ounces of juice or milk.  See Figure I.

    Figure I

    Figure I

    Step 9.  Stir the EMFLAZA oral suspension and juice or milk with a spoon to mix well.  See Figure J.

    Figure J

    Figure J

    Step 10.  Immediately drink the juice or milk that is mixed with EMFLAZA oral suspension.

    Step 11.  Replace the cap tightly on the bottle by turning the cap in a clockwise direction (to the right).  See Figure K.

    Figure K

    Figure K

    Step 12.  Wash the oral dispenser after each use.  The oral dispenser should be taken apart by pulling back on the plunger and removing it from the barrel of the oral dispenser.  See Figure L.

    Figure L

    Figure L

    Step 13.  After the barrel and plunger are dry, put the oral dispenser back together by pushing the plunger back into the barrel.


    How should I store EMFLAZA oral suspension?

    • Store the bottle upright at room temperature between 68°F to 77°F (20°C to 25°C).
    • Throw away (discard) any unused EMFLAZA oral suspension after 1 month of first opening the bottle.

    What are the ingredients in EMFLAZA oral suspension?
    Active ingredient: deflazacort
    Inactive ingredients: acetic acid, aluminum magnesium silicate, benzyl alcohol, carboxymethylcellulose sodium, polysorbate 80, purified water, and sorbitol.


    Manufactured for: PTC Therapeutics, Inc., South Plainfield, NJ 07080, U.S.A.

    This Instructions for Use has been approved by the U.S. Food and Drug Administration.  EMFLAZA™ is a trademark of PTC Therapeutics, Inc.

    Issued: April 2019



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-501-01 - 6 mg Tablet 100-Count Bottle Label

    NDC: 52856-501-01
    100 Tablets
    Emflaza™
    (deflazacort)
    Tablets
    for oral use
    6 mg
    Rx Only

    6 mg Tablet 100-Count Bottle Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-501-01 - 6 mg Tablet 100-Count Carton Label

    NDC: 52856-501-01
    100 Tablets
    Emflaza™
    (deflazacort)
    Tablets
    for oral use
    6 mg
    Rx Only

    6 mg Tablet 100-Count Carton Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-502-03 - 18 mg Tablet 30-Count Bottle Label

    NDC: 52856-502-03
    30 Tablets
    Emflaza™
    (deflazacort)
    Tablets
    for oral use
    18 mg
    Rx Only

    18 mg Tablet 30-Count Bottle Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-502-03 - 18 mg Tablet 30-Count Carton Label

    NDC: 52856-502-03
    30 Tablets
    Emflaza™
    (deflazacort)
    Tablets
    for oral use
    18 mg
    Rx Only

    18 mg Tablet 30-Count Carton Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-503-03 - 30 mg Tablet 30-Count Bottle Label

    NDC: 52856-503-03
    30 Tablets
    Emflaza™
    (deflazacort)
    Tablets
    for oral use
    30 mg
    Rx Only

    30 mg Tablet 30-Count Bottle Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-503-03 - 30 mg Tablet 30-Count Carton Label

    NDC: 52856-503-03
    30 Tablets
    Emflaza™
    (deflazacort)
    Tablets
    for oral use
    30 mg
    Rx Only

    30 mg Tablet 30-Count Carton Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-504-03 - 36 mg Tablet 30-Count Bottle Label

    NDC: 52856-504-03
    30 Tablets
    Emflaza™
    (deflazacort)
    Tablets
    for oral use
    36 mg
    Rx Only

    36 mg Tablet 30-Count Bottle Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-504-03 - 36 mg Tablet 30-Count Carton Label

    NDC: 52856-504-03
    30 Tablets
    Emflaza™
    (deflazacort)
    Tablets
    for oral use
    36 mg
    Rx Only

    36 mg Tablet 30-Count Carton Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-505-21 - 22.75 mg/mL Oral Suspension 13 mL Bottle Label

    NDC: 52856-505-21
    13 mL
    Emflaza™
    (deflazacort)
    Oral Suspension
    Rx only
    22.75 mg/mL
    For Oral Administration Only

    22.75 mg/mL Oral Suspension 13 mL Bottle Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-505-21 - 22.75 mg/mL Oral Suspension 13 mL Carton Label

    NDC: 52856-505-21
    13 mL
    Emflaza™
    (deflazacort)
    Oral Suspension
    22.75 mg/mL
    For Oral Administration Only
    Rx only

    22.75 mg/mL Oral Suspension 13 mL Carton Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-505-22 - 22.75 mg/mL Oral Suspension 13 mL Bottle Label

    NDC: 52856-505-22
    13 mL
    Emflaza®
    (deflazacort)
    Oral Suspension
    Rx only
    22.75 mg/mL
    For Oral Administration Only

    22.75 mg/mL Oral Suspension 13 mL Bottle Label



  • PRINCIPAL DISPLAY PANEL - NDC: 52856-505-22 - 22.75 mg/mL Oral Suspension 13 mL Carton Label

    NDC: 52856-505-22
    13 mL
    Emflaza®
    (deflazacort)
    Oral Suspension
    22.75 mg/mL
    For Oral Administration Only
    Rx only

    22.75 mg/mL Oral Suspension 13 mL Carton Label



  • INGREDIENTS AND APPEARANCE
    EMFLAZA 
    deflazacort tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 52856-501
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEFLAZACORT (UNII: KR5YZ6AE4B) (DEFLAZACORT - UNII:KR5YZ6AE4B) DEFLAZACORT6 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeROUNDSize6mm
    FlavorImprint Code 6
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 52856-501-01100 in 1 BOTTLE; Type 0: Not a Combination Product09/10/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20868409/10/2018
    EMFLAZA 
    deflazacort tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 52856-502
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEFLAZACORT (UNII: KR5YZ6AE4B) (DEFLAZACORT - UNII:KR5YZ6AE4B) DEFLAZACORT18 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code 18
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 52856-502-0330 in 1 BOTTLE; Type 0: Not a Combination Product09/10/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20868409/10/2018
    EMFLAZA 
    deflazacort tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 52856-503
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEFLAZACORT (UNII: KR5YZ6AE4B) (DEFLAZACORT - UNII:KR5YZ6AE4B) DEFLAZACORT30 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize15mm
    FlavorImprint Code 30
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 52856-503-0330 in 1 BOTTLE; Type 0: Not a Combination Product09/10/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20868409/10/2018
    EMFLAZA 
    deflazacort tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 52856-504
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEFLAZACORT (UNII: KR5YZ6AE4B) (DEFLAZACORT - UNII:KR5YZ6AE4B) DEFLAZACORT36 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize17mm
    FlavorImprint Code 36
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 52856-504-0330 in 1 BOTTLE; Type 0: Not a Combination Product09/10/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20868409/10/2018
    EMFLAZA 
    deflazacort suspension
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 52856-505
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEFLAZACORT (UNII: KR5YZ6AE4B) (DEFLAZACORT - UNII:KR5YZ6AE4B) DEFLAZACORT22.75 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACETIC ACID (UNII: Q40Q9N063P)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 52856-505-2113 mL in 1 BOTTLE; Type 0: Not a Combination Product09/10/2018
    2NDC: 52856-505-2213 mL in 1 BOTTLE; Type 0: Not a Combination Product08/30/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20868509/10/2018
    Labeler - PTC Therapeutics, Inc. (124371951)

    • Trademark Results [EMFLAZA]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    EMFLAZA
    EMFLAZA
    86639624 5261599 Live/Registered
    PTC THERAPEUTICS, INC.
    2015-05-22
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