Efmody 5mg modified release hard capsules

Efmody is indicated in adolescents aged 12 years and over and adults for the:

• Treatment of adrenal insufficiency (AI)

• Treatment of congenital adrenal hyperplasia (CAH)

Posology

Treatment should be initiated by physicians experienced in the management of AI and/or CAH.

As maintenance therapy the dose must be individualised according to the response of the individual patient. The lowest possible dose should be used.

Monitoring of the clinical response is necessary and patients should be observed closely for signs that might require dose adjustment, including changes in clinical status resulting from remissions or exacerbations of the disease, changes in electrolytes particularly hypokalaemia (see section 4.4) or hyponatraemia, individual responsiveness to the medicinal product, and the effect of stress (e.g. surgery, infection, trauma). As the treatment has a modified release profile when, in CAH, blood tests are used to monitor clinical response, assessment of the evening dose should be done with a morning blood test and assessment of the morning dose should be done with an early afternoon blood test.

During excessive physical and/or mental stress it may be necessary to increase the dose of Efmody, and/or add additional immediate release hydrocortisone especially in the afternoon or evening.

Dose adjustments should be considered in case of concomitant use of potent CYP3A4 inducers or inhibitors (see section 4.5).

Treatment in AI and CAH

Recommended replacement doses of hydrocortisone are 10-15 mg/m²/day (CAH) and 8‑10 mg/m2/day (other forms of AI) in adolescents aged 12 years and over who have not completed growth, and 15-25 mg/day in adolescents who have completed growth and adult patients with AI or CAH. In patients with some remaining endogenous cortisol production a lower dose may be sufficient.

At initiation the total daily dose should be split into two doses with two thirds to three quarters of the dose given in the evening at bedtime and the rest given in the morning. Patients should then be titrated based on their individual response.

The morning dose should be taken on an empty stomach at least 1 hour before a meal and the evening dose taken at bedtime at least 2 hours after the last meal of the day.

Changing from conventional oral glucocorticoid treatment to Efmody

When changing patients from other oral hydrocortisone replacement therapy to Efmody, the identical total daily dose should be given, but the dose should be given in two doses with two thirds to three quarters of the dose given in the evening at bedtime and the rest given in the morning.

When changing patients from other glucocorticoids to Efmody an appropriate conversion factor should be used, and the patient monitored for response carefully.

Conversion to Efmody might elicit symptoms of adrenal insufficiency or overreplacement during dose optimisation.

A starting dose exceeding 40 mg per day of hydrocortisone is not recommended.

During serious trauma, intercurrent illness or periods of stress

In severe situations, an increase in dose is immediately required and oral administration of hydrocortisone must be replaced with parenteral treatment (see section 4.4).

In less severe situations when parenteral administration of hydrocortisone is not required, during periods of physical and/or mental stress, additional immediate release hydrocortisone at the same total daily dose as Efmody should be given in three divided doses; Efmody should be continued as well with the usual regimen (i.e. a doubled daily dose of hydrocortisone) to allow for easy return to the normal replacement dose of Efmody once additional hydrocortisone is no longer required.

In case of long-term increases in hydrocortisone daily dose due to prolonged periods of stress or illness, the additional hydrocortisone should be carefully weaned off.

Missed doses

If a dose of Efmody is missed it is recommended that it be taken as soon as possible.

Special populations

Elderly

Limited clinical data on the safety and efficacy of Efmody are available in elderly patients (over the age of 65 years) with AI or with CAH. There are no data available in very elderly patients (over the age of 75 years).

Renal impairment

There is no need for dose adjustment in patients with mild to moderate renal impairment. In patients with severe renal impairment monitoring of the clinical response is recommended and adjustment of dose may be necessary (see section 4.4).

Hepatic impairment

There is no need for dose adjustment in patients with mild to moderate hepatic impairment. In patients with severe hepatic impairment monitoring of the clinical response is recommended and adjustment of dose may be necessary (see section 4.4).

Paediatric population

No clinical data on the safety and efficacy of Efmody are available in children aged below 12 years. Other hydrocortisone containing medicinal products are available for children below 12 years.

Adolescents

Limited clinical data on the safety and efficacy of Efmody are available in adolescents aged 12-18 years.

In the clinical development programme 2 patients ≤ 18 years of age have been treated with Efmody. Their response was comparable to that of patients > 18 years of age.

Method of administration

The capsules must be given orally.

Patients should be advised to swallow the capsules with water to wash the capsules down.

The capsules should not be chewed as chewing the capsule could affect the release profile.

Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.

Adrenal crisis

Acute adrenal insufficiency may develop in patients with known adrenal insufficiency or CAH who are on inadequate daily doses or in situations with increased cortisol need.

Therefore, patients should be advised of the signs and symptoms of acute adrenal insufficiency and of adrenal crisis and the need to seek immediate medical attention. Sudden discontinuation of therapy with hydrocortisone risks triggering an adrenal crisis and death.

During adrenal crisis parenteral, preferably intravenous administration of hydrocortisone in high doses, together with sodium chloride 9 mg/ml (0.9%) solution for infusion, should be administered according to current treatment guidelines.

Pre-operatively, during serious trauma or during intercurrent illness

Pre-operatively, anaesthetists must be informed if the patient is taking corticosteroids or has previously taken corticosteroids.

Parenteral administration of hydrocortisone is warranted during transient illness episodes such as severe infections, in particular gastroenteritis associated with vomiting and/or diarrhoea, high fever of any aetiology or extensive physical stress, such as for instance serious accidents and surgery under general anaesthesia. Where parenteral hydrocortisone is required, the patient should be treated in a facility with resuscitation facilities in case of evolving adrenal crisis.

In less severe situations when parenteral administration of hydrocortisone is not required, for instance low grade infections, moderate fever of any aetiology and stressful situations such as minor surgical procedures, there should be high awareness of the risk of developing acute adrenal insufficiency.

Infections

Infection should not be more likely at a replacement dose of hydrocortisone, but all infections should be taken seriously, and an increase in steroid dose be initiated early (see section 4.2). Patients with AI or CAH are at risk of life-threatening adrenal crisis during infection so clinical suspicion of infection should be high and specialist advice should be sought early.

Immunisation

Treatment schedules of corticosteroids for people with AI or CAH do not cause immunosuppression and are not, therefore, contraindications for administration of live vaccines.

Undesirable effects of corticosteroid replacement therapy

Most undesirable effects of corticosteroids are dose and duration of exposure related. Undesirable effects are therefore less likely when using corticosteroids as replacement therapy. High (supra-physiological) dosages of hydrocortisone can cause elevation of blood pressure, salt and water retention, and increased excretion of potassium.

Long-term treatment with higher than physiological hydrocortisone doses can lead to clinical features resembling Cushing´s syndrome with increased adiposity, abdominal obesity, hypertension and diabetes, and thus result in an increased risk of cardiovascular morbidity and mortality.

Patients should be warned of the signs of diabetes and the need to seek medical advice if they occur.

All glucocorticoids increase calcium excretion and reduce the bone-remodelling rate. Long-term glucocorticoid replacement therapy may therefore reduce bone mineral density (see section 4.8).

Patients should be warned that potentially severe psychiatric adverse reactions; euphoria, mania, psychosis with hallucinations and delirium have been seen in adult patients at replacement doses of hydrocortisone (see section 4.8). Symptoms typically emerge within a few days or weeks of starting the treatment. Risks may be higher with high doses/systemic exposure (see also section 4.5), although dose levels do not allow prediction of the onset, type, severity or duration of reactions. Most reactions recover after either dose reduction or withdrawal, although specific treatment may be necessary. Patients should be encouraged to seek medical advice if worrying psychological symptoms develop, especially if depressed mood or suicidal ideation is suspected. Patients should also be alert to possible psychiatric disturbances that may occur either during or immediately after dose tapering/withdrawal of systemic steroids, although such reactions have been reported infrequently.

Rare instances of anaphylactoid reactions have occurred in patients receiving corticosteroids, medical advice should be sought immediately in the case of anaphylactoid symptoms (see section 4.8).

Gastric emptying and motility disorders

Modified-release formulations, such as Efmody are not recommended in patients with increased gastrointestinal motility, i.e. chronic diarrhoea, due to the risk of impaired cortisol exposure. There are no data in patients with confirmed slow gastric emptying or decreased motility disease/disorder. The clinical response should be monitored in patients with these conditions.

Growth retardation

Corticosteroids may cause growth retardation in childhood and adolescence; this may be irreversible. Treatment should be limited to the minimum dose required to achieve desired clinical response and when reduction in dose is possible, the reduction should be gradual. Excessive weight gain with decreased height velocity or other symptoms or signs of Cushing syndrome indicate excessive glucocorticoid replacement.

Children require frequent assessment to assess growth, blood pressure, and general well-being.

Accelerated sexual maturation

Adolescents with CAH may show accelerated sexual maturation. Patients should be closely monitored; and if signs of early puberty or accelerated sexual maturation are present, an increase in dose considered. Careful and regular monitoring of adolescent patients with dose adjustment according to the response of the individual patient is recommended.

Visual disturbance

Visual disturbance may be reported with systemic and topical corticosteroid use. If a patient presents with symptoms such as blurred vision or other visual disturbances, the patient should be considered for referral to an ophthalmologist for evaluation of possible causes which may include cataract, glaucoma or rare diseases such as central serous chorioretinopathy which have been reported after use of systemic and topical corticosteroids.

Hypokalaemia

Treatment of AI or CAH often warrants additional treatment with mineralocorticosteroids. Potassium should be monitored (see sections 4.5 and 4.8).

Precaution

In both men and women who have lower fertility, fertility may be restored shortly after beginning treatment with Efmody, which can lead to unexpected pregnancies. Patients should be informed of the potential for restored fertility when starting treatment with Efmody, to be able to consider if a contraceptive measure is needed (see section 4.6).

Hydrocortisone is metabolised by cytochrome P450 3A4 (CYP3A4). Concomitant administration of medicinal products that are inhibitors or inducers of CYP3A4 may therefore lead to unwanted alterations in serum concentrations of hydrocortisone with the risk of adverse reactions, particularly adrenal crisis. The need for dose adjustment when such medicinal products are used can be anticipated and patients should be closely monitored.

Medicinal products inducing CYP3A4, requiring a potential increase in Efmody dosing, include but are not limited to:

- Anticonvulsants: phenytoin, carbamazepine and oxcarbazepine

- Antibiotics: rifampicin and rifabutin

- Barbiturates including phenobarbital and primidone

- Antiretroviral medicinal products: efavirenz and nevirapine

- Herbal medicinal products such as St. John's Wort

Medicinal products/substances inhibiting CYP3A4, requiring a potential decrease in hydrocortisone dosing, include but are not limited to:

- Anti-fungals: itraconazole, posaconazole, voriconazole

- Antibiotics: erythromycin and clarithromycin

- Antiretroviral medicinal products: ritonavir

- Grapefruit juice

- Liquorice

The desired actions of hypoglycaemic medicinal products including insulin are antagonised by corticosteroids.

Medicinal products/substances that affect the electrolyte balance may increase the risk of hypokalaemia in patients taking Efmody. These include hypokalaemic diuretics, stimulant laxatives, mineralocorticosteroids (fludrocortisone), tetracosactide (Synacthen), IV amphotericin B and liquorice.

Pregnancy

Hydrocortisone crosses the placenta. Hydrocortisone is preferentially metabolised by placental 11βHSD2 to inactive cortisone reducing the fetal exposure. There are no indications that replacement therapy with hydrocortisone in pregnant women is associated with adverse consequences for the fetus. Hydrocortisone for replacement therapy can be used during pregnancy.

Studies in animals have shown reproductive toxicity of corticosteroids (see section 5.3).

Breast-feeding

Hydrocortisone is excreted in breast milk. However, the doses of hydrocortisone used for replacement therapy probably do not clinically significantly affect the child.

Hydrocortisone for replacement therapy can be used during breast-feeding.

Fertility

In both men and women who have lower fertility, fertility may be restored shortly after beginning treatment with Efmody. In women, a reduction of 17- OH progesterone and androstenedione will lead to a corresponding fall in progesterone and testosterone which may restore menses/fertility. (see section 4.4).

Efmody has minor influence on the ability to drive and use machines. Fatigue and dizziness have been reported. Untreated and poorly replaced adrenal insufficiency may affect the ability to drive and use machines.

Summary of safety profile

The adverse drug reactions reported to Efmody in the clinical trial programmes for AI and CAH, and from post-marketing surveillance of CAH are discussed in this section.

In the clinical trial programmes of AI and CAH, 284 adverse reactions have been reported from 203 Efmody-treated patients. Unexpected therapeutic benefits and fatigue were both reported very commonly, affecting 23.6% and 14.3% of patients, respectively. The most frequently reported unexpected therapeutic benefits of Efmody included feeling more alert, reduced tiredness, better sleep, improved menstrual cyclicity, and increased bone density. Headache (6.4%), and Dizziness (5.9%) were reported commonly.

Events of adrenal insufficiency, including acute events, were reported in 7.9% of clinical trial participants without causal attribution. Acute adrenal insufficiency has been reported in CAH patients as a post-marketing ADR for Efmody.

Tabulated list of adverse reactions

The commonest reactions reported to Efmody in the pooled population in the clinical trial population (n = 203), and spontaneous reporting are tabulated below. Frequencies are defined as very common (≥ 1/10), common (≥ 1/100 to < 1/10), uncommon (≥ 1/1,000 to < 1/100).

Table 1-Tabulated summary of adverse reactions

¹frequency based on postmarketing reports

²Includes events of; feeling more alert/less tired/better sleep; improved menstrual cyclicity; increased bone density

Description of selected adverse reactions

Adrenal Insufficiency (including acute events).

Events of acute adrenal insufficiency were reported during the clinical trial programme but none were considered related to Efmody. Acute adrenal insufficiency should be monitored for and treated promptly in patients with adrenal insufficiency (see sections 4.2 and 4.4).

Rare instances of anaphylactoid reactions have occurred in patients receiving corticosteroids especially when a patient has a history of allergies to medicinal products.

Historical cohorts of adults treated from childhood for AI and CAH have been found to have reduced bone mineral density and increased fracture rates (see section 4.4) - it is unclear if these relate to hydrocortisone therapy using current replacement regimens.

Historical cohorts of adults treated from childhood for AI and CAH have been found to have raised cardiovascular risk factors and a higher risk of cerebrovascular disease than the general population - it is unclear if these relate to hydrocortisone therapy using current replacement regimens.

Paediatric population

No paediatric patients (<16 years) were included in the clinical development programme for Efmody. Hydrocortisone has been used for more than 60 years in paediatrics with a safety profile similar to that in adults. Growth retardation has been seen in children treated with hydrocortisone for CAH and can be caused by both the disorder and hydrocortisone. Accelerated sexual maturation has been seen in hydrocortisone-treated paediatric CAH patients and is associated with excess adrenal androgen production (see section 4.4).

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

Reports of acute toxicity and/or deaths following hydrocortisone overdose are rare. No antidote is available. Treatment is probably not indicated for reactions due to chronic poisoning unless the patient has a condition that would render him/her unusually susceptible to ill effects from hydrocortisone. In which case, symptomatic treatment should be instituted as necessary.

Pharmacotherapeutic group: Corticosteroids for systemic use; glucocorticoids. ATC code: H02AB09.

Mechanism of action

Hydrocortisone is a glucocorticoid. Glucocorticoids have multiple effects in multiple tissues through actions on the intracellular steroid receptors.

Pharmacodynamic effects

Hydrocortisone is a glucocorticoid and the synthetic form of endogenously produced cortisol. Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastro-intestinal tract. Cortisol is the principal corticosteroid secreted by the adrenal cortex. Naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. They are also used for their potent anti-inflammatory effects in disorders of many organ systems. Glucocorticoids cause profound and varied metabolic effects. In addition, they modify the body's immune responses to diverse stimuli.

Clinical efficacy and safety

AI

Fifty-eight participants were enrolled in a double-blind, double- dummy crossover study to compare the efficacy, safety and tolerability of twice daily Efmody compared with once-daily Plenadren over a treatment period of up to two months, with two 4-week treatment periods. Participants were randomly assigned to either Efmody in Treatment Period 1 and Plenadren in Treatment Period 2 (Efmody /Plenadren), or Plenadren in Treatment Period 1 and Efmody in Treatment Period 2 (Plenadren/ Efmody). At the end of 4 weeks treatment (periods 1 and 2), the median serum cortisol was higher at the 07:00 timepoint during Efmody treatment (417.0 nmol/L) compared to Plenadren treatment (6.04 nmol/L), with this difference being highly statistically significant (p<0.0001) and showing superiority of Efmody to Plenadren. (See Table 2). The number of participants who achieved a physiological morning cortisol level (defined as a 07:00 hour serum cortisol before the morning dose of >140 nmol/L after 4 weeks of treatment) was 95.7% in Period 1 and 88.5% in Period 2 for Efmody compared to 0% in Period 1 and 8.7% in period 2 for Plenadren. If cortisol is poorly controlled overnight, then high adrenocorticotropic hormone (ACTH) levels will be seen in the morning. In this study, median ACTH levels at the end of 4 weeks treatment were 19.0 pmol/L following Efmody treatment and 169.6 pmol/L following Plenadren treatment, with the results being statistically significant in favour of Efmody.

Table 2. Serum Cortisol (nmol/L) in phase 2 study DIUR‑016-AI (Efficacy Evaluable Analysis Set)

^aEfmody 10 mg was taken in the morning on waking (typically between 06:00 and 08:00 hours) and Efmody 15 mg was taken at night just prior to going to bed (typically between 22:00 hours and midnight).

^bPlenadren 25 mg was taken in the morning on waking (typically between 06:00 and 08:00 hours).

^cAs all participants were randomised to receive Efmody and Plenadren, the baseline values are the same for both treatments.

A profile plot of daytime salivary cortisone values from 7 to 22 hours clock time in different treatment groups is provided in Figure 1.

Figure 1. Profile Plot of Daytime Salivary Cortisone levels in IRHC, Plenadren and Efmody (Chronocort) -treated subjects in Study DIUR-016-AI with overlaid Normative Data

Shaded area represents normative data from 14 healthy adults

IRHC: immediate-release hydrocortisone (Baseline)

CAH

A double blind study(DIUR-014) of 53 participants with 21 hydroxylase deficiency CAH randomised to twice daily Efmody or twice daily immediate release hydrocortisone (IRHC) with blinded titration of dose demonstrated that more participants were biochemical responders (i.e had improvements in androgen control or maintenance of control with dose reduction) following 28 weeks of Efmody treatment (40.0%) compared to IHRC treatment (14.3%) (p=0.015). Overall, participants had a lower mean daily dose following Efmody treatment (20.2 mg) compared to IHRC treatment (26.0 mg) (p<0.001). A total of 92 adverse events were reported in 24 [85.7%] participants in the IRHC group and 100 events in 22 [88.0%] participants in the Chronocort group.

An open label study(DIUR-005) in 122 participants with 21-hydroxylase deficiency CAH randomised to Efmody or continuation of standard care with blinded titration of dose and regular overnight profiles failed to meet its primary endpoint of superiority in change from baseline to 24 weeks of the mean of the 24-hour standard deviation score (SDS) profile for 17-hydroxyprogesterone (17-OHP). The 17-OHP SDS was lower in the Efmody cohort than standard therapy at 4 and 12 weeks. At 24 weeks the 17-OHP SDS was lower in the morning period (07:00 hrs to 15:00 hrs) but not in the evening or overnight (see also Figure 2 for the geometric mean 24-hour profile of 17-OHP after 24 weeks intensive treatment). A reduction in the 17-OHP area under the curve occurred in both groups, with greater reduction in the Efmody cohort. The percentage of patients with controlled 09:00 hrs 17-OHP (<36nmol/l) was 50% at baseline and at 24 weeks was 91% in the Efmody cohort and 71% in the standard therapy cohort. Efmody patients suffered no adrenal crises (compared to 3 in the control arm) and had fewer sick day episodes where increased dosing due to stress was required (26 vs 36 in the control arm) despite reporting more episodes of intercurrent infective or gastro-intestinal illness. Glucocorticoid daily dose, measured as a hydrocortisone equivalent dose, increased in most subjects during the study (see Table 3).

Table3. Glucocorticoid daily dose changes during the phase 3 study DIUR-005

Figure 2. End of study geometric mean 24-hour profile of 17-OHP after 24 weeks intensive treatment with either Efmody (closed circles) or standard therapy (open circles).

A safety extension study of 91 CAH patients with titration by investigators (DIUR-006) was characterised by dose reductions with median daily dose of Efmody at 18 months interim analysis (n=50) being 20 mg (from a median baseline daily dose of 30 mg) with 17-OHP levels remaining in the clinically determined optimal range and androstenedione at or below the reference range for normal individual.

Overall in the CAH clinical trial programme, the cumulative exposure was 417.7 treatment years (TY) and the incidence of adrenal crisis was 2.9 per 100 TY. All events of adrenal crisis were assessed as unrelated.

In the safety assessment of clinical studies, differences between the treatment arms in treatment related AEs were reported (by preferred term [PT]). The most notable differences between the Efmody and standard glucocorticoid therapy pools, respectively were observed for weight increased (6.9% vs 1.1%), decreased appetite (4.1% vs 0.0%), headache (6.9% vs 3.4%), dizziness (5.5% vs 2.2%) and fatigue (13.1% vs 10.1%).

Absorption

Following a single oral administration in fasted dexamethasone-suppressed healthy adults, the rate of absorption of hydrocortisone from Efmody 20 mg was delayed and reduced compared to immediate release hydrocortisone tablets 20 mg, as reflected by a lower C_max and a significantly longer T_max for Efmody (median T_max for serum cortisol of 4.5 hours and 0.88 hours for Efmody and hydrocortisone tablets respectively). Efmody appeared to be more bioavailable relative to immediate release hydrocortisone tablets, with overall exposure to serum cortisol and derived free cortisol approximately 19% and 13% higher respectively for Efmody.

In the same population, food (high fat meal started 30 minutes before dosing) was found to delay and reduce the rate of absorption of hydrocortisone from Efmody 20 mg, as reflected by a longer T_max (median T_max for serum cortisol of 6.75 hours and 4.5 hours for fed and fasted subjects respectively) and lower C_max (reduced by approximately 20% in fed subjects). Overall exposure appeared similar in fed and fasted subjects (90% confidence intervals for the fed/fasted ratio of the geometric least square mean of AUC_0-t and AUC_0-inf were within 80-125%). This effect is therefore not considered clinically significant.

Distribution

90% or more of circulating hydrocortisone is reversibly bound to protein.

The binding is accounted for by two protein fractions. One, corticosteroid-binding globulin is a glycoprotein; the other is albumin.

Biotransformation

Hydrocortisone is metabolised in the liver and most body tissues to hydrogenated and degraded forms such as tetrahydrocortisone and tetrahydrocortisol which are excreted in the urine, mainly conjugated as glucuronides, together with a very small proportion of unchanged hydrocortisone. Hydrocortisone is both metabolised by and a regulator of CYP3A4.

Elimination

In the fasted dexamethasone-suppressed healthy adult population described above, terminal elimination half-life values were similar for Efmody and hydrocortisone tablets (geometric mean t_1/2 for serum cortisol of 1.38 hours and 1.40 hours respectively). Clearance appeared higher for hydrocortisone tablets relative to Efmody (geometric mean CL/F for serum cortisol of 22.24 L/h and 18.48 L/h respectively).

Paediatrics

The pharmacokinetics of Efmody have not been studied in the paediatric population.

Other populations

No studies have been conducted in patients with hepatic or renal impairment.

Administration of corticosteroids to pregnant animals can cause abnormalities of fetal development including cleft palate, intrauterine growth retardation and effects on brain growth and development.

Granules

Microcrystalline cellulose

Povidone

Methacrylic acid-methyl methacrylate copolymer (1:2)

Methacrylic acid-methyl methacrylate copolymer (1:1)

Talc

Dibutyl sebacate

Capsule

Gelatin

Efmody 5 mg modified-release hard capsules (white/blue)

Titanium dioxide (E171)

Indigotine (E132)

Printing ink

Shellac

Black iron oxide (E172)

Propylene glycol

Potassium hydroxide

Not applicable

3 years

Store in the original package.

Keep the bottle tightly closed as the product is sensitive to moisture.

This medicinal product does not require any special temperature storage conditions.

The capsules are provided in high-density polyethylene bottles with child resistant, tamper evident polypropylene screw cap with integrated desiccant. Each bottle contains 50 modified-release hard capsules.

Pack sizes:

Carton containing 1 bottle of 50 modified-release hard capsules.

Carton containing 2 bottles of 50 modified-release hard capsules (100 capsules).

Not all pack sizes may be marketed.

Any unused medicinal product or waste material should be disposed of in accordance with local requirements.