Prednisolone 20mg/100ml Rectal Solution

Prednisolone Rectal Solution provides local corticosteroid treatment and is indicated for rectal and rectosigmoidal disease in ulcerative colitis and Crohn's disease.

Posology

Adults

1 enema used nightly, for 2 to 4 weeks. Treatment may be continued in patients showing progressive improvement, but it should not be persisted with if the response has been inadequate. Some patients may relapse after an interval but are likely to respond equally well to a repeated course of treatment.

The enema is used each night on retiring. It may be warmed before administration by placing the bottle in a vessel of warm water for a few minutes. Before use, lie in bed on the left side with knees drawn up. Hold the bottle upwards. Place hand in the protective plastic cover and remove the cap from the bottle. Attach the nozzle and lubricate with petroleum jelly. Gently insert about half the length of the nozzle into the rectum. The bottle should then be squeezed gently until it is emptied, taking a minute or two to do so. The nozzle should then be removed from the rectum. Invert the plastic protective cover around the bottle and discard the whole unit. The patient should then roll over to lie face down for 3 to 5 minutes but may sleep in any comfortable position.

Although Prednisolone Rectal Solution is applied locally, it should be borne in mind that there is likely to be substantial systemic absorption, especially when the bowel is inflamed.

The volume of the enema is considered to be the optimum to ensure maximum coverage of the affected area. However, undesirable effects may be minimised by using for the minimum period. Frequent patient review is required to monitor therapeutic effect against disease activity.

Children

Prednisolone Rectal Solution as packed is not suitable for use in children.

Method of Administration

Rectal

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

Systemic or local infection unless specific anti-infective therapy is employed.

Although Prednisolone Rectal Solution is applied locally, it should be borne in mind that there is likely to be substantial systemic absorption, especially when the bowel is inflamed.

The volume of the enema is considered to be the optimum to ensure maximum coverage of the affected area, however, undesirable effects may be minimised by using for the minimum period. Frequent patient review is required to monitor therapeutic effect against disease activity (see 'Posology and Method of Administration').

Suppression of the inflammatory response and immune system increases the susceptibility to infections and their severity. The clinical presentation may often be atypical and serious infections such as septicaemia and tuberculosis may be masked and may reach an advanced stage before being recognised.

Chickenpox is of particular concern since this normally minor illness may be fatal in immunosuppressed patients. Patients without a definite history of chickenpox should be advised to avoid close contact with chickenpox or herpes zoster and if exposed they should seek medical attention. Passive immunisation with varicella zoster immunoglobulin (VZIG) is needed by exposed non-immune patients who are receiving systemic corticosteroids or who have used them within the previous 3 months; this should be given within 10 days of exposure to chickenpox. If a diagnosis of chickenpox is confirmed, the illness warrants special care and urgent treatment. Corticosteroids should not be stopped and the dose may need to be increased.

Patients should be advised to take particular care to avoid exposure to measles and to seek immediate medical advice if exposure occurs. Prophylaxis with intramuscular normal immunoglobulin may be needed.

Live vaccines should not be given to individuals with impaired immune responsiveness. The antibody response to other vaccines may be diminished.

Corticosteroid treatment may reduce the response of the pituitary adrenal axis to stress, and relative insufficiency can persist for up to a year after withdrawal of prolonged therapy. Withdrawal of corticosteroids after prolonged therapy must therefore always be gradual to avoid acute adrenal insufficiency, being tapered off over weeks or months according to the dose and the duration of treatment. During prolonged therapy any intercurrent illness, trauma or surgical procedure will require a temporary increase in dosage; if corticosteroids have been stopped following prolonged therapy they may need to be temporarily re-introduced.

Use with caution in patients with myasthenia gravis, non-specific ulcerative colitis, diverticulitis and fresh intestinal anastamoses.

Special precautions

Particular care is required when considering the use of systemic corticosteroids in patients with the following conditions and frequent patient monitoring is necessary.

A. Osteoporosis (post-menopausal females are particularly at risk).

B. Hypertension or congestive heart failure.

C. Existing or previous history of severe affective disorders (especially previous steroid psychosis).

D. Diabetes mellitus (or a family history of diabetes).

E. History of tuberculosis.

F. Glaucoma (or a family history of glaucoma).

G. Previous corticosteroid-induced myopathy.

H. Liver failure - blood levels of corticosteroid may be increased, as with other drugs which are metabolised in the liver.

I. Renal insufficiency.

J. Epilepsy.

K. Peptic ulceration.

L. Hypothroidism

M. Recent myocardial infarction.

Patients should carry “ Steroid treatment” cards which give clear guidance on the precautions to be taken to minimise risk and which provide details of the prescriber, drug, dosage and the duration of treatment.

Patients/and or carers should be warned that potentially severe psychiatric adverse reactions may occur with systemic steroids (see section 4.8). Symptoms typically emerge within a few days or weeks of starting treatment. Risks may be higher with high doses/systemic exposure (see also section 4.5 pharmacokinetic interactions that can increase the risk of side effects), 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/carers should be encouraged to seek medical advice if worrying psychological symptoms develop, especially if depressed mood or suicidal ideation is suspected. Patients/carers 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.

Particular care is required when considering the use of systemic corticosteroids in patients with existing or previous history of severe affective disorders in themselves or in their first degree relatives. These would include depressive or manic-depressive illness and previous steroid psychosis.

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 (CSCR) which have been reported after use of systemic and topical corticosteroids.

Use in the Elderly

The common adverse effects of systemic corticosteroids may be associated with more serious consequences in old age, especially osteoporosis, hypertension, hypokalaemia, diabetes, susceptibility to infection and thinning of the skin. Close clinical supervision is required to avoid life-threatening reactions.

Systemic absorption of prednisolone should be borne in mind, especially when there is local inflammation. Thus the following interactions are possible:

Analgesics:

Increased risk of gastro-intestinal bleeding and ulceration with aspirin and NSAIDs; the renal clearance of salicylates is increased by corticosteroids and steroid withdrawal may result in salicylate intoxication.

Antibacterials:

Rifamycins accelerate metabolism of corticosteroids (reduced effect); erythromycin inhibits metabolism of methylprednisolone and possibly other corticosteroids. Fluoroquinolones - Increased risk of tendon rupture.

Anticoagulants:

The efficacy of coumarin anticoagulants may be enhanced by concurrent corticosteroid therapy and close monitoring of the INR or prothrombin time is required to avoid spontaneous bleeding.

Antidiabetics:

Antagonism of hypoglycaemic effect.

Antiepileptics:

Carbamazepine, phenobarbital, phenytoin and primidone accelerate metabolism of corticosteroids (reduced effect).

Antifungals:

Increased risk of hypokalaemia with amphotericin (avoid concomitant use unless corticosteroids are required to control reactions); ketoconazole inhibits metabolism of methylprednisolone and possibly other corticosteroids.

Antihypertensives:

Antagonism of hypotensive effect.

Anticholinesterases:

Decreased effect of anticholinesterases in myasthenia gravis.

Antivirals:

Ritonavir possibly increases plasma concentration of prednisolone.

Cardiac Glycosides:

Increased toxicity if hypokalaemia occurs with corticosteroids.

Ciclosporin:

Increased plasma concentrations of prednisolone.

Cytotoxics:

Increased risk of haematological toxicity with methotrexate.

Diuretics:

Antagonism of diuretic effect; acetazolamide, loop diuretics, and thiazides increased risk of hypokalaemia.

Hormone antagonists:

Aminoglutethimide accelerates metabolism of corticosteroids (reduced effect).

Licorice:

Increased corticosteroid levels.

Mifepristone:

Effects of corticosteroids may be reduced for 3-4 days after mifepristone.

Neuromuscular blockers:

Antagonism of the neuromuscular blockade.

Oral Contraceptives:

Alteration in the plasma protein binding and metabolism of prednisolone caused by oestrogens, with or without progesterone, can result in exposure of women to increased levels of unbound prednisolone for prolonged periods of time.

Somatropin:

The growth promoting effect of somatropin may be inhibited.

Sympathomimetics:

Increased risk of hypokalaemia if high doses of corticosteroids given with high doses of bambuterol, fenoterol, formoterol, ritodrine, salbutamol, salmeterol, and terbutaline.

Theophylline:

Increased risk of hypokalaemia.

Ulcer-healing drugs:

Carbenoxolone increases the risk of hypokalaemia.

Vaccines:

Live vaccines should not be given to individuals with impaired immune response as a result of treatment with large doses of corticosteroids.

CYP3A inhibitors, including cobicistat-containing products:

Co-treatment with CYP3A inhibitors, including cobicistat-containing products, is expected to increase the risk of systemic side-effects. The combination should be avoided unless the benefit outweighs the increased risk of systemic corticosteroid side-effects, in which case patients should be monitored for systemic corticosteroid side-effects.

Pregnancy

Topical administration of corticosteroids to pregnant animals can cause abnormalities of foetal development including cleft palate and intrauterine growth retardation. There may therefore be a very small risk of such effects in the human foetus. Also, hypoadrenalism may occur in the neonate. When corticosteroids are essential however, patients with normal pregnancies may be treated as though they were in the non-gravid state. Patients with pre-eclampsia or fluid retention require close monitoring.

Breast-feeding

Corticosteroids are excreted in small amounts in breast milk and infants of mothers taking pharmacological doses of steroids should be monitored carefully for signs of adrenal suppression.

Fertility

No fertility data is available.

Prednisolone Rectal Solution has no influence on the ability to drive and use machines.

The incidence of predictable undesirable effects, including hypothalamic - pituitary - adrenal suppression correlates with the relative systemic potency of the drug, dosage, timing of administration and the duration of treatment (see 'Special Warnings and Precautions for Use').

Common: (≥ 1/100 to 1/10)

Common: (≥ 1/100 to 1/10): Psychiatric disorders

Affective disorder (such as irritable, euphoric, depressed and labile mood and suicidal thoughts), psychotic reactions (including mania, delusions, hallucinations and aggravation of schizophrenia), behavioural disturbances, irritability, anxiety, sleep disturbances and cognitive dysfunction including confusion and amnesia have been reported. Reactions are common, any may occur in both adults and children. In adults, the frequency of severe reactions has been estimated to the 5-6%.

Not known: (frequency cannot be estimated from the available data)

Not known: Infections and infestations

Increased susceptibility and severity of infections with suppression of clinical symptoms and signs. Opportunistic infections, recurrence of dormant tuberculosis (see 'Special Warnings and Precautions for Use').

Not known: Blood and lymphatic system disorders

Alteration in lipid levels (increases in total cholesterol, low density lipoproteins and triglycerides), leukemoid reactions and hypertension.

Not known: Endocrine disorders

Suppression of the hypothalamic - pituitary - adrenal axis, growth suppression in infancy, childhood and adolescence, menstrual irregularity and amenorrhoea. Cushingoid Facies, hirsutism.

Not known: Metabolism and nutrition disorders

Weight gain, impaired carbohydrate tolerance with increased requirement for antidiabetic therapy. Negative protein and calcium balance. Increased appetite.

A 'withdrawal syndrome' may also occur including loss of weight.

Not known: Psychiatric disorders

Psychological effects have been reported on withdrawal of corticosteroids.

Psychological dependence. Aggravation of epilepsy.

Not known: Eye disorders

Increased intra-ocular pressure, glaucoma, papilloedema, posterior subcapsular cataracts, corneal or scleral thinning, exacerbation of ophthalmic viral or fungal diseases. Chorioretinopathy.

A 'withdrawal syndrome' may also occur including conjunctivitis.

Vision, blurred (see also section 4.4)

Not known: Cardiac disorders

Myocardial rupture following recent myocardial infarction.

Not known: Gastrointestinal disorders

Nausea, hiccups, dyspepsia, peptic ulceration with perforation and haemorrhage, acute pancreatitis, candidiasis.

Not known: Skin and subcutaneous tissue disorders

Impaired healing, skin atrophy, bruising, telangiectasia, striae, acne, dermatitis and toxic epidermal necrolysis.

A 'withdrawal syndrome' may also occur including rhinitis and painful itchy skin nodules.

Not known: Musculoskeletal and connective tissue disorders

Osteoporosis, vertebral and long bone fractures, avascular osteonecrosis, tendon rupture, proximal myopathy.

A 'withdrawal syndrome' may also occur including myalgia and arthralgia.

Not known: Renal and urinary disorders

Sodium and water retention, potassium loss, hypokalaemic alkalosis.

Too rapid a reduction of corticosteroid dosage following prolonged treatment can lead to acute adrenal insufficiency, hypotension and in severe cases this could be fatal.

Not known: General disorders and administration site conditions

Hypersensitivity including anaphylaxis, has been reported. Leucocytosis. Thrombo-embolism.

A 'withdrawal syndrome' may also occur including fever.

Paediatric Population

Increased intra-cranial pressure with papilloedema in children (pseudotumour cerebri), usually after treatment withdrawal.

Reporting of suspected adverse reactions

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

Treatment is unlikely to be needed in cases of acute overdosage.

Pharmacotherapeutic group – Corticosteroids acting locally

ATC Code: A07E A01

Not applicable.

None stated

Novapreserve B5

Disodium edetate

Sodium acid phosphate

Disodium phosphate anhydrous

Sodium hydroxide

Purified water

None known.

24 months

Do not store above 25° C. Keep the bottle in the outer carton in order to protect from light.

Each 100ml single dose is supplied in a low density polythene bottle with a low density polythene cap, with a separate LDPE nozzle. Seven bottles, seven nozzles, seven protective plastic bags and instructions for use are supplied in each box.

No special requirements for disposal.