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Ifosfamide Injection 2g

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SUMMARY OF PRODUCT CHARACTERISTICS

1 NAME OF THE MEDICINAL PRODUCT

Ifosfamide Injection 2g

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Each vial contains 2g of ifosfamide

When reconstituted as directed, each milliliter of concentrate contains 80 mg Ifosfamide.

3    PHARMACEUTICAL FORM

Powder for concentrate for solution for infusion. White powder.

4    CLINICAL PARTICULARS

4.1 Therapeutic indications

Ifosfamide is a cytotoxic drug for the treatment of malignant disease. As a single agent it has successfully produced objective remissions in a wide range of malignant conditions. Ifosfamide is also frequently used in combination with other cytotoxic drugs, radiotherapy and surgery.

Children and adolescents - see section 5.1-Paediatric population

4.2 Posology and method of administration

Ifosfamide should only be administered when there are facilities for regular monitoring of clinical, biochemical and haematological parameters before, during and after administration and under the direction of a specialist oncology service by physicians experienced with this drug.

Dosage must be individualized. Doses and duration of treatment and/or treatment intervals depend on the therapeutic indication, the scheme of a combination therapy, the patient’s general state of health and organ function, and the results of laboratory monitoring.

In combination with other agents of similar toxicity, a dose reduction or extension of the therapy-free intervals may be necessary.

Method of administration

A guide to the dosage regimens used for most indications is given below:

a)    8 - 12 g/m2 equally fractionated as single daily doses over 3 - 5 days every 2-4 weeks.

b)    5 - 6 g/m2 (maximum 10 g) given as a 24 hour infusion every 3 - 4 weeks.

The frequency of dosage is determined by the degree of myelosuppression and the time taken to recover adequate bone marrow function. The usual number of courses given is 4, but up to 7 (6 by 24 hour infusion) courses have been given. Re-treatment has been given following relapse.

During or immediately after administration, adequate amounts of fluid should be ingested or infused to force diuresis in order to reduce the risk of urothelial toxicity. See Section 4.4.

For prophylaxis of hemorrhagic cystitis, ifosfamide should be used in combination with mesna.

Use in Patients with Renal Impairment

In patients with renal impairment, particularly in those with severe renal impairment, decreased renal excretion may result in increased plasma levels of ifosfamide and its metabolites. This may result in increased toxicity (e.g., neurotoxicity, nephrotoxicity, haematotoxicity) and should be considered when determining the dosage in such patients. See section 4.3.

Ifosfamide and its metabolites are dialyzable.

Use in Patients with Hepatic Impairment

Hepatic impairment, particularly if severe, may be associated with decreased activation of ifosfamide. This may alter the effectiveness of ifosfamide treatment.

Low serum albumin and hepatic impairment are also considered risk factors for the development of CNS toxicity. Hepatic impairment may increase the formation of a metabolite that is believed to cause or contribute to CNS toxicity and also contribute to nephrotoxicity. This should be considered when selecting the dose and interpreting response to the dose selected. See section 4.3.

Use in Paediatric Patients

In children, the dosage and administration should be determined by the tumour type, tumour stage, the general condition of the patient, any previous cytotoxic therapy, and whether chemotherapy or radiotherapy is to be administered concurrently. Clinical trials have involved doses of:

a)    5 g/m2 over 24 hours

b)    9 g/m2 equally fractionated as single daily doses over 5 days

c)    9 g/m2 as a continuous infusion over 72 hours- repeated at three weekly intervals.

In general, dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy (See Section 5.2).

Administration

Ifosfamide is inert until activated by enzymes in the liver. However, safe handling is required and advice is included under Pharmaceutical Precautions. The dry contents of a vial should be dissolved in Water for Injections as follows:

2 g vial: add 25 ml of Water for Injections

The resultant solution of 8% of ifosfamide should not be injected directly into the vein. The solution may be:

1.    diluted to less than a 4% solution and injected directly into the vein, with the patient supine.

2.    infused in 5% dextrose-saline or normal saline over 30-120 mins.

3.    injected directly into a fast-running infusion,

4.    made up in 3 x 1 litres of dextrose-saline or normal saline and infused over 24 hours. Each litre should be given over eight hours, and should be freshly made up immediately before infusion.

Care should be taken that extravasation does not take place, however, should it occur local tissue damage is unlikely and no specific measures need be taken. Repeated intravenous injections of large doses of Ifosfamide have resulted in local irritation.

Mesna should be used to prevent urothelial toxicity.

Where Ifosfamide is used as an i.v. bolus, increased dosages of mesna are recommended in children, patients whose urothelium may be damaged from previous therapies and those who are not adequately protected by the standard dose of mesna.

The patient should be well hydrated and maintained in fluid balance, replacement fluids being given as necessary to achieve this. The fluid intake of patients on the intermittent regimen should be at least 2 litres in 24 hours. As Ifosfamide may exert an antidiuretic effect, a diuretic may be necessary to ensure an adequate urinary output.

Urine should be sent for laboratory analysis before, and at the end of, each course of treatment, and the patient should be monitored for output and evidence of proteinuria and haematuria at regular intervals (4-hourly if possible) throughout the treatment period. The patient should be instructed to report any signs or symptoms of cystitis. Ifosfamide should be avoided in patients with cystitis from any cause until it has been treated.

Antiemetics given before, during and after therapy may reduce nausea and vomiting. Oral hygiene is important.

If leucocyte count is below 4,000/mm3 or the platelet count is below 100,000/mm3, treatment with Ifosfamide should be withheld until the blood count returns to normal.

There should be no signs or symptoms of urothelial toxicity or renal or hepatic impairment prior to the start of each course of Ifosfamide.

4.3 Contraindications

Ifosfamide is contra-indicated in patients with :

•    known hypersensitivity to ifosfamide. See section 4.4

•    urinary outflow obstruction.

•    severely impaired bone-marrow function (especially in patients previously treated with cytotoxic agents or radiotherapy)

•    inflammation of the urinary bladder (cystitis)

•    impaired renal function

•    hepatic impairment

•    acute infections

4.4 Special warnings and precautions for use

In individual patients, risk factors for ifosfamide toxicities and their sequelae described here and in other sections may constitute contraindications. In such situations, individual assessment of risk and expected benefits is necessary. Adverse reactions, depending on their severity, may require dosage modification or discontinuation of treatment

WARNINGS

Myelosuppression, Immunosuppression, Infections

Treatment with ifosfamide may cause myelosuppression and significant suppression of immune responses, which can lead to severe infections. Fatal outcome of ifosfamide-associated myelosuppression has been reported.

Administration of ifosfamide is normally followed by a reduction in the leukocyte count. The nadir of the leukocyte count tends to be reached approximately during the second week after administration. Subsequently, the leukocyte count rises again.

Severe myelosuppression and immunosuppression must be expected particularly in patients pre-treated with and/or receiving concomitant chemotherapy/haematotoxic agents, immunosuppressants and/or radiation therapy( See Section 4.5).

Where indicated, use of haematopoiesis-stimulating agents (colonystimulating factors and erythropoiesis-stimulating agents) may be considered to reduce the risk of myelosuppressive complications and/or help facilitate the delivery of the intended dosing. For information on a potential interaction with G-CSF and GM-CSF (granulocyte colonystimulating factor, granulocyte macrophage colony-stimulating factor) (See section 4.5).

The risk of myelosuppression is dosedependent and is increased with administration of a single high dose compared to fractionated administration.

The risk of myelosuppression is increased in patients with reduced renal function.

Severe immunosuppression has led to serious, sometimes fatal, infections. Infections reported with ifosfamide include pneumonias, as well as other bacterial, fungal, viral, and parasitic infections. Sepsis and septic shock also have been reported.

Latent infections can be reactivated. In patients treated with ifosfamide, reactivation has been reported for various viral infections.

Close hematologic monitoring is recommended. White blood cell count, platelet count, and haemoglobin levels should be obtained prior to each administration and at appropriate intervals after administration.

Central Nervous System Toxicity, Neurotoxicity

Administration of ifosfamide can cause CNS toxicity and other neurotoxic effects (see Section 4.8).

Ifosfamide neurotoxicity may become manifest within a few hours to a few days after first administration and in most cases resolves within 48 to 72 hours of ifosfamide discontinuation. Symptoms may persist for longer periods of time. Occasionally, recovery has been incomplete. Fatal outcome of CNS toxicity has been reported.

Recurrence of CNS toxicity after several uneventful treatment courses has been reported.

CNS toxicity appears to be dose dependent.

Other risk factors that have been demonstrated or discussed in the literature include:

-    Renal dysfunction, elevated serum creatinine

-    Low serum albumin

-    Hepatic dysfunction

-    Low bilirubin, low haemoglobin levels, decreased white blood cell count

-    Acidosis, low serum bicarbonate

-    Electrolyte imbalances, hyponatraemia and inappropriate ADH (vasopressin) secretion, low fluid intake

-    Presence of brain metastases, prior CNS disease, brain irradiation

-    Cerebral sclerosis, peripheral vasculopathy

-    Presence of tumour in lower abdomen, bulky abdominal disease

-    Poor performance status, advanced age

-    Obesity, female gender

-    Interactions with other medicines (e.g., aprepitant, CYP 3A4 inhibitors), alcohol, drug abuse, or pretreatment with cisplatin

If encephalopathy develops, administration of ifosfamide should be discontinued.

Publications report both successful and unsuccessful use of methylene blue for the treatment and prophylaxis of ifosfamide-associated encephalopathy.

Due to the potential for additive effects, drugs acting on the CNS (such as antiemetics, sedatives, narcotics, or antihistamines) must be used with particular caution or, if necessary, be discontinued in case of ifosfamide induced encephalopathy.

Renal and Urothelial Toxicity Ifosfamide is both nephrotoxic and urotoxic.

Glomerular and tubular kidney function must be evaluated and checked before commencement of therapy, as well as during and after treatment.

Close clinical monitoring of serum and urine chemistries, including phosphorus, potassium, and other laboratory parameters appropriate for identifying nephrotoxicity and urothelial toxicity is recommended, see section 4.3.

Nephrotoxic Effects

Fatal outcome from nephrotoxicity has been documented.

Disorders of renal function (glomerular and tubular) following ifosfamide administration are very common. ( See 4.8).

Development of a syndrome resembling SIADH (syndrome of inappropriate antidiuretic hormone secretion) has been reported with ifosfamide.

Tubular damage may become apparent during therapy, months or even years after cessation of treatment.

Glomerular or tubular dysfunction may resolve with time, remain stable, or progress over a period of months or years, even after completion of ifosfamide treatment.

The risk of developing clinical manifestations of nephrotoxicity is increased with, for example:

-    large cumulative doses of ifosfamide

-    pre-existing renal impairment

-    prior or concurrent treatment with potentially nephrotoxic agents

-    younger age in children

-    reduced nephron reserve as in patients with renal tumours and those having undergone renal radiation or unilateral nephrectomy.

Urothelial Effects

Ifosfamide administration is associated with urotoxic effects, which can be reduced by prophylactic use of mesna.

Hemorrhagic cystitis requiring blood transfusion has been reported with ifosfamide.

The risk of hemorrhagic cystitis is dose-dependent and increased with administration of single high doses compared to fractionated administration.

Hemorrhagic cystitis after a single dose of ifosfamide has been reported.

Before starting treatment, it is necessary to exclude or correct any urinary tract obstructions.

During or immediately after administration, adequate amounts of fluid should be ingested or infused to force diuresis in order to reduce the risk of urinary tract toxicity.

Ifosfamide should be used with caution, if at all, in patients with active urinary tract infections.

Past or concomitant radiation of the bladder or busulfan treatment may increase the risk for hemorrhagic cystitis.

Cardiotoxicity, Use in Patients With Cardiac Disease

Fatal outcome of ifosfamide-associated cardiotoxicity has been reported.

The risk of developing cardiotoxic effects is dose-dependent. It is increased in patients with prior or concomitant treatment with other cardiotoxic agents or radiation of the cardiac region and, possibly, renal impairment.

Particular caution should be exercised when ifosfamide is used in patients with risk factors for cardiotoxicity and in patients with pre-existing cardiac disease.

Manifestations of cardiotoxicity reported with ifosfamide treatment (see Section 4.8) and include:

-    Supraventricular or ventricular arrhythmias, including atrial/supraventricular tachycardia, atrial fibrillation, pulseless ventricular tachycardia

-    Decreased QRS voltage and STsegment or T-wave changes

-    Toxic cardiomyopathy leading to heart failure with congestion and hypotension

-    Pericardial effusion, fibrinous pericarditis, and epicardial fibrosis

Pulmonary Toxicity

Pulmonary toxicity leading to respiratory failure as well as fatal outcome has been reported.Interstitial pneumonitis and pulmonary fibrosis have been reported with ifosfamide treatment.

Secondary Malignancies

As with all cytotoxic therapy, treatment with ifosfamide involves the risk of secondary tumours and their precursors . The secondary malignancy may develop several years after chemotherapy has been discontinued.

The risk of myelodysplastic alterations, some progressing to acute leukemias, is increased.

Veno-occlusive Liver Disease

Veno-occlusive liver disease has been reported with chemotherapy that included ifosfamide and also is a known complication with another oxazaphosphorine cytotoxic agent.

Genotoxicity See section 4.6 Effects on Fertility See section 4.6

Female Patients

Amenorrhea has been reported in patients treated with ifosfamide. In addition, with another oxazaphosphorine cytotoxic agent, oligomenorrhea has been reported, see section 4.6.

The risk of permanent chemotherapy-induced amenorrhea is increased in older women.

Male Patients

Men treated with ifosfamide may develop oligospermia or azoospermia, see section 4.6.

Anaphylactic/Anaphylactoid Reactions, Cross-sensitivity

Anaphylactic/anaphylactoid reactions have been reported in association with ifosfamide.

Cross-sensitivity between oxazaphosphorine cytotoxic agents has been reported.

Impairment of Wound Healing

Ifosfamide may interfere with normal wound healing.

Paravenous Administration

The cytotoxic effect of ifosfamide occurs after its activation, which takes place mainly in the liver. Therefore, the risk of tissue injury from accidental paravenous administration is low.

In case of accidental paravenous administration of ifosfamide, the infusion should be stopped immediately, the extravascular ifosfamide solution should be aspirated with the cannula in place, and other measures should be instituted as appropriate.

Use in Patients With Renal Impairment

In patients with renal impairment, particularly in those with severe renal impairment, decreased renal excretion may result in increased plasma levels of ifosfamide and its metabolites. This may result in increased toxicity (e.g., neurotoxicity, nephrotoxicity,

hematotoxicity) and should be considered when determining the dosage in such patients.

Use in Patients With Hepatic Impairment

Hepatic impairment, particularly if severe, may be associated with decreased activation of ifosfamide. This may alter the effectiveness of ifosfamide treatment. Low serum albumin and hepatic impairment are also considered risk factors for the development of CNS toxicity. Hepatic impairment may increase the formation of a metabolite that is believed to cause or contribute to CNS toxicity and also contribute to nephrotoxicity.

This should be considered when selecting the dose and interpreting response to the dose selected.

4.5 Interaction with other medicinal products and other forms of interaction

Planned co administration or sequential administration of other substances or treatments that could increase the likelihood or severity of toxic effects (by means of pharmacodynamic or pharmacokinetic interactions) requires careful individual assessment of the expected benefit and the risks. Patients receiving such combinations must be monitored closely for signs of toxicity to permit timely intervention.

Patients being treated with ifosfamide and agents that reduce its activation should be monitored for a potential reduction of therapeutic effectiveness and the need for dose adjustment.

Increased haematotoxicity and/or immunosuppression may result from a combined effect of ifosfamide and, for example:

-    ACE inhibitors: ACE inhibitors can cause leukopenia.

-    Carboplatin

-    Cisplatin

-    Natalizumab

Increased cardiotoxicity may result from a combined effect of ifosfamide and, for example:

-    Anthracyclines

-    Irradiation of the cardiac region

Increased pulmonary toxicity may result from a combined effect of ifosfamide and, for example:

-    Amiodarone

-    G-CSF, GM-CSF (granulocyte colonystimulating factor, granulocyte macrophage colony-stimulating factor)

Increased nephrotoxicity may result from a combined effect of ifosfamide and, for example: - Acyclovir

-    Aminoglycosides

-    Amphotericin B

-    Carboplatin

-    Cisplatin

An increased risk of developing hemorrhagic cystitis may result from a combined effect of ifosfamide and, for example:

-    Busulfan

Irradiation of the bladder

Additive CNS effects may result from a combined effect of ifosfamide and, for example:

-    Antiemetics

-    Antihistamines

-    Narcotics

-    Sedatives

Inducers of human hepatic and extrahepatic microsomal enzymes (e.g.,cytochrome P450 enzymes):

The potential for increased formation of metabolites responsible for cytotoxicity and other toxicities (depending on the enzymes induced) must be considered in case of prior or concomitant treatment with, for example:

-    Carbamazepine

-    Corticosteroids

-    Rifampin

-    Phenobarbital

-    Phenytoin

-    St. John’s Wort

See also aprepitant below.

Inhibitors of CYP 3A4: Reduced activation and metabolism of ifosfamide may alter the effectiveness of ifosfamide treatment. Inhibition of CYP 3A4 can also lead to increased formation of an ifosfamide metabolite associated with CNS and nephrotoxicity. CYP 3A4 inhibitors include:

-    Ketoconazole

-    Fluconazole

-    Itraconazole

-    Sorafenib

See also aprepitant below.

Aprepitant: Reports suggest increased ifosfamide neurotoxicity in patients receiving antiemetic prophylaxis with aprepitant, which is both an inducer and a moderate inhibitor of CYP 3A4.

Docetaxel: Increased gastrointestinal toxicity has been reported when ifosfamide was administered before docetaxel infusion.

Coumarin derivatives: Increased INR (increased international normalized ratio) has been reported in patients receiving ifosfamide and warfarin.

Vaccines: The immunosuppressive effects of ifosfamide can be expected to reduce the response to vaccination. Use of live vaccines may lead to vaccine induced infection.

Tamoxifen: Concomitant use of tamoxifen and chemotherapy may increase the risk of thromboembolic complications.

Cisplatin: Cisplatin-induced hearing loss can be exacerbated by concurrent ifosfamide therapy (see also interactions above).

Irinotecan: Formation of the active metabolite of irinotecan may be reduced when irinotecan is administered with ifosfamide.

Alcohol: In some patients, alcohol may increase ifosfamide-induced nausea and vomiting.

Concurrent administration of antidiabetic agents, such as sulfonylureas and ifosfamide may enhance the hypoglycaemic effects of the former drugs.

Theoretical interactions of ifosfamide and allopurinol resulting in an increased severity of bone marrow depression.

4.6 Fertility, pregnancy and lactation

Pregnancy

The administration of ifosfamide during organogenesis has been shown to have a fetotoxic effect in mice, rats, and rabbits and therefore may cause fetal damage when administered to pregnant women.

There are only very limited data available on the use of ifosfamide during pregnancy in humans. Fetal growth retardation and neonatal anaemia have been reported following exposure to ifosfamide-containing chemotherapy regimens during pregnancy. Multiple congenital deviations have been reported after use during the first trimester of pregnancy. Animal data generated with cyclophosphamide, another oxazaphosphorine cytotoxic agent suggest that an increased risk of failed pregnancy and malformations may persist after discontinuation of the agent as long as oocytes/follicles exist that were exposed to the agent during any of their maturation phases.

In addition, exposure to cyclophosphamide has been reported to cause miscarriage, malformations (following exposure during the first trimester), and neonatal effects, including leukopenia, pancytopenia, severe bone marrow hypoplasia, and gastroenteritis.

Based on the results of animal studies, human case reports and the substance's mechanism of action, the use of Ifosfamide during pregnancy, particularly in the first trimester, is advised against.

In every individual case, the benefits of the treatment will have to be weighed against possible risks for the fetus.

If ifosfamide is used during pregnancy, or if the patient becomes pregnant while taking this drug or after treatment, the patient should be apprised of the potential hazard to a fetus.

Breast-feeding

Ifosfamide is passed into the breast milk and may cause neutropenia, thrombocytopenia, low hemoglobin concentrations and diarrhea in children. Ifosfamide is contra-indicated for breast-feeding (see section 4.3).

Fertility

Ifosfamide interferes with oogenesis and spermatogenesis. It may cause sterility in both sexes.

Development of sterility appears to depend on the dose of ifosamide, duration of therapy, and state of gonadal function at the time of treatment.

Ifosfamide may cause transient or permanent amenorrhea in women and oligospermia or azoospermia in men.

Female patients

Women treated with ifosamide should be informed prior to treatment about the possibility to save and preserve their eggs.

The risk of permanent chemotherapy-induced amenorrhea is increased in older women.

Girls treated with ifosfamide during prepubescence may develop secondary sexual characteristics normally and have regular menses.

Girls treated with ifosfamide during prepubescence subsequently have conceived. Girls who have retained ovarian function after completing treatment are at increased risk of developing premature menopause.

Male Patients

Men treated with Ifosfamide should be informed prior to treatment about the possibility to save pre-produced sperm kept in proper conditions.

Sexual function and libido generally are unimpaired in these patients.

Boys treated with ifosfamide during prepubescence may develop secondary sexual characteristics normally, but may have oligospermia or azoospermia.

Some degree of testicular atrophy may occur.

Azoospermia may be reversible in some patients, though the reversibility may not occur for several years after cessation of therapy.

Men treated with ifosfamide have subsequently fathered children.

Genotoxicity

Ifosfamide is genotoxic and mutagenic in male and female germ cells. Therefore, women should not become pregnant and men should not father a child during therapy with ifosfamide.

Women treated with ifosfamide should take contraceptive measures for at least 1 year after discontinuation of ifosfamide therapy.

Men should not father a child for up to 6 months after the end of therapy.

Sexually active women and men should use effective methods of contraception during these periods of time.

4.7 Effects on Ability to Drive and Use Machines

Potential side-effects on the central nervous system may transiently impair the ability to operate machinery and motor vehicles.

4.8 Undesirable effects

The adverse reactions and frequencies below are based on publications describing clinical experience with fractionated administration of ifosfamide as monotherapy with a total dose of 4 to 12 g/m2 per course.

ADR frequency is based upon the following scale: Very common (>1/10); Common (>1/100 - <1/10), Uncommon (>1/1,000 - <1/100), Rare (>1/10,000 - <1/1,000), Very

rare (<1/10,000), Not known (adverse reactions reported in the post-marketing experience).

System Organ Class (SOC)

Adverse Reaction

Frequency

Category

INFECTIONS AND

Infections (including reactivation of

Common

INFESTATIONS

latent infections)

Sepsis (septic shock )*

Not known

NEOPLASMS BENIGN,

Secondary tumors*

Not known

MALIGNANT AND

(including Urinary tract carcinoma,

UNSPECIFIED (INCL

- Myelodysplastic syndrome,

CYCTS AND POLYPS)

Acute leukaemia, Acute lymphocytic leukemia, Lymphoma (Non-Hodgkin’s lymphoma), Sarcomas, Renal cell carcinoma,

Thyroid cancer)

Progressions of underlying malignancies*

Not known

BLOOD AND LYMPHATIC

Myelosuppression

Very

SYSTEM DISORDERS

- Leukopenia

common

- Thrombocytopenia*

Very

- Anemia

common

- Agranulocytosis

Very

Hematotoxicity*

common

- Hemolytic anemia

Not known

- Methaemoglobinaemia

Not known

Febrile bone marrow aplasia

Not known

Disseminated intravascular

Not known

coagulation Hemolytic uremic

Not known

syndrome

Not known

Neonatal anemia

Not known Not known Not known

IMMUNE SYSTEM

Angioedema*

Not known

DISORDERS

Anaphylactic reaction

Not known

Immunosuppression

Not known

Urticaria

Not known

Hypersensitivity reaction

Not known

ENDOCRINE DISORDERS

Syndrome of inappropriate antidiuretic hormone secretion (SIADH)

Not known

METABOLISM AND

Decreased Appetite

Common

NUTRITION DISORDERS

Tumor lysis syndrome

Not known

Metabolic acidosis

Not known

Hypokalemia

Not known

Hypocalcemia

Not known

Hypophosphatemia

Not known

Hyperglycemia

Not known

Polydipsia

Not known

System Organ Class (SOC)

Adverse Reaction

Frequency

Category

PSYCHIATRIC

Mutism

Not known

DISORDERS

Mental status change (including

Not known

mania, paranoia, delusion, delirium,

Not known

catatonia, amnesia, panic attack)

Not known

Echolalia

Not known

Perseveration

Not known

NERVOUS SYSTEM

Central nervous system toxicity

Not known

DISORDERS

- Encephalopathy

Not known

- Faecal incontinence

Not known

- Status epilepticus* (convulsive and nonconvulsive)

Not known

- Movement disorder

Not known

- Extrapyramidal disorder

Not known

- Gait disturbance

Not known

- Dysarthia

Not known

Peripheral neuropathy

Not known

- Hypoesthesia

Not known

- Paresthesia

Not known

- Asterixis

Not known

- Neuralgia

Not known

EYE DISORDERS

Visual impairment

Not known

Conjunctivitis

Not known

Eye irritation

Not known

EAR AND LABYRINTH

Deafness

Not known

DISORDERS

Vertigo

Not known

Tinnitus

Not known

CARDIAC DISORDERS

Cardiotoxicity*

Uncommon

Arrythmia (including

Not known

supraventricular and ventricular

Not known

arrhythmia)

Not known

Atrial fibrillation

Not known

Premature atrial contractions

Not known

Bradycardia

Not known

Cardiac arrest*

Not known

Myocardial infarction

Not known

Cardiac failure*

Not known

Myocardial hemorrhage

Not known

Angina pectoris

Not known

Cardiomyopathy* (including

Not known

congestive cardiomyopathy)

Not known

Electrocardiogram ST-segment

Not known

abnormal

Electrocardiogram T- wave inversion Electrocardiogram QRS complex abnormal

Not known

System Organ Class (SOC)

Adverse Reaction

Frequency

Category

VASCULAR DISORDERS

Hypotension7

Uncommon

Pulmonary embolism

Not known

Deep vein thrombosis

Not known

Capillary leak syndrome

Not known

Vasculitis

Not known

Hypertension

Not known

Flushing

Not known

RESPIRATORY,

Respiratory failure*

Not known

THORACIC, AND

Acute respiratory distress

Not known

MEDIASTINAL

syndrome* Pulmonary

Not known

DISORDERS

hypertension

Interstitial lung disease* (as

Not known

manifested by Pulmonary fibrosis)

Not known

Pneumonitis*

Not known

Pulmonary oedema*

Not known

Pleural effusion

Not known

Dyspnea

Not known

Hypoxia

Cough

Not known

GASTROINTESTINAL

Nausea/Vomiting

Very

DISORDERS

Diarrhea

common

Stomatitis

Uncommon

Enterocolitis

Uncommon

Pancreatitis

Not known

Ileus

Not known

Gastrointestinal hemorrhage

Not known

Mucosal ulceration

Not known

Constipation

Not known

Abdominal pain

Not known

Salivary hypersecretion

Not known Not known

HEPATOBILIARY

Hepatotoxicity

Common

DISORDERS

- Hepatic failure

Not known

Veno-occlusive liver disease

Not known

Portal vein thrombosis

Not known

Cytolytic hepatitis

Not known

SKIN AND

Alopecia

Very

SUBCUTANEOUS TISSUE

Dermatitis

common

DISORDERS

Papular rash

Rare

Toxic epidermal necrolysis

Rare

Stevens-Johnson syndrome

Not known

Palmar-plantar erythrodysesthesia

Not known

syndrome

Not known

Radiation recall dermatitis

Not known

Skin necrosis

Not known

Facial swelling

Not known

Rash

Not known

Pruritus

Not known

Erythema

Not known

Skin hyperpigmentation

Not known

Hyperhidrosis

Not known

Nail disorder

Not known

System Organ Class (SOC)

Adverse Reaction

Frequency

Category

MUSCULOSKELETAL

Rhabdomyolysis

Not known

AND CONNECTIVE

Osteomalacia

Not known

TISSUE DISORDERS

Rickets

Not known

Growth retardation

Not known

Myalgia

Not known

Arthralgia

Not known

Muscle twitching

Not known

RENAL AND URINARY

Hemorrhagic cystitis

Very

DISORDERS

Hematuria

common

Renal dysfunction1

Very

- Acute renal failure

common

- Chronic renal failure

Very

- Aminoaciduria

common

- Phosphaturia

Very

- Fanconi syndrome

common

- Tubulointerstitial nephritis

Not known

Renal structural damage

Not known

Nephrogenic diabetes insipidus

Not known

Polyuria

Not known

Enuresis

Not known

Feeling of residual urine

Not known Not known Not known Not known Not known

REPRODUCTIVE SYSTEM

Infertility

Not known

AND BREAST DISORDERS

Ovarian failure

Not known

Premature menopause

Not known

Amenorrhea

Not known

Ovulation disorder

Not known

Azoospermia

Not known

Oligospermia

Not known

CONGENITAL, FAMILIAL AND GENETIC DISORDERS

Fetal growth retardation

Not known

GENERAL DISORDERS

Phlebitis

Common

AND ADMINISTRATIVE

Fatigue

Uncommon

SITE CONDITIONS

Malaise

Not known

Multiorgan failure1

Not known

General physical deterioration

Not known

Injection/Infusion site reactions

Not known

Edema

Not known

Pain

Not known

Pyrexia

Not known

Chills

Not known

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 website: www.mhra.gov.uk/yellowcard

4.9 Overdose

Serious consequences of overdosage include manifestations of dose-dependent toxicities such as CNS toxicity, nephrotoxicity, myelosuppression, and mucositis. See Section 4.4.

Patients who received an overdose should be closely monitored for the development of toxicities.

No specific antidote for ifosfamide is known.

Overdosage should be managed with supportive measures, including appropriate, state-of-the-art treatment for any concurrent infection, myelosuppression, or other toxicity, should it occur.

Ifosfamide as well as ifosfamide metabolites are dialyzable. Consider haemodialysis in cases of severe overdose presenting early, particularly in patients with renal impairment.

Cystitis prophylaxis with mesna may be helpful in preventing or limiting urotoxic effects with overdose.

5 PHARMACOLOGICAL PROPERTIES

5.1 Pharmacodynamic properties

Ifosfamide is an antineoplastic, a cytotoxic alkylating agent. It is a prodrug and shows no in vitro cytotoxic activity until activated by microsomal enzymes. The cytotoxic activity of Ifosfamide (alkylation of the nucleophilic centres in the cells) is associated with the activated oxazaphosphorine ring hydroxylated at the C4 atom which interacts with DNA-DNA cross linking. This activity manifests itself by blocking the late S and early G2 phases of the cell cycle.

Paediatric population Ewing’s sarcoma

In a randomized controlled trial, 518 patients (87% under 17 years of age) with Ewing’s Sarcoma, primitive neuroectodermal tumour of bone or primitive sarcoma of bone were randomized to ifosfamide/etoposide alternating with standard treatment, or to standard treatment alone. In those with no metastases at baseline, there was a statistically significant improvement in 5 year survival for those receiving ifosfamide /etoposide (69%) compared to those on standard treatment alone (54%). Overall survival at 5 years was 72% in the ifosfamide/etoposide group compared to 61% in the standard treatment group. Similar toxicities were observed in both treatment arms. In those with metastases at baseline, there was no difference in 5 year event-free survival or 5 year overall survival between treatment groups.

In a randomized comparative study of ifosfamide (VAIA regimen) and cyclophosphamide (VACA regimen) in 155 patients with standard risk Ewing’s sarcoma (83% under 19 years of age), no difference in event free survival or overall survival was demonstrated. Less toxicity was demonstrated for the ifosfamide regimen.

Other paediatric cancers

Ifosfamide has been widely investigated in uncontrolled prospective exploratory studies in children. Various dosage schedules and regimens, in combination with other antitumour agents, have been used. The following paediatric cancers have been investigated: rhabdomyosarcoma, non-rhabdomyosarcoma soft tissue sarcoma, germ cell tumours, osteosarcoma, non-Hodgkins lymphoma, Hodgkins Disease, acute lymphoblastic leukaemia, neuroblastoma, Wilms tumour, and malignant CNS tumours. Favourable partial responses, complete responses and survival rates have been documented.

A variety of dosage schedules and regimens of ifosfamide in combination with other antitumor agents, are used. The prescriber should refer to chemotherapy regimens for specific tumour type in choosing a specific dosage, mode of administration and schedules.

Usually the doses of ifosfamide in pediatric tumors range from 0.8 to 3 g/m2/day for 2-5 days for a total dose of 4-12 g/m2 for chemotherapy course.

Fractionated administration of ifosfamide is performed as intravenous infusion over a period ranging between 30 minutes and 2 hours, depending on the infusion volume or recommendations of protocol:

Uroprotection with mesna is mandatory during ifosfamide administration with a dose equivalent to 80-120 % of ifosfamide. It is recommended to prolong Mesna infusion to 12-48 hours after the end of ifosfamide infusion. 20 % of the whole Mesna dose should be given as i.v start bolus. Hyperhydration with at least 3000 ml/m2 is required during ifosfamide infusion and for 24-48 hours after the end of ifosfamide administration.

Under treatment with ifosfamide, especially in case of long-term treatment, sufficient diuresis and regular control of renal function will be required. Children 5 years of age or younger may be more susceptible to ifosfamide-induced renal toxicity than older children or adults. Severe nephrotoxicity leading to Fanconi’s syndrome has been reported. Progressive tubular damage resulting in potentially debilitating hypophosphatemia and rickets has been reported rarely but should be taken into consideration.

Paediatric data from randomized controlled clinical studies are limited.

5.2 Pharmacokinetic properties

Ifosfamide is rapidly absorbed from the site of administration, activation of Ifosfamide is primarily in the liver by microsomal mixed function oxidases. Elimination of metabolised Ifosfamide is primarily via the kidneys. The serum halflife ranges between 4 - 8 hours depending on the dose and dosage regimen. Over 80% of a single dose of ifosfamide was excreted in the urine within 24 hours. Approximately 80% of the dose was excreted as parent compound. Significant quantities of unchanged ifosfamide were found in the cerebrospinal fluid consistent with the high lipid solubility of the drug.

Pre-clinical Safety Data

5.3


Not relevant

6. PHARMACEUTICAL PARTICULARS

6.1    List of Excipients

None

6.2    Incompatibilities

Benzyl alcohol-containing solutions can reduce the stability of ifosfamide.

6.3 Shelf-Life

Five years.

The reconstituted solution should be used immediately. The product does not contain a preservative, therefore microbial stability cannot be guaranteed. When prepared under strict aseptic conditions, ifosfamide is, as a 4% solution, however, chemically stable for 7 days at room temperature with Water for Injections, 0.9% saline, dextrose/saline and dextrose solutions. Ifosfamide and mesna when prepared under strict aseptic conditions at the recommended dilutions are chemically stable with:

(i)    0.9% saline and dextrose/saline solution for one week at room temp.

(ii)    Water for Injections for one week under refrigeration

(iii)    5% dextrose solution for 24 hours at room temperature, and

(iv)    0.9% saline solution for 28 days at room temperature.

6.4 Special Precautions for Storage

Do not store above 25°C.

Keep container in outer carton.

6.5


Nature and Content of Container

Type I or Type III glass injection vial with bromobutyl rubber closure and beading cap. Vials are packed singly in a cardboard box.

6.6 Special precautions for disposal

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration.

Before parenteral administration, the substance must be completely dissolved.

The following protective recommendations are advised during handling due to the toxic nature of the substance:

Reconstitution and administration must be undertaken only by trained personnel. Pregnant staff and breastfeeding mothers should be excluded.

Protective clothing, goggles, masks and disposable PVC or latex gloves should be worn.

A designated area should be defined for reconstitution (preferably under a laminar-airflow system). The work surface should be protected by a disposable, plastic backed absorbent paper. Accidental contact with the skin or eyes should be treated immediately by copious lavage with water. Soap and water should then be used on non-mucous membranes. Spillage should be removed by dry or moist disposable towels.

Care must be taken in the disposal of all waste material (syringes, needles and disposable towels etc.) Used items should be placed in appropriate secure containers in readiness for destruction in an appropriate high-temperature incinerator with an after-burner.

7. MARKETING AUTHORISATION HOLDER

Baxter Healthcare Ltd

Caxton Way

Theford

Norfolk

IP24 3SE

United Kingdom

8    MARKETING AUTHORISATION NUMBER(S)

PL 00116/0395

DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION 04/04/2012

10


DATE OF REVISION OF THE TEXT

20/02/2014

1

including fatal outcomes

Reporting of suspected adverse reactions