Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
The electronic medicines compendium (emc) no longer publishes a Summary of Product Characteristics for this product, which usually means it is no longer marketed in the UK. The patient leaflet below is kept for reference, but the product may not be available.
If you were prescribed this medicine, other products containing Mitomycin may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.
for
Mitomycin is a medicine for the treatment of cancer, i.e. a medicine which prevents or considerably delays the division of active cells by influencing their metabolism in various ways. The therapeutic application of medicinal products for the treatment of cancer is based on the fact that one way in which cancer cells differ from normal cells in the body is that the rate of cell division is increased due to a lack of control of their growth. Therapeutic Indications Mitomycin is used in cancer therapy for the relief of symptoms (palliative cancer therapy). Intravenous application When administered intravenously it is used in monochemotherapy, i.e. treatment with only one active substance, or in combined cytostatic chemotherapy, i.e. treatment with several active substances. Mitomycin is effective in the case of the following tumours:
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2.
e Mitocin
Do not use Mitocin in the case of systemic or intravesical use
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You should not get vaccinated, especially with live vaccines during mitomycin treatment. Please note that the above also applies to medications used in the recent past. Pregnancy, breastfeeding and fertility Mitomycin should not be used during pregnancy. Your doctor has to evaluate the benefit against the risk of harmful effects on your child, if mitomycin treatment during pregnancy is necessary. Women of child-bearing age should avoid becoming pregnant. Contraceptive measures must be taken by both male and female patients during and for at least six months after cessation of therapy. Still, if you become pregnant during this period you must immediately inform your doctor. Breast-feeding must be discontinued before you start to use mitomycin. Driving and using machines Even when used in accordance with instructions this medicine may cause nausea and vomiting and thereby reduce your reaction times to such an extent that the ability to drive a motor vehicle or operate machinery is impaired. This applies in particular in conjunction with alcohol.
3.
Mitocin
Mitomycin should only be administered by healthcare professionals experienced in this kind of therapy. Mitomycin is intended to be used for injection or infusion into a blood vessel (intravenous use) or for introduction into the urinary bladder (intravesical instillation) after being dissolved. Your doctor will prescribe a dose and treatment regimen that is right for you. Before you receive mitomycin as injection or infusion into a vein a blood test, check of lung, kidney and liver function is recommended to exclude any diseases, which could worsen during mitomycin therapy. The needle must remain in the vein while mitomycin is being given. If the needle comes out or becomes loose, or the medicinal product is going into the tissue outside the vein (you may feel discomfort or pain) – tell the doctor or nurse immediately. If you use more Mitocin than you should If you have been accidentally given a higher dose you may experience symptoms such as fever, nausea, vomiting and blood disorders. Your doctor may give you supportive treatment for any symptoms that may occur. If you have any further questions on the use of this medicine, please ask your doctor or pharmacist.
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4.
Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them. Possible side effects following administration into a vein Severe lung disease presenting as shortness of breath, dry cough and crackles during breath-in (interstitial pneumonia) as well as severe renal dysfunction (nephrotoxicity) may occur. If you notice any of the above reactions please inform your doctor immediately because mitomycin therapy must be stopped. Very common (may affect more than 1 in 10 people)
following installation in the bladder Common (may affect up to 1 in 10 people)
Mitocin
Do not store above 25°C. Keep the vial in the outer carton in order to protect from light. Chemical and physical in-use stability of reconstituted solution has been demonstrated at room temperature and light effect with: • 0.9% sodium chloride solution for 2 hours 5
•
water for injections for 1 hour.
From a microbiological point of view, the product must be used immediately. In the event of non-immediate use, the user is responsible for storage times and conditions during use.
Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date which is stated on the label and folding box after "EXP". The expiry date refers to the last day of that month. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment
6.
What Mitocin contains The active substance is mitomycin. 1 vial powder for solution for injection/infusion or intravesical use contains 20 mg mitomycin. After reconstitution with 40 ml water for injections 1 ml solution for injection/infusion contains 0.5 mg mitomycin. After reconstitution with 20 ml solvent 1 ml solution for intravesical use contains 1 mg mitomycin The other excipients are: Mannitol, hydrochloric acid 36% and sodium hydroxide for pH adjustment What Mitocin looks like and contents of the pack Mitomycin is a grey powder. Mitocin, powder for solution for injection/infusion or intravesical use is available in packs containing 1 amber glass vial and packs containing 5 amber glass vials with powder for solution for injection/infusion or intravesical use Not all pack sizes may be marketed. Marketing Authorisation Holder and Manufacturer Marketing Authorisation Holder Vygoris Limited 930 High Road London N12 9RT United Kingdom Tel: +44 (0)12 2339 5301 Manufacturer Creapharm Clinical Supplies 6
ZA Air-Space, Avenue de Magudas CS 2007, Le Haillan Cedex, 33187, France This package leaflet was last revised in 29/11/2024.
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——————————————————————————————————The following information is intended for healthcare professionals only: General Information It is essential that the injection is administered intravenous. If the medicinal product is injected perivasally, extensive necrosis occurs in the area concerned. To avoid necrosis following recommendations apply:
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Mitocin 20 mg, powder for solution for injection/infusion or intravesical use comes as injection containing 20mg. Always follow the dose your doctor or pharmacist has given you, and read the leaflet that comes with the medicine.
The active substance in Mitocin 20 mg, powder for solution for injection/infusion or intravesical use is mitomycin.
This leaflet reproduces the patient information leaflet approved for Mitocin 20 mg, powder for solution for injection/infusion or intravesical use, as published on the electronic medicines compendium (emc). The version printed inside your medicine’s packaging is the one that applies to you.
Whether a medicine is available over the counter or on prescription only depends on its licence. Check the leaflet, or ask your pharmacist — they can tell you straight away.
The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.
Mitomycin is used in palliative tumour therapy.
Mitomycin is administered intravenously as monochemotherapy or in combined cytostatic chemotherapy in the case of:
• advanced metastatic gastric carcinoma
• advanced and/or metastatic breast cancer
Furthermore mitomycin is administered intravenously in combined chemotherapy in the case of:
• non-small cell bronchial carcinoma
• advanced pancreatic carcinoma
Intravesical administration for relapse prevention in superficial urinary bladder carcinoma after transurethral resection.
Posology
Mitomycin should only be used by doctors experienced in this therapy if there is a strict indication and with continual monitoring of the haematological parameters. It is essential that the injection is administered intravenous. If the medicinal product is injected perivasally, extensive necrosis occurs in the area concerned.
Unless otherwise prescribed, mitomycin is dosed as follows:
Intravenous administration
In cytostatic monochemotherapy mitomycin is usually administered intravenously as a bolus injection. The recommended dosage is 10 - 20 mg/m2 of body surface every 6 - 8 weeks, 8 - 12 mg/m2 of body surface every 3 - 4 weeks or 5-10 mg/m2 of body surface every 1-6 weeks, depending on the therapeutic scheme used.
In combination therapy the dosage is considerably lower. Because of the risk of additive myelotoxicity, proven treatment protocols may not be deviated from without a specific reason.
Intravesical administration
In intravesical therapy, 20 - 40 mg of mitomycin, corresponding to 1 - 2 vials of Mitocin 20 mg in 20 - 40 ml of water for injections or sodium chloride (0.9%) solution, is instilled weekly into the bladder. In the case of intravesical administration the urine pH should be higher than pH 6.
Alternative dose recommendation in the prevention of recurrent superficial bladder tumours is 4-10 mg (0.06-0.15 mg/kg of body weight) instilled into the bladder though a urethral catheter 1 or 3 times per week.
Special population
The dose must be reduced in patients who have undergone extensive previous cytostatic therapy, in case of myelosuppression or in elderly patients.
Insufficient data from clinical studies are available concerning the use of mitomycin in patients ≥65 years of age.
The product should not be used in patients with renal impairment (see section 4.3)
The product is not recommended in patients with hepatic impairment due to lack efficacy and safety data in this group of patients.
Paediatric population
The safety and efficacy of mitomycin in children have not been established.
Method of administration
Mitomycin is intended for intravenous injection or infusion or for intravesical instillation after being dissolved. Partial use is applicable.
Preparation of ready-to-use solution for injection or infusion
The contents of one vial of Mitocin 20 mg are dissolved in 40 ml of water for injections by swirling.
Shake until the reconstituted solution becomes clear and free of particles.
For intravenous infusion the solution of Mitocin 20 mg in 40 ml of water for injections can be diluted with isotonic sodium chloride infusion solution down to a concentration of 20 - 40 micrograms of mitomycin/ml.
Preparation of ready-to-use solution for intravesical administration
The contents of 1 - 2 vials of Mitocin 20 mg (equivalent to 20 – 40 mg of mitomycin) are dissolved in 20 – 40 ml of water for injections or sodium chloride (0.9%) solution.
Notes
• Mitocin 20 mg must not be used in mixed injections.
• Other injection solutions or infusion solutions must be administered separately.
• It is essential that the injection is administered intravenous
• Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
• Breastfeeding
Systemic therapy
Pancytopenia or isolated leucopoenia/thrombopenia, haemorrhagic diathesis and acute infections are absolute contraindications.
Restrictive or obstructive disturbances to pulmonary ventilation, renal function, liver function and/or a poor general state of health are relative contraindications. Temporal connection with radiotherapy or other cytostatic may be a further contraindication.
Intravesical therapy
Perforation of the bladder wall is an absolute contraindication.
Cystitis is a relative contraindication.
Due to the toxic effects on the bone marrow of mitomycin, other myelotoxic therapy modalities (in particular other cytostatics, radiation) must be administered with particular caution in order to minimise the risk of additive myelosuppression.
It is essential that the injection is administered intravenous. If the medicinal product is injected perivasally, extensive necrosis occurs in the area concerned. To avoid necrosis following recommendations apply:
• Always inject into large veins in the arms.
• Do not directly inject intravenously, but rather into the tube of a good and securely running infusion.
• Before removing the cannula after central venous administration, flush it through for a few minutes using the infusion in order to release any residual mitomycin.
If extravasation occurs, it is recommended that the area is immediately infiltrated with sodium bicarbonate 8.4% solution, followed by an injection of 4 mg dexamethasone. A systemic injection of 200 mg of Vitamin B6 may be of some value in promoting the regrowth of tissues that have been damaged.
Long-term therapy may result in cumulative bone marrow toxicity. Bone marrow suppression may only manifest itself after a delay, being expressed most strongly after 4 - 6 weeks, accumulating after prolonged use and therefore often requiring an individual dose adjustment.
Elderly patients often have reduced physiological function, bone marrow depression, which may be protracted, so administer mitomycin with special caution in this population while closely monitoring patient's condition.
Mitomycin is a mutagenic and potentially carcinogenic substance in humans. Contact with the skin and mucous membranes is to be avoided.
In the case of pulmonary symptoms, which cannot be attributed to the underlying disease, therapy should be stopped immediately. Pulmonary toxicity can be well treated with steroids.
Therapy should be stopped immediately also if there are symptoms of haemolysis or indications of renal dysfunction (nephrotoxicity).
At doses of > 30 mg of mitomycin/m2 of body surface microangiopathic-haemolytic anaemia has been observed. Close monitoring of renal function is recommended.
New findings suggest a therapeutic trial may be appropriate for the removal of immune complexes that seem to play a significant role in the onset of symptoms by means of staphylococcal protein A.
Occurrence of acute leukaemia (in some cases following preleukaemic phase) and myelodysplastic syndrome has been reported in the patients treated concomitantly with other antineoplastic agents.
Extravasation following intravesical administration
Symptoms of extravasation after intravesical mitomycin administration might present straight after the application or weeks or months later. It can be unclear if the extravasation occurred due to unnoticed perforation, a thinned muscularis propria or if the medicinal product was not administered correctly.
First symptoms present as pelvic or abdominal pain that are refractory to simple analgesia. (Fat) tissue necrosis in the surrounding area as a consequence of the extravasation was observed in most cases. Bladder perforation or development of fistula and/or abscess has also been reported (see section 4.8).
Therefore, physicians should consider the possibility that extravasation occurred if the patient complains about pelvic or abdominal pain to prevent serious consequences.
Recommended check-ups and safety measures in the case of intravenous administration:
Before the start of treatment
• Complete blood count
• Pulmonary function test if pre-existing lung dysfunction is suspected
• Renal function test in order to exclude renal insufficiency
• Liver function test in order to exclude liver insufficiency
During therapy
• Regular checks of the blood count
• Close monitoring of renal function
Myelotoxic interactions with other bone marrow-toxic treatment modalities (especially other cytotoxic medicinal products, radiation) are possible.
Combination with vinca alkaloids or bleomycin may reinforce pulmonary toxicity.
An increased risk of haemolytic-uremic syndrome has been reported in patients receiving a concomitant administration of mitomycin and fluorouracil or tamoxifen.
In animal experiments, pyridoxine hydrochloride (vitamin B6) resulted in the loss of effect of mitomycin.
No injections with live vaccines should be carried out in connection with mitomycin treatment.
The cardiotoxicity of Adriamycin (doxorubicin) may be reinforced by mitomycin
Pregnancy
There are no data from the use of mitomycin in pregnant women. Studies in animals have shown reproductive toxicity (see section 5.3). Mitomycin has a mutagenic, teratogenic and carcinogenic effect and therefore may impair the development of an embryo. Mitomycin should not be used during pregnancy. In the case of a vital indication for the treatment of a pregnant patient a medical consultation should be carried out with respect to the risk of the harmful effects on the child, which are associated with the treatment.
Breastfeeding
It is suggested that mitomycin is excreted in breast milk. Due to its proven mutagenic, teratogenic and carcinogenic effects, mitomycin may not be administered during breastfeeding and therefore Mitocinis contraindicated during breastfeeding (see section 4.3).
Fertility/ Contraception in males and females
Female patients of a sexually mature age should take contraceptive measures during and up to 6 months after the end of chemotherapy or refrain from sexual intercourse.
Mitomycin has a genetically harmful effect. Men who are being treated with mitomycin are therefore advised not to father a child during treatment and up to 6 months thereafter and to seek advice on the preservation of sperm before the start of therapy due to the possibility of irreversible infertility caused by the therapy with mitomycin.
Even when used in accordance with instructions these medicinal products may cause nausea and vomiting and thereby impair alertness to such an extent that the ability to drive a motor vehicle or operate machinery is impaired. This applies even more in connection with alcohol.
Undesirable effects are listed below by system organ class and frequency. Frequencies below are defined as:
Very common (≥ 1/10), common (≥ 1/100 to < 1/10), uncommon (≥ 1/1,000 to < 1/100), rare (≥ 1/10,000 to < 1/1,000), very rare (< 1/10,000) or not known (cannot be estimated from the available data)
Possible side-effects under systemic therapy
The most common side effects of mitomycin administered systemically are gastrointestinal symptoms like nausea and vomiting and bone marrow suppression with leukopenia and mostly dominant thrombocytopenia. This bone marrow suppression occurs in up to 65% of patients.
In up to 10% of patients serious organ toxicity in the form of interstitial pneumonia or nephrotoxicity must be expected.
Mitomycin is potentially hepatotoxic.
Blood and the lymphatic system disorders
Very common
Bone marrow suppression, leucopenia thrombocytopenia
Rare
Life-threatening infection, sepsis, haemolytic anaemia
Immune system disorders
Very rare
Severe allergic reaction
Cardiac disorders
Rare
Heart failure after previous therapy with anthracyclines
Respiratory, thoracic and mediastinal disorders
Common
Interstitial pneumonia,dyspnoe, cough, shortness of breath
Rare
Pulmonary hypertension, pulmonary veno-occlusive disease (PVOD)
Gastrointestinal disorders
Very common
Nausea, vomiting,
Uncommon
Mucositis, stomatitis, diarrhoea, anorexia
Hepatobiliary disorders
Rare
Liver dysfunction, increased transaminases, jaundice, veno-occlusive disease (VOD) of the liver
Skin and subcutaneous tissue disorders
Common
Exanthema, allergic skin rash, contact dermatitis, palmar-plantar erythema
Uncommon
Alopecia
Rare
Generalised exanthema
Renal and urinary disorders
Common
Renal dysfunction, increase in serum creatinine, glomerulopathy, Nephrotoxicity
Rare
Haemolytic uraemic syndrome (HUS) (commonly fatal), microangiopathic-haemolytic anaemia (MAHA syndrome)
General disorders and administration site conditions
Common
Following Extravasation:
Cellulitis, tissue necrosis
Uncommon
Fever
Possible side-effects under intravesical therapy
Skin and subcutaneous tissue disorders
Common
Pruritus, allergic skin rash, contact dermatitis, palmar-plantar erythema
Rare
Generalised exanthema
Renal and urinary disorders
Common
Cystitis (possibly haemorrhagic), dysuria, nocturia, pollakisuria, hematuria, local irritation of the bladder wall.
Very rare
Necrotizing cystitis, allergic (eosinophilic) cystitis, stenosis of the efferent urinary tract, reduction in bladder capacity, bladder wall calcification, bladder wall fibrosis, bladder perforation.
Not known
in case of extravasation:
Bladder perforation, (fat) tissue necrosis of the surrounding area, vesical fistula, abscesses.
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.
In case of overdose severe myelotoxicity or even myelophthisis must be expected, with the full-blown clinical effect only appearing after approximately 2 weeks.
The period until which the number of leucocytes falls to the lowest value may be 4 weeks. Prolonged close haematological monitoring therefore also has to be carried out if an overdose is suspected.
As there are no effective antidotes available, the greatest level of caution is required during each application.
Medicines sold in Poland with the same active substance: W Polsce znany jako
Same active substance. The strength, the form and whether you need a prescription can differ. Always ask a pharmacist before you switch. Polish medicines in the UK →
Ask anything about Mitocin 20 mg, powder for solution for injection/infusion or intravesical use. The assistant answers only from this leaflet — if the leaflet does not cover it, it will say so. It does not give medical advice.
Answers come from the patient leaflet published on the electronic medicines compendium (emc). They are not medical advice. Ask a pharmacist or your GP if you are unsure. For urgent help call NHS 111, or 999 in an emergency.
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