VISTIDE Concentrate for solution for infusion Ref.[6674] Active ingredients: Cidofovir

Cidofovir 75 mg/ml Concentrate for Solution for Infusion is formulated for intravenous infusion only and must not be administered by other methods including intraocular injection or topically. It should be infused only into veins with adequate blood flow to permit rapid dilution and distribution.

The safety and efficacy of cidofovir has not been demonstrated in diseases other than CMV retinitis in adults with AIDS.

Renal insufficiency/Haemodialysis

Treatment with cidofovir must not be initiated in patients with creatinine clearance ≤55 ml/min, or ≥2+ proteinuria (≥100 mg/dl), as the optimum induction and maintenance doses for patients with moderate to severe renal impairment are not known. The efficacy and safety of cidofovir in such conditions has not been established.

High flux haemodialysis has been shown to reduce the serum levels of cidofovir by approximately 75%. The fraction of the dose extracted during haemodialysis is 51.9 ± 11.0%.

Nephrotoxicity

Dose-dependent nephrotoxicity is the major dose-limiting toxicity related to administration of cidofovir (see section 4.8). The safety of cidofovir has not been evaluated in patients receiving other known potentially nephrotoxic agents (e.g. tenofovir, aminoglycosides, amphotericin B, foscarnet, intravenous pentamidine, adefovir and vancomycin).

Cidofovir should not be administered concurrently with medicinal products containing tenofovir disoproxil fumarate due to the risk of Fanconi syndrome (see section 4.5).

It is recommended to discontinue potentially nephrotoxic agents at least 7 days before starting cidofovir.

Patients treated at 3.0 mg/kg, 5.0 mg/kg or 10 mg/kg without concomitant probenecid developed evidence of proximal tubular cell injury, including glycosuria, and decreases in serum phosphate, uric acid and bicarbonate, and elevations in serum creatinine. The signs of nephrotoxicity were partially reversible in some patients. Concomitant use of probenecid is essential for reducing the pronounced nephrotoxicity of cidofovir to an extent that results in an acceptable benefit/risk balance of cidofovir therapy.

Prevention of nephrotoxicity

Therapy must be accompanied by administration of oral probenecid and adequate intravenous saline prehydration (see section 6.6 for information on obtaining probenecid) with each cidofovir dose. All clinical trials relevant to clinical efficacy evaluation were performed using probenecid concomitantly with cidofovir. Two grams of probenecid should be administered 3 hours prior to the cidofovir dose and one gram administered at 2 and again at 8 hours after completion of the 1 hour cidofovir infusion (for a total of 4 grams). In order to reduce the potential for nausea and/or vomiting associated with administration of probenecid, patients should be encouraged to eat food prior to each dose of probenecid. The use of an anti-emetic may be necessary.

In patients who develop allergic or hypersensitivity symptoms to probenecid (e.g., rash, fever, chills and anaphylaxis), prophylactic or therapeutic use of an appropriate antihistamine and/or paracetamol should be considered.

Cidofovir administration is contraindicated in patients unable to receive probenecid because of a clinically significant hypersensitivity to the active substance or medicinal product or to other sulfa containing medicines. Use of cidofovir without concomitant probenecid has not been clinically investigated. A probenecid desensitisation program is not recommended for use.

In addition to probenecid, patients must receive a total of one litre of 0.9% (normal) saline solution intravenously immediately prior to each infusion of cidofovir. Patients who can tolerate the additional fluid load may receive up to a total of 2 litres of 0.9% saline intravenously with each dose of cidofovir. The first litre of saline solution should be infused over a 1 hour period immediately before the cidofovir infusion, and the second litre, if given, infused over a 1-3 hour period beginning simultaneously with the cidofovir infusion or starting immediately after the infusion of cidofovir.

Cidofovir therapy should be discontinued and intravenous hydration is advised if serum creatinine increases by ≥44 μmol/l (≥0.5 mg/dl), or if persistent proteinuria ≥ 2+ develops. In patients exhibiting ≥2+ proteinuria, intravenous hydration should be performed and the test repeated. If following hydration, a ≥2+ proteinuria is still observed, cidofovir therapy should be discontinued. Continued administration of cidofovir to patients with persistent ≥2+ proteinuria following intravenous hydration may result in further evidence of proximal tubular injury, including glycosuria, decreases in serum phosphate, uric acid and bicarbonate, and elevations in serum creatinine.

Interruption, and possibly discontinuation, is required for changes in renal function. For those patients who fully recover from cidofovir associated renal toxicity, the benefits-risk balance of reintroducing cidofovir has not yet been evaluated.

Patient monitoring

Proteinuria appears to be an early and sensitive indicator of cidofovir-induced nephrotoxicity. Patients receiving cidofovir must have their serum creatinine and urine protein levels determined on specimens obtained within 24 hours prior to the administration of each dose of cidofovir. Differential white blood cell counts should also be performed prior to each dose of cidofovir (see section 4.8).

Ocular events

Patients receiving cidofovir should be advised to have regular follow-up ophthalmologic examinations for possible occurrence of uveitis/iritis and ocular hypotony. In case of uveitis/iritis cidofovir should be discontinued if there is no response to treatment with a topical corticosteroid or the condition worsens, or if iritis/uveitis reoccurs after successful treatment.

Other

Cidofovir should be considered a potential carcinogen in humans (see section 5.3).

Caution should be applied when considering cidofovir treatment of patients with diabetes mellitus due to the potential increased risk of developing ocular hypotony.

Male patients should be advised that cidofovir caused reduced testes weight and hypospermia in animals. Although not observed in clinical studies of cidofovir, such changes may occur in humans and cause infertility. Men should be advised to practice barrier contraceptive methods during and for 3 months after treatment with cidofovir (see sections 4.6 and 5.3).

Appropriate precautions should continue to be employed to prevent transmission of HIV.

Excipients

This medicinal product contains approximately 2.5 mmol (or 57 mg) sodium per vial which should be taken into consideration by patients on a controlled sodium diet.

There is a risk that concomitant treatment of cidofovir with products containing tenofovir disoproxil fumarate may give rise to a pharmacodynamic interaction and increase the risk of Fanconi syndrome (see section 4.4).

Probenecid increases the AUC of zidovudine. Patients receiving both medicinal products should be closely monitored for zidovudine induced haematological toxicity.

For other nucleoside reverse transcriptase inhibitors (NRTI) administered concomitantly with probenecid, reference should be made to their respective prescribing information for any appropriate recommendations.

Interactions of cidofovir/probenecid and anti-HIV medicinal products or medicinal products used to treat common chronic viral infections in this population, such as HCV- and HBV-related hepatitis, have not been investigated in clinical trials.

Probenecid is known to increase the exposure of many substances (e.g., paracetamol, acyclovir, angiotensin-converting enzyme inhibitors, aminosalicyclic acid, barbiturates, benzodiazepines, bumetanide, clofibrate, methotrexate, famotidine, furosemide, nonsteroidal anti-inflammatory agents, theophylline, and zidovudine).

Therefore, when co-prescribing cidofovir/probenecid with other drugs, it is important for prescribers to consult the current probenecid SmPC (or an appropriate medicinal product reference source) and the respective prescribing information of the other co-administered products for full information regarding drug interactions and other features of that product.

Women of childbearing potential/Contraception in males and females

Women of childbearing potential have to use effective contraception during and after treatment with cidofovir. Men should be advised to practice barrier contraceptive methods during and for 3 months after treatment with cidofovir (see section 4.4).

Pregnancy

There are no data from the use of cidofovir in pregnant women. Studies in animals have shown reproductive toxicity (see section 5.3).

Cidofovir is not recommended during pregnancy and in women of childbearing potential not using contraception.

Breast-feeding

It is unknown whether cidofovir/metabolites are excreted in human milk. A risk to the newborns/infants cannot be excluded. Breast-feeding should be discontinued during treatment with cidofovir.

Fertility

There are no studies of cidofovir on the fertility of men or women. Male patients should be advised that cidofovir caused reduced testes weight and hypospermia in animals. Although not observed in clinical studies of cidofovir, such changes may occur in humans and cause infertility.

Cidofovir has negligible influence on the ability to drive and use machines. Adverse reactions such as asthenia may occur during cidofovir therapy. The physician is advised to discuss this issue with the patient, and based upon the condition of the disease and the tolerance of medication, give his recommendation in the individual case.

The table below lists the adverse reactions identified through clinical trials or post-marketing surveillance by system organ class (SOC) and frequency. Within each frequency grouping, adverse reactions are presented in order of decreasing seriousness. Frequencies 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). Adverse reactions identified from post-marketing experience are included in italics.

Adverse reactions possibly or probably related to cidofovir based on clinical trial experience and post-marketing surveillance:

Blood and lymphatic system disorders

Very common: Neutropenia

Nervous system disorders

Very common: Headache

Eye disorders

Common: Iritis, uveitis, hypotony of the eye (see section 4.4)

Ear and labyrinth disorders

Not known: Hearing impaired

Respiratory, thoracic and mediastinal disorders

Common: Dyspnea

Gastrointestinal disorders

Very common: Nausea, vomiting

Common: Diarrhoea

Not known: Pancreatitis

Skin and subcutaneous tissue disorders

Very common: Alopecia, rash

Renal and urinary disorders

Very common: Proteinuria, blood creatinine increased (see section 4.4)

Common: Renal failure

Uncommon: Fanconi syndrome acquired

General disorders and administration site conditions

Very common: Asthenia, fever

Common: Chills

Reports of renal failure (plus events possibly caused by renal failure, e.g. blood creatinine increased, proteinuria, glycosuria) received during post-marketing surveillance include some which were fatal. Cases of acute renal failure have been reported after only one or two doses of cidofovir.

The finding of any glycosuria, proteinuria/aminoaciduria, hypouricemia, hypophosphatemia and/or hypokalemia, should prompt for the consideration of cidofovir-related Fanconi syndrome.

The following table lists adverse reactions possibly or probably related to probenecid based on clinical trial experience:

Nervous system disorders

Common: Headache

Gastrointestinal disorders

Very common: Nausea, vomiting

Skin and subcutaneous tissue disorders

Very common: Rash

General disorders and administration site conditions

Very common: Fever

Common: Asthenia, chills

In addition probenecid may also cause other adverse reactions including anorexia, gingival pain, flushing, alopecia, dizziness, anaemia, and pollakiuria. Hypersensitivity reactions, with dermatitis, pruritus, urticaria and, rarely, anaphylaxis, and Stevens-Johnson syndrome have occurred. There have been reports of leukopenia, hepatic necrosis, nephrotic syndrome, and aplastic anaemia. Haemolytic anaemia has also occurred, and may be associated with G6DP deficiency. Therefore, when co-prescribing probenecid with cidofovir, it is important for prescribers to consult the current probenecid SmPC (or an appropriate drug reference source) for full information on the safety profile and other features of that product.

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 www.mhra.gov.uk/yellowcard.

This medicinal product must not be mixed with other medicinal products or diluents except those mentioned in section 6.6.