CAV\/VVHD      :Not dialysed. Dose as in normal renal function; adjust according to levels IMPORTANT DRUG INTERACTIONS <\/H3>Potentially hazardous interactions with other drugsIncreased risk of hyperkalaemia with ACE inhibitors, angiotensin-II antagonists, potassium-sparing diuretics, potassium saltsIncreased risk of nephrotoxicity with aciclovir, aminoglycosides, amphotericin, colchicine, co-trimoxazole, disopyramide, foscarnet, melphalan, NSAIDs, polymyxins, quinolones, sulphonamides, thiazide diuretics, trimethoprim and vancomycinIncreased plasma ciclosporin levels with aciclovir, amiodarone, atazanavir, carvedilol, chloramphenicol, chloroquine, cimetidine, clarithromycin, colchicine, danazol, diltiazem, doxycycline, erythromycin, famotidine, fluconazole, fluoxetine, fluvoxamine, glibenclamide, glipizide, grapefruit juice, hydroxychloroquine, itraconazole, ketoconazole, lercanidipine (concentration of both drugs increased \u2013 avoid), miconazole, high-dose methylprednisolone, metoclopramide, metronidazole, muromonab-CD3, nelfinavir, nicardipine, nifedipine, posaconazole, progestogens, propafenone, .CiCLosPorin 151quinupristin\/dalfopristin, ritonavir, saquinavir (concentration of both drugs increased), tacrolimus, telithromycin, verapamil and voriconazoleDecreased plasma ciclosporin levels with barbiturates, bupropion, carbamazepine, griseofulvin, lanreotide, modafinil, octreotide, phenytoin, primidone, quinine, red wine, rifampicin, St John\u2019s wort, sulfadiazine, IV sulfadimidine, sulfasalazine, sulfinpyrazone, ticlopidine and IV trimethoprimAntibacterials: increased risk of myopathy with daptomycin \u2013 try to avoid concomitant useBasiliximab: may alter ciclosporin levels Bosentan: co-administration of ciclosporin and bosentan is contraindicated. When ciclosporin and bosentan are co-administered, initial trough concentrations of bosentan are 30 times higher than normal. At steady state, trough levels are 3\u20134 times higher than normal. Blood concentrations of ciclosporin decreased by 50%Calcium-channel blockers: increased nifedipine concentration and toxicityCardiac glycosides: increased digoxin concentration and toxicityCasponfungin: caspofungin concentration increased \u2013 avoid concomitant useColchicine: risk of myopathy or rhabdomyolysis; also increased blood-ciclosporin concentrations and nephrotoxicityCytotoxics: increased risk of neurotoxicity with doxorubicin; increased toxicity with methotrexate; seizures have been reported in bone marrow transplants taking busulfan and cyclophosphamide; concentration of etoposide possibly increased (increased risk of toxicity); possible interaction with docetaxolLipid-lowering agents: increased risk of myopathy with statins (max dose of simvastatin and atorvastatin should be 10 mg1); avoid with rosuvastatin; increased risk of nephrotoxicity with fenofibrate; bezafibrate may increase creatinine and reduce ciclosporin levels; concentration of both drugs may be increased with ezetimibeMycophenolate mofetil: some studies show that ciclosporin decreases plasma MPA AUC levels \u2013 no dose change requiredNSAIDs: diclofenac concentration increased \u2013 reduce diclofenac dose. Omeprazole: may alter ciclosporin concentrationOrlistat: absorption of ciclosporin possibly reducedOxcarbazepine: may reduce ciclosporin concentrationPrednisolone: increased prednisolone concentrationSirolimus: increased absorption of sirolimus \u2013 give sirolimus 4 hours after ciclosporin; sirolimus concentration increased; long-term concomitant administration may be associated with deterioration in renal functionSitaxentan: concentration of sitaxentan increased \u2013 avoid concomitant useTacrolimus: increased tacrolimus concentration and toxicity \u2013 avoid concomitant useUrsodeoxycholic acid: unpredictably increased absorption and raised ciclosporin levels in some patients ADMINISTRATION <\/H3> Reconstition<\/H4>Dilute 50 mg in 20\u2013100 mL with sodium chloride 0.9% or glucose 5% Route <\/H4>Oral, IV peripherally or centrally Rate of Administration <\/H4>Over 2\u20136 hours peripherally or 1 hour centrallyComments<\/H4>\u2013 OTHER INFORMATION <\/H4>To convert from IV to oral multiply by 2\u20133 (usually 2.5). Dose and monitor blood levels in accordance with local protocol
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