Ferinject

Fe deficiency when oral Fe prep are ineffective or cannot be used or there is clinical need to deliver Fe rapidly.

Adult & adolescent ≥14 yr Should not exceed 15 mg Fe/kg IV inj or 20 mg Fe/kg IV infusion. Max recommended cumulative dose: 1,000 mg Fe/wk (20 mL). If total Fe need is higher, then administration of additional dose should be min 7 days apart from 1st dose. Patients w/ haemodialysis-dependent CKD Max daily dose: 200 mg. Childn & adolescent 1-13 yr 15 mg Fe/kg. Max recommended cumulative dose: 750 mg Fe/wk (15 mL). If total Fe need is higher, then administration of additional dose should be min 7 days apart from 1st dose. IV inj (undiluted) Rate: >10-20 mL (>500-1,000 mg Fe) for at least 15 min; >4-10 mL (>200-500 mg Fe) for at least 100 mg Fe/min; 2-4 mL (100-200 Fe) w/ no minimal prescribed time. IV infusion Conc: Not <2 mg Fe/mL (not including vol of ferric carboxymaltose dispersion). Rate: >10-20 mL (>500-1,000 mg Fe) diluted soln for at least 15 min infusion time; >4-10 mL (>200-500 mg Fe) diluted soln for at least 6 min infusion time; 2-4 mL (100-200 mg Fe) diluted soln w/ no minimal prescribed infusion time.

Hypersensitivity to ferric carboxymaltose or to other parenteral Fe products. Anaemia not attributed to Fe deficiency eg, other microcytic anaemia. Evidence of Fe overload or disturbances in the utilization of Fe.

Do not administer by SC or IM route. Hypersensitivity reactions including serious & potentially fatal anaphylactic/anaphylactoid reactions; after previously uneventful doses of parenteral Fe complexes; which progressed to Kounis syndrome; patients w/ known allergies including drug allergies & w/ history of severe asthma, eczema or other atopic allergy; immune or inflammatory conditions (eg, SLE, RA). Observe for at least 30 min following each administration; stop immediately if hypersensitivity reactions or signs of intolerance occur. Hypophosphataemia (mostly transient & w/o clinical symptoms) in patients w/ existing risk factors & after prolonged exposure to high-dose IV Fe; reports of symptomatic hypophosphataemia leading to hypophosphataemic osteomalacia & fracture requiring clinical intervention. Re-evaluate treatment in case of persistent hypophosphataemia. Liver dysfunction. Avoid in patients w/ hepatic dysfunction where Fe overload is a precipitating factor, in particular porphyria cutanea tarda; careful monitoring of Fe status is recommended. Acute or chronic infection. Discontinue in patients w/ ongoing bacteremia. Avoid paravenous leakage. Contains 5.5 mg Na equiv to max daily intake of 2 g Na for adult. Should not be used during pregnancy unless clearly necessary. Not recommended in childn <1 yr.

Hypophosphataemia; headache, dizziness; flushing, HTN; nausea; inj/infusion site reactions.

Reduced absorption of oral Fe.

Vitamins & Minerals (Pre & Post Natal) / Antianemics

B03AC - Iron, parenteral preparations ; Used in the treatment of anemia

Rx