Maxfer 500 mg/10 ml (IV Injection or Infusion)
10 ml vial: ৳ 700.00
Medicine Details
Category | Details |
---|---|
Generic | Ferric carboxymaltose |
Company | Eskayef pharmaceuticals ltd |
Also available as |
Indications
- Treatment of iron deficiency anaemia in adult patients with intolerance to oral iron
- Treatment of iron deficiency anaemia in adult patients with unsatisfactory response to oral iron
- Treatment of iron deficiency anaemia in adult patients with non-dialysis dependent chronic kidney disease
Description
- Colloidal iron (III) hydroxide in complex with Carboxymaltose
Dosage & Administration
- Stepwise approach for determination and administration of individual iron need
- Individual iron need based on body weight and haemoglobin level
- Calculation and administration of maximum individual iron dose(s)
- Post-iron repletion assessments by the clinician
Interaction
- Formal drug interaction studies not performed
Contraindications
- Hypersensitivity to the active substance or any of its excipients
- Serious hypersensitivity to other parenteral iron products
- Anaemia not attributed to iron deficiency
- Evidence of iron overload or disturbances in the utilisation of iron
Side Effects
- Infrequent and mild side effects
- Nausea
- Headache
- Dizziness
- Hypertension
- Injection site reactions
- Nausea
- Hypophosphataemia
- Hypersensitivit
- Dysgeusia
- Tachycardia
- Hypotension
- Flushing
- Dyspnoea
- Dyspepsia
- Abdominal pain
- Constipation
- Diarrhea
- Pruritus
- Urticaria
- Erythema
- Rash
- Myalgia
- Back pain
- Arthralgia
- Muscle spasms
- Pyrexia
- Fatigue
- Chest pain
- Edema peripheral
- Chills
- Anaphylactoid reactions
- Loss of consciousness
- Anxiety
- Phlebitis
- Syncope
- Presyncope
- Bronchospasm
- Flatulence
- Angioedema
- Pallor
- Face edema
- Rigors
- Malaise
- Influenza like illness
Pregnancy & Lactation
- No adequate and well-controlled trials in pregnant women
- Careful benefit/risk evaluation required before use during pregnancy
- Unlikely risk to the breast-fed child
Precautions & Warnings
- Serious hypersensitivity reactions reported
- Monitoring for signs and symptoms of hypersensitivity
- Administering only when immediate treatment for serious hypersensitivity reactions is available
- Transient elevations in systolic blood pressure
- Monitoring for signs and symptoms of hypertension
- Laboratory test alterations in the 24 hours following administration
- Laboratory assays may overestimate serum iron and transferrin bound iron
Use in Special Populations
- Limit on the maximum daily injection dose for haemodialysis-dependent chronic kidney disease patients
- Not recommended in children under 14 years
Overdose Effects
- Accumulation of iron in storage sites potentially leading to hemosiderosis
- Monitoring of iron parameters may assist in recognising iron accumulation
- Consideration of iron chelator in case of iron accumulation
Therapeutic Class
- Parenteral Iron Preparations
Storage Conditions
- Store in a cool and dry place below 30°C
- Keep away from light
- Do not freeze
- Keep out of the reach of children
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